Department of Biophysics, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
Department of Cell Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
Development. 2024 Nov 15;151(22). doi: 10.1242/dev.202892.
Ventral furrow (VF) formation in Drosophila melanogaster is an important model of epithelial folding. Previous models of VF formation require cell volume conservation to convert apically localized constriction forces into lateral cell elongation and tissue folding. Here, we have investigated embryonic morphogenesis in anillin knockdown (scra RNAi) embryos, where basal cell membranes fail to form and therefore cells can lose cytoplasmic volume through their basal side. Surprisingly, the mesoderm elongation and subsequent folding that comprise VF formation occurred essentially normally. We hypothesized that the effects of viscous shear may be sufficient to drive membrane elongation, providing effective volume conservation, and thus driving tissue folding. Since this hypothesis may not be possible to test experimentally, we turned to a computational approach. To test whether viscous shear is a dominant force for morphogenesis in vivo, we developed a 3D computational model incorporating both accurate cell and tissue geometry, and experimentally measured material parameters. Results from this model demonstrate that viscous shear generates sufficient force to drive cell elongation and tissue folding in vivo.
果蝇中 ventral furrow(VF)的形成是上皮折叠的重要模型。之前的 VF 形成模型需要细胞体积守恒,将局部的顶端收缩力转化为横向细胞伸长和组织折叠。在这里,我们研究了 anillin 敲低(scra RNAi)胚胎中的胚胎形态发生,其中基底细胞膜无法形成,因此细胞可以通过基底侧失去细胞质体积。令人惊讶的是,构成 VF 形成的中胚层伸长和随后的折叠基本上正常发生。我们假设粘性剪切的影响可能足以驱动膜伸长,提供有效的体积守恒,从而驱动组织折叠。由于这个假设可能无法通过实验来验证,我们转向了一种计算方法。为了测试粘性剪切是否是体内形态发生的主要力,我们开发了一个 3D 计算模型,该模型结合了精确的细胞和组织几何形状以及实验测量的材料参数。该模型的结果表明,粘性剪切产生的力足以在体内驱动细胞伸长和组织折叠。