Gortat Anna
Department of Anatomical Pathology, Pharmacology and Microbiology, University of Barcelona, Casanova 143, Barcelona, 08036, Spain,
Methods Mol Biol. 2016;1336:95-109. doi: 10.1007/978-1-4939-2926-9_9.
The role of cyclin-dependent kinase inhibitors (CDKIs) is to negatively regulate cyclin-dependent kinases as a mechanism of control of cell proliferation. As such, CDKIs are being used to induce apoptosis in cancer cells to prevent their excessive reproduction. This chapter describes procedures to study apoptosis induction upon treatment with any CDKI through the evaluation of morphological and functional mitochondrial alterations, in particular, how to measure the mitochondrial membrane potential (ΔΨm) using TMRE dye, determine the content of intracellular ATP, observe mitochondrial network morphology using HeLa cells stably expressing fluorescent reporter DsRed targeting mitochondrial matrix, observe ultrastructure of the organelle using transmission electron microscopy, and, finally, assure that mitochondrial outer membrane permeabilization takes place by assessing the subcellular localization of cyt C in HeLa cells stably expressing fluorescent cyt C-GFP.
细胞周期蛋白依赖性激酶抑制剂(CDKIs)的作用是负向调节细胞周期蛋白依赖性激酶,作为控制细胞增殖的一种机制。因此,CDKIs正被用于诱导癌细胞凋亡以防止其过度增殖。本章描述了通过评估形态学和功能性线粒体改变来研究用任何CDKI处理后凋亡诱导的程序,特别是如何使用TMRE染料测量线粒体膜电位(ΔΨm)、确定细胞内ATP含量、使用稳定表达靶向线粒体基质的荧光报告基因DsRed的HeLa细胞观察线粒体网络形态、使用透射电子显微镜观察细胞器的超微结构,以及最后通过评估稳定表达荧光细胞色素C-GFP的HeLa细胞中细胞色素C的亚细胞定位来确保线粒体外膜通透性发生。