检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]沈阳医学院附属第二医院心内科,沈阳110002 [2]北京军区北戴河疗养院康复医学科
出 处:《临床心血管病杂志》2015年第2期213-215,共3页Journal of Clinical Cardiology
基 金:辽宁省教育厅(No:L20105500);沈阳市科委(No:112222);辽宁省科委(No:2011225032);辽宁省人事厅百千万人才资助(No:2008921064);沈阳市科委(No:071481-2)
摘 要:目的:探讨组织蛋白酶B(CTSB)对人脐静脉血管内皮细胞系(HUVEC)增殖及凋亡的影响。方法:慢病毒转染HUVEC,获得稳定过表达CTSB的HUVEC细胞系HU-CTSB。CCK-8法检测转染前后各组细胞的增殖情况;流式细胞法检测各组细胞的凋亡情况;实时定量PCR法检测各组细胞内凋亡基因Bax;蛋白质印迹法检测各组细胞被剪切的内caspase3表达差异。结果:CCK8法检测发现,与转染前及空病毒对照组HU-MOCK相比,HU-CTSB细胞的生存率明显下降(P<0.01);流式细胞法检测发现,HU-CTSB细胞的凋亡率明显增高(P<0.01);实时定量PCR法检测发现,HU-CTSB细胞中Bax mRNA水平增高(P<0.01);蛋白质印迹法检测发现,HU-CTSB细胞中Bcl蛋白表达下降,且被剪切的caspase3的量最多。结论:CTSB可以抑制HUVEC的生长,并通过上调Bax的表达,激活caspase3通路诱导HUVEC发生凋亡。Objective:To study the roles of cathepsin B (CTSB) in the proliferation and apoptosis of human umbilical vein endothelial cell (HUVEC). Method:Lentiviral CTSB vector was transfected into HUVEC cell line for the construction of stable HUVEC cell line expressing CTSB (HU-CTSB). Proliferation of cells before and after the transfection were detected with CCK8 method; the apoptosis rates were assayed by flow cytometryl bax gene was determined with qPCR method; and the expression of cleaved caspase-3 protein of each group was detec- ted with Western Blot method. Result: Compared with those before transfection and empty virus control group HU-MOCK, the viability of HU-CTSB cells was significantly decreased (P〈0.01) and the apoptosis rate of HU- CTSB ceils was significantly increased (P〈0.01); Results from qPCR and Western Blot showed that both the hax mRNA level and the expression of cleaved caspase-3 protein in HU-CTSB cells were obviously increased (P〈 0.01). Conclusion:CTSB could inhibit the growth of HUVEC cells and induce the cellular apoptosis through the upregulation of bax gene and the activation of the caspase-3 pathway.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.117