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Deletion of IL-18 Expression Ameliorates Spontaneous Kidney Failure in MRLlpr Mice

  • Bastian Schirmer ,

    Contributed equally to this work with: Bastian Schirmer, Dirk Wedekind

    Affiliation Institute of Pharmacology, Hannover Medical School, Hannover, Germany

  • Dirk Wedekind ,

    Contributed equally to this work with: Bastian Schirmer, Dirk Wedekind

    Affiliation Institute of Laboratory Animal Science, Hannover Medical School, Hannover, Germany

  • Silke Glage,

    Affiliation Institute of Laboratory Animal Science, Hannover Medical School, Hannover, Germany

  • Detlef Neumann

    neumann.detlef@mh-hannover.de

    Affiliation Institute of Pharmacology, Hannover Medical School, Hannover, Germany

Deletion of IL-18 Expression Ameliorates Spontaneous Kidney Failure in MRLlpr Mice

  • Bastian Schirmer, 
  • Dirk Wedekind, 
  • Silke Glage, 
  • Detlef Neumann
PLOS
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Abstract

The role of IL-18 in the pathogenesis of systemic lupus erythematosus is still not definitively solved. In this study, we generated MRLlpr mice, which develop a disease resembling systemic lupus erythematosus, genetically devoid of IL-18 expression. These mice in comparison to IL-18-competent MRLlpr mice show reduced signs of renal pathogenesis, while other parameters such as mean survival time, lymphadenopathy, constitutive interferon-γ production, and frequency of CD3+B220+ abnormal T cells were without differences. We conclude that in the systemic lupus erythematosus syndrom IL-18 is involved specifically in the renal pathogenesis.

Introduction

The interleukin (IL)-1 family member IL-18, originally referred to as ‘interferon (IFN)-γ-inducing factor (IGIF)’, is a proinflammatory cytokine [1]. Major cellular targets of IL-18 are T helper (Th) 1 cells, natural killer (NK) cells, and CD8+ T cells, in which it increases proliferation, lytic activity and IFNγ production [24]. IL-18 by itself does not induce IFN-γ expression, but rather acts synergistically with e.g. IL-12, which induces expression of the IL-18 receptor [5, 6].

The participation of IL-18 in inflammatory diseases including autoimmunity has been demonstrated in several animal models and also in humans [79]. Of those, the predominant ones are type 1 diabetes, multiple sclerosis, rheumatoid arthritis, psoriasis, and possibly also systemic lupus erythematosus (SLE). SLE is characterized by hyper-gammaglobulinemia, autoantibody production and immune complex formation, eventually leading to end-organ damage, including vasculitis and fatal renal failure [10]. The disease is associated with genetic polymorphisms in the il18 gene in diverse populations [1113]. In plasma of SLE patients the concentration of IL-18 is enhanced and correlates with the disease activity [1416].

Homozygous MRL/Mp-Tnfrsf6lpr/lpr (MRLlpr) mice serve as model for human SLE [17]. Th-cells, characterized by the expression of CD4, centrally contribute to the pathogenesis of MRLlpr mice [18]. Of those, IL-17-expressing cells constitute a decisive effector population [19]; however, also Th1- and Th2-derived cytokines are apparently involved: IFN-γ, the prototypical Th1-cytokine, is detected at rather high concentrations in serum of MRLlpr mice and deletion of IFN-γ or IFN-γ receptor expression leads to reduced pathological signs [2023]. In accordance with these observations, administration of IFN-γ exacerbates the disease [24]. The contribution of IL-18 to the syndrome of MRLlpr mice is still discussed controversially. Lymph node cells or autoreactive T-cell lines obtained from MRLlpr mice are hyper-reactive to IL-18 stimulation due to a constitutive high expression of the IL-18 receptor [25]. Consequently, administration of IL-18 to MRLlpr mice worsened the disease [26] and MRLlpr mice vaccinated against IL-18 demonstrated reduced pathological signs [27, 28]. However, IL-18 administration by itself is unable to induce a lupus-like pathogenesis in MRL/Mp-Tnfrsf6+/+ mice [26].

Genetic deletion of the IL-18 receptor in MRLlpr mice has been described in two independent studies with contradictory conclusions [29, 30]. While the first one claimed the amelioration of the lupus-like disease due to the absence of the IL-18 receptor expression [30], the second one could not find any consequences of the deletion [29]. Moreover, there are indications, that the IL-18 receptor can be engaged not only by IL-18 itself, but also by another, yet unidentified ligand [31].

Thus, in the present study, we genetically deleted IL-18 expression in MRLlpr mice in order to specifically analyze the contribution of IL-18 to the lupus-like disease. We demonstrate that IL-18 is involved mainly in the autoimmune lupus nephritis.

Materials and Methods

Mice

Homozygous MRL/MpOlaHsd-Tnfrs6lpr/lpr mice and MRL/MpOlaHsd (MRL+/+) mice were purchased from Harlan/Winkelmann (Borchen, Germany) and housed and bred in the animal facility of the Hannover Medical School. IL-18 deficient MRLlpr mice were obtained by ten generations of backcrossing of the Il18tm/tmAki genotype from C57BL/6 mice (generously provided by S. Akira, Osaka, Japan [32]) onto the MRLlpr strain. Backcrossing was assisted by genetic diagnoses of the Il18 locus and SNPs (small nuclear polymorphism) analyses discriminating the C57Bl/6 and MRLlpr strains. Resulting strains were homozygous MRL/Mp-Tnfrs6lprIl18tm/tm (MRLlprIL18tm/tm) and heterozygous MRL/Mp-Tnfrs6lprIl18+/tm (MRLlprIL18+/tm). Mice were inspected daily and their health and constitution was ranked using a scoring system as detailed in table 1 (Table 1; [33]). Due to the autoimmune lupus-like disease, the mice acquired a moribund state rather quickly; however mice did not die unexpectedly or spontaneously since those which ranked score ≥4 were euthanized by CO2 inhalation followed by cervical dislocation. The age of mice when ranking score ≥4 are the bases for calculating their survival times. For all other analyses (except measurement of proteinuria), mice at pre-defined ages anaesthetized by CO2 inhalation and killed by exsanguination via cardiac puncture. Otherwise, analgesics and anaesthetics were not used in this study. Experimental procedures were performed according to the German Animal Welfare Act (Tierschutzgesetz, § 4) and approved by the Local Institutional Animal Care and Research Advisory Committee of the Hannover Medical School and the Lower Saxony State Office for Consumer Protection and Food Safety (Approval ID: 2012/8).

Serum preparation

The blood obtained by exsanguination was clotted for either one hour at room temperature or overnight at 4°C. Serum was separated by centrifugation at 10,000 g, 4°C for 20 min, aliquoted and stored at– 80°C until use.

Organ and cell preparation

Axillary and inguinal lymph nodes, spleens, and kidneys were removed and dissociated into single cell suspensions using the gentleMACS dissociator system (Miltenyi Biotech, Bergisch Gladbach, Germany).

Lymphadenopathy and splenomegaly

Lymphocyte proliferation in lymph nodes and spleen was assessed in parallel with two methods. Weights of lymph nodes and spleens were evaluated routinely to assess the macroscopic lymphadenopathy. In addition, nucleated cell counts were performed after organ dissociation.

Proteinuria

Urine protein levels were assessed semi-quantitatively using Combur Test strips (Boehringer-Mannheim, Mannheim, Germany). Small volumes (20 μl) of spontaneously voided urine were taken at weekly intervals.

Determination of renal damage

Renal tissue was either fixed in formalin and embedded in paraffin or was prepared for cryo-conservation. Sections were stained with hematoxylin and eosin (H&E), periodic acid-Schiff (PAS), or silver based reticulin. Kidney lesions were scored according to Table 2, analyzing at least 2 sections of each kidney and 55 +/- 5 glomeruli of each section.

Statistical analysis

Where appropriate, data are presented as individual values and the mean ± SD. Statistical significance was determined using Student’s t test or one- or two-way ANOVA with Bonferroni’s post-test. Proteinuria data were analyzed by Kruskal-Wallis test with Dunn’s post-test, whereas survival analysis was performed using Kaplan-Meier method and significance of differences in survival was determined using Mantle-Cox and Gehan-Breslow-Wilcoxon tests.

Results

In order to analyze a possible role of IL-18 in the pathogenesis of the lupus-like disease in MRL/Mp-Tnfrs6lpr (MRLlpr) mice, we intensively backcrossed the Il18tm/tmAki genotype from C57BL/6 mice onto the MRLlpr strain to obtain MRL/Mp-Tnfrs6lprIl18tm/tm (MRLlprIL18tm/tm) and MRL/Mp-Tnfrs6lprIl18+/tm (MRLlprIL18+/tm) mice. Differences in the mean survival time of MRLlpr mice due to the genetic deletion of IL-18 expression (MRLlpr: 163 days, MRLlprIL18+/tm: 125 days; MRLlprIL18tm/tm 150 days; Fig 1) were statistically not significant.

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Fig 1. Deletion of IL-18 expression does not affect survival.

MRLlpr mice displaying an IL-18 expression status as indicated were housed as described in the methods section. Individual ages (weeks) when they reached a health status ranking score ≥4 (table 1) were documented. Presented are pooled data from n = 23, 38, and 51 individuals of MRLlpr, MRLlprIl18+/tm, and MRLlprIl18tm/tm mice, respectively. The three data sets were analysed by Log-rank (Mantel-Cox) test and revealed no statistically significant differences.

https://doi.org/10.1371/journal.pone.0140173.g001

A major symptom occurring in MRLlpr mice is the eponymous lymphoproliferation, resulting in strongly enlarged secondary lymphoid organs. Analyses of spleen and lymph nodes weights and cell numbers revealed no statistically significant differences between MRLlpr and MRLlprIL18tm/tm mice (data not shown).

IL-18, which promotes IFN-γ production [5] is constitutively expressed in e.g. macrophages and dendritic cells. Thus, we measured constitutive IFN-γ concentrations in sera, but, again, could not detect statistically significant differences depending on the IL-18 genotype (Fig 2). Differences were also absent when comparing age-matched subgroups of mice (not shown).

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Fig 2. Deletion of IL-18 expression does not affect constitutive IFNγ production.

Mice, aged between 11 and 35 weeks, were bled and IFNγ concentrations in sera were measured by ELISA. Presented are data from n = 15, 10, and 8 individuals of MRLlpr, MRLlprIl18+/tm, and MRLlprIl18tm/tm mice, respectively, and the respective means +/- SD. The three data sets were analysed by ANOVA with Bonferroni’s post test and revealed no statistically significant differences.

https://doi.org/10.1371/journal.pone.0140173.g002

The lupus-like disease in MRLlpr mice is paralleled by the persistence of CD3+B220+CD4-CD8- cells, identified by the co-expression of CD3 and B220 and referred to as the DN T-cell population [34]. DN T-cells are numerously present in peripheral blood of MRLlpr mice, however, in MRLlprIL18tm/tm mice their number is not statistically significantly different (Fig 3A). Also the other leukocyte subsets identified by the markers CD3, B220, CD4, and CD8 demonstrated no quantitative differences in peripheral blood between the mouse strains (data not shown).

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Fig 3. Flow cytometric analyses of T-cells.

(A) MRLlpr, MRLlprIl18+/tm, and MRLlprIl18tm/tm mice were bled and frequencies of blood cells were analysed using antibodies recognizing CD3 and B220. Presented are individual data from 3–23 evaluations and the respective means +/- SD. The three data sets were analysed by ANOVA with Bonferroni’s post test and revealed no statistically significant differences. (B) Single cell suspensions were prepared from kidneys of 19–29 week old MRLlpr and MRLlprIl18tm/tm mice, and frequencies of CD3++, CD4+, and CD8+ cells within the CD45+ population were determined. Presented are data of individual evaluations and the respective means +/- SD. The data sets (n = 9 and 13, respectively) were analysed by Student’s T-test and revealed no statistically significant differences.

https://doi.org/10.1371/journal.pone.0140173.g003

The kidney is one of the mainly affected organs in the lupus-like disease of MRLlpr mice [17]. Single cell suspensions prepared from kidneys of MRLlpr and MRLlprIL18tm/tm mice consisted of about 10% CD45+ leukocytes. Within these, DN T-cells were absent, while the subsets identified by Ly-6G/C, CD11b, and F4/80 were readily detectable, however, without statistically significant quantitative differences between MRLlpr+ and MRLlprIL18tm/tm mice (not shown). In contrast, CD3+B220- T-cells, both CD4+ and CD8+, were less frequent in the kidney cell suspensions of MRLlprIL18tm/tm mice as compared to that of MRLlpr mice (Fig 3B).

Since we found CD3+ T-cells less frequently in the kidneys of MRLlpr mice due to the absence of IL-18, we analyzed urine protein concentration as a measure for functional kidney integrity in MRLlpr, MRLlprIL18+/tm, and MRLlprIL18tm/tm mice. As a further control, in this experiment we also included wild type MRL (MRL+/+) mice, lacking the disease accelerating lpr mutation. While in MRL+/+ mice the progression of proteinuria was rather slow, it was significantly faster in MRLlpr mice (Fig 4). In heterozygous mice (MRLlprIL18+/tm) protein concentrations in urine increased as fast as in MRLlpr mice. In MRLlprIL18tm/tm mice, in contrast, the kinetics of proteinuria development were significantly slower, virtually resembling that observed in MRL+/+ mice (Fig 4).

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Fig 4. Deletion of IL-18 expression reduces proteinuria.

Protein concentrations in spontaneously voided urine from MRLlpr, MRLlprIl18+/tm, MRLlprIl18tm/tm, and MRL+/+ mice were measured in weekly intervals. Within each strain, mice were grouped according to their age on a weekly base. Each symbol represents the mean of at least two individual evaluations, performed using a total of 13–39 individuals per strain. Lines show the linear regressions of the data of each strain. Statistical differences between the transformed data of each strain were analysed by ANOVA Kruskal Wallis test with Dunn’s post test (ns, not significant; *, p < 0.05; **, p < 0.01; ***, p < 0.005).

https://doi.org/10.1371/journal.pone.0140173.g004

Next, we evaluated the kidneys histologically, both by light (Fig 5A) and by electron microscopy (data not shown). Kidney sections obtained from young (< 20 weeks) and old (> 20 weeks) MRLlpr, MRLlprIL18+/tm, and MRLlprIL18tm/tm mice (chosen independently of their health status) were analyzed for several aspects as detailed in the materials and methods section. Of these, sclerotic changes of the mesangium, protein casts in distal tubuli, and lobular accentuation of glomerulopathy increased age-dependently in MRLlpr and MRLlprIL18+/tm mice (Fig 5B). Importantly, while sclerotic changes of the mesangium and protein casts in distal tubuli increased age-dependently also in MRLlprIL18tm/tm mice, the lobular accentuation of glomerulopathy was significantly reduced in old MRLlprIL18tm/tm as compared to old MRLlpr mice (Fig 5B).

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Fig 5. Histological analyses of kidney sections.

Kidneys of MRLlpr, MRLlprIl18+/tm, and MRLlprIl18tm/tm mice were removed, processed, and histologically analysed. (A) Presented are representative pictures of PAS-stained kidney sections obtained from MRLlpr (+/+), MRLlprIl18+/tm, (+/tm), and MRLlprIl18tm/tm (tm/tm) mice. (B) Quantitative evaluations of the sections were performed using the scoring system as detailed in Table 2. Presented are individual data for three evaluated parameters from 5–11 mice per strain and the respective means +/- SD. Differences between the three strains were analysed by ANOVA with Bonferroni’s post test (*, p < 0.05; no indication: no significance).

https://doi.org/10.1371/journal.pone.0140173.g005

Discussion

Several studies point to a contribution of IL-18 to symptoms associated with human lupus and the lupus-like disease in mouse models [7, 3538]. In the MRLlpr mouse model resembling human SLE such evidence based on a genomic approach is discussed very controversially [29, 30]. These studies, in order to eliminate IL-18 bioactivity, deleted the IL-18 receptor, but more recently it has also been reported that the IL-18 receptor is necessary not only for IL-18 bioactivity but also for a yet not identified ligand [31], probably similar to the human IL-18 receptor ligand IL-37 [39]. Thus, in order to specifically analyze the function of IL-18 in murine SLE, in the present study, we deleted the gene encoding IL-18 in MRLlpr mice and compared pathological and immunological manifestations with those of IL-18-competent MRLlpr mice.

In MRLlpr mice serum concentrations of IFN-γ are enhanced in comparison to not autoimmune-prone mouse strains and IFN signaling is essential for lupus development [2023]. Blockade of IFN-γ signaling by deleting expression of the cytokine itself or its receptor results in reduced double-stranded DNA-directed autoantibody production and prolonged survival. Interestingly, lymphadenopathy and the number of DN T-cells are reduced in MRLlpr only due to IFN-γ-deficiency, while it is unaffected by the lack of the IFN-γ receptor. IL-18 promotes IFN-γ expression in T-cells and NK cells [1], however, since IL-18-deficiency in MRLlpr mice does not reduce IFN-γ concentration in blood, the constitutively enhanced production of IFN-γ is not a consequence of IL-18 function [25]. Probably due to the unaffected IFN-γ concentration, IL-18 deficiency in MRLlpr mice affects neither survival nor the accumulation of DN T-cells accompanied by lymphadenopathy and splenomegaly. These data are in contrast to our previous ones obtained by a cDNA vaccination technique [27], probably reflecting that vaccination of MRLlpr mice with an IL18-encoding plasmid not only led to the reduction of IL-18 bioactivity but also to additional beneficial effects, e.g. TLR9 activation [40, 41], leading to an amelioration of clinical parameters.

Thus, the effect of IL-18 in MRLlpr mice seems to be restricted to the kidney inflammation and probably other organs as well, which we have not analyzed in this study. Such a specific function for IL-18 in autoimmune lupus nephritis as well as in other kidney diseases already has been proposed previously [39, 4244]. Interestingly, deletion of IL-18 expression in MRLlpr mice selectively reduced the intra-renal frequency of T-cells, both CD4+ and CD8+, while other leukocyte populations, such as granulocytes, monocytes, and macrophages were unaffected. This is in contrast to data provided by an ‘intra-renal IL-18 overexpression’ model [43], and may reflect an IL-18 concentration exceeding the physiologic range in the latter study.

Using a flow cytometric approach, we could not detect infiltrating DN T-cells, identified by the co-expression of CD3 and B220, in the kidneys of MRLlpr mice, aged up to 4 months, while in cell suspensions obtained from spleens they were readily detectable (not shown). This result is in direct contradiction to the histological observation of CD3+IL-17+ cells in the kidneys of 5 months old MRLlpr mice, which are claimed to be of the DN T-cell population [19]. Unfortunately, in the latter publication the CD4-CD8- phenotype of the kidney infiltrating CD3+IL-17+ cells was not documented, but deduced from analyses using peripheral CD3+IL-17+ cells.

Surprisingly, the fast worsening general health status, quantified as ‘survival’, is unaffected by deletion of IL-18 expression, although specific parameters of nephritis are ameliorated. This may be due to the fact that only a few specific kidney pathological parameters were reduced due to IL-18 deletion, while others and also the gross inflammatory pathology remained unaffected.

In summary, using a genetic approach, we provide evidence that IL-18 plays a minor role in the autoimmune disease in MRLlpr mice, essentially confirming the data observed in IL-18-deficient lupus-prone C57Bl/6 mice [45]. In our model, IL-18 does not affect the lupus-like pathogenesis generally, but specifically some parameters of affected end-organs, i.e. the kidneys.

Acknowledgments

We are also grateful for intriguing and stimulating discussions with Drs. Klaus Resch and Roland Seifert. The excellent technical help of Anna Bauer and Marzena Wyschkon is highly acknowledged.

Author Contributions

Conceived and designed the experiments: BS DW SG DN. Performed the experiments: BS DW SG. Analyzed the data: BS DW SG DN. Contributed reagents/materials/analysis tools: DW SG DN. Wrote the paper: DW DN.

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