Loading…
GLUT4 and UBC9 protein expression is reduced in muscle from type 2 diabetic patients with severe insulin resistance
Subgroups of patients with type 2 diabetes mellitus demand large insulin doses to maintain euglycemia. These patients are characterized by severe skeletal muscle insulin resistance and the underlying pathology remains unclear. The purpose of this study was to examine protein expression of the princi...
Saved in:
Published in: | PloS one 2011-11, Vol.6 (11), p.e27854-e27854 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c691t-275099e4ea9857cd9fe646c8be801cacf775f295016483c651ad15207c9488413 |
---|---|
cites | cdi_FETCH-LOGICAL-c691t-275099e4ea9857cd9fe646c8be801cacf775f295016483c651ad15207c9488413 |
container_end_page | e27854 |
container_issue | 11 |
container_start_page | e27854 |
container_title | PloS one |
container_volume | 6 |
creator | Kampmann, Ulla Christensen, Britt Nielsen, Thomas Svava Pedersen, Steen Bønløkke Ørskov, Lotte Lund, Sten Møller, Niels Jessen, Niels |
description | Subgroups of patients with type 2 diabetes mellitus demand large insulin doses to maintain euglycemia. These patients are characterized by severe skeletal muscle insulin resistance and the underlying pathology remains unclear. The purpose of this study was to examine protein expression of the principal glucose transporter, GLUT4, and associated proteins in skeletal muscle from type 2 diabetic patients characterized by severe insulin resistance.
Seven type 2 diabetic patients with severe insulin resistance (mean insulin dose 195 IU/day) were compared with seven age matched type 2 diabetic patients who did not require insulin treatment, and with an age matched healthy control group. Protein expression of GLUT4 and associated proteins was assessed in muscle and fat biopsies using standard western blotting techniques.
GLUT4 protein expression was significantly reduced by ∼30 pct in skeletal muscle tissue from severely insulin resistant type 2 diabetic subjects, compared with both healthy controls and type 2 diabetic subjects that did not require insulin treatment. In fat tissue, GLUT4 protein expression was reduced in both diabetic groups. In skeletal muscle, the reduced GLUT4 expression in severe insulin resistance was associated with decreased ubiquitin-conjugating enzyme 9 (UBC9) expression while expression of GLUT1, TBC1D1 and AS160 was not significantly different among type 2 diabetic patients and matched controls.
Type 2 diabetic patients with severe insulin resistance have reduced expression of GLUT4 in skeletal muscle compared to patients treated with oral antidiabetic drugs alone. GLUT4 protein levels may therefore play a role in the pathology behind type 2 diabetes mellitus among subgroups of patients, and this may explain the heterogeneous response to insulin treatment. This new finding contributes to the understanding of the underlying mechanisms for the development of extreme insulin resistance. |
doi_str_mv | 10.1371/journal.pone.0027854 |
format | article |
fullrecord | <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1311930204</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A476862891</galeid><doaj_id>oai_doaj_org_article_506360e739634c15a006bc077697addc</doaj_id><sourcerecordid>A476862891</sourcerecordid><originalsourceid>FETCH-LOGICAL-c691t-275099e4ea9857cd9fe646c8be801cacf775f295016483c651ad15207c9488413</originalsourceid><addsrcrecordid>eNqNk-FvEyEYxi9G4-b0PzBKYqLxQyscBxxfTGajs0mTJbr6lVDuvZbmetyAm9t_L7W3pWf2wfABAr_nAR54s-w1wVNCBfm0db1vdTPtXAtTjHNRsuJJdkokzSc8x_Tp0fgkexHCFmNGS86fZyd5TkghCDnNwsVieVUg3VZo-WUmUeddBNsiuO08hGBdi2xAHqreQIXSwq4PpgFUe7dD8a4DlKPK6hVEa1Cno4U2BvTbxg0KcAMekib0TRImOxuibg28zJ7VugnwaujPsuW3r1ez75PF5cV8dr6YGC5JnOSCYSmhAC1LJkwla-AFN-UKSkyMNrUQrM4lw4QXJTWcEV0RlmNhZFGWBaFn2duDb9e4oIa8giKUpGBwjotEzA9E5fRWdd7utL9TTlv1d8L5tdI-3awBxTCnHIOgktPCEKYx5iuDheBS6KoyyevzsFu_2kFlUhBeNyPT8UprN2rtbhTNSYmZTAYfBgPvrnsIUe1sMNA0ugXXByUxJ4xyyhL57h_y8csN1Fqn89u2dmlbs_dU54XgJc9LuQ9p-giVWgU7a9Lfqm2aHwk-jgSJiXAb17oPQc1__vh_9vLXmH1_xG5AN3ETXNPH9AfDGCwOoPEuBA_1Q8YEq31p3Keh9qWhhtJIsjfH7_Mguq8F-geaiweA</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1311930204</pqid></control><display><type>article</type><title>GLUT4 and UBC9 protein expression is reduced in muscle from type 2 diabetic patients with severe insulin resistance</title><source>Open Access: PubMed Central</source><source>Publicly Available Content (ProQuest)</source><creator>Kampmann, Ulla ; Christensen, Britt ; Nielsen, Thomas Svava ; Pedersen, Steen Bønløkke ; Ørskov, Lotte ; Lund, Sten ; Møller, Niels ; Jessen, Niels</creator><contributor>Calbet, Jose A. L.</contributor><creatorcontrib>Kampmann, Ulla ; Christensen, Britt ; Nielsen, Thomas Svava ; Pedersen, Steen Bønløkke ; Ørskov, Lotte ; Lund, Sten ; Møller, Niels ; Jessen, Niels ; Calbet, Jose A. L.</creatorcontrib><description>Subgroups of patients with type 2 diabetes mellitus demand large insulin doses to maintain euglycemia. These patients are characterized by severe skeletal muscle insulin resistance and the underlying pathology remains unclear. The purpose of this study was to examine protein expression of the principal glucose transporter, GLUT4, and associated proteins in skeletal muscle from type 2 diabetic patients characterized by severe insulin resistance.
Seven type 2 diabetic patients with severe insulin resistance (mean insulin dose 195 IU/day) were compared with seven age matched type 2 diabetic patients who did not require insulin treatment, and with an age matched healthy control group. Protein expression of GLUT4 and associated proteins was assessed in muscle and fat biopsies using standard western blotting techniques.
GLUT4 protein expression was significantly reduced by ∼30 pct in skeletal muscle tissue from severely insulin resistant type 2 diabetic subjects, compared with both healthy controls and type 2 diabetic subjects that did not require insulin treatment. In fat tissue, GLUT4 protein expression was reduced in both diabetic groups. In skeletal muscle, the reduced GLUT4 expression in severe insulin resistance was associated with decreased ubiquitin-conjugating enzyme 9 (UBC9) expression while expression of GLUT1, TBC1D1 and AS160 was not significantly different among type 2 diabetic patients and matched controls.
Type 2 diabetic patients with severe insulin resistance have reduced expression of GLUT4 in skeletal muscle compared to patients treated with oral antidiabetic drugs alone. GLUT4 protein levels may therefore play a role in the pathology behind type 2 diabetes mellitus among subgroups of patients, and this may explain the heterogeneous response to insulin treatment. This new finding contributes to the understanding of the underlying mechanisms for the development of extreme insulin resistance.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0027854</identifier><identifier>PMID: 22114711</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Antidiabetics ; Biology ; Biopsy ; Blotting, Western ; Case-Control Studies ; Diabetes ; Diabetes mellitus ; Diabetes Mellitus, Type 2 - genetics ; Diabetes Mellitus, Type 2 - metabolism ; Diabetes Mellitus, Type 2 - pathology ; Diabetes therapy ; Diabetics ; Drugs ; Endocrinology ; Enzymes ; Female ; Glucose ; Glucose transporter ; Glucose Transporter Type 4 - genetics ; Glucose Transporter Type 4 - metabolism ; Humans ; Hypoglycemic agents ; Insulin ; Insulin Resistance ; Internal medicine ; Kinases ; Male ; Medical research ; Medicine ; Metabolism ; Middle Aged ; Muscle, Skeletal - cytology ; Muscle, Skeletal - metabolism ; Musculoskeletal system ; Pathology ; Patients ; Protein expression ; Proteins ; Real-Time Polymerase Chain Reaction ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - genetics ; Rodents ; Skeletal muscle ; Subgroups ; Trends ; Type 2 diabetes ; Ubc9 protein ; Ubiquitin ; Ubiquitin-conjugating enzyme ; Ubiquitin-Conjugating Enzymes - genetics ; Ubiquitin-Conjugating Enzymes - metabolism ; Western blotting</subject><ispartof>PloS one, 2011-11, Vol.6 (11), p.e27854-e27854</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Kampmann et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Kampmann et al. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c691t-275099e4ea9857cd9fe646c8be801cacf775f295016483c651ad15207c9488413</citedby><cites>FETCH-LOGICAL-c691t-275099e4ea9857cd9fe646c8be801cacf775f295016483c651ad15207c9488413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1311930204/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1311930204?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22114711$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Calbet, Jose A. L.</contributor><creatorcontrib>Kampmann, Ulla</creatorcontrib><creatorcontrib>Christensen, Britt</creatorcontrib><creatorcontrib>Nielsen, Thomas Svava</creatorcontrib><creatorcontrib>Pedersen, Steen Bønløkke</creatorcontrib><creatorcontrib>Ørskov, Lotte</creatorcontrib><creatorcontrib>Lund, Sten</creatorcontrib><creatorcontrib>Møller, Niels</creatorcontrib><creatorcontrib>Jessen, Niels</creatorcontrib><title>GLUT4 and UBC9 protein expression is reduced in muscle from type 2 diabetic patients with severe insulin resistance</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Subgroups of patients with type 2 diabetes mellitus demand large insulin doses to maintain euglycemia. These patients are characterized by severe skeletal muscle insulin resistance and the underlying pathology remains unclear. The purpose of this study was to examine protein expression of the principal glucose transporter, GLUT4, and associated proteins in skeletal muscle from type 2 diabetic patients characterized by severe insulin resistance.
Seven type 2 diabetic patients with severe insulin resistance (mean insulin dose 195 IU/day) were compared with seven age matched type 2 diabetic patients who did not require insulin treatment, and with an age matched healthy control group. Protein expression of GLUT4 and associated proteins was assessed in muscle and fat biopsies using standard western blotting techniques.
GLUT4 protein expression was significantly reduced by ∼30 pct in skeletal muscle tissue from severely insulin resistant type 2 diabetic subjects, compared with both healthy controls and type 2 diabetic subjects that did not require insulin treatment. In fat tissue, GLUT4 protein expression was reduced in both diabetic groups. In skeletal muscle, the reduced GLUT4 expression in severe insulin resistance was associated with decreased ubiquitin-conjugating enzyme 9 (UBC9) expression while expression of GLUT1, TBC1D1 and AS160 was not significantly different among type 2 diabetic patients and matched controls.
Type 2 diabetic patients with severe insulin resistance have reduced expression of GLUT4 in skeletal muscle compared to patients treated with oral antidiabetic drugs alone. GLUT4 protein levels may therefore play a role in the pathology behind type 2 diabetes mellitus among subgroups of patients, and this may explain the heterogeneous response to insulin treatment. This new finding contributes to the understanding of the underlying mechanisms for the development of extreme insulin resistance.</description><subject>Antidiabetics</subject><subject>Biology</subject><subject>Biopsy</subject><subject>Blotting, Western</subject><subject>Case-Control Studies</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus, Type 2 - genetics</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Diabetes Mellitus, Type 2 - pathology</subject><subject>Diabetes therapy</subject><subject>Diabetics</subject><subject>Drugs</subject><subject>Endocrinology</subject><subject>Enzymes</subject><subject>Female</subject><subject>Glucose</subject><subject>Glucose transporter</subject><subject>Glucose Transporter Type 4 - genetics</subject><subject>Glucose Transporter Type 4 - metabolism</subject><subject>Humans</subject><subject>Hypoglycemic agents</subject><subject>Insulin</subject><subject>Insulin Resistance</subject><subject>Internal medicine</subject><subject>Kinases</subject><subject>Male</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Metabolism</subject><subject>Middle Aged</subject><subject>Muscle, Skeletal - cytology</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Musculoskeletal system</subject><subject>Pathology</subject><subject>Patients</subject><subject>Protein expression</subject><subject>Proteins</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - genetics</subject><subject>Rodents</subject><subject>Skeletal muscle</subject><subject>Subgroups</subject><subject>Trends</subject><subject>Type 2 diabetes</subject><subject>Ubc9 protein</subject><subject>Ubiquitin</subject><subject>Ubiquitin-conjugating enzyme</subject><subject>Ubiquitin-Conjugating Enzymes - genetics</subject><subject>Ubiquitin-Conjugating Enzymes - metabolism</subject><subject>Western blotting</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk-FvEyEYxi9G4-b0PzBKYqLxQyscBxxfTGajs0mTJbr6lVDuvZbmetyAm9t_L7W3pWf2wfABAr_nAR54s-w1wVNCBfm0db1vdTPtXAtTjHNRsuJJdkokzSc8x_Tp0fgkexHCFmNGS86fZyd5TkghCDnNwsVieVUg3VZo-WUmUeddBNsiuO08hGBdi2xAHqreQIXSwq4PpgFUe7dD8a4DlKPK6hVEa1Cno4U2BvTbxg0KcAMekib0TRImOxuibg28zJ7VugnwaujPsuW3r1ez75PF5cV8dr6YGC5JnOSCYSmhAC1LJkwla-AFN-UKSkyMNrUQrM4lw4QXJTWcEV0RlmNhZFGWBaFn2duDb9e4oIa8giKUpGBwjotEzA9E5fRWdd7utL9TTlv1d8L5tdI-3awBxTCnHIOgktPCEKYx5iuDheBS6KoyyevzsFu_2kFlUhBeNyPT8UprN2rtbhTNSYmZTAYfBgPvrnsIUe1sMNA0ugXXByUxJ4xyyhL57h_y8csN1Fqn89u2dmlbs_dU54XgJc9LuQ9p-giVWgU7a9Lfqm2aHwk-jgSJiXAb17oPQc1__vh_9vLXmH1_xG5AN3ETXNPH9AfDGCwOoPEuBA_1Q8YEq31p3Keh9qWhhtJIsjfH7_Mguq8F-geaiweA</recordid><startdate>20111116</startdate><enddate>20111116</enddate><creator>Kampmann, Ulla</creator><creator>Christensen, Britt</creator><creator>Nielsen, Thomas Svava</creator><creator>Pedersen, Steen Bønløkke</creator><creator>Ørskov, Lotte</creator><creator>Lund, Sten</creator><creator>Møller, Niels</creator><creator>Jessen, Niels</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20111116</creationdate><title>GLUT4 and UBC9 protein expression is reduced in muscle from type 2 diabetic patients with severe insulin resistance</title><author>Kampmann, Ulla ; Christensen, Britt ; Nielsen, Thomas Svava ; Pedersen, Steen Bønløkke ; Ørskov, Lotte ; Lund, Sten ; Møller, Niels ; Jessen, Niels</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c691t-275099e4ea9857cd9fe646c8be801cacf775f295016483c651ad15207c9488413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Antidiabetics</topic><topic>Biology</topic><topic>Biopsy</topic><topic>Blotting, Western</topic><topic>Case-Control Studies</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus, Type 2 - genetics</topic><topic>Diabetes Mellitus, Type 2 - metabolism</topic><topic>Diabetes Mellitus, Type 2 - pathology</topic><topic>Diabetes therapy</topic><topic>Diabetics</topic><topic>Drugs</topic><topic>Endocrinology</topic><topic>Enzymes</topic><topic>Female</topic><topic>Glucose</topic><topic>Glucose transporter</topic><topic>Glucose Transporter Type 4 - genetics</topic><topic>Glucose Transporter Type 4 - metabolism</topic><topic>Humans</topic><topic>Hypoglycemic agents</topic><topic>Insulin</topic><topic>Insulin Resistance</topic><topic>Internal medicine</topic><topic>Kinases</topic><topic>Male</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Metabolism</topic><topic>Middle Aged</topic><topic>Muscle, Skeletal - cytology</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Musculoskeletal system</topic><topic>Pathology</topic><topic>Patients</topic><topic>Protein expression</topic><topic>Proteins</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - genetics</topic><topic>Rodents</topic><topic>Skeletal muscle</topic><topic>Subgroups</topic><topic>Trends</topic><topic>Type 2 diabetes</topic><topic>Ubc9 protein</topic><topic>Ubiquitin</topic><topic>Ubiquitin-conjugating enzyme</topic><topic>Ubiquitin-Conjugating Enzymes - genetics</topic><topic>Ubiquitin-Conjugating Enzymes - metabolism</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kampmann, Ulla</creatorcontrib><creatorcontrib>Christensen, Britt</creatorcontrib><creatorcontrib>Nielsen, Thomas Svava</creatorcontrib><creatorcontrib>Pedersen, Steen Bønløkke</creatorcontrib><creatorcontrib>Ørskov, Lotte</creatorcontrib><creatorcontrib>Lund, Sten</creatorcontrib><creatorcontrib>Møller, Niels</creatorcontrib><creatorcontrib>Jessen, Niels</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale_Opposing Viewpoints In Context</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest advanced technologies & aerospace journals</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials science collection</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kampmann, Ulla</au><au>Christensen, Britt</au><au>Nielsen, Thomas Svava</au><au>Pedersen, Steen Bønløkke</au><au>Ørskov, Lotte</au><au>Lund, Sten</au><au>Møller, Niels</au><au>Jessen, Niels</au><au>Calbet, Jose A. L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GLUT4 and UBC9 protein expression is reduced in muscle from type 2 diabetic patients with severe insulin resistance</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2011-11-16</date><risdate>2011</risdate><volume>6</volume><issue>11</issue><spage>e27854</spage><epage>e27854</epage><pages>e27854-e27854</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Subgroups of patients with type 2 diabetes mellitus demand large insulin doses to maintain euglycemia. These patients are characterized by severe skeletal muscle insulin resistance and the underlying pathology remains unclear. The purpose of this study was to examine protein expression of the principal glucose transporter, GLUT4, and associated proteins in skeletal muscle from type 2 diabetic patients characterized by severe insulin resistance.
Seven type 2 diabetic patients with severe insulin resistance (mean insulin dose 195 IU/day) were compared with seven age matched type 2 diabetic patients who did not require insulin treatment, and with an age matched healthy control group. Protein expression of GLUT4 and associated proteins was assessed in muscle and fat biopsies using standard western blotting techniques.
GLUT4 protein expression was significantly reduced by ∼30 pct in skeletal muscle tissue from severely insulin resistant type 2 diabetic subjects, compared with both healthy controls and type 2 diabetic subjects that did not require insulin treatment. In fat tissue, GLUT4 protein expression was reduced in both diabetic groups. In skeletal muscle, the reduced GLUT4 expression in severe insulin resistance was associated with decreased ubiquitin-conjugating enzyme 9 (UBC9) expression while expression of GLUT1, TBC1D1 and AS160 was not significantly different among type 2 diabetic patients and matched controls.
Type 2 diabetic patients with severe insulin resistance have reduced expression of GLUT4 in skeletal muscle compared to patients treated with oral antidiabetic drugs alone. GLUT4 protein levels may therefore play a role in the pathology behind type 2 diabetes mellitus among subgroups of patients, and this may explain the heterogeneous response to insulin treatment. This new finding contributes to the understanding of the underlying mechanisms for the development of extreme insulin resistance.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22114711</pmid><doi>10.1371/journal.pone.0027854</doi><tpages>e27854</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2011-11, Vol.6 (11), p.e27854-e27854 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1311930204 |
source | Open Access: PubMed Central; Publicly Available Content (ProQuest) |
subjects | Antidiabetics Biology Biopsy Blotting, Western Case-Control Studies Diabetes Diabetes mellitus Diabetes Mellitus, Type 2 - genetics Diabetes Mellitus, Type 2 - metabolism Diabetes Mellitus, Type 2 - pathology Diabetes therapy Diabetics Drugs Endocrinology Enzymes Female Glucose Glucose transporter Glucose Transporter Type 4 - genetics Glucose Transporter Type 4 - metabolism Humans Hypoglycemic agents Insulin Insulin Resistance Internal medicine Kinases Male Medical research Medicine Metabolism Middle Aged Muscle, Skeletal - cytology Muscle, Skeletal - metabolism Musculoskeletal system Pathology Patients Protein expression Proteins Real-Time Polymerase Chain Reaction Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - genetics Rodents Skeletal muscle Subgroups Trends Type 2 diabetes Ubc9 protein Ubiquitin Ubiquitin-conjugating enzyme Ubiquitin-Conjugating Enzymes - genetics Ubiquitin-Conjugating Enzymes - metabolism Western blotting |
title | GLUT4 and UBC9 protein expression is reduced in muscle from type 2 diabetic patients with severe insulin resistance |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T05%3A30%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=GLUT4%20and%20UBC9%20protein%20expression%20is%20reduced%20in%20muscle%20from%20type%202%20diabetic%20patients%20with%20severe%20insulin%20resistance&rft.jtitle=PloS%20one&rft.au=Kampmann,%20Ulla&rft.date=2011-11-16&rft.volume=6&rft.issue=11&rft.spage=e27854&rft.epage=e27854&rft.pages=e27854-e27854&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0027854&rft_dat=%3Cgale_plos_%3EA476862891%3C/gale_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c691t-275099e4ea9857cd9fe646c8be801cacf775f295016483c651ad15207c9488413%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1311930204&rft_id=info:pmid/22114711&rft_galeid=A476862891&rfr_iscdi=true |