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Microgravity-induced programmed cell death in astrocytes

机译:微重力诱导的星形胶质细胞程序性死亡

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Cultured astrocytes were submitted to simulated microgravity using a Fokker clinostat under continuous rotation (60 rpm) for 15', 30', 1h, 20h and 32h. Samples processing included (ⅰ) nuclear stainings using Propidium Iodide and 4,6-diamidino-2-phenilindole, dihydro chloride, (ⅱ) immunohistochemical identification of Caspase-7, (ⅲ) identification of DNA fragmentation using the terminal dUTP nick end labelling and (ⅳ) Scanning Electron Microscope analysis. After 30' at simulated microgravity the glial cells showed morphological evidence of apoptosis: cell shrinkage, chromatin condensation, nuclear blebs and fragmentation. The enzyme caspase-7 was present and DNA fragmentation was evident. After 32h the density of the cell population was much lower than that observed in controls.
机译:在连续旋转(60 rpm)下使用Fokker clinostat将培养的星形胶质细胞置于模拟微重力下15',30',1h,20h和32h。样品处理包括(ⅰ)使用碘化丙啶和4,6-二mid基-2-苯并吲哚,二氢氯化物进行核染色,(ⅱ)Caspase-7的免疫组化鉴定,(ⅲ)使用末端dUTP缺口末端标记鉴定DNA片段和(ⅳ)扫描电子显微镜分析。在模拟微重力作用下30'后,神经胶质细胞显示出凋亡的形态学证据:细胞萎缩,染色质凝集,核泡和碎片。存在caspase-7酶,DNA片段明显。 32小时后,细胞群的密度远低于对照中观察到的密度。

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