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小胶质细胞中S100B与晚期糖基化终末产物受体(RAGE)结合会刺激环氧化酶-2(COX-2)的表达。

S100B binding to RAGE in microglia stimulates COX-2 expression.

作者信息

Bianchi Roberta, Adami Cecilia, Giambanco Ileana, Donato Rosario

机构信息

department of Experimental Medicine and Biochemical Sciences, Sect. Anatomy, University of Perugia, Via del Giochetto C.P. 81 Succ. 3, 06122 Perugia, Italy.

出版信息

J Leukoc Biol. 2007 Jan;81(1):108-18. doi: 10.1189/jlb.0306198. Epub 2006 Oct 5.

Abstract

Besides exerting regulatory roles within astrocytes, the Ca2+-modulated protein of the EF-hand type S100B is released into the brain extracellular space, thereby affecting astrocytes, neurons, and microglia. However, extracellular effects of S100B vary, depending on the concentration attained and the protein being trophic to neurons up to nanomolar concentrations and causing neuronal apoptosis at micromolar concentrations. Effects of S100B on neurons are transduced by receptor for advanced glycation end products (RAGE). At high concentrations, S100B also up-regulates inducible NO synthase in and stimulates NO release by microglia by synergizing with bacterial endotoxin and IFN-gamma, thereby participating in microglia activation. We show here that S100B up-regulates cyclo-oxygenase-2 expression in microglia in a RAGE-dependent manner in the absence of cofactors through independent stimulation of a Cdc42-Rac1-JNK pathway and a Ras-Rac1-NF-kappaB pathway. Thus, S100B can be viewed as an astrocytic endokine, which might participate in the inflammatory response in the course of brain insults, once liberated into the brain extracellular space.

摘要

除了在星形胶质细胞内发挥调节作用外,EF 手型钙结合蛋白 S100B 还会释放到脑细胞外空间,从而影响星形胶质细胞、神经元和小胶质细胞。然而,S100B 的细胞外效应各不相同,这取决于其达到的浓度,该蛋白在纳摩尔浓度时对神经元具有营养作用,而在微摩尔浓度时会导致神经元凋亡。S100B 对神经元的作用是通过晚期糖基化终产物受体(RAGE)转导的。在高浓度时,S100B 还会上调诱导型一氧化氮合酶的表达,并通过与细菌内毒素和γ干扰素协同作用刺激小胶质细胞释放一氧化氮,从而参与小胶质细胞的激活。我们在此表明,在没有辅助因子的情况下,S100B 通过独立刺激 Cdc42-Rac1-JNK 途径和 Ras-Rac1-NF-κB 途径,以 RAGE 依赖的方式上调小胶质细胞中环氧合酶-2 的表达。因此,S100B 可被视为一种星形胶质细胞内源性因子,一旦释放到脑细胞外空间,它可能参与脑部损伤过程中的炎症反应。

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