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可逆性脑缺血后大鼠脑中膜联蛋白A3上调异构体的蛋白质组学鉴定

Proteomic identification of an upregulated isoform of annexin A3 in the rat brain following reversible cerebral ischemia.

作者信息

Junker Heike, Suofu Yalikun, Venz Simone, Sascau Magdalena, Herndon James G, Kessler Christof, Walther Reinhard, Popa-Wagner Aurel

机构信息

Molecular Neurobiology Laboratory, Clinic of Neurology, Ernst-Moritz-Arndt-University, Greifswald, Germany.

出版信息

Glia. 2007 Dec;55(16):1630-7. doi: 10.1002/glia.20581.

Abstract

We used proteomics to identify regulated proteins following cerebral ischemia in a rat model. Young rats were subjected to reversible middle cerebral artery (MCA) occlusion and proteins were extracted from the peri-infarcted and the corresponding contralateral area at days 3 and 14 postischemia. Proteins were analyzed by two-dimensional polyacrylamide gel electrophoresis followed by mass spectrometry. We report for the first time that an isoform of annexin A3 (ANXA3) was among the upregulated proteins in the postischemic rat brain. The results were confirmed by real-time PCR and by western blotting. Double- and triple-immunostaining with neuronal and microglia/macrophagic markers demonstrated that ANXA3 is produced by resting microglia in control tissue and by activated microglial/macrophage cells in the infarcted area. 3D-images of the infarcted area suggest that ANXA3 is associated with a phagocytic phenotype. Our study identifies ANXA3 as a novel marker of brain microglia, which should be of substantial value in future studies of microglial cells and its role in the postischemic brain.

摘要

我们运用蛋白质组学技术,在大鼠模型中鉴定脑缺血后发生调控的蛋白质。对幼年大鼠实施可逆性大脑中动脉(MCA)闭塞,在缺血后第3天和第14天,从梗死灶周围区域和相应的对侧区域提取蛋白质。通过二维聚丙烯酰胺凝胶电泳,随后进行质谱分析来分析蛋白质。我们首次报道,膜联蛋白A3(ANXA3)的一种亚型是缺血后大鼠脑中上调的蛋白质之一。通过实时PCR和蛋白质印迹法证实了该结果。用神经元和小胶质细胞/巨噬细胞标志物进行双重和三重免疫染色表明,在对照组织中,静息小胶质细胞产生ANXA3,而在梗死区域,活化的小胶质细胞/巨噬细胞产生ANXA3。梗死区域的三维图像表明,ANXA3与吞噬表型相关。我们的研究将ANXA3鉴定为脑小胶质细胞的一种新型标志物,这在未来关于小胶质细胞及其在缺血后脑中作用的研究中应具有重要价值。

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