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Vol. 291, Issue 2, 555-561, November 1999
Department of Physiological Sciences, University of Florida,
College of Veterinary Medicine, Gainesville, Florida
The interaction of the cysteine conjugate
S-(1-chloro-1,2,2,-trifluoroethyl)-L-cysteine
(CTFC) with organic anion and amino acid transport in the basolateral
and apical membranes was examined with rabbit renal proximal tubule
suspensions and primary cultures of rabbit renal proximal tubule cells.
The apparent Ki for CTFC inhibition of the
1-min uptake of [3H]p-aminohippurate in
tubule suspensions was 105 ± 3 µM and suggests that CTFC
interacts with basolateral organic anion transport. Also, the addition
of 1 mM CTFC decreased the secretion and intracellular accumulation of
fluorescein by ~70 to 75%. The addition of 1 mM CTFC to the apical
compartment decreased the reabsorption and intracellular accumulation
of the amino acid [3H]phenylalanine by ~60 to 70%.
Similar to CTFC, saturating concentrations of the organic anion
[3H]p-aminohippurate and the amino acid
phenylalanine reduced by ~75% fluorescein secretion and
[3H]phenylalanine reabsorption, respectively, by ~60 to
70%. Thus, the cysteine conjugate CTFC appears to be a potent
inhibitor of basolateral organic anion and apical amino acid
transepithelial transport. In contrast to its effects on apical
phenylalanine uptake, CTFC had no effect on the basal uptake of
[3H]phenylalanine by primary cultures. The presence of
CTFC in the external bath did trans-stimulate the efflux
of fluorescein and [3H]phenylalanine across the basal and
apical membrane in tubule suspensions or primary cultures,
respectively, grown on plastic. Collectively, these data demonstrate
that CTFC interacts with, and is transported by, two anatomically and
functionally distinct transporters, the basolateral organic anion and
apical neutral amino acid pathways, in the rabbit renal proximal tubule cell.
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