PUBLICATION

Stochastic contraction of myosin minifilaments drives evolution of microridge protrusion patterns in epithelial cells

Authors
van Loon, A.P., Erofeev, I.S., Goryachev, A.B., Sagasti, A.
ID
ZDB-PUB-210604-3
Date
2021
Source
Molecular biology of the cell   32(16): 1501-1513 (Journal)
Registered Authors
Sagasti, Alvaro
Keywords
none
MeSH Terms
  • Actins/metabolism*
  • Animals
  • Cytoskeleton/metabolism*
  • Epithelial Cells/cytology
  • Epithelial Cells/metabolism
  • Epithelial Cells/physiology*
  • Myosin Type II/metabolism*
  • Zebrafish
PubMed
34081537 Full text @ Mol. Biol. Cell
Abstract
Actin-based protrusions vary in morphology, stability, and arrangement on cell surfaces. Microridges are laterally-elongated protrusions on mucosal epithelial cells, where they form evenly spaced, maze-like patterns that dynamically remodel by fission and fusion. To characterize how microridges form their highly ordered, subcellular patterns and investigate the mechanisms driving fission and fusion, we imaged microridges in the maturing skin of zebrafish larvae. After their initial development, microridge spacing and alignment became increasingly well ordered. Imaging F-actin and Non-Muscle Myosin II (NMII) revealed that microridge fission and fusion were associated with local NMII activity in the apical cortex. Inhibiting NMII blocked fission and fusion rearrangements, reduced microridge density, and altered microridge spacing. High-resolution imaging allowed us to image individual NMII minifilaments in the apical cortex of cells in live animals, revealing that minifilaments are tethered to protrusions and often connect adjacent microridges. NMII minifilaments connecting the ends of two microridges fused them together, whereas minifilaments oriented perpendicular to microridges severed them or pulled them closer together. These findings demonstrate that as cells mature, cortical NMII activity orchestrates a remodeling process that creates an increasingly orderly microridge arrangement. [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text].
Genes / Markers
Figures
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Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
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