首页 | 本学科首页   官方微博 | 高级检索  
检索        

脂联素对高糖中hRPE细胞活性及T—cad表达的影响
引用本文:张鹏,李兴.脂联素对高糖中hRPE细胞活性及T—cad表达的影响[J].医学研究通讯,2010(5):87-89.
作者姓名:张鹏  李兴
作者单位:山西医科大学第二医院内分泌科,太原030001
摘    要:目的观察脂联素对高糖环境下人视网膜色素上皮(hRPE)细胞活性及T-钙黏蛋白(T—cad)表达的影响,以阐明脂联素和T—cad对糖尿病视网膜病变(DR)的影响。方法①将hRPE细胞随机分为正常对照组(5.5mmo~L葡萄糖)、高糖组(33mmol/L葡萄糖)、脂联素组(33mmol/L+2.5μg/m1脂联素),运用MTT法测定不同情况下48h后对细胞活性的影响;②再将上述各组细胞分别培养24h、48h、72h后,运用荧光定量PCR测定T—cad的表达水平。结果①高糖组细胞活性降低,加入脂联素后细胞活力比高糖组升高;②随时间的延长,高糖组T—cad表达下降,脂联素组T—cad表达增加。结论脂联素可通过Tcad保护hRPE细胞的功能。

关 键 词:脂联素  视网膜色素上皮细胞  T-钙黏蛋白

Effects of Adiponectin on Cell Activity and Expression of T - cadherin in Human RPE Cells Cultured with High D - glucose
Zhang Peng,Li Xing.Effects of Adiponectin on Cell Activity and Expression of T - cadherin in Human RPE Cells Cultured with High D - glucose[J].Bulletin of Medical Research,2010(5):87-89.
Authors:Zhang Peng  Li Xing
Institution:.( Department of Endocrinology, Second Clinical Medical College, Shanxi Medical University, Shanxi 030001, China)
Abstract:Objective To investigate the effects of adiponectin on cell activity and expression of T - cadherin in human retinal pigment epithelial(hRPE) cells cultured with high glucose. Methods ①The hRPE cells were divided into three groups: normal glucose group(5.5mmol/L glucose) , high glucose group (33mmol/L glucose) , high glucose plus adiponectin group ( 33mmol/L glucose + 2.5ug/ ml adiponectin). 48h later, the cell activity was observed by MTT assay. ②After the above groups were cultured respectively for 24h ,48h, 72h again, the expression of T - cadherin mRNA was observed by RT - PCR. Results ①Cell activity in high glucose group significantly decreased. Cell activity adiponectin group was higher than that in the high glucose group.②With the extension of time , the expression of T- cadherin decreased in high glucose group, but increased in adiponectin group. Conclusion Adiponectin may be protect the hRPE cells by T - cadherin.
Keywords:Adiponectin  Human retinal pigment epithelial(hRPE) cells  T - cadherin
本文献已被 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号