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 WOHLMAN, A.
Right arrow Articles by ALLEN, R. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by WOHLMAN, A.
Right arrow Articles by ALLEN, R. D.

Journal of Cell Science, Vol 3, 105-114, Copyright © 1968 by Company of Biologists

Submitted on April 26, 1967
Revised on August 1, 1967

Structural Organization Associated with Pseudopod Extension and Contraction During Cell Locomotion in Difflugia

A. WOHLMAN 1 and R. D. ALLEN 2

1 Department of Biology, Princeton University Princeton, New Jersey, U.S.A.; Bell-Craig Laboratories for Medical Research, 451 Alliance Avenue, Toronto 9, Ontario, Canada.
2 Department of Biology, Princeton University Princeton, New Jersey, U.S.A.; Department of Biological Sciences, State University of New York at Albany, Albany, New York, U.S.A.

In Difflugia corona, a free-living amoeboid cell, locomotion is hampered by a heavy shell or test made of sand grains and other debris. Locomotion involves pseudopod extension, attachment to the substratum, and forcible pseudopod retraction which pulls the shelled cell body forward.

When observed through a polarizing microscope, the extending pseudopodia appear isotropic or very weakly birefringent. Upon attachment to the substratum a positively birefringent fibrillar array develops rapidly at the attachment point and extends from this region bade to the cell body within the test. These birefringent fibrils extend through and parallel to the long axis of the pseudopod. As the pseudopod retracts, the birefringent fibrillar array disappears, and hyaline blebs, suggestive of syneresis, appear on the pseudopodial surface. The birefringent fibrils correspond in position and approximate diameter (1 µ) to retractile fibrils visible with the Nomarski differential interference microscope.

Individual organisms were fixed for electron microscopy at a time when the pseudopodia were firmly attached to the substratum. Electron-microscopic examination of thin sections of pseudopodia revealed many 1-µ bundles of intimately associated, aligned, 55-75 Å microfilaments. The orientation and size of the bundles indicate that they probably correspond to the birefringent, refractile fibrils observed in living cells. Microfilaments have also been observed both as randomly oriented and dispersed cytoplasmic components, and as aligned filaments in the ectoplasm adjacent to the plasmalemma.

During pseudopod extension with sporadic streaming, birefringent ‘flashes’ have been observed at the front of the pseudopod. These flashes are believed to represent a photo-elastic phenomenon.

Submitted on April 26, 1967
Revised on August 1, 1967




This article has been cited by other articles:


Home page
ScienceHome page
R. D. Goldman and E. A. C. Follett
Birefringent Filamentous Organelle in BHK-21 Cells and Its Possible Role in Cell Spreading and Motility
Science, July 17, 1970; 169(3942): 286 - 288.
[Abstract] [PDF]




© The Company of Biologists Ltd 1968