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血小板源性生长因子下调肌浆网Ca^(2+)-ATP酶促进人气道平滑肌细胞表型转化

Platelet derived growth factor down-regulated sarcoplasmic reticulum Ca^(2+) atpase to promote the phenotype modulation of human airway smooth muscle cells
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摘要 目的:探讨肌浆网Ca^(2+)-ATP酶(SERCA2)对人气道平滑肌细胞(cells,HASMCs)表型转化的作用及其机制。方法 :原代培养HASMCs并饥饿5 d后进行分组,分别从显微镜下检测细胞的形态变化、采用Western Blot检测a-actin、SERCA2及ERK通路蛋白的变化、CCK-8检测各组细胞的增殖状态。结果 :与对照组相比,PDGF刺激后可诱导HASMCs收缩蛋白表达减少、增殖能力增加,TSG可显著抑制其作用(P<0.01);PDGF显著抑制SERCA2并促进磷酸化ERK的表达(P<0.01),U0126显著抑制了上述效应(P<0.01)。结论 :PDGF可能通过调节肌浆网Ca^(2+)-ATP酶及ERK通路蛋白的表达诱导HASMCs表型转化。 Objective To investigate of the effect and mechanisman of SERCA2 on the phenotype modulation of HASMCs. Methods HASMCs were starved for 5 days and divided into different groups,then we observed morphology change of the cells from the microscope and detected a-actin,SERCA2 and p-ERK by Western Blot,cells proliferation was observed by CCK-8 method. Results Compared with the control group,PDGF could reduce a-actin of HASMCs and increased the cells proliferation ability,TSG could significantly inhibit the effect (P 〈 0.01), PDGF could also significantly inhibit SERCA2 protein and increased the expression p-ERK (P 〈 0.01), while U0126 significantly inhibited the effect (P 〈 0.01 ). Conclusion PDGF may induce HASMCs phenotype modulation through the regulation of SERCA2 and p-ERK.
出处 《实用医学杂志》 CAS 北大核心 2016年第13期2133-2137,共5页 The Journal of Practical Medicine
基金 广东省自然科学基金资助项目(编号:s2012010009036) 南方医院院长基金资助项目(编号:2014A001)
关键词 人气道平滑肌细胞 细胞表型 肌浆网CA^2+-ATP酶 ERK通路 Human airway smooth muscle cells Cell phenotype Sarcoplasmic reticulum Ca^2+ atpase ERK pathway
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