spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ireland, G. W.
Right arrow Articles by Voon, F. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ireland, G. W.
Right arrow Articles by Voon, F. C.

Journal of Cell Science, Vol 52, Issue 1 55-69, Copyright © 1981 by Company of Biologists


JOURNAL ARTICLES

Polygonal networks in living chick embryonic cells

GW Ireland and FC Voon

Regular polygonal networks have been found in explants and dissociated cells of early chick embryos. These networks are readily observable in live cells with phase-contrast optics thus allowing time-lapse cinemicroscopy. They consisted of a regular pattern of nodes and radiating struts found predominantly in the lamelliplasm of the free edges of the cells bordering explants. At the outer edge, the network was terminated by radial struts associated with substrate-attached retraction processes whilst toward the centre of the cells it faded out. The network was also associated with stress fibres running across the cell and with microextensions on the dorsal surface. Even within one cell the network varied in size. Time-lapse films showed that microvilli were protruded from the dorsal surface over the nodes. Although the cells containing the networks were poorly motile the network itself was a mobile structure. Many explants from regions differing in prospective fates developed these networks after 2-4 days in culture. They appeared earlier in the smaller less yolky cells of definitive endoblast and epiblast. Experiments with dissociated and reaggregated cells confirmed their occurrence mainly in free edges of cells. The relationship between these networks seen in living chick embryo cells and those seen in other cell types using immunofluorescent techniques is discussed and a mechanism is proposed for their formation.


This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
A. M. Malek, C. Xu, E. S. Kim, and S. L. Alper
Hypertonicity triggers RhoA-dependent assembly of myosin-containing striated polygonal actin networks in endothelial cells
Am J Physiol Cell Physiol, May 1, 2007; 292(5): C1645 - C1659.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
M. S. Filla, A. Woods, P. L. Kaufman, and D. M. Peters
{beta}1 and {beta}3 Integrins Cooperate to Induce Syndecan-4-Containing Cross-linked Actin Networks in Human Trabecular Meshwork Cells
Invest. Ophthalmol. Vis. Sci., May 1, 2006; 47(5): 1956 - 1967.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1981