Ophthalmology and Visual Sciences Research Center, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Proc Natl Acad Sci U S A. 2012 Sep 25;109(39):15799-804. doi: 10.1073/pnas.1210992109. Epub 2012 Sep 10.
Purse-string healing is driven by contraction of actin/myosin cables that span cells at wound edges, and it is the predominant mode of closing small round wounds in embryonic and some adult epithelia. Wounds can also heal by cell crawling, and my colleagues and I have shown previously that the presence of unconstrained, straight edges in sheets of epithelial cells is a sufficient signal to induce healing by crawling. Here, it is reported that the presence of highly concave edges, which are free or physically constrained by an inert material (agarose), is sufficient to induce formation of purse strings. It was determined that neither of the two types of healing required cell damage or other potential stimuli by using the particularly gentle procedure of introducing gaps by digesting agarose blocks imbedded in the cell sheets. Movement by crawling depends on signaling by the EGF receptor (EGFR); however, this was not required for purse-string contraction. A migrating epithelial cell sheet usually produces finger-like projections of crawling cells. The cells between fingers contain continuous actin cables, which were also determined to contain myosin IIA and exhibit additional characteristics of purse strings. When crawling was blocked by inhibition of EGFR signaling, the concave regions continued to move, suggesting that both mechanisms contribute to propel the sheets forward. Wounding epithelial cell sheets causes activation of the EGFR, which triggers movement by crawling. The EGFR was found to be activated only at straight and convex edges, which explains how both types of movement can coexist at leading epithelial edges.
套索式愈合是由跨越伤口边缘细胞的肌动蛋白/肌球蛋白电缆收缩驱动的,它是胚胎和一些成人上皮细胞闭合小圆形伤口的主要方式。伤口也可以通过细胞爬行来愈合,我的同事和我之前已经表明,上皮细胞片中存在无约束的、直的边缘是诱导爬行愈合的充分信号。在这里,据报道,高度凹形边缘(自由的或被惰性材料(琼脂糖)物理约束的)足以诱导套索的形成。通过使用特别温和的方法,即用消化嵌入细胞片的琼脂糖块来引入间隙,确定这两种愈合方式都不需要细胞损伤或其他潜在的刺激。爬行运动依赖于表皮生长因子受体(EGFR)的信号;然而,这对于套索收缩并不是必需的。迁移的上皮细胞片通常会产生爬行细胞的指状突起。指间的细胞含有连续的肌动蛋白电缆,这些电缆也被确定含有肌球蛋白 IIA,并表现出套索的其他特征。当通过抑制 EGFR 信号传导来阻止爬行时,凹形区域继续移动,这表明这两种机制都有助于推动细胞向前移动。创伤上皮细胞片会导致 EGFR 的激活,从而触发爬行运动。发现 EGFR 仅在直的和凸的边缘处被激活,这解释了两种运动如何在领先的上皮边缘共存。