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作 者:朱焕勉 陈然[1] 薛峰[1] 申屠杨萍[1] 范小芳[1] 龚永生[1] 张宏宇[2] 孔晓霞[1]
机构地区:[1]温州医科大学基础医学院低氧医学研究所 [2]温州医科大学药学院,浙江温州325035
出 处:《中国应用生理学杂志》2014年第1期8-12,共5页Chinese Journal of Applied Physiology
基 金:国家自然科学基金资助项目(81200010;81200958);浙江省自然科学基金资助项目(LY12H01003)
摘 要:目的:探讨自噬抑制剂氯喹(CQ)在低氧(hypoxia)调节肺动脉平滑肌细胞(PASMCs)增殖中的作用。方法:将体外培养的大鼠PASMCs分为4组:正常对照组、1%低氧组、50μmol/L氯喹+1%低氧组、50μmol/L氯喹组。MTT方法检测各组的PASMCs增殖率;MDC染色检测细胞自噬空泡的变化;Western blot方法检测微管相关蛋白轻链3(LC3)蛋白的表达变化;划痕法检测细胞迁移的变化。结果:与对照组比较,氯喹组的PASMCs细胞增殖率无明显变化。与对照组比较,1%低氧组PASMCs增殖率明显增加,细胞内出现大量自噬空泡,细胞迁移速度明显增加。细胞LC3-II蛋白表达增强。与1%低氧组比较,氯喹与低氧联合作用时细胞自噬空泡的积聚以及LC3-II蛋白表达增强,但细胞增殖率和迁移明显降低。结论:低氧激活自噬过程并促进了PASMCs增殖和迁移,而自噬抑制剂氯喹在一定程度上通过抑制自噬进程,达到抑制肺动脉平滑肌细胞增殖和迁移的作用。Objective: To investigate the role of autophagy inhibitor chloroquine (CQ) in the proliferation of pulmonary arterial smooth muscle ceUs (PASMCs)in hypoxia conditions. Methods: The following groups in this study were sot up: control group, hypoxia group, 50 /~mol/L CQ + hypoxia group, 50 p.mol/L CQ group. The viability of PASMCs in every group was detected by MIT assay. Autophagic vac- uoles in the cells were observed by MDC staining. Protein expression of microtubule associated protein light chain 3 (LC3) was measured by Western blot. Migration of PASMCs was detected by wound healing assay. Results: Compared with control group, no effect on the viability of PASMCs was observed treated by CQ alone. In 1% hypoxia group, cell viability increased significantly compared with that in control group. The number of autophagic vacuoles and the rate of cell migration and also protein expression of LC3-II were also markedly increased. Compared with hypoxia group, addition of CQ increased the number of autophagic vacuoles and the levels of LC3-II protein, but decreased the prolifera- tion and migration of PASMCs. Conclusion: Hypoxia could activates autophagy and contributes to proliferation and migration of PASMCs, and autophagy inhibitor CQ could decrease the effect of hypoxia on PASMCs through inhibiting autophagy process.
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