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


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search    

The fully linked HTML version of this article has now been published.
Development ePress online publication date 19 May 2004
doi: 10.1242/dev.01160


This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
dev.01160v1
131/12/2887    most recent
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 Rupp, P. A.
Right arrow Articles by Little, C. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rupp, P. A.
Right arrow Articles by Little, C. D.

Research article

{alpha}v{beta}3 integrin-dependent endothelial cell dynamics in vivo


Paul A. Rupp, András Czirók, and Charles D. Little*
* Author for correspondence (e-mail: clittle{at}kumc.edu)

A major challenge confronting developmental cell biologists is to understand how individual cell behaviors lead to global tissue organization. Taking advantage of an endothelial cell-specific marker and scanning time-lapse microscopy, we have examined the formation of the primary vascular pattern during avian vasculogenesis. Five types of distinguishable endothelial cell motion are observed during formation of a vascular plexus: (1) global tissue deformations that passively convect endothelial cells; (2) vascular drift, a sheet-like medial translocation of the entire vascular plexus; (3) structural rearrangements, such as vascular fusion; (4) individual cell migration along existing endothelial structures; and (5) cell process extension into avascular areas, resulting in new links within the plexus. The last four types of motion are quantified and found to be reduced in the presence of an {alpha}v{beta}3 integrin inhibitor. These dynamic cell motility data result in new hypotheses regarding primordial endothelial cell behavior during embryonic vasculogenesis.




This article has been cited by other articles:


Home page
Mol. Biol. CellHome page
P. A. Rupp, R. P. Visconti, A. Czirok, D. A. Cheresh, and C. D. Little
Matrix Metalloproteinase 2-Integrin {alpha}v{beta}3 Binding Is Required for Mesenchymal Cell Invasive Activity but Not Epithelial Locomotion: A Computational Time-Lapse Study
Mol. Biol. Cell, December 1, 2008; 19(12): 5529 - 5540.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
A. Szabo, E. Mehes, E. Kosa, and A. Czirok
Multicellular Sprouting In Vitro
Biophys. J., September 15, 2008; 95(6): 2702 - 2710.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
M. Murga, O. Fernandez-Capetillo, and G. Tosato
Neuropilin-1 regulates attachment in human endothelial cells independently of vascular endothelial growth factor receptor-2
Blood, March 1, 2005; 105(5): 1992 - 1999.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2004