Cellular stress causes accumulation of the glucose transporter at the surface of cells independently of their insulin sensitivity

The stimulation of glucose transport in response to various types of stress has been studied. There is no relationship between effects of stress-inducing agents on glucose transport and their effects on cellular protein synthesis. Although the effect of stress on glucose transport appears analogous...

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Veröffentlicht in:The Journal of membrane biology 1996-01, Vol.149 (2), p.133-140
Hauptverfasser: Sviderskaya, E V, Jazrawi, E, Baldwin, S A, Widnell, C C, Pasternak, C A
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Sprache:eng
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Zusammenfassung:The stimulation of glucose transport in response to various types of stress has been studied. There is no relationship between effects of stress-inducing agents on glucose transport and their effects on cellular protein synthesis. Although the effect of stress on glucose transport appears analogous to its stimulation by insulin, cells that are slightly insulin-sensitive in terms of glucose transport (BHK cells) show a similar degree of stimulation as highly insulin-sensitive cells (differentiated 3T3-L1 cells). External labeling of the transporter protein with a photoactivatable derivative of mannose, 2-N-4-(1-azi-2,2,2-trifluoroethyl) benzoyl-1, 3-bis-(D-mannos-4-yloxy)-propylamine, shows that most of the increased glucose transport activity correlates with an increase in the amount of the transporter on the cell surface. Cells subjected to K(+)-depletion, which inhibits endocytosis and results in an accumulation of receptors at the cell surface, show the same increase in glucose transport as cells exposed to stress; stressed cells show no further increase in glucose transport when subjected to K+ depletion. These results support the view (Widnell, C.C., Baldwin, S.A., Davies, A., Martin, S., Pasternak, C.A. 1990. FASEB J 4:1634-1637) that cellular stress increases glucose transport by promoting the accumulation of glucose transporter molecules at the cell surface.
ISSN:0022-2631
1432-1424
DOI:10.1007/s002329900014