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IGF-1 and Bone: New Discoveries From Mouse Models

Insulin-like growth factor-1 (IGF-1) plays a central role in cellular growth, differentiation, survival, and cell cycle progression. It is expressed early during development and its effects are mediated through binding to a tyrosine kinase receptor, the insulin-like growth factor-1 receptor (IGF-1R)...

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Autores principales: Yakar, Shoshana, Courtland, Hayden-William, Clemmons, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Subscription Services, Inc., A Wiley Company 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3179280/
https://www.ncbi.nlm.nih.gov/pubmed/20836088
http://dx.doi.org/10.1002/jbmr.234
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author Yakar, Shoshana
Courtland, Hayden-William
Clemmons, David
author_facet Yakar, Shoshana
Courtland, Hayden-William
Clemmons, David
author_sort Yakar, Shoshana
collection PubMed
description Insulin-like growth factor-1 (IGF-1) plays a central role in cellular growth, differentiation, survival, and cell cycle progression. It is expressed early during development and its effects are mediated through binding to a tyrosine kinase receptor, the insulin-like growth factor-1 receptor (IGF-1R). In the circulation, the IGFs bind to IGF-binding proteins (IGFBPs), which determine their bioavailability and regulate the interaction between the IGFs and IGF-1R. Studies in animal models and in humans have established critical roles for IGFs in skeletal growth and development. In this review we present new and old findings from mouse models of the IGF system and discuss their clinical relevance to normal and pathological skeletal physiology. © 2010 American Society for Bone and Mineral Research.
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spelling pubmed-31792802011-12-01 IGF-1 and Bone: New Discoveries From Mouse Models Yakar, Shoshana Courtland, Hayden-William Clemmons, David J Bone Miner Res Review Insulin-like growth factor-1 (IGF-1) plays a central role in cellular growth, differentiation, survival, and cell cycle progression. It is expressed early during development and its effects are mediated through binding to a tyrosine kinase receptor, the insulin-like growth factor-1 receptor (IGF-1R). In the circulation, the IGFs bind to IGF-binding proteins (IGFBPs), which determine their bioavailability and regulate the interaction between the IGFs and IGF-1R. Studies in animal models and in humans have established critical roles for IGFs in skeletal growth and development. In this review we present new and old findings from mouse models of the IGF system and discuss their clinical relevance to normal and pathological skeletal physiology. © 2010 American Society for Bone and Mineral Research. Wiley Subscription Services, Inc., A Wiley Company 2010-12 2010-08-23 /pmc/articles/PMC3179280/ /pubmed/20836088 http://dx.doi.org/10.1002/jbmr.234 Text en Copyright © 2010 American Society for Bone and Mineral Research http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Review
Yakar, Shoshana
Courtland, Hayden-William
Clemmons, David
IGF-1 and Bone: New Discoveries From Mouse Models
title IGF-1 and Bone: New Discoveries From Mouse Models
title_full IGF-1 and Bone: New Discoveries From Mouse Models
title_fullStr IGF-1 and Bone: New Discoveries From Mouse Models
title_full_unstemmed IGF-1 and Bone: New Discoveries From Mouse Models
title_short IGF-1 and Bone: New Discoveries From Mouse Models
title_sort igf-1 and bone: new discoveries from mouse models
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3179280/
https://www.ncbi.nlm.nih.gov/pubmed/20836088
http://dx.doi.org/10.1002/jbmr.234
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