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Transforming growth factor-β in stem cells and tissue homeostasis
TGF-β 1–3 are unique multi-functional growth factors that are only expressed in mammals, and mainly secreted and stored as a latent complex in the extracellular matrix (ECM). The biological functions of TGF-β in adults can only be delivered after ligand activation, mostly in response to environmenta...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802812/ https://www.ncbi.nlm.nih.gov/pubmed/29423331 http://dx.doi.org/10.1038/s41413-017-0005-4 |
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author | Xu, Xin Zheng, Liwei Yuan, Quan Zhen, Gehua Crane, Janet L. Zhou, Xuedong Cao, Xu |
author_facet | Xu, Xin Zheng, Liwei Yuan, Quan Zhen, Gehua Crane, Janet L. Zhou, Xuedong Cao, Xu |
author_sort | Xu, Xin |
collection | PubMed |
description | TGF-β 1–3 are unique multi-functional growth factors that are only expressed in mammals, and mainly secreted and stored as a latent complex in the extracellular matrix (ECM). The biological functions of TGF-β in adults can only be delivered after ligand activation, mostly in response to environmental perturbations. Although involved in multiple biological and pathological processes of the human body, the exact roles of TGF-β in maintaining stem cells and tissue homeostasis have not been well-documented until recent advances, which delineate their functions in a given context. Our recent findings, along with data reported by others, have clearly shown that temporal and spatial activation of TGF-β is involved in the recruitment of stem/progenitor cell participation in tissue regeneration/remodeling process, whereas sustained abnormalities in TGF-β ligand activation, regardless of genetic or environmental origin, will inevitably disrupt the normal physiology and lead to pathobiology of major diseases. Modulation of TGF-β signaling with different approaches has proven effective pre-clinically in the treatment of multiple pathologies such as sclerosis/fibrosis, tumor metastasis, osteoarthritis, and immune disorders. Thus, further elucidation of the mechanisms by which TGF-β is activated in different tissues/organs and how targeted cells respond in a context-dependent way can likely be translated with clinical benefits in the management of a broad range of diseases with the involvement of TGF-β. |
format | Online Article Text |
id | pubmed-5802812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58028122018-02-08 Transforming growth factor-β in stem cells and tissue homeostasis Xu, Xin Zheng, Liwei Yuan, Quan Zhen, Gehua Crane, Janet L. Zhou, Xuedong Cao, Xu Bone Res Review Article TGF-β 1–3 are unique multi-functional growth factors that are only expressed in mammals, and mainly secreted and stored as a latent complex in the extracellular matrix (ECM). The biological functions of TGF-β in adults can only be delivered after ligand activation, mostly in response to environmental perturbations. Although involved in multiple biological and pathological processes of the human body, the exact roles of TGF-β in maintaining stem cells and tissue homeostasis have not been well-documented until recent advances, which delineate their functions in a given context. Our recent findings, along with data reported by others, have clearly shown that temporal and spatial activation of TGF-β is involved in the recruitment of stem/progenitor cell participation in tissue regeneration/remodeling process, whereas sustained abnormalities in TGF-β ligand activation, regardless of genetic or environmental origin, will inevitably disrupt the normal physiology and lead to pathobiology of major diseases. Modulation of TGF-β signaling with different approaches has proven effective pre-clinically in the treatment of multiple pathologies such as sclerosis/fibrosis, tumor metastasis, osteoarthritis, and immune disorders. Thus, further elucidation of the mechanisms by which TGF-β is activated in different tissues/organs and how targeted cells respond in a context-dependent way can likely be translated with clinical benefits in the management of a broad range of diseases with the involvement of TGF-β. Nature Publishing Group UK 2018-01-31 /pmc/articles/PMC5802812/ /pubmed/29423331 http://dx.doi.org/10.1038/s41413-017-0005-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Article Xu, Xin Zheng, Liwei Yuan, Quan Zhen, Gehua Crane, Janet L. Zhou, Xuedong Cao, Xu Transforming growth factor-β in stem cells and tissue homeostasis |
title | Transforming growth factor-β in stem cells and tissue homeostasis |
title_full | Transforming growth factor-β in stem cells and tissue homeostasis |
title_fullStr | Transforming growth factor-β in stem cells and tissue homeostasis |
title_full_unstemmed | Transforming growth factor-β in stem cells and tissue homeostasis |
title_short | Transforming growth factor-β in stem cells and tissue homeostasis |
title_sort | transforming growth factor-β in stem cells and tissue homeostasis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802812/ https://www.ncbi.nlm.nih.gov/pubmed/29423331 http://dx.doi.org/10.1038/s41413-017-0005-4 |
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