Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Phosphorylation state of the glucose transporter from 3T3-L1 adipocytes: effect of insulin and phorbol ester

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5230538

Polyclonal antibodies against the purified human erythrocyte glucose transporter (GT) were used to study the phosphorylation state of GT in (/sup 32/P)orthophosphate-labeled 3T3-L1 adipocytes that were exposed to insulin or phorbol ester. Conditions were established in which the recovery of GT (identified as a polypeptide of M/sub r/ 51,000) after immunoprecipitation from detergent-solubilized adipocytes was about 50% of total cellular transporter, as quantitated by immunoblot analysis. Exposure of adipocytes to insulin (100 nM) for 10 min after prelabeling in /sup 32/P for 90 min, followed by the addition of phorbol myristate acetate (PMA; 1 ..mu..M) for 20 min elicited a marked phosphorylation of GT. Addition of excess purified human erythrocyte GT completely abolished the immunoprecipitation of the 51 K phosphoprotein; this finding validates the conclusion that this phosphoprotein is GT. Treatment with PMA alone resulted in only 30% of the incorporation of /sup 32/P into the 51 K region of the gel compared to that seen with the combination of PMA and insulin. Insulin alone gave only about 20% /sup 32/P incorporation into this region compared to the combination treatment. It remains to be determined if the phosphorylation into the 51 K region of the gel seen after treatment with either of the two agonists alone is into GT. The authors tentative hypothesis is that GT is not phosphorylated in basal cells, and that insulin causes little or no increase in the phosphorylation state. On the other hand, PMA elicits some phosphorylation of GT that can be increased about 3-fold by prior treatment with insulin. Presumably, this increase is due to the translocation of GT to the plasma membrane where it is a better substrate for activated protein kinase C.

Research Organization:
Dartmouth Medical School, Hanover, NH
OSTI ID:
5230538
Report Number(s):
CONF-8606151-
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Journal Name: Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States) Vol. 45:6; ISSN FEPRA
Country of Publication:
United States
Language:
English

Similar Records

Isoproterenol stimulates phosphorylation of the insulin-regulatable glucose transporter in rat adipocytes
Journal Article · Tue Oct 31 23:00:00 EST 1989 · Proceedings of the National Academy of Sciences of the United States of America; (USA) · OSTI ID:6906576

Threonine 1336 of the human insulin receptor is a major target for phosphorylation by protein kinase C
Journal Article · Mon Feb 19 23:00:00 EST 1990 · Biochemistry; (USA) · OSTI ID:6897378

Effect of growth hormone on protein phosphorylation in isolated rat hepatocytes
Journal Article · Mon Feb 09 23:00:00 EST 1987 · Biochemistry; (United States) · OSTI ID:6616975