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出 处:《医学研究杂志》2015年第5期111-113,共3页Journal of Medical Research
摘 要:目的建立PDGF-BB诱导的原代大鼠肺动脉平滑肌细胞(pulmonary vascular smooth musclecells,PASMCs)的增殖细胞模型,通过AMPK激动剂AICAR干预,探讨AICAR对PASMCs细胞周期和增殖的影响及其机制,为肺血管重构防治寻找靶点。方法通过20ng/mlPDGF-BB刺激诱导PASMCs增殖建立细胞模型,采用AICAR(0.5mmol/L)干预PDGF-BB诱导的PASMCs增殖,Westernblot法检测总的和磷酸化的AMPK,CCK-8检测PASMCs增殖,流式细胞仪分析细胞周期,实时定量PCR(RT-PCR)检测cyclinDl、cyclinE、CDK2/4/6mRNA的表达。结果Westernblot法检测表明AICAR可以活化AMPK,CCK-8检测结果表明AICAR能够抑制PDGF-BB诱导的PASMCs增殖;流式细胞仪检测结果表明AICAR能够抑制细胞周期于G0/G1期,RT-PCR结果表明AICAR可以抑制cyclinDl、cyclinE、CDK2、CDK4和CDK6的mRNA的表达。结论AICAR通过抑制cy-clinDl、cyclinE、CDK2/4/6的mRNA表达阻滞细胞周期于G0/G1-S期,抑制PASMCs增殖。Objective To establish the PDGF -BB -induced proliferation of rat pulmonary artery smooth muscle cells(PAbMGs) , and investigate the effects of the AMPK agonist AICAR on the cell cycle of PASMCs, in order to search new drugs for prevention of pulmo- nary vascular remodeling. Methods 20ng/ml PDGF - BB was used to induced the proliferation of PASMCs, and the effect of 0.5mmol/ L AICAR on the proliferation of PASMCs was observed. Western blot was used to detect the total and phosphorylated AMPK. The prolifer- ation of PASMCs was determined by CCK - 8. The mRNA expression of cyclinD1, cyclinE and CDK2/4/6 were detected by flow cytome- try analysis cell cycle, quantitative real - time PCR. Results Western blot results indicated AICAR could promote the activation of AMPK. CCK - 8 test results showed that AICAR blocked the proliferation of PASMCs induced by PDGF - BB. Flow cytometry analysis in- dicated that AICAR arrested the cell cycle in G0/G1 to S phase. RT - PCR results demonstrated that AICAR inhibited the mRNA expres- sion of cyclinD1, cyclinE and CDK2/4/6. Conclusion The AMPK agonist AICAR can block the proliferation of PASMCs induced through arrest cell cycle in Go/G1 - S phase by regulation the mRNA expression of cyclin D1, cyclinE, CDK2/4/6, and AICAR has a po- tential application in preventing pulmonary vascular remodeling.
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