Apoptotic cells inhibit LPS-induced cytokine and chemokine production and IFN responses in macrophages

被引:42
作者
Tassiulas, Ioannis
Park-Min, Kyung-Hyun
Hu, Yang
Kellerman, Lisa
Mevorach, Dror
Ivashkiv, Lionel B.
机构
[1] Hosp Special Surg, Arthrit & Tissue Degenerat Program, New York, NY 10021 USA
[2] Hosp Special Surg, Dept Med, New York, NY 10021 USA
[3] Cornell Univ, Weill Grad Sch Med Sci, Grad Program Immunol & Microbial Pathogenesis, New York, NY 10021 USA
[4] Hadassah Hebrew Univ Hosp, Dept Med, Rheumatol Unit, Cellular & Mol Immunol Lab, IL-91120 Jerusalem, Israel
[5] Hebrew Univ Jerusalem, IL-91120 Jerusalem, Israel
关键词
autoimmunity; inflammation; signaling; interferon; STAT;
D O I
10.1016/j.humimm.2006.12.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Apoptosis is a critical process in tissue homeostasis and results in immediate removal of the dying cell by professional phagocytes such as macrophages and dendritic cells. Phagocytosis of apoptotic cells actively suppresses production of proinflarnmatory growth factors and cytokines. Impaired phagocytosis of apoprotic cells has been implicated in the pathogenesis of chronic inflammatory and autoimmune diseases. In this study we found that, in addition to suppressing lipopolysaccharide (LPS)-induced production of TNF-alpha and IL-6, phagocytosis of apoptotic cells by macrophages suppressed production of the chemokine CXCL10 that is activated by LPS-induced autocrine-acting type I IFNs. Inhibition of cytokine and chemokine production was not universally affected because LPS-induced production of IL-10 and IL-8 was not significantly affected. Apoptotic cells had minimal effects on LPS-induced activation of NF-kappa B and MAPKs, but induced expression of SOCS proteins and substantially suppressed induction of CXCL10 expression by IFN-alpha. In addition to suppressing LPS responses, apoptotic cells inhibited macrophage responses to another major macrophage activator IFN-gamma by attenuating IFN-gamma-induced STAT1 activation and downstream gene expression. These results identify suppressive effects of apoptotic cells on signal transduction, and extend our understanding of the anti-inflammatory effects of apoptotic cells to include suppression of Jak-STAT signaling.
引用
收藏
页码:156 / 164
页数:9
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