Department of Cardiology, The Fourth Affiliated Hospital, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.
Am J Physiol Renal Physiol. 2013 Aug 1;305(3):F304-13. doi: 10.1152/ajprenal.00074.2013. Epub 2013 May 29.
We used mouse cortical collecting duct principal cells (mpkCCDc14 cell line) as a model to determine whether statins reduce the harmful effects of cyclosporine A (CsA) on the distal nephron. The data showed that treatment of cells with CsA increased transepithelial resistance and that the effect of CsA was abolished by lovastatin. Scanning ion conductance microscopy showed that CsA significantly increased the height of cellular protrusions near tight junctions. In contrast, lovastatin eliminated the protrusions and even caused a modest depression between cells. Western blot analysis and confocal microscopy showed that lovastatin also abolished CsA-induced elevation of both zonula occludens-1 and cholesterol in tight junctions. In contrast, a high concentration of CsA induced apoptosis, which was also attenuated by lovastatin, elevated intracellular ROS via activation of NADPH oxidase, and increased the expression of p47phox. Sustained treatment of cells with lovastatin also induced significant apoptosis, which was attenuated by CsA, but did not elevate intracellular ROS. These results indicate that both CsA and lovastatin are harmful to principal cells of the distal tubule, but via ROS-dependent and ROS-independent apoptotic pathways, respectively, and that they counteract probably via mobilization of cellular cholesterol levels.
我们使用鼠皮质集合管主细胞(mpkCCDc14 细胞系)作为模型,以确定他汀类药物是否能降低环孢素 A(CsA)对远曲小管的有害影响。数据表明,CsA 处理细胞会增加跨上皮电阻,而 lovastatin 可消除 CsA 的作用。扫描离子电导显微镜显示,CsA 显著增加了紧密连接附近细胞突起的高度。相比之下,lovastatin 消除了突起,甚至导致细胞之间出现轻微凹陷。Western blot 分析和共聚焦显微镜显示,lovastatin 还消除了 CsA 诱导的紧密连接中 zonula occludens-1 和胆固醇的升高。相比之下,高浓度的 CsA 诱导细胞凋亡,这也被 lovastatin 减弱,通过激活 NADPH 氧化酶增加细胞内 ROS 的表达,并增加 p47phox 的表达。持续 lovastatin 处理也会诱导明显的细胞凋亡,这被 CsA 减弱,但不会增加细胞内 ROS。这些结果表明,CsA 和 lovastatin 都对远曲小管的主细胞有害,但分别通过 ROS 依赖和 ROS 非依赖的凋亡途径,它们可能通过动员细胞胆固醇水平来相互拮抗。