Inflammatory arthritis increases the susceptibility to acute immune-mediated hepatitis in mice through enhancing leptin expression in T cells. (December 2021)

• Record Type: Journal Article
• Authors: Wang, Youyi; Wang, Ping; Xu, Qishan; Dong, Lijun; Liu, Yunzhi; Chen, Yu; Zhou, Jia; Lu, Xiao; Zuo, Daming; Chen, Qingyun
• Is Part Of: Molecular immunology. Volume 140(2021)
• Page Start: 97
• Page End: 105
• Publication Date: 2021-12
• Subjects: AIA adjuvant-induced arthritis -- AIH autoimmune hepatitis -- ALT alanine aminotransferase -- AS ankylosing spondylitis -- CFA complete Freund's adjuvant -- CFSE 5-(and-6)-carboxyfluorescein diacetate succinimidyl ester -- Con A concanavalin A -- ESR erythrocyte sedimentation rate -- GGT gamma-glutamyl transferase -- JIA juvenile idiopathic arthritis -- MNCs mononuclear cells -- PsA psoriatic arthritis -- PVDF polyvinylidene fluoride -- RA rheumatoid arthritis; Inflammatory arthritis -- Immune-mediated hepatitis -- Concanavalin A -- T cells -- Leptin; Immunochemistry -- Periodicals; Molecular biology -- Periodicals; Immunochemistry -- Periodicals; Allergy and Immunology -- Periodicals; Molecular Biology -- Periodicals; Immunochimie -- Périodiques; Biologie moléculaire -- Périodiques; Immunochemistry; Molecular biology; Periodicals; Electronic journals; 571.96
• DOI: 10.1016/j.molimm.2021.09.015
• Languages: English
• ISSNs: 0161-5890

Abstract

Graphical abstract: Highlights: Arthritis mice are highly susceptible to Con A-induced hepatitis. Hepatic T cells from arthritis mice are more sensitive to Con A stimulation. Leptin might be responsible for the difference in Con A-induced T cell activation between control and arthritis mice. Abstract: Liver function abnormalities are common in patients with inflammatory arthritis. However, the precise mechanism is still unclear. In this study, inflammatory arthritis was established in mice by subcutaneous injection of complete Freund's adjuvant, and the intravenous injection of concanavalin A (Con A) was employed to induce acute immune-mediated hepatitis in mice. The result showed that the arthritis mice were more susceptible to ConA-induced hepatitis than the control mice, as evidenced by increased hepatic necrosis, elevated serum alanine aminotransferase activity, and raised inflammatory cytokines. Besides, the in vitro assay demonstrated that the T cells from arthritis mice were more sensitive to the Con A stimulation than those from control mice. Moreover, we determined that the level of leptin, a kind of adipokine, was significantly increased in the serum and hepatic T cells of arthritis mice. Interestingly, the data indicated that the enhanced expression of leptin in hepatic T cells is responsible for the hypersensitivity of arthritis mice-derived T cells to Con A challenge. Collectively, our findings demonstrate an unexpected role of leptin in the connection between inflammatory arthritis and acute immune-mediated hepatitis, thus providing new insight into the clinical therapy of arthritis-related liver dysfunction.