Journal of Immunology Research

Journal of Immunology Research / 2015 / Article

Research Article | Open Access

Volume 2015 |Article ID 269610 | 11 pages | https://doi.org/10.1155/2015/269610

An Animal Model Using Metallic Ions to Produce Autoimmune Nephritis

Academic Editor: Kurt Blaser
Received04 Jan 2015
Accepted19 Mar 2015
Published30 Apr 2015

Abstract

Autoimmune nephritis triggered by metallic ions was assessed in a Long-Evans rat model. The parameters evaluated included antinuclear autoantibody production, kidney damage mediated by immune complexes detected by immunofluorescence, and renal function tested by retention of nitrogen waste products and proteinuria. To accomplish our goal, the animals were treated with the following ionic metals: HgCl2, CuSO4, AgNO3, and Pb(NO3)2. A group without ionic metals was used as the control. The results of the present investigation demonstrated that metallic ions triggered antinuclear antibody production in 60% of animals, some of them with anti-DNA specificity. Furthermore, all animals treated with heavy metals developed toxic glomerulonephritis with immune complex deposition along the mesangium and membranes. These phenomena were accompanied by proteinuria and increased concentrations of urea. Based on these results, we conclude that metallic ions may induce experimental autoimmune nephritis.

1. Introduction

Autoimmunity induced by metallic ions was previously described in experimental animals and humans suffering from chronic intoxication by heavy metals. However, the pathogenic mechanisms are only partially understood. One possibility is that interactions between metallic ions and normal proteins may trigger a self-immune-response characterized by autoantibody production and cell hypersensitivity. A second possibility is that stereochemical alteration of normal proteins results in the exposition of cryptic self-epitopes or neoepitope formation capable of activating autoreactive clones. A third possibility is related to the increased production of apoptotic remains, resulting in externalization of intracellular antigens onto apoptotic cell membranes. Regardless of how autoantigens are produced, they are processed and presented via MHC molecules to the TCR, resulting in polyclonal activation and autoimmunity [1].

Different examples of autoimmune responses triggered by ionic metals have been reported. For instance, cadmium ions induce autoantibodies to laminin, chromium and platinum trigger antinuclear antibodies (ANA), copper induces antibodies against red blood cells, lithium is associated with ANA and antithyroid antibodies, gold stimulates the production of ANA with Ro specificity and antiplatelet autoantibodies, and finally silver salts induce antifibrillarin antibodies [2]. As a consequence, it is widely accepted that metallic ions are potential inducers of autoimmune responses.

The kidneys are sensitive organs involved in autoimmune diseases, especially lupus erythematosus. Thus, this interesting topic deserves our attention. Previous works demonstrated that exposure to mercury was associated with autoimmune nephritis accompanied by autoantibody production and increased levels of proinflammatory cytokines such as TNFα, IL-1, and IFNγ. Similarly, animals that suffer contamination with mercury ions or their derivatives display membranous nephropathy [36].

In the present study, we induced autoimmune nephritis in inbred Long-Evans rats by intoxication with heavy metals; this model was chosen because other researchers previously reported nephrotoxicity in rats including Brown Norway (BN) and Sprague-Dawley; also lower doses of mercuric chloride administrated to outbreed Wistar rats resulted in renal toxicity [7]. We used inbred Long-Evans strains to maintain homozygosis; therefore, we observed in this particular strain high sensitivity to heavy metals injuries; therefore, this animal model was used to induce autoimmunity and we assessed antinuclear antibodies, kidney damage, and abnormalities in glomerular function. Main results of present work indicate that metallic ions can trigger glomerulonephritis associated with autoantibodies.

2. Material and Methods

2.1. Animals

Male Long-Evans rats that were 8 weeks of age with an average weight between 198 and 258 g were used for the present experiments. The animals were maintained under standard conditions at the animal facility unit of our research institute with free access to food and water. The animals were exposed to metallic ions by a weekly injection. Serum and urine samples were collected simultaneously with the weekly injections, and tissue biopsies were obtained at the end of the intoxication trial. The kidneys were collected immediately after sacrifice. Experiments were conducted according to the guidelines for ethical conduct in the care and use of animals developed by the American Psychological Association (APA) (http://www.apa.org/science/anguide.html).

2.2. Experimental Groups

Animals were grouped () according to the treatments with metallic ions as follows: Group (I), the control group treated with 100 μL of sterile 0.9% NaCl; Group (II) treated with HgCl2 (1.5 mg/100 g of weight); Group (III) treated with CuSO4 (3 mg/100 g of weight); Group (IV) treated with AgNO3 (3 mg/100 g of weight); and Group (V) treated with Pb(NO3)2 (6 mg/100 g of weight). The metallic ions were dissolved in distilled water and administered subcutaneously weekly over a period of 8 weeks. Urine and serum samples were obtained to determinate proteinuria and urea concentrations by conventional methods. At the end of the trial the animals were anesthetized with ether and sacrificed, followed by kidney excision. The organs were rinsed with PBS. One tissue fragment was included in Tissue-tek, frozen at −20°C, and then used for direct immunofluorescence. The other kidney fragment was fixed in 10% formalin and processed for H&E staining and immunohistochemistry.

2.3. Antinuclear Antibodies

Commercial slides containing HEp-2 cells (Immuno Concepts NA, Ltd, Sacramento, CA) were incubated for 30 minutes with serum diluted from 1 : 80 to 1 : 1280, followed by three times of PBS washing and a 30-minute incubation with FITC-labeled goat anti-rat polyvalent gamma globulin (IgG, IgA, and IgM; SAB3700662 Sigma). After another round of washing, the slides were mounted in glycerol-PBS and evaluated with fluorescence microscopy. And anti-DNA antibodies by immunofluorescence using Crithidia luciliae (Immuno Concepts NA, Ltd, Sacramento, CA). The fine specificity of sera samples was tested by ELISA against the following recombinant proteins: Ro60, La, and Sm/RNP (Euroimmun AG, Lübeck, Germany, and Orgentec Diagnostics GmbH, Mainz, Germany). Goat anti-rat polyvalent HRP-labeled anti-IgG and -IgM antibodies were used as the secondary antibodies (Sigma, SAB3700666-2MG).

2.4. Direct Immunofluorescence

A 4 μm slice of renal tissue was obtained using cryosectioning. The tissues were rinsed in 0.15 M PBS, and any possible immune depositions were detected after incubation with FITC-labeled goat anti-rat polyvalent gamma globulin (IgG, IgA, and IgM; SAB3700662 Sigma). After 30-minute incubation, the slides were rinsed, mounted in glycerol-PBS, and evaluated using fluorescent microscopy.

2.5. Immunohistochemistry

To investigate intracellular autoantigen exposition in the kidneys, the tissues were tagged with monoclonal antibodies against the follow ribonucleoproteins: Sm (Pierce MA5-13449), RNP (Pierce MA1-34962), Ro60 (Santa Cruz Biotechnology, sc-100844), and La (Mybiosource MBS533624) as follows. Slides containing 4 μm sections of renal tissue were dewaxed, permeabilized, and washed three times with PBS. Endogenous peroxidase was blocked with 3% horse serum inactivated at 56°C. After washing, the tissues were incubated for 1 hour with the monoclonal antibody diluted in 10% fetal calf serum/PBS according to the manufacturer’s recommendations. The slides were washed with PBS and then incubated for 1 hour with HRP-labeled rabbit anti-mouse IgG. After washing, the color reaction was induced by 3,3′-diaminobenzidine-0.06% H2O2 (Sigma, Catalog number A9044), and finally the reaction was stopped with 2 N sulfuric acid. Assays were performed in duplicate and evaluated by two observers using a light microscope. The intensity of the color reaction obtained from kidneys by immunohistochemistry displays an intensity signal which was expressed in pixels and was analyzed with the software Image-Pro Plus Version 7.0. (Media Cybernetics, USA).

2.6. Double Fluorescence Labeling Assays

To assess the presence of intracellular antigens on apoptotic glomerular membranes, we colocalized the possible target proteins using a double fluorescence assay. Briefly, the autoantigens were tagged in red via 120-minute incubation with monoclonal anti-Sm and anti-RNP, anti-Ro60, or anti-La antibody. Next, the samples were incubated for 120 minutes with goat anti-mouse Texas red-labeled antibody (IgG-TR) (Catalog number sc-2781. Santa Cruz Biotechnology, Inc. Santa Cruz, CA). Apoptotic membranes were stained in green with FITC Annexin V (BD Pharmigen) (this assay is based on the property of cells to lose membrane asymmetry in the early phases of apoptosis because annexin V is a calcium-dependent phospholipid binding protein that binds with high affinity to phosphatidylserine). The tissues were rinsed with 1x binding buffer and then incubated for 15 minutes with 10 μg of FITC-labeled recombinant annexin, followed by PBS washing. Finally, the slides were counterstained with DAPI, mounted, and evaluated under a fluorescence microscope using the appropriate filters for the dyes.

2.7. Podocyte Involvement

To investigate whether podocytes were affected by metallic ions, the tissues were blocked with 3% fetal bovine serum in PBS for 30 minutes and incubated for one hour with monoclonal anti-WT1 antibody (Catalog number sc-7385 Santa Cruz, Biotechnology Inc., Santa Cruz, CA) 1 : 100 in 10% FBS-PBS. After washing with PBS, the presence of the bound antibody was identified with goat anti-mouse IgG-TR. Additionally, following the washes some slides were counterstained with 4′,6-diamidino-2-phenylindole (DAPI). Finally, the slides were mounted and examined using fluorescent microscopy [8].

2.8. Statistical Analyses

The data were processed using nonparametric statistics (ANOVA and -test) and chi-square test using Graph Pad Prism version 6.0 Software. A value <0.05 was considered statistically significant.

3. Results

3.1. Kidney Pathology

The group of control animals did not develop any renal histology abnormalities. In contrast, the kidneys of animals treated with metallic ions developed tubular degeneration, glomerular swelling, and cell hypertrophy at the end of the trial. Furthermore, the urinary space was enhanced as a consequence of the glomerular atrophy, and many samples exhibited acute tubular edema and glomerular changes characterized by glomerular inflammation in varying degrees (Table 1).


ControlGlomeruli conserved, tubules, interstice, and blood vessels normal

AgNO3Glomeruli with mesangial moderate hypercellularity, interstitial lymphocyte infiltration, congested blood vessels, edema of convoluted tubules, and the presence of proteinaceous material

CuSO4Glomerular size increased as Bowman space decreased; podocytes with enlarged volume, thickened membranes, and discrete lymphocytic infiltrates, tubular edema with the luminal presence of proteinaceous material, and diffuse vascular congestion

HgCl2Glomerulus and Bowman space enlarged, mesangial cell proliferation, podocytes with increased volume, increase in membrane thickness, interstitium with inflammatory infiltrate of neutrophils, and tubules with epithelial edema and presence of acidophilus material

Pb(NO3)2Glomeruli with slight increase in size, increased Bowman space, increased membrane thickness, discrete inflammatory infiltrate, and tubular edema

The control group maintained normal renal function without proteinuria. The animals injected with different metallic ions developed renal dysfunction manifested by nitrogen waste product retention in all animals and in 50% of the animals display proteinuria at the second week but at the end of the trial all animals display proteinuria (Figure 1).

3.2. Autoantibody Production

Most of the animals displayed negative ANA titers at the beginning of the trial; however, all sera collected from animals treated with metallic ions tested positive for ANA determination four weeks after treatment, and the ANA titers increased at the end of the trial, and most of the ANA exhibited a cytoplasmic and speckled pattern. An interesting finding was that rats treated with mercury developed anti-nucleoli antibodies (Figure 2). Anti-La antibodies were ubiquitously present in all groups treated with different metallic ions, while anti-DNA and anti-Sm antibodies were ubiquitously present except in animals treated with HgCl2 (Figure 3).

3.3. Immune Complexes at the Glomerular Level

A total of 60% of treated animals showed localization of immune complexes (IC) in their kidneys. These complexes were composed of IgG in complex with antigens from mesangium and/or membranes. This finding was common in different groups of animals treated with different metals; however, the IC trapping in the glomeruli of animals treated with AgNO3 and Pb(NO3)2 was remarkable. In spite of the fact that immune complex deposition was demonstrated at glomerular level only in the 60% of animals, the renal damage was evident by histopathology in all animals treated with metallic ions; furthermore, all intoxicated animals exhibited increased levels of urea and proteinuria and positive antinuclear antibodies or immune complex immune deposition at tubuli regardless of the metallic ion used in the trial (Figure 4).

3.4. Renal Autoantigen

Two assays were performed to assess the expression and externalization effect induced by metals on the exposure of Sm, RNP, Ro, and La autoantigens on apoptotic membranes of glomerular and tubular cells: immunohistochemistry and double fluorescence. (a) All ribonucleoproteins were strongly expressed following intoxication with all tested metallic ions (Figures 5 and 6), whereas the Ro antigen was detected in animals treated with AgNO3 and Pb(NO3)2 and the Sm ribonucleoprotein was overexpressed in animals treated with CuSO4 and AgNO3. (b) Interestingly, the Ro and La autoantigens were distributed on the apoptotic membranes of mesangial cells and podocytes (Figures 7 and 8). Autoantigens are normally expressed inside of tubular and glomerular cells rather than externalized onto apoptotic membranes, as was the case for the animals treated with heavy metals (Figure 9). This type of apoptotic process involves the podocytes, as shown in the podocyte marker WT1 (Figure 10).

4. Discussion

Exposure to metal ions is the result of human activities such as mining, industrial processes, and other activities; this produce contamination of water sources, food, and consequently the inadvertent exposure or accidental contamination with heavy metals may affect humans or animals which can develop autoimmunity. The experimental models of autoimmunity induced by metal ions are important because they allow us to explore the pathophysiological mechanisms that trigger autoimmunity, and using this approach makes it possible to clarify clinically manifestations observed in human beings who are accidentally or inadvertently exposed to these pollutants.

The present study was undertaken to address the possible role of metallic ions in autoimmunity. Autoimmunity was triggered using an experimental rat model based on treatment with different heavy metals. The main findings can be summarized as follows. (1) Metallic ions such as mercury, lead, silver, and copper trigger the production of antinuclear antibodies. (2) The animals develop kidney damage demonstrated by proteinuria and urea retention. (3) Morphology changes including glomerular swelling and tubular degeneration were induced by the metals. (4) Immune glomerular damage was mediated by immune complexes. Taken together, we can conclude that heavy metals are capable of triggering autoimmune nephritis.

Experimental nephritis induced by mercury chloride [9], cadmium, and gold was previously reported [1012]; additionally other reports suggest that lead might alter the clearance of immune complexes at the mesangial level [13]. In current investigation doses reported by other authors were used in the trial [14, 15], and our results agree with previous reports demonstrating that metallic ions may induce autoantibodies in serum and cause immune complex deposition along the mesangium and glomerular base membranes [16]. The original contribution of the present work demonstrates that the overexpression of intracellular ribonucleoproteins such as Ro, La, RNP, and Sm is caused by apoptosis; therefore, based on the results of our double fluorescence assays, we demonstrate that intracellular antigens are externalized onto the surface of apoptotic membranes and the externalization of autoantigen might contribute to disrupt the tolerance. Another original observation is that the toxic effect of ionic metals decreases the podocyte number and also modifies its diaphragm function resulting in proteinuria; this is a new finding that was not previously reported. Another important observation of this study indicates that homozygous animals are more susceptible to the nephrotoxic effects of metal ions; in this sense we previously found (unpublished observations) that heterozygous animals showed reduced susceptibility to renal injury by metal salts. The biggest limitation is the small number of animals included in each experimental group, which does not rule conceptual observation that metal salts induce apoptosis, helping to outsource autoantigens which triggers autoimmunity that favors the in situ immune complex formation which promotes renal failure and proteinuria.

In addition to the acute toxic effect of metallic ions on glomerular and tubular cells, it appears that subacute intoxication induces an autoimmune process in the kidneys. The mechanism responsible for this phenomenon that modifies the immune tolerance is still under investigation.

The effects of metallic ions on the immune response can be demarcated in at least two aspects. First, the metallic salts directly affect the conformation of proteins, resulting in autoantigen production; and, second, the adjuvant effect on the immune cells induces polyclonal cell activation. Both possibilities are mutual but not exclusive. A third factor involved in immunogenicity is the conformational changes that directly cause the metal ions on protein; so, it is important to understand that the metal binding sites on proteins are diverse and involve factors such as geometries, ligands, and metal preferences for certain protein domains. Nevertheless, metals commonly affect the highly hydrophobic centers [17]. Proteins with cysteine or histidine residues are modified by metal bonding and such interactions disrupt disulfide bonds or salt bridges. This type of disruption results in conformational changes in the secondary and tertiary structures, which can modify protein properties. Moreover, these stereochemical changes can expose cryptic antigens or induce the formation of neoantigens, resulting in better accommodation of “antigenic peptides” inside class II molecules of antigen presenting cells. These changes, together with the stimulation of autoimmune repertoires, render a breakdown of immune tolerance.

To predict the residues of autoantigens that are susceptible to metal binding, the Uniprot KB/Swiss-Prot data bank and the NCBI graphical sequence viewer were used to analyze metal-ion dependent adhesion sites (MIDAS) in the Ro60, La, Sm and RNP ribonucleoproteins. The Ro60 ribonucleoprotein (Uniprot KB/Swiss-Prot: P10155.2) displayed three binding sites at positions 378, and 380 (serine), and 445 (threonine), suggesting that there is a molecular basis to assume that Ro60 can be modified by metal bonding (Table 2). Thus, modification of its behavior as an autoantigen is theoretically possible based on our findings of the presence of anti-Ro antibodies in the serum and deposited along the glomeruli of experimental animals.


P10155455, 60 kDa SS-A/Ro ribonucleoprotein, Homo sapiens
10
MEESVNQMQP
20
LNEKQIANSQ
30
DGYVWQVTDM
40
NRLHRFLCFG
50
SEGGTYYIKE
60
QKLGLENAEA
70
LIRLIEDGRG
80
CEVIQEIKSF
90
SQEGRTTKQE
100
PMLFALAICS
110
QCSDISTKQA
120
AFKAVSEVCR
130
IPTHLFTFIQ
140
FKKDLKESMK
150
CGMWGRALRK
160
AIADWYNEKG
170
GMALALAVTK
180
YKQRNGWSHK
190
DLLRLSHLKP
200
SSEGLAIVTK
210
YITKGWKEVH
220
ELYKEKALSV
230
ETEKLLKYLE
240
AVEKVKRTRD
250
ELEVIHLIEE
260
HRLVREHLLT
270
NHLKSKEVWK
280
ALLQEMPLTA
290
LLRNLGKMTA
300
NSVLEPGNSE
310
VSLVCEKLCN
320
EKLLKKARIH
330
PFHILIALET
340
YKTGHGLRGK
350
LKWRPDEEIL
360
KALDAAFYKT
370
FKTVEPTGKR
380
FLLAVDVSAS
390
MNQRVLGSIL
400
NASTVAAAMC
410
MVVTRTEKDS
420
YVVAFSDEMV
430
PCPVTTDMTL
440
QQVLMAMSQI
450
PAGGTDCSLP
460
MIWAQKTNTP
470
ADVFIVFTDN
480
ETFAGGVHPA
490
IALREYRKKM
500
DIPAKLIVCG
510
MTSNGFTIAD
520
PDDRGMLDMC
530
GFDTGALDVI

RNFTLDMI
Divalent metal cation

In contrast, the La, RNP, and Sm ribonucleoproteins did not display any MIDAS; however, this negative prediction did not rule out the possibility of stereochemical modification through interaction with –SH and carboxylate groups (which result in protein denaturation) as another potential source of antigenic peptides.

Metallic ions directly affect the immune system by working like an adjuvant. It is well known that the administration of subtoxic doses of mercury and other metals induces polyclonal activation of lymphocytes, yielding highly specific autoantibodies [3, 18].

In present work the cellular pathway involved in autoimmunity elicited by mercury salts encompasses endosomal TLR signaling; in turn, this signaling stimulates transcription factor NF-kB and promotes the transcription of the pro-IL-1B and IL-6 genes. Then, pro-IL-1B is activated by caspase 1 at the inflammasome, and both cytokines promote autoimmunity [1921]. Additionally, the lymphocyte activation gene-3 (LAG-3) is an important regulator of autoimmunity in response to mercury [22].

5. Conclusions

In conclusion, this study focused on the analysis of environmentally induced autoimmunity using an animal model. Based on the present findings, we can suggest that metallic ions induce autoreactive clones that trigger autoantibody production against intracellular ribonucleoproteins. These ribonucleoproteins are then exposed on apoptotic membranes, enabling the formation of immune complexes along the glomeruli. Based on this experimental approach, we conclude that metallic ions induce autoimmune nephritis.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This work was supported by COZCYT-FOMIX Grant ZAC-2011-C01-172788 and PROMEP UAZ-CA5 Autoinmunidad.

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Copyright © 2015 Roxana Ramírez-Sandoval et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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