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Role of E-cadherin and other cell adhesion molecules in survival and differentiation of human pluripotent stem cells

The survival, proliferation, self-renewal and differentiation of human pluripotent stem cells (hPSCs, including human embryonic stem cells and human induced pluripotent stem cells) involve a number of processes that require cell-cell and cell-matrix interactions. The cell adhesion molecules (CAMs),...

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Detalles Bibliográficos
Autores principales: Li, Li, Bennett, Steffany A.L., Wang, Lisheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364139/
https://www.ncbi.nlm.nih.gov/pubmed/22647941
http://dx.doi.org/10.4161/cam.19583
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author Li, Li
Bennett, Steffany A.L.
Wang, Lisheng
author_facet Li, Li
Bennett, Steffany A.L.
Wang, Lisheng
author_sort Li, Li
collection PubMed
description The survival, proliferation, self-renewal and differentiation of human pluripotent stem cells (hPSCs, including human embryonic stem cells and human induced pluripotent stem cells) involve a number of processes that require cell-cell and cell-matrix interactions. The cell adhesion molecules (CAMs), a group of cell surface proteins play a pivotal role in mediating such interactions. Recent studies have provided insights into the essential roles and mechanisms of CAMs in the regulation of hPSC fate decisions. Here, we review the latest research progress in this field and focus on how E-cadherin and several other important CAMs including classic cadherins, Ig-superfamily CAMs, integrins and heparin sulfate proteoglycans control survival and differentiation of hPSCs
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spelling pubmed-33641392012-06-05 Role of E-cadherin and other cell adhesion molecules in survival and differentiation of human pluripotent stem cells Li, Li Bennett, Steffany A.L. Wang, Lisheng Cell Adh Migr Review The survival, proliferation, self-renewal and differentiation of human pluripotent stem cells (hPSCs, including human embryonic stem cells and human induced pluripotent stem cells) involve a number of processes that require cell-cell and cell-matrix interactions. The cell adhesion molecules (CAMs), a group of cell surface proteins play a pivotal role in mediating such interactions. Recent studies have provided insights into the essential roles and mechanisms of CAMs in the regulation of hPSC fate decisions. Here, we review the latest research progress in this field and focus on how E-cadherin and several other important CAMs including classic cadherins, Ig-superfamily CAMs, integrins and heparin sulfate proteoglycans control survival and differentiation of hPSCs Landes Bioscience 2012-01-01 /pmc/articles/PMC3364139/ /pubmed/22647941 http://dx.doi.org/10.4161/cam.19583 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Li, Li
Bennett, Steffany A.L.
Wang, Lisheng
Role of E-cadherin and other cell adhesion molecules in survival and differentiation of human pluripotent stem cells
title Role of E-cadherin and other cell adhesion molecules in survival and differentiation of human pluripotent stem cells
title_full Role of E-cadherin and other cell adhesion molecules in survival and differentiation of human pluripotent stem cells
title_fullStr Role of E-cadherin and other cell adhesion molecules in survival and differentiation of human pluripotent stem cells
title_full_unstemmed Role of E-cadherin and other cell adhesion molecules in survival and differentiation of human pluripotent stem cells
title_short Role of E-cadherin and other cell adhesion molecules in survival and differentiation of human pluripotent stem cells
title_sort role of e-cadherin and other cell adhesion molecules in survival and differentiation of human pluripotent stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364139/
https://www.ncbi.nlm.nih.gov/pubmed/22647941
http://dx.doi.org/10.4161/cam.19583
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