Influence of Different Levels of Lipoic Acid Synthase Gene Expression on Diabetic Nephropathy

Longquan Xu; Sylvia Hiller; Stephen Simington; Volker Nickeleit; Nobuyo Maeda; Leighton R. James; Xianwen Yi

doi:10.1371/journal.pone.0163208

Abstract

Oxidative stress is implicated in the pathogenesis of diabetic nephropathy (DN) but outcomes of many clinical trials are controversial. To define the role of antioxidants in kidney protection during the development of diabetic nephropathy, we have generated a novel genetic antioxidant mouse model with over- or under-expression of lipoic acid synthase gene (Lias). These models have been mated with Ins2^Akita/+ mice, a type I diabetic mouse model. We compare the major pathologic changes and oxidative stress status in two new strains of the mice with controls. Our results show that Ins2^Akita/+ mice with under-expressed Lias gene, exhibit higher oxidative stress and more severe DN features (albuminuria, glomerular basement membrane thickening and mesangial matrix expansion). In contrast, Ins2^Akita/+ mice with highly-expressed Lias gene display lower oxidative stress and less DN pathologic changes. Our study demonstrates that strengthening endogenous antioxidant capacity could be an effective strategy for prevention and treatment of DN.

Citation: Xu L, Hiller S, Simington S, Nickeleit V, Maeda N, James LR, et al. (2016) Influence of Different Levels of Lipoic Acid Synthase Gene Expression on Diabetic Nephropathy. PLoS ONE 11(10): e0163208. https://doi.org/10.1371/journal.pone.0163208

Editor: Jian Fu, University of Kentucky, UNITED STATES

Received: October 1, 2015; Accepted: September 6, 2016; Published: October 5, 2016

Copyright: © 2016 Xu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: All relevant data are within the paper.

Funding: The study design, data collection and analysis, decision to publish, or preparation of the manuscript are supported by Juvenile Diabetes Research Foundation (5-2011-471) and Diabetic Complications Consortium DCC)3U24DK076169-0452 grants.

Competing interests: The authors have declared that no competing interests exist.

Abbreviations: DN, diabetic nephropathy; Lias, LA, α-lipoic acid; lipoic acid synthase gene; 3’-UTR, 3’-untranslated region; ROS, reactive oxygen species; MME, mesangial matrix expansion; 4-HNE, 4-Hydroxynonenal; Sod2, superoxide dismutase 2; Tgfβ1, transforming growth factor β1; Nrf2, nuclear factor (erythroid-derived 2)-like 2; Nox4, NADPH oxidase 4

Introduction

Alpha-lipoid acid (1, 2-dithiolane-3-pentanoic acid, LA) is a potent antioxidant produced in mitochondria by lipoic acid synthase (LIAS) [1]. Among all natural antioxidants, LA plays a central role in the antioxidant network. It has several unique characteristics that include: 1) serving as a powerful antioxidant in both the oxidized and reduced forms; 2) quenching of a variety of reactive oxygen species (ROS); and 3) regenerating other antioxidants such as oxidized vitamins C and E, coenzyme Q10 and glutathione [2, 3]. LA is also a cofactor for several mitochondrial enzymes such as pyruvate dehydrogenase complex and α-ketoglutarate dehydrogenase complex, both of which participate in energy generation [4]. Complete lack of the Lias gene leads to mouse embryonic death, further underscoring the pivotal role LA plays in antioxidant defense and as a metabolic requirement [5].

Diabetic nephropathy (DN) is a leading cause of end-stage renal disease [6]. Oxidative stress has been suggested to play an important role in the development of DN [7, 8]. On the basis of epidemiological evidence, antioxidant therapy is a plausible strategy for treatment of this oxidative stress-related disease. However, there are conflicting reports regarding the effect of chronic dietary supplementation with antioxidants on outcomes of diabetic kidney disease in clinical trials [9–12]. An explanation for these observations is that natural genetic variation leads to inter-individual variations with respect to basic endogenous antioxidant levels. Indeed, it is well known that natural genetic variation affects gene expression levels and thus impacts molecular and physiological phenotypes such as protein expression levels. As a consequence, different endogenous antioxidant levels in tested individuals may influence experimental results and outcome of clinical trials aimed at examining the impact of antioxidant therapy on disease course. Thus, we hypothesize that the extent of oxidative damage is mainly dependent on endogenous antioxidant levels, especially in the initiation stage of diseases in which oxidative stress is implicated. To test our hypothesis, we have generated a group of unique lipoic acid hypomorphic and hypermorphic antioxidant mice by genetically modifying the 3’-untranslated region (3’-UTR) of lipoic acid synthase; this strategy is a similar approach that has been previously reported [13]. By comparing the major parameters of DN and oxidative stress in Ins2^Akita/+ type 1 diabetic mice with different levels of endogenous Lias gene expression, we sought to define the role of oxidative stress in the onset and development of DN and obtain a better understanding of impact of antioxidants.

Materials and Methods

Creation of Lias^Low/+ and Lias^High/+ Mice by Changing 3’ untranslated region (3’-UTR) Sequences

The targeting construct prior to recombination consisted of a 3’-UTR of the endogenous Lias gene and was replaced after recombination with a cassette. The cassette consisted of the 3’-UTR sequences of bovine growth hormone gene (bGH) and a Neo gene, two lox P sites flanking the two fragments, and followed by the 3’-UTR of cFos gene. Colonies surviving after selection with G418 and ganciclovir were first screened by PCR with the following primers: a common primer (5′-CTA AAG TGT AGC CAA GCC CT-3′), a primer for screening Lias 3’-UTR (5′-CCT CCT CAG CTA CTG ACA TT-3′), a primer for bGH 3’-UTR (5′-GAG GCA AAC AAC AGA TGG CT-3’) and a primer for cFos 3’-UTR (5′-CTT CTC TGA CTG CAG ATC CT-3’). Targeted Embryonic stem (ES) cells were identified by the presence of approximately 200 bp PCR product for bGH 3’-UTR, and 300 bp after Cre recombinase-mediated recombination. Germline recombination was achieved using the B6.FVB-Tg (EIIa-Cre) stock (JAX#3724). These results were confirmed by Southern blot analysis.

The hypomorphic (Lias^Low/Low) and hypermorphic (Lias^High/High) Lias mice in C57BL/6 genetic background, with 25% or 150% of wildtype Lias gene expression respectively, were mated with C57BL/6-Ins2^Akita/+ diabetic mice (JAX#3548), an established mouse model of type I diabetes mellitus [14, 15]. The Ins2^Akita/+ mice have a mutation changing cysteine 96 to tyrosine in the insulin 2 gene and exhibit marked hyperglycemia as early as 4 weeks of age [15]. Eight B6-Lias^Low/LowIns2^Akita/+ males and 9 B6-Lias^High/HighIns2^Akita/+ males were obtained from crossing C57BL/6-Ins2^Akita/+ female mice and Lias^Low/Low or Lias^High/High male mice. Only males were phenotyped in this study because Ins2^Akita/+ females on the B6 genetic background displayed much less severe diabetic phenotype than the males [16]. Lias^+/+Ins2^Akita/+ mice served as a control. In addition, the mice were fed normal mouse chow (Research Diets, Inc. New Brunswick, NJ) and had ad libitum access to autoclaved water. All animal protocols were approved by the University of North Carolina at Chapel Hill Institutional Animal Care and Use Committee (Protocol numbers: 13-208-0 and16-153-0).

Biochemical Parameters

Blood glucose was monitored monthly in the mice from 7 to 28 weeks using the One-Touch Lifescan meter (Lifescan Inc, Milpitas, CA) on samples obtained after a 5-hour fasting period. Plasma glucose, total cholesterol and triglyceride were examined using assay kits (Wako, Richmond, VA). Lactic acid concentration in tissues was determined as described [17]. Pyruvate concentration was measured using a pyruvate assay kit (BioVision, Mountain View, CA).

Urinary Albumin Excretion

At 28 weeks of age, individual mice were placed in metabolic cages to record food consumption, water intake, body weight, and urine output for 48 hours prior to sacrifice. Urine albumin in Lias^High/High Ins2^Akita/+ and Lias^Low/LowIns2^Akita/+ mice was assessed by ELISA using Albuwell according to the manufacturer’s instructions (Exocell, Philadelphia, PA). Urinary creatinine levels were determined by the Creatinine Kit (Exocell) according to the manufacturer’s instructions.

Urinary MCP-1 assay

Urinary monocyte chemoattractant protein-1 (MCP-1) excretion was measured as markers of renal inflammation. The MCP-1 concentration was measured using an ELISA assay kit (Research & Diagnostic Systems, Minneapolis, MN) according to the manufacturer’s instructions. The ELISA kit was specific for mouse MCP-1 and sensitive down to 2 pg/ml. The MCP-1 concentration was normalized to the urinary creatinine concentration.

Blood Pressure Measurement

Systolic blood pressure (BP) was determined in conscious mice using a tail-cuff method [18]. The first 10 readings were discarded, and 30 readings were taken to obtain daily BP. Average BP on 5 consecutive days was taken to represent BP of each mouse.

Renal Function and Morphometric Analyses

Mice were perfused at 120 mmHg with 0.9% saline containing heparin, followed by 4% paraformaldehyde and then embedded in paraffin and 3-μm sections were cut. Sections were stained with hematoxylin and eosin (H&E) and Periodic acid-Schiff's base (PAS) for examination by light microscopy. Mesangial matrix expansion (MME) was examined in a blinded fashion and scored from 0 to 4 according to the ratio of glomerular expansion area/normal area: score 0, a normal glomerulus; score 1, increased mesangial matrix <25% of glomerular tuft; score 2, MME of 25%–50% of glomerular tuft; score 3, MME of 50%–75%; and score 4, MME of >75% of the tuft. MME was derived from assessment of three glomerular profiles on each mouse. Next, the kidney cortex was conventionally prepared for transmission electron microscopy. The samples were examined with an electron microscope (Model LEO 910; LEO Electron Microscopy Inc, Thornwood, NY). Three to four kidney samples from each experimental group were randomly chosen for electron microscopic observation. Thickness of glomerular basement membranes (GBM) was measured from transmission electron microscopy photos (magnification, x12,000) at 5 specific points along each of 10 randomly selected glomerular capillaries to determine an average GBM thickness for 5 mice in each group. Mitochondrial damage in proximal tubules was examined in each genotypic group. Briefly, under the same magnification (x10,000), about 200–300 mitochondria from 10–12 randomly selected fields in each genotypic group were observed. The Degree of the mitochondrial damage was assessed according to the following scale from 0 to 3: 0) indicating a normal structure, 1) normal with slight swelling, 2) mitochondrial swelling and cristae dilated/disorder, and 3) mitochondrial vacuolization. On the basis of the above criteria, the degree of mitochondrial damage in the different groups of mice were scored and the total scores of mitochondria per group were summarized and then divided by total counted mitochondrion number in each group to get the ratio of damaged over total counted mitochondrion number. The ratio indicates the degree of mitochondrial damage.

Assessment of Oxidative Stress

To evaluate oxidative stress, the concentration of urinary 8-isoprostane was measured using an enzyme immunoassay and expressed relative to the level of urine creatinine following the manufacturer’s protocol (Cayman Chemical Inc., Ann Arbor, MI). Systemic oxidative stress in blood was determined using 4-Hydroxynonenal (4-HNE) assay kit in accordance with manufacturer’s specifications (Cell Biolabs, Inc. San Diego, CA).

Western Blot Analysis

Total protein was extracted from the renal cortical tissues with RIPA buffer and protein concentration was determined by BCA protein assay method (Thermo Scientific, Rockford, IL) following manufacturer’s instructions. Western blot analysis was performed using a rabbit polyclonal antibody against mouse LIAS (GeneTex, Inc.Irvine, CA), and (voltage-dependent anion-selective channel protein 1) VDAC1 as mitochondrial loading control (Abcam, Cambridge, MA) and the protein bands were quantified with Image Quant LAS4000 software (GE Healthcare, Piscataway, NJ).

Reverse Transcription and Quantitative Real-Time Polymerase Chain Reaction (RT-PCR)

Total RNA was extracted from kidney cortex using an ABI 6700 Automated Nucleic Acid Workstation following the manufacturer’s protocol (Applied Biosystems, Foster City, CA). Relative mRNA amounts were determined using real-time quantitative reverse transcriptase-PCR (Applied Biosystems) with β-actin as the reference gene in each reaction [18]. The expression of the genes Lias, superoxide dismutase 2 (Sod2), transforming growth factor β1 (Tgfβ1), nuclear factor (erythroid-derived 2)-like 2 (Nrf2) and NADPH oxidase 4 (Nox4) were examined.

Statistical Analyses

Data were expressed as mean ± standard error of the mean (SEM). P<0.05 was considered significant. P values are obtained for comparisons among Lias^Low/LowIns2^Akita//+, Lias^High/HighIns2^Akita/+ and Lias^+/+Ins2^Akita/+ mice using one-way or two-way ANOVA. Post hoc pairwise comparisons were performed by Tukey–Kramer honestly significant differences (HSD) test (JUM, SAS Institute, Cary, NC).

Results

Model Construction

As described in methods, the gene targeting strategy for engineering the hyper- and hypomorphic Lias mice with over- or under-expression of the Lias gene was based on genetic modification of the 3’-UTR (Fig 1A). The DNA sequence result showed that the orientation of the 3'UTR sequences of both bGH and c-Fos are replaced in the transcriptional orientation (data not shown). ES cell lines with a correctly targeted 3’-UTR were identified and injected into C57BL/6J recipient blastocysts, which were transferred to the uteri of CD-1 pseudopregnant dams. These mice initially produced stabilized transcripts of the Lias gene using the 3’-UTR sequence of bGH, but were changed to unstable transcripts using the 3’-UTR from the cFos gene after Cre-LoxP recombination was induced. The Lias^High/+ mice were crossed with Tg (Ella-cre) mice that expressed Cre-recombinase in testis and thus the homozygous offspring (Lias^Low/Low) generated from these Lias^Low/+ founder males expressed low levels of Lias. Since plasma and tissue LA were not directly measured due to a technical difficulty [19], changes in organ LA levels were inferred by demonstrating changes in Lias gene expression using RT-PCR (Fig 1B) or Western blot (Fig 1C). Western blot results for kidney LIAS, quantitatively assessed by densitometry, showed that LIAS protein concentrations were about 150% in Lias^High/High mice and around 25% in Lias^Low/low mice, compared with those in Lias^+/+ mice (Fig 1D).

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Fig 1. Characterizations of the new mouse model.

(A) Generation of mice with genetically graded expression of lipoic acid synthase (Lias). Wild type (top line): Endogenous Lias gene 3’-UTR (white column) is located after exon 11 of Lias gene. The targeting construct (second line): consisted of the 3’-UTR sequences of bovine growth hormone (bGH) gene and a Neo gene, two lox P sites flanking the two fragments, and followed by the 3’-UTR of cFos gene and thymidine kinase gene (TK). H/H (third line): The locus after homologous recombination. Lias expression is now controlled by the 3’-UTR of bGH, which stabilizes Lias mRNA. L/L (bottom line): The locus after Cre-lox P recombination. Lias expression is controlled by the 3-UTR of cFos, which destabilizes the Lias mRNA. (B) The kidney mRNA levels of Lias in 12-week-old L/L, H/H and WT male mice and in 28-week-old diabetic L/L, H/H and WT male mice. Lias gene expression in the non-diabetic WT mice as a reference for the all six groups of mice. (C) Lipoic acid synthase (LIAS) concentrations of kidney cortex mitochondria, measured by Western blot, and VDAC1 as loading control, in 12-week-old L/L, H/H and WT male mice. n = 5, in each group. (D) The amounts of lipoic acid in non-diabetic Lias^High/High and Lias^Low/Low kidney, detected by Western blot, were quantified by Image Quant software. Data are expressed as the mean ± SE.

https://doi.org/10.1371/journal.pone.0163208.g001

Systemic Pathological Changes

The hypomorphic (Lias^Low/Low) and hypermorphic (Lias^High/High) Lias mice, with 25% or 150% of wildtype Lias gene expression, respectively, were mated with Ins2^Akita/+ diabetic mice, an established mouse model of diabetes mellitus that can mimic early stages of DN [14, 15]. Lias^High/High Ins2^Akita/+ and Lias^Low/LowIns2^Akita/+ mice exhibited the different diabetic phenotypes. Lias^Low/LowIns2^Akita/+ mice had significantly lower body weight compared to both Lias^High/HighIns2^Akita/+ and Lias^+/+Ins2^Akita/+ mice as shown in Table 1 (P<0.05). Both Lias^High/HighIns2^Akita/+ and Lias^Low/LowIns2^Akita//+ mice manifested hyperglycemia at 28 weeks of age but there was no significant difference between the two groups of mice. In addition, plasma total cholesterol and triglyceride levels were similar among Lias^High/HighIns2^Akita/+, Lias^Low/LowIns2^Akita/+, and Lias^+/+Ins2^Akita/+ mice (Table 1).

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Table 1. Laboratory data in experimental animals.

https://doi.org/10.1371/journal.pone.0163208.t001

Kidney Pathologic Changes

Urinary albumin/creatinine ratio in Lias^Low/LowIns2^Akita/+ mice was 2.6-fold higher than Lias^+/+Ins2^Akita/+ mice at 28 weeks of age whereas, the ratio in Lias^High/HighIns2^Akita/+ mice was about 30% lower than Lias^+/+Ins2^Akita mice but was not statistically significant (Fig 2). Dietary intake and water consumption in Lias^Low/LowIns2^Akita/+ and Lias^High/HighIns2^Akita/+ mice were not significantly different compared with Lias^+/+Ins2^Akita mice (Table 1). The ratio of kidney weight-to-body weight (KW/BW) in Lias^Low/LowIns2^Akita/+ mice was higher than control Lias^+/+Ins2^Akita/+ mice whereas this ratio was lower in Lias^High/HighIns2^Akita/+ mice than in control Lias^+/+Ins2^Akita/+ mice. Kidney levels of lactate and pyruvate were similar in all three diabetic groups (Table 1).

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Fig 2. Changes of urine albumin in the mice.

Urine albumin/creatinine ratio in Lias^Low/LowIns2^Akita//+ mice is significantly elevated (P<0.01) whereas the ratio in Lias^High/HighIns2^Akita/+ mice is reduced but does not reach significance, compared with Lias^+/+Ins2^Akita/+ mice at 28 weeks of age. The numbers inside the bars indicate the number of animals.

https://doi.org/10.1371/journal.pone.0163208.g002

Renal pathological changes were assessed by light and transmission electron microscopy. Moderate mesangial matrix expansion, as evidenced by increased accumulation of PAS positive material in the mesangial area, was observed in 28-week-old Lias^Low/LowIns2^Akita/+ mice (Fig 3A), whereas mesangial expansion was milder in Lias^High/HighIns2^Akita/+ mice (Fig 3C), compared to the Lias^+/+Ins2^Akita control (Fig 3B). Semi-quantitative analysis of PAS-stained kidney sections revealed a higher mesangial expansion score (P<0.05) in Lias^Low/LowIns2^Akita/+ mice as compared with Lias^High/HighIns2^Akita/+ and Lias^+/+Ins2^Akita/+ mice (Fig 3D). Electron microscopic examination showed thickening of the GBM in Lias^Low/LowIns2^Akita/+ mice (Fig 4A), compared to Lias^+/+Ins2^Akita/+ mice (Fig 4C). Quantitative examination using Image J showed the thickening of the GBM significantly increased (0.36 ± 0.04 μm versus 0.27 ± 0.04 μm in, P<0.05, Fig 4G). Foot process effacement was primarily detected in Lias^Low/LowIns2^Akita/+ mice (Fig 4A) but podocyte slit pore width did not exhibit significant differences among three groups of the mice. Considerable numbers of mitochondria within proximal tubules in Lias^Low/LowIns2^Akita/+ mice were damaged as revealed by mitochondrial structural irregularities with swelling, disruption of cisternae and vacuolization. In contrast, few damaged mitochondria were observed in Lias^High/HighIns2^Akita/+ mice (Fig 4B and 4E) compared with Lias^Low/LowIns2^Akita/+ and Lias^+/+Ins2^Akita/+ mice (Fig 4D and 4F). Damaged mitochondria were quantified in Lias^High/HighIns2^Akita/+ and Lias^+/+Ins2^Akita/+ mice at 28 weeks of age. As shown in Fig 4H, the average number of damaged mitochondria in proximal tubules of Lias^Low/LowIns2^Akita/+ mice were significantly increased whereas damaged mitochondria in Lias^High/HighIns2^Akita/+ mice were significantly decreased compared to Lias^+/+Ins2^Akita/+ mice. Glomerulosclerosis, arteriolar hyalinosis and focal tubulointerstitial fibrosis were not detectable in all diabetic Ins2^Akita/+ mice at 28 weeks of age regardless of Lias transcript level. In addition, no electron dense deposits were observed in the glomeruli in all mice.

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Fig 3. Changes of Lias gene expression influences mesangial matrix expansion (MME).

Representative PAS staining of glomeruli in diabetic Ins2^Akita//+ mice at 28 weeks of age. (A) Lias^Low/LowIns2^Akita//+ mice. (B) Lias^+/+Ins2^Akita/+ mice. (C) Lias^High/HighIns2^Akita/+ mice. Original magnification x400, Bars = 50μm. (D) MME score, quantified as the region of positive PAS staining, is expressed as a function of total glomerular tuft area. The numbers inside the bars indicate the number of animals. Lias^Low/LowIns2^Akita//+ and Lias^High/HighIns2^Akita/+ mice are compared with Lias^+/+Ins2^Akita/+ mice. Values are expressed as the mean ± SEM.

https://doi.org/10.1371/journal.pone.0163208.g003

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Fig 4. Representative electron micrographs from diabetic Ins2^Akita//+ mice at 28 weeks of age.

(A) Segmentally thickened glomerular basement membrane (GBM) with minor irregularities along the lamina rara externa (“undulations”) and segmental podocyte foot process effacement in Lias^Low/LowIns2^Akita//+ mice. Original magnification, x8,000. (B) Lias^High/HighIns2^Akita/+ mice. Original magnification, x8,000. (C) Lias^+/+Ins2^Akita/+ mice. Original magnification, x8,000. (D) Illustrated is the basal part of a tubular epithelial cell containing distorted mitochondria. Cristae are disrupted and mitochondria filled presumably with lipid products vaguely resembling zebra-bodies in Lias^Low/LowIns2^Akita//+ mice. Original Magnification, x5,000. (E) A small number of damaged mitochondria in proximal tubular cells of Lias^High/HighIns2^Akita/+ mice. Original magnification, x8,000. (F) Damaged mitochondria in proximal tubular cells of Lias^+/+Ins2^Akita/+ mice. Magnification, x8,000. (G) Electron microscopic quantitative examination using Image J showed thickening of the GBM significant increase in Lias^Low/LowIns2^Akita/+ mice compared to Lias^+/+Ins2^Akita/+ mice. (H) Ratio of average damaged mitochondrion over entire counted mitochondria in proximal tubules of Lias^Low/LowIns2^Akita//+, Lias^High/HighIns2^Akita/+ and Lias^+/+Ins2^Akita/+ mice, using one-way ANOVA for the comparison.

https://doi.org/10.1371/journal.pone.0163208.g004

Oxidative Stress and Inflammation

Systemic oxidative stress, assessed by measuring 4-HNE, a well-known product of lipid peroxidation and a measure of oxidative stress, was significantly different in Lias^High/HighIns2^Akita/+ and Lias^+/+Ins2^Akita/+ mice compared with Lias^+/+Ins2^Akita/+ mice (Fig 5A). Another reliable lipid peroxidation marker, 8-isoprostane, was examined in urine. Lias^Low/LowIns2^Akita/+ mice at 28-weeks-old showed noticeably higher levels than Lias^+/+Ins2^Akita/+ mice (Fig 5B). On the contrary, Lias^High/HighIns2^Akita/+ mice manifested significantly lower urinary 8-isoprostane levels than Lias^+/+Ins2^Akita/+ mice (Fig 5B).

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Fig 5. Alternated oxidative stress.

(A). Oxidative stress in kidney cortex is associated with plasma concentration of lipid perioxidation marker, 4-hydroxynonenal (4-HNE), in diabetic Ins2^Akita//+ mice and non-diabetic mice with differential Lias gene expression. Lias^+/+ mice as a control. Data were analyzed using two-way ANOVA. (B). Urine 8-isoprostane varies with Lias expression in diabetic mice. Data were analyzed using one-way ANOVA. The numbers inside the bars indicate the number of animals in each group. Results are expressed as mean ±SEM.

https://doi.org/10.1371/journal.pone.0163208.g005

Consistent with Western blot results for LIAS protein, RT-PCR analysis of kidney cortex showed significantly increased Lias gene expression in Lias^High/HighIns2^Akita/+ and significantly reduced expression in Lias^Low/LowIns2^Akita/+ mice at 28 weeks of age (Table 2). Interestingly, gene expression of mitochondrial Sod2, a major antioxidant enzyme which responds to enhanced superoxide production in mitochondria, was significantly higher in Lias^Low/LowIns2^Akita/+ mice, likely reflecting an attempt to compensate for reduced LIAS-generated LA in Lias^Low/LowIns2^Akita/+ kidney. The data confirm our previous observation that Sod2 expression also markedly increases in Lias^+/-Ins2^Akita/+ mice [20]. To identify the ROS sources, we examined Nox4 gene expression in kidney cortex. Our result showed that Nox4 gene expression was significantly increased at 28-weeks of age in Lias^Low/LowIns2^Akita/+ whereas a significant decrease in Lias^High/HighIns2^Akita/+ kidney suggests that NADPH oxidase is a target for the antioxidant effects of lipoic acid (Table 2). In addition, significantly reduced Tgfβ1 gene expression in Lias^High/HighIns2^Akita mice (Table 2) suggests that increased Lias gene expression likely attenuates adverse effect(s) of TGF-β1.

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Table 2. Gene expression in kidney cortex.

https://doi.org/10.1371/journal.pone.0163208.t002

NRF2 is a key transcription factor for regulation of antioxidant defense [21] and LA has been shown to stimulate NRF2 nuclear accumulation [22]. To test whether endogenous LA can affect NRF2, we examined Nrf2 gene expression in 28-week-old Lias^Low/LowIns2^Akita/+ and Lias^High/HighIns2^Akita/+ mouse kidney. Unlike Sod2, Nox4 and Tgfb1 transcripts, no significant changes in Nrf2 expression were observed in response to Lias gene manipulation (Table 2).

Inflammation is thought to be a pathogenic factor in the initiation of DN and monocyte chemoattractant protein-1 (MCP-1) is considered as a major mediator of inflammation in DN patients. To further probe the underlying mechanism(s) of endogenous oxidant injury in relation to inflammation in diabetes mellitus, we measured urinary MCP-1. Our results showed that there were significantly increased urinary MCP-1 levels in Lias^Low/LowIns2^Akita/+ mice compared with Lias^+/+Ins2^Akita/+ and Lias^High/HighIns2^Akita/+ mice (Fig 6).

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Fig 6. Kideny inflammation.

Urinary MCP-1 levels in Lias^Low/LowIns2^Akita/+, Lias^+/+Ins2^Akita/+ and Lias^High/HighIns2^Akita/+ mice. The numbers inside the bars indicate the number of animals in each group. Results are expressed as mean ±SEM.

https://doi.org/10.1371/journal.pone.0163208.g006

Discussion

In our previous study, the pathologic changes of diabetic nephropathy (DN) were exacerbated in Lias^+/-Ins2^Akita/+ mice with an approximately 50% reduced Lias gene expression, and the aforementioned pathology was associated with significantly enhanced oxidative stress [20]. To verify the central role of LIAS in generating endogenous LA for antioxidant defenses, we manipulated Lias transcript stability to generate two lines of novel antioxidant mouse models. In one, Lias gene expression was reduced to roughly 25% of normal, a level sufficient to maintain viability (Lias null mice are embryonic lethal). In the other, Lias gene expression was increased to approximately 150% of normal expression level, which is anticipated to afford better protection, than wildtype mice, against oxidative stress. When combined with the diabetogenic Ins2^Akita mutation, the double mutants allow evaluation of the impact of two different antioxidant baselines (Low or High) on the development of DN. As hypothesized, the new diabetic models exhibited divergent renal responses to diabetogenic stress when compared with Lias^+/+Ins2^Akita/+ mice. Major DN pathological changes such as albuminuria and mesangial expansion in Lias^Low/LowIns2^Akita/+ mice were significantly worse than those in Lias^+/+Ins2^Akita/+ mice whereas the two pathological changes were less severe in Lias^High/HighIns2^Akita/+ mice. The data further support the correlation between Lias transcript abundance and inferred endogenous LA concentration; levels of two reliable common oxidative stress biomarkers, plasma 4-NHE and urine 8-isoprostane, were both significantly higher in Lias^Low/LowIns2^Akita/+ mice and significantly lower in Lias^High/HighIns2^Akita/+ mice compared to Lias^+/+Ins2^Akita/+ controls. These results are consistent with our previous data where we used different lipid peroxidation markers, like TBARS and, antioxidant marker such as ratio of GSH/GSSG to reveal significantly increased oxidative stress and decreased endogenous antioxidant capacity in Lias^+/-Ins2^Akita/+ mice. Since lipoic acid plays a central role in the antioxidant network, the significantly increased oxidative stress and decreased endogenous antioxidant capacity observed in Lias^+/-Ins2^Akita/+ mice were very likely due to the impairment of the antioxidant defense system. In addition, our data demonstrate that Lias overexpression effectively attenuates albuminuria and kidney disorders without exerting a significant hypoglycemic effect in Lias^High/HighIns2^Akita/+ mice, suggesting that the protective effect of LA results primarily from its antioxidant capacity rather than from a direct hypoglycemic effect. These findings confirm that LIAS-generated lipoic acid plays a vital role in the early development of DN by demonstrating that diabetic mice with low endogenous antioxidant capacity manifestly increased ROS-mediated renal stress. In particular, the new models provide very strong proof-of-principle that an increased antioxidant reservoir could represent a powerful new tool in the prevention and / or treatment of diabetic kidney disease. A novel finding obtained from our current study underlines the importance of antioxidants for mitochondrial protection in the retardation of DN. Growing evidence indicates that mitochondria play a critical role in the initiation and development of DN. Mitochondria are believed to be the major organelles involved in superoxide generation. They consume approximately 85% of the oxygen used by cells and overproduction of superoxide anions may occur by excessive electron leak in the mitochondrial electron transport chain during diabetes [21]. On the other hand, mitochondria are the primary targets for oxidative stress because they lack protection from histone and are incapable of performing DNA repair functions by themselves [22]. Our previous observations have shown that the number of damaged mitochondrion in kidney proximal tubules was significantly higher in Ins2^Akita/+ mice with 50% of reduced Lias gene expression than Lias^+/+Ins2^Akita/+ littermate controls. In the current studies, we consolidate our previous observation that mitochondrial damage in proximal tubules is a predominant pathological feature of DN by demonstrating that reduction in Lias gene expression in Lias^Low/LowIns2^Akita/+ mice and increased Lias expression in Lias^High/HighIns2^Akita/+ mice impact mitochondrial integrity and function. Through use of in vitro LIAS knockdown studies it has been reported that ROS may decrease the mitochondrial membrane potential [23]. Given that mitochondrial dysfunction is postulated to be an initiator for diabetic complications [24], we presume that attenuation of DN by endogenous LA is likely, through preservation of mitochondrial function, to mediate reduction in mitochondrial ROS and mitochondrial damage. Thus, strengthening mitochondrial antioxidant capacity could be an effective means for prevention and treatment of DN. Our results are similar to a recent report indicating that Ins2^Akita/+ mice specifically overexpressing catalase, a key antioxidant enzyme in renal proximal tubular cells, had reduced renal oxidative stress and attenuated progression of DN without changing blood glucose concentration [25]. Our contention, that mitochondrial damage mediates DN and that lipoic acid mitigates this injury, is further supported by another recent report that Ins2^Akita/+ derived β-cells have increased mitochondrial dysfunction, oxidative stress, mitochondrial DNA damage, and alterations in mitochondrial protein levels that contribute to β-cell dysfunction [26].

LIAS synthesizes lipoic acid in mitochondria. Lipoic acid has a high reductive capacity and actively participates in the recycling of vitamin C and E. Diabetes mellitus is characterized by increased oxidative stress that negatively impacts mitochondrial integrity and function. Hence the physiologic importance of LIAS in diabetes is through its role in lipoic acid synthesis; lipoic acid may play a vital role in mitochondrial protection from oxidative stress and thus maintain energy balance during diabetes. Our previous data obtained from in Lias^+/-Ins2^Akita/+ mice showed that systemic and urinary oxidative stress markers significantly increased, whereas endogenous antioxidant capacity significantly decreased, when Lias gene expression levels was approximately 50%. Furthermore, reduced Lias gene expression in Lias^+/-Ins2^Akita/+ mice was associated with more severe DN pathological changes compared with Lias^+/+Ins2^Akita/+ mice. In particular, a large number of damaged mitochondria were detected in mouse proximal tubule epithelial cells as a unique phenomenon. The results observed in Lias^Low/LowIns2^Akita/+ mice have confirmed that reduced Lias gene expression leads to decreased endogenous antioxidant capacity and mitochondrial damage in the proximal tubules. On the other hand, in Lias^High/HighIns2^Akita/+ mice harboring increased Lias gene expression, endogenous oxidant capacity and mitochondrial integrity are protected. Our data also indicate that kidney proximal tubules can serve as a window via which alternation of mitochondrial status due to oxidative stress can be assessed in diabetic nephropathy.

Based on ours and, other investigator’s data [23], we propose that several mechanisms are involved in the changes of kidney Lias expression and LA levels under diabetic conditions:

Excess ROS generated in diabetic mellitus impairs the antioxidant defense system, indicated by decline of reduced GSH levels, leading to further accumulation of ROS. The latter is reflected by a significantly enhanced lipid peroxidation levels in body and urine. Our new animal model with low expression of Lias gene further highlights this relationship between endogenous antioxidant levels, ROS concentrations and DN pathologic changes. That is, low endogenous antioxidant capacity will result in high levels of ROS and more severe DN.
Excessive ROS in diabetes mellitus damages mitochondria. Mitochondria are a major site of ROS generation and are vulnerable targets for ROS; hence, accumulated ROS due to insufficient LA protection in Lias^Low/LowIns2^Akita/+ mice could damage mitochondria. We found that significant mitochondrial damage in Lias^Low/LowIns2^Akita/+ mice; other investigators have also demonstrated decreased mitochondrial membrane potential using in vitro LASY knockdown method [23].

To investigate the mechanisms through which lipoic acid protects mitochondria in kidney proximal tubules, we examined gene expression of several common antioxidant enzymes in kidney cortex, including Sod series and glutathione peroxidase. Our data, using these novel mouse models, identify Sod2 as an antioxidant target by showing that expression of Sod2 (a major antioxidant enzyme which responds to enhanced superoxide production in mitochondria) markedly increases in kidney cortex of Lias^Low/LowIns2^Akita/+ mice; the latter observation has been previously reported in the Lias^+/-Ins2^Akita/+ diabetic mice with 50% reduced LIAS [20]. SOD2 co-exists with Lias in mitochondria and is a major antioxidant enzyme that responds to enhanced superoxide production in mitochondria; hence, the observation that SOD2 increases in kidney cortex of Lias^Low/LowIns2^Akita/+ mice with increased ROS is not surprising.

We attempted to identify antioxidant targets of LA in the diabetic kidney cortex. In addition to dysfunctional mitochondria, one of the most prominent sources of ROS is from the NADPH oxidase (NOX) activity [27–29]. Amongst these, the Nox4 gene, a biomarker of oxidative stress in the diabetic mellitus, has particularly high expression in the kidney [30]. Our result showed that Nox4 gene expression was significantly increased in Lias^Low/LowIns2^Akita/+ and decreased in Lias^High/HighIns2^Akita/+ kidney cortex, respectively, suggesting that NADPH oxidase 4 is an antioxidant target of lipoic acid.

NRF2 is a key transcription factor for regulation of antioxidant defense [31]. Although it has been reported that LA stimulated NRF2 nuclear accumulation [32], our result do not detect any significant changes of Nrf2 gene expression in 28-week-old Lias^Low/LowIns2^Akita/+ and Lias^High/HighIns2^Akita/+ mouse kidney. Hence, the renal protective action mediated by increased LIAS-generated LA is not accompanied by Nrf2 transcription alternation.

Several studies have revealed increased expression of TGF-β1 in renal glomeruli in experimental models of diabetes [34]. TGF-β1 is a critical mediator of podocyte injury and kidney hypertrophy characteristic of DN [33]. Thus, significantly reduced Tgfβ1 gene expression in Lias^High/HighIns2^Akita mice may play a role in attenuation of the adverse effect of diabetes mellitus on kidney structure and function. In addition, our results obtained from previous and the current studies using different degrees of Lias deficiency mouse models have clearly demonstrated that renal proximal tubules, with numerous mitochondria required for their important absorption functions, are sensitive to mitochondrion damage and that they are an ideal region of the nephron for assessment of mitochondria status during development of diabetic nephropathy. It is also worth studying the impact of mitochondrial damage on resorption in order to ascertain which mitochondrial component(s) is/are injured and the mechanism through which the deficiency of endogenous antioxidant protection develops.

Accumulating evidence support a role for inflammation in DN. In particular, the inflammatory cells infiltrate (like increased renal macrophage infiltration) and significantly higher levels of cytokines (chemokines) including monocyte chemoattractant protein-1 (MCP-1), accompanies DN [35]. MCP-1 is considered as a major mediator of inflammation process in DN patients [36]. It is a member of the CC chemokine family synthesized by a variety of cell types including glomerular endothelial cells, mesangial cells, tubular epithelial cells, and monocytes [37]. Studies suggest that MCP-1 production in mesangial cells and renal tubular epithelial cells are induced by advanced glycated end products (AGEs) through NF-κB activation [38, 39]. The promoters of MCP-1 gene contain binding sites for NF-kB [40]. Since urinary MCP-1 is upregulated in many renal diseases, including DN patients, we measured urinary MCP-1 levels in the three groups of mice. Our results showed that there were significantly increased urinary MCP-1 levels in Lias^Low/LowIns2^Akita/+ mice compared with Lias^+/+Ins2^Akita/+ and Lias^High/HighIns2^Akita/+ mice. This observation indicates that increased inflammation occurs in Lias^Low/LowIns2^Akita/+ mice. The increased MCP-1 is likely mediated by NF-kB in response to enhanced kidney oxidative stress [41, 42]. This result provides further evidence that increasing the endogenous antioxidant capacity could be an effective strategy for prevention and treatment of DN.

In a previous study, we showed that plasma glucose levels in Lias^+/-Ins2^Akita/+ mice are significantly greater than those in Lias^+/+Ins2^Akita/+ mice [20]. However, we did not detect any significant differences among the three groups of mice in the current study. We believe genetic background of the mice plays a major role in this discrepancy [43, 44]. We used mice with B6 genetic background for the current project, whereas we used F1 genetic background for the previous one. Thus, it is likely that even the same level of Lias gene expression in the different genetic background could exhibit different traits.

In summary, our data clearly indicate that Lias^High/HighIns2^Akita/+ and Lias^Low/LowIns2^Akita/+ mice manifest variations in levels of endogenous antioxidant capacity in kidneys that lead to different degrees of diabetic pathologic changes. The results have clarified the role of antioxidants in the early development of diabetic nephropathy and strongly suggest that protection of mitochondria is a novel therapeutic target for effective antioxidant therapy of DN.

We conclude that these new antioxidant mouse models are suitable to elucidate the contributions of oxidative stress in the pathogenesis of diabetic kidney disease.

Acknowledgments

We thank Drs. Edward Leiter and Racheal Wallace of the Jackson Laboratory for assisting with mouse model development. The authors thank Dr. Edward H. Leiter for critical review. =

Author Contributions

Conceptualization: XY.
Data curation: XY.
Formal analysis: XY LRJ VN NM.
Funding acquisition: XY LRJ.
Investigation: XY.
Methodology: XY LX SH SS.
Project administration: XY.
Supervision: XY.
Validation: XY LRJ VN.
Visualization: XY.
Writing – original draft: XY.
Writing – review & editing: XY LRJ VN LX SH.

References

1. Packer L, Witt EH, Tritschler HJ. alpha-Lipoic acid as a biological antioxidant. Free Radic Biol Med. 1995 Aug;19(2):227–50. pmid:7649494
- View Article
- PubMed/NCBI
- Google Scholar
2. Biewenga G, Haenen GR, Bast A. The role of lipoic acid in the treatment of diabetic polyneuropathy. Drug Metab Rev. 1997 Nov;29(4):1025–54. pmid:9421684
- View Article
- PubMed/NCBI
- Google Scholar
3. Shay KP, Hagen TM. Age-associated impairment of Akt phosphorylation in primary rat hepatocytes is remediated by alpha-lipoic acid through PI3 kinase, PTEN, and PP2A. Biogerontology. 2009 Aug;10(4):443–56. pmid:18931933
- View Article
- PubMed/NCBI
- Google Scholar
4. Reed LJ. From lipoic acid to multi-enzyme complexes. Protein Sci. 1998 Jan;7(1):220–4. pmid:9514279
- View Article
- PubMed/NCBI
- Google Scholar
5. Yi X, Maeda N. Endogenous production of lipoic acid is essential for mouse development. Mol Cell Biol. 2005 Sep;25(18):8387–92. pmid:16135825
- View Article
- PubMed/NCBI
- Google Scholar
6. Raptis AE, Viberti G. Pathogenesis of diabetic nephropathy. Exp Clin Endocrinol Diabetes. 2001;109 Suppl 2:S424–37. pmid:11460589
- View Article
- PubMed/NCBI
- Google Scholar
7. Baynes JW. Role of oxidative stress in development of complications in diabetes. Diabetes. 1991 Apr;40(4):405–12. pmid:2010041
- View Article
- PubMed/NCBI
- Google Scholar
8. Ha H, Hwang IA, Park JH, Lee HB. Role of reactive oxygen species in the pathogenesis of diabetic nephropathy. Diabetes Res Clin Pract. 2008 Nov 13;82 Suppl 1:S42–5. pmid:18845352
- View Article
- PubMed/NCBI
- Google Scholar
9. Darko D, Dornhorst A, Kelly FJ, Ritter JM, Chowienczyk PJ. Lack of effect of oral vitamin C on blood pressure, oxidative stress and endothelial function in Type II diabetes. Clin Sci (Lond). 2002 Oct;103(4):339–44. pmid:12241530
- View Article
- PubMed/NCBI
- Google Scholar
10. Lonn E, Yusuf S, Hoogwerf B, Pogue J, Yi Q, Zinman B, et al. Effects of vitamin E on cardiovascular and microvascular outcomes in high-risk patients with diabetes: results of the HOPE study and MICRO-HOPE substudy. Diabetes Care. 2002 Nov;25(11):1919–27. pmid:12401733
- View Article
- PubMed/NCBI
- Google Scholar
11. Blum S, Vardi M, Levy NS, Miller-Lotan R, Levy AP. The effect of vitamin E supplementation on cardiovascular risk in diabetic individuals with different haptoglobin phenotypes. Atherosclerosis. 2010 Jul;211(1):25–7. pmid:20223458
- View Article
- PubMed/NCBI
- Google Scholar
12. Gaede P, Poulsen HE, Parving HH, Pedersen O. Double-blind, randomized study of the effect of combined treatment with vitamin C and E on albuminuria in Type 2 diabetic patients. Diabet Med. 2001 Sep;18(9):756–60. pmid:11606175
- View Article
- PubMed/NCBI
- Google Scholar
13. Doherty HE, Kim HS, Hiller S, Sulik KK, Maeda N. A mouse strain where basal connective tissue growth factor gene expression can be switched from low to high. PLOS ONE. 2010 Sep;5(9):1–14. pmid:20877562
- View Article
- PubMed/NCBI
- Google Scholar
14. Brosius FC 3rd, Alpers CE, Bottinger EP, Breyer MD, Coffman TM, Gurley SB, et al. Mouse models of diabetic nephropathy. J Am Soc Nephrol. 2009 Dec;20(12):2503–12. pmid:19729434
- View Article
- PubMed/NCBI
- Google Scholar
15. Breyer MD, Bottinger E, Brosius FC 3rd, Coffman TM, Harris RC, Heilig CW, et al. Mouse models of diabetic nephropathy. J Am Soc Nephrol. 2005 Jan;16(1):27–45. pmid:15563560
- View Article
- PubMed/NCBI
- Google Scholar
16. Yoshioka M, Kayo T, Ikeda T, Koizumi A. A novel locus, Mody4, distal to D7Mit189 on chromosome 7 determines early-onset NIDDM in nonobese C57BL/6 (Akita) mutant mice. Diabetes. 1997 May;46(5):887–94. pmid:9133560
- View Article
- PubMed/NCBI
- Google Scholar
17. Valero E, Garcia-Carmona F. Optimizing enzymatic cycling assays: spectrophotometric determination of low levels of pyruvate and L-lactate. Anal Biochem. 1996 Jul 15;239(1):47–52. pmid:8660624
- View Article
- PubMed/NCBI
- Google Scholar
18. Kim HS, Lee G, John SW, Maeda N, Smithies O. Molecular phenotyping for analyzing subtle genetic effects in mice: application to an angiotensinogen gene titration. Proc Natl Acad Sci U S A. 2002 Apr 2;99(7):4602–7. pmid:11904385
- View Article
- PubMed/NCBI
- Google Scholar
19. Carlson DA, Smith AR, Fischer SJ, Young KL, Packer L. The plasma pharmacokinetics of R-(+)-lipoic acid administered as sodium R-(+)-lipoate to healthy human subjects. Altern Med Rev. 2007 Dec;12(4):343–51. pmid:18069903
- View Article
- PubMed/NCBI
- Google Scholar
20. Yi X, Xu L, Hiller S, Kim HS, Nickeleit V, James LR, et al. Reduced expression of lipoic acid synthase accelerates diabetic nephropathy. J Am Soc Nephrol. 2012 Jan;23(1):103–11. pmid:22021711
- View Article
- PubMed/NCBI
- Google Scholar
21. Forbes JM, Coughlan MT, Cooper ME. Oxidative stress as a major culprit in kidney disease in diabetes. Diabetes 2008 57: 1446–1454. pmid:18511445
- View Article
- PubMed/NCBI
- Google Scholar
22. Shigenaga MK, Hagen TM, Ames BN. Oxidative damage and mitochondrial decay in aging. Proc Natl Acad Sci U S A. 1994 Nov 8;91(23):10771–8. pmid:7971961
- View Article
- PubMed/NCBI
- Google Scholar
23. Padmalayam I, Hasham S, Saxena U, Pillarisetti S. Lipoic acid synthase (LASY): a novel role in inflammation, mitochondrial function, and insulin resistance. 2009 Mar;58(3):600–8. pmid:19074983
- View Article
- PubMed/NCBI
- Google Scholar
24. Brownlee M. The pathobiology of diabetic complications: a unifying mechanism. Diabetes. 2005 Jun;54(6):1615–25. pmid:15919781
- View Article
- PubMed/NCBI
- Google Scholar
25. hi Y, Lo CS, Chenier I, Maachi H, Filep JG, Ingelfinger JR, et al. Overexpression of catalase prevents hypertension and tubulointerstitial fibrosis and normalization of renal angiotensin-converting enzyme-2 expression in Akita mice. Am J Physiol Renal Physiol. 2013 Jun 1;304(11):F1335–46. pmid:23552863
- View Article
- PubMed/NCBI
- Google Scholar
26. Mitchell T, Johnson MS, Ouyang X, Chacko BK, Mitra K, Lei X, et al. Dysfunctional mitochondrial bioenergetics and oxidative stress in Akita(+/Ins2)-derived beta-cells. Am J Physiol Endocrinol Metab. 2013 Sep 1;305(5):E585–99. pmid:23820623
- View Article
- PubMed/NCBI
- Google Scholar
27. Bedard K, Krause KH. The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiol Rev. 2007 Jan;87(1):245–313. pmid:17237347
- View Article
- PubMed/NCBI
- Google Scholar
28. Gill PS, Wilcox CS. NADPH oxidases in the kidney. Antioxid Redox Signal. 2006 Sep-Oct;8(9–10):1597–607. pmid:16987014
- View Article
- PubMed/NCBI
- Google Scholar
29. Asaba K, Tojo A, Onozato ML, Goto A, Quinn MT, Fujita T, et al. Effects of NADPH oxidase inhibitor in diabetic nephropathy. Kidney Int. 2005 May;67(5):1890–8. pmid:15840036
- View Article
- PubMed/NCBI
- Google Scholar
30. Gorin Y, Block K, Hernandez J, Bhandari B, Wagner B, Barnes JL, et al. Nox4 NAD(P)H oxidase mediates hypertrophy and fibronectin expression in the diabetic kidney. J Biol Chem. 2005 Nov 25;280(47):39616–26. pmid:16135519
- View Article
- PubMed/NCBI
- Google Scholar
31. Pickering AM, Linder RA, Zhang H, Forman HJ, Davies KJ. Nrf2-dependent induction of proteasome and Pa28alphabeta regulator are required for adaptation to oxidative stress. J Biol Chem. 2012 Mar 23;287(13):10021–31. pmid:22308036
- View Article
- PubMed/NCBI
- Google Scholar
32. Shay KP, Moreau RF, Smith EJ, Smith AR, Hagen TM. Alpha-lipoic acid as a dietary supplement: molecular mechanisms and therapeutic potential. Biochim Biophys Acta. 2009 Oct;1790(10):1149–60. pmid:19664690
- View Article
- PubMed/NCBI
- Google Scholar
33. Herman-Edelstein M, Thomas MC, Thallas-Bonke V, Saleem M, Cooper ME, Kantharidis P. Dedifferentiation of immortalized human podocytes in response to transforming growth factor-beta: a model for diabetic podocytopathy. Diabetes. 2011 Jun;60(6):1779–88. pmid:21521871
- View Article
- PubMed/NCBI
- Google Scholar
34. Park IS, Kiyomoto H, Abboud SL, Abboud HE. Expression of transforming growth factor-beta and type IV collagen in early streptozotocin-induced diabetes. Diabetes. 1997 Mar;46(3):473–80. pmid:9032105
- View Article
- PubMed/NCBI
- Google Scholar
35. Sancar-Bas S, Gezginci-Oktayoglu S, Bolkent S. Exendin-4 attenuates renal tubular injury by decreasing oxidative stress and inflammation in streptozotocin-induced diabetic mice. Growth Factors. 2015 Oct;33(5–6):419–29. pmid:26728502
- View Article
- PubMed/NCBI
- Google Scholar
36. Navarro-González JF, Mora-Fernández C, de Fuentes MM, García-Pérez J. Inflammatory molecules and pathways in the pathogenesis of diabetic nephropathy. Nat Rev Neprol. 2011 Jun;7:327–40. pmid:21537349
- View Article
- PubMed/NCBI
- Google Scholar
37. Rovin BH, Yoshimura T, Tan L. Cytokine-induced production of monocyte chemoattractant protein-1 by cultured human mesangial cells. J Immunol 1992 Apr;148:2148–2153. pmid:1532001
- View Article
- PubMed/NCBI
- Google Scholar
38. Wu J, Guan TJ, Zheng S, Grosjean F, Liu W, Xiong H, et al. Inhibition of inflammation by pentosan polysulfate impedes the development and progression of severe diabetic nephropathy in aging C57B6 mice. Lab Invest. 2011 Oct; 91:1459–1471. pmid:21808238
- View Article
- PubMed/NCBI
- Google Scholar
39. Morri T, Fujita H, Narita T, Shimotomai T, Fujishima H, Yoshioka N, et al. Association of monocyte chemoattractant protein-1 with renal tubular damage in diabetic nephropathy. J Diabetes Complicate. 2003 Jan;17:11–15.
- View Article
- Google Scholar
40. Zhang Z, Yuan W, Sun L, Szeto FL, Wong KE, Li X, Kong J, Li YC. 1,25-Dihydroxyvitamin D3 targeting of NF-kappaB suppresses high glucose-induced MCP-1 expression in mesangial cells. Kidney Int. 2007 Jul;72:193–201. pmid:17507908
- View Article
- PubMed/NCBI
- Google Scholar
41. Kowluru RA, Koppolu P, Chakrabarti S, Chen S. Diabetes-induced activation of nuclear transcriptional factor in the retina, and its inhibition by antioxidants. Free Radic Res. 2003 Nov;37:1169–1180. pmid:14703729
- View Article
- PubMed/NCBI
- Google Scholar
42. Cooper ME. Pathogenesis, prevention and treatment of diabetic nephropathy. Lancet. 1998 July;352:213–219. pmid:9683226
- View Article
- PubMed/NCBI
- Google Scholar
43. Gurley SB, Mach CL, Stegbauer J, Yang J, Snow KP, Hu A, et al. Influence of genetic background on albuminuria and kidney injury in Ins2(+/C96Y) (Akita) mice. Am J Physiol Renal Physiol. 2010 Mar;298(3):F788–95. pmid:20042456
- View Article
- PubMed/NCBI
- Google Scholar
44. Gurley SB, Clare SE, Snow KP, Hu A, Meyer TW, Coffman TM. Impact of genetic background on nephropathy in diabetic mice. Am J Physiol Renal Physiol. 2006 Jan;290(1):F214–22. pmid:16118394
- View Article
- PubMed/NCBI
- Google Scholar

[ref1] 1. Packer L, Witt EH, Tritschler HJ. alpha-Lipoic acid as a biological antioxidant. Free Radic Biol Med. 1995 Aug;19(2):227–50. pmid:7649494
View Article
PubMed/NCBI
Google Scholar

[2] View Article

[3] PubMed/NCBI

[4] Google Scholar

[ref2] 2. Biewenga G, Haenen GR, Bast A. The role of lipoic acid in the treatment of diabetic polyneuropathy. Drug Metab Rev. 1997 Nov;29(4):1025–54. pmid:9421684
View Article
PubMed/NCBI
Google Scholar

[6] View Article

[7] PubMed/NCBI

[8] Google Scholar

[ref3] 3. Shay KP, Hagen TM. Age-associated impairment of Akt phosphorylation in primary rat hepatocytes is remediated by alpha-lipoic acid through PI3 kinase, PTEN, and PP2A. Biogerontology. 2009 Aug;10(4):443–56. pmid:18931933
View Article
PubMed/NCBI
Google Scholar

[10] View Article

[11] PubMed/NCBI

[12] Google Scholar

[ref4] 4. Reed LJ. From lipoic acid to multi-enzyme complexes. Protein Sci. 1998 Jan;7(1):220–4. pmid:9514279
View Article
PubMed/NCBI
Google Scholar

[14] View Article

[15] PubMed/NCBI

[16] Google Scholar

[ref5] 5. Yi X, Maeda N. Endogenous production of lipoic acid is essential for mouse development. Mol Cell Biol. 2005 Sep;25(18):8387–92. pmid:16135825
View Article
PubMed/NCBI
Google Scholar

[18] View Article

[19] PubMed/NCBI

[20] Google Scholar

[ref6] 6. Raptis AE, Viberti G. Pathogenesis of diabetic nephropathy. Exp Clin Endocrinol Diabetes. 2001;109 Suppl 2:S424–37. pmid:11460589
View Article
PubMed/NCBI
Google Scholar

[22] View Article

[23] PubMed/NCBI

[24] Google Scholar

[ref7] 7. Baynes JW. Role of oxidative stress in development of complications in diabetes. Diabetes. 1991 Apr;40(4):405–12. pmid:2010041
View Article
PubMed/NCBI
Google Scholar

[26] View Article

[27] PubMed/NCBI

[28] Google Scholar

[ref8] 8. Ha H, Hwang IA, Park JH, Lee HB. Role of reactive oxygen species in the pathogenesis of diabetic nephropathy. Diabetes Res Clin Pract. 2008 Nov 13;82 Suppl 1:S42–5. pmid:18845352
View Article
PubMed/NCBI
Google Scholar

[30] View Article

[31] PubMed/NCBI

[32] Google Scholar

[ref9] 9. Darko D, Dornhorst A, Kelly FJ, Ritter JM, Chowienczyk PJ. Lack of effect of oral vitamin C on blood pressure, oxidative stress and endothelial function in Type II diabetes. Clin Sci (Lond). 2002 Oct;103(4):339–44. pmid:12241530
View Article
PubMed/NCBI
Google Scholar

[34] View Article

[35] PubMed/NCBI

[36] Google Scholar

[ref10] 10. Lonn E, Yusuf S, Hoogwerf B, Pogue J, Yi Q, Zinman B, et al. Effects of vitamin E on cardiovascular and microvascular outcomes in high-risk patients with diabetes: results of the HOPE study and MICRO-HOPE substudy. Diabetes Care. 2002 Nov;25(11):1919–27. pmid:12401733
View Article
PubMed/NCBI
Google Scholar

[38] View Article

[39] PubMed/NCBI

[40] Google Scholar

[ref11] 11. Blum S, Vardi M, Levy NS, Miller-Lotan R, Levy AP. The effect of vitamin E supplementation on cardiovascular risk in diabetic individuals with different haptoglobin phenotypes. Atherosclerosis. 2010 Jul;211(1):25–7. pmid:20223458
View Article
PubMed/NCBI
Google Scholar

[42] View Article

[43] PubMed/NCBI

[44] Google Scholar

[ref12] 12. Gaede P, Poulsen HE, Parving HH, Pedersen O. Double-blind, randomized study of the effect of combined treatment with vitamin C and E on albuminuria in Type 2 diabetic patients. Diabet Med. 2001 Sep;18(9):756–60. pmid:11606175
View Article
PubMed/NCBI
Google Scholar

[46] View Article

[47] PubMed/NCBI

[48] Google Scholar

[ref13] 13. Doherty HE, Kim HS, Hiller S, Sulik KK, Maeda N. A mouse strain where basal connective tissue growth factor gene expression can be switched from low to high. PLOS ONE. 2010 Sep;5(9):1–14. pmid:20877562
View Article
PubMed/NCBI
Google Scholar

[50] View Article

[51] PubMed/NCBI

[52] Google Scholar

[ref14] 14. Brosius FC 3rd, Alpers CE, Bottinger EP, Breyer MD, Coffman TM, Gurley SB, et al. Mouse models of diabetic nephropathy. J Am Soc Nephrol. 2009 Dec;20(12):2503–12. pmid:19729434
View Article
PubMed/NCBI
Google Scholar

[54] View Article

[55] PubMed/NCBI

[56] Google Scholar

[ref15] 15. Breyer MD, Bottinger E, Brosius FC 3rd, Coffman TM, Harris RC, Heilig CW, et al. Mouse models of diabetic nephropathy. J Am Soc Nephrol. 2005 Jan;16(1):27–45. pmid:15563560
View Article
PubMed/NCBI
Google Scholar

[58] View Article

[59] PubMed/NCBI

[60] Google Scholar

[ref16] 16. Yoshioka M, Kayo T, Ikeda T, Koizumi A. A novel locus, Mody4, distal to D7Mit189 on chromosome 7 determines early-onset NIDDM in nonobese C57BL/6 (Akita) mutant mice. Diabetes. 1997 May;46(5):887–94. pmid:9133560
View Article
PubMed/NCBI
Google Scholar

[62] View Article

[63] PubMed/NCBI

[64] Google Scholar

[ref17] 17. Valero E, Garcia-Carmona F. Optimizing enzymatic cycling assays: spectrophotometric determination of low levels of pyruvate and L-lactate. Anal Biochem. 1996 Jul 15;239(1):47–52. pmid:8660624
View Article
PubMed/NCBI
Google Scholar

[66] View Article

[67] PubMed/NCBI

[68] Google Scholar

[ref18] 18. Kim HS, Lee G, John SW, Maeda N, Smithies O. Molecular phenotyping for analyzing subtle genetic effects in mice: application to an angiotensinogen gene titration. Proc Natl Acad Sci U S A. 2002 Apr 2;99(7):4602–7. pmid:11904385
View Article
PubMed/NCBI
Google Scholar

[70] View Article

[71] PubMed/NCBI

[72] Google Scholar

[ref19] 19. Carlson DA, Smith AR, Fischer SJ, Young KL, Packer L. The plasma pharmacokinetics of R-(+)-lipoic acid administered as sodium R-(+)-lipoate to healthy human subjects. Altern Med Rev. 2007 Dec;12(4):343–51. pmid:18069903
View Article
PubMed/NCBI
Google Scholar

[74] View Article

[75] PubMed/NCBI

[76] Google Scholar

[ref20] 20. Yi X, Xu L, Hiller S, Kim HS, Nickeleit V, James LR, et al. Reduced expression of lipoic acid synthase accelerates diabetic nephropathy. J Am Soc Nephrol. 2012 Jan;23(1):103–11. pmid:22021711
View Article
PubMed/NCBI
Google Scholar

[78] View Article

[79] PubMed/NCBI

[80] Google Scholar

[ref21] 21. Forbes JM, Coughlan MT, Cooper ME. Oxidative stress as a major culprit in kidney disease in diabetes. Diabetes 2008 57: 1446–1454. pmid:18511445
View Article
PubMed/NCBI
Google Scholar

[82] View Article

[83] PubMed/NCBI

[84] Google Scholar

[ref22] 22. Shigenaga MK, Hagen TM, Ames BN. Oxidative damage and mitochondrial decay in aging. Proc Natl Acad Sci U S A. 1994 Nov 8;91(23):10771–8. pmid:7971961
View Article
PubMed/NCBI
Google Scholar

[86] View Article

[87] PubMed/NCBI

[88] Google Scholar

[ref23] 23. Padmalayam I, Hasham S, Saxena U, Pillarisetti S. Lipoic acid synthase (LASY): a novel role in inflammation, mitochondrial function, and insulin resistance. 2009 Mar;58(3):600–8. pmid:19074983
View Article
PubMed/NCBI
Google Scholar

[90] View Article

[91] PubMed/NCBI

[92] Google Scholar

[ref24] 24. Brownlee M. The pathobiology of diabetic complications: a unifying mechanism. Diabetes. 2005 Jun;54(6):1615–25. pmid:15919781
View Article
PubMed/NCBI
Google Scholar

[94] View Article

[95] PubMed/NCBI

[96] Google Scholar

[ref25] 25. hi Y, Lo CS, Chenier I, Maachi H, Filep JG, Ingelfinger JR, et al. Overexpression of catalase prevents hypertension and tubulointerstitial fibrosis and normalization of renal angiotensin-converting enzyme-2 expression in Akita mice. Am J Physiol Renal Physiol. 2013 Jun 1;304(11):F1335–46. pmid:23552863
View Article
PubMed/NCBI
Google Scholar

[98] View Article

[99] PubMed/NCBI

[100] Google Scholar

[ref26] 26. Mitchell T, Johnson MS, Ouyang X, Chacko BK, Mitra K, Lei X, et al. Dysfunctional mitochondrial bioenergetics and oxidative stress in Akita(+/Ins2)-derived beta-cells. Am J Physiol Endocrinol Metab. 2013 Sep 1;305(5):E585–99. pmid:23820623
View Article
PubMed/NCBI
Google Scholar

[102] View Article

[103] PubMed/NCBI

[104] Google Scholar

[ref27] 27. Bedard K, Krause KH. The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiol Rev. 2007 Jan;87(1):245–313. pmid:17237347
View Article
PubMed/NCBI
Google Scholar

[106] View Article

[107] PubMed/NCBI

[108] Google Scholar

[ref28] 28. Gill PS, Wilcox CS. NADPH oxidases in the kidney. Antioxid Redox Signal. 2006 Sep-Oct;8(9–10):1597–607. pmid:16987014
View Article
PubMed/NCBI
Google Scholar

[110] View Article

[111] PubMed/NCBI

[112] Google Scholar

[ref29] 29. Asaba K, Tojo A, Onozato ML, Goto A, Quinn MT, Fujita T, et al. Effects of NADPH oxidase inhibitor in diabetic nephropathy. Kidney Int. 2005 May;67(5):1890–8. pmid:15840036
View Article
PubMed/NCBI
Google Scholar

[114] View Article

[115] PubMed/NCBI

[116] Google Scholar

[ref30] 30. Gorin Y, Block K, Hernandez J, Bhandari B, Wagner B, Barnes JL, et al. Nox4 NAD(P)H oxidase mediates hypertrophy and fibronectin expression in the diabetic kidney. J Biol Chem. 2005 Nov 25;280(47):39616–26. pmid:16135519
View Article
PubMed/NCBI
Google Scholar

[118] View Article

[119] PubMed/NCBI

[120] Google Scholar

[ref31] 31. Pickering AM, Linder RA, Zhang H, Forman HJ, Davies KJ. Nrf2-dependent induction of proteasome and Pa28alphabeta regulator are required for adaptation to oxidative stress. J Biol Chem. 2012 Mar 23;287(13):10021–31. pmid:22308036
View Article
PubMed/NCBI
Google Scholar

[122] View Article

[123] PubMed/NCBI

[124] Google Scholar

[ref32] 32. Shay KP, Moreau RF, Smith EJ, Smith AR, Hagen TM. Alpha-lipoic acid as a dietary supplement: molecular mechanisms and therapeutic potential. Biochim Biophys Acta. 2009 Oct;1790(10):1149–60. pmid:19664690
View Article
PubMed/NCBI
Google Scholar

[126] View Article

[127] PubMed/NCBI

[128] Google Scholar

[ref33] 33. Herman-Edelstein M, Thomas MC, Thallas-Bonke V, Saleem M, Cooper ME, Kantharidis P. Dedifferentiation of immortalized human podocytes in response to transforming growth factor-beta: a model for diabetic podocytopathy. Diabetes. 2011 Jun;60(6):1779–88. pmid:21521871
View Article
PubMed/NCBI
Google Scholar

[130] View Article

[131] PubMed/NCBI

[132] Google Scholar

[ref34] 34. Park IS, Kiyomoto H, Abboud SL, Abboud HE. Expression of transforming growth factor-beta and type IV collagen in early streptozotocin-induced diabetes. Diabetes. 1997 Mar;46(3):473–80. pmid:9032105
View Article
PubMed/NCBI
Google Scholar

[134] View Article

[135] PubMed/NCBI

[136] Google Scholar

[ref35] 35. Sancar-Bas S, Gezginci-Oktayoglu S, Bolkent S. Exendin-4 attenuates renal tubular injury by decreasing oxidative stress and inflammation in streptozotocin-induced diabetic mice. Growth Factors. 2015 Oct;33(5–6):419–29. pmid:26728502
View Article
PubMed/NCBI
Google Scholar

[138] View Article

[139] PubMed/NCBI

[140] Google Scholar

[ref36] 36. Navarro-González JF, Mora-Fernández C, de Fuentes MM, García-Pérez J. Inflammatory molecules and pathways in the pathogenesis of diabetic nephropathy. Nat Rev Neprol. 2011 Jun;7:327–40. pmid:21537349
View Article
PubMed/NCBI
Google Scholar

[142] View Article

[143] PubMed/NCBI

[144] Google Scholar

[ref37] 37. Rovin BH, Yoshimura T, Tan L. Cytokine-induced production of monocyte chemoattractant protein-1 by cultured human mesangial cells. J Immunol 1992 Apr;148:2148–2153. pmid:1532001
View Article
PubMed/NCBI
Google Scholar

[146] View Article

[147] PubMed/NCBI

[148] Google Scholar

[ref38] 38. Wu J, Guan TJ, Zheng S, Grosjean F, Liu W, Xiong H, et al. Inhibition of inflammation by pentosan polysulfate impedes the development and progression of severe diabetic nephropathy in aging C57B6 mice. Lab Invest. 2011 Oct; 91:1459–1471. pmid:21808238
View Article
PubMed/NCBI
Google Scholar

[150] View Article

[151] PubMed/NCBI

[152] Google Scholar

[ref39] 39. Morri T, Fujita H, Narita T, Shimotomai T, Fujishima H, Yoshioka N, et al. Association of monocyte chemoattractant protein-1 with renal tubular damage in diabetic nephropathy. J Diabetes Complicate. 2003 Jan;17:11–15.
View Article
Google Scholar

[154] View Article

[155] Google Scholar

[ref40] 40. Zhang Z, Yuan W, Sun L, Szeto FL, Wong KE, Li X, Kong J, Li YC. 1,25-Dihydroxyvitamin D3 targeting of NF-kappaB suppresses high glucose-induced MCP-1 expression in mesangial cells. Kidney Int. 2007 Jul;72:193–201. pmid:17507908
View Article
PubMed/NCBI
Google Scholar

[157] View Article

[158] PubMed/NCBI

[159] Google Scholar

[ref41] 41. Kowluru RA, Koppolu P, Chakrabarti S, Chen S. Diabetes-induced activation of nuclear transcriptional factor in the retina, and its inhibition by antioxidants. Free Radic Res. 2003 Nov;37:1169–1180. pmid:14703729
View Article
PubMed/NCBI
Google Scholar

[161] View Article

[162] PubMed/NCBI

[163] Google Scholar

[ref42] 42. Cooper ME. Pathogenesis, prevention and treatment of diabetic nephropathy. Lancet. 1998 July;352:213–219. pmid:9683226
View Article
PubMed/NCBI
Google Scholar

[165] View Article

[166] PubMed/NCBI

[167] Google Scholar

[ref43] 43. Gurley SB, Mach CL, Stegbauer J, Yang J, Snow KP, Hu A, et al. Influence of genetic background on albuminuria and kidney injury in Ins2(+/C96Y) (Akita) mice. Am J Physiol Renal Physiol. 2010 Mar;298(3):F788–95. pmid:20042456
View Article
PubMed/NCBI
Google Scholar

[169] View Article

[170] PubMed/NCBI

[171] Google Scholar

[ref44] 44. Gurley SB, Clare SE, Snow KP, Hu A, Meyer TW, Coffman TM. Impact of genetic background on nephropathy in diabetic mice. Am J Physiol Renal Physiol. 2006 Jan;290(1):F214–22. pmid:16118394
View Article
PubMed/NCBI
Google Scholar

[173] View Article

[174] PubMed/NCBI

[175] Google Scholar

Figures

Abstract

Introduction

Materials and Methods

Creation of LiasLow/+ and LiasHigh/+ Mice by Changing 3’ untranslated region (3’-UTR) Sequences

Biochemical Parameters

Urinary Albumin Excretion

Urinary MCP-1 assay

Blood Pressure Measurement

Renal Function and Morphometric Analyses

Assessment of Oxidative Stress

Western Blot Analysis

Reverse Transcription and Quantitative Real-Time Polymerase Chain Reaction (RT-PCR)

Statistical Analyses

Results

Model Construction

Systemic Pathological Changes

Kidney Pathologic Changes

Oxidative Stress and Inflammation

Discussion

Acknowledgments

Author Contributions

References

Creation of Lias^Low/+ and Lias^High/+ Mice by Changing 3’ untranslated region (3’-UTR) Sequences