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PMID: 2243134 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Reduced beta-cell glucose transporter in new onset diabetic BB rats.

The Journal of clinical investigation ·Vol. 86 ·No. 5 ·1990-11-00 ·Pages 1615-22

Orci L, Unger RH, Ravazzola M, Ogawa A, Komiya I, Baetens D, Lodish HF, Thorens B

Abstract

Previous studies from our laboratories have suggested a defect in glucose transport in islets isolated from BB rats on the first day of overt diabetes. To quantitate by immunostaining the glucose transporter of beta-cells (GLUT-2) before and at the onset of autoimmune diabetes we employed an antibody to its COOH-terminal octapeptide. On the first day of overt diabetes, defined as the day the daily blood glucose first reached 200 mg/dl, the volume density ratio of GLUT-2-positive to insulin-positive beta-cells was only 0.48 +/- 0.06, compared to 0.91 +/- 0.02 in age-matched nondiabetic diabetes-resistant controls (P less than 0.001). In age-matched nondiabetic diabetes-prone rats, most of which would have become diabetic, the ratio was 0.85 +/- 0.02, also less than the controls (P less than 0.05). Protein A-gold labeling of GLUT-2 in beta-cells of day 1 diabetic rats revealed 2.17 +/- 0.16 gold particles per micrometer length of microvillar plasma membranes compared to 3.91 +/- 0.14 in controls (P less than 0.001) and 2.87 +/- 0.24 in the nondiabetic diabetes-prone rats (P less than 0.02). Reduction in GLUT-2 correlates temporally with and may contribute to the loss of glucose-stimulated insulin secretion that precedes profound beta-cell depletion of autoimmune diabetes.

MeSH Terms
Animals B-Lymphocytes/metabolism,ultrastructure Diabetes Mellitus, Experimental/metabolism Fluorescent Antibody Technique Glucose/metabolism,pharmacology Immunohistochemistry Insulin/metabolism Male Microscopy, Electron Monosaccharide Transport Proteins/metabolism Rats Rats, Inbred Strains
Chemicals
Insulin Monosaccharide Transport Proteins Glucose
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Orci L
Gifford Laboratories, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235.
Unger R H
Ravazzola M
Ogawa A
Komiya I
Baetens D
Lodish H F
Thorens B
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1990-11-00
Pages
1615-22
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC296911
Subset
IM
Grants
NIDDK NIH HHS · DK02700-30 · United States
NIGMS NIH HHS · GM40916 · United States
NHLBI NIH HHS · HL41484 · United States
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