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Journal Article
Effects of insulin on intracellular GLUT4 vesicles in adipocytes: evidence for a secretory mode of regulation
S. Martin, C.A. Millar, C.T. Lyttle, T. Meerloo, B.J. Marsh, G.W. Gould, D.E. James
Journal of Cell Science 2000 113: 3427-3438;
S. Martin
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C.A. Millar
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C.T. Lyttle
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T. Meerloo
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B.J. Marsh
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G.W. Gould
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D.E. James
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Summary

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.

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Journal Article
Effects of insulin on intracellular GLUT4 vesicles in adipocytes: evidence for a secretory mode of regulation
S. Martin, C.A. Millar, C.T. Lyttle, T. Meerloo, B.J. Marsh, G.W. Gould, D.E. James
Journal of Cell Science 2000 113: 3427-3438;
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Journal Article
Effects of insulin on intracellular GLUT4 vesicles in adipocytes: evidence for a secretory mode of regulation
S. Martin, C.A. Millar, C.T. Lyttle, T. Meerloo, B.J. Marsh, G.W. Gould, D.E. James
Journal of Cell Science 2000 113: 3427-3438;

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Mole – The Corona files

“Despite everything, it's just incredible that we get to do science.”

Mole continues to offer his wise words to researchers on how to manage during the COVID-19 pandemic.


JCS and COVID-19

For more information on measures Journal of Cell Science is taking to support the community during the COVID-19 pandemic, please see here.

If you have any questions or concerns, please do not hestiate to contact the Editorial Office.

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