期刊
MICROSCOPY AND MICROANALYSIS
卷 29, 期 2, 页码 675-685出版社
OXFORD UNIV PRESS
DOI: 10.1093/micmic/ozac046
关键词
acetylated lysine; chronic kidney disease; inflammatory cytokine; interleukin 36; lupus nephritis; MRL; MpJ-Fas(lpr lpr); systemic autoimmune disease
Systemic autoimmune diseases often lead to lupus nephritis, which alters the balance and expression of IL-36R ligands in the kidneys. In a mouse model of lupus nephritis, it was found that IL-36R knockout significantly improved renal pathology, particularly mesangial matrix expansion and fibrosis.
Systemic autoimmune diseases frequently induce lupus nephritis, causing altered balance and expression of interleukin 36 receptor (IL-36R) ligands, including agonists (IL-36 alpha, beta, gamma) and antagonists (IL-36Ra, IL-38), in kidneys. Here, we established and analyzed a mouse model of lupus nephritis, MRL/MpJ-Fas(lpr/lpr) with IL-36R-knockout (KO), compared to wild-type (WT) mice. In both genotypes, indices for immune abnormalities and renal functions were comparable, although female WT mice showed higher serum autoantibody levels than males. IL-36R ligand expression did not differ significantly between genotypes at the mRNA level or in IL-36 alpha and IL-38 scores. However, glomerular lesions, especially mesangial matrix expansion, were significantly ameliorated in both sexes of IL-36R-KO mice compared to WT mice. Cell infiltration into the tubulointerstitium with the development of tertiary lymphoid structures was comparable between genotypes. However, the positive correlation with the IL-36 alpha score in WT mice was not evident in IL-36R-KO mice. Fibrosis was less in female IL-36R-KO mice than in WT mice. Importantly, some IL-36 alpha(+) nuclei co-localized with acetylated lysine and GCN5 histone acetyltransferase, in both genotypes. Therefore, IL-36R ligands, especially IL-36 alpha, contribute to the progression of renal pathology in lupus nephritis via IL-36R-dependent and IL-36R-independent pathways.
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