Post-Natal Inhibition of NF-κB Activation Prevents Renal Damage Caused by Prenatal LPS Exposure

Prenatal exposure to an inflammatory stimulus has been shown to cause renal damage in offspring. Our present study explored the role of intra-renal NF-κB activation in the development of progressive renal fibrosis in offspring that underwent prenatal exposure to an inflammatory stimulus. Time-dated pregnant rats were treated with saline (control group) or 0.79 mg/kg lipopolysaccharide (LPS) through intra-peritoneal injection on gestational day 8, 10 and 12. At the age of 7 weeks, offspring from control or LPS group were treated with either tap water (Con+Ve or LPS+Ve group) or pyrollidine dithiocarbamate (PDTC, 120mg/L), a NF-κB inhibitor, via drinking water starting (Con+PDTC or LPS+PDTC group), respectively, till the age of 20 or 68 weeks. The gross structure of kidney was assessed by hematoxylin-eosin, periodic acid–Schiff staining and Sirius red staining. The expression levels of TNF-α, IL-6, α-smooth muscle actin (α-SMA) and renin-angiotensin system (RAS) genes were determined by real time polymerase chain reaction and/or immunohistochemical staining. Our data showed that post-natal persistent PDTC administration efficiently repressed intra-renal NF-κB activation, TNF-α and IL-6 expression. Post-natal PDTC also prevented intra-renal glycogen deposition and collagenous fiber generation as evident by the reduced expression of collagen III and interstitial α-SMA in offspring of prenatal LPS exposure. Furthermore, post-natal PDTC administration reversed the intra-renal renin-angiotensin system (RAS) over-activity in offspring of prenatal LPS exposure. In conclusion, prenatal inflammatory exposure results in offspring’s intra-renal NF-κB activation along with inflammation which cross-talked with excessive RAS activation that caused exacerbation of renal fibrosis and dysfunction in the offspring. Thus, early life prevention of NF-κB activation may be a potential preventive strategy for chronic renal inflammation and progressive renal damage.


Introduction
The incidence and morbidity rates of cardiovascular disease (CVD) such as hypertension continue to rise despite ongoing research efforts in regard to primary and secondary prevention [1]. Therefore, exploring novel mechanisms yielding new biological targets are of great significance to improve prevention and treatment of hypertension as well as to reduce the incidence of CVD.
The association of adverse intra-uterine environment with adult chronic diseases in offspring has attracted significant attention worldwide [2]. Based on an epidemiological study in England, they showed that women with bacterial vaginosis had a fivefold increased risk of preterm delivery independent of age, race, marital status, education, income and history of preterm birth [3]. The children born with pre-term birth showed the characteristic risk factors for the development of cardiovascular disease, such as higher blood pressure, higher fasting levels of serum free fatty acids [4]. A recent epidemiological study had also demonstrated that the population involved with the prenatal exposure to the 1918 influenza pandemic showed~20% excess cardiovascular disease [4]. These findings provide supportive evidence that prenatal inflammation is epidemiologically relevant to CVD. We previously found that prenatal exposure to inflammatory stimuli, such as lipopolysaccharides (LPS), the main component of gramnegative bacteria cellular wall [5], resulted in the development of hypertension in Sprague-Dawley (SD) rats [6]. As such, this may be indirectly caused by maternal derived pro-inflammatory cytokines exposure, rather than directly LPS exposure in utero [7]. As prenatal inflammatory exposure, such as infection [8], hepatitis [9] as well as arthritis [10], is still the most common public health problems during pregnancy, further research is required in this area to uncover the mechanisms of prenatal programmed hypertension and other CVD complications.
Interestingly, our research group has shown that prenatal exposure to LPS resulted in significantly lower glomerular numbers, creatinine clearance rates and higher urinary protein in adult offspring [11]. Our reported findings in this area was also confirmed by another independent research group [12]. Mechanistic studies found that abnormality of intra-renal reninangiotensin system (RAS) [11] and oxidative stress [12] might be involved. However, the relative mechanisms of prenatal LPS exposure induced renal damage are still largely unknown.
We previously found an increased renal infiltrating monocytes/macrophages and lymphocytes at the age of 7 weeks [13], and also an intra-renal NF-κB activation in offspring of prenatal exposure to LPS at the age of 25 weeks [11]. A specific IκBα degradation inhibitor, pyrollidine dithiocarbamate (PDTC) [14], which can prevent NF-κB activation [15], treated simultaneously with prenatal LPS stimulation significantly attenuated prenatal LPS exposureinduced offspring's renal damage [11]. These findings indicate that intra-renal NF-κB activation may have an important role in renal damage. However, PDTC simultaneously with LPS administration mainly blocks maternal NF-κB activation and inflammation response, which could only suggest that prenatal LPS exposure induced high levels of maternal inflammation may have a very important role in the development of renal damage in offspring. Thus, the physiological role of NF-κB activation in postnatal progressive renal damage in offspring of prenatal exposure to LPS is still uncertain.
Renal fibrosis is a common manifestation of various chronic kidney diseases, characterized by an excessive accumulation of extracellular matrix. The pathogenesis of renal fibrosis is a progressive process, which could ultimately lead to end-stage renal failure. In a simplistic view, renal fibrosis represents a failure of a wound-healing process in the kidney tissue responding to chronic, sustained injury [16]. We recently found that an early life and persistent NF-κB activation existed in the thoracic aorta [7] and increased renal collagen I expression [13] of prenatal LPS-induced offspring. Several researches showed that PDTC treatment could be a potential method to prevent renal damage in several animal models of chronic kidney diseases, such as doxorubicin hydrochloride induced nonimmune proteinuric tubulointerstitial inflammation [17], zymosan induced multiple organ failure [18], chronic tacrolimus (FK506) induced nephrotoxicity [19] and human renin and angiotensinogen genes double-transgenic rats [20]. As such, in the current study, we used PDTC to persistently inhibit the in vivo NF-κB activity of prenatal LPS-induced offspring postnatally in order to explore the role of NF-κB activation in the process of progressive renal fibrosis and its relationship with intra-renal RAS activation in offspring of prenatal LPS exposure.

Material and Methods Animals
The study protocol was approved by the Ethical Committee for Animal Experimentation of Third Military Medical University. Nulliparous pregnant time-mated SD rats were obtained from the Experimental Animal Center of the Third Military Medical University (Chongqing, China). All animals had free access to standard laboratory rat chow and tap water. Until parturition, rats were housed individually in a room at constant temperature (24°C) and under a 12 hour light-dark cycle. The pups were raised with a lactating mother until 4 weeks of age, at which time they were removed to cages containing three or four pups. The present study conformed to the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85-23, revised 1996, revised 2011; www.nap.edu/ catalog/5140.html).
The pregnant rats received an intraperitoneal (i.p) injection with saline (Control group) or 0.79 mg/kg LPS (Sigma Chemical, St. Louis, MO, USA) (LPS group), respectively, at gestational day 8, 10 and 12, as described previously (n = 8 for each group) [11,21,22]. The pregnant rats were used only once. After birth, the litter size was then reduced to eight pups to ensure equal nutrient access for all of the offspring. Neonatal rats were cared for by their mothers until they were weaned at the age of 4 weeks, after which they received standard rat chow. As both male and female offspring of prenatal exposure to LPS showed increased renal damage, equal size of male and female offspring rats were selected for each experiments in current study [11]. Offspring that received saline or LPS prenatally were treated with PDTC (120 mg/L, Sigma Chemical) [23,24] through drinking water from postnatal 7 weeks to 20 or 68 weeks, defined as Con+PDTC or LPS+PDTC groups, respectively, by random selection. Offspring received saline or LPS prenatally without any additional post-natal treatment, identified as Con+Ve or LPS+Ve groups respectively. At the end of treatment, offspring were anesthetized using chloral hydrate (0.35 g/kg, 7% in saline) and sacrificed by decapitation. Kidneys were collected for future analysis.
During the period of treatment, the physical condition of all the animals was monitored every day. Some animals were dead prior to the experimental endpoint [S1 Fig], and some of which might be caused by long-term PDTC treatment. Once the animal showed reduced locomotive activity and any other weakness, such as arching, it will be supplied with mush food in the petri dish. Humane endpoints/early euthanasia with CO 2 followed by cervical dislocation was used for animals who exhibited moribund states. The moribund states were identified as followings: weight loss (> 20%); inability to roll over from side to chest; dyspnea or labored breathing.
Systolic blood pressure (SBP) measurement SBP was assessed by the non-invasive tail-cuff method with computer-assisted BP-2010 Series tail measurement equipment (Softron Beijing Biotechnology Co., Ltd, Beijing, China), as described previously [6]. The investigators were blinded during the measuring of the blood pressure. SBP was calculated from three consecutive recordings.

Ratio of kidney weight/body weight
Ratio of kidney weight/body weight was calculated by using the value of kidney weight divided by the value of whole body weight for each animal.

Urine collection and analysis of 24 hour urine volume
Seven days ahead of sacrificing, each rat was housed in individual metabolic cage with free access to water and food for the collection of 24 hour urine. The mean value of 24 hour urine volume for each rat was calculated by using the 7 days consecutive data of urine volume.

Histopathological evaluations
Renal tissue samples from offspring of 68 week-old were fixed with 4% para-formaldehyde, embedded in paraffin, and sectioned into 4-μm-thick sections. Hematoxylineosin (HE) staining was used to summarize the gross morphology of renal glomerulus, tubes and interstitium by using our standard in house protocol. Periodic acid-Schiff (PAS) stain was used for detecting saccharides, glomerulus basilar membrane and neutral mucus material by using PAS Kit, according to the manufacturer's instructions (Sigma-Aldrich). Glomerular damage and tubulo-interstitial injury were semi-quantitatively scored, according to reported literature [27][28][29], by two independent examiners who were blinded as to animal groups. Briefly, randomly selected microscopic fields (6)(7)(8) at 100 × magnification per slide were used to count damaged glomerular or tubulo-interstitial injury.
Renal tissue samples from 68-week-old offspring were used for Sirius red staining. After dewaxing and re-hydration, slices were stained with Sirius red saturation picric acid for 30 minutes. After washed within water, nuclei were stained with hematoxylin. Slices were viewed with both light microscope (Olympus BH-2) and polarized microscope (Olympus BX-51). Collagen fibers appear as red under white microscope. Under polarized microscope, collagen I appears as yellow or red color with strong double refraction, while collagen III presents as green color with light double refraction.
The area of positive Sirius red staining was measured in 6-8 randomly chosen microscopic fields at 100 × magnification per offspring using NIH Image J software, according to the reported literature [30].

Statistical analysis
For multiple comparisons, a two-way ANOVA model followed by LSD or Dunnett T3 test for inter-group comparison, when appropriated, was performed by PASW Statistic software 18.0. Data are shown as mean ± S.D. A P value less than 0.05 was considered statistically significant.

Results
Prenatal inflammatory exposure leads to NF-κB activation along with increased pro-inflammatory cytokines in renal tissue of offspring Our previously finding had shown that NF-κB activation existed in kidney of offspring that received prenatal LPS exposure at the age of 25 weeks [11]. We first assessed NF-κB activity by determining the protein level of p-p65 and p65 at the age of 20 weeks. The protein levels of p-p65 and total p65 were significantly increased in renal tissue of offspring that received prenatal exposure to LPS (Fig 1A), which indicates that intra-renal NF-κB was activated in adult offspring of prenatal exposure to LPS. Interestingly, post-natal administration of specific IκBα degradation inhibitor PDTC reversed the NF-κB activation, and was therefore consistent with our previous finding [11]. TNF-α, IL-1β and IL-6 are the main downstream pro-inflammatory cytokines of NF-κB activation [15,32]. To find more evidence of NF-κB activation and in vivo effect of PDTC on NF-κB inhibition, we next determined the mRNA expression of TNF-α, and IL-6 in renal tissue. We found that prenatal LPS exposure significantly increased the mRNA expression of TNF-α and IL-6 in renal tissue of offspring at the age of 20 weeks, whereas postnatal PDTC administration significantly reduced the mRNA expression of TNF-α and IL-6 ( Fig 1B and 1C). This data demonstrates that NF-κB activation along with increased proinflammatory cytokines exists in the renal tissue of offspring that received prenatal exposure to LPS, whereas post-natal PDTC administration effectively blocks the NF-κB activation. NF-κB activation and increased expression of pro-inflammatory cytokines existed in the renal tissue of offspring that received prenatal LPS exposure. Relative protein expression of phospho-p65 ser536 and total p65 at the age of 20 weeks was determined by immunoblotting. Representative plots in each group and statistical data of relative densitometry, normalized by GAPDH, were shown (A). The mRNA expressions of TNF-α (B) and IL-6 (C) in the kidney at the age of 20 weeks were determined by realtime RT-PCR. Data are presented as mean ± SD. n = 6 offspring per group for (A); n = 7 offspring in each group for (B) and (C). * and ** indicate P<0.05 and P<0.01, respectively, which denote statistical comparison between the two marked treatment groups (Two-way ANOVA for followed by Dunnett T3 test for inter-group comparison (A, B and C)). Con+Ve group, offspring rats from maternal saline treatment together with post-natal saline treatment; LPS+Ve group, offspring rats from maternal LPS exposure together with post-natal saline treatment; LPS +PDTC group, offspring rats from maternal LPS exposure together with post-natal PDTC treatment; Con+PDTC group, offspring rats from maternal saline treatment together post-natal PDTC treatment. Post-natal NF-κB inhibition represses offspring's blood pressure elevation, increased kidney/body weight ratio and reduced urine volume (24 hour) induced by prenatal LPS exposure Consistent with our previous findings, the current model also showed that offspring of prenatal exposure to LPS showed increased SBP, whereas post-natal PDTC treatment reversed this elevation (Fig 2A). Prenatal LPS exposure significantly increased offspring's the ratio of kidney Post-natal inhibition of NF-κB activity by PDTC prevents blood pressure elevation (A), reverses the increased kidney/body weight ratio (B) and the reduced 24 hour urine volume (C). Systolic blood pressure (SBP) was measured by a noninvasive tail-cuff method at indicated time points after PDTC treatment (A). Relative kidney weight was calculated as a ratio of kidney wet weight to whole body weight after animals were sacrificed at indicated time-point (B). 24 hour urine volume was calculated by collecting urine for 24 hour by using metabolic cage at the indicated time-point (C). Data are presented as mean ± SD. n = 16 offspring for each group for (A, B, C).*P<0.05 or **P<0.01, Con+Ve vs LPS+Ve; #P<0.05 or ##P<0.01, LPS+PDTC vs LPS+Ve (A); * and ** indicate P<0.05 and P<0.01, respectively, which denote statistical comparison between the two marked treatment groups (B, C) (Two-way ANOVA followed by LSD test for inter-group comparison (A) or Dunnett T3 test (B and C) for inter-group comparison). Indications of Con+Ve, LPS+Ve, LPS+PDTC and Con+PDTC are as described in Fig 1. doi:10.1371/journal.pone.0153434.g002 Post-Natal NF-κB Activation and Prenatal LPS-Induced Renal Fibrogenesis in Offspring weight to whole body weight at the age of both 20 and 68 weeks, while post-natal PDTC treatment reversed this increment at the age of 68 weeks (Fig 2B, left panel). Since urine volume is one of the most direct indications of renal function, we also collected the urine by metabolic cage to assess the 24 hour urine volume. There were no significant changes in 24 hour urine volume among these groups at the age of 20 weeks. At the age of 68 weeks, the 24 hour urine volume was significantly reduced in offspring of prenatal exposure to LPS, whereas post-natal PDTC reversed it [ Fig 2C]. Though this decreased 24 hour urine volume did not meet the diagnosing criterion of oliguria [33], it may be an indication of impaired kidney function in offspring of prenatal exposure to LPS, whereas post-natal NF-κB inhibition showed a protective effect.
Prenatal LPS exposure induced offspring's renal gross morphology damages could be reversed by post-natal NF-κB inhibition HE staining of renal morphology at the age of 68 weeks showed an obvious increased infiltration of inflammatory cell, increased mesangial matrix fraction as well as the swelling of renal proximal tubules in the renal tissue of prenatal LPS-induced offspring when compared to that of control animals. This damage was prevented by post-natal PDTC administration (Fig 3A). PAS staining showed that offspring from prenatal LPS exposure presented with an increased mesangial matrix in glomeruli and also a few glomeruli undergoing sclerosis. This indicated increased glycoprotein accumulation in glomeruli. We also demonstrated that post-natal PDTC administration reversed this change [ Fig 3B]. Semi-quantitation of glomerular damage and tubulo-interstitial injury further supported our idea that post-natal NF-κB activation plays an important role in progressive renal damage [ Fig 3C and 3D].

Inhibition of NF-κB activation protects offspring of prenatal LPS exposure from renal fibrosis
Inflammation plays an important role in the progress of renal fibrosis [34]. As such we then explored the role of NF-κB activation in offspring's renal fibrosis. We first determined renal fibrosis by Sirius red staining and viewed the slices under both light microscope (Fig 4A, top panel) and polarized microscope (Fig 4A, bottom panel). Our results showed that prenatal LPS exposure led to increased Sirius red positive area, which was mainly type III collagen fibers in renal tissue of offspring at the age of 68 weeks, whereas post-natal NF-κB inhibition by PDTC reversed this damage [ Fig 4A and 4B]. Analysis of the mRNA expression of collagen 1 and collagen 3 at an earlier age of 20 weeks showed that renal collagen 1 and collagen 3 transcripts were significantly increased in offspring of prenatal exposure to LPS, whereas post-natal PDTC treatment repressed these increments [ Fig 4C].
α-SMA, predominantly existing in vasculature [35], is the actin isoform that plays an important role in fibrogenesis [36]. In health kidney, α-SMA is only expressed in the middle or adventitia layer of vasculature, while it occurs at the renal interstitial during renal fibrosis [37,38]. During the medical condition of glomerular nephritis, inflammatory cells in glomerular and renal interstitial can be activated, leading to an increase in actin synthesis (indicated by the expression of α-SMA). As such, inflammatory injuries can be aggravated leading to further fibrogenesis of the kidney [39,40]. To find more evidence of renal fibrosis in offspring of prenatal LPS exposure, we next determined the α-SMA expression in renal tissue by IHC. Our data showed that little cells in kidney expressed α-SMA in control offspring at the age of 68 weeks, whereas much higher level of α-SMA appeared at the interstitial in offspring of prenatal LPS exposure. As expected, post-natal PDTC administration obviously prevented the increased expression of α-SMA in the interstitial of renal tissue (Fig 5). All this data above Post-natal NF-κB inhibition reverses the morphological changes in offspring of prenatal LPS exposure. Renal gross morphology was determined by Hematoxylin-eosin (HE) staining (A) and periodic acid-Schiff (PAS) staining (B) at the age of 68 weeks. Semi-quantitation of renal glomerular damage index and tubulo-interstitial injury index were semi-quantitatively from HE staining (C) and of relative glomerular matrix glycoprotein accumulation from PAS staining (D) were shown. The black arrows indicate obvious damaged glomerulus (A) or glomerulus with obvious mesangial matrix accumulation (B). The white arrows indicate the swelling of renal proximal tubules. Data are presented as mean ± SD. n = 8 offspring in each group for (A) and (B). n = 8 offspring and at least 100 glomeruli were counted from each offspring for (C) and (D). * and ** indicate P<0.05 and P<0.01, respectively, which denote statistical comparison between the two marked treatment groups (Two-way ANOVA followed by Dunnett T3 test (C) or LSD test (D) for inter-group comparison). Indications of Con+Ve, LPS+Ve, LPS+PDTC and Con+PDTC are as described in Fig 1. suggests that post-natal NF-κB activation along with pro-inflammatory status has a critical role in the process of gradual interstitial renal fibrosis and post-natal NF-κB inhibition could be a potential therapeutic target for renal damage of prenatal inflammation stimulated offspring. . Relative mRNA expressions of collagen type1 (Col1a1) and collagen type 3 (Col3a1) (C) were determined by realtime RT-PCR in kidney at the age of 20 weeks. Data are presented as mean ± SD. n = 7 offspring and 4-5 pictures from each offspring were quantified for (B). n = 7 offspring in each group for (C). * and ** indicate P<0.05 and P<0.01, respectively, which denote statistical comparison between the two marked treatment groups (Two-way ANOVA followed by Dunnett T3 test (B) or LSD test (C) for inter-group comparison). Indications of Con+Ve, LPS+Ve, LPS+PDTC and Con+PDTC are as described in Fig 1. doi:10.1371/journal.pone.0153434.g004 Post-Natal NF-κB Activation and Prenatal LPS-Induced Renal Fibrogenesis in Offspring RAS over-activity could be reversed by post-natal NF-κB inhibition in offspring of prenatal LPS exposure Inflammation leads to over activation of RAS, while enhanced RAS activity positively aggravates inflammation response in local tissue through NF-κB signal pathway. This positive feedback cycle is critical in causing tissue damage [41]. In addition, the cross-talk among RAS,  Post-Natal NF-κB Activation and Prenatal LPS-Induced Renal Fibrogenesis in Offspring NF-κB and pro-inflammatory cytokines obviously exacerbates the progress of renal fibrosis [42]. So we next detected the role of post-natal NF-κB inhibition by PDTC on renal RAS activity of prenatal LPS exposed offspring. As expected, post-natal PDTC treatment restored the increased protein expression of renal Ang II and ACE in offspring of prenatal LPS exposure [Figs 6 and 7]. Unexpectedly, the mRNA expression of RAS family components showed the similar trend as the protein expressions without statistical significance [Fig 8]. This might due to the large variations of the samples or the limited sample size for each group.

Discussion
Inflammation plays a critical role in the process of progressive renal malfunction, fibrosis and chronic renal failure [43]. However, the exact mechanisms for initiation and development of persistent inflammation status are largely unknown. Our research laboratory previously found that prenatal inflammatory exposure led to higher level of pro-inflammatory cytokines in fetus, renal damage in newborns [44] and NF-κB activation in adult [11]. Our current study showed that intra-renal elevated levels of pro-inflammatory cytokines, such as TNF-α and IL-6, were found in offspring that were exposed to an inflammatory stimuli during the prenatal period. All these findings suggest that prenatal inflammatory exposure should be a momentous but also easily ignored etiology of chronic renal inflammation. As such, prevention of inflammation during earlier life may have a great significance on reducing the incidence of several kidney diseases related to chronic renal inflammation, such as renal malfunction and renal failure.
Previous studies have demonstrated that higher levels of inflammatory activity are positively correlated with renal fibrosis and renal hypo-function [45]. In this study, we show that prenatal inflammatory exposure led to obvious offspring's intra-renal damage, such as increased infiltration of inflammatory cell and mesangial matrix fraction, as well as accumulation of glycogen in both glomeruli and interstitial area. Post-natal NF-κB inhibition, through daily drinking water with PDTC, strikingly repressed the expression level of pro-inflammatory cytokines together with obvious protection of progressive kidney damage. As such, our results suggest that NF-κB-dependent persistent inflammatory activation might drive the progressive pathology of renal damage in offspring of prenatal inflammatory exposure. Previous findings showed that prenatal inflammatory exposure led to increased collagen I expression [13], which was significantly increased when renal fibrosis occurred. Our current study provides additional supportive in regard to our finding of intra-renal fibrosis as evident by increased expression of collagen III, α-SMA and collagen hyperplasia in kidney of prenatal LPS-induced offspring. All these changes related to renal fibrosis were reversed by post-natal NF-κB inhibition. Together with our previously finding that prenatal inflammatory exposure directly led to reduced total number of glomeruli during the developmental stage [11,13], our results suggest that prenatal inflammatory stimulus cause both direct micro-structural damage and proneness to activation of inflammatory response. In the adult, these two factors cross-talk with each other, which in turn aggravate and worsen the resultant renal damage.
Mechanistically, we found that the protective effects of NF-κB inhibition on renal fibrosis in offspring of prenatal LPS exposure might be attributed to repressed RAS over-activity. The RAS is described as a cascade of biochemical reactions, whose activity is essential for cardiovascular homeostasis [46]. Cross-talk of pro-inflammatory status and RAS over-activation plays a critical role in progressive renal fibrosis [47,48]. We previously found that prenatal LPS exposure led to decreased renal cortex renin and Ang II expression in offspring at 1 day of age, but significantly increased at 7, 16 and 25 weeks [11]. Our current finding showed that post-natal PDTC treatment significantly reduced the intra-renal expression level of ACE and Ang II in offspring exposed to prenatal inflammatory stimulus. All these findings suggests that the Higher level of Ang II positive cell in kidney in offspring of prenatal LPS exposure is reversed by post-natal NF-κB inhibition. The protein expression of Ang II in renal tissue of offspring at the age of 20 weeks was determined by immunohistochemistry staining. Representative picture from each group (A) and semi-quantitation of its positive area and density (B) are shown. Data are shown as mean ± SD. n = 7 offspring and 4-5 pictures from each offspring were quantified for (B). * and ** indicate P<0.05 and P<0.01, respectively, which denote statistical comparison between the two marked treatment groups (Two-way ANOVA followed by LSD test (B) for inter-group comparison). Indications of Con+Ve, LPS+Ve, LPS+PDTC and Con+PDTC are as described in Fig 1. doi:10.1371/journal.pone.0153434.g006 Post-Natal NF-κB Activation and Prenatal LPS-Induced Renal Fibrogenesis in Offspring cross-talk between RAS abnormality and NF-κB activation interact with each other thereby accelerating the progressive renal damage in offspring of prenatal exposure to LPS.
In summary, the activation of the offspring's intra-renal NF-κB activation caused by prenatal inflammatory exposure cross-talks with excessive RAS activation, exaggerates offspring's renal inflammation status, renal fibrosis and further damage of renal function. Thus, early life Post-natal NF-κB inhibition protects offspring of prenatal LPS exposure from ACE overexpression in kidney. The protein level of ACE in kidney of offspring at the age of 20 weeks was assessed by immunohistochemistry staining. Representative picture from each group (A) and semiquantitation of its positive area and density (B) are shown. Data are presented as mean ± SD. n = 7 offspring and 4-5 pictures from each offspring were quantified for (B). * and ** indicate P<0.05 and P<0.01, respectively, which denote statistical comparison between the two marked treatment groups (Twoway ANOVA followed by LSD test (B) for inter-group comparison). Indications of Con+Ve, LPS+Ve, LPS+PDTC and Con+PDTC are as described in Fig 1. doi:10.1371/journal.pone.0153434.g007  Post-Natal NF-κB Activation and Prenatal LPS-Induced Renal Fibrogenesis in Offspring prevention of excessive NF-κB activation may be a potential preventive strategy for chronic renal inflammation and progressive renal injury.
Supporting Information S1 Fig. Kaplan-Meier survival curve of offspring that received saline or prenatal LPS exposure together with post-natal PDTC treatment. Con+Ve group, offspring rats from maternal saline treatment together with post-natal saline treatment; LPS+Ve group, offspring rats from maternal LPS exposure together with post-natal saline treatment; LPS+PDTC group, offspring rats from maternal LPS exposure together with post-natal PDTC treatment; Con+PDTC group, offspring rats from maternal saline treatment together post-natal PDTC treatment.