| Literature DB >> 29396116 |
Steven J Del Signore1, Rodrigo Cilla1, Victor Hatini2.
Abstract
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.Entities:
Keywords: Abi; Arp2/3 complex; PI(3,4,5)P3; SCAR; WAVE regulatory complex; actomyosin contractility; branched F-actin; cell shape change; epithelial morphogenesis; small Rho GTPases
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Year: 2018 PMID: 29396116 PMCID: PMC5856465 DOI: 10.1016/j.devcel.2017.12.025
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270