ZFIN ID: ZDB-PUB-150130-4
In vivo imaging and characterization of actin microridges
Lam, P.Y., Mangos, S., Green, J.M., Reiser, J., Huttenlocher, A.
Date: 2015
Source: PLoS One   10: e0115639 (Journal)
Registered Authors: Huttenlocher, Anna, Lam, Pui Ying, Mangos, Steve
Keywords: none
MeSH Terms:
  • Actins/metabolism*
  • Actins/ultrastructure*
  • Animals
  • Cytokinesis
  • Epithelial Cells/metabolism
  • Epithelial Cells/ultrastructure
  • Molecular Imaging*
  • Time-Lapse Imaging
  • Zebrafish
PubMed: 25629723 Full text @ PLoS One
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ABSTRACT
Actin microridges form labyrinth like patterns on superficial epithelial cells across animal species. This highly organized assembly has been implicated in mucus retention and in the mechanical structure of mucosal surfaces, however the mechanisms that regulate actin microridges remain largely unknown. Here we characterize the composition and dynamics of actin microridges on the surface of zebrafish larvae using live imaging. Microridges contain phospho-tyrosine, cortactin and VASP, but not focal adhesion kinase. Time-lapse imaging reveals dynamic changes in the length and branching of microridges in intact animals. Transient perturbation of the microridge pattern occurs before cell division with rapid re-assembly during and after cytokinesis. Microridge assembly is maintained with constitutive activation of Rho or inhibition of myosin II activity. However, expression of dominant negative RhoA or Rac alters microridge organization, with an increase in distance between microridges. Latrunculin A treatment and photoconversion experiments suggest that the F-actin filaments are actively treadmilling in microridges. Accordingly, inhibition of Arp2/3 or PI3K signaling impairs microridge structure and length. Taken together, actin microridges in zebrafish represent a tractable in vivo model to probe pattern formation and dissect Arp2/3-mediated actin dynamics in vivo.
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