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Bifurcation of Cell Migratory and Proliferative Signaling by the Adaptor Protein Shc

Cytokines and extracellular matrix proteins initiate signaling cascades that regulate cell migration and proliferation. Evidence is provided that the adaptor protein Shc can differentially regulate these processes. Specifically, under growth factor–limiting conditions, Shc stimulates haptotactic cel...

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Detalles Bibliográficos
Autores principales: Collins, Lila R., Ricketts, William A., Yeh, Linda, Cheresh, David
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174237/
https://www.ncbi.nlm.nih.gov/pubmed/10613912
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author Collins, Lila R.
Ricketts, William A.
Yeh, Linda
Cheresh, David
author_facet Collins, Lila R.
Ricketts, William A.
Yeh, Linda
Cheresh, David
author_sort Collins, Lila R.
collection PubMed
description Cytokines and extracellular matrix proteins initiate signaling cascades that regulate cell migration and proliferation. Evidence is provided that the adaptor protein Shc can differentially regulate these processes. Specifically, under growth factor–limiting conditions, Shc stimulates haptotactic cell migration without affecting anchorage-dependent proliferation. However, when growth factors are present, Shc no longer influences cell migration; rather, Shc is crucial for DNA synthesis. Mutational analysis of Shc demonstrates that, while tyrosine phosphorylation is required for both DNA synthesis and cell migration, the switch in Shc signaling is associated with differential use of Shc's phosphotyrosine interacting domains; the PTB domain regulates haptotaxis, while the SH2 domain is selectively required for proliferation.
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spelling pubmed-21742372008-05-01 Bifurcation of Cell Migratory and Proliferative Signaling by the Adaptor Protein Shc Collins, Lila R. Ricketts, William A. Yeh, Linda Cheresh, David J Cell Biol Original Article Cytokines and extracellular matrix proteins initiate signaling cascades that regulate cell migration and proliferation. Evidence is provided that the adaptor protein Shc can differentially regulate these processes. Specifically, under growth factor–limiting conditions, Shc stimulates haptotactic cell migration without affecting anchorage-dependent proliferation. However, when growth factors are present, Shc no longer influences cell migration; rather, Shc is crucial for DNA synthesis. Mutational analysis of Shc demonstrates that, while tyrosine phosphorylation is required for both DNA synthesis and cell migration, the switch in Shc signaling is associated with differential use of Shc's phosphotyrosine interacting domains; the PTB domain regulates haptotaxis, while the SH2 domain is selectively required for proliferation. The Rockefeller University Press 1999-12-27 /pmc/articles/PMC2174237/ /pubmed/10613912 Text en © 1999 The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Original Article
Collins, Lila R.
Ricketts, William A.
Yeh, Linda
Cheresh, David
Bifurcation of Cell Migratory and Proliferative Signaling by the Adaptor Protein Shc
title Bifurcation of Cell Migratory and Proliferative Signaling by the Adaptor Protein Shc
title_full Bifurcation of Cell Migratory and Proliferative Signaling by the Adaptor Protein Shc
title_fullStr Bifurcation of Cell Migratory and Proliferative Signaling by the Adaptor Protein Shc
title_full_unstemmed Bifurcation of Cell Migratory and Proliferative Signaling by the Adaptor Protein Shc
title_short Bifurcation of Cell Migratory and Proliferative Signaling by the Adaptor Protein Shc
title_sort bifurcation of cell migratory and proliferative signaling by the adaptor protein shc
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174237/
https://www.ncbi.nlm.nih.gov/pubmed/10613912
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