Tufts University School of Medicine, Department of Developmental, Molecular & Chemical Biology, Program in Cell, Molecular and Developmental Biology and Program in Genetics, 150 Harrison Avenue, Jaharis 322, Boston, MA 02111, USA.
Tufts University School of Medicine, Department of Developmental, Molecular & Chemical Biology, Program in Cell, Molecular and Developmental Biology and Program in Genetics, 150 Harrison Avenue, Jaharis 322, Boston, MA 02111, USA.
Dev Cell. 2018 Feb 26;44(4):471-483.e4. doi: 10.1016/j.devcel.2017.12.025. Epub 2018 Jan 27.
Contractile forces eliminate cell contacts in many morphogenetic processes. However, mechanisms that balance contractile forces to promote subtler remodeling remain unknown. To address this gap, we investigated remodeling of Drosophila eye lattice cells (LCs), which preserve cell contacts as they narrow to form the edges of a multicellular hexagonal lattice. We found that during narrowing, LC-LC contacts dynamically constrict and expand. Similar to other systems, actomyosin-based contractile forces promote pulses of constriction. Conversely, we found that WAVE-dependent branched F-actin accumulates at LC-LC contacts during expansion and functions to expand the cell apical area, promote shape changes, and prevent elimination of LC-LC contacts. Finally, we found that small Rho GTPases regulate the balance of contractile and protrusive dynamics. These data suggest a mechanism by which WAVE regulatory complex-based F-actin dynamics antagonize contractile forces to regulate cell shape and tissue topology during remodeling and thus contribute to the robustness and precision of the process.
收缩力在许多形态发生过程中消除细胞间的接触。然而,平衡收缩力以促进更微妙的重塑的机制仍然未知。为了解决这一差距,我们研究了果蝇眼睛晶格细胞(LC)的重塑,这些细胞在变窄形成多细胞六边形晶格时保持细胞间的接触。我们发现,在变窄过程中,LC-LC 接触会动态收缩和扩张。与其他系统类似,基于肌动球蛋白的收缩力会促进收缩脉冲。相反,我们发现 WAVE 依赖性分支 F-肌动蛋白在扩张过程中积累在 LC-LC 接触处,并发挥扩大细胞顶面积、促进形状变化和防止 LC-LC 接触消除的功能。最后,我们发现小 Rho GTPases 调节收缩和伸出动力学的平衡。这些数据表明,基于 WAVE 调节复合物的 F-肌动蛋白动力学通过拮抗收缩力来调节重塑过程中的细胞形状和组织拓扑结构的机制,从而为该过程的稳健性和精确性做出贡献。