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Tissue-Specific GHR Knockout Mice: Metabolic Phenotypes

In addition to its major role in the regulation of somatic growth, growth hormone (GH) signaling has profound effects on function of various tissues in the body. However, the cellular location where the GH signaling exerts its effect on metabolic homeostasis remains largely unknown. Here, we briefly...

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Detalles Bibliográficos
Autores principales: Sun, Liou Y., Bartke, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298218/
https://www.ncbi.nlm.nih.gov/pubmed/25646092
http://dx.doi.org/10.3389/fendo.2014.00243
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author Sun, Liou Y.
Bartke, Andrzej
author_facet Sun, Liou Y.
Bartke, Andrzej
author_sort Sun, Liou Y.
collection PubMed
description In addition to its major role in the regulation of somatic growth, growth hormone (GH) signaling has profound effects on function of various tissues in the body. However, the cellular location where the GH signaling exerts its effect on metabolic homeostasis remains largely unknown. Here, we briefly review recent progress and insights from mice with GH receptor deletion specifically in adipocytes, macrophages, hepatocytes, pancreatic β-cells, and skeletal muscle cell types. These studies have greatly enhanced our understanding of the GH–IGF-I physiological function.
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spelling pubmed-42982182015-02-02 Tissue-Specific GHR Knockout Mice: Metabolic Phenotypes Sun, Liou Y. Bartke, Andrzej Front Endocrinol (Lausanne) Endocrinology In addition to its major role in the regulation of somatic growth, growth hormone (GH) signaling has profound effects on function of various tissues in the body. However, the cellular location where the GH signaling exerts its effect on metabolic homeostasis remains largely unknown. Here, we briefly review recent progress and insights from mice with GH receptor deletion specifically in adipocytes, macrophages, hepatocytes, pancreatic β-cells, and skeletal muscle cell types. These studies have greatly enhanced our understanding of the GH–IGF-I physiological function. Frontiers Media S.A. 2015-01-19 /pmc/articles/PMC4298218/ /pubmed/25646092 http://dx.doi.org/10.3389/fendo.2014.00243 Text en Copyright © 2015 Sun and Bartke. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Sun, Liou Y.
Bartke, Andrzej
Tissue-Specific GHR Knockout Mice: Metabolic Phenotypes
title Tissue-Specific GHR Knockout Mice: Metabolic Phenotypes
title_full Tissue-Specific GHR Knockout Mice: Metabolic Phenotypes
title_fullStr Tissue-Specific GHR Knockout Mice: Metabolic Phenotypes
title_full_unstemmed Tissue-Specific GHR Knockout Mice: Metabolic Phenotypes
title_short Tissue-Specific GHR Knockout Mice: Metabolic Phenotypes
title_sort tissue-specific ghr knockout mice: metabolic phenotypes
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298218/
https://www.ncbi.nlm.nih.gov/pubmed/25646092
http://dx.doi.org/10.3389/fendo.2014.00243
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