Department of Cytology & Histology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikatacho, Okayama 700-8558, Japan.
J Clin Biochem Nutr. 2008 Jan;42(1):35-44. doi: 10.3164/jcbn.2008006.
The membrane permeability transition (MPT) of mitochondria plays an important role in the mechanism of apoptotic cell death in various cells. Classic type MPT is induced by Ca(2+) in the presence of inorganic phosphate and respiratory substrate, and is characterized by various events including generation of reactive oxygen species (ROS), membrane depolarization, swelling, release of Ca(2+) and high sensitivity to cyclosporine A. However, the sequence of these events and the effect of antioxidants on their events remain obscure. Flow cytometry is a convenient method to investigate the order of events among various functions occurring in MPT using a limited amount of mitochondria (200 microl of 0.02 mg protein/ml) without contamination by other organelles. Flow cytometric analysis revealed that Ca(2+) sequentially induced ROS generation, depolarization, swelling and Ca(2+) release in mitochondria by a cyclosporine A-inhibitable mechanism. These results were supported by the finding that Ca(2+)-induced MPT was inhibited by antioxidants, such as glutathione and N-acetylcysteine. It was also revealed that various inhibitors of Ca(2+)-induced phospholipase A(2) suppressed all of the events associated with Ca(2+)-induced MPT. These results suggested that ROS generation and phospholipase A(2) activation by Ca(2+) underlie the mechanism of the initiation of MPT.
线粒体的膜通透性转变(MPT)在各种细胞的细胞凋亡死亡机制中起着重要作用。经典的 MPT 是在存在无机磷酸盐和呼吸底物的情况下由 Ca(2+) 诱导的,其特征是各种事件,包括活性氧(ROS)的产生、膜去极化、肿胀、Ca(2+)的释放以及对环孢菌素 A 的高敏感性。然而,这些事件的顺序以及抗氧化剂对其事件的影响仍然不清楚。流式细胞术是一种方便的方法,可使用有限量的线粒体(200 μl 为 0.02mg 蛋白/ml),无需其他细胞器的污染,研究 MPT 中发生的各种功能之间的事件顺序。流式细胞术分析表明,Ca(2+) 通过环孢菌素 A 抑制机制依次诱导线粒体中 ROS 的产生、去极化、肿胀和 Ca(2+)的释放。抗氧化剂,如谷胱甘肽和 N-乙酰半胱氨酸,抑制 Ca(2+)-诱导的 MPT,这一发现支持了这些结果。还发现 Ca(2+)-诱导的磷脂酶 A(2)的各种抑制剂抑制了与 Ca(2+)-诱导的 MPT 相关的所有事件。这些结果表明,Ca(2+)诱导的 ROS 生成和磷脂酶 A(2)的激活是 MPT 起始机制的基础。