Yw. Shi et al., MODULATION OF GLUT1 INTRINSIC ACTIVITY IN CLONE-9 CELLS BY INHIBITIONOF OXIDATIVE-PHOSPHORYLATION, The Journal of biological chemistry, 270(37), 1995, pp. 21772-21778
Brief (1-2 h) exposure of Clone 9 cells to inhibitors of oxidative pho
sphorylation such as azide is known to markedly increase glucose uptak
e. Clone 9 cells express GLUT1 but not GLUT2, -3, and -4, and the azid
e effect was not accompanied by any increase in cellular or plasma mem
brane GLUT1 level. To identify the molecular event underlying this app
arent increase in GLUT1 intrinsic activity, we studied the acute effec
ts of azide on the substrate binding activity of GLUT1 in Clone 9 cell
s by measuring glucose-sensitive cytochalasin B binding. The glucose-d
isplaceable, cytochalasin B binding activity was barely detectable in
membranes isolated from Clone 9 cells under control conditions but was
readily detectable after a 60-min incubation of cells in the presence
of 5 mM azide showing a 3-fold increase in binding capacity with no c
hange in binding affinity. Furthermore, the cytochalasin B binding act
ivity of purified human erythrocyte GLUT1 reconstituted in liposomes w
as significantly reduced in the presence of cytosol derived from azide
-treated Clone 9 cells but not in the presence of cytosol from control
cells; this effect was heat-labile and abolished by the presence of t
he peptide corresponding to the GLUT1 COOH-terminal sequence. These re
sults suggest that a cytosolic protein in Clone 9 cells binds to GLUT1
at its COOH-terminal domain and inhibits its substrate binding and th
at azide-induced metabolic alteration releases GLUT1 from this inhibit
ory interaction. Studying the binding of cytosolic proteins derived fr
om S-35-labeled Clone 9 cells to glutathione S-transferase fusion prot
ein containing glucose transporter COOH-terminal sequences, we identif
ied 28- and 70-kDa proteins that bind specifically to the cytoplasmic
domain of GLUT1 and GLUT4 in vitro. We also found a P-32-labeled, 85-k
Da protein that binds to GLUT4 but not to GLUT1 and only in cytosol de
rived from azide-treated cells, The roles, if any, of these glucose tr
ansporter-binding proteins in the azide-sensitive modulation of GLUT1
substrate binding activity in Clone 9 cells are yet to be determined.