| Altered glucose homeostasis in mice with liver-specific deletion of Src homology phosphatase 2. | |
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MedLine Citation:
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PMID: 20841350 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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The Src homology 2 domain-containing protein-tyrosine phosphatase Shp2 has been implicated in a variety of growth factor signaling pathways, but its role in insulin signaling has remained unresolved. In vitro studies suggest that Shp2 is both a negative and positive regulator of insulin signaling, although its physiological function in a number of peripheral insulin-responsive tissues remains unknown. To address the metabolic role of Shp2 in the liver, we generated mice with either chronic or acute hepatic Shp2 deletion using tissue-specific Cre-LoxP and adenoviral Cre approaches, respectively. We then analyzed insulin sensitivity, glucose tolerance, and insulin signaling in liver-specific Shp2-deficient and control mice. Mice with chronic Shp2 deletion exhibited improved insulin sensitivity and increased glucose tolerance compared with controls. Acute Shp2 deletion yielded comparable results, indicating that the observed metabolic effects are directly caused by the lack of Shp2 in the liver. These findings correlated with, and were most likely caused by, direct dephosphorylation of insulin receptor substrate (IRS)1/2 in the liver, accompanied by increased PI3K/Akt signaling. In contrast, insulin-induced ERK activation was dramatically attenuated, yet there was no effect on the putative ERK site on IRS1 (Ser(612)) or on S6 kinase 1 activity. These studies show that Shp2 is a negative regulator of hepatic insulin action, and its deletion enhances the activation of PI3K/Akt pathway downstream of the insulin receptor. |
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Authors:
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Kosuke Matsuo; Mirela Delibegovic; Izumi Matsuo; Naoto Nagata; Siming Liu; Ahmed Bettaieb; Yannan Xi; Kazushi Araki; Wentian Yang; Barbara B Kahn; Benjamin G Neel; Fawaz G Haj |
Publication Detail:
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Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't Date: 2010-09-14 |
Journal Detail:
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Title: The Journal of biological chemistry Volume: 285 ISSN: 1083-351X ISO Abbreviation: J. Biol. Chem. Publication Date: 2010 Dec |
Date Detail:
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Created Date: 2010-12-14 Completed Date: 2011-01-11 Revised Date: 2011-12-19 |
Medline Journal Info:
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Nlm Unique ID: 2985121R Medline TA: J Biol Chem Country: United States |
Other Details:
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Languages: eng Pagination: 39750-8 Citation Subset: IM |
Affiliation:
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Department of Nutrition, University of California, Davis, California 95616, USA. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Animals Extracellular Signal-Regulated MAP Kinases / genetics, metabolism Gene Deletion Glucose / genetics, metabolism* Homeostasis / physiology* Insulin / genetics, metabolism Insulin Receptor Substrate Proteins / genetics, metabolism Liver / enzymology* Mice Mice, Transgenic Phosphatidylinositol 3-Kinases / genetics, metabolism Protein Tyrosine Phosphatase, Non-Receptor Type 11 / genetics, metabolism* Proto-Oncogene Proteins c-akt / genetics, metabolism Receptor, Insulin / genetics, metabolism Ribosomal Protein S6 Kinases / genetics, metabolism Signal Transduction / physiology |
| Grant Support | |
ID/Acronym/Agency:
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R01DK60838/DK/NIDDK NIH HHS; R3749512//PHS HHS |
| Chemical | |
Reg. No./Substance:
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0/Insulin; 0/Insulin Receptor Substrate Proteins; 0/Irs1 protein, mouse; 0/Irs2 protein, mouse; 50-99-7/Glucose; EC 2.7.1.-/Phosphatidylinositol 3-Kinases; EC 2.7.10.1/Receptor, Insulin; EC 2.7.11.1/Proto-Oncogene Proteins c-akt; EC 2.7.11.1/Ribosomal Protein S6 Kinases; EC 2.7.11.24/Extracellular Signal-Regulated MAP Kinases; EC 3.1.3.48/Protein Tyrosine Phosphatase, Non-Receptor Type 11; EC 3.1.3.48/Ptpn11 protein, mouse |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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