spacer gif spacer gif spacer gif spacer gif ARCHIVE ANNOUNCEMENT! 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 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 Google Scholar
Google Scholar
Right arrow Articles by Crawford, V. D.
Right arrow Articles by Burke, R. D.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Crawford, V. D.
Right arrow Articles by Burke, R. D.

Development, Vol 120, Issue 11 3227-3234, Copyright © 1994 by Company of Biologists


JOURNAL ARTICLES

YIGSR domain of laminin binds surface receptors of mesenchyme and stimulates migration during gastrulation in sea urchins

V. D. Crawford and R. D. Burke

During gastrulation in sea urchins, cells at the tip of the archenteron extend filopodia that attach to the blastocoel wall and are thought to assist in the elongation of the archenteron. Upon completion of gastrulation, these cells migrate into the blastocoel. Time-lapse video records were made of preparations from which ectodermal cells have been removed, leaving the archenteron, mesenchyme cells and blastocoelar extracellular matrix (ECM) bounded by the basal lamina. In preparations of late gastrulae, cells at the tip of the archenteron extend filopodia that attach to the basal lamina and pull it inward, collapsing the preparation. This collapse does not occur in preparations made prior to the elongation phase and can be inhibited with cytochalasin B and azide, but not with colchicine. Migratory behavior increased in preparations treated with the laminin-derived peptide Tyr-Ile-Gly-Ser- Arg (YIGSR). Cells extend and retract filopodia, collapse the ECM and migrate out of the preparation. This behavior was not observed in preparations treated with whole laminin, fibronectin or Arg-Gly- Asp-Ser (RGDS) peptides. Cells in preparations treated with YIGSR extend significantly more processes than those incubated in RGDS, laminin, fibronectin or BSA. This effect is titratable between 10-3 and 10-6 M. Whole laminin has a significant inhibitory effect on the number of cell processes observed. Double labelling experiments with biotinylated laminin or biotinylated CDPGYIGSR and a mesenchyme-specific monoclonal antibody (Sp12) reveal that laminin and CDPGYIGSR label mesenchymal and non-mesenchymal cells. A CDPGYIGSR affinity column binds a 125I-labelled cell surface component, which elutes with YIGSR and has an Mr of about 80x103 on SDS-PAGE. We propose that cells at the tip of the archenteron attach to the basal lamina during archenteron elongation, and that domains of laminin containing YIGSR in the basal lamina of the target region stimulate migratory behavior in these cells.





© The Company of Biologists Ltd 1994