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α6-Integrin alternative splicing: distinct cytoplasmic variants in stem cell fate specification and niche interaction
α6-Integrin subunit (also known as CD49f) is a stemness signature that has been found on the plasma membrane of more than 30 stem cell populations. A growing body of studies have focused on the critical role of α6-containing integrins (α6β1 and α6β4) in the regulation of stem cell properties, lineag...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930856/ https://www.ncbi.nlm.nih.gov/pubmed/29720266 http://dx.doi.org/10.1186/s13287-018-0868-3 |
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author | Zhou, Zijing Qu, Jing He, Li Peng, Hong Chen, Ping Zhou, Yong |
author_facet | Zhou, Zijing Qu, Jing He, Li Peng, Hong Chen, Ping Zhou, Yong |
author_sort | Zhou, Zijing |
collection | PubMed |
description | α6-Integrin subunit (also known as CD49f) is a stemness signature that has been found on the plasma membrane of more than 30 stem cell populations. A growing body of studies have focused on the critical role of α6-containing integrins (α6β1 and α6β4) in the regulation of stem cell properties, lineage-specific differentiation, and niche interaction. α6-Integrin subunit can be alternatively spliced at the post-transcriptional level, giving rise to divergent isoforms which differ in the cytoplasmic and/or extracellular domains. The cytoplasmic domain of integrins is an important functional part of integrin-mediated signals. Structural changes in the cytoplasmic domain of α6 provide an efficient means for the regulation of stem cell responses to biochemical stimuli and/or biophysical cues in the stem cell niche, thus impacting stem cell fate determination. In this review, we summarize the current knowledge on the structural variants of the α6-integrin subunit and spatiotemporal expression of α6 cytoplasmic variants in embryonic and adult stem/progenitor cells. We highlight the roles of α6 cytoplasmic variants in stem cell fate decision and niche interaction, and discuss the potential mechanisms involved. Understanding of the distinct functions of α6 splicing variants in stem cell biology may inform the rational design of novel stem cell-based therapies for a range of human diseases. |
format | Online Article Text |
id | pubmed-5930856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59308562018-05-09 α6-Integrin alternative splicing: distinct cytoplasmic variants in stem cell fate specification and niche interaction Zhou, Zijing Qu, Jing He, Li Peng, Hong Chen, Ping Zhou, Yong Stem Cell Res Ther Review α6-Integrin subunit (also known as CD49f) is a stemness signature that has been found on the plasma membrane of more than 30 stem cell populations. A growing body of studies have focused on the critical role of α6-containing integrins (α6β1 and α6β4) in the regulation of stem cell properties, lineage-specific differentiation, and niche interaction. α6-Integrin subunit can be alternatively spliced at the post-transcriptional level, giving rise to divergent isoforms which differ in the cytoplasmic and/or extracellular domains. The cytoplasmic domain of integrins is an important functional part of integrin-mediated signals. Structural changes in the cytoplasmic domain of α6 provide an efficient means for the regulation of stem cell responses to biochemical stimuli and/or biophysical cues in the stem cell niche, thus impacting stem cell fate determination. In this review, we summarize the current knowledge on the structural variants of the α6-integrin subunit and spatiotemporal expression of α6 cytoplasmic variants in embryonic and adult stem/progenitor cells. We highlight the roles of α6 cytoplasmic variants in stem cell fate decision and niche interaction, and discuss the potential mechanisms involved. Understanding of the distinct functions of α6 splicing variants in stem cell biology may inform the rational design of novel stem cell-based therapies for a range of human diseases. BioMed Central 2018-05-02 /pmc/articles/PMC5930856/ /pubmed/29720266 http://dx.doi.org/10.1186/s13287-018-0868-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Zhou, Zijing Qu, Jing He, Li Peng, Hong Chen, Ping Zhou, Yong α6-Integrin alternative splicing: distinct cytoplasmic variants in stem cell fate specification and niche interaction |
title | α6-Integrin alternative splicing: distinct cytoplasmic variants in stem cell fate specification and niche interaction |
title_full | α6-Integrin alternative splicing: distinct cytoplasmic variants in stem cell fate specification and niche interaction |
title_fullStr | α6-Integrin alternative splicing: distinct cytoplasmic variants in stem cell fate specification and niche interaction |
title_full_unstemmed | α6-Integrin alternative splicing: distinct cytoplasmic variants in stem cell fate specification and niche interaction |
title_short | α6-Integrin alternative splicing: distinct cytoplasmic variants in stem cell fate specification and niche interaction |
title_sort | α6-integrin alternative splicing: distinct cytoplasmic variants in stem cell fate specification and niche interaction |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930856/ https://www.ncbi.nlm.nih.gov/pubmed/29720266 http://dx.doi.org/10.1186/s13287-018-0868-3 |
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