Characterization of two distinct intracellular GLUT4 membrane populations in muscle fiber: differential protein composition and sensivity to insulin

dc.contributor.author
Sevilla, Lidia
dc.contributor.author
Tomàs, Eva
dc.contributor.author
Muñoz Moruno, Purificación
dc.contributor.author
Gumà i Garcia, Anna Maria
dc.contributor.author
Fischer, Yvan
dc.contributor.author
Thomas, Julia
dc.contributor.author
Ruiz-Montasell, Bonaventura
dc.contributor.author
Testar, Xavier
dc.contributor.author
Palacín Prieto, Manuel
dc.contributor.author
Blasi Cabús, Joan
dc.contributor.author
Zorzano Olarte, Antonio
dc.date.issued
2019-06-03T15:19:20Z
dc.date.issued
2019-06-03T15:19:20Z
dc.date.issued
1997-07
dc.date.issued
2019-06-03T15:19:20Z
dc.identifier
0013-7227
dc.identifier
https://hdl.handle.net/2445/134424
dc.identifier
119735
dc.identifier
9202246
dc.description.abstract
A major objective for the understanding of muscle glucose disposal is the elucidation of the intracellular trafficking pathway of GLUT4 glucose carriers in the muscle fiber. In this report, we provide functional and biochemical characterization of two distinct intracellular GLUT4 vesicle pools obtained from rat skeletal muscle. The two pools showed a differential response to insulin; thus, one showed a marked decrease in GLUT4 levels but the other did not. They also showed a markedly different protein composition as detected by quantitative vesicle immunoisolation analysis. The GLUT4 pool showing no response to insulin contained SCAMP proteins and the vSNARE proteins VAMP2 and cellubrevin, whereas only VAMP2 was found in the insulin-recruitable GLUT4 pool. SDS-PAGE and further silver staining of the immunoprecipitates revealed discrete polypeptide bands associated to the insulin-sensitive pool, and all these polypeptide bands were found in the insulin-insensitive population. Furthermore, some polypeptide bands were exclusive to the insulin-insensitive population. The presence of cellubrevin and SCAMP proteins, endosomal markers, suggest that the insulin-insensitive GLUT4 membrane population belongs to an endosomal compartment. In addition, we favor the view that the insulin-sensitive GLUT4 membrane pool is segregated from the endosomal GLUT4 population and is undergoes exocytosis to the cell surface in response to insulin. Intracellular GLUT4 membranes obtained from skeletal muscle contain cellubrevin, and VAMP2 and GLUT4-vesicles from cardiomyocytes also contain cellubrevin. This suggests that vSNARE proteins are key constituents of GLUT4 vesicles. The presence of the tSNARE protein SNAP25 in skeletal muscle membranes and SNAP25 and syntaxin 1A and syntaxin 1B in cardiomyocyte plasma membranes further suggest a role of the SNAREs in GLUT4 trafficking in muscle.
dc.format
10 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Association for the Study of Internal Secretions
dc.relation
Reproducció del document publicat a: https://doi.org/10.1210/endo.138.7.5235
dc.relation
Endocrinology, 1997, vol. 138, num. 7, p. 3006-3015
dc.relation
https://doi.org/10.1210/endo.138.7.5235
dc.rights
(c) Association for the Study of Internal Secretions, 1997
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Bioquímica i Biomedicina Molecular)
dc.subject
Insulina
dc.subject
Farmacologia
dc.subject
Metabolisme
dc.subject
Proteïnes
dc.subject
Transport
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Cèl·lules musculars
dc.subject
Insulin
dc.subject
Pharmacology
dc.subject
Metabolism
dc.subject
Proteins
dc.subject
Transportation
dc.subject
Muscle cells
dc.title
Characterization of two distinct intracellular GLUT4 membrane populations in muscle fiber: differential protein composition and sensivity to insulin
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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