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 References
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 Coan, D. E.
Right arrow Articles by Sauvage, L. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Coan, D. E.
Right arrow Articles by Sauvage, L. R.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Journal of Cell Science, Vol 104, Issue 4 1145-1153, Copyright © 1993 by Company of Biologists


JOURNAL ARTICLES

Effect of shear stress upon localization of the Golgi apparatus and microtubule organizing center in isolated cultured endothelial cells

DE Coan, AR Wechezak, RF Viggers and LR Sauvage
Hope Heart Research Institute, Seattle, Washington 98122.

Despite substantial evidence to suggest that directed cell migration is dependent upon positioning of the Golgi apparatus (GA) and the microtubule organizing center (MTOC), some controversy exists about whether such a relationship is relevant to endothelial cells under flow. The present study was undertaken to provide an indepth investigation of the relationship between shear stress, GA/MTOC localization, cell migration and nuclear position. Bovine carotid endothelial cells were exposed to 22 or 88 dynes/cm2 for 0.5, 2, 8 or 24 h, and localization of their GA/MTOCs was determined relative to the direction of flow. In no-flow control specimens, (0, 0.5, 2, 8 and 24 h) there was no change in the equally distributed GA/MTOCs. In contrast, during the first 8 h at 88 dynes/cm2 and by 2 h at 22 dynes/cm2 there was a significant increase in the number of cells with GA/MTOCs localized upstream to flow direction. The effect was temporary, however, and by 24 h there was no significant difference between the no-flow, 22 and 88 dynes/cm2 specimens. Analysis of GA/MTOC localization with respect to the direction of cell migration determined that 72.5% of no-flow cells possessed GA/MTOCs localized to the sides of nuclei nearest the direction of migration. In contrast, 64% of the specimens shear stressed over the same time period had GA/MTOCs localized to the sides of nuclei opposite the direction of migration. These results suggest that positioning of the GA/MTOC in endothelial cells is not dependent completely upon the direction of migration.(ABSTRACT TRUNCATED AT 250 WORDS)
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J. Cell Sci.Home page
F. Pouthas, P. Girard, V. Lecaudey, T. B. N. Ly, D. Gilmour, C. Boulin, R. Pepperkok, and E. G. Reynaud
In migrating cells, the Golgi complex and the position of the centrosome depend on geometrical constraints of the substratum
J. Cell Sci., July 15, 2008; 121(14): 2406 - 2414.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
P. Uttayarat, M. Chen, M. Li, F. D. Allen, R. J. Composto, and P. I. Lelkes
Microtopography and flow modulate the direction of endothelial cell migration
Am J Physiol Heart Circ Physiol, February 1, 2008; 294(2): H1027 - H1035.
[Abstract] [Full Text] [PDF]


Home page
Molecular Cancer TherapeuticsHome page
K. A. Hotchkiss, A. W. Ashton, R. Mahmood, R. G. Russell, J. A. Sparano, and E. L. Schwartz
Inhibition of Endothelial Cell Function in Vitro and Angiogenesis in Vivo by Docetaxel (Taxotere): Association with Impaired Repositioning of the Microtubule Organizing Center
Mol. Cancer Ther., November 1, 2002; 1(13): 1191 - 1200.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
Y.-L. Hu, S. Li, J. Y.-J. Shyy, and S. Chien
Sustained JNK activation induces endothelial apoptosis: studies with colchicine and shear stress
Am J Physiol Heart Circ Physiol, October 1, 1999; 277(4): H1593 - H1599.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. P. Irigoyen, D. Besser, and Y. Nagamine
Cytoskeleton Reorganization Induces the Urokinase-type Plasminogen Activator Gene via the Ras/Extracellular Signal-regulated Kinase (ERK) Signaling Pathway
J. Biol. Chem., January 17, 1997; 272(3): 1904 - 1909.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
A. Malek and S Izumo
Mechanism of endothelial cell shape change and cytoskeletal remodeling in response to fluid shear stress
J. Cell Sci., January 4, 1996; 109(4): 713 - 726.
[Abstract] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
D. S. Ettenson and A. I. Gotlieb
Basic Fibroblast Growth Factor Is a Signal for the Initiation of Centrosome Redistribution to the Front of Migrating Endothelial Cells at the Edge of an In Vitro Wound
Arterioscler Thromb Vasc Biol, April 1, 1995; 15(4): 515 - 521.
[Abstract] [Full Text]




© The Company of Biologists Ltd 1993