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Potential conflict of interest: Nothing to report.
Financial support provided by National Institutes of Health grant DK090019.
Mice with a dominant-negative transforming growth factor β receptor restricted to T cells (dnTGFβRII mice) develop an inflammatory biliary ductular disease that strongly resembles human primary biliary cirrhosis (PBC). Furthermore, deletion of the gene encoding interleukin (IL)-12p40 resulted in a strain (IL-12p40−/−dnTGFβRII) with dramatically reduced autoimmune cholangitis. To further investigate the role of the IL-12 cytokine family in dnTGFβRII autoimmune biliary disease, we deleted the gene encoding the IL-12p35 subunit from dnTGFβRII mice, resulting in an IL-12p35−/− dnTGFβRII strain which is deficient in two members of the IL-12 family, IL-12 and IL-35. In contrast to IL-12p40−/− mice, the IL-12p35−/−mice developed liver inflammation and bile duct damage with similar severity but delayed onset as the parental dnTGFβRII mice. The p35−/− mice also demonstrated a distinct cytokine profile characterized by a shift from a T-helper 1 (Th1) to a Th17 response. Strikingly, liver fibrosis was frequently observed in IL-12p35−/− mice. In conclusion, IL-12p35−/− dnTGFβRII mice, histologically and immunologically, reflect key features of PBC, providing a useful generic model to understand the immunopathology of human PBC. (HEPATOLOGY 2013;)
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Primary biliary cirrhosis (PBC) is an organ- specific autoimmune disease characterized by destruction of intrahepatic small bile duct biliary epithelial cells.1 The serological hallmark of PBC is the presence of antimitochondrial autoantibodies (AMA) directed against the pyruvate dehydrogenase E2 complex (PDC-E2) located within the inner membrane of mitochondria.2-4 We previously reported that mice transgenic for directed expression of a dominant-negative form of transforming growth factor beta receptor type II (dnTGFβRII), under the control of the CD4 promoter lacking the CD8 silencer, spontaneously develop an autoimmune biliary ductular disease.5 This disease is associated with the spontaneous production of AMAs directed to the same mitochondrial autoantigens recognized by sera from PBC patients6 with lymphocytic liver infiltration and periportal inflammation analogous to human PBC. The murine serum cytokine profile is similar to sera of patients with PBC. These findings indicate that the dnTGFβRII mice are a useful animal model for studying the pathogenic mechanisms of human PBC. We have demonstrated that deleting the p40 chain of interleukin (IL)-12 from dnTGFβRII mice produced a marked diminution in the levels of proinflammatory T helper 1 (Th1) cytokines in livers with accompanying reductions in cellular infiltrates in portal tracts and diminished bile duct damage.7
IL-12, the prototypic member of the heterodimeric family of cytokines, consists of a p40 and a p35 subunit covalently linked by two disulfide linkages. Both p35 and p40 are components of two heterodimeric cytokines in the IL-12 family.8 In order to further examine and differentiate the role of the p35- and p40-containing members of the IL-12 cytokine family in dnTGFβRII disease, we generated an IL-12p35−/− mouse strain on the dnTGFβRII background. Our results indicate that, in contrast to the IL-12p40−/− mice that were protected from liver inflammation, the IL-12p35−/− mice developed liver inflammation with similar severity but delayed onset compared to the parental dnTGFβRII mice. The p35−/− mice demonstrate a distinct cytokine profile, with enhanced IL-17, compared to parental dnTGFβRII and p40−/− mice. Strikingly, deletion of the IL-12p35 subunit from dnTGFβRII mice resulted in frequent development of liver fibrosis. This model is unique in that it has a resemblance to a number of immunological and histological features of human PBC. Although we do not opine that it recapitulates PBC faithfully, we submit that it is a useful system to dissect the cellular and molecular basis of loss of tolerance and liver damage.
AMA, antimitochondrial autoantibodies; dnTGFβRII, dominant-negative form of transforming growth factor beta receptor type II; MNCs, mononuclear cells; PBD, primary biliary cirrhosis; PDC-E2, pyruvate dehydrogenase E2 complex.
Materials and Methods
The dnTGFβRII colony on a B6 background (B6.Cg-Tg(Cd4-TGF BR2)16Flv/J) was maintained at the University of California at Davis animal facility (Davis, CA) and bred as hemizygotes due to the severe inflammatory bowel disease of homozygotes. The dnTGFβRII mice used herein are on a B6 background. Essentially, the transgenic founder mice were backcrossed to B10.BR mice for three generations and thence backcrossed to C57BL/6 mice for 15 generations.9 Further descriptions of the genetics of these mice are found in http://jaxmice.jax.org/strain/005551.html. B6.129S1-Il12btm1Jm/J (IL-12p40−/−) and B6.129S1-Il12atm1Jm/J (IL-12p35−/−) mice were purchased from the Jackson Laboratory (Bar Harbor, ME). IL-12p40−/−dnTGFβRII mice were generated as described.5, 7 Similarly, male dnTGFβRII mice were mated with female IL-12p35−/− mice to obtain IL-12p35+/−dnTGFβRII mice, which were subsequently backcrossed with female IL-12p35−/− mice to obtain IL-12p35−/−dnTGFβRII mice. The parental dnTGFβRII and the derived IL-12p35−/−dnTGFβRII mice at 3 to 4 weeks of age were genotyped to confirm the dnTGFβRII gene and IL-12p35−/− in their genomic DNA.5 Male hemizygous dnTGFβRII, hemizygous IL-12p35−/−dnTGFβRII mice, and hemizygous IL-12p40−/−dnTGFβRII mice were backcrossed onto female C57BL/6 (B6), IL-35−/− and p40−/− mice, respectively.5 All mice were fed sterile rodent Helicobacter Medicated Dosing System (three-drug combination) diets (Bio-Serv, Frenchtown, NJ) and maintained in individually ventilated cages under specific pathogen-free conditions. Sulfatrim (Hi-tech Pharmacal, Amityville, NY) was delivered through drinking water according to the manufacturer's instructions. At 12 and 24 weeks of age, animals were sacrificed and their liver and colon tissues were processed as outlined below. In addition, liver mononuclear cells were isolated and analyzed as below. The experimental protocols were approved by the University of California Animal Care and Use Committee.
Serum samples collected at different ages were tested for levels of anti-PDC-E2 antibodies using an enzyme-linked immunosorbent assay (ELISA). Briefly, 96-well ELISA plates were coated with 5 mg/mL of purified recombinant PDC-E2 in carbonate buffer (pH 9.6) at 4°C overnight, washed with Tris-buffered saline Tween-20 (TBS-T), and blocked with 5% skim milk in TBS for 30 minutes. Serum samples at 1:100 dilution were added to individual wells of the microtiter plate and incubated for 1 hour at room temperature (RT). After washing, horseradish peroxidase (HRP)-conjugated antihuman immunoglobulin (A+M+G) (H+L) (1:2,000) (Zymed, San Francisco, CA) was added. The plates were incubated for 1 hour at RT, then washed. OD450nm was measured after addition of TMB peroxidase substrate (BD Biosciences, San Jose, CA) and incubation at RT for 15 minutes. Previously calibrated positive and negative standards were included with each assay.
The harvested liver and colon tissues were fixed in 4% paraformaldehyde at RT for 2 days, embedded in paraffin, and cut into 4-mm sections. The sections were deparaffinized, stained with hematoxylin and eosin (H&E), and evaluated by a “blinded” pathologist for pathological changes. To evaluate the severity of fibrosis, the images of the H&E-stained slides were captured using a microscope at a magnification of 40×. A standard 1063 × 797 pixel region of interest (ROI) was taken from each sample by the “blinded” pathologist and analyzed using ImageJ software (National Institutes of Health, Bethesda, MD), which provides the percentage of fibrosis area in each ROI. Masson's trichrome and Sirius Red stain was also used for visualizing fibrosis on liver tissue sections.
Liver infiltrating mononuclear cells (MNCs) were isolated as described.10 The cells were resuspended in staining buffer (0.2% bovine serum albumin [BSA], 0.04% ethylenediaminetetraacetic acid [EDTA] and 0.05% sodium azide in phosphate-buffered saline [PBS]), divided into 25-μL aliquots, and incubated with antihuman FcR blocking reagent (eBioscience) for 15 minutes at 4°C. Cells were then washed and stained for 30 minutes at 4°C with cocktails containing combinations of fluorochrome-conjugated monoclonal antibodies for different cell surface markers including CD8a, CD4, NK1.1 (Biolegend, San Diego, CA), CD19 and TCRβ (eBioscience, San Diego, CA). IgG isotype antibodies with matching conjugates were used as negative controls. The cells were then washed once with PBS containing 0.2% BSA. For intracellular cytokine staining, cells were resuspended in 10% FBS RPMI and stimulated with Leukocyte Activation Cocktail in the presence of BD GolgiPlug (BD Pharmingen, San Diego, CA) at 37°C for 4 hours. The cells were stained for surface CD4, NK1.1, and TCRβ, fixed, and permeabilized with BD Cytofix/Cytoperm Solution (BD Biosciences, San Diego, CA), then stained for intracellular interferon γ (IFN-γ), IL-4, and IL-17 (BioLegend). Normal IgG isotype controls were used in parallel. A FACScan flow cytometer (BD Immunocytometry Systems, San Jose, CA) upgraded for the detection of five colors by Cytek Development (Fremont, CA) was used to acquire data, which were analyzed with Cellquest PRO software (BD Immunocytometry Systems).
Cell Culture and Cytokine Detection.
For analysis of secreted cytokines, 2.0 × 105 hepatic MNCs were cultured in 96-well round-bottom plates in 200 μL of RPMI supplemented with 10% heat-inactivated FBS (GIBCO-Invitrogen, Grand Island, NY), 100 μg/mL streptomycin, 100 U/mL penicillin, and 0.5 μg/mL each of anti-CD3 (BioLegend) and anti-CD28 (BioLegend). The cells were incubated for 72 hours at 37°C in a humidified 5% CO2 incubator, then centrifuged. The supernatant was collected and analyzed for concentration of cytokines. IL-22 level was measured using an ELISA kit (BioLegend). The levels of IFN-γ, tumor necrosis factor α (TNF-α), IL-6, and IL-17 were measured simultaneously with a mouse cytometric bead array (CBA) kit (BD Biosciences), using a FACScan flow cytometer with CBA software (BD Biosciences).
Assay of Hepatic Hydroxyproline Content.
Hepatic hydroxyproline content was quantified using a hydroxyproline assay kit (BioVision, Mountain View, CA). Briefly, frozen liver tissue from 24-week-old mice, in groups of 5-8 mice, were weighed and homogenized in distilled H2O and hydrolyzed. Ten μL of hydrolysate was transferred to a 96-well plate and evaporated to dryness under vacuum; a standard curve was applied following the kit protocol. Total hydroxyproline content was measured and data presented per gram of wet weight liver tissue.
Liver Fibrosis of qPCR Array.
A murine fibrosis PCR array (SABiosciences/Qiagen, Frederick, MD) was performed to assess the expression of 84 key genes involved in fibrogenesis or fibronolysis in liver. Briefly, total RNA was extracted from individual liver tissues using the Qiagen RNAeasy Mini Kit (Qiagen, Valencia, CA). For quantitative polymerase chain reaction (qPCR) array analysis, 1 μg of total RNA was reverse transcribed and then quantified on an ABI ViiA 7 Real-Time PCR System (Applied Biosystems, Foster City, CA). Amplification was performed for 40 cycles in a total volume of 10 μL and products were detected using SYBR Green (Applied Biosystems). The relative level of expression of each target gene was determined by normalizing its messenger RNA (mRNA) level to internal control genes.
Cytokine production, portal inflammation, and bile duct damage in different mouse strains were compared by a two-tailed unpaired Mann-Whitney test. The frequency of fibrosis in the different mouse strains was compared using Fisher's exact test. In addition, the Tukey-Kramer Multiple Comparisons Test was performed to compare the quantification of fibrosis in different groups. Hypothesis tests were declared statistically significant for attained significance levels of P < 0.05.
IL-12p35−/−dnTGFβRII Mice Developed Liver Inflammation with Similar Severity but Delayed Onset.
To distinguish the role of IL-12p35 from that of IL-12p40 in dnTGFβRII biliary disease, we generated IL-12p35−/−dnTGFβRII mice and compared the data with the parental dnTGFβRII mice and IL-12p40−/−dnTGFβRII mice (Fig. 1). Histological examination of liver demonstrated that at 12 weeks both the p40−/− and p35−/− mice had significantly milder portal inflammation compared with the parental dnTGFβRII mice (P < 0.05). By 24 weeks, however, the p35−/− mice and the parental dnTGFβRII mice had similar portal tract lymphocyte infiltration; both were significantly more severe than the p40−/− mice (P < 0.001) (Fig. 1A,B). Biliary duct damage was not observed at 12 weeks in any group except for one out of nine animals in the dnTGFβRII group (Fig. 1B), but at 24 weeks was readily detectable in the p35−/− and dnTGFβRII mice but not p40−/− mice (Fig. 1A,B). In addition, histological analysis of colonic tissues demonstrated the absence of lymphocyte infiltration in both p40−/− and p35−/− mice compared to parental dnTGFβRII mice (P < 0.001) (Fig. 1C,D), indicating that deletion of p35 differentially affected the liver versus colonic inflammatory response compared to dnTGFβRII mice.
The liver histological data were largely correlated with the number of MNCs recovered from the liver tissues. At 12 weeks, only dnTGFβRII mice had a significantly enlarged spleen (Fig. 2A). However, a significantly reduced liver weight was observed in p35−/− mice at 12 and 24 weeks (Fig. 2A). Both the p40−/− mice and the p35−/− mice had significantly fewer intrahepatic MNCs than dnTGFβRII mice (P < 0.05); by 24 weeks no significant difference was detected between p35−/− mice and dnTGFβRII mice, whereas the hepatic MNCs in the p40−/− mice remained at significantly lower levels (Fig. 2B). Although the numbers of liver-infiltrating CD4 T cells were reduced in both the p40−/− and p35−/− mice compared to the dnTGFβRII mice (P < 0.01), the numbers of p35−/− CD8 T cells increased by 24 weeks and was significantly higher than in p40−/− or dnTGFβRII mice (P < 0.05) (Fig. 2B). The numbers of intrahepatic B cells, natural killer (NK) cells, and NKT cells were all significantly lower in p40−/− mice than dnTGFβRII mice at both 12 and 24 weeks, whereas those of the p35−/− mice were in general intermediate between the other two mouse strains (data not shown). In summary, these results indicate that the absence of IL-12 p35 resulted in reduced liver inflammation at 12 weeks but not 24 weeks of age compared to dnTGFβRII mice. In contrast, deletion of the IL-12 p40 resulted in complete protection against liver inflammation and bile duct damage at both 12 and 24 weeks.
Enhanced Liver Fibrosis in IL-12p35−/−dnTGFβRII Mice.
Liver fibrosis is characteristic of human PBC but has not been previously reported in murine models of PBC. To assess the extent of fibrosis, Masson's trichrome staining (Fig. 3B) and Sirius Red staining (Fig. 3D) were performed to detect collagen distribution. At 24 weeks fibrosis was detected in 54% (7/13) of the p35−/− mice but none of 14 dnTGFβRII mice (P < 0.05, Fisher's exact test) (Fig. 3C). The results of liver fibrosis quantification with image analysis of Sirius Red staining sections further confirmed the presence of fibrosis in p35−/− mice (Fig. 3E). Mild fibrosis was also observed in one out of eight p40−/− mice. However, the severity of fibrosis in this mouse was substantially lower than the p35−/− mice with fibrosis, based on the area of fibrosis (Fig. 3C,E). The hepatic hydroxyproline content was significantly higher in p35−/− mice than p40−/− (P = 0.016) and dnTGFβRII mice (P = 0.007) at 24 weeks (Fig. 3F).
Enhanced Liver Fibrosis Is Associated with Decreased Expression of Th1 Response-Related Genes.
To address the potential mechanism of fibrosis in IL-12p35−/− dnTGFβRII mice, we examined 84 genes associated with dysregulated wound healing, tissue repair, and remodeling in three groups using a PCR array. A total of 13 genes were significantly down-regulated in the IL-12p35−/−dnTGFβRII group (Table 1), including the important negative regulators in liver fibrosis STAT1, IFN-γ, and hepatocyte growth factor (HGF), suggesting that reduced expression levels of IFN-γ/STAT1 signaling and antifibrotic factor-HGF are involved in development of fibrosis in IL-12p35−/−dnTGFβRII mice.
Table 1. PCR Array Analysis of Fibrosis-Related Gene Expression in Liver Tissue
IL-12p35−/−dnTGFβRII Versus dnTGFβRII Mice
IL-12p35−/−dnTGFβRII Versus IL-12p40−/−dnTGFβRII Mice
Elevated Serum AMA Level in IL-12p35−/−dnTGFβRII Mice.
There were no significant differences in the level of serum AMAs among the three mice strains at 12 weeks. By 24 weeks, the serum AMA level was significantly higher in p35−/− mice compared to the other two strains (P < 0.05) (Fig. 4).
Increased Th17 Response in IL-12p35−/−dnTGFβRII Mice.
To further confirm decreased IFN-γ/STAT1 signaling and compare Th1, Th2, and Th17 differentiation in the hepatic CD4 T cells of the three strains, we stimulated hepatic MNC and stained for intracellular cytokines IFN-γ, IL-4, and IL-17. As shown in Fig. 5, the frequency of Th1 (IFN-γ+) cells was significantly lower in both p35−/− and p40−/− mice than the dnTGFβRII mice (P < 0.001) at 12 weeks. The relative frequencies of Th2 (IL-4+) cells, in comparison to the Th1 (IFN-γ+) cells, were significantly higher in p40−/− and p35−/− mice (P < 0.05) at both 12 weeks and 24 weeks. Most strikingly, the relative frequency of the Th17 (IL-17+) cells, in comparison to the Th1 (IFN-γ+) cells, was significantly higher in the p35−/− mice than either the p40−/− or dnTGFβRII mice at both timepoints (P < 0.05).
Consistent with increased frequency of intrahepatic Th17 cells, the p35−/− mice demonstrated increased concentrations of Th17 cytokines secreted from the cultured hepatic MNCs. As shown in Fig. 6, whereas the concentration of secreted IFN-γ was significantly higher in dnTGFβRII mice than the p35−/− and p40−/− mice (P < 0.05), the concentrations of IL-17 and IL-22 were both significantly higher in p35−/− mice than p40−/− and dnTGFβRII mice (P < 0.05). The level of secreted IL-6 was also significantly higher in p35−/− mice than the other strains at 12 weeks. By 24 weeks, the secreted IL-6 level was significantly lower in p40−/− mice than the other two strains, although in all three strains the IL-6 levels are substantially lower than that of 12 weeks. Taken together, these results show an enhanced Th17 response in p35−/− mice.
The IL-12 family, composed of IL-12, IL-23, IL-27, and IL-35, is an important group of secreted proteins in the cytokine network of the innate and adaptive immune system.8, 11 All four IL-12 family cytokines are heterodimers constructed with an α chain and a β chain, and each cytokine shares at least one chain with another member of the family. Specifically, p40 is shared by IL-12 and IL-23, whereas p35 is shared by IL-12 and IL-35. We previously reported that p40 deficiency eliminated biliary disease in dnTGFβRII mice,7 suggesting that IL-12 and IL-23 are important in the development of biliary disease. The goal of the current study was to examine the role of the p35-containing cytokines in the pathogenesis of dnTGFβRII mice.
IL-12, IL-23, and IL-27 were initially described as proinflammatory/stimulatory cytokines, and have been implicated in various autoimmune diseases including experimental colitis,12 collagen-induced arthritis,13 insulin-dependent diabetes,14 experimental autoimmune encephalomyelitis (EAE),15 PBC,16 and inflammatory bowel disease.17 In contrast, IL-35, the newest member of the IL-12 family, is distinct from the other three members. Within the CD4 T cell population, IL-35 is expressed by resting and activated T regulatory cells (Tregs) but not effector T cells, hence considered an inhibitory cytokine that contributes to Treg function.11 The role of IL-35 in infection and autoimmune diseases is a largely uncharted territory. We previously reported that autoimmune cholangitis in dnTGFβRII mice has features strikingly similar to human PBC, and have documented the role of different mononuclear subsets and cytokines in this PBC model.5, 18-21 In particular, dnTGFβRII IL-12p40 knockouts, lacking the proinflammatory cytokines IL-12 and IL-23, have no biliary disease.7
IL-12 is a major cytokine involved in prototype Th1 responses and plays a role in both innate and adaptive immunity.22 A genomewide association analysis of DNA samples from 536 patients with PBC and 1,536 controls revealed significant associations between PBC and common genetic variants at IL12A locus (encoding p35 subunit) and IL12RB2 (encoding IL-12 receptor β2) locus, suggesting that the IL-12 signaling pathway is relevant to the pathophysiology of PBC.16 A case report of biliary cirrhosis in an IL-12 deficiency child further suggests that the alteration of IL-12 immunomodulatory signaling is critical to the pathogenesis of PBC.23 We demonstrate herein that, similar to IL-12p40−/−dnTGFβRII mice, the IL-12p35−/−dnTGFβRII mice had significantly milder portal inflammation at 12 weeks compared to dnTGFβRII mice. Because the presence of the proinflammatory IL-23 alone without IL-12, as in the case of the p35−/− mice, is not sufficient to cause early onset of portal inflammation in dnTGFβRII mice, this suggests that IL-12 plays a dominant role in portal inflammation. However, in the p35−/− mice the IL-12 deficiency in the presence of IL-23 but absence of IL-35 did not prevent dnTGFβRII biliary disease at 24 weeks (Fig. 1), suggesting that the pathological role of IL-23 can be enhanced by the deficiency of IL-35 related Treg functions. Unexpectedly, the absence of both IL-12 and IL-35 resulted in a strikingly high frequency (>50%) of liver fibrosis in the IL-12p35−/−dnTGFβRII mice (Fig. 3), which has not been seen in any other mouse models of PBC. Because IL-35 is expressed only by Tregs, whereas dnTGFβRII mice clearly lack the ability to regulate the immune response by way of TGFβ, an important mechanism of Treg-mediated tolerance, adding an IL-35 deficiency might cripple the Treg mechanisms further; it points to a role for Treg activity in control of liver pathogenesis including fibrosis.
In PBC, a predominance of prototype Th1 cytokines and Th1 cells have been reported, and the Th1 response has been highly correlated with the degree of bile duct destruction.24-26 Furthermore, a significant decline of Th2 response has been reported during the late stage of PBC.27 Similar observations have also been reported in other organ-specific autoimmune diseases in which a Th2-type response prevented tissue damage.28, 29 However, the role of the newer IL-12 family cytokines in PBC is not yet clear. We should note that the cell isolation techniques used herein are similar to our previous work; we avoided enzymatic digestion because NK1.1 and the DX5 marker are significantly down-regulated after isolation using enzymatic digestion.30 Our focus was on the correlation between Th1, Th17, and liver fibrosis and thus we used our established technique of mechanical dissection for isolation of mononuclear cells. We do, however, note that cellular infiltration was demonstrated not only by cell counting, but also by histologic examination. Indeed, although a significant decrease was found in hepatic MNC in dnTGFβRII p35−/− mice at 12 weeks of age in comparison with dnTGFβRII mice, no significant difference was found at 24 weeks of age, indicating that the liver infiltration at 24 weeks in the p35−/− mice was as severe as dnTGFβRII mice; such data were supported by histologic examinations.
In the current study we observed a reduced IFN-γ/STAT1 signaling at the mRNA level (Table 1) and a lower IFN-γ production in p35−/− mice compared to dnTGFβRII mice (Fig. 5), which is in agreement with previous reports on these mutations on a different genetic background31, 32 and is compatible with the presence of liver inflammation in dnTGFβRII mice but not p35−/− and p40−/− mice at 12 weeks (Fig. 1). The similar levels of liver disease in p35−/− and the parent dnTGFβRII mice at 24 weeks, however, cannot be directly attributed to the Th1/Th2 balance. The most prominent feature in the cytokine profile of p35−/− mice is the significantly enhanced IL-6 and Th17 responses (Figs. 5, 6).
IL-17 producing CD4 T cells, or Th17 cells, have attracted attention because of their potent pathogenic role in autoimmune and inflammatory diseases including rheumatoid arthritis, experimental autoimmune encephalomyelitis (EAE), colitis,33-36 and liver disease.37, 38 The pathogenic potential of Th17 cells is conferred by the cytokines they produce, including IL-17A, IL-I7F, IL-21, and IL-22.39 Recent studies have shown that IL-21 and IL-22 are important in the pathogenesis of inflammatory responses.40 A close relationship between levels of Th17 and PBC has been found in several studies, including a significant increase in the frequency of IL-17+ lymphocytes41 and the periductal production of IL-17 in association with biliary innate immunity, which has been shown to contribute to the pathogenesis of cholangiopathy.42, 43 The elevated level of Th17 cells and Th17-produced cytokines may be one of the contributing factors for the liver disease observed in the 24-week-old p35−/− mice. In particular, IL-17 up-regulates the expression of CXCL3 on biliary epithelial cells,42 which promotes migration of T cells into the liver, including CD8 T cells that play a pathogenic role in dnTGFβRII biliary damage.44, 45 Consistent with these previous findings, we demonstrate a significantly increased number of intrahepatic CD8 T cells in p35−/− mice by 24 weeks (Fig. 2). In addition, Th17 cells have been shown to participate in the production of autoantibodies.46 This is in agreement with the higher levels of AMA in p35−/− mice compared to the p40−/− and dnTGFβRII mice (Fig. 4).
The association of the distinct cytokine profile and the extensive liver fibrosis in the p35−/− mice is of interest because a similar correlation between Th17 and fibrosis has been documented in patients with autoimmune hepatitis, hepatitis B virus-related liver disease, and alcoholic liver disease.37, 47, 48 The expression level of IL-17 strongly correlates with the degree of fibrosis in patients with hepatitis B virus (HBV)-related chronic liver diseases.47 IL-17A-activated fibroblasts enhances production of IL-6 in one of the mouse models.49 In addition, IL-17A independently induces the activation of collagen-producing cells contributing to BDL- or CCL4-induced liver fibrosis in mice. Thus, it is likely that Th17 and IL-6 also play a role in p35−/− liver fibrosis. Of note, IL-22 has recently been shown to be primarily synthesized by the Th17, Th22, γδT, NK, and NKT cell lineages.39 A weakness of the study herein is the failure to study the mechanism of amplified fibrinogenesis in these mice. Our initial efforts were placed on defining the specific roles of the p35 versus p40 subunits in modulating the inflammatory disease we previously reported in dnTGFβRII mice. Hence, the appearance of fibrosis was unexpected and must become a subject of future studies. We note the role of IL-22 in tissue fibrosis remains unclear or controversial50, 51 and suggest that the fibrosis in p35−/− mice is most likely due to a reduction in IFN-γ and the increase in IL-17. Future directions will focus on the generation of IL-17, p35 double knockout mice as a model to explore these issues including fibrinogenesis and cytokine interactions with hepatic stellate cells.
Interestingly, Th17 cells have been classified as an independent T-helper cell subset through the identification of their differentiation factors IL-6 and TGFβ1.52 Recent studies demonstrate that Th17 cells can also be induced without TGFβ1 but by way of the effects of IL-6, IL-1β, and IL23. These “alternative” Th17 cells are thought to be more pathogenic than the “classical” Th17 cells.53 Because the TGFβ pathway is disrupted in the dnTGFβRII mice, the Th17 cells in the IL-12p35−/−dnTGFβRII are likely to be the “alternative” type with elevated pathogenic character.
In summary, our results reveal distinct phenotypes in terms of fibrosis, liver inflammation, and cytokine profile among the dnTGFβRII strain and its two derivative strains, IL-12p35−/− and IL-12p40−/− mice. Importantly, because the deletion of p35 gene disrupts IL-12 and IL-23, whereas deletion of p40 gene disrupts IL-12 and IL-35, the different phenotypes of 12p35−/− and 12p40−/− reflect the differential effects of a proinflammatory cytokine, IL-23, versus a presumably inhibitory cytokine, IL-35, in the absence of IL-12 and a functional TGFβ pathway. In particular, our results suggest a potential role of IL-35 in protection against development of fibrosis. Further investigation of the IL-12 family members, especially the poorly studied IL-35, should shed more light on the immunopathogenic mechanism of the PBC-like liver disease in the dnTGFβRII mice, especially pathogenesis of liver fibrosis.