Regulation of Proteins Involved in Insulin Signaling Pathways in Differentiating Human Adipocytes
In the present study we have examined the proteins involved in the insulin signaling cascade during and after differentiation of human adipocyte precursor cells and their correlation with glucose uptake. The differentiation of human adipocytes was characterized by a two- to threefold stimulation of...
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Veröffentlicht in: | Biochemical and biophysical research communications 2000-09, Vol.276 (1), p.162-168 |
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description | In the present study we have examined the proteins involved in the insulin signaling cascade during and after differentiation of human adipocyte precursor cells and their correlation with glucose uptake. The differentiation of human adipocytes was characterized by a two- to threefold stimulation of glucose transport in response to insulin and a marked increase protein expression for the insulin receptor, IRS-1, GLUT-4, PI 3-kinase, and PKB, with respect to undifferentiated cells. In contrast, there were small changes in the protein expression of IRS-2, and no changes in PKC zeta and MAP kinases, although basal MAP kinase activity and GLUT-1 protein were reduced during differentiation. In conclusion, there are quantitative differences in the regulation of IRS-1 and other proteins during differentiation which may contribute to more efficient insulin signaling leading to glucose uptake in mature fat cells. Alterations in this pattern may reflect or contribute to an insulin-resistant state. |
doi_str_mv | 10.1006/bbrc.2000.3429 |
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The differentiation of human adipocytes was characterized by a two- to threefold stimulation of glucose transport in response to insulin and a marked increase protein expression for the insulin receptor, IRS-1, GLUT-4, PI 3-kinase, and PKB, with respect to undifferentiated cells. In contrast, there were small changes in the protein expression of IRS-2, and no changes in PKC zeta and MAP kinases, although basal MAP kinase activity and GLUT-1 protein were reduced during differentiation. In conclusion, there are quantitative differences in the regulation of IRS-1 and other proteins during differentiation which may contribute to more efficient insulin signaling leading to glucose uptake in mature fat cells. Alterations in this pattern may reflect or contribute to an insulin-resistant state.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1006/bbrc.2000.3429</identifier><identifier>PMID: 11006100</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adipocytes - cytology ; Adipocytes - physiology ; Biological Transport - physiology ; Cell Differentiation - physiology ; Cells, Cultured ; differentiation ; Glucose - physiology ; glucose transport ; Glucose Transporter Type 4 ; human adipocytes ; Humans ; Insulin - physiology ; insulin signaling proteins ; MAP Kinase Signaling System ; Monosaccharide Transport Proteins - physiology ; Muscle Proteins ; Receptor, Insulin - physiology ; Signal Transduction</subject><ispartof>Biochemical and biophysical research communications, 2000-09, Vol.276 (1), p.162-168</ispartof><rights>2000 Academic Press</rights><rights>Copyright 2000 Academic Press.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-de7e43c2b8626702ee437ad3c9e2b79d11650a760173f76d218af73c955e6b363</citedby><cites>FETCH-LOGICAL-c340t-de7e43c2b8626702ee437ad3c9e2b79d11650a760173f76d218af73c955e6b363</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/bbrc.2000.3429$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11006100$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pederson, Terry</creatorcontrib><creatorcontrib>Rondinone, Cristina M.</creatorcontrib><title>Regulation of Proteins Involved in Insulin Signaling Pathways in Differentiating Human Adipocytes</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>In the present study we have examined the proteins involved in the insulin signaling cascade during and after differentiation of human adipocyte precursor cells and their correlation with glucose uptake. The differentiation of human adipocytes was characterized by a two- to threefold stimulation of glucose transport in response to insulin and a marked increase protein expression for the insulin receptor, IRS-1, GLUT-4, PI 3-kinase, and PKB, with respect to undifferentiated cells. In contrast, there were small changes in the protein expression of IRS-2, and no changes in PKC zeta and MAP kinases, although basal MAP kinase activity and GLUT-1 protein were reduced during differentiation. In conclusion, there are quantitative differences in the regulation of IRS-1 and other proteins during differentiation which may contribute to more efficient insulin signaling leading to glucose uptake in mature fat cells. Alterations in this pattern may reflect or contribute to an insulin-resistant state.</description><subject>Adipocytes - cytology</subject><subject>Adipocytes - physiology</subject><subject>Biological Transport - physiology</subject><subject>Cell Differentiation - physiology</subject><subject>Cells, Cultured</subject><subject>differentiation</subject><subject>Glucose - physiology</subject><subject>glucose transport</subject><subject>Glucose Transporter Type 4</subject><subject>human adipocytes</subject><subject>Humans</subject><subject>Insulin - physiology</subject><subject>insulin signaling proteins</subject><subject>MAP Kinase Signaling System</subject><subject>Monosaccharide Transport Proteins - physiology</subject><subject>Muscle Proteins</subject><subject>Receptor, Insulin - physiology</subject><subject>Signal Transduction</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1LAzEQxYMotlavHmVP3nZNstukeyz1o4WCxQ_wFrLJbI1sk5rsVvrfm6UFTx6Gmcx78yA_hK4JzgjG7K6qvMooxjjLC1qeoCHBJU4pwcUpGsY1S2lJPgboIoQvjAkpWHmOBqS_jTVE8gXWXSNb42zi6mTlXQvGhmRhd67ZgU6MjXPomthfzdrKOKyTlWw_f-Q-9Oq9qWvwYFsTU6I27zbSJlNttk7tWwiX6KyWTYCrYx-h98eHt9k8XT4_LWbTZaryArepBg5Frmg1YZRxTCG-uNS5KoFWvNSEsDGWnGHC85ozTclE1jzK4zGwKmf5CN0ecrfefXcQWrExQUHTSAuuC4JTWtIxodGYHYzKuxA81GLrzUb6vSBY9GBED1X0UEUPNR7cHJO7agP6z36kGA2TgwHi_3YGvAjKgFWgjQfVCu3Mf9m_oz6GSg</recordid><startdate>20000916</startdate><enddate>20000916</enddate><creator>Pederson, Terry</creator><creator>Rondinone, Cristina M.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20000916</creationdate><title>Regulation of Proteins Involved in Insulin Signaling Pathways in Differentiating Human Adipocytes</title><author>Pederson, Terry ; Rondinone, Cristina M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-de7e43c2b8626702ee437ad3c9e2b79d11650a760173f76d218af73c955e6b363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adipocytes - cytology</topic><topic>Adipocytes - physiology</topic><topic>Biological Transport - physiology</topic><topic>Cell Differentiation - physiology</topic><topic>Cells, Cultured</topic><topic>differentiation</topic><topic>Glucose - physiology</topic><topic>glucose transport</topic><topic>Glucose Transporter Type 4</topic><topic>human adipocytes</topic><topic>Humans</topic><topic>Insulin - physiology</topic><topic>insulin signaling proteins</topic><topic>MAP Kinase Signaling System</topic><topic>Monosaccharide Transport Proteins - physiology</topic><topic>Muscle Proteins</topic><topic>Receptor, Insulin - physiology</topic><topic>Signal Transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pederson, Terry</creatorcontrib><creatorcontrib>Rondinone, Cristina M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pederson, Terry</au><au>Rondinone, Cristina M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of Proteins Involved in Insulin Signaling Pathways in Differentiating Human Adipocytes</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2000-09-16</date><risdate>2000</risdate><volume>276</volume><issue>1</issue><spage>162</spage><epage>168</epage><pages>162-168</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>In the present study we have examined the proteins involved in the insulin signaling cascade during and after differentiation of human adipocyte precursor cells and their correlation with glucose uptake. The differentiation of human adipocytes was characterized by a two- to threefold stimulation of glucose transport in response to insulin and a marked increase protein expression for the insulin receptor, IRS-1, GLUT-4, PI 3-kinase, and PKB, with respect to undifferentiated cells. In contrast, there were small changes in the protein expression of IRS-2, and no changes in PKC zeta and MAP kinases, although basal MAP kinase activity and GLUT-1 protein were reduced during differentiation. In conclusion, there are quantitative differences in the regulation of IRS-1 and other proteins during differentiation which may contribute to more efficient insulin signaling leading to glucose uptake in mature fat cells. Alterations in this pattern may reflect or contribute to an insulin-resistant state.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11006100</pmid><doi>10.1006/bbrc.2000.3429</doi><tpages>7</tpages></addata></record> |
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subjects | Adipocytes - cytology Adipocytes - physiology Biological Transport - physiology Cell Differentiation - physiology Cells, Cultured differentiation Glucose - physiology glucose transport Glucose Transporter Type 4 human adipocytes Humans Insulin - physiology insulin signaling proteins MAP Kinase Signaling System Monosaccharide Transport Proteins - physiology Muscle Proteins Receptor, Insulin - physiology Signal Transduction |
title | Regulation of Proteins Involved in Insulin Signaling Pathways in Differentiating Human Adipocytes |
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