自身抗体
下调和上调
抗体
免疫系统
免疫学
流式细胞术
细胞凋亡
分子生物学
巨噬细胞
医学
生物
体外
生物化学
基因
作者
Akira Iizuka,Seiji Segawa,Yuya Kondo,Shunta Kaneko,Masahiro Yokosawa,Kotona Furuyama,Haruka Miki,Satoko Tahara‐Hanaoka,Akira Shibuya,Hiroto Tsuboi,Daisuke Goto,Isao Matsumoto,Shiro Shibayama,Takayuki Sumida
标识
DOI:10.1111/1756-185x.13381
摘要
Allergy inhibitory receptor-1 (Allergin-1) is a newly identified immune regulatory molecule thought to influence autoantibody production. Autoantibody production, like that observed in Allergin-1-deficient mice, is crucial in the pathogenesis of several autoimmune diseases such as systemic lupus erythematosus. The purpose of this study is to clarify the regulatory role of Allergin-1-mediated autoantibody production using a murine model of thymocytic anaphylaxis.C57BL/6 (WT) and Allergin-1-deficient mice were treated with apoptotic cells from naive thymocytes stimulated by dexamethasone. Antibody titers of total or immunoglobulin G (IgG) subclass of anti-double-stranded DNA (anti-dsDNA) and anti-histone antibody from serum were measured using an enzyme-linked immunosorbent assay. Macrophages from wild-type (WT) or Allergin-1-deficient mice were co-cultured with fluorescence-labeled apoptotic thymocytes or fluorogenic reagent and resultant phagocytic activity was quantified by with flow cytometry.After apoptotic cells injection, antibody titers of total and IgG3 anti-dsDNA and total anti-histone from serum were significantly increased in Allergin-1-deficient versus WT mice. Phagocytic activity was significantly lower in macrophages from Allergin-1-deficient mice versus WT mice.Allergin-1 might play an inhibitory role in autoantibody production via upregulation of macrophage phagocytosis.
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