Cooper Sandra T, McNeil Paul L
Institute for Neuroscience and Muscle Research, Kids Research Institute, The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Discipline of Paediatrics and Child Health, Faculty of Medicine, University of Sydney, Sydney, New South Wales, Australia; and Department of Cellular Biology and Anatomy, Institute of Molecular Medicine and Genetics, Georgia Regents University, Augusta, Georgia.
Physiol Rev. 2015 Oct;95(4):1205-40. doi: 10.1152/physrev.00037.2014.
Eukaryotic cells have been confronted throughout their evolution with potentially lethal plasma membrane injuries, including those caused by osmotic stress, by infection from bacterial toxins and parasites, and by mechanical and ischemic stress. The wounded cell can survive if a rapid repair response is mounted that restores boundary integrity. Calcium has been identified as the key trigger to activate an effective membrane repair response that utilizes exocytosis and endocytosis to repair a membrane tear, or remove a membrane pore. We here review what is known about the cellular and molecular mechanisms of membrane repair, with particular emphasis on the relevance of repair as it relates to disease pathologies. Collective evidence reveals membrane repair employs primitive yet robust molecular machinery, such as vesicle fusion and contractile rings, processes evolutionarily honed for simplicity and success. Yet to be fully understood is whether core membrane repair machinery exists in all cells, or whether evolutionary adaptation has resulted in multiple compensatory repair pathways that specialize in different tissues and cells within our body.
真核细胞在其整个进化过程中一直面临着潜在的致命性质膜损伤,包括由渗透应激、细菌毒素和寄生虫感染以及机械和缺血应激所造成的损伤。如果能够迅速启动修复反应以恢复边界完整性,受伤的细胞就能存活下来。钙已被确定为激活有效膜修复反应的关键触发因素,该反应利用胞吐作用和胞吞作用来修复膜撕裂或去除膜孔。我们在此回顾关于膜修复的细胞和分子机制的已知情况,特别强调修复与疾病病理学的相关性。综合证据表明,膜修复采用了原始但强大的分子机制,如囊泡融合和收缩环,这些过程在进化中经过优化,以实现简单性和有效性。核心膜修复机制是否存在于所有细胞中,或者进化适应是否导致了多种补偿性修复途径,这些途径专门针对我们体内不同的组织和细胞,这些问题还有待充分了解。