The Journal of Neuroscience, August 1, 1999, 19(15):6290-6297
L-Proline and L-Pipecolate Induce
Enkephalin-Sensitive Currents in Human Embryonic Kidney 293 Cells
Transfected with the High-Affinity Mammalian Brain
L-Proline Transporter
Aurelio
Galli2,
Lankupalle D.
Jayanthi1,
I.
Scott
Ramsey1,
Joshua W.
Miller3,
Robert T.
Fremeau Jr3, and
Louis J.
DeFelice1
1 Department of Pharmacology and Center for Molecular
Neuroscience, Vanderbilt University Medical Center, Nashville,
Tennessee 37232-6600, 2 Department of Pharmacology,
University of Texas, Health Science Center, San Antonio, Texas
78284-7764, and 3 Department of Pharmacology and Cancer
Biology and Neurobiology, Duke University Medical Center, Durham, North
Carolina 27710
The high-affinity mammalian brain L-proline transporter
(PROT) belongs to the GAT1 gene family, which includes Na- and
Cl-dependent plasma membrane carriers for neurotransmitters, osmolites,
and metabolites. These transporters couple substrate flux to
transmembrane electrochemical gradients, particularly the Na gradient.
In the nervous system, transporters clear synapses and help to
replenish transmitters in nerve terminals. The localization of PROT to
specific excitatory terminals in rat forebrain suggests a role for this carrier in excitatory transmission (Renick et al., 1999). We
investigated the voltage regulation and electrogenicity of this novel
transporter, using human embryonic kidney (HEK) 293 cells stably
transfected with rat PROT cDNA. In physiological solutions between
140 and
40 mV, L-proline (PRO) and its six-member ring
congener L-pipecolate (PIP) induced inward current. The
current-voltage relationship and the variance of current fluctuations
were similar for PRO- and PIP-induced current, and the ratio of induced
variance to the mean current ranged from 20 to 60 fA.
Des-Tyr-Leu-enkephalin (GGFL), a competitive peptide inhibitor of PROT,
reduced the rat PROT-associated current to control levels. GGFL alone
did not elicit currents, and the GGFL-sensitive substrate-induced
current was absent in nontransfected cells. Finally, GGFL inhibited
PROT-mediated transport only when applied to the extracellular face of
PROT. These data suggest that (1) PROT uptake is electrogenic, (2)
individual transporter currents are voltage-independent, and (3) GGFL
is a nonsubstrate inhibitor that interacts either with an extracellular domain of PROT or in an externally accessible pore.
Key words:
proline; pipecolic acid; transporter; enkephalin; voltage-clamp; uptake; current; HEK-293 cells
Copyright © 1999 Society for Neuroscience 0270-6474/99/19156290-08$05.00/0