Literature DB >> 2689883

Expression of an insulin-regulatable glucose carrier in muscle and fat endothelial cells.

S Vilaró1, M Palacín, P F Pilch, X Testar, A Zorzano.   

Abstract

Insulin rapidly stimulates glucose use in the major target tissues, muscle and fat, by modulating a tissue-specific glucose transporter isoform. Access of glucose to the target tissue is restricted by endothelial cells which line the walls of nonfenestrated capillaries of fat and muscle. Thus, we examined whether the capillary endothelial cells are actively involved in the modulation of glucose availability by these tissues. We report here the abundant expression of the muscle/fat glucose transporter isoform in endothelial cells, using an immunocytochemical analysis with a monoclonal antibody specific for this isoform. This expression is restricted to endothelial cells from the major insulin target tissues, and it is not detected in brain and liver where insulin does not activate glucose transport. The expression of the muscle/fat transporter isoform in endothelial cells is significantly greater than in the neighbouring muscle and fat cells. Following administration of insulin to animals in vivo, there occurs a rapid increase in the number of muscle/fat transporters present in the lumenal plasma membrane of the capillary endothelial cells. These results document that insulin promotes the translocation of the muscle/fat glucose transporter in endothelial cells. It is therefore likely that endothelial cells play an important role in the regulation of glucose use by the major insulin target tissues in normal and diseased states.

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Year:  1989        PMID: 2689883     DOI: 10.1038/342798a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  12 in total

1.  Gi-mediated translocation of GLUT4 is independent of p85/p110alpha and p110gamma phosphoinositide 3-kinases but might involve the activation of Akt kinase.

Authors:  L Wang; H Hayashi; K Kishi; L Huang; A Hagi; K Tamaoka; P T Hawkins; Y Ebina
Journal:  Biochem J       Date:  2000-02-01       Impact factor: 3.857

2.  Insulin responsiveness in skeletal muscle is determined by glucose transporter (Glut4) protein level.

Authors:  M Kern; J A Wells; J M Stephens; C W Elton; J E Friedman; E B Tapscott; P H Pekala; G L Dohm
Journal:  Biochem J       Date:  1990-09-01       Impact factor: 3.857

Review 3.  Pathways for oxidative fuel provision to working muscles: ecological consequences of maximal supply limitations.

Authors:  J M Weber
Journal:  Experientia       Date:  1992-06-15

4.  Immunoelectron microscopic demonstration of insulin-stimulated translocation of glucose transporters to the plasma membrane of isolated rat adipocytes and masking of the carboxyl-terminal epitope of intracellular GLUT4.

Authors:  R M Smith; M J Charron; N Shah; H F Lodish; L Jarett
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-01       Impact factor: 11.205

5.  Characterisation of glucose transporters in the intact coronary artery endothelium in rats: GLUT-2 upregulated by long-term hyperglycaemia.

Authors:  N Gaudreault; D R L Scriven; E D W Moore
Journal:  Diabetologia       Date:  2004-12-10       Impact factor: 10.122

6.  Effect of diabetes and fasting on GLUT-4 (muscle/fat) glucose-transporter expression in insulin-sensitive tissues. Heterogeneous response in heart, red and white muscle.

Authors:  M Camps; A Castelló; P Muñoz; M Monfar; X Testar; M Palacín; A Zorzano
Journal:  Biochem J       Date:  1992-03-15       Impact factor: 3.857

Review 7.  Proton-linked sugar transport systems in bacteria.

Authors:  P J Henderson
Journal:  J Bioenerg Biomembr       Date:  1990-08       Impact factor: 2.945

8.  Decreased in vivo glucose uptake but normal expression of GLUT1 and GLUT4 in skeletal muscle of diabetic rats.

Authors:  B B Kahn; L Rossetti; H F Lodish; M J Charron
Journal:  J Clin Invest       Date:  1991-06       Impact factor: 14.808

9.  Glucose regulates its transport in L8 myocytes by modulating cellular trafficking of the transporter GLUT-1.

Authors:  R Greco-Perotto; E Wertheimer; B Jeanrenaud; E Cerasi; S Sasson
Journal:  Biochem J       Date:  1992-08-15       Impact factor: 3.857

10.  MiR-3138 deteriorates the insulin resistance of HUVECs via KSR2/AMPK/GLUT4 signaling pathway.

Authors:  Yan Chen; Da Lin; Changxuan Shi; Liang Guo; Linhua Liu; Lin Chen; Ting Li; Ying Liu; Chengchao Zheng; Xintong Chi; Chun Meng; Yaoming Xue
Journal:  Cell Cycle       Date:  2021-01-28       Impact factor: 4.534

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