Jp. Charon et al., CHARACTERIZATION OF SODIUM-DEPENDENT GLUCOSE-TRANSPORT IN SHEEP TRACHEAL EPITHELIUM, American journal of physiology. Lung cellular and molecular physiology, 11(4), 1994, pp. 120000390-120000397
The nonmetabolizable glucose analogue methyl(alpha-D-[U-C-14]gluco)pyr
anoside ([C-14]AMG) was used to study sodium-dependent glucose transpo
rt in two preparations: 1) discs punched from strips of sheep tracheal
epithelium, and 2) freshly enzyme-isolated sheep tracheal epithelial
cells. In discs, cellular accumulation of [C-14]AMG was saturable and
exhibited a Michaelis-Menten constant (K-m) for AMG of 0.63 +/- 0.15 m
M. Uptake was linear over 30 min and was inhibited maximally by 100 mu
M phlorizin [inhibition constant (K-i) approximate to 20 nM], by repl
acement of external sodium with choline or by addition of 10 mM D-gluc
ose (K-i = 0.19 +/- 0.02 mM). Accumulative uptake was activated, in a
concentration-dependent manner, by external sodium [affinity constant
(K-a) approximate to 23 mM] with a Hill coefficient of greater than on
e but was abolished on depolarizing with high external potassium. In t
he presence of sodium, D-galactose and AMG both inhibited uptake of [C
-14]AMG, whereas L-glucose, D-fructose, and D-mannose were ineffective
. In isolated cells, [C-14]AMG accumulated only in the presence of ext
ernal sodium and uptake was inhibited by the addition of D-glucose (K-
i approximate to 0.2 mM), D-galactose, and AMG but not by L-glucose or
D-xylose. We conclude that sheep tracheal epithelium exhibits sodium-
dependent glucose uptake with a very high affinity for phlorizin, whic
h indicates the presence of a novel isoform of the transporter.