Nowak Grażyna, Bakajsova Diana
Department of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Arkansas, USA.
J Vis Exp. 2013 Jan 7(71):4301. doi: 10.3791/4301.
The protein kinase C (PKC) family of isozymes is involved in numerous physiological and pathological processes. Our recent data demonstrate that PKC regulates mitochondrial function and cellular energy status. Numerous reports demonstrated that the activation of PKC-a and PKC-ε improves mitochondrial function in the ischemic heart and mediates cardioprotection. In contrast, we have demonstrated that PKC-α and PKC-ε are involved in nephrotoxicant-induced mitochondrial dysfunction and cell death in kidney cells. Therefore, the goal of this study was to develop an in vitro model of renal cells maintaining active mitochondrial functions in which PKC isozymes could be selectively activated or inhibited to determine their role in regulation of oxidative phosphorylation and cell survival. Primary cultures of renal proximal tubular cells (RPTC) were cultured in improved conditions resulting in mitochondrial respiration and activity of mitochondrial enzymes similar to those in RPTC in vivo. Because traditional transfection techniques (Lipofectamine, electroporation) are inefficient in primary cultures and have adverse effects on mitochondrial function, PKC-ε mutant cDNAs were delivered to RPTC through adenoviral vectors. This approach results in transfection of over 90% cultured RPTC. Here, we present methods for assessing the role of PKC-ε in: 1. regulation of mitochondrial morphology and functions associated with ATP synthesis, and 2. survival of RPTC in primary culture. PKC-ε is activated by overexpressing the constitutively active PKC-ε mutant. PKC-ε is inhibited by overexpressing the inactive mutant of PKC-ε. Mitochondrial function is assessed by examining respiration, integrity of the respiratory chain, activities of respiratory complexes and F0F1-ATPase, ATP production rate, and ATP content. Respiration is assessed in digitonin-permeabilized RPTC as state 3 (maximum respiration in the presence of excess substrates and ADP) and uncoupled respirations. Integrity of the respiratory chain is assessed by measuring activities of all four complexes of the respiratory chain in isolated mitochondria. Capacity of oxidative phosphorylation is evaluated by measuring the mitochondrial membrane potential, ATP production rate, and activity of F0F1-ATPase. Energy status of RPTC is assessed by determining the intracellular ATP content. Mitochondrial morphology in live cells is visualized using MitoTracker Red 580, a fluorescent dye that specifically accumulates in mitochondria, and live monolayers are examined under a fluorescent microscope. RPTC viability is assessed using annexin V/propidium iodide staining followed by flow cytometry to determine apoptosis and oncosis. These methods allow for a selective activation/inhibition of individual PKC isozymes to assess their role in cellular functions in a variety of physiological and pathological conditions that can be reproduced in in vitro.
蛋白激酶C(PKC)同工酶家族参与众多生理和病理过程。我们最近的数据表明,PKC调节线粒体功能和细胞能量状态。大量报告表明,PKC-α和PKC-ε的激活可改善缺血心脏中的线粒体功能并介导心脏保护作用。相比之下,我们已经证明PKC-α和PKC-ε参与肾毒性物质诱导的肾细胞线粒体功能障碍和细胞死亡。因此,本研究的目的是建立一种维持活跃线粒体功能的肾细胞体外模型,在该模型中可以选择性激活或抑制PKC同工酶,以确定它们在调节氧化磷酸化和细胞存活中的作用。肾近端小管细胞(RPTC)的原代培养在改良条件下进行,使其线粒体呼吸和线粒体酶活性与体内RPTC相似。由于传统的转染技术(脂质体转染、电穿孔)在原代培养中效率低下且对线粒体功能有不利影响,因此通过腺病毒载体将PKC-ε突变体cDNA导入RPTC。这种方法可使超过90%的培养RPTC转染。在此,我们介绍评估PKC-ε在以下方面作用的方法:1. 调节与ATP合成相关的线粒体形态和功能;2. 原代培养中RPTC的存活。通过过表达组成型活性PKC-ε突变体激活PKC-ε。通过过表达PKC-ε的无活性突变体抑制PKC-ε。通过检测呼吸作用、呼吸链完整性、呼吸复合体和F0F1-ATP酶的活性、ATP产生速率以及ATP含量来评估线粒体功能。在洋地黄皂苷通透的RPTC中评估呼吸作用,作为状态3(存在过量底物和ADP时的最大呼吸作用)和解偶联呼吸作用。通过测量分离线粒体中呼吸链所有四个复合体的活性来评估呼吸链的完整性。通过测量线粒体膜电位、ATP产生速率和F0F1-ATP酶的活性来评估氧化磷酸化能力。通过测定细胞内ATP含量来评估RPTC的能量状态。使用MitoTracker Red 580(一种特异性积聚在线粒体中的荧光染料)在活细胞中观察线粒体形态,并在荧光显微镜下检查活细胞单层。使用膜联蛋白V/碘化丙啶染色,随后通过流式细胞术评估RPTC活力,以确定细胞凋亡和胀亡。这些方法允许选择性激活/抑制单个PKC同工酶,以评估它们在各种生理和病理条件下细胞功能中的作用,这些条件可在体外重现。