Innate immune responses regulate morphogenesis and degeneration: roles of Toll-like receptors and Sarm1 in neurons

被引:42
作者
Liu, Hsin-Yu [1 ,2 ]
Chen, Chiung-Ya [1 ]
Hsueh, Yi-Ping [1 ,2 ]
机构
[1] Acad Sinica, Inst Mol Biol, Taipei 115, Taiwan
[2] Natl Def Med Ctr, Grad Inst Life Sci, Taipei 114, Taiwan
关键词
axon; cytokines; dendrite; innate immunity; interleukin-6; Sarm1; toll-like receptor; NEGATIVE REGULATOR; ACTIVATION; PROTEIN; TLR7; NEURODEGENERATION; EXPRESSION; INFECTION; CELLS; DEATH; NEUROFIBROMIN;
D O I
10.1007/s12264-014-1445-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The central nervous system is recognized as an immunoprivileged site because peripheral immune cells do not typically enter it. Microglial cells are thought to be the main immune cells in brain. However, recent reports have indicated that neurons express the key players of innate immunity, including Toll-like receptors (TLRs) and their adaptor proteins (Sarm1, Myd88, and Trif), and may produce cytokines in response to pathogen infection. In the absence of an immune challenge, neuronal TLRs can detect intrinsic danger signals and modulate neuronal morphology and function. In this article, we review the recent findings on the involvement of TLRs and Sarm1 in controlling neuronal morphogenesis and neurodegeneration. Abnormal behaviors in TLR- and Sarm1-deficient mice are also discussed.
引用
收藏
页码:645 / 654
页数:10
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