Inoue Makoto, Shinohara Mari L
Department of Immunology, Duke University Medical Center, DUMC-3010, Durham, NC 27710, USA.
Autoimmune Dis. 2013;2013:859145. doi: 10.1155/2013/859145. Epub 2013 Jan 8.
Inflammasomes are cytosolic sensors that detect pathogens and danger signals in the innate immune system. The NLRP3 inflammasome is currently the most fully characterized inflammasome and is known to detect a wide array of microbes and endogenous damage-associated molecules. Possible involvement of the NLRP3 inflammasome (or inflammasomes) in the development of multiple sclerosis (MS) was suggested in a number of studies. Recent studies showed that the NLRP3 inflammasome exacerbates experimental autoimmune encephalomyelitis (EAE), an animal model of MS, although EAE can also develop without the NLRP3 inflammasome. In this paper, we discuss the NLRP3 inflammasome in MS and EAE development.
炎性小体是先天性免疫系统中检测病原体和危险信号的胞质传感器。NLRP3炎性小体是目前特征最明确的炎性小体,已知其能检测多种微生物和内源性损伤相关分子。多项研究提示NLRP3炎性小体(或炎性小体)可能参与多发性硬化症(MS)的发病过程。最近的研究表明,NLRP3炎性小体可加重实验性自身免疫性脑脊髓炎(EAE),这是MS的一种动物模型,不过即使没有NLRP3炎性小体,EAE也可能发生。在本文中,我们讨论了NLRP3炎性小体在MS和EAE发病过程中的作用。