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PMID: 2649887 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Activation of glucose uptake by insulin and insulin-like growth factor I in Xenopus oocytes.

Janicot M, Lane MD

Abstract

Xenopus laevis oocytes possess a glucose transport system that is activated 3- to 5-fold by insulin-like growth factor I (Ka = 3 nM) and insulin (Ka = 200-250 nM), properties suggesting activation mediated by an insulin-like growth factor I receptor. This activation increases the Vmax of hexose uptake and has little or no effect on the Km for deoxyglucose (Km = 1-2 mM). Activation by hormone requires about 60 min and is inhibited by cytochalasin B but not by cycloheximide. The dependence of hexose uptake rate on hexose concentration exhibits cooperativity with Hill coefficients of 1.8 and 1.4 for the basal and hormone-activated states, respectively. Microinjection of a monoclonal antibody directed against the tyrosine kinase domain of the human insulin receptor blocks activation of hexose uptake by insulin-like growth factor I and insulin but has no effect on basal uptake. Taken together the results implicate the tyrosine-specific protein kinase activity of a cell-surface insulin-like growth factor I receptor in the activation of glucose transport in the Xenopus oocyte.

MeSH Terms
Animals Biological Transport Dose-Response Relationship, Drug Glucose/metabolism Hexoses/metabolism Insulin/pharmacology Insulin-Like Growth Factor I/pharmacology Kinetics Monosaccharide Transport Proteins/metabolism Oocytes Protein-Tyrosine Kinases/physiology Somatomedins/pharmacology Xenopus laevis/physiology
Chemicals
Hexoses Insulin Monosaccharide Transport Proteins Somatomedins Insulin-Like Growth Factor I Protein-Tyrosine Kinases Glucose
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Janicot M
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Lane M D
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20 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1989-04-00
Pages
2642-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC286973
Subset
IM
Grants
NIDDK NIH HHS · DK-14574 · United States
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