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 Toyoizumi, R.
Right arrow Articles by Takeuchi, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Toyoizumi, R.
Right arrow Articles by Takeuchi, S.
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 108, Issue 2 557-567, Copyright © 1995 by Company of Biologists


JOURNAL ARTICLES

The behavior of chick gastrula mesodermal cells under the unidirectional tractive force parallel to the substrata

R Toyoizumi and S Takeuchi
Department of Biological Sciences, Faculty of Science, Kanagawa University, Hiratsuka City, Japan.

Advancement of leading lamellae of a migratory cell inevitably causes a strain inside the cell body. We investigated the effect of the tension arisen inside a mesodermal cell on its behavior by pulling the cell body unidirectionally along the substratum. Chick gastrula mesodermal cells, known as highly migratory, were dissociated into single cells in sodium citrate buffer, conjugated with paramagnetic beads activated by tosyl-residue (4.5 microns in diameter) and seeded onto coverglasses coated with fibronectin. After the cells spread on the substratum and protruded cellular processes in all directions, they were exposed to a non-uniform magnetic field by a magnet. Thus the cells bearing the beads were pulled with a force in the order of 10(-10) N. The behavior of such cells was recorded with a time-lapse video taperecorder and assessed quantitatively. Shortly after the magnetic force was applied, the beads stuck to the cells were aligned in tandem along the line of magnetic force at the site for the magnet. Subsequently, they frequently came to extend their leading lamella precisely counter to the traction on the line of the beads. Observation with scanning electron microscope revealed that a large part of the beads attached to the cells were wrapped in the cell membrane. In this condition, the cells were stretched locally between the attachment site of the beads and adhesion plaques beneath the leading edge, which was formed in a direction away from the traction. It was proved statistically that such cells tended to locomote away from the magnet at the 0.1% significance level with Hotelling's T2-test. In contrast, the mesodermal cells free of the artificial traction in three kinds of control experiments did not show such a preference in the direction of locomotion. These results proved that migratory cells tended to move in the direction away from the tractive force parallel to the substratum, suggesting that advancement of a leading lamella is accelerated when it is stretched along the direction of projection by a mechanical force of sufficient strength. Implication of this finding to the mechanism of cell locomotion will be discussed.
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
L. Vonna, A. Wiedemann, M. Aepfelbacher, and E. Sackmann
Local force induced conical protrusions of phagocytic cells
J. Cell Sci., March 1, 2003; 116(5): 785 - 790.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1995