scholarly journals Regulation of Organic Cation Transport in Isolated Mouse Proximal Tubules Involves Complex Changes in Protein Trafficking and Substrate Affinity

2012 ◽  
Vol 30 (1) ◽  
pp. 269-281 ◽  
Author(s):  
Denise Guckel ◽  
Giuliano Ciarimboli ◽  
Hermann Pavenstädt ◽  
Eberhard Schlatter
1994 ◽  
Vol 266 (3) ◽  
pp. F450-F458 ◽  
Author(s):  
C. E. Groves ◽  
K. K. Evans ◽  
W. H. Dantzler ◽  
S. H. Wright

The physiological characteristics of peritubular organic cation transport were examined by measuring the transport of the organic cation tetraethylammonium (TEA) in rabbit renal proximal tubule suspensions and isolated nonperfused rabbit renal proximal tubules. Peritubular organic cation transport in both single S2 segments and suspensions of isolated renal proximal tubules was found to be a high-capacity, high-affinity, carrier-mediated process. For tubule suspensions, the maximal capacity of the carrier for TEA (Jmax) and the concentration of TEA at 1/2 Jmax (Kt) (1.49 +/- 0.21 nmol.min-1.mg dry wt-1 and 131 +/- 16 microM, respectively), did not differ significantly from those measured in single S2 segments (Jmax, 1.16 +/- 0.075 nmol.min-1.mg dry wt-1; Kt, 108 +/- 10 microM). In addition, the pattern of inhibition of peritubular TEA transport by long-chain n-tetraalkylammonium compounds (n = 1-5) was both qualitatively and quantitatively similar in single S2 segments and tubule suspensions, exhibiting an increase in inhibitory potency with increasing alkyl chain length. For example, in tubule suspensions, apparent Michaelis constants for inhibition of TEA uptake ranged from 1.3 mM for tetramethylammonium (TMA) to 0.8 microM for tetrapentylammonium (TPeA). To determine whether these compounds were substrates for the peritubular organic cation transporter, their effect on the efflux of [14C]TEA from tubule suspensions was examined. A concentration of 0.5 mM of the short-chain tetraalkyls TMA or TEA increased the efflux of [14C]TEA (i.e., trans-stimulated) from tubules in suspension. The longer-chain tetraalkyls tetrapropylammonium, tetrabutylammonium, and TPeA all decreased the efflux of [14C]TEA from tubules in suspension; TPeA completely blocked efflux.(ABSTRACT TRUNCATED AT 250 WORDS)


2005 ◽  
Vol 34 (3) ◽  
pp. 339-342 ◽  
Author(s):  
Frank Pietruck ◽  
Markus Horbelt ◽  
Thorsten Feldkamp ◽  
Katrin Engeln ◽  
Stefan Herget-Rosenthal ◽  
...  

2001 ◽  
Vol 276 (36) ◽  
pp. 33741-33746 ◽  
Author(s):  
Gesine Pietig ◽  
Thomas Mehrens ◽  
Jochen R. Hirsch ◽  
Ibrahim Çetinkaya ◽  
Hansjürgen Piechota ◽  
...  

1996 ◽  
Vol 270 (5) ◽  
pp. R1025-R1030
Author(s):  
Y. K. Kim ◽  
W. H. Dantzler

We examined the specificity of basolateral organic cation transport in isolated snake (Thamnophis spp.) renal proximal tubules by determining the inhibitory effect of a series of n-tetraalkylammonium (n-TAA) compounds (n = 1-5) on the basolateral uptake of [3H]tetraethylammonium (TEA). The inhibitory potency increased with increasing alkyl chain length, with the apparent Michaelis constants for inhibition of TEA uptake ranging from 3.3 mM for tetramethylammonium (TMA) to 1.0 microM for tetrapentylammonium (TPeA). Thus the apparent affinity of the carrier for n-TAA compounds increases with their increasing hydrophobicity. Because previous data suggested that TEA transport across the basolateral membrane may be asymmetrical and that the exit step may be regulated differently from the entry step, we examined the kinetics of [3H]TEA efflux across the basolateral membrane, Efflux, like entry, occurred by a saturable process that could be described adequately by Michaelis-Menten kinetics. However, the concentration of TEA at one-half Jmax (Kt) for efflux (approximately 110 microM) was about six times the Kt for uptake (approximately 18 muM), indicating that the affinity of the carrier for TEA is greater in the uptake direction than in the efflux direction or that there are separate carriers with different affinities for uptake and efflux. In either case, this difference would favor movement of TEA taken up at the basolateral side across the cells and into the lumen over movement back into the peritubular fluid.


2011 ◽  
Vol 462 (2) ◽  
pp. 359-369 ◽  
Author(s):  
Svenja K. Holle ◽  
Giuliano Ciarimboli ◽  
Bayram Edemir ◽  
Ute Neugebauer ◽  
Hermann Pavenstädt ◽  
...  

2002 ◽  
Vol 90 (4) ◽  
pp. 181-186 ◽  
Author(s):  
Brett Grover ◽  
Christopher Auberger ◽  
Rangaprasad Sarangarajan ◽  
William Cacini

2004 ◽  
Vol 449 (5) ◽  
pp. 423-441 ◽  
Author(s):  
Giuliano Ciarimboli ◽  
Eberhard Schlatter

1998 ◽  
Vol 37 (2) ◽  
pp. 131-136 ◽  
Author(s):  
F. MARTEL ◽  
M.J. MARTINS ◽  
C. CALHAU ◽  
C. HIPÓLITO-REIS ◽  
I. AZEVEDO

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