4.7 Article

GABA reverse transport by the neuronal cotransporter GAT1: influence of internal chloride depletion

Journal

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 301, Issue 5, Pages C1064-C1073

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00120.2011

Keywords

gamma-aminobutyric acid; KCC2; Xenopus oocytes

Funding

  1. Compagnia di San Paolo, Torino, Programma Neuroscienze

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Bertram S, Cherubino F, Bossi E, Castagna M, Peres A. GABA reverse transport by the neuronal cotransporter GAT1: influence of internal chloride depletion. Am J Physiol Cell Physiol 301: C1064-C1073, 2011. First published July 20, 2011; doi:10.1152/ajpcell.00120.2011.-The role of intracellular ions on the reverse GABA transport by the neuronal transporter GAT1 was studied using voltage-clamp and [H-3]GABA efflux determinations in Xenopus oocytes transfected with heterologous mRNA. Reverse transport was induced by intracellular GABA injections and measured in terms of the net outward current generated by the transporter. Changes in various intracellular ionic conditions affected the reverse current: higher concentrations of Na+ enhanced the ratio of outward over inward transport current, while a considerable decrease of the outward current and a parallel reduction of the transporter-mediated GABA efflux were observed after treatments causing a diminution of the intracellular Cl- concentration. Particularly interesting was the impairment of the reverse transport observed after depletion of internal Cl- generated by the activity of a coexpressed K+-Cl- exporter KCC2. This finding suggests that reverse GABA transport may be physiologically regulated during early neuronal development, similarly to the functional alterations seen in GABA receptors caused by KCC2 activity.

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