Sodium-gradient-driven, high-affinity, uphill transport of succinate in human placental brush-border membrane vesicles
- PMID: 3342005
- PMCID: PMC1148682
- DOI: 10.1042/bj2490179
Sodium-gradient-driven, high-affinity, uphill transport of succinate in human placental brush-border membrane vesicles
Abstract
Brush-border membrane vesicles isolated from normal human term placentas were shown to accumulate succinate transiently against a concentration gradient, when an inward-directed Na+ gradient was imposed across the membrane. This uptake was almost totally due to transport into intravesicular space, non-specific binding to the membranes being negligible. The dependence of the initial uptake rate of succinate on Na+ concentration exhibited sigmoidal kinetics, indicating interaction of more than one Na+ ion with the carrier system. The Hill coefficient for this ion was calculated to be 2.7. The Na+-dependent uptake of succinate was electrogenic, resulting in the transfer of positive charge across the membrane. Kinetic analysis showed that succinate uptake in these vesicles occurred via a single transport system, with an apparent affinity constant of 4.8 +/- 0.2 microM and a maximal velocity of 274 +/- 4 pmol/20 s per mg of protein. Uptake of succinate was strongly inhibited by various C4 or C5 dicarboxylic acids, whereas monocarboxylic acids, amino acids and glucose showed little or no effect. Li+ and K+ could not substitute for Na+ in the uptake process. Instead, Li+ was found to have a significant inhibitory effect on the Na+-dependent uptake of succinate.
Similar articles
-
Dicarboxylate transport in renal basolateral and brush-border membrane vesicles.Can J Physiol Pharmacol. 1992 Jan;70(1):106-12. doi: 10.1139/y92-015. Can J Physiol Pharmacol. 1992. PMID: 1581843
-
A proton gradient is the driving force for uphill transport of lactate in human placental brush-border membrane vesicles.J Biol Chem. 1988 Sep 25;263(27):13823-30. J Biol Chem. 1988. PMID: 2843538
-
Dicarboxylate transport in human placental brush-border membrane vesicles.Biochim Biophys Acta. 1989 Apr 14;980(2):248-54. doi: 10.1016/0005-2736(89)90406-9. Biochim Biophys Acta. 1989. PMID: 2930791
-
Na+ + Cl- -gradient-driven, high-affinity, uphill transport of taurine in human placental brush-border membrane vesicles.FEBS Lett. 1988 Apr 11;231(1):263-7. doi: 10.1016/0014-5793(88)80744-0. FEBS Lett. 1988. PMID: 3360130
-
Succinate and citrate transport in renal basolateral and brush-border membranes.Am J Physiol. 1987 Sep;253(3 Pt 2):F432-9. doi: 10.1152/ajprenal.1987.253.3.F432. Am J Physiol. 1987. PMID: 3631279
Cited by
-
Drug transfer and metabolism by the human placenta.Clin Pharmacokinet. 2004;43(8):487-514. doi: 10.2165/00003088-200443080-00001. Clin Pharmacokinet. 2004. PMID: 15170365 Review.
-
Cryo-EM structures reveal the H+/citrate symport mechanism of Drosophila INDY.Life Sci Alliance. 2025 Jan 30;8(4):e202402992. doi: 10.26508/lsa.202402992. Print 2025 Apr. Life Sci Alliance. 2025. PMID: 39884835 Free PMC article.
-
Complex, coordinated and highly regulated changes in placental signaling and nutrient transport capacity in IUGR.Biochim Biophys Acta Mol Basis Dis. 2020 Feb 1;1866(2):165373. doi: 10.1016/j.bbadis.2018.12.024. Epub 2019 Jan 23. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 30684642 Free PMC article. Review.
-
Sodium-coupled dicarboxylate and citrate transporters from the SLC13 family.Pflugers Arch. 2014 Jan;466(1):119-30. doi: 10.1007/s00424-013-1369-y. Epub 2013 Oct 10. Pflugers Arch. 2014. PMID: 24114175 Review.
-
Computational modelling of amino acid exchange and facilitated transport in placental membrane vesicles.J Theor Biol. 2015 Jan 21;365:352-64. doi: 10.1016/j.jtbi.2014.10.042. Epub 2014 Nov 11. J Theor Biol. 2015. PMID: 25451528 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous