Id. Millar et al., THE MECHANISM OF L-GLUTAMATE TRANSPORT BY LACTATING RAT MAMMARY TISSUE, Biochimica et biophysica acta. Biomembranes, 1282(2), 1996, pp. 200-206
The transport of L-glutamate by lactating rat mammary gland has been e
xamined using both tissue explants and a perfused mammary preparation.
L-Glutamate uptake by mammary tissue explants was predominantly via a
Na+-dependent pathway: Li+, choline(+) and NMDG(+) could not substitu
te for Na+. L-Glutamate efflux from preloaded explants was also influe
nced by the transmembrane Na+-gradient. These results are consistent w
ith (Na+-glutamate) cotransport. The Naf-dependent system for L-glutam
ate transport in tissue explants was saturable (K-m = 112.5 +/- 19.7 m
u M; V-max = 71.3 +/- 10.4 nmol/min per g cells) and selective for ani
onic amino acids. Thus, D- and L-aspartate were high affinity inhibito
rs of L-glutamate uptake whereas neutral amino acids were relatively i
neffective. a-Aspartate inhibited L-glutamate uptake in a competitive
fashion. L-Glutamate uptake by the perfused mammary gland was (a) Naf-
dependent (b) saturable (K-m = 18.1 +/- 4.9 mu M; V-max = 40.3 +/- 3.7
nmol/min per g tissue) and (c) selective for anionic amino acids. The
results suggest that the (Na+-glutamate) cotransporter is situated in
the blood-facing aspect of the mammary epithelium.