转化生长因子-β1促血管内皮细胞向间质细胞转化的作用研究简宇1.DOCVIP

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转化生长因子-β1促血管内皮细胞向间质细胞转化的作用研究简宇1.DOC

转化生长因子-β1促血管内皮细胞向间质细胞转化的作用研究简宇1

转化生长因子-β1促血管内皮细胞向间质细胞转化的作用研究 简宇1,简华刚1,黄宏2,徐祥2,郭敏1,代卉2,崔文慧2,蒋建新2,朱佩芳2,王正国2 (400016重庆,重庆医科大学第二附属医院创伤烧伤科1;400042重庆,第三军医大学第三附属医院野战外科研究所,创伤、烧伤与复合伤国家重点实验室2) [摘要] 目的 观察转化生长因子-β1(transforming growth factor-β1,TGF-β1)对促进内皮细胞向间质细胞转化(endothelial-mesenchymal (myofibroblast) transition,EnMT)的效应,探讨肌成纤维细胞的来源以及纤维化疾病发生的新机制。方法 分离培养人脐静脉内皮细胞,采用不同浓度的TGF-β1(10、25、和50 ng/ml)刺激细胞 72 h后,倒置显微镜观察诱导后细胞形态变化,免疫荧光方法检测第Ⅷ因子相关抗原和α-SMA表达变化,RT-PCR检测VE-钙粘蛋白(VE-Cadherin),α-SMA和Ⅰ型胶原基因表达变化。 结果 正常对照组内皮细胞呈铺路石样生长,TGF-β1刺激组内皮细胞由铺路石样形态向梭形转化。免疫荧光检测可见对照组含有少量FⅧ,α-SMA双阳性细胞。TGF-β1组FⅧ,α-SMA双阳性细胞明显增多,并且具有明显的浓度依赖性(P0.05,P0.01)。RT-PCR检测结果显示,TGF-β1刺激导致内皮细胞特异性标记物VE-钙粘蛋白(VE-cadherin)基因的表达显著减少(P0.05),随着TGF-β1刺激浓度的增加,VE-钙粘蛋白基因表达呈明显的下降趋势;相反,内皮细胞间质性标记物α-SMA和I型胶原基因的表达显著增加(P0.05,P0.01),并且具有明显的浓度依赖性。结论TGF-β1刺激内皮细胞后,细胞表型和功能均表现为间质细胞特性,提示TGF-β1具有促进内皮细胞向间质细胞转化(EnMT)的作用,并且其促EnMT效应具有明显的浓度依赖性。 [关键词] 内皮细胞;肌成纤维细胞;转分化;转化生长因子-β1 TGF-β1-induced transformation of endothelial into myofibroblast : a study of role Jian Yu1, Huang Hong2, Jian Hua-gang1, Guo Min1, Dai Hui2, Cui Wen-hui2, Zhang Bo2, Jiang Jian-xin2, Zhu Pei-fang2, Wang Zheng-guo2(1Department of burn and trauma, The Second Affiliated Hospital, Chongqing Medical University, Chongqing 400016; 2State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Surgery Research, The Third Affiliated Hospital, Third Military Medical University, Chongqing, 400042, China) Abstract: Objective To explore the effect of endothelial-mesenchymal (myofibroblast)transition of human umbilical vein endothelial cells induced by different concentration TGF-β1, and the changes of cell phenotype and function. Methods Human umbilical vein endothelial cells (HUVECs) were isolated and cultured and then prepared as experiment cells after 3 passages. HUVECs were divided into four groups randomly: PBS was added to culture medium in control group; 10, 25 and 50 ng/mL TGF-β1 were added to culture medium in TGF-β1 groups respectively. At culturing for 72 hours.The changes of cell morpholgy were observed w

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