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Apoptotic microtubules delimit an active caspase free area in the cellular cortex during the execution phase of apoptosis

机译:凋亡微管在细胞凋亡的执行阶段划定了细胞皮层中一个活跃的caspase游离区域

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Apoptotic microtubule network (AMN) is organized during apoptosis, forming a cortical structure beneath plasma membrane, which has an important role in preserving cell morphology and plasma membrane permeability. The aim of this study was to examine the role of AMN in maintaining plasma membrane integrity during the execution phase of apoptosis. We demonstrated in camptothecin-induced apoptosis in H460 cells that AMN delimits an active caspase free area beneath plasma membrane that permits the preservation of cellular cortex and transmembrane proteins. AMN depolymerization in apoptotic cells by a short exposure to colchicine allowed active caspases to reach the cellular cortex and cleave many key proteins involved in plasma membrane structural support, cell adhesion and ionic homeostasis. Cleavage of cellular cortex and plasma membrane proteins, such as α -spectrin, paxilin, focal adhesion kinase (FAK), E-cadherin and integrin subunit β 4 was associated with cell collapse and cell detachment. Otherwise, cleavage-mediated inactivation of calcium ATPase pump (PMCA-4) and Na+/Ca2+ exchanger (NCX) involved in cell calcium extrusion resulted in calcium overload. Furthermore, cleavage of Na+/K+ pump subunit β was associated with altered sodium homeostasis. Cleavage of cell cortex and plasma membrane proteins in apoptotic cells after AMN depolymerization increased plasma permeability, ionic imbalance and bioenergetic collapse, leading apoptotic cells to secondary necrosis. The essential role of caspase-mediated cleavage in this process was demonstrated because the concomitant addition of colchicine that induces AMN depolymerization and the pan-caspase inhibitor z-VAD avoided the cleavage of cortical and plasma membrane proteins and prevented apoptotic cells to undergo secondary necrosis. Furthermore, the presence of AMN was also critical for proper phosphatidylserine externalization and apoptotic cell clearance by macrophages. These results indicate that AMN is essential to preserve an active caspase free area in the cellular cortex of apoptotic cells that allows plasma membrane integrity during the execution phase of apoptosis.
机译:凋亡微管网络(AMN)在细胞凋亡期间组织,在质膜下形成皮质结构,这在保持细胞形态和质膜通透性方面具有重要作用。这项研究的目的是检查在细胞凋亡执行阶段AMN在维持质膜完整性方面的作用。我们在喜树碱诱导的H460细胞凋亡中证明AMN限定了质膜下的一个活跃的caspase游离区域,从而可以保留细胞皮质和跨膜蛋白。短时暴露于秋水仙碱可使凋亡细胞中的AMN解聚,从而使活性半胱氨酸蛋白酶到达细胞皮层并裂解涉及质膜结构支持,细胞粘附和离子稳态的许多关键蛋白质。细胞皮质和质膜蛋白(例如α-血影蛋白,paxilin,粘着斑激酶(FAK),E-钙粘蛋白和整联蛋白亚基β4)的裂解与细胞萎缩和细胞脱离有关。否则,裂解介导的钙ATP酶泵(PMCA-4)和Na + / Ca 2 + 交换剂(NCX)的失活会导致钙超负荷。此外,Na + / K + 泵亚基β的裂解与钠稳态的改变有关。 AMN解聚后,凋亡细胞中细胞皮质和质膜蛋白的裂解会增加血浆通透性,离子失衡和生物能崩溃,从而导致凋亡细胞继发性坏死。证实了胱天蛋白酶介导的裂解在该过程中的重要作用,因为伴随加入秋水仙碱诱导AMN解聚和泛胱天蛋白酶抑制剂z-VAD避免了皮质和质膜蛋白的裂解,并防止凋亡细胞继发性坏死。此外,AMN的存在对于适当的磷脂酰丝氨酸外在化和巨噬细胞清除凋亡细胞也至关重要。这些结果表明,AMN对于在凋亡细胞的细胞皮层中保留活性caspase游离区域至关重要,该区域在凋亡执行阶段允许质膜完整性。

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