PUBLICATION

Formation of the zebrafish midbrain-hindbrain boundary constriction requires laminin-dependent basal constriction

Authors
Gutzman, J.H., Graeden, E.G., Lowery, L.A., Holley, H.S., and Sive, H.
ID
ZDB-PUB-080825-24
Date
2008
Source
Mechanisms of Development   125(11-12): 974-983 (Journal)
Registered Authors
Gutzman, Jennifer, Lowery, Laura Anne, Sive, Hazel
Keywords
basal constriction, apical expansion, zebrafish morphogenesis, laminin, brain ventricle, midbrain-hindbrain boundary, midbrain-hindbrain boundary constriction (MHBC), cell shape
MeSH Terms
  • Actins/metabolism
  • Animals
  • Brain/pathology
  • Cell Shape
  • Cell Size
  • Cytoskeleton/metabolism
  • Epithelium/metabolism
  • Immunohistochemistry/methods
  • Laminin/genetics
  • Laminin/metabolism*
  • Mesencephalon/embryology*
  • Mesencephalon/physiology
  • Models, Biological
  • Mutation
  • Neural Crest/metabolism
  • Rhombencephalon/embryology*
  • Rhombencephalon/physiology
  • Zebrafish
PubMed
18682291 Full text @ Mech. Dev.
Abstract
The midbrain-hindbrain boundary (MHB) is a highly conserved fold in the vertebrate embryonic brain. We have termed the deepest point of this fold the MHB constriction (MHBC) and have begun to define the mechanisms by which it develops. In the zebrafish, the MHBC is formed soon after neural tube closure, concomitant with inflation of the brain ventricles. The MHBC is unusual, as it forms by bending the basal side of the neuroepithelium. At single cell resolution, we show that zebrafish MHBC formation involves two steps. The first is a shortening of MHB cells to approximately 75% of the length of surrounding cells. The second is basal constriction, and apical expansion, of a small group of cells that contribute to the MHBC. In the absence of inflated brain ventricles, basal constriction still occurs, indicating that the MHBC is not formed as a passive consequence of ventricle inflation. In laminin mutants, basal constriction does not occur, indicating an active role for the basement membrane in this process. Apical expansion also fails to occur in laminin mutants, suggesting that apical expansion may be dependent on basal constriction. This study demonstrates laminin-dependent basal constriction as a previously undescribed molecular mechanism for brain morphogenesis.
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