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Physiological and molecular effects of interleukin-18 administration on the mouse kidney

  • Kyosuke Yamanishi1,
  • Keiichiro Mukai1,
  • Takuya Hashimoto1,
  • Kaoru Ikubo1,
  • Keiji Nakasho2,
  • Yosif El-Darawish3,
  • Wen Li3,
  • Daisuke Okuzaki4, 5,
  • Yuko Watanabe6,
  • Tetsu Hayakawa3,
  • Hiroshi Nojima4, 5,
  • Hiromichi Yamanishi6,
  • Haruki Okamura3 and
  • Hisato Matsunaga1Email author
Journal of Translational Medicine201816:51

https://doi.org/10.1186/s12967-018-1426-6

Received: 6 February 2017

Accepted: 27 February 2018

Published: 7 March 2018

Abstract

Background

The cytokine interleukin-18 was originally identified as an interferon-γ-inducing proinflammatory factor; however, there is increasing evidence to suggest that it has non-immunological effects on physiological functions. We previously investigated the potential pathophysiological relationship between interleukin-18 and dyslipidemia, non-alcoholic fatty liver disease, and non-alcoholic steatohepatitis, and suggested interleukin-18 as a possible novel treatment for not only these diseases but also for cancer immunotherapy. Before clinical application, the effects of interleukin-18 on the kidney need to be determined. In the current study, we examined the kidney of interleukin-18 knockout (Il18−/−) mice and the effects of interleukin-18 on the kidney following intravenous administration of recombinant interleukin-18.

Methods

Il18−/− male mice were generated on the C57Bl/6 background and littermate C57Bl/6 Il18+/+ male mice were used as controls. To assess kidney damage, serum creatinine and blood urea nitrogen levels were measured and histopathological analysis was performed. For molecular analysis, microarray and quantitative reverse transcription PCR was performed using mice 6 and 12 weeks old. To evaluate the short- and long-term effects of interleukin-18 on the kidney, recombinant interleukin-18 was administered for 2 and 12 weeks, respectively.

Results

Compared with Il18+/+ mice, Il18/ mice developed kidney failure in their youth-6 weeks of age, but the condition was observed to improve as the mice aged, even though dyslipidemia, arteriosclerosis, and higher insulin resistance occurred. Analyses of potential molecular mechanisms involved in the onset of early kidney failure in Il18−/− mice identified a number of associated genes, such as Itgam, Nov, and Ppard. Intravenous administration of recombinant interleukin-18 over both the short and long term showed no effects on the kidney despite significant improvement in metabolic diseases.

Conclusions

Short- and long-term administration of interleukin-18 appeared to have no adverse effects on the kidney in these mice, suggesting that administration may be a safe and novel treatment for metabolic diseases and cancer.

Keywords

Interleukin-18Interleukin-18 knockoutKidneyClinical translationKidney injuryMicroarrayQuantitative reverse transcription polymerase chain reaction

Background

The cytokine interleukin-18 (IL-18) was originally identified as an interferon-γ-inducing proinflammatory factor; however, there is increasing evidence to support its non-immunological effects on physiological functions [13]. IL-18 is produced as an inactive 24-kDa precursor and is processed by inflammasomes to an active 18-kDa mature form [47]. Previous studies have reported that mice deficient in IL-18 developed hyperphagia, obesity, and insulin resistance [8]. IL-18-knockout (Il18−/−) mice also showed dyslipidemia, non-alcoholic fatty liver disease (NAFLD), or non-alcoholic steatohepatitis (NASH) [3]. In human studies, the serum concentration of IL-18 was found to be significantly higher in patients with metabolic syndrome, type 2 diabetes mellitus, or diabetic nephropathy compared with healthy control participants [911].

The development of structural and functional changes in the kidney in patients with diabetes mellitus has been known for more than 20 years [12]. Diabetic nephropathy is considered the most frequent cause of end-stage renal failure in the United States [13]. A previous study found that Il18−/− mice showed severe insulin resistance resulting in diabetes mellitus [8]; however, specific renal complications remain uncertain.

We previously reported on a novel cancer immunotherapy with IL-18 [14]. Intravenous administration of recombinant IL-18 (rIL-18) for Il18−/− mice significantly improved dyslipidemia and prevented the onset of NASH. IL-18 may therefore be a promising factor that will contribute to novel treatment options for NAFLD or NASH mainly through correction of energy unbalances by lipids or glucose in the liver [3]. It is important that before clinical application, possible side effects of rIL-18 on the kidney are examined.

This study investigated whether Il18−/− mice develop kidney failure as they age and whether IL-18 has beneficial or damaging effects on the kidney. We analyzed the role of IL-18 in the kidney by histopathological observation and by measuring serum concentrations of several markers in Il18−/− mice during growth. The molecular mechanisms affected during growth were analyzed and the influence of short- and long-term administration of rIL-18 was assessed.

Methods

Animals

Il18−/− male mice were generated on the C57Bl/6 background as previously described [15]. Littermate C57Bl/6 Il18+/+ male mice were used as controls. Mice were housed in groups of 3–5 in polycarbonate cages in a colony room that was maintained at a constant temperature (22 ± 1 °C) and humidity (50–60%) on a 12-h light/dark cycle (lights on at 8 a.m.) with free access to standard food (MF; Oriental Yeast Co., Ltd., Tokyo, Japan) and water. Mice were killed at 10 a.m. were used and Samples from Il18+/+ and Il18−/− mice were taken for molecular, biochemical, and histological analyses at the same time points (n = 4–11). Additionally, five to six and three mice per group were included in the short- and long-term rIL-18 treatment groups, respectively. Details of the rIL-18 treatment are given in “Short- and long-term treatment of mice with rIL-18” section.

Animal experiments were conducted according to the “Guide for Care and Use of Laboratory Animals” published by the National Institutes of Health and approved by the Animal Care Committee of Hyogo College of Medicine (#28041 and #14-020).

Histological analysis

Three to four mice per group were used for histopathological analysis. Mice were anesthetized with isoflurane and perfused in a transcardial manner with periodate–lysine-paraformaldehyde fixative at 10 a.m. Fixed kidneys were removed and immersed in the same fixative at 4 °C overnight. Specimens were processed for histological staining. Paraffin-embedded sections were used for hematoxylin–eosin, periodic acid–Schiff, azan, and periodic acid methenamine silver staining (all Muto Pure Chemicals Co., Ltd., Tokyo, Japan). Staining was performed according to the manufacturer’s instructions detection was achieved using the VECTASTAIN ABC Standard Kit (PK-4000; Vector Laboratories, INC., Burlingame, CA, USA) according to the manufacturer’s instructions. Paraffin-embedded sections were also stained with primary antibodies against F4/80 [product T-2008 (lot 20PO0309); dianova GmbH, Hamburg, Germany] and CD4 (553043; BD Biosciences, Tokyo, Japan). The antigen retrieval methods of F4/80 and CD4 were 4 µg/ml proteinase K (Nacalai Tesque, Inc., Kyoto, Japan) treatment at room temperature for 10 min and 0.01 M citrate buffer pH 6.0 for 10 min at 100 °C respectively referring to manufacturer’s instructions. Antibodies were diluted 1:200 and 1:125, respectively, and 5 µg/ml was used for an overnight incubation at 4 °C according to the manufacturer’s instructions, followed by incubation with 1.5 µg/ml rabbit anti-rat secondary antibody (BA-4000; Vector Laboratories, Inc.) diluted 1:1000. Stained tissues were mounted and pathological diagnosis was determined in a blind fashion by pathological specialists. Tissues were photographed using an optical microscope and CCD camera (AX-80 and DP-71; Olympus, Tokyo, Japan).

Serum analysis

Levels of creatinine (CREA) and blood urea nitrogen (BUN) in sera were measured using enzymatic methods. Serum analysis was performed by LSI Medience Corp., Tokyo, Japan.

Molecular analysis

The protocols for sample collection, mRNA purification, microarray, Ingenuity® Pathway Analysis (IPA; Ingenuity® Systems; http://www.ingenuity.com), and quantitative reverse transcription polymerase chain reaction (RT-qPCR) have been described previously [3, 16]. Mice were euthanized by decapitation at 10 a.m. and the kidneys were removed and immediately placed in liquid nitrogen and stored at − 80 °C until use.

Total RNA was purified from 12 samples using a miRNeasy mini kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions, and treated with five units of RNase free DNase I at 37 °C for 30 min to remove genomic DNA contamination. After phenol/chloroform extraction and ethanol precipitation, total RNA was dissolved in de-ionized distilled water. RNA concentrations were determined by NanoDrop-1000 spectrophotometry (NanoDrop Technologies, Wilmington, DE, USA).

For microarray analysis, expression profiling was performed using a SurePrint G3 Mouse GE 8x60K Microarray G4852A (Agilent Technologies, Inc., Santa Clara, CA, USA). Twelve microarrays (three for Il18+/+ mice and three for Il18−/− mice at both 6 and 12 weeks of age) for one color experiment were performed as biological triplicates. Each gene expression profile was compared between Il18+/+ and Il18−/− mice at 6 and 12 weeks of age. Total RNA (200 ng) was reverse-transcribed into double-stranded cDNA using AffinityScript multiple temperature reverse transcriptase (Agilent Technologies, Inc.) and amplified. The resulting cDNA was used for in vitro transcription by T7-polymerase and labeled with cyanine-3-labeled cytosine triphosphate (Perkin Elmer, Wellesley, MA, USA) using a Low Input Quick-Amp Labeling Kit (Agilent Technologies, Inc.). After labeled cDNA had been fragmented, each cRNA sample was hybridized on a SurePrint G3 Mouse GE 8x60K Microarray (#028005; Agilent Technologies, Inc.). After washing, slides were scanned with a microarray scanner (G2505C; Agilent Technologies, Inc.). Feature extraction software (ver. 10.5.1.1) was used to convert images into gene expression data. For microarray data analysis, raw data were imported into the Subio platform (ver. 1.18; Subio Inc., Kagoshima, Japan), and raw intensity data were normalized to the 75th‰ intensity of probes above background levels (gIsWellAbove = 1). Kidney genes in Il18+/+ and Il18−/− mice were defined to show signal ratios with a greater than twofold increase or a less than 0.5-fold decrease. Details of microarray analysis and results can be found in Gene Expression Omnibus (Accession No. GSE64310).

IPA software was used for microarray analyses to provide functionality for the interpretation of gene expression data. To investigate molecular mechanism on the kidney by IL-18, core analysis was performed with the setting for “Tissues” being only “Kidney”. This software for molecular analysis was based on that described in previous studies [17, 18].

For RT-qPCR, kidney samples at 6 and 12 weeks of age were obtained from the same mice used for microarray analyses. Total RNA (10 ng/reaction) was used in the RNA-direct SYBR Green Real-Time PCR Master Mix (One-step qPCR Kit; Toyobo Co., Ltd., Tokyo, Japan). Samples were put in duplicate reactions in 384-well plates and run on a QuantStudio 12K Flex PCR system (Thermo Fisher Scientific, Waltham, MA, USA). Median threshold cycle values were used to calculate the fold change between samples from two groups. Fold change values were normalized to glyceraldehyde-3-phosphate dehydrogenase (Gapdh). The following temperature profile was used: 30 s at 90 °C and 20 min at 61 °C for reverse transcription, according to the manufacturer’s instructions, followed by 45 cycles at 98 °C for 1 s, 67 °C for 15 s, and 74 °C for 35 s. The primer sequences for RT-qPCR are shown in Additional file 1.

Short- and long-term treatment of mice with rIL-18

To determine treatment responses to IL-18, mice were administered 2 µg/mouse rIL-18 dissolved in saline containing heat-inactivated normal mouse serum (0.5%). Mice were injected twice a week via the caudal vein for 2 weeks (short-term study) from 10 weeks of age, and for 12 weeks (long-term study) from 37 weeks of age, as previously reported [3]. For control experiments, saline was injected by the same procedure. Five to six and three mice per group were included in the short- and long-term treatment groups, respectively.

Statistical analysis

All statistical analysis was performed as previously described [3, 8]. Sigmaplot™ (ver. 11.0; Systat Software, Inc., San Jose, CA, USA) was used for statistical analyses. RT-qPCR was analyzed using the Student’s t test after the equal variances test or Mann–Whitney U-test were performed as appropriate. Equal variances results are expressed as mean ± SD, and Mann–Whitney results as medians and ranges. Serum measurements and effects of rIL-18 administration was analyzed by two-way analysis of variance. A p-value < 0.05 was considered statistically significant. All analyses were performed at least in duplicate to confirm the results.

Results

Histopathological and serum observations of the kidney

Histopathological changes were observed in Il18−/− mice at 6 weeks of age, especially around glomeruli (Fig. 1a–c, Additional file 2). Enucleated epithelial cells of the Bowman’s capsule and collapse of glomerular capillaries were observed at 6 weeks of age in Il18−/− mice, and serum levels of CREA and BUN in Il18−/− mice increased compared with Il18+/+ mice at 6 and 12 weeks of age. As mice aged, there were no comparable differences (Fig. 1d, e). Moreover, in the interstitium there were also no remarkable findings such as macrophage or T cell infiltration, as shown by F4/80 and CD4 staining at 6, 12, and 24 weeks of age (Additional files 2, 3). Il18−/− mice at 6 weeks old showed renal impairment but there was no evidence of kidney injury at 48 weeks old between groups.
Figure 1
Fig. 1

Il18−/− mice showed renal impairment in youth but no injury was observed at 48 weeks. a Hematoxylin–eosin, b periodic acid–Schiff, and c periodic acid methenamine silver staining were performed at 6, 12, and 48 weeks of age. Arrows in ac at 6 weeks old indicate enucleated epithelial cells of the Bowman’s capsule and the collapse of glomerular capillaries. Scale bars represent 50 μm (ac). To assess the degree of damage to the kidney, serum BUN (d) and CREA (e) were measured (n = 6–8 mice per group). Data are mean ± SD. *p < 0.05, **p < 0.01. BUN: blood urea nitrogen; CREA: creatinine

Microarray and IPA

To identify the genes responsible for kidney failure (including dyslipidemia and diabetes mellitus but not renal function degeneration) in mice at 6 and 12 weeks old, gene expression profiles in Il18−/− mice were compared with control mice at 6 and 12 weeks old. For Il18/ mice, 158 genes at 6 weeks and 142 genes at 12 weeks showed a greater than twofold increase or a less than 0.5-fold decrease, respectively (p < 0.05 for both age groups). Among these genes, eight and four molecules at 6 and 12 weeks old, respectively, involved in kidney function were identified from core analysis using IPA. These were paired box gene 2 (Pax2), interleukin 18 (Il18), integrin alpha M (Itgam), peroxisome proliferator activator receptor delta (Ppard), lecithin-retinol acyltransferase (Lrat), mitogen-activated protein kinase 8 (Mapk8), stabilin 2 (Stab 2), and nephroblastoma overexpressed gene (Nov) at 6 weeks old and Il18, C-X-C motif chemokine 10 (Cxcl10), Notch homolog 1 (Notch1), and cytochrome P450, family 4, subfamily a, polypeptide 14 (Cyp4a14) at 12 weeks old (Tables 1, 2, Additional file 1).
Table 1

Core analysis of the kidney in 6-week-old mice

Diseases or functions annotation

p-value

Molecules

Delayed hypersensitive reaction of renal glomerulus

4.92E−03

Il18

Injury of kidney

3.50E−02

Il18, Ppard

Injury of endothelial cells

4.92E−03

Itgam

Thrombosis of blood

4.92E−03

Itgam

Recruitment of neutrophils

9.83E−03

Itgam

Accumulation of neutrophils

1.96E−02

Itgam

Generation of reactive oxygen species

2.92E−02

Itgam

Concentration of retinol

9.83E−03

Lrat

Hypertrophy of renal glomerulus

1.27E−02

Mapk8, Stab 2

Congestion of vasculature

1.96E−02

Nov

Aggregation of mesenchymal cells

4.92E−03

Pax2

Abnormal morphology of renal calyx

9.83E−03

Pax2

Development of renal calyx

9.83E−03

Pax2

Organogenesis of kidney

9.83E−03

Pax2

Size of renal medulla

9.83E−03

Pax2

Hypoplasia of renal cortex

1.47E−02

Pax2

Development of epithelial cells

1.96E−02

Pax2

Injury of outer medulla

4.92E−03

Ppard

Injury of renal cortex

9.83E−03

Ppard

Fibrosis of renal glomerulus

3.87E−02

Stab 2

Table 2

Core analysis of the kidney in 12-week-old mice

Diseases or functions annotation

p-value

Molecules

Mitogenesis of mesangial cells

1.47E−02

Cxcl10

Synthesis of DNA

3.87E−02

Cxcl10

Migration of mesangial cells

4.35E−02

Cxcl10

Renal vascular resistance

1.96E−02

Cyp4a14

Flow of blood

4.82E−02

Cyp4a14

Delayed hypersensitive reaction of renal glomerulus

4.92E−03

Il18

Transformation of kidney cells

1.47E−02

Notch1

Gene expression comparison between groups by RT-qPCR

To confirm mRNA expression by microarray, RT-qPCR was performed. At 6 weeks old, expression of Itgam, Nov, and Stab 2 in Il18−/− mice significantly increased compared with Il18+/+ mice (Table 3). Expression of Il18, Lrat, and Ppard significantly decreased in Il18−/− mice compared with Il18+/+ mice (Table 3). At 12 weeks old, expression of Cxcl10, Cyp4a14, and Il18 was lower in Il18−/− mice compared with Il18+/+ mice (Table 4).
Table 3

Comparison of molecular expression between microarray and RT-qPCR analysis in 6-week-old mice

Gene

Microarray

RT-qPCR

Il18

0.280 ± 0.11

0.154 ± 0.024*

Itgam

3.02 ± 0.15

1.77 ± 0.39*

Lrat

0.478 ± 0.12

0.416 ± 0.068*

Mapk8

0.370 ± 0.28

0.991 ± 0.19

Nov

2.60 ± 0.31

1.643 ± 0.10*

Pax2

2.13 ± 0.28

1.17 ± 0.35

Ppard

0.426 ± 0.10

0.572 ± 0.099*

Stab 2

2.08 ± 0.21

1.39 ± 0.067*

Comparison between microarray and RT-qPCR analysis at 6 weeks old is shown as a ratio (Il18−/−/Il18+/+). Data are mean ± SD. * p < 0.05 (n = 3 per group)

Table 4

Comparison of molecular expression between microarray and RT-qPCR analysis in 12-week-old mice

Gene

Microarray

RT-qPCR

Cxcl10

0.495 ± 0.50

0.573 ± 0.036*

Cyp4a14

0.461 ± 0.10

0.386 ± 0.16*

Il18

0.241 ± 0.11

0.129 ± 0.069*

Notch1

0.481 ± 0.10

0.740 ± 0.28

Comparison of molecular expression between microarray and RT-qPCR analysis at 12 weeks old is shown as a ratio (Il18−/−/Il18+/+). Data are mean ± SD.* p < 0.05 (n = 3 per group)

At 6 weeks old, Itgam, Il18, Lrat, Nov, and Ppard appeared to be expressed differently with microarray analysis, which might be related to kidney function. At 12 weeks old, Cxcl10, Cyp4a14, and Il18 showed similar tendencies in terms of differences between the groups.

To validate the correlation between microarray and RT-qPCR analysis, Spearman’s rank correlation coefficient analysis was performed for each group (6-week-old group: p = 0.0038, rs = 0.881; 12-week-old group: p = 0.0016, rs = 0.827).

Effect of short-term rIL-18 treatment on kidney function

To verify the effects of IL-18 on the kidney, especially any potential side effects, Il18+/+ and Il18−/− mice were treated with rIL-18. Serum BUN and CREA were not affected by rIL-18 administration (Fig. 2a, b). No histological changes in glomeruli were observed between groups (Fig. 2c–e). Short-term treatment with rIL-18 appeared to have no influence on the kidney, including any side effects.
Figure 2
Fig. 2

No side effects were observed with rIL-18 administration for 2 weeks. To analyze the effects on renal function, mice were injected with rIL-18 twice a week for 2 weeks from 10 weeks of age (short-term treatment). Serum levels of BUN (a) and CREA (b) are shown. Data are mean ± SD (a, b: n = 8 per group). c Hematoxylin–eosin, d periodic acid–Schiff, and e periodic acid methenamine silver staining. Scale bars represent 50 μm (ce). BUN: blood urea nitrogen; CREA: creatinine

Effect of long-term rIL-18 treatment on the kidney in Il18 −/− mice

To determine the efficacy of rIL-18 in Il18−/− mice, we administered rIL-18 to Il18−/− mice twice a week for 12 weeks from 37 weeks old and found that the kidneys of Il18−/− mice did not show any differential changes (Fig. 3a–d).
Figure 3
Fig. 3

Effects of long-term treatment with rIL-18 on the kidney. Histopathological analysis was conducted to assess renal damage with rIL-18 exposure for 12 weeks. a Hematoxylin–eosin, b periodic acid–Schiff, c periodic acid methenamine silver, and d azan staining. Scale bars represent 50 μm (ad)

Discussion

In the current study, we found that: (1) Il18−/− mice showed renal impairment in their youth-6 weeks of age, but improved naturally as they aged; (2) even though no renal damage was observed at 48 weeks of age, Il18−/− mice showed diabetes mellitus, dyslipidemia, and arteriosclerosis; (3) several molecules related to renal function were affected by a lack of IL-18; and (4) the administration of IL-18 exerted few effects on the kidney regardless of short or long-term administration.

IL-18 is associated with the pathogenesis of a number of renal disorders, such as autoimmune diseases [19, 20]. In humans, IL-18 in the urine is one of the early markers of renal tubular disease [21]. IL-18 deficiency protects against renal fibrosis by aldosterone-salt treatment [22]. In human mesangial cells, inhibition of 5-lipoxygenase and cyclooxygenase, which play important roles in the pathogenesis of glomerulonephritis in childhood, resulted in IL-18-induced proinflammatory cytokine release and cellular proliferation of these cells [2332]. It is possible that IL-18 has a substantial impact on the kidney, including renal tubules, glomeruli, and mesangial cells.

No remarkable changes were observed in renal tubules during initial growth in the current study. In youth, however, enucleated epithelial cells of the Bowman’s capsule and collapse of glomerular capillaries were detected despite a deficiency of IL-18 (Fig. 1a–c). Serum BUN levels in Il18−/− mice increased significantly compared with Il18+/+ mice. These results suggest that a deficiency in IL-18 led to temporary kidney damage during youth, however this damage might improve naturally over time.

Il18−/− mice show dyslipidemia at 6 weeks old, develop diabetes mellitus, and show high glucose and insulin levels and arteriosclerosis at 6 months old, and NAFLD or NASH at 48 weeks old [3, 8]. Structural and functional changes in the kidney develop with diabetes mellitus [12]. In the current study, at over 6 months old, no remarkable changes to the kidney were observed (Fig. 1a–e). Down-regulation of IL-18 expression can protect renal function and prevent the development of diabetic nephropathy [33]. It is suggested that IL-18 deficiency can result in an energy unbalance, such as some sort of metabolic disorder, despite preserving renal function.

With regard to possible molecular mechanisms, eight and four genes at 6 and 12 weeks old, respectively, were identified by core analysis using IPA (Tables 1, 2). Expression of Il18, Itgam, Lrat, Nov, Ppard, and Stab 2 were significantly different between Il18+/+ and Il18−/− mice at 6 weeks old using RT-qPCR (Table 3). Similar to that observed in 6-week-old mice, 12-week-old mice showed significantly different expression of Cxcl10, Cyp4a14, and Il18 between groups (Table 4).

At 6 weeks of age, renal impairment was observed in Il18−/− mice. As reported previously, inhibition of IL-18 protects renal function, such as prevention of the development of diabetic nephropathy [33]. Itgam induces kidney macrophage recruitment, and glomerular histological changes, and contributes to kidney injury in diabetic nephropathy [34]. Nov shows reduced expression levels with inflammation and renal fibrosis after nephropathy in mice [35]. Ppard plays an important role in energy metabolism and Ppard agonist decreases insulin and glucose levels by increasing glucose transport and possibly affecting subsequent chronic kidney disease risks [36]. Polymorphisms in PPARD is significantly associated with the risk for chronic kidney disease in Japanese [36]. A deficit in Stab 1 and Stab 2 exhibit the development of severe glomerular fibrosis [37]. In the current study, expression of Itgam, Nov, and Stab 2 increased and Ppard decreased in Il18−/− mice (Table 3), suggesting that increased levels of Itgam and Nov and decreased expression of Ppard led to kidney damage in youth-aged mice, although high levels of Stab 2 might show some protective effects.

At 12 weeks old, renal impairment showed signs of improvement compared with 6-week-old mice (Fig. 1a–e). The affected molecules at 6 weeks old normalized, excluding Il18, and expression of Cxcl10 and Cyp4a14 in Il18−/− mice was lower compared with Il18+/+ mice (Table 4). CXCL10/Cxcl10 can be expressed by mesangial cells [38, 39] and tubular epithelial cells [40] in the kidney by stimulation of proinflammatory cytokines, such as interferon-γ [38]. Cyp4a14-deficient mice exhibit deterioration of renal disease with increased albuminuria, mesangial expansion, and glomerular matrix deposition [41]. Consequently, loss of IL-18 might result in loss of the ability to induce normal inflammatory responses or to decrease Cxcl10 levels or to protect the kidney.

In a previous study, we found that dyslipidemia in Il18−/− mice recovered with short-term (2 weeks) administration of rIL-18 [3]. Additionally, Il18−/− mice that received rIL-18 for 12 weeks recovered from conditions corresponding to NAFLD or NASH [3]. In another study, we suggested a new cancer immunotherapy using IL-18 [14]. Therefore, it appears that IL-18 is not only essential for the synthesis of lipids, for maintaining an energy balance, and for promoting normal lipolysis, but also plays a role in boosting immunological functions.

Before clinical application, the effects of IL-18 on the kidney require study. We found that short-term intravascular administration of IL-18 (2 weeks) induced no kidney damage, and appeared to improve dyslipidemia in Il18−/− mice (Fig. 2a–e) [3]. With long-term administration of rIL-18 in Il18−/− mice, we observed no remarkable findings (Fig. 3a–d). These results suggest that IL-18 administration had little effect on the kidney in these mice, but did show a number of beneficial effects, such as maintaining energy balance and cancer immunotherapy.

This study was limited in that only IL-18 and no other medication was administered. It is possible that IL-18 combined with other medication may have other effects on the kidney including side effects. Moreover, this study only focused on the kidney. However, we are currently investigating the relationship between IL-18 and physiological homeostasis [3], with particular emphasis on not only other remodeling of the kidney but also other organs such as adipose tissue and the pancreas.

Conclusion

We observed a novel influence of IL-18 on the kidney. A deficiency in IL-18 resulted in kidney injury in younger mice but protection from renal damage was observed in mice aged 48 weeks even though Il18−/− mice showed signs of diabetes mellitus, dyslipidemia, and arteriosclerosis. Because IL-18 is considered a possible novel clinical treatment for some conditions, such as cancer immunotherapy, assessment of adverse effects are required. In this study, we found that short- and long-term administration of IL-18 had no adverse effects on the kidney in this population of mice.

Abbreviations

BUN: 

blood urea nitrogen

CREA: 

creatinine

Cxcl10/CXCL10: 

C-X-C motif chemokine 10

Cyp4a14

cytochrome P450, family 4, subfamily a, polypeptide 14

Gapdh

glyceraldehyde-3-phosphate dehydrogenase

IL-18: 

interleukin 18

Il18

interleukin 18

Il18 −/−

IL-18 knockout

IPA: 

Ingenuity® Pathway Analysis

Itgam

integrin alpha M

Lrat

lecithin-retinol acyltransferase

Mapk8

mitogen-activated protein kinase 8

NAFLD: 

non-alcoholic fatty liver disease

NASH: 

non-alcoholic steatohepatitis

Notch1

Notch homolog 1

Nov

nephroblastoma overexpressed gene

Pax2

paired box gene 2

Ppard/PPARD

peroxisome proliferator activator receptor delta

RT-qPCR: 

quantitative reverse transcription polymerase chain reaction

rIL-18: 

recombinant IL-18

Stab 2

stabilin 2

Declarations

Authors’ contributions

KY, KM, TH, KI, and HM conducted the study. KY, KM, TH, KI, YE, DO, and HN performed the experiments. KY, KN, YW, HY, and HM analyzed the data. KY and HM prepared the tables and figures and wrote the manuscript. All authors read and approved the final manuscript.

Acknowledgements

We thank Mr. Nobutaka Okamura, Mrs. Naomi Gamachi, and Ms. Emi Yamaguchi for their technical support; Mr. Nobutaka Okamura for his assistance in the care of animals, accurate collection of samples, and perfusion fixation; Mrs. Naomi Gamachi for molecular analysis and staining techniques; and Ms. Emi Yamaguchi for RNA purification and clerical support. We are grateful to all staff at the Research Facilities for Common Use, Hyogo College of Medicine for allowing us to use resources for RT-qPCR and histological analysis. We are thankful to the editing staff of Edanz Group Japan (Fukuoka, Japan) for their instruction in the use of English language, editorial support, and proofreading.

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

The dataset supporting the conclusions of this article is available in the Gene Expression Omnibus Repository, (GSE64310 at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE64310).

Consent for publication

Not applicable.

Ethics approval and consent to participate

Animal experiments were conducted according to the “Guide for Care and Use of Laboratory Animals” published by the National Institutes of Health and approved by the Animal Care Committee of Hyogo College of Medicine (Nishinomiya, Hyogo, Japan) (#28041 and #14-020).

Funding

There are no sources of funding.

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Authors’ Affiliations

(1)
Department of Neuropsychiatry, Hyogo College of Medicine, Nishinomiya, Japan
(2)
Department of Pathology, Hyogo College of Medicine, Nishinomiya, Japan
(3)
Laboratory of Tumor Immunology and Cell Therapy, Hyogo College of Medicine, Nishinomiya, Japan
(4)
DNA-Chip Development Center for Infectious Diseases, Research Institute for Microbial Diseases, Osaka University, Suita, Japan
(5)
Department of Molecular Genetics, Research Institute for Microbial Diseases, Osaka University, Suita, Japan
(6)
Hirakata General Hospital for Developmental Disorders, Hirakata, Japan

References

  1. Okamura H, Tsutsi H, Komatsu T, Yutsudo M, Hakura A, Tanimoto T, Torigoe K, Okura T, Nukada Y, Hattori K, et al. Cloning of a new cytokine that induces IFN-gamma production by T cells. Nature. 1995;378:88–91.View ArticlePubMedGoogle Scholar
  2. Reddy P. Interleukin-18: recent advances. Curr Opin Hematol. 2004;11:405–10.View ArticlePubMedGoogle Scholar
  3. Yamanishi K, Maeda S, Kuwahara-Otani S, Watanabe Y, Yoshida M, Ikubo K, Okuzaki D, El-Darawish Y, Li W, Nakasho K, et al. Interleukin-18-deficient mice develop dyslipidemia resulting in nonalcoholic fatty liver disease and steatohepatitis. Transl Res. 2016;173(101–114):e107.Google Scholar
  4. Ghayur T, Banerjee S, Hugunin M, Butler D, Herzog L, Carter A, Quintal L, Sekut L, Talanian R, Paskind M, et al. Caspase-1 processes IFN-gamma-inducing factor and regulates LPS-induced IFN-gamma production. Nature. 1997;386:619–23.View ArticlePubMedGoogle Scholar
  5. Okamura H, Tsutsui H, Kashiwamura S, Yoshimoto T, Nakanishi K. Interleukin-18: a novel cytokine that augments both innate and acquired immunity. Adv Immunol. 1998;70:281–312.View ArticlePubMedGoogle Scholar
  6. Sugawara S, Uehara A, Nochi T, Yamaguchi T, Ueda H, Sugiyama A, Hanzawa K, Kumagai K, Okamura H, Takada H. Neutrophil proteinase 3-mediated induction of bioactive IL-18 secretion by human oral epithelial cells. J Immunol. 2001;167:6568–75.View ArticlePubMedGoogle Scholar
  7. Tsutsui H, Kayagaki N, Kuida K, Nakano H, Hayashi N, Takeda K, Matsui K, Kashiwamura S, Hada T, Akira S, et al. Caspase-1-independent, Fas/Fas ligand-mediated IL-18 secretion from macrophages causes acute liver injury in mice. Immunity. 1999;11:359–67.View ArticlePubMedGoogle Scholar
  8. Netea MG, Joosten LA, Lewis E, Jensen DR, Voshol PJ, Kullberg BJ, Tack CJ, van Krieken H, Kim SH, Stalenhoef AF, et al. Deficiency of interleukin-18 in mice leads to hyperphagia, obesity and insulin resistance. Nat Med. 2006;12:650–6.View ArticlePubMedGoogle Scholar
  9. Moriwaki Y, Yamamoto T, Shibutani Y, Aoki E, Tsutsumi Z, Takahashi S, Okamura H, Koga M, Fukuchi M, Hada T. Elevated levels of interleukin-18 and tumor necrosis factor-alpha in serum of patients with type 2 diabetes mellitus: relationship with diabetic nephropathy. Metabolism. 2003;52:605–8.View ArticlePubMedGoogle Scholar
  10. Yamaoka-Tojo M, Tojo T, Wakaume K, Kameda R, Nemoto S, Takahira N, Masuda T, Izumi T. Circulating interleukin-18: a specific biomarker for atherosclerosis-prone patients with metabolic syndrome. Nutr Metab (Lond). 2011;8:3.View ArticleGoogle Scholar
  11. Liu F, Guo J, Zhang Q, Liu D, Wen L, Yang Y, Yang L, Liu Z. The expression of tristetraprolin and its relationship with urinary proteins in patients with diabetic nephropathy. PLoS ONE. 2015;10:e0141471.View ArticlePubMedPubMed CentralGoogle Scholar
  12. Forbes JM, Cooper ME. Mechanisms of diabetic complications. Physiol Rev. 2013;93:137–88.View ArticlePubMedGoogle Scholar
  13. Gilbertson DT, Liu J, Xue JL, Louis TA, Solid CA, Ebben JP, Collins AJ. Projecting the number of patients with end-stage renal disease in the United States to the year 2015. J Am Soc Nephrol. 2005;16:3736–41.View ArticlePubMedGoogle Scholar
  14. Ma Z, Li W, Yoshiya S, Xu Y, Hata M, El-Darawish Y, Markova T, Yamanishi K, Yamanishi H, Tahara H, et al. Augmentation of immune checkpoint cancer immunotherapy with IL18. Clin Cancer Res. 2016;22:2969–80.View ArticlePubMedGoogle Scholar
  15. Takeda K, Tsutsui H, Yoshimoto T, Adachi O, Yoshida N, Kishimoto T, Okamura H, Nakanishi K, Akira S. Defective NK cell activity and Th1 response in IL-18-deficient mice. Immunity. 1998;8:383–90.View ArticlePubMedGoogle Scholar
  16. Yamanishi K, Doe N, Sumida M, Watanabe Y, Yoshida M, Yamamoto H, Xu Y, Li W, Yamanishi H, Okamura H, Matsunaga H. Hepatocyte nuclear factor 4 alpha is a key factor related to depression and physiological homeostasis in the mouse brain. PLoS ONE. 2015;10:e0119021.View ArticlePubMedPubMed CentralGoogle Scholar
  17. Buonomo T, Carraresi L, Rossini M, Martinelli R. Involvement of aryl hydrocarbon receptor signaling in the development of small cell lung cancer induced by HPV E6/E7 oncoproteins. J Transl Med. 2011;9:2.View ArticlePubMedPubMed CentralGoogle Scholar
  18. Ghiabi P, Jiang J, Pasquier J, Maleki M, Abu-Kaoud N, Halabi N, Guerrouahen BS, Rafii S, Rafii A. Breast cancer cells promote a notch-dependent mesenchymal phenotype in endothelial cells participating to a pro-tumoral niche. J Transl Med. 2015;13:27.View ArticlePubMedPubMed CentralGoogle Scholar
  19. Faust J, Menke J, Kriegsmann J, Kelley VR, Mayet WJ, Galle PR, Schwarting A. Correlation of renal tubular epithelial cell-derived interleukin-18 up-regulation with disease activity in MRL-Faslpr mice with autoimmune lupus nephritis. Arthritis Rheum. 2002;46:3083–95.View ArticlePubMedGoogle Scholar
  20. Parikh CR, Jani A, Melnikov VY, Faubel S, Edelstein CL. Urinary interleukin-18 is a marker of human acute tubular necrosis. Am J Kidney Dis. 2004;43:405–14.View ArticlePubMedGoogle Scholar
  21. Parikh CR, Abraham E, Ancukiewicz M, Edelstein CL. Urine IL-18 is an early diagnostic marker for acute kidney injury and predicts mortality in the intensive care unit. J Am Soc Nephrol. 2005;16:3046–52.View ArticlePubMedGoogle Scholar
  22. Tanino A, Okura T, Nagao T, Kukida M, Pei Z, Enomoto D, Miyoshi K, Okamura H, Higaki J. Interleukin-18 deficiency protects against renal interstitial fibrosis in aldosterone/salt-treated mice. Clin Sci (Lond). 2016;130:1727–39.View ArticleGoogle Scholar
  23. Cheng H, Fan X, Guan Y, Moeckel GW, Zent R, Harris RC. Distinct roles for basal and induced COX-2 in podocyte injury. J Am Soc Nephrol. 2009;20:1953–62.View ArticlePubMedPubMed CentralGoogle Scholar
  24. Kastner C, Pohl M, Sendeski M, Stange G, Wagner CA, Jensen B, Patzak A, Bachmann S, Theilig F. Effects of receptor-mediated endocytosis and tubular protein composition on volume retention in experimental glomerulonephritis. Am J Physiol Renal Physiol. 2009;296:F902–11.View ArticlePubMedGoogle Scholar
  25. Datta PK, Dhupar S, Lianos EA. Regulatory effects of inducible nitric oxide synthase on cyclooxygenase-2 and heme oxygenase-1 expression in experimental glomerulonephritis. Nephrol Dial Transplant. 2006;21:51–7.View ArticlePubMedGoogle Scholar
  26. Coppo R, Amore A. New perspectives in treatment of glomerulonephritis. Pediatr Nephrol. 2004;19:256–65.View ArticlePubMedGoogle Scholar
  27. Waldner C, Heise G, Schror K, Heering P. COX-2 inhibition and prostaglandin receptors in experimental nephritis. Eur J Clin Invest. 2003;33:969–75.View ArticlePubMedGoogle Scholar
  28. Montero A, Uda S, Kelavkar U, Yoshimura A, Badr KF, Munger KA. Increased 5-lipoxygenase activating protein in immune-mediated experimental nephritis. J Nephrol. 2003;16:682–90.PubMedGoogle Scholar
  29. Menegatti E, Roccatello D, Fadden K, Piccoli G, De Rosa G, Sena LM, Rifai A. Gene expression of 5-lipoxygenase and LTA4 hydrolase in renal tissue of nephrotic syndrome patients. Clin Exp Immunol. 1999;116:347–53.View ArticlePubMedPubMed CentralGoogle Scholar
  30. Clarkson MR, McGinty A, Godson C, Brady HR. Leukotrienes and lipoxins: lipoxygenase-derived modulators of leukocyte recruitment and vascular tone in glomerulonephritis. Nephrol Dial Transplant. 1998;13:3043–51.View ArticlePubMedGoogle Scholar
  31. Rodriguez-Barbero A, Dorado F, Velasco S, Pandiella A, Banas B, Lopez-Novoa JM. TGF-beta1 induces COX-2 expression and PGE2 synthesis through MAPK and PI3K pathways in human mesangial cells. Kidney Int. 2006;70:901–9.View ArticlePubMedGoogle Scholar
  32. Wu YJ, Xue M, Chen H. Licofelone inhibits interleukin-18-induced pro-inflammatory cytokine release and cellular proliferation in human mesangial cells. Basic Clin Pharmacol Toxicol. 2012;111:166–72.PubMedGoogle Scholar
  33. Luo C, Li T, Zhang C, Chen Q, Li Z, Liu J, Wang Y. Therapeutic effect of alprostadil in diabetic nephropathy: possible roles of angiopoietin-2 and IL-18. Cell Physiol Biochem. 2014;34:916–28.View ArticlePubMedGoogle Scholar
  34. You H, Gao T, Cooper TK, Brian Reeves W, Awad AS. Macrophages directly mediate diabetic renal injury. Am J Physiol Renal Physiol. 2013;305:F1719–27.View ArticlePubMedPubMed CentralGoogle Scholar
  35. Marchal PO, Kavvadas P, Abed A, Kazazian C, Authier F, Koseki H, Hiraoka S, Boffa JJ, Martinerie C, Chadjichristos CE. Reduced NOV/CCN3 expression limits inflammation and interstitial renal fibrosis after obstructive nephropathy in mice. PLoS ONE. 2015;10:e0137876.View ArticlePubMedPubMed CentralGoogle Scholar
  36. Hishida A, Wakai K, Naito M, Tamura T, Kawai S, Hamajima N, Oze I, Imaizumi T, Turin TC, Suzuki S, et al. Polymorphisms in PPAR Genes (PPARD, PPARG, and PPARGC1A) and the risk of chronic kidney disease in Japanese: cross-sectional data from the J-MICC study. PPAR Res. 2013;2013:980471.View ArticlePubMedPubMed CentralGoogle Scholar
  37. Schledzewski K, Geraud C, Arnold B, Wang S, Grone HJ, Kempf T, Wollert KC, Straub BK, Schirmacher P, Demory A, et al. Deficiency of liver sinusoidal scavenger receptors stabilin-1 and -2 in mice causes glomerulofibrotic nephropathy via impaired hepatic clearance of noxious blood factors. J Clin Invest. 2011;121:703–14.View ArticlePubMedPubMed CentralGoogle Scholar
  38. Banas B, Luckow B, Moller M, Klier C, Nelson PJ, Schadde E, Brigl M, Halevy D, Holthofer H, Reinhart B, Schlondorff D. Chemokine and chemokine receptor expression in a novel human mesangial cell line. J Am Soc Nephrol. 1999;10:2314–22.PubMedGoogle Scholar
  39. Duque N, Gomez-Guerrero C, Egido J. Interaction of IgA with Fc alpha receptors of human mesangial cells activates transcription factor nuclear factor-kappa B and induces expression and synthesis of monocyte chemoattractant protein-1, IL-8, and IFN-inducible protein 10. J Immunol. 1997;159:3474–82.PubMedGoogle Scholar
  40. Gomez-Chiarri M, Ortiz A, Gonzalez-Cuadrado S, Seron D, Emancipator SN, Hamilton TA, Barat A, Plaza JJ, Gonzalez E, Egido J. Interferon-inducible protein-10 is highly expressed in rats with experimental nephrosis. Am J Pathol. 1996;148:301–11.PubMedPubMed CentralGoogle Scholar
  41. Gangadhariah MH, Luther JM, Garcia V, Paueksakon P, Zhang MZ, Hayward SW, Love HD, Falck JR, Manthati VL, Imig JD, et al. Hypertension is a major contributor to 20-hydroxyeicosatetraenoic acid-mediated kidney injury in diabetic nephropathy. J Am Soc Nephrol. 2015;26:597–610.View ArticlePubMedGoogle Scholar

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