Center for Stem Cell and Regenerative Medicine and Department of Cardiology of the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310058, China.
State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China.
Dev Cell. 2020 Sep 14;54(5):624-638.e5. doi: 10.1016/j.devcel.2020.06.027. Epub 2020 Jul 14.
Membrane repair is essential for cell and organism survival. Exocytosis and endocytosis facilitate membrane repair in small wounds within a single cell; however, it remains unclear how large wounds in the plasma membrane are repaired in metazoans. Here, we show that wounding triggers rapid transcriptional upregulation and dynamic recruitment of the fusogen EFF-1 to the wound site in C. elegans epidermal cells. EFF-1 recruitment at the wounded membrane depends on the actin cytoskeleton and is important for membrane repair. We identified syntaxin-2 (SYX-2) as an essential regulator of EFF-1 recruitment. SYX-2 interacts with the C terminus of EFF-1 to promote its recruitment, facilitating both endoplasmic and exoplasmic membrane repair. Furthermore, we show that SYX-2-EFF-1 repair machinery acts downstream of the ESCRT III signal. Together, our findings identify a key pathway underlying membrane repair and provide insights into tissue repair and regenerative medicine after injury.
膜修复对于细胞和生物的生存至关重要。胞吐作用和胞吞作用有助于单个细胞中小伤口处的膜修复;然而,真核生物中如何修复质膜上的大伤口仍不清楚。在这里,我们表明,在 C. elegans 表皮细胞中,损伤会触发融合蛋白 EFF-1 在伤口部位的快速转录上调和动态募集。在受伤的膜上的 EFF-1 募集依赖于肌动蛋白细胞骨架,对于膜修复很重要。我们确定了突触素-2(SYX-2)是 EFF-1 募集的必需调节剂。SYX-2 与 EFF-1 的 C 末端相互作用,促进其募集,促进内质网和外质膜的修复。此外,我们表明,SYX-2-EFF-1 修复机制作用于 ESCRT III 信号的下游。总之,我们的发现确定了膜修复的关键途径,并为损伤后的组织修复和再生医学提供了见解。