Crossref journal-article
Rockefeller University Press
The Journal of cell biology (291)
Abstract

The Wnt-1 gene plays an essential role in fetal brain development and encodes a secreted protein whose signaling mechanism is presently unknown. In this report we have investigated intracellular mechanisms by which the Wnt-1 gene induces morphological changes in PC12 pheochromocytoma cells. PC12 cells expressing Wnt-1 show increased steady-state levels of the adhesive junction protein plakoglobin, and an altered distribution of this protein within the cell. This effect appears similar to a modulation of the plakoglobin homolog, Armadillo, that occurs in Drosophila embryos in response to the Wnt-1 homolog, wingless (Riggleman, B., P. Schedl, and E. Wieschaus. 1990. Cell. 63:549-560). In addition, PC12/Wnt-1 cells show elevated expression of E-cadherin and increased calcium-dependent cell-cell adhesion. These results imply evolutionary conservation of cellular responses to Wnt-1/wingless and indicate that in certain cell types Wnt-1 may act to modulate cell adhesion mechanisms.

Authors 3
  1. R S Bradley (first)
  2. P Cowin (additional)
  3. A M Brown (additional)
References 0 Referenced 191

None

Dates
Type When
Created 21 years, 3 months ago (May 14, 2004, 8:22 p.m.)
Deposited 2 years, 1 month ago (July 22, 2023, 2:11 a.m.)
Indexed 11 hours, 5 minutes ago (Sept. 3, 2025, 6:48 a.m.)
Issued 31 years, 8 months ago (Dec. 15, 1993)
Published 31 years, 8 months ago (Dec. 15, 1993)
Published Online 31 years, 8 months ago (Dec. 15, 1993)
Published Print 31 years, 8 months ago (Dec. 15, 1993)
Funders 0

None

@article{Bradley_1993, title={Expression of Wnt-1 in PC12 cells results in modulation of plakoglobin and E-cadherin and increased cellular adhesion.}, volume={123}, ISSN={1540-8140}, url={http://dx.doi.org/10.1083/jcb.123.6.1857}, DOI={10.1083/jcb.123.6.1857}, number={6}, journal={The Journal of cell biology}, publisher={Rockefeller University Press}, author={Bradley, R S and Cowin, P and Brown, A M}, year={1993}, month=dec, pages={1857–1865} }