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首页> 外文期刊>Clinical hemorheology and microcirculation >Down-regulation of hepatocyte growth factor mRNA in rat cardiac myocytes under hypoxia mimicked by cobalt chloride.
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Down-regulation of hepatocyte growth factor mRNA in rat cardiac myocytes under hypoxia mimicked by cobalt chloride.

机译:氯化钴模拟的低氧条件下大鼠心肌细胞中肝细胞生长因子mRNA的下调。

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摘要

Hypoxia is generally considered to represent a fundamental stimulus for angiogenesis. Most angiogenic factors were up-regulated by hypoxia, but as a strong angiogenic and antiapoptotic factor, hepatocyte growth factor (HGF) was down-regulated by hypoxia. In order to investigate whether hypoxia inducible factor 1a (HIF-1alpha) participate in the transcriptional regulation of HGF under hypoxia, rat cardiac myocytes were treated with cobalt chloride (CoCl2), the specific inducer of HIF-1alpha, for different times, and total RNA and protein were isolated to perform RT-PCR and Western blot. Results show the expression of HGF mRNA in cardiac myocytes decreased distinctively after treating with CoCl2 for 12 hours. However, at the same time, the expression of HIF-1alpha protein was up-regulated. HIF-1alpha may be participate in the transcriptional regulation of HGF indirectly.
机译:低氧通常被认为是血管生成的基本刺激。缺氧可上调大多数血管生成因子,但缺氧下调肝细胞生长因子(HGF)作为强血管生成和抗凋亡因子。为了研究缺氧条件下低氧诱导因子1a(HIF-1alpha)是否参与HGF的转录调控,分别用HIF-1alpha的特异性诱导剂氯化钴(CoCl2)处理大鼠心肌细胞不同时间和总量。分离RNA和蛋白质以进行RT-PCR和蛋白质印迹。结果显示,用CoCl2处理12小时后,心肌细胞中HGF mRNA的表达明显下降。但是,与此同时,HIF-1α蛋白的表达被上调。 HIF-1alpha可能间接参与HGF的转录调控。

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