Interferon-inducible immunity-related GTPase Irgm1 regulates IFNγ-dependent host defense, lymphocyte survival and autophagy

被引:42
作者
Feng, Carl G. [1 ]
Zheng, Lixin [2 ]
Lenardo, Michael J. [2 ]
Sher, Alan
机构
[1] NIAID, Immunobiol Sect, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
关键词
autophagy; cell death; IFN gamma; Th1; lymphocyte homeostasis; GTPase; Irgm1; CELL-DEATH; INTRACELLULAR PATHOGENS; MICE DEFICIENT; P47; GTPASES; LRG-47; PROLIFERATION; TUBERCULOSIS; RESISTANCE;
D O I
10.4161/auto.5.2.7445
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
IFN gamma is a pleiotropic cytokine that plays a key role in host resistance, yet when not properly regulated can become detrimental to the host. The interferon-inducible Immunity Related GTPase family M member I (Irgm1), previously characterized as an effector molecule required for macrophage microbicidal activity has been shown recently to control IFN gamma-dependent cell survival and host resistance. Irgm1 regulates the expansion/survival of mature effector CD4(+) T lymphocytes by protecting them from IFN gamma-induced autophagic cell death. Importantly, mice deficient in both IFN gamma and Irgm1 were rescued from the lymphocyte depletion and increased mortality that typically occurs in Irgm1(-/-) animals following pathogen exposure. We propose that Irgm1 plays a major role in maintaining T lymphocyte homeostasis during host IFN gamma responses by protecting these cells from autophagy-dependent cell death.
引用
收藏
页码:232 / 234
页数:3
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