Regulation of Interleukin-10 Gene Expression in Macrophages Engulfing Apoptotic Cells

被引:31
作者
Zhang, Yan [1 ]
Kim, Ha-Jeong [1 ]
Yamamoto, Soichiro [1 ]
Kang, Xiaoyan [1 ]
Ma, Xiaojing [1 ,2 ,3 ]
机构
[1] Cornell Univ, Weill Med Coll, Dept Microbiol & Immunol, New York, NY 10065 USA
[2] Cornell Univ, Weill Med Coll, Dept Pediat, New York, NY 10065 USA
[3] Cornell Univ, Weill Grad Sch Med Sci, Program Immunol & Microbial Pathogenesis, New York, NY 10065 USA
关键词
SINGLE-NUCLEOTIDE POLYMORPHISMS; SYSTEMIC-LUPUS-ERYTHEMATOSUS; TUMOR-NECROSIS-FACTOR; ARREST-SPECIFIC GENE; POLY(ADP-RIBOSE) POLYMERASE; IL-10; PROMOTER; CYTOKINE PRODUCTION; INFLAMMATORY RESPONSE; RECEPTOR ANTAGONIST; AUTOANTIBODY LEVELS;
D O I
10.1089/jir.2010.0004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis and the rapid clearance of apoptotic cells (ACs) by professional or nonprofessional phagocytes are normal and coordinated processes that ensure controlled cell growth and stress response with nonpathological outcomes. Uptake of ACs by phagocytes is thought to suppress autoimmune responses through the release of anti-inflammatory cytokines such as interleukin-10 (IL-10), transforming growth factor-beta (TGF-beta), and inhibition of proinflammatory cytokines. The production of pro-and anti-inflammatory cytokines by phagocytes is highly regulated as part of an intrinsic mechanism to prevent inflammatory and autoimmune reactions in a physiological state. Production of IL-10 by phagocytes during clearance of ACs is critical to ensuring cellular homeostasis and suppression of autoimmunity. The molecular mechanism whereby IL-10 production is induced by ACs is only beginning to be understood. This review summarizes our recent work in this aspect of an essential physiological and homeostatic process.
引用
收藏
页码:113 / 121
页数:9
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