Department of Biomolecular Science, Toho University, Miyama, Funabashi, Chiba, Japan.
Cell Tissue Res. 2011 Sep;345(3):379-90. doi: 10.1007/s00441-011-1219-1. Epub 2011 Aug 17.
Re-epithelialization in skin wound healing is a process in which epidermal sheets grow and close the wound. Although the actin-myosin system is thought to have a pivotal role in re-epithelialization, its role is not clear. In fish skin, re-epithelialization occurs around 500 μm/h and is 50 times faster than in mammalian skin. We had previously reported that leading-edge cells of the epidermal outgrowth have both polarized large lamellipodia and "purse string"-like actin filament cables in the scale-skin culture system of medaka fish, Oryzias latipes (Cell Tissue Res, 2007). The actin purse-string (APS) is a supracellular contractile machinery in which adherens junctions (AJs) link intracellular myosin II-including actin cables between neighboring cells. In this study, we developed a modified "face-to-face" scale-skin culture system as an ex vivo model to study epidermal wound healing, and examined the role of the actin-myosin system in the rapid re-epithelialization using a myosin II ATPase inhibitor, blebbistatin. A low level of blebbistatin suppressed the formation of APS and induced the dissociation of keratocytes from the leading edge without attenuating the growth of the epidermal sheet or the migration rate of solitary keratocytes. AJs in the superficial layer showed no obvious changes elicited by blebbistatin. However, two epidermal sheets without APSs did not make a closure with each other, which was confirmed by inhibiting the connecting AJs between the superficial layers. These results suggest that myosin II activity is required for functional leading-edge cells and for epidermal closure.
皮肤创伤愈合中的再上皮化过程是指表皮细胞生长并封闭伤口的过程。尽管肌动球蛋白系统被认为在再上皮化过程中起着关键作用,但它的作用尚不清楚。在鱼类皮肤中,再上皮化速度约为 500 μm/h,比哺乳动物皮肤快 50 倍。我们之前曾报道过,在斑马鱼(Oryzias latipes)的鳞片-皮肤培养系统中,表皮突起的前缘细胞既有极化的大片状伪足,也有“束口袋状”的肌动蛋白丝电缆(Cell Tissue Res,2007)。肌动蛋白束口袋(APS)是一种超细胞收缩机制,其中黏着连接(AJs)将细胞内包含肌球蛋白 II 的肌动蛋白电缆连接在相邻细胞之间。在这项研究中,我们开发了一种改良的“面对面”鳞片-皮肤培养系统作为体外模型来研究表皮创伤愈合,并使用肌球蛋白 II ATP 酶抑制剂 blebbistatin 研究肌动球蛋白系统在快速再上皮化中的作用。低浓度的 blebbistatin 抑制 APS 的形成,并诱导角质细胞从前缘解离,而不会减弱表皮片的生长或孤立角质细胞的迁移率。浅层的 AJs 没有明显变化。然而,两个没有 APS 的表皮片彼此不能闭合,这可以通过抑制浅层之间的连接 AJs 来证实。这些结果表明,肌球蛋白 II 活性对于功能性前缘细胞和表皮闭合是必需的。