Nephron

Physiology: Original Paper

SPAK and OSR1 Sensitivity of Excitatory Amino Acid Transporter EAAT3

Borrás J. · Salker M.S. · Elvira B. · Warsi J. · Fezai M. · Hoseinzadeh Z. · Lang F.

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Department of Physiology I, University of Tübingen, Tubingen, Germany

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Nephron 2015;130:221-228

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Article / Publication Details

First-Page Preview
Abstract of Physiology: Original Paper

Received: March 26, 2015
Accepted: May 20, 2015
Published online: June 25, 2015
Issue release date: July 2015

Number of Print Pages: 8
Number of Figures: 7
Number of Tables: 0

ISSN: 1660-8151 (Print)
eISSN: 2235-3186 (Online)

For additional information: https://www.karger.com/NEF

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 (spaktg/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 spaktg/tg mice. Conclusion: Both, SPAK and OSR1 are negative regulators of EAAT3 activity.

© 2015 S. Karger AG, Basel




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References

  1. Rafiqi FH, Zuber AM, Glover M, Richardson C, Fleming S, Jovanović S, Jovanović A, O'Shaughnessy KM, Alessi DR: Role of the WNK-activated SPAK kinase in regulating blood pressure. EMBO Mol Med 2010;2:63-75.
  2. Castañeda-Bueno M, Gamba G: SPAKling insight into blood pressure regulation. EMBO Mol Med 2010;2:39-41.
  3. Yang SS, Lo YF, Wu CC, Lin SW, Yeh CJ, Chu P, Sytwu HK, Uchida S, Sasaki S, Lin SH: SPAK-knockout mice manifest Gitelman syndrome and impaired vasoconstriction. J Am Soc Nephrol 2010;21:1868-1877.
  4. Lin SH, Yu IS, Jiang ST, Lin SW, Chu P, Chen A, Sytwu HK, Sohara E, Uchida S, Sasaki S, Yang SS: Impaired phosphorylation of Na(+)-K(+)-2Cl() cotransporter by oxidative stress-responsive kinase-1 deficiency manifests hypotension and Bartter-like syndrome. Proc Natl Acad Sci U S A 2011;108:17538-17543.
  5. Villa F, Deak M, Alessi DR, van Aalten DM: Structure of the OSR1 kinase, a hypertension drug target. Proteins 2008;73:1082-1087.
  6. Vitari AC, Deak M, Morrice NA, Alessi DR: The WNK1 and WNK4 protein kinases that are mutated in Gordon's hypertension syndrome phosphorylate and activate SPAK and OSR1 protein kinases. Biochem J 2005;391:17-24.
  7. Vitari AC, Thastrup J, Rafiqi FH, Deak M, Morrice NA, Karlsson HK, Alessi DR: Functional interactions of the SPAK/OSR1 kinases with their upstream activator WNK1 and downstream substrate NKCC1. Biochem J 2006;397:223-231.
  8. Glover M, Zuber AM, O'Shaughnessy KM: Hypertension, dietary salt intake, and the role of the thiazide-sensitive sodium chloride transporter NCCT. Cardiovasc Ther 2011;29:68-76.
  9. O'Reilly M, Marshall E, Speirs HJ, Brown RW: WNK1, a gene within a novel blood pressure control pathway, tissue-specifically generates radically different isoforms with and without a kinase domain. J Am Soc Nephrol 2003;14:2447-2456.
  10. Kahle KT, Rinehart J, Lifton RP: Phosphoregulation of the Na-K-2Cl and K-Cl cotransporters by the WNK kinases. Biochim Biophys Acta 2010;1802:1150-1158.
  11. Flatman PW: Cotransporters, WNKs and hypertension: an update. Curr Opin Nephrol Hypertens 2008;17:186-192.
  12. Furgeson SB, Linas S: Mechanisms of type I and type II pseudohypoaldosteronism. J Am Soc Nephrol 2010;21:1842-1845.
  13. Uchida S: Pathophysiological roles of WNK kinases in the kidney. Pflugers Arch 2010;460:695-702.
  14. Wilson FH, Disse-Nicodème S, Choate KA, Ishikawa K, Nelson-Williams C, Desitter I, Gunel M, Milford DV, Lipkin GW, Achard JM, Feely MP, Dussol B, Berland Y, Unwin RJ, Mayan H, Simon DB, Farfel Z, Jeunemaitre X, Lifton RP: Human hypertension caused by mutations in WNK kinases. Science 2001;293:1107-1112.
  15. Delpire E, Gagnon KB: SPAK and OSR1, key kinases involved in the regulation of chloride transport. Acta Physiol (Oxf) 2006;187:103-113.
  16. Delpire E, Gagnon KB: SPAK and OSR1: STE20 kinases involved in the regulation of ion homoeostasis and volume control in mammalian cells. Biochem J 2008;409:321-331.
  17. Giménez I: Molecular mechanisms and regulation of furosemide-sensitive Na-K-Cl cotransporters. Curr Opin Nephrol Hypertens 2006;15:517-523.
  18. Richardson C, Sakamoto K, de los Heros P, Deak M, Campbell DG, Prescott AR, Alessi DR: Regulation of the NKCC2 ion cotransporter by SPAK-OSR1-dependent and -independent pathways. J Cell Sci 2011;124:789-800.
  19. Gagnon KB, Delpire E: On the substrate recognition and negative regulation of SPAK, a kinase modulating Na+-K+-2Cl- cotransport activity. Am J Physiol Cell Physiol 2010;299:C614-C620.
  20. Glover M, O'Shaughnessy KM: SPAK and WNK kinases: a new target for blood pressure treatment? Curr Opin Nephrol Hypertens 2011;20:16-22.
  21. Huang CL, Yang SS, Lin SH: Mechanism of regulation of renal ion transport by WNK kinases. Curr Opin Nephrol Hypertens 2008;17:519-525.
  22. Mercier-Zuber A, O'Shaughnessy KM: Role of SPAK and OSR1 signalling in the regulation of NaCl cotransporters. Curr Opin Nephrol Hypertens 2011;20:534-540.
  23. Richardson C, Alessi DR: The regulation of salt transport and blood pressure by the WNK-SPAK/OSR1 signalling pathway. J Cell Sci 2008;121:3293-3304.
  24. Achard JM, Disse-Nicodeme S, Fiquet-Kempf B, Jeunemaitre X: Phenotypic and genetic heterogeneity of familial hyperkalaemic hypertension (Gordon syndrome). Clin Exp Pharmacol Physiol 2001;28:1048-1052.
  25. Capasso G, Cantone A, Evangelista C, Zacchia M, Trepiccione F, Acone D, Rizzo M: Channels, carriers, and pumps in the pathogenesis of sodium-sensitive hypertension. Semin Nephrol 2005;25:419-424.
  26. Alessi DR, Zhang J, Khanna A, Hochdörfer T, Shang Y, Kahle KT: The WNK-SPAK/OSR1 pathway: master regulator of cation-chloride cotransporters. Sci Signal 2014;7:re3.
  27. Pathare G, Föller M, Michael D, Walker B, Hierlmeier M, Mannheim JG, Pichler BJ, Lang F: Enhanced FGF23 serum concentrations and phosphaturia in gene targeted mice expressing WNK-resistant SPAK. Kidney Blood Press Res 2012;36:355-364.
  28. Bailey CG, Ryan RM, Thoeng AD, Ng C, King K, Vanslambrouck JM, Auray-Blais C, Vandenberg RJ, Bröer S, Rasko JE: Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria. J Clin Invest 2011;121:446-453.
  29. Peghini P, Janzen J, Stoffel W: Glutamate transporter EAAC-1-deficient mice develop dicarboxylic aminoaciduria and behavioral abnormalities but no neurodegeneration. EMBO J 1997;16:3822-3832.
  30. O'Kane RL, Martínez-López I, DeJoseph MR, Viña JR, Hawkins RA: Na(+)-dependent glutamate transporters (EAAT1, EAAT2, and EAAT3) of the blood-brain barrier. A mechanism for glutamate removal. J Biol Chem 1999;274:31891-31895.
  31. Amara SG, Fontana AC: Excitatory amino acid transporters: keeping up with glutamate. Neurochem Int 2002;41:313-318.
  32. Schniepp R, Kohler K, Ladewig T, Guenther E, Henke G, Palmada M, Boehmer C, Rothstein JD, Bröer S, Lang F: Retinal colocalization and in vitro interaction of the glutamate transporter EAAT3 and the serum- and glucocorticoid-inducible kinase SGK1 [correction]. Invest Ophthalmol Vis Sci 2004;45:1442-1449.
  33. Maragakis NJ, Dietrich J, Wong V, Xue H, Mayer-Proschel M, Rao MS, Rothstein JD: Glutamate transporter expression and function in human glial progenitors. Glia 2004;45:133-143.
  34. Miralles VJ, Martínez-López I, Zaragozá R, Borrás E, García C, Pallardó FV, Viña JR: Na+ dependent glutamate transporters (EAAT1, EAAT2, and EAAT3) in primary astrocyte cultures: effect of oxidative stress. Brain Res 2001;922:21-29.
  35. Schmitt A, Zink M, Petroianu G, May B, Braus DF, Henn FA: Decreased gene expression of glial and neuronal glutamate transporters after chronic antipsychotic treatment in rat brain. Neurosci Lett 2003;347:81-84.
  36. van Landeghem FK, Weiss T, von Deimling A: Expression of PACAP and glutamate transporter proteins in satellite oligodendrocytes of the human CNS. Regul Pept 2007;142:52-59.
  37. Grewer C, Gameiro A, Zhang Z, Tao Z, Braams S, Rauen T: Glutamate forward and reverse transport: from molecular mechanism to transporter-mediated release after ischemia. IUBMB Life 2008;60:609-619.
  38. Dowd LA, Coyle AJ, Rothstein JD, Pritchett DB, Robinson MB: Comparison of Na+-dependent glutamate transport activity in synaptosomes, C6 glioma, and Xenopus oocytes expressing excitatory amino acid carrier 1 (EAAC1). Mol Pharmacol 1996;49:465-473.
    External Resources
  39. Dowd LA, Robinson MB: Rapid stimulation of EAAC1-mediated Na+-dependent L-glutamate transport activity in C6 glioma cells by phorbol ester. J Neurochem 1996;67:508-516.
  40. Fezai M, Elvira B, Borras J, Ben-Attia M, Hoseinzadeh Z, Lang F: Negative regulation of the creatine transporter SLC6A8 by SPAK and OSR1. Kidney Blood Press Res 2014;39:546-554.
  41. Almilaji A, Munoz C, Hosseinzadeh Z, Lang F: Upregulation of Na+,Cl(-)-coupled betaine/γ-amino-butyric acid transporter BGT1 by Tau tubulin kinase 2. Cell Physiol Biochem 2013;32:334-343.
  42. Munoz C, Pakladok T, Almilaji A, Elvira B, Decher N, Shumilina E, Lang F: Up-regulation of Kir2.1 (KCNJ2) by the serum & glucocorticoid inducible SGK3. Cell Physiol Biochem 2014;33:491-500.
  43. Pakladok T, Almilaji A, Munoz C, Alesutan I, Lang F: PIKfyve sensitivity of hERG channels. Cell Physiol Biochem 2013;31:785-794.
  44. Strutz-Seebohm N, Henrion U, Schmitt N, Schulze-Bahr E, Seebohm G: A common structural component for β-subunit mediated modulation of slow inactivation in different KV channels. Cell Physiol Biochem 2013;31:968-980.
  45. Almilaji A, Honisch S, Liu G, Elvira B, Ajay SS, Hosseinzadeh Z, Ahmed M, Munoz C, Sopjani M, Lang F: Regulation of the voltage gated K channel Kv1.3 by recombinant human klotho protein. Kidney Blood Press Res 2014;39:609-622.
  46. Hosseinzadeh Z, Dong L, Bhavsar SK, Warsi J, Almilaji A, Lang F: Upregulation of peptide transporters PEPT1 and PEPT2 by Janus kinase JAK2. Cell Physiol Biochem 2013;31:673-682.
  47. Almilaji A, Sopjani M, Elvira B, Borras J, Dërmaku-Sopjani M, Munoz C, Warsi J, Lang UE, Lang F: Upregulation of the creatine transporter Slc6A8 by Klotho. Kidney Blood Press Res 2014;39:516-525.
  48. Almilaji A, Szteyn K, Fein E, Pakladok T, Munoz C, Elvira B, Towhid ST, Alesutan I, Shumilina E, Bock CT, Kandolf R, Lang F: Down-regulation of Na/K+ atpase activity by human parvovirus B19 capsid protein VP1. Cell Physiol Biochem 2013;31:638-648.
  49. Warsi J, Elvira B, Bissinger R, Shumilina E, Hosseinzadeh Z, Lang F: Downregulation of peptide transporters PEPT1 and PEPT2 by oxidative stress responsive kinase OSR1. Kidney Blood Press Res 2014;39:591-599.
  50. Elvira B, Munoz C, Borras J, Chen H, Warsi J, Ajay SS, Shumilina E, Lang F: SPAK and OSR1 dependent down-regulation of murine renal outer medullary K channel ROMK1. Kidney Blood Press Res 2014;39:353-360.
  51. Warsi J, Dong L, Elvira B, Salker MS, Shumilina E, Hosseinzadeh Z, Lang F: SPAK dependent regulation of peptide transporters PEPT1 and PEPT2. Kidney Blood Press Res 2014;39:388-398.
  52. Warsi J, Hosseinzadeh Z, Elvira B, Bissinger R, Shumilina E, Lang F: Regulation of ClC-2 activity by SPAK and OSR1. Kidney Blood Press Res 2014;39:378-387.
  53. Dërmaku-Sopjani M, Almilaji A, Pakladok T, Munoz C, Hosseinzadeh Z, Blecua M, Sopjani M, Lang F: Down-regulation of the Na+-coupled phosphate transporter NaPi-IIa by AMP-activated protein kinase. Kidney Blood Press Res 2013;37:547-556.
  54. Elvira B, Blecua M, Luo D, Yang W, Shumilina E, Munoz C, Lang F: SPAK-sensitive regulation of glucose transporter SGLT1. J Membr Biol 2014;247:1191-1197.
  55. Yang L, Cai X, Zhou J, Chen S, Chen Y, Chen Z, Wang Q, Fang Z, Zhou L: STE20/SPS1-related proline/alanine-rich kinase is involved in plasticity of GABA signaling function in a mouse model of acquired epilepsy. PLoS One 2013;8:e74614.
  56. Crino PB, Jin H, Shumate MD, Robinson MB, Coulter DA, Brooks-Kayal AR: Increased expression of the neuronal glutamate transporter (EAAT3/EAAC1) in hippocampal and neocortical epilepsy. Epilepsia 2002;43:211-218.
  57. Mathern GW, Mendoza D, Lozada A, Pretorius JK, Dehnes Y, Danbolt NC, Nelson N, Leite JP, Chimelli L, Born DE, Sakamoto AC, Assirati JA, Fried I, Peacock WJ, Ojemann GA, Adelson PD: Hippocampal GABA and glutamate transporter immunoreactivity in patients with temporal lobe epilepsy. Neurology 1999;52:453-472.
  58. Proper EA, Hoogland G, Kappen SM, Jansen GH, Rensen MG, Schrama LH, van Veelen CW, van Rijen PC, van Nieuwenhuizen O, Gispen WH, de Graan PN: Distribution of glutamate transporters in the hippocampus of patients with pharmaco-resistant temporal lobe epilepsy. Brain 2002;125:32-43.
  59. Rakhade SN, Loeb JA: Focal reduction of neuronal glutamate transporters in human neocortical epilepsy. Epilepsia 2008;49:226-236.
  60. Simantov R, Crispino M, Hoe W, Broutman G, Tocco G, Rothstein JD, Baudry M: Changes in expression of neuronal and glial glutamate transporters in rat hippocampus following kainate-induced seizure activity. Brain Res Mol Brain Res 1999;65:112-123.
  61. Deng X, Shibata H, Takeuchi N, Rachi S, Sakai M, Ninomiya H, Iwata N, Ozaki N, Fukumaki Y: Association study of polymorphisms in the glutamate transporter genes SLC1A1, SLC1A3, and SLC1A6 with schizophrenia. Am J Med Genet B Neuropsychiatr Genet 2007;144B:271-278.
  62. Huerta I, McCullumsmith RE, Haroutunian V, Giménez-Amaya JM, Meador-Woodruff JH: Expression of excitatory amino acid transporter interacting protein transcripts in the thalamus in schizophrenia. Synapse 2006;59:394-402.
  63. Kim JH, Do SH, Kim YL, Zuo Z: Effects of chronic exposure to ethanol on glutamate transporter EAAT3 expressed in Xenopus oocytes: evidence for protein kinase C involvement. Alcohol Clin Exp Res 2005;29:2046-2052.
  64. Lang UE, Puls I, Muller DJ, Strutz-Seebohm N, Gallinat J: Molecular mechanisms of schizophrenia. Cell Physiol Biochem 2007;20:687-702.
  65. McCullumsmith RE, Meador-Woodruff JH: Striatal excitatory amino acid transporter transcript expression in schizophrenia, bipolar disorder, and major depressive disorder. Neuropsychopharmacology 2002;26:368-375.
  66. Nudmamud-Thanoi S, Piyabhan P, Harte MK, Cahir M, Reynolds GP: Deficits of neuronal glutamatergic markers in the caudate nucleus in schizophrenia. J Neural Transm Suppl 2007;72:281-285.
  67. Smith RE, Haroutunian V, Davis KL, Meador-Woodruff JH: Expression of excitatory amino acid transporter transcripts in the thalamus of subjects with schizophrenia. Am J Psychiatry 2001;158:1393-1399.
  68. Chan H, Zwingmann C, Pannunzio M, Butterworth RF: Effects of ammonia on high affinity glutamate uptake and glutamate transporter EAAT3 expression in cultured rat cerebellar granule cells. Neurochem Int 2003;43:137-146.
  69. Hoffmann EK: Ion channels involved in cell volume regulation: effects on migration, proliferation, and programmed cell death in non adherent EAT cells and adherent ELA cells. Cell Physiol Biochem 2011;28:1061-1078.
  70. Hoffmann EK, Lambert IH, Pedersen SF: Physiology of cell volume regulation in vertebrates. Physiol Rev 2009;89:193-277.
  71. Lang F: Mechanisms and significance of cell volume regulation. J Am Coll Nutr 2007;26​(5 suppl):613S-623S.

Article / Publication Details

First-Page Preview
Abstract of Physiology: Original Paper

Received: March 26, 2015
Accepted: May 20, 2015
Published online: June 25, 2015
Issue release date: July 2015

Number of Print Pages: 8
Number of Figures: 7
Number of Tables: 0

ISSN: 1660-8151 (Print)
eISSN: 2235-3186 (Online)

For additional information: https://www.karger.com/NEF


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