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NLRP3炎症小体在MS/EAE发病机制中的作用及其靶向治疗
引用本文:杨一凡,刘立丽,聂作明,吕正兵,王丹. NLRP3炎症小体在MS/EAE发病机制中的作用及其靶向治疗[J]. 中国病理生理杂志, 2020, 0(1): 181-187
作者姓名:杨一凡  刘立丽  聂作明  吕正兵  王丹
作者单位:浙江理工大学浙江省家蚕生物反应器与生物医药重点实验室;浙江理工大学生命科学与医药学院
基金项目:浙江省公益技术研究计划社会发展项目(No.LGF19H250002);国家自然科学基金资助项目(No.31772677);浙江理工大学科研启动基金资助项目(No.16042187-Y)
摘    要:<正>多发性硬化症(multiple sclerosis,MS)是由免疫细胞攻击中枢神经系统(central nervous system,CNS)而造成的一种自身免疫性疾病,其具有神经元脱髓鞘、神经胶质细胞增生和轴突损伤等病理特征[1]。NLRP3炎症小体作为一种能识别病原体和危险信号的传感器,近年来被发现与许多自身免疫性疾病的发病关系密切[2]。本文从NLRP3炎症小体激活的主要途径出发,综述了NLRP3炎症小体在MS及其动物模型——实验

关 键 词:NLRP3炎症小体  多发性硬化症  实验性自身免疫性脑脊髓炎

NLRP3 inflammasome in pathogenesis of MS/EAE and its targeted therapy
YANG Yi-fan,LIU Li-li,NIE Zuo-ming,LV Zheng-bing,WANG Dan. NLRP3 inflammasome in pathogenesis of MS/EAE and its targeted therapy[J]. Chinese Journal of Pathophysiology, 2020, 0(1): 181-187
Authors:YANG Yi-fan  LIU Li-li  NIE Zuo-ming  LV Zheng-bing  WANG Dan
Affiliation:(Zhejiang Provincial Key Laboratory of Silkworm Bioreactor and Biomedicine,Zhejiang Sci-Tech University,Hangzhou 310018,China;College of Life Sciences and Medicine,Zhejiang Sci-Tech University,Hangzhou 310018,China)
Abstract:Inflammasomes,the important component of innate immune system,play an important role in inflammatory diseases.NLRP3,the most studied inflammasome,is activated after recognizing danger-associated molecular patterns and pathogen-associated molecular patterns.The activated NLRP3 inflammasome promotes inflammation by maturation and release of the pro-inflammatory cytokines interleukin(IL)-1βand IL-18.Involvement of the NLRP3 inflammasome in the development of multiple sclerosis(MS)and experimental autoimmune encephalomyelitis(EAE)was suggested in a number of studies.Therefore,targeting on NLRP3 inflammasome is one of the promising methods for treatment of related diseases.In this review,we summarize the main ways by which the NLRP3 inflammasome is activated in the cytosol.We also discuss the development and treatment of NLRP3 inflammasome in MS and EAE,and expect to provide reference for the treatment of MS.
Keywords:NLRP3 inflammasome  Multiple sclerosis  Experimental autoimmune encephalomyelitis
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