The WAVE Regulatory Complex and Branched F-Actin Counterbalance Contractile Force to Control Cell Shape and Packing in the Drosophila Eye

被引:25
作者
Del Signore, Steven J. [1 ,2 ,3 ]
Cilla, Rodrigo [1 ,2 ]
Hatini, Victor [1 ,2 ]
机构
[1] Tufts Univ, Sch Med, Dept Dev Mol & Chem Biol, Program Cell Mol & Dev Biol, 150 Harrison Ave,Jaharis 322, Boston, MA 02111 USA
[2] Program Genet, 150 Harrison Ave,Jaharis 322, Boston, MA 02111 USA
[3] Brandeis Univ, Dept Biol, Waltham, MA 02453 USA
关键词
ADHERENS JUNCTIONS; TISSUE MORPHOGENESIS; APICAL CONSTRICTION; C-ELEGANS; EPITHELIAL MORPHOGENESIS; CADHERIN ENGAGEMENT; ACTOMYOSIN NETWORK; PATTERN-FORMATION; DORSAL CLOSURE; ALPHA-CATENIN;
D O I
10.1016/j.devcel.2017.12.025
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 amulticellular hexagonal lattice. Wefound 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 smallRho 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.
引用
收藏
页码:471 / +
页数:17
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