文章摘要
单冬凯 邹路路 宋晓伟 赵仙先 荆清.小鼠不同组织及缺氧损伤后的大鼠心肌细胞中RIP3的表达[J].,2014,14(16):3001-3004
小鼠不同组织及缺氧损伤后的大鼠心肌细胞中RIP3的表达
Expression Profile of Receptor Interacting Protein 3 in Different MouseTissues and Rat's Myocardial Cells with Hypoxia Injury
  
DOI:
中文关键词: 丝氨酸/ 苏氨酸蛋白激酶家族  心肌细胞  缺氧  坏死
英文关键词: Receptor interacting proteins(RIPs)  Myocardial cells  Hypoxia  Necrosis
基金项目:国家自然科学基金项目(81130005,31100830)
作者单位
单冬凯 邹路路 宋晓伟 赵仙先 荆清 第二军医大学长海医院心血管内科 
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中文摘要:
      目的:检测小鼠组织中受体相互作用丝氨酸/ 苏氨酸蛋白激酶家族(RIPs)表达谱,并检测RIP3 在大鼠心肌细胞缺氧损伤后 的表达。方法:① 采用荧光实时定量PCR 分别检测RIPs家族基因在小鼠组织(心、肝、肺、肾、脑、小肠、骨骼肌、脾和主动脉)中的 mRNA 表达谱,并采用Western blot进一步检测RIP3 在小鼠组织的蛋白表达谱。② 将培养的大鼠心肌细胞分为缺氧组和对照 组,缺氧组置于缺氧环境中培养48 h,采用western blot 检测其中RIP3 的表达变化。结果:① mRNA水平:RIP1 mRNA在脑组织 中表达最高,心脏、肺、肾、骨骼肌较低;RIP2在心脏和肺表达量较其他组织高;RIP3在肠中表达较其他组织高出4 倍以上,脑组 织中未检测到RIP3 表达;RIP4 的表达以肺最高,而骨骼肌、脑和血管中表达量低。② 蛋白水平:在小鼠组织中,RIP3 表达以脑、骨 骼肌中最高,心脏、肝、肺中表达较低。③ 培养的大鼠心肌细胞中,缺氧组心肌细胞的RIP3 表达量显著高于对照组(P<0.05)。结论: RIPs在小鼠组织中呈现差异表达,而在培养的大鼠心肌细胞缺氧损伤后RIP3表达升高。
英文摘要:
      Objective: To detect the expression profile of receptor interacting proteins (RIPs) in mouse tissues, and to detect the expression of RIP3 in rat's myocardial cells with hypoxia injury.Methods:① We detected the expression profile of RIPs family in mouse tissues (heart, liver, lung, kidney, brain, intestine, skeletal muscles, spleen and aorta) by real-time fluorescent quantitative PCR, then detected the expression profile of RIP3 protein. ② The myocardial cells of rat were divided into hypoxia group and control. We treated the first group for 48 h on hypoxia to obtain hypoxia injured models, then quantitated the expression of RIP3 by western blot.Results:① On mRNA level, the expression of RIP1 was highest in brain, but lower in heart, lung, kidney and skeletal muscle; the expression of RIP2 was higher in heart and lung than other tissues; RIP3 in the intestine was 4 times higher than other, but it was very low expression in brain; the expression of RIP4 was highest in lung, and was lowest in skeletal muscle, brain, spleen, and vessel. ② Western blot results showed the expression of RIP3 at protein level. It was higher expressed in brain, skeletal muscle, however, lower in heart, liver and lung. ③ After treated on hypoxia, RIP3 of hypoxia group was significantly higher than control in the cultured rat myocardial cell (P<0.05).Conclusion:The expression of RIPs represented various level in mouse tissues. RIP3 increased in rat myocardial cells under hypoxia injured condition.
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