SPAK and OSR1 Sensitivity of Excitatory Amino Acid Transporter EAAT3

Abstract

Background/Aims: Kinases involved in the regulation of epithelial transport include SPAK (SPS1-related proline/alanine-rich kinase) and OSR1 (oxidative stress-responsive kinase 1). SPAK and OSR1 are both regulated by WNK (with-no-K(Lys)) kinases. The present study explored whether SPAK and/or OSR1 influence the excitatory amino acid transporter EAAT3, which accomplishes glutamate and aspartate transport in kidney, intestine and brain. Methods: cRNA encoding EAAT3 was injected into Xenopus laevis oocytes with or without additional injection of cRNA encoding wild-type SPAK, constitutively active ^T233ESPAK, WNK insensitive ^T233ASPAK, catalytically inactive ^D212ASPAK, wild-type OSR1, constitutively active ^T185EOSR1, WNK insensitive ^T185AOSR1 and catalytically inactive ^D164AOSR1. Glutamate-induced current was taken as measure of electrogenic glutamate transport and was quantified utilizing dual electrode voltage clamp. Furthermore, Ussing chamber was employed to determine glutamate transport in the intestine from gene-targeted mice carrying WNK insensitive SPAK (spak^tg/tg) and from corresponding wild-type mice (spak^+/+). Results: EAAT3 activity was significantly decreased by wild-type SPAK and ^T233ESPAK, but not by ^T233ASPAK and ^D212ASPAK. SPAK decreased maximal transport rate without affecting significantly affinity of the carrier. Similarly, EAAT3 activity was significantly downregulated by wild-type OSR1 and ^T185EOSR1, but not by ^T185AOSR1 and ^D164AOSR1. Again OSR1 decreased maximal transport rate without affecting significantly affinity of the carrier. Intestinal electrogenic glutamate transport was significantly lower in spak^+/+ than in spak^tg/tg mice. Conclusion: Both, SPAK and OSR1 are negative regulators of EAAT3 activity.

Down-Regulation of the Na+,Cl- Coupled Creatine Transporter CreaT (SLC6A8) by Glycogen Synthase Kinase GSK3ß

“…Observations made utilizing this experimental approach have frequently been confirmed by analysing gene targeted mice lacking or overexpressing the respective kinase or mutants [35,41,42,[54][55][56][57][58][59]. Nevertheless, the present study does not allow safe predictions as to the functional significance of GSK3ß-sensitive CreaT activity.…”