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Expression and localization of Fas-associated proteins following focal cerebral ischemia in rats.

机译:大鼠局灶性脑缺血继局灶性脑缺血后Fas相关蛋白的表达与定位。

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The aim of this study was to investigate the changes of expression of Fas-associated proteins and its cellular localization in the peri-infarct region following transient focal cerebral ischemia. Adult male Sprague-Dawley rats underwent right middle cerebral artery occlusion (MCAo) for 2 h and reperfusion for 1, 3, 6, 12 and 24 h. The expression of Fas-associated death domain protein (FADD), Fas-associated phosphatase-1 (FAP-1) caspase-8 and death-associated protein (Daxx), the pro-apoptotic genes, were examined by methods of RT-PCR, immunohistochemistry and Western blot. The results showed that the expression levels of mRNA and protein for FADD and caspase-8 increased significantly at 1-3 h after reperfusion, peaked at 12 h, then declined markedly at 24 h. The time course change of FAP-1 was consistent with that of FADD. The expression level of mRNA and protein for death-associated protein (Daxx) increased significantly at 3 h after reperfusion and persisted for 24 h at a high level. Immunofluorescence double-staining laser scanning showed that the immunoreactivity of FADD was localized in cytoplasm, and Daxx immunoreactivity was translocated from nucleus to cytoplasm at 3 h after reperfusion. The TUNEL-positive cells could be found in peri-infarct region at 3 h and increased with time after reperfusion. Our findings suggest a possible association between expression of FADD, caspase-8, Daxx and FAP-1 genes and apoptosis following ischemia.
机译:本研究的目的是探讨瞬时焦点脑缺血后PERI-INFARCT区域中FAS相关蛋白质表达及其细胞定位的变化。成年男性Sprague-Dawley大鼠接受右中脑动脉闭塞(MCAO),2小时,再灌注1,3,6,12和24小时。通过RT-PCR的方法检查Fas相关的死亡结构域蛋白(FADD),Fas相关的磷酸酶-1(FAP-1)Caspase-8和死亡相关蛋白(Daxx)的促凋亡基因的表达,免疫组化和蛋白质印迹。结果表明,在再灌注后,FADD和Caspase-8的mRNA和蛋白的表达水平在1-3小时内显着增加,12小时达到峰值,然后在24小时下显着下降。 FAP-1的时间过程变化与FADD的时间变化一致。在再灌注后3小时,死亡相关蛋白(Daxx)的mRNA和蛋白的表达水平显着增加,并且在高水平下持续24小时。免疫荧光双染力激光扫描表明,在再灌注后,FADD的免疫反应性在细胞质中定位在细胞质中,并且在再灌注后3小时将Daxx免疫反应性从核转移到细胞质。可以在3小时的Peri-Infarct区域中发现TUNEL阳性细胞并随着再灌注后的时间而增加。我们的研究结果表明FADD,Caspase-8,Daxx和FAP-1基因表达与缺血后凋亡之间的可能关联。

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