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Mitochondrial cell death effectors

机译:线粒体细胞死亡效应子

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Programmed cell death (apoptosis) is crucial for embryogenesis and tissue homeostasis. Deregulated apoptosis leads to immunodeficiency, autoimmune disorders or cancer. The two main routes to apoptosis are the extrinsic and intrinsic (mitochondrial) pathways. Both involve caspase activation that leads to the cleavage of multiple intracellular substrates [1,9]. This review highlights recent advances in our understanding of the intrinsic pathway. We describe how BCL-2-family members preserve or disrupt mitochondrial integrity, the contribution of BH3-only proteins to this process, and the importance of cytotoxic factors released by the mitochondria. The growing evidence that the intrinsic pathway is crucial for tumourigenesis makes this an intriguing field. In particular, the finding that BCL-2 homologues are inhibited by BH3-only proteins may have future therapeutic applications.
机译:程序性细胞死亡(细胞凋亡)对于胚胎发生和组织稳态至关重要。凋亡失调会导致免疫缺陷,自身免疫性疾病或癌症。凋亡的两个主要途径是外在途径和内在途径(线粒体)。两者都涉及胱天蛋白酶激活,导致多种细胞内底物的裂解[1,9]。这篇综述突出了我们对内在途径的理解的最新进展。我们描述了BCL-2-家族成员如何保存或破坏线粒体完整性,仅BH3蛋白对该过程的贡献以及线粒体释放的细胞毒性因子的重要性。越来越多的证据表明内源性途径对于肿瘤发生至关重要,这使这一领域引人入胜。特别地,仅BH3蛋白抑制BCL-2同源物的发现可能具有未来的治疗应用。

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