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 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 Kawamura, K.
Right arrow Articles by Sugino, Y. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kawamura, K.
Right arrow Articles by Sugino, Y. M.

Development, Vol 113, Issue 3 995-1005, Copyright © 1991 by Company of Biologists


JOURNAL ARTICLES

Budding-specific lectin induced in epithelial cells is an extracellular matrix component for stem cell aggregation in tunicates

K Kawamura, S Fujiwara and YM Sugino
Department of Biology, Faculty of Science, Kochi University, Japan.

We have examined immunocytochemically the expression, localization and in vivo function of a calcium-dependent and galactose-binding 14 x 10(3) Mr lectin purified from the budding tunicate, Polyandrocarpa misakiensis. Lectin granules first appeared in the inner epithelium of a double-walled bud vesicle. Soon after the bud entered the developmental phase, the granules were secreted into the mesenchymal space, where the lectin-positive extracellular matrix (ECM) developed. The lectin was also produced and secreted by granular leucocytes during budding. Hemoblasts, pluripotent stem cells in the blood, were often found in association with the ECM and they aggregated with epithelial cells to form organ rudiments. The lectin showed a high binding affinity for hemoblast precursors. The blockage of epithelial transformation of stem cells by galactose in in vivo bioassy was ineffective in the presence of the lectin. Polyclonal anti-lectin antibody prevented the hemoblasts spreading on the ECM and moving toward the epithelium, but it did not block the cell-cell adhesion of hemoblasts. By three days of bud development, lectin granules and ECM have almost disappeared from the developing bud together with a cessation of hemoblast aggregation. These results show that Polyandrocarpa lectin is a component of the ECM induced specifically in budding and suggest strongly that it plays a role in bud morphogenesis by directing the migration of pluripotent stem cells to the epithelium.


This article has been cited by other articles:


Home page
Integr. Comp. Biol.Home page
M. S. Quesenberry, H. Ahmed, M. T. Elola, N. O'Leary, and G. R. Vasta
Diverse Lectin Repertoires in Tunicates Mediate Broad Recognition and Effector Innate Immune Responses
Integr. Comp. Biol., April 1, 2003; 43(2): 323 - 330.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. Matsumoto, C. Nakamoto, S. Fujiwara, T. Yubisui, and K. Kawamura
A novel C-type lectin regulating cell growth, cell adhesion and cell differentiation of the multipotent epithelium in budding tunicates
Development, September 1, 2001; 128(17): 3339 - 3347.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1991