spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Martin, S.
Right arrow Articles by James, D. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Martin, S.
Right arrow Articles by James, D. E.

Journal of Cell Science, Vol 113, Issue 19 3427-3438, Copyright © 2000 by Company of Biologists


JOURNAL ARTICLES

Effects of insulin on intracellular GLUT4 vesicles in adipocytes: evidence for a secretory mode of regulation

S Martin, CA Millar, CT Lyttle, T Meerloo, BJ Marsh, GW Gould and DE James
Centre for Molecular and Cellular Biology & Dept Physiology and Pharmacology, University of Queensland, St Lucia, Brisbane, QLD 4072, Australia. s.martin@cmcb.uq.edu.au

The facilitative glucose transporter, GLUT4 undergoes insulin-dependent movement to the cell surface in adipocytes. The magnitude of the insulin effect is much greater for GLUT4 than other recycling proteins such as the CD-MPR. In the present study we have studied the colocalisation of these proteins in adipocytes in an effort to explain this selective insulin-dependent recruitment of GLUT4. Using immunofluorescence microscopy or immuno-EM on 3T3-L1 adipocytes we find that there is considerable colocalisation between these proteins particularly within the area of the TGN. However, the distribution of CD-MPR was not significantly effected by insulin. The insulin-dependent recruitment of GLUT4 was concomitant with a selective decrease in GLUT4 labelling of cytoplasmic vesicles whereas the amount of GLUT4 in the TGN region (approx. 50% of total GLUT4) was relatively unaffected. To explore the possibility that the cytoplasmic GLUT4(+) vesicles represent an intracellular insulin-responsive storage compartment we performed quantitative immuno-EM on whole mounts of intracellular vesicles isolated from basal and insulin-stimulated adipocytes. These studies revealed that: (1) GLUT4 and CD-MPR were concentrated in small (30-200 nm) vesicles at a labelling density of 1-20+ gold particles/vesicle; (2) there was significant overlap between both proteins in that 70% of the total GLUT4 pool colocalised with CD-MPR; (3) a significant amount of GLUT4 (approx. 50% of total) was found in a subpopulation of vesicles that contained as little as 5% of the total CD-MPR pool; (4) the GLUT4(+)/CD-MPR(-) vesicles were highly insulin-responsive, and (5) the total number of GLUT4(+) vesicles, but not CD-MPR(+) vesicles, decreased by approx. 30% in response to insulin treatment. These data are consistent with a model in which GLUT4 is selectively sorted into a vesicular compartment in adipocytes that is recruited to the plasma membrane by insulin stimulation.


This article has been cited by other articles:


Home page
Mol. Endocrinol.Home page
M. Larance, G. Ramm, and D. E. James
The GLUT4 Code
Mol. Endocrinol., February 1, 2008; 22(2): 226 - 233.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
S. Huang, L. M. Lifshitz, C. Jones, K. D. Bellve, C. Standley, S. Fonseca, S. Corvera, K. E. Fogarty, and M. P. Czech
Insulin Stimulates Membrane Fusion and GLUT4 Accumulation in Clathrin Coats on Adipocyte Plasma Membranes
Mol. Cell. Biol., May 1, 2007; 27(9): 3456 - 3469.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. C. Hou, S. Shigematsu, H. C. Crawford, P. Z. Anastasiadis, and J. E. Pessin
Dual Regulation of Rho and Rac by p120 Catenin Controls Adipocyte Plasma Membrane Trafficking
J. Biol. Chem., August 18, 2006; 281(33): 23307 - 23312.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
D. J. Hernandez-Deviez, S. Martin, S. H. Laval, H. P. Lo, S. T. Cooper, K. N. North, K. Bushby, and R. G. Parton
Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3
Hum. Mol. Genet., January 1, 2006; 15(1): 129 - 142.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Larance, G. Ramm, J. Stockli, E. M. van Dam, S. Winata, V. Wasinger, F. Simpson, M. Graham, J. R. Junutula, M. Guilhaus, et al.
Characterization of the Role of the Rab GTPase-activating Protein AS160 in Insulin-regulated GLUT4 Trafficking
J. Biol. Chem., November 11, 2005; 280(45): 37803 - 37813.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Bose, A. Guilherme, S. Huang, A. C. Hubbard, C. R. Lane, N. A. Soriano, and M. P. Czech
The v-SNARE Vti1a Regulates Insulin-stimulated Glucose Transport and Acrp30 Secretion in 3T3-L1 Adipocytes
J. Biol. Chem., November 4, 2005; 280(44): 36946 - 36951.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
A. Zeigerer, M. K. McBrayer, and T. E. McGraw
Insulin Stimulation of GLUT4 Exocytosis, but Not Its Inhibition of Endocytosis, Is Dependent on RabGAP AS160
Mol. Biol. Cell, October 1, 2004; 15(10): 4406 - 4415.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
H. K. I. Perera, M. Clarke, N. J. Morris, W. Hong, L. H. Chamberlain, and G. W. Gould
Syntaxin 6 Regulates Glut4 Trafficking in 3T3-L1 Adipocytes
Mol. Biol. Cell, July 1, 2003; 14(7): 2946 - 2958.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
K. H. Pfenninger, L. Laurino, D. Peretti, X. Wang, S. Rosso, G. Morfini, A. Caceres, and S. Quiroga
Regulation of membrane expansion at the nerve growth cone
J. Cell Sci., April 1, 2003; 116(7): 1209 - 1217.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
A. M. Shewan, E. M. van Dam, S. Martin, T. B. Luen, W. Hong, N. J. Bryant, and D. E. James
GLUT4 Recycles via a trans-Golgi Network (TGN) Subdomain Enriched in Syntaxins 6 and 16 But Not TGN38: Involvement of an Acidic Targeting Motif
Mol. Biol. Cell, March 1, 2003; 14(3): 973 - 986.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
Y. Xu, S. Martin, D. E. James, and W. Hong
GS15 Forms a SNARE Complex with Syntaxin 5, GS28, and Ykt6 and Is Implicated in Traffic in the Early Cisternae of the Golgi Apparatus
Mol. Biol. Cell, October 1, 2002; 13(10): 3493 - 3507.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. C. Molero, J. P. Whitehead, T. Meerloo, and D. E. James
Nocodazole Inhibits Insulin-stimulated Glucose Transport in 3T3-L1 Adipocytes via a Microtubule-independent Mechanism
J. Biol. Chem., November 16, 2001; 276(47): 43829 - 43835.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
J. S. Bogan, A. E. McKee, and H. F. Lodish
Insulin-Responsive Compartments Containing GLUT4 in 3T3-L1 and CHO Cells: Regulation by Amino Acid Concentrations
Mol. Cell. Biol., July 15, 2001; 21(14): 4785 - 4806.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
S. Mora, C. Yang, J. W. Ryder, D. Boeglin, and J. E. Pessin
The MEF2A and MEF2D Isoforms Are Differentially Regulated in Muscle and Adipose Tissue during States of Insulin Deficiency
Endocrinology, May 1, 2001; 142(5): 1999 - 2004.
[Abstract] [Full Text]




© The Company of Biologists Ltd 2000