小胶质细胞极化在多发性硬化发病中的作用机制研究进展
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国家自然科学基金项目(81273497,81301208);北京市卫生系统高层次卫生技术人才-学科骨干(2014-3-052)。


Advances in research of the role of microglia polarization in the mechanisms of pathogenesis of multiple sclerosis
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    摘要:

    多发性硬化(multiple sclerosis,MS)是一种以中枢神经系统(central nervous system,CNS)炎症反应和髓鞘脱失为主要病理特征的自身免疫性疾病,具有青壮年高发、致残率高等特点,具体发病机制尚不明确。研究发现,MS发病时CNS固有的免疫细胞-小胶质细胞向促炎态M1型极化,导致体内小胶质细胞M1/M2比率失衡,形成CNS促炎态的微环境,损害神经组织。受损神经组织进一步促进小胶质细胞极化,构成恶性循环,最终加重病情。小胶质细胞极化状态失衡是启动MS的关键病因,为此,本文将综述近年来国内外小胶质细胞在MS发病中作用机制的研究进展,旨在为进一步阐明MS发病机制及寻找潜在的治疗靶点提供借鉴。

    Abstract:

    Multiple sclerosis (MS) is an autoimmune disease of the central nervous system (CNS) characterized by demyelination and inflammation lesions. MS predominantly affects young adults with a high incidence of disability. However, the exact pathogenesis of MS is still not clear. Studies found that microglia polarization tending to pro-inflammatory M1-like state during the onset of MS, causing the M1/M2 ratio imbalance, forming pro-inflammatory microenvironment state, and which further leading to nervous tissue damage ultimately. Microglia polarization may be considered as the initiator of pathologic alterations by releasing pro-inflammatory cytokines and secondarily trigger the initial microglia response. Given the pivotal role of imbalanced microglia polarization in MS initiation, a critical review of microglia polarization is presented here, in order to elucidate the pathogenesis of MS and highlight the noteworthy candidate therapeutic targets for clinic treatment.

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张明,刘江红,洪浩,尹琳琳.小胶质细胞极化在多发性硬化发病中的作用机制研究进展[J].中国比较医学杂志,2016,26(4):79~82.

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  • 最后修改日期:2015-12-29
  • 在线发布日期: 2016-04-28
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