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首页> 外文期刊>European journal of neurology: the official journal of the European Federation of Neurological Societies >Gene expression profiling in the human middle cerebral artery after cerebral ischemia.
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Gene expression profiling in the human middle cerebral artery after cerebral ischemia.

机译:脑缺血后人中脑动脉的基因表达谱。

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We have investigated the gene expression in human middle cerebral artery (MCA) after ischemia. Ischemic stroke affects the perfusion in the affected area and experimental cerebral ischemia results in upregulation of vasopressor receptors in the MCA leading to the ischemic area. We obtained human MCA samples distributing to the ischemic area, 7-10 days post-stroke. The gene expression was examined with real-time polymerase chain reaction (PCR) and microarray, proteins were studied with immunohistochemistry.We investigated genes previously shown to be upregulated in animal models of cerebral ischemia (e.g. ET(A), ET(B), AT1, AT2, and 5-HT(2A/1B/1D)). Their mRNA expression was increased compared with controls, consistent with findings in experimental stroke. Immunohistochemistry showed upregulation of the receptors localized on the smooth muscle cells. The gene expression was profiled with microarray and seven genes chosen for further investigation with real-time PCR; ELK3, LY64, Metallothionin IG, POU3F4, Actin alpha2, RhoA and smoothelin. Six of these were regulated the same way when confirming array expression with real-time PCR. Gene expression studies in the human MCA leading to the ischemic region is similar to that seen after MCA occlusion in rats. We found new genes that support the dynamic changes that occur in the MCA distributing to the ischemic region.
机译:我们已经研究了缺血后人大脑中动脉(MCA)中的基因表达。缺血性中风会影响患处的血流灌注,实验性脑缺血会导致MCA中导致血管局部缺血的血管升压受体上调。我们在中风后7-10天获得了分布到缺血区域的人MCA样品。通过实时聚合酶链反应(PCR)和微阵列检查基因表达,通过免疫组织化学研究蛋白质。我们调查了先前显示在脑缺血动物模型中被上调的基因(例如ET(A),ET(B), AT1,AT2和5-HT(2A / 1B / 1D))。与对照组相比,它们的mRNA表达增加,与实验性卒中的发现一致。免疫组织化学显示位于平滑肌细胞上的受体的上调。用微阵列分析基因表达,并选择七个基因用于实时PCR的进一步研究。 ELK3,LY64,金属硫蛋白IG,POU3F4,肌动蛋白alpha2,RhoA和Smoothelin。当通过实时PCR确认阵列表达时,对其中的六个进行了相同的调节。导致缺血区域的人MCA中的基因表达研究与大鼠MCA闭塞后所见相似。我们发现新的基因支持MCA分布到缺血区域的动态变化。

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