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Molecular and Cellular Biology, March 2001, p. 1573-1580, Vol. 21, No. 5
Department of Physiology and
Biophysics1 and Department of Internal
Medicine,3 The University of Iowa, Iowa
City, Iowa 52242, and Department of Cell Biology, Pfizer
Global Research and Development, Ann Arbor, Michigan
481052
Received 19 September 2000/Returned for modification 28 September
2000/Accepted 27 November 2000
To investigate the physiological function of the VAMP3 vesicle
SNARE (v-SNARE) isoform in the regulation of GLUT4 vesicle trafficking,
we generated homozygotic VAMP3 null mice by targeted gene disruption.
The VAMP3 null mice had typical growth rate and weight gain, with
normal maintenance of fasting serum glucose and insulin levels.
Analysis of glucose disposal and insulin sensitivity demonstrated
normal insulin and glucose tolerance, with no evidence for insulin
resistance. Insulin stimulation of glucose uptake in isolated primary
adipocytes was essentially the same for the wild-type and VAMP3 null
mice. Similarly, insulin-, hypoxia-, and exercise-stimulated glucose
uptake in isolated skeletal muscle did not differ significantly. In
addition, other general membrane trafficking events including
phagocytosis, pinocytosis, and transferrin receptor recycling were also
found to be unaffected in the VAMP3 null mice. Taken together, these
data demonstrate that VAMP3 function is not necessary for either
regulated GLUT4 translocation or general constitutive membrane recycling.
0270-7306/01/$04.00+0 DOI: 10.1128/MCB.21.5.1573-1580.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
VAMP3 Null Mice Display Normal Constitutive,
Insulin- and Exercise-Regulated Vesicle Trafficking

*
Corresponding author. Mailing address: Department of
Physiology and Biophysics, The University of Iowa, Iowa City, IA 52242. Phone: (319) 335-7823. Fax: (319) 335-7886. E-mail:
Jeffrey-Pessin{at}uiowa.edu.
Present address: Lexicon Genetics Incorporated, The Woodlands, TX 77381.
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