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吴珊珊, 谢亮, 刘翰旻, 等. PDGF-BB诱导肺动脉平滑肌细胞表型转换时细胞骨架的变化[J]. 四川大学学报(医学版), 2018, 49(4): 524-529.
引用本文: 吴珊珊, 谢亮, 刘翰旻, 等. PDGF-BB诱导肺动脉平滑肌细胞表型转换时细胞骨架的变化[J]. 四川大学学报(医学版), 2018, 49(4): 524-529.
WU Shan-shan, XIE Liang, LIU Han-min, et al. The Changes of Cytoskeleton during Phenotypic Transition of Pulmonary Artery Smooth Muscle Cells Induced by PDGF-BB[J]. Journal of Sichuan University (Medical Sciences), 2018, 49(4): 524-529.
Citation: WU Shan-shan, XIE Liang, LIU Han-min, et al. The Changes of Cytoskeleton during Phenotypic Transition of Pulmonary Artery Smooth Muscle Cells Induced by PDGF-BB[J]. Journal of Sichuan University (Medical Sciences), 2018, 49(4): 524-529.

PDGF-BB诱导肺动脉平滑肌细胞表型转换时细胞骨架的变化

The Changes of Cytoskeleton during Phenotypic Transition of Pulmonary Artery Smooth Muscle Cells Induced by PDGF-BB

  • 摘要: 目的 研究血小板衍生生长因子(PDGF-BB)诱导大鼠肺动脉平滑肌细胞(PASMCs)表型转换时细胞骨架构象的改变,探讨PASMCs表型转换的机制。 方法 原代培养并鉴定SD大鼠PASMCs,将PASMCs分为对照组(细胞不加诱导剂培养24 h)、实验组(细胞用PDGF-BB 10 ng/mL诱导培养24 h);实时荧光定量PCR(RT-qPCR)及Western blot检测细胞表型转化标志基因α-肌动蛋白(α-SMA)、平滑肌22α蛋白(SM22α)mRNA及相关蛋白的表达;免疫荧光法检测细胞骨架微丝F-actin及微管α-tubulin、β-tubulin的构象;CCK-8法检测细胞增殖能力及划痕实验观察细胞迁移能力。 结果 与对照组相比,PDGF-BB下调α-SMA及SM22α表达水平;细胞骨架荧光强度明显减弱,F-actin排列紊乱、边缘不规则、呈毛刺样,α-tubulin、β-tubulin形态模糊,表现为共定位;明显增强PASMCs增殖与迁移能力。 结论 PDGF-BB可能通过影响细胞骨架构象诱导PASMCs表型转换,进而改变细胞增殖及迁移能力。

     

    Abstract: Objective To study the changes of cytoskeleton during the phenotypic transition of rat pulmonary artery smooth muscle cells (PASMCs) induced by platelet-derived growth factor (PDGF-BB), and to explore the mechanism involved in the process of phenotypic transition of PASMCs. Methods PASMCs of Sprague Dawley (SD) rats were cultured and identified by immunohistochemistry (IHC) method. The cells were randomly divided into control group and PDGF-BB treated group (10 ng/mL). RT-qPCR and Western blot were used to detect the mRNA and protein level of marker genes (α-SMA and SM22α) during the process of phenotypic transition of PASMCs. The changes of cytoskeleton were observed by fluorescent microscopy, cell proliferation was measured by CCK-8 method; and cell migration was observed by wound healing assay. Results Compared with control group, PDGF-BB down-regulated the mRNA and protein expression of α-SMA and SM22α. The fluorescence intensity of cytoskeletal protein was significantly reduced after the treatment of PDGF-BB. In addition, the structure of F-actin was disorganized with a burr-like appearance, and the structures of α-tubulin and β-tubulin were irregular with co-location appearance. PDGF-BB significantly enhanced the proliferation and migration of PASMCs. Conclusion PDGF-BB could induce a conformation change in cytoskeletal proteins for PASMCs phenotypic transition, and enhance the ability of proliferation and migration of PASMCs.

     

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