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Molecular and Cellular Biology, January 2000, p. 379-388, Vol. 20, No. 1
0270-7306/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Munc18c Function Is Required for Insulin-Stimulated
Plasma Membrane Fusion of GLUT4 and Insulin-Responsive Amino
Peptidase Storage Vesicles
Debbie C.
Thurmond,
Makoto
Kanzaki,
Ahmir H.
Khan, and
Jeffrey E.
Pessin*
Department of Physiology and Biophysics, The
University of Iowa, Iowa City, Iowa 52242
Received 10 May 1999/Returned for modification 11 June
1999/Accepted 18 August 1999
To examine the functional role of the interaction between Munc18c
and syntaxin 4 in the regulation of GLUT4 translocation in 3T3L1
adipocytes, we assessed the effects of introducing three different
peptide fragments (20 to 24 amino acids) of Munc18c from evolutionarily
conserved regions of the Sec1 protein family predicted to be solvent
exposed. One peptide, termed 18c/pep3, inhibited the binding of
full-length Munc18c to syntaxin 4, whereas expression of the other two
peptides had no effect. In parallel, microinjection of 18c/pep3 but not
a control peptide inhibited the insulin-stimulated translocation of
endogenous GLUT4 and insulin-responsive amino peptidase (IRAP) to the
plasma membrane. In addition, expression of 18c/pep3 prevented the
insulin-stimulated fusion of endogenous and enhanced green fluorescent
protein epitope-tagged GLUT4- and IRAP-containing vesicles into the
plasma membrane, as assessed by intact cell immunofluorescence.
However, unlike the pattern of inhibition seen with full-length Munc18c
expression, cells expressing 18c/pep3 displayed discrete clusters of
GLUT4 abd IRAP storage vesicles at the cell surface which were not
contiguous with the plasma membrane. Together, these data suggest that
the interaction between Munc18c and syntaxin 4 is required for the integration of GLUT4 and IRAP storage vesicles into the plasma membrane
but is not necessary for the insulin-stimulated trafficking to and
association with the cell surface.
*
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.
Molecular and Cellular Biology, January 2000, p. 379-388, Vol. 20, No. 1
0270-7306/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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