Literature DB >> 3619087

Cell cycle and neuroepithelial cell shape during bending of the chick neural plate.

J L Smith, G C Schoenwolf.   

Abstract

Neuroepithelial cells change shape from spindle-like to wedge-like within three restricted areas (hinge points) of the bending neural plate. The mechanisms underlying these localized cell shape changes and the specific role that these changes play in bending are unclear. This study was designed to determine whether changes in neuroepithelial cell shape involve basal cellular expansion owing to alteration of the cell cycle. Neurulating chick embryos were treated with colchicine to arrest and accumulate cells in metaphase, and colchicine indices and cell generation times were calculated for the neural plate. During bending of the neural plate, cell generation time in the median hinge point, which contains predominantly wedge-shaped cells, was significantly longer than that in adjacent lateral areas of the neural plate, which contain predominantly spindle-shaped cells. In addition, cell generation time in the flat neural plate, which contains predominantly spindle-shaped cells and has not yet differentiated into the median hinge point and lateral subdivisions, was identical to that in lateral areas of the bending neural plate but was significantly shorter than that in the median hinge point. These results support the hypothesis that changes in neuroepithelial cell shape from spindle-like to wedge-like involve basal cellular expansion owing to alteration of the cell cycle. Additional tests of this hypothesis and studies on the role of localized cell shape changes in neurulation are in progress.

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Year:  1987        PMID: 3619087     DOI: 10.1002/ar.1092180215

Source DB:  PubMed          Journal:  Anat Rec        ISSN: 0003-276X


  21 in total

1.  Early neuronal development in the spinal cord of a reptile assessed by neurofilament protein immunoreactivity.

Authors:  E Marti; M A Batista; A R Bello; A Lancha; D Dahl
Journal:  J Anat       Date:  1990-12       Impact factor: 2.610

2.  Development of floor plate, neurons and axonal outgrowth pattern in the early spinal cord of the notochord-deficient chick embryo.

Authors:  H W van Straaten; J W Hekking
Journal:  Anat Embryol (Berl)       Date:  1991

Review 3.  The genesis of avian neural crest cells: a classic embryonic induction.

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Journal:  Proc Natl Acad Sci U S A       Date:  1996-09-03       Impact factor: 11.205

4.  Bone morphogenetic proteins regulate neural tube closure by interacting with the apicobasal polarity pathway.

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Journal:  Development       Date:  2011-08       Impact factor: 6.868

5.  Axial structures control laterality in the distribution pattern of endothelial cells.

Authors:  S Klessinger; B Christ
Journal:  Anat Embryol (Berl)       Date:  1996-04

Review 6.  G-protein-coupled receptor signaling and neural tube closure defects.

Authors:  Issei S Shimada; Saikat Mukhopadhyay
Journal:  Birth Defects Res       Date:  2017-01-30       Impact factor: 2.344

7.  Immunohistochemistry of laminin in early chicken and quail blastoderms.

Authors:  H Bortier; G De Bruyne; M Espeel; L Vakaet
Journal:  Anat Embryol (Berl)       Date:  1989

8.  Role of cell-cycle in regulating neuroepithelial cell shape during bending of the chick neural plate.

Authors:  J L Smith; G C Schoenwolf
Journal:  Cell Tissue Res       Date:  1988-06       Impact factor: 5.249

Review 9.  From proliferation to target innervation: signaling molecules that direct sympathetic nervous system development.

Authors:  W H Chan; C R Anderson; David G Gonsalvez
Journal:  Cell Tissue Res       Date:  2017-10-02       Impact factor: 5.249

Review 10.  Morphogenesis of epithelial tubes: Insights into tube formation, elongation, and elaboration.

Authors:  Deborah J Andrew; Andrew J Ewald
Journal:  Dev Biol       Date:  2009-09-22       Impact factor: 3.582

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