2-Hydroxypropyl-beta-cyclodextrin enhances phorbol ester effects on glucose transport and/or protein kinase C-beta translocation to the plasma membrane in rat adipocytes and soleus muscles

J Biol Chem. 1993 Sep 25;268(27):19949-55.

Abstract

In rat adipocytes and soleus muscles, 2-hydroxypropyl-beta-cyclodextrin (CD) was found to have a relatively small or no effect on basal or insulin-stimulated hexose uptake, but markedly enhanced hexose uptake effects of phorbol esters and/or diacylglycerol. In rat adipocytes, the CD-induced enhancement of hexose uptake during concurrent phorbol ester treatment was not associated with an increase in GLUT4 glucose transporter translocation to the plasma membrane, which was stimulated comparably by insulin and phorbol esters. Moreover, CD appeared to activate or facilitate the activation of glucose transporters subsequent to their translocation to the plasma membrane during ongoing phorbol ester treatment. In rat adipocytes, CD also enhanced the translocation of protein kinase C (PKC)-beta to the plasma membrane during the action of phorbol esters, which alone had little or no effect on this specific PKC translocation. Although it is uncertain how CD alters the function of plasma membranes to enhance the translocation of PKC-beta to, and the activation of glucose transporters within, this subcellular fraction during phorbol ester treatment, our findings provide direct support for a two-step model in the activation of glucose transport. In addition, it seems clear that, at least in some cell types, simple phorbol ester treatment does not necessarily serve as a ubiquitous activator of all activable PKC pools and all potential PKC-mediated responses.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 2-Hydroxypropyl-beta-cyclodextrin
  • 3-O-Methylglucose
  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism*
  • Alkaloids / pharmacology
  • Animals
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cyclodextrins / pharmacology*
  • Cytosol / drug effects
  • Cytosol / metabolism
  • Deoxyglucose / metabolism*
  • Epididymis
  • Insulin / pharmacology
  • Isoenzymes / metabolism*
  • Kinetics
  • Male
  • Methylglucosides / metabolism*
  • Monosaccharide Transport Proteins / metabolism*
  • Muscles / drug effects
  • Muscles / metabolism*
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / metabolism*
  • Rats
  • Staurosporine
  • Tetradecanoylphorbol Acetate / pharmacology*
  • beta-Cyclodextrins*

Substances

  • Alkaloids
  • Cyclodextrins
  • Insulin
  • Isoenzymes
  • Methylglucosides
  • Monosaccharide Transport Proteins
  • beta-Cyclodextrins
  • 3-O-Methylglucose
  • 2-Hydroxypropyl-beta-cyclodextrin
  • Deoxyglucose
  • Protein Kinase C
  • Staurosporine
  • Tetradecanoylphorbol Acetate