Andrews Norma W, Almeida Patricia E, Corrotte Matthias
Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD 20742-5815, USA.
Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD 20742-5815, USA; Department of Biology, Federal University of Juiz de Fora, Juiz de Fora, Minas Gerais, Brazil.
Trends Cell Biol. 2014 Dec;24(12):734-42. doi: 10.1016/j.tcb.2014.07.008. Epub 2014 Aug 20.
When wounded, eukaryotic cells reseal in a few seconds. Ca(2+) influx induces exocytosis of lysosomes, a process previously thought to promote repair by 'patching' wounds. New evidence suggests that resealing involves direct wound removal. Exocytosis of lysosomal acid sphingomyelinase (ASM) triggers endocytosis of lesions followed by intracellular degradation. Characterization of injury-induced endosomes revealed a role for caveolae, sphingolipid-enriched plasma membrane invaginations that internalize toxin pores and are abundant in mechanically stressed cells. These findings provide a novel mechanistic explanation for the muscle pathology associated with mutations in caveolar proteins. Membrane remodeling by the ESCRT complex was also recently shown to participate in small-wound repair, emphasizing that cell resealing involves previously unrecognized mechanisms for lesion removal that are distinct from the patch model.
受伤时,真核细胞会在几秒钟内重新封闭。钙离子内流会诱导溶酶体胞吐,这一过程以前被认为是通过“修补”伤口来促进修复的。新证据表明,重新封闭涉及直接去除伤口。溶酶体酸性鞘磷脂酶(ASM)的胞吐会触发损伤的内吞作用,随后进行细胞内降解。对损伤诱导的内体的表征揭示了小窝(富含鞘脂的质膜内陷,可内化毒素孔且在机械应激细胞中大量存在)的作用。这些发现为与小窝蛋白突变相关的肌肉病理学提供了一种新的机制解释。ESCRT复合物介导的膜重塑最近也被证明参与小伤口修复,这强调了细胞重新封闭涉及以前未被认识的损伤去除机制,这些机制不同于修补模型。