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作 者:严莉莎 霍建云 董宇华[2] 潘娅[1] 王晋星一[1] 陈妮[1] 臧贵勇[3] 胡晓霞[1] 陈腾祥[1]
机构地区:[1]贵阳医学院生理学教研室,贵州贵阳550004 [2]贵阳医学院机能学实验室,贵州贵阳550004 [3]贵阳医学院人体解剖学教研室,贵州贵阳550004
出 处:《贵阳医学院学报》2015年第1期6-9,共4页Journal of Guiyang Medical College
基 金:国家自然科学基金资助项目(NO.81060176);贵阳医学院院基金(院基金合同字第2012005号);贵州省高层次人才科研条件特助经费(TZJF-2009年38号)
摘 要:目的:研究细胞培养密度对MCF7乳腺癌细胞integrinβ4水解机制。方法:常规培养高密度和低密度MCF7乳腺癌细胞,分别给予钙离子螯合剂和肝素处理,用Western blot检测不同培养密度MCF7细胞integrinβ4的水解情况;用Fluo-3 AM作为钙离子荧光探针,激光共聚焦扫描显微镜检测细胞内钙离子的分布。结果:Western blot检测结果显示,在低密度和高密度培养的MCF7细胞中,integrinβ4的水解模式不同;在高浓度培养的细胞中,200 k D integrinβ4片段产生增多;激光共聚焦扫描显微镜观察发现,低密度培养MCF7细胞中,钙离子的绿色荧光主要成团或颗粒状分布,而且与红色荧光有较多的重合,部分钙离子分布于细胞核内;在高密度培养的细胞中,钙离子在细胞质膜和细胞核中的定位较少;钙离子螯合剂BAPTA-AM处理可使200 k D integrinβ4明显减少;10-6mol/L的肝素能够减少MCF7细胞200 k D水解片段的增多,随着肝素浓度的增高,抑制效果有所增强;相对于BAPTA-AM,10-4mol/L肝素的抑制效应减弱。结论:高密度培养的MCF7细胞中,钙离子从钙库中释放,细胞外内流增多,激活calpain 2,导致200 k D integrinβ4水解片段增多。Objective: To investigate the role and itg mechanism of cell density in culture on the pro- teolysis of integrin β4. Methods: MCF7 was cultured to reach 70% (sparse) and 100% (dense) and then treated with calcium ion chelator and heparin. Western blot was utilized to detected the proteolysis of integrin β4, and Fluo-3 AM was used as fluorescence probe for calcium ion to observe its localiza- tion inside cell. Results: As Western blot results showing, the proteolysis profile of integrin β4 was different between cells cultured as sparse and dense. In dense, 200 kD integrin β4 fragment was in- creased, which could be attenuated by BAPTA-AM (calcium ion chelator) and heparin. However, the inhibitor effects of heparin was dose-dependent, but reached to its platform as 10-5 mol/L, which was less than BAPTA-AM even if heparin reached to10-4 mol/L. Conclusions: In MCF7 ceils with high density, calcium ion release from ion bank inside and inflow h'om outside of cells, leading to activation of calpain 2 and increase of product of integrin β4 fragment with 200 kD.
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