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脑刺伤处的小胶质细胞表达连接蛋白43,在经γ干扰素和肿瘤坏死因子-α处理后,在体外形成功能性缝隙连接。

Microglia at brain stab wounds express connexin 43 and in vitro form functional gap junctions after treatment with interferon-gamma and tumor necrosis factor-alpha.

作者信息

Eugenín E A, Eckardt D, Theis M, Willecke K, Bennett M V, Saez J C

机构信息

Departamento de Ciencias Fisiológicas, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago 340, Chile.

出版信息

Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):4190-5. doi: 10.1073/pnas.051634298. Epub 2001 Mar 20.

Abstract

Gap junctional communication between microglia was investigated at rat brain stab wounds and in primary cultures of rat and mouse cells. Under resting conditions, rat microglia (FITC-isolectin-B4-reactive cells) were sparsely distributed in the neocortex, and most (95%) were not immunoreactive for Cx43, a gap junction protein subunit. At brain stab wounds, microglia progressively accumulated over several days and formed aggregates that frequently showed Cx43 immunoreactivity at interfaces between cells. In primary culture, microglia showed low levels of Cx43 determined by Western blotting, diffuse intracellular Cx43 immunoreactivity, and a low incidence of dye coupling. Treatment with the immunostimulant bacterial lipopolysaccharide (LPS) or the cytokines interferon-gamma (INF-gamma) or tumor necrosis factor-alpha (TNF-alpha) one at a time did not increase the incidence of dye coupling. However, microglia treated with INF-gamma plus LPS showed a dramatic increase in dye coupling that was prevented by coapplication of an anti-TNF-alpha antibody, suggesting the release and autocrine action of TNF-alpha. Treatment with INF-gamma plus TNF-alpha also greatly increased the incidence of dye coupling and the Cx43 levels with translocation of Cx43 to cell-cell contacts. The cytokine-induced dye coupling was reversibly inhibited by 18 alpha-glycyrrhetinic acid, a gap junction blocker. Cultured mouse microglia also expressed Cx43 and developed dye coupling upon treatment with cytokines, but microglia from homozygous Cx43-deficient mice did not develop significant dye coupling after treatment with either INF-gamma plus LPS or INF-gamma plus TNF-alpha. This report demonstrates that microglia can communicate with each other through gap junctions that are induced by inflammatory cytokines, a process that may be important in the elaboration of the inflammatory response.

摘要

在大鼠脑刺伤处以及大鼠和小鼠细胞的原代培养物中,研究了小胶质细胞之间的缝隙连接通讯。在静息条件下,大鼠小胶质细胞(FITC-异凝集素B4反应性细胞)稀疏分布于新皮层,且大多数(95%)对缝隙连接蛋白亚基Cx43无免疫反应性。在脑刺伤处,小胶质细胞在数天内逐渐聚集并形成聚集体,这些聚集体在细胞间界面处常显示Cx43免疫反应性。在原代培养中,通过蛋白质印迹法测定,小胶质细胞显示出低水平的Cx43、弥漫性细胞内Cx43免疫反应性以及低发生率的染料偶联。一次用免疫刺激剂细菌脂多糖(LPS)、细胞因子干扰素-γ(INF-γ)或肿瘤坏死因子-α(TNF-α)处理,并未增加染料偶联的发生率。然而,用INF-γ加LPS处理的小胶质细胞显示染料偶联显著增加,而同时应用抗TNF-α抗体可阻止这种增加,提示TNF-α的释放和自分泌作用。用INF-γ加TNF-α处理也极大地增加了染料偶联的发生率以及Cx43水平,且Cx43转位至细胞-细胞接触部位。细胞因子诱导的染料偶联可被缝隙连接阻滞剂18α-甘草次酸可逆性抑制。培养的小鼠小胶质细胞也表达Cx43,并在用细胞因子处理后形成染料偶联,但来自纯合Cx43缺陷小鼠的小胶质细胞在用INF-γ加LPS或INF-γ加TNF-α处理后未形成显著的染料偶联。本报告表明,小胶质细胞可通过炎症细胞因子诱导的缝隙连接相互通讯,这一过程在炎症反应的形成中可能很重要。

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