Bement W M, Mandato C A, Kirsch M N
Department of Zoology, Program in Cellular and Molecular Biology, University of Wisconsin-Madison, 1117 West Johnson Street, Madison, Wisconsin 53706, USA.
Curr Biol. 1999 Jun 3;9(11):579-87. doi: 10.1016/s0960-9822(99)80261-9.
Both single cells and multicellular systems rapidly heal physical insults but are thought to do so by distinctly different mechanisms. Wounds in single cells heal by calcium-dependent membrane fusion, whereas multicellular wounds heal by a variety of different mechanisms, including circumferential contraction of an actomyosin 'purse string' that assembles around wound borders and is dependent upon the small GTPase Rho.
We investigated healing of puncture wounds made in Xenopus oocytes, a single-cell system. Oocyte wounds rapidly assumed a circular morphology and constricted circumferentially, coincident with the recruitment of filamentous actin (F-actin) and myosin-II to the wound borders. Surprisingly, recruitment of myosin-II to wound borders occurred before that of F-actin. Further, experimental disruption of F-actin prevented healing but did not prevent myosin-II recruitment. Actomyosin purse-string assembly and closure was dependent on Rho GTPases and extracellular calcium. Wounding resulted in reorganization of microtubules into an array similar to that which forms during cytokinesis in Xenopus embryos. Experimental perturbation of oocyte microtubules before wounding inhibited actomyosin recruitment and wound closure, whereas depolymerization of microtubules after wounding accelerated wound closure.
We conclude the following: actomyosin purse strings can close single-cell wounds; myosin-II is recruited to wound borders independently of F-actin; purse-string assembly is dependent on a Rho GTPase; and purse-string assembly and closure are controlled by microtubules. More generally, the results indicate that actomyosin purse strings have been co-opted through evolution to dispatch a broad variety of single-cell and multicellular processes, including wound healing, cytokinesis and morphogenesis.
单细胞和多细胞系统都能迅速修复物理损伤,但人们认为它们的修复机制截然不同。单细胞中的伤口通过钙依赖性膜融合来愈合,而多细胞伤口则通过多种不同机制愈合,包括围绕伤口边缘组装的肌动球蛋白“束带”的周向收缩,这种收缩依赖于小GTP酶Rho。
我们研究了非洲爪蟾卵母细胞(一种单细胞系统)中穿刺伤口的愈合情况。卵母细胞伤口迅速呈现圆形形态并周向收缩,同时丝状肌动蛋白(F-肌动蛋白)和肌球蛋白-II被募集到伤口边缘。令人惊讶的是,肌球蛋白-II在F-肌动蛋白之前就被募集到伤口边缘。此外,F-肌动蛋白的实验性破坏阻止了愈合,但没有阻止肌球蛋白-II的募集。肌动球蛋白束带的组装和闭合依赖于Rho GTP酶和细胞外钙。伤口导致微管重新组织成类似于非洲爪蟾胚胎胞质分裂期间形成的阵列。在伤口形成前对卵母细胞微管进行实验性扰动会抑制肌动球蛋白的募集和伤口闭合,而在伤口形成后微管解聚则加速伤口闭合。
我们得出以下结论:肌动球蛋白束带可以闭合单细胞伤口;肌球蛋白-II独立于F-肌动蛋白被募集到伤口边缘;束带组装依赖于Rho GTP酶;束带组装和闭合受微管控制。更普遍地说,结果表明肌动球蛋白束带在进化过程中被用于多种单细胞和多细胞过程,包括伤口愈合、胞质分裂和形态发生。