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Probing Mitochondrial Permeability Transition Pore Activity in Nucleated Cells and Platelets by High-Throughput Screening Assays Suggests Involvement of Protein Phosphatase 2B in Mitochondrial Dynamics

机译:通过高通量筛选测定探测核细胞和血小板中的线粒体渗透率过渡孔活性表明蛋白质磷酸酶2b在线粒体动力学中的参与

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Mitochondrial permeability transition pore (mPTP) formation is well documented in isolated mitochondria. However, convincing detection of mPTP in whole cells remains elusive. In this study, we describe a high-throughput assay for Ca2+-activated mPTP opening in platelets using HyperCyt flow cytometry. In addition, we demonstrate that in several nucleated cells, using multiple approaches, the detection of cyclophilin D-dependent mPTP opening is highly challenging. Results with the mitochondrial-targeted Ca2+-sensing green fluorescent protein (mito-Case12) suggest the involvement of protein phosphatase 2B (PP2B; calcineurin) in regulating mitochondrial dynamics. Our results highlight the danger of relying on cyclosporine A alone as a pharmacological tool, and the need for comprehensive studies of mPTP in the cell.
机译:线粒体渗透率过渡孔(MPTP)形成在分离的线粒体中有很好的记录。 然而,在整个细胞中令人信服地检测MPTP仍然难以捉摸。 在这项研究中,我们描述了使用Hypercyt流式细胞术中血小板中CA2 +活化的MPTP开口的高通量测定。 此外,我们证明,在几种核细胞中,使用多种方法,对细胞素D依赖性MPTP开口的检测具有高度挑战性。 用线粒体靶向CA2 + - 溶解绿色荧光蛋白(MITO-CASE12)表明蛋白质磷酸酶2b(pp2b; carchineurin)在调节线粒体动力学中的累积。 我们的结果突出了单独依赖环孢菌素A作为药理学工具的危险,以及对细胞中MPTP的综合研究的需求。

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