Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, VIC, 3086, Australia.
The Walter and Eliza Hall Institute for Medical Research, Parkville, VIC, 3052, Australia.
Cell Death Differ. 2020 Jan;27(1):102-116. doi: 10.1038/s41418-019-0342-5. Epub 2019 May 1.
Many cell types are known to undergo a series of morphological changes during the progression of apoptosis, leading to their disassembly into smaller membrane-bound vesicles known as apoptotic bodies (ApoBDs). In particular, the formation of circular bulges called membrane blebs on the surface of apoptotic cells is a key morphological step required for a number of cell types to generate ApoBDs. Although apoptotic membrane blebbing is thought to be regulated by kinases including ROCK1, PAK2 and LIMK1, it is unclear whether these kinases exhibit overlapping roles in the disassembly of apoptotic cells. Utilising both pharmacological and CRISPR/Cas9 gene editing based approaches, we identified ROCK1 but not PAK2 or LIMK1 as a key non-redundant positive regulator of apoptotic membrane blebbing as well as ApoBD formation. Functionally, we have established an experimental system to either inhibit or enhance ApoBD formation and demonstrated the importance of apoptotic cell disassembly in the efficient uptake of apoptotic materials by various phagocytes. Unexpectedly, we also noted that ROCK1 could play a role in regulating the onset of secondary necrosis. Together, these data shed light on both the mechanism and function of cell disassembly during apoptosis.
许多细胞类型在凋亡过程中被已知会经历一系列形态变化,导致它们分解成更小的膜结合囊泡,称为凋亡小体(ApoBDs)。特别是,在凋亡细胞表面形成称为膜泡的圆形膨出物是许多细胞类型生成 ApoBDs 的关键形态步骤。尽管凋亡细胞膜起泡被认为受包括 ROCK1、PAK2 和 LIMK1 在内的激酶调节,但这些激酶在凋亡细胞解体中是否表现出重叠作用尚不清楚。我们利用药理学和基于 CRISPR/Cas9 的基因编辑方法,鉴定 ROCK1 而不是 PAK2 或 LIMK1 是凋亡细胞膜起泡以及 ApoBD 形成的关键非冗余正向调节因子。在功能上,我们建立了一个实验系统来抑制或增强 ApoBD 的形成,并证明了凋亡细胞解体在各种吞噬细胞有效摄取凋亡物质中的重要性。出乎意料的是,我们还注意到 ROCK1 可能在调节继发性坏死的开始中发挥作用。总之,这些数据阐明了细胞在凋亡过程中解体的机制和功能。