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中枢神经系统革兰氏阳性菌感染模型中的神经退行性变。

Neurodegeneration in models of Gram-positive bacterial infections of the central nervous system.

作者信息

Neher J J, Brown G C

机构信息

Department of Biochemistry, University of Cambridge, Downing Site, Tennis Court Road, Cambridge CB2 1QW, U.K.

出版信息

Biochem Soc Trans. 2007 Nov;35(Pt 5):1166-7. doi: 10.1042/BST0351166.

Abstract

Gram-positive bacterial infections of the central nervous system, such as meningitis, induce an extensive inflammatory response, which in turn may damage neurons. LTA (lipoteichoic acid) is a component of the Gram-positive bacterial cell wall that induces glial inflammatory activation in vitro and in vivo. It does so by binding to Toll-like receptor-2 on microglia and astrocytes, rapidly activating ERK1/2 (extracellular-signal-regulated kinase 1/2) and p38 MAPKs (mitogen-activated protein kinases), causing NF-kappaB (nuclear factor kappaB) activation and leading to the production of pro-inflammatory cytokines and expression of inducible nitric oxide synthase (in synergy with muramyl dipeptide). LTA-activated microglia kill co-cultured neurons apparently via nitric oxide, superoxide and peroxynitrite, which may induce apoptosis of neurons that are then phagocytosed by microglia.

摘要

革兰氏阳性菌引起的中枢神经系统感染,如脑膜炎,会引发广泛的炎症反应,进而可能损害神经元。脂磷壁酸(LTA)是革兰氏阳性菌细胞壁的一种成分,在体外和体内均可诱导胶质细胞发生炎症激活。它通过与小胶质细胞和星形胶质细胞上的Toll样受体2结合来实现这一点,迅速激活细胞外信号调节激酶1/2(ERK1/2)和p38丝裂原活化蛋白激酶(MAPKs),导致核因子κB(NF-κB)激活,并引发促炎细胞因子的产生以及诱导型一氧化氮合酶的表达(与胞壁酰二肽协同作用)。LTA激活的小胶质细胞显然通过一氧化氮、超氧化物和过氧亚硝酸盐杀死共培养的神经元,这些物质可能诱导神经元凋亡,随后被小胶质细胞吞噬。

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