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Fibronectin at select sites binds multiple growth factors (GF) and enhances their activity: expansion of the collaborative ECM-GF paradigm
Intensive research has demonstrated that extracellular matrix (ECM) molecules and growth factors (GF) collaborate at many different levels. The ability of ECM to modulate GF signals has important implications in tissue formation and homeostasis as well as novel therapies for acute and chronic wounds...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961531/ https://www.ncbi.nlm.nih.gov/pubmed/24335899 http://dx.doi.org/10.1038/jid.2013.484 |
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author | Zhu, Jia Clark, Richard A.F. |
author_facet | Zhu, Jia Clark, Richard A.F. |
author_sort | Zhu, Jia |
collection | PubMed |
description | Intensive research has demonstrated that extracellular matrix (ECM) molecules and growth factors (GF) collaborate at many different levels. The ability of ECM to modulate GF signals has important implications in tissue formation and homeostasis as well as novel therapies for acute and chronic wounds. Recently, a number of GF binding sites were identified in fibronectin and were shown to provide another layer of regulation on GF signaling. Here, we review these new findings on fibronectin interaction with GF in context of general ways ECM molecules regulate GF signaling. |
format | Online Article Text |
id | pubmed-3961531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-39615312014-10-01 Fibronectin at select sites binds multiple growth factors (GF) and enhances their activity: expansion of the collaborative ECM-GF paradigm Zhu, Jia Clark, Richard A.F. J Invest Dermatol Article Intensive research has demonstrated that extracellular matrix (ECM) molecules and growth factors (GF) collaborate at many different levels. The ability of ECM to modulate GF signals has important implications in tissue formation and homeostasis as well as novel therapies for acute and chronic wounds. Recently, a number of GF binding sites were identified in fibronectin and were shown to provide another layer of regulation on GF signaling. Here, we review these new findings on fibronectin interaction with GF in context of general ways ECM molecules regulate GF signaling. 2013-12-12 2014-04 /pmc/articles/PMC3961531/ /pubmed/24335899 http://dx.doi.org/10.1038/jid.2013.484 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Zhu, Jia Clark, Richard A.F. Fibronectin at select sites binds multiple growth factors (GF) and enhances their activity: expansion of the collaborative ECM-GF paradigm |
title | Fibronectin at select sites binds multiple growth factors (GF) and enhances their activity: expansion of the collaborative ECM-GF paradigm |
title_full | Fibronectin at select sites binds multiple growth factors (GF) and enhances their activity: expansion of the collaborative ECM-GF paradigm |
title_fullStr | Fibronectin at select sites binds multiple growth factors (GF) and enhances their activity: expansion of the collaborative ECM-GF paradigm |
title_full_unstemmed | Fibronectin at select sites binds multiple growth factors (GF) and enhances their activity: expansion of the collaborative ECM-GF paradigm |
title_short | Fibronectin at select sites binds multiple growth factors (GF) and enhances their activity: expansion of the collaborative ECM-GF paradigm |
title_sort | fibronectin at select sites binds multiple growth factors (gf) and enhances their activity: expansion of the collaborative ecm-gf paradigm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961531/ https://www.ncbi.nlm.nih.gov/pubmed/24335899 http://dx.doi.org/10.1038/jid.2013.484 |
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