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连接蛋白 43 C 端结构域在脑卒中时发挥神经保护作用。

The connexin43 C-terminal region mediates neuroprotection during stroke.

机构信息

Department of Cellular and Physiological Sciences, Life Sciences Institute, University of British Columbia, Canada.

出版信息

J Neuropathol Exp Neurol. 2010 Feb;69(2):196-206. doi: 10.1097/NEN.0b013e3181cd44df.

DOI:10.1097/NEN.0b013e3181cd44df
PMID:20084014
Abstract

Connexin43 plays an important role in neuroprotection in experimental stroke models; reducing the expression of this gap junction protein in astrocytes enhances injury upon middle cerebral artery occlusion (MCAO). Because the C-terminal region of connexin43 isimportant for channel activity, we carried out MCAO stroke experiments in mice expressing a truncated form of connexin43 (Cx43DeltaCT mice). Brain sections were analyzed for infarct volume, astrogliosis, and inflammatory cell invasion 4 days after MCAO. Adult cortices and astrocyte cultures were examined for connexin43 (Cx43) expression by immunohistochemistry and Western blot. Cultured astrocytes were also examined for dye coupling, channel conductance, hemichannel activity, and Ca wave propagation. The Cx43DeltaCT mice exhibit enhanced cerebral injury after stroke. Astrogliosis was reduced and inflammatory cell invasion was increased inthe peri-infarct region in these mice compared with controls; Cx43 expression was also altered. Lastly, cultured astrocytes from Cx43DeltaCT mice were less coupled and displayed alterations in channel gating, hemichannel activity, and Ca wave properties. These results suggest that astrocytic Cx43 contributed to the regulation of cell death after stroke and support the view that the Cx43 C-terminal region is important in protection in cerebral ischemia.

摘要

间隙连接蛋白 43(Connexin43,Cx43)在实验性中风模型中具有重要的神经保护作用;减少星形胶质细胞中这种缝隙连接蛋白的表达会加重大脑中动脉闭塞(MCAO)后的损伤。由于 Cx43 的 C 末端区域对于通道活性很重要,我们在表达 Cx43 截断形式的小鼠中进行了 MCAO 中风实验(Cx43DeltaCT 小鼠)。在 MCAO 后 4 天,对脑切片进行梗死体积、星形胶质细胞增生和炎性细胞浸润分析。通过免疫组织化学和 Western blot 检查成年皮质和星形胶质细胞培养物中的 Cx43(Connexin43)表达。还检查了培养的星形胶质细胞中的染料偶联、通道电导、半通道活性和 Ca 波传播。与对照相比,Cx43DeltaCT 小鼠在中风后表现出增强的脑损伤。这些小鼠的梗死周围区域的星形胶质细胞增生减少,炎性细胞浸润增加;Cx43 的表达也发生了改变。最后,来自 Cx43DeltaCT 小鼠的培养星形胶质细胞的偶联减少,并表现出通道门控、半通道活性和 Ca 波特性的改变。这些结果表明,星形胶质细胞的 Cx43 有助于调节中风后的细胞死亡,并支持 Cx43 C 末端区域在脑缺血保护中很重要的观点。

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