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 McCoy, J. P.
Right arrow Articles by Varani, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McCoy, J. P.
Right arrow Articles by Varani, J.

Journal of Cell Science, Vol 65, Issue 1 139-151, Copyright © 1984 by Company of Biologists


JOURNAL ARTICLES

Identification of a laminin-like substance on the surface of high-malignant murine fibrosarcoma cells

JP McCoy, RV Lloyd, MS Wicha and J Varani

High- and low-malignant murine fibrosarcoma cells were stained with anti-laminin antibodies using immunoperoxidase techniques and examined by electron microscopy. With the high-malignant cells, specific staining was observed along the cell surface. Use of normal rabbit serum in place of the rabbit anti-laminin or pretreatment of the anti-laminin with soluble laminin completely eliminated this staining. No immunoperoxidase staining was observed with the low-malignant cells. In additional studies, membrane fractions were prepared from the high- and low-malignant cells and used to immunize rabbits. The animals immunized with the membrane fractions from the high-malignant cells produced antibodies that reacted by enzyme-linked immunosorbent assay (ELISA) with murine laminin obtained from the EHS sarcoma. The animals immunized with membrane fractions from the low-malignant cells did not. These studies provide strong evidence that the high-malignant cells (but not the low) express on their cell surface a substance that is immunologically cross-reactive with laminin. In addition, the high-malignant cells (but not the low) secreted a material into the cell culture fluid that could be specifically immunoprecipitated with antilaminin antibodies. The immunoprecipitated material co-migrated with purified laminin when examined by sodium dodecyl sulphate/polyacrylamide gel electrophoresis under reducing conditions. The existence of this substance associated with the surface of the high-malignant cells and its absence from that of the low-malignant cells may explain the previously noted difference between these cells in their ability to attach to type IV collagen. This difference may also contribute to the dissimilarity between these cells in their metastatic potential.


This article has been cited by other articles:


Home page
ScienceHome page
Y Iwamoto, F. Robey, J Graf, M Sasaki, H. Kleinman, Y Yamada, and G. Martin
YIGSR, a synthetic laminin pentapeptide, inhibits experimental metastasis formation
Science, November 20, 1987; 238(4830): 1132 - 1134.
[Abstract] [PDF]


Home page
ScienceHome page
V. Terranova, J. Williams, L. Liotta, and G. Martin
Modulation of the metastatic activity of melanoma cells by laminin and fibronectin
Science, November 23, 1984; 226(4677): 982 - 985.
[Abstract] [PDF]




© The Company of Biologists Ltd 1984