Open Access
A lateral protrusion latticework connects neuroepithelial cells and is regulated during neurogenesis
Author(s) -
Ioannis Kasioulis,
Alwyn Dady,
John James,
Alan R. Prescott,
Pamela A. Halley,
Kate G. Storey
Publication year - 2022
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.259897
Subject(s) - neuroepithelial cell , biology , filopodia , microbiology and biotechnology , anatomy , neurogenesis , pseudopodia , morphogenesis , actin , lamellipodium , neurulation , cell migration , cell , gastrulation , embryo , embryogenesis , neural stem cell , stem cell , biochemistry , gene , genetics
Dynamic contacts between cells within the developing neuroepithelium are poorly understood but play important roles in cell and tissue morphology and cell signalling. Here, using live-cell imaging and electron-microscopy we reveal multiple protrusive structures in neuroepithelial apical endfeet of the chick embryonic spinal cord, including sub-apical protrusions that extend laterally within the tissue, and observe similar structures in human neuroepithelium. We characterise the dynamics, shape, and cytoskeleton of these lateral protrusions and distinguish them from cytonemes/filopodia and tunnelling nanotubes. We demonstrate that lateral protrusions form a latticework of membrane contacts between non-adjacent cells, depend on actin but not microtubule dynamics and provide a lamellipodial-like platform for further extending fine actin-dependent filipodia. We find that lateral protrusions depend on actin-binding protein WAVE1: mutant-WAVE1 misexpression attenuated protrusion and generated a round-ended apical endfoot morphology. However, this did not alter apico-basal cell polarity nor tissue integrity. During normal neuronal delamination lateral protrusions were withdrawn, but mutant-WAVE1-induced precocious protrusion loss was insufficient to trigger neurogenesis. This study uncovers a new form of cell-cell contact within the developing neuroepithelium regulation of which prefigures neuronal delamination.