Toyama Yusuke, Peralta Xomalin G, Wells Adrienne R, Kiehart Daniel P, Edwards Glenn S
Physics Department and Free Electron Laser Laboratory, Duke University, Durham, NC 27708, USA.
Science. 2008 Sep 19;321(5896):1683-6. doi: 10.1126/science.1157052.
Understanding cell morphogenesis during metazoan development requires knowledge of how cells and the extracellular matrix produce and respond to forces. We investigated how apoptosis, which remodels tissue by eliminating supernumerary cells, also contributes forces to a tissue (the amnioserosa) that promotes cell-sheet fusion (dorsal closure) in the Drosophila embryo. We showed that expression in the amnioserosa of proteins that suppress or enhance apoptosis slows or speeds dorsal closure, respectively. These changes correlate with the forces produced by the amnioserosa and the rate of seam formation between the cell sheets (zipping), key processes that contribute to closure. This apoptotic force is used by the embryo to drive cell-sheet movements during development, a role not classically attributed to apoptosis.
了解后生动物发育过程中的细胞形态发生需要知道细胞和细胞外基质如何产生并响应力。我们研究了细胞凋亡如何通过消除多余细胞来重塑组织,同时也为促进果蝇胚胎中细胞层融合(背侧闭合)的组织(羊膜浆膜)贡献力量。我们发现,在羊膜浆膜中表达抑制或增强细胞凋亡的蛋白质分别会减缓或加速背侧闭合。这些变化与羊膜浆膜产生的力以及细胞层之间形成接缝(拉链化)的速率相关,而这些是促成闭合的关键过程。胚胎利用这种凋亡力在发育过程中驱动细胞层运动,这一作用并非传统上认为的细胞凋亡所具有的。