Background: Both single cells and multicellular systems rapidly heal physic
al insults but are thought to do so by distinctly different mechanisms. Wou
nds in single cells heal by calcium-dependent membrane fusion, whereas mult
icellular wounds heal by a variety of different mechanisms, including circu
mferential contraction of an actomyosin 'purse string' that assembles aroun
d wound borders and is dependent upon the small GTPase Rho.
Results: 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 fila
mentous actin (F-actin) and myosin-ll to the wound borders. Surprisingly, r
ecruitment of myosin-ll to wound borders occurred before that of F-actin, F
urther, experimental disruption of F-actin prevented healing but did not pr
event myosin-ll recruitment. Actomyosin purse-string assembly and closure w
as dependent on Rho GTPases and extracellular calcium. Wounding resulted in
reorganization of microtubules into an array similar to that which forms d
uring cytokinesis in Xenopus embryos. Experimental perturbation of oocyte m
icrotubules before wounding inhibited actomyosin recruitment and wound clos
ure, whereas depolymerization of microtubules after wounding accelerated wo
und closure.
Conclusions: We conclude the following: actomyosin purse strings can close
single-cell wounds; myosin-ll is recruited to wound borders independently o
f F-actin; purse-string assembly is dependent on a Rho GTPase; and purse-st
ring assembly and closure are controlled by microtubules. More generally, t
he results indicate that actomyosin purse strings have been co-opted throug
h evolution to dispatch a broad variety of single-cell and multicellular pr
ocesses, including wound healing, cytokinesis and morphogenesis.