Pten, PI3K, and PtdIns(3,4,5)P < sub > 3 < /sub > dynamics control pulsatile actin branching in Drosophila retina morphogenesis

Dev Cell. 2024 Apr 17:S1534-5807(24)00203-X. doi: 10.1016/j.devcel.2024.03.035. Online ahead of print.ABSTRACTEpithelial remodeling of the Drosophila retina depends on the pulsatile contraction and expansion of apical contacts between the cells that form its hexagonal lattice. Phosphoinositide PI(3,4,5)P3 (PIP3) accumulates around tricellular adherens junctions (tAJs) during contact expansion and dissipates during contraction, but with unknown function. Here, we found that manipulations of Pten or PI3-kinase (PI3K) that either decreased or increased PIP3 resulted in shortened contacts and a disordered lattice, indicating a requirement for PIP3 dynamics and turnover. These phenotypes are caused by a loss of branched actin, resulting from impaired activity of the Rac1 Rho GTPase and the WAVE regulatory complex (WRC). We additionally found that during contact expansion, PI3K moves into tAJs to promote the cyclical increase of PIP3 in a spatially and temporally precise manner. Thus, dynamic control of PIP3 by Pten and PI3K governs the protrusive phase of junctional remodeling, which is essential for planar epithelial morphogenesis.PMID:38640926 | DOI:10.1016/j.devcel.2024.03.035

Source: Developmental Cell - April 19, 2024 Category: Cytology Authors: Jacob Malin Christian Rosa-Birriel Victor Hatini Source Type: research