Marroquin Lisa, Swiss Rachel, Will Yvonne
Compound Safety Prediction, Worldwide Medicinal Chemistry, Pfizer Inc, Groton, Connecticut.
Curr Protoc Toxicol. 2014 May 27;60:25.4.1-17. doi: 10.1002/0471140856.tx2504s60.
The mitochondrial permeability transition pore (MPTP) is a protein pore that forms in the inner mitochondrial membrane and allows the membrane to be permeable to all molecules of less than 1500 Da. Ca(2+), numerous reactive chemicals, and oxidative stress induce MPTP opening, whereas cyclosporin A (CsA) or bongkrekic acid block it. In addition, several drugs have been shown to induce MPTP opening, leading to the loss of mitochondrial membrane potential, swelling of the matrix because of water accumulation, rupture of the outer mitochondrial membrane, and release of intermembrane space proteins into the cytosol. This ultimately leads to the rupture of the outer mitochondrial membrane and cell demise. Here, we describe an assay using isolated rat liver mitochondria that can detect Ca(2+)-dependent drug-induced opening of the MPTP, providing protocols for screening in both cuvette and 96-well format.
线粒体通透性转换孔(MPTP)是一种形成于线粒体内膜的蛋白质孔道,它能使内膜对所有分子量小于1500 Da的分子具有通透性。钙离子、多种活性化学物质以及氧化应激均可诱导MPTP开放,而环孢素A(CsA)或硼酸可对其产生阻断作用。此外,已有研究表明,多种药物可诱导MPTP开放,进而导致线粒体膜电位丧失、基质因水分蓄积而肿胀、线粒体外膜破裂以及膜间隙蛋白释放至胞质溶胶中。这最终会导致线粒体外膜破裂和细胞死亡。在此,我们描述了一种利用分离的大鼠肝脏线粒体进行的检测方法,该方法能够检测钙离子依赖性药物诱导的MPTP开放,并提供了在比色皿和96孔板两种形式下进行筛选的实验方案。