Skip to main content
Log in

GlyT1 and GlyT2 in brain astrocytes: expression, distribution and function

  • Original Article
  • Published:
Brain Structure and Function Aims and scope Submit manuscript

Abstract

GlyT1 and GlyT2 are the transporters responsible for glycine uptake from the synaptic cleft. The expression and function of these two glycine transporters in rat cortical cultured astrocytes over several maturation stages (10, 18 and 24 days in vitro) were herein investigated. Quantitative PCR and western blot showed that both GlyT1 and GlyT2 transcripts and protein were expressed in astrocytes in the examined maturation stages. Double detection of Glial fibrillary acidic protein (GFAP) and GlyT1/GlyT2 revealed that both transporters were detected in the cell body and in the processes of astrocytes. Furthermore, the double immunofluorescence analysis carried out in P21 rat brain slices corroborated the presence of both transporters in cortical and hippocampal astrocytes. The functional characterization of GlyT1 and GlyT2 in cultured astrocytes performed by [3H]glycine uptake experiments revealed that both transporters take up glycine in a concentration-dependent way, but with a very distinct affinity. Kinetic analysis revealed a K m of 51.15 ± 4.96 μM and a V max of 379.30 ± 10.31 pmol/min/mg for GlyT1 and a K m of 1,801 ± 148.9 μM and a V max of 5,730 ± 200.2 pmol/min/mg for GlyT2. It is concluded that astrocytes express functional GlyT2, which challenge previous findings that those cells would express only GlyT1, whereas GlyT2 was supposed to be restricted to the glycinergic nerve terminals. Therefore, the work herein reported provides new insights about glycinergic neurotransmission in the brain.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

References

  • Adams RH, Sato K, Shimada S, Tohyama M, Pϋschel AW, Betz H (1995) Gene structure and glial expression of the glycine transporter GLYT1 in embryonic and adult rodents. J Neurosci 15:2524–2532

    CAS  PubMed  Google Scholar 

  • Allaman I, Bélanger M, Magistretti PJ (2011) Astrocyte–neuron metabolic relationships: for better and for worse. Trends Neurosci 34:76–87

    Article  CAS  PubMed  Google Scholar 

  • Andersen P, Morris R, Amaral D, Bliss T, O’Keefe J (eds) (2007) The hippocampus book. Oxford University Press, USA

    Google Scholar 

  • Araque A, Parpura V, Sanzgiri RP, Haydon PG (1999) Tripartite synapses: glia, the unacknowledged partner. Trends Neurosci 22:208–215

    Article  CAS  PubMed  Google Scholar 

  • Aroeira RI, Ribeiro JA, Sebastião AM, Valente CA (2011) Age-related changes of glycine receptor at the rat hippocampus: from the embryo to the adult. J Neurochem 118:339–353

    Article  CAS  PubMed  Google Scholar 

  • Atkinson BN, Bell SC, De Vivo M, Kowalski LR, Lechner SM, Ognyanov VI, Tham CS, Tsai C, Jia J, Ashton D, Klitenick MA (2001) ALX 5407: a potent, selective inhibitor of the hGlyT1 glycine transporter. Mol Pharmacol 60:1414–1420

    CAS  PubMed  Google Scholar 

  • Barker GA, Wilkins RJ, Golding S, Ellory JC (1999) Neutral amino acid transport in bovine articular chondrocytes. J Physiol 514(3):795–808

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Belachew S, Malgrange B, Rigo JM, Rogister B, Leprince P, Hans G, Nguyen L, Moonen G (2000) Glycine triggers an intracellular calcium influx in oligodendrocyte progenitor cells which is mediated by the activation of both the ionotropic glycine receptor and Na+-dependent transporters. Eur J Neurosci 12:1924–1930

    Article  CAS  PubMed  Google Scholar 

  • Betz H, Gomeza J, Armsen W, Scholze P, Eulenburg V (2006) Glycine transporters: essential regulators of synaptic transmission. Biochem Soc Trans 34:55–58

    Article  CAS  PubMed  Google Scholar 

  • Biber K, Klotz KN, Berger M, Gebicke-Härter PJ, van Calker D (1997) Adenosine A1 receptor-mediated activation of phospholipase C in cultured astrocytes depends on the level of receptor expression. J Neurosci 17:4956–4964

    CAS  PubMed  Google Scholar 

  • Borowsky B, Mezey E, Hoffman BJ (1993) Two glycine transporter variants with distinct localization in the CNS and peripheral tissues are encoded by a common gene. Neuron 10:851–863

    Article  CAS  PubMed  Google Scholar 

  • Bowery NG, Smart TG (2006) GABA and glycine as neurotransmitters: a brief history. Br J Pharmacol 147:S109–S119

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Brown A, Carlyle I, Clark J, Hamilton W, Gibson S, McGarry G, McEachen S, Rae D, Thorn S, Walker G (2001) Discovery and SAR of Org 24598-A selective glycine uptake inhibitor. Bioorg Med Chem Lett 11:2007–2009

    Article  CAS  PubMed  Google Scholar 

  • Castagna M, Shayakul C, Trotti D, Sacchi VF, Harvey WR, Hediger MA (1997) Molecular Characteristics of mammalian and insect amino acid transporters: implications for amino acid homeostasis. J Exp Biol 200:269–286

    CAS  PubMed  Google Scholar 

  • Cubelos B, Gimenez C, Zafra F (2005) Localization of the GlyT1 glycine transporter at glutamatergic synapses in the rat brain. Cereb Cortex 15:448–459

    Article  PubMed  Google Scholar 

  • Dohi T, Morita K, Kitayama T, Motoyama N, Morioka N (2009) Glycine transporter inhibitors as a novel drug discovery strategy for neuropathic pain. Pharmacol Therap 123:54–79

    Article  CAS  Google Scholar 

  • Du F, Qian ZM, Zhu L, Wu XM, Qian C, Chan R, Ke Y (2010) Purity, cell viability, expression of GFAP and bystin in astrocytes cultured by different procedures. J Cell Biochem 109:30–37

    CAS  PubMed  Google Scholar 

  • Ebihara S, Yamamoto T, Obata K, Yanagawa Y (2004) Gene structure and alternative splicing of the mouse glycine transporter type-2. Biochem Biophys Res Commun 317:857–864

    Article  CAS  PubMed  Google Scholar 

  • Eichler SA, Kirischuk S, Jϋttner R, Schaäfermeier PK, Legendre P, Lehmann TN, Gloveli T, Grantyn R, Meier JC (2008) Glycinergic tonic inhibition of hippocampal neurons with depolarising GABAergic transmission elicits histopathological signs of temporal lobe epilepsy. J Cell Mol Med 12:2848–2866

    Article  CAS  PubMed  Google Scholar 

  • Eulenburg V, Armsen W, Betz H, Gomeza J (2005) Glycine transporters: essential regulators of neurotransmission. Trends Biochem Sci 30(6):325–333

    Article  CAS  PubMed  Google Scholar 

  • Eulenburg V, Retiounskaia M, Papadopoulos T, Gomeza J, Betz H (2010) Glial glycine transporter 1 function is essential for early postnatal survival but dispensable in adult mice. Glia 58:1066–1073

    Article  PubMed  Google Scholar 

  • Fornés A, Núñez E, Alonso-Torres P, Aragón C, López-Corcuera B (2008) Trafficking properties and activity regulation of the neuronal glycine transporter GLYT2 by protein kinase C. Biochem J 412:495–506

    Article  PubMed  Google Scholar 

  • Gabryel B, Adamczyk J, Huzarska M, Pudełko A, Trzeciak HI (2002) Aniracetam attenuates apoptosis of astrocytes aubjected to simulated ischemia in vitro. Neurotoxic 23:385–395

    Article  CAS  Google Scholar 

  • Geerlings A, Núñez E, López-Corcuera B, Aragón C (2001) Calcium- and syntaxin 1-mediated trafficking of the neuronal glycine transporter GLYT2. J Biol Chem 276:17584–17590

    Article  CAS  PubMed  Google Scholar 

  • Gingras M, Gagnon V, Minotti S, Durham HD, Berthod F (2007) Optimized protocols for isolation of primary motor neurons, astrocytes and microglia from embryonic mouse spinal cord. J Neurosci Method 163:111–118

    Article  CAS  Google Scholar 

  • Gomeza J, Hulsmann S, Ohno K, Eulenburg V, Szoke K, Richter D, Betz H (2003a) Inactivation of the glycine transporter 1 gene discloses vital role of glial glycine uptake in glycinergic inhibition. Neuron 40:785–796

    Article  CAS  PubMed  Google Scholar 

  • Gomeza J, Ohno K, Hulsmann S, Armsen W, Eulenburg V, Richter DW, Laube B, Betz H (2003b) Deletion of the mouse glycine transporter 2 results in a hyperekplexia phenotype and postnatal lethality. Neuron 40:797–806

    Article  CAS  PubMed  Google Scholar 

  • Guastella J, Brecha N, Weigmann C, Lester A, Davidson N (1992) Cloning, expression and localization of a rat brain high-affinity glycine transporter. Proc Natl Acad Sci USA 89:7189–7193

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Hamilton NB, Attwell D (2010) Do astrocytes really exocytose neurotransmitters? Nat Rev Neurosci 11(4):227–238

    Article  CAS  PubMed  Google Scholar 

  • Harvey RJ, Carta E, Pearce BR, Chung SK, Supplisson S, Rees MI, Harvey K (2008) A critical role for glycine transporters in hyperexcitability disorders. Front Mol Neurosci 1:1–6

    Article  PubMed Central  PubMed  Google Scholar 

  • Jursky F, Nelson N (1995) Localization of glycine neurotransmitter transporter (GLYT2) reveals correlation with the distribution of glycine receptor. J Neurochem 64:1026–1033

    Article  CAS  PubMed  Google Scholar 

  • Jursky F, Nelson N (1996) Developmental expression of the glycine transporters GLYT1 and GLYT2 in mouse brain. J Neurochem 67(1):336–344

    CAS  PubMed  Google Scholar 

  • Jursky F, Tamura S, Tamura A, Mandiyan S, Nelson H, Nelson N (1994) Structure, function and brain localization of neurotransmitter transporters. J Exp Biol 196:283–295

    CAS  PubMed  Google Scholar 

  • Liu QR, Nelson H, Mandiyan S, López-Corcuera B, Nelson N (1992) Cloning and expression of a glycine transporter from mouse brain. FEBS Lett 305:110–114

    Article  CAS  PubMed  Google Scholar 

  • Luccini E, Raiteri L (2007) Mechanisms of [3H]glycine release from mouse spinal cord synaptosomes selectively labeled through GLYT2 transporters. J Neurochem 103:2439–2448

    Article  CAS  PubMed  Google Scholar 

  • Martinez-Maza R, Poyatos I, López-Corcuera B, Núñez E, Giménez C, Zafra F, Aragón C (2001) The role of N-glycosylation in transport to the plasma membrane and sorting of the neuronal glycine transporter GLYT2. J Biol Chem 276:2168–2173

    Article  CAS  PubMed  Google Scholar 

  • McCarthy KD, de Vellis J (1980) Preparation of separate astroglial and ligodendroglial cell cultures from rat cerebral tissue. J Cell Biol 85(3):890–902

    Article  CAS  PubMed  Google Scholar 

  • Nagaraja TN, Brookes N (1996) Glutamine transport in mouse cerebral astrocytes. J Neurochem 66:1665–1674

    Article  CAS  PubMed  Google Scholar 

  • Núñez E, López-Corcuera B, Vázquez J, Giménez C, Aragón C (2000) Differential effects of the tricyclic antidepressant amoxapine on glycine uptake mediated by the recombinant GLYT1 and GLYT2 glycine transporters. Br J Pharmacol 129(1):200–206

    Article  PubMed Central  PubMed  Google Scholar 

  • Olivares L, Aragón C, Giménez C, Zafra F (1995) The role of N-glycosylation in the targeting and activity of the GLYT1 glycine transporter. J Biol Chem 270:9437–9442

    Article  CAS  PubMed  Google Scholar 

  • Paxinos G, Watson C (1998) The rat brain in stereotaxic coordinates, 4th edn. Academic Press, San Diego

    Google Scholar 

  • Perea G, Navarrete M, Araque A (2009) Tripartite synapses: astrocytes process and control synaptic information. Trends Neurosci 32(8):421–431

    Article  CAS  PubMed  Google Scholar 

  • Peterson GL (1979) Review of the folin phenol protein quantitation method of Lowry, Rosebrough, Farr and Randall. Anal Biochem 100:201–220

    Article  CAS  PubMed  Google Scholar 

  • Pfaffl MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29(9):2002–2007

    Article  Google Scholar 

  • Raiteri L, Stigliani S, Usai C, Diaspro A, Paluzzi S, Milanese M, Raiteri M, Bonanno G (2008) Functional expression of release-regulating glycine transporters GLYT1 on GABAergic neurons and GLYT2 on astrocytes in mouse spinal cord. Neurochem Int 52:103–112

    Article  CAS  PubMed  Google Scholar 

  • Rees MI, Harvey K, Pearce BR, Chung SK, Duguid IC, Thomas P, Beatty S, Graham GE, Armstrong L, Shiang R, Abbott KJ, Zuberi SM, Stephenson JBP, Owen MJ, Tijssen MAJ, van den Maagdenberg AMJM, Smart TG, Supplisson S, Harvey RJ (2006) Mutations in the gene encodingGlyT2 (SLC6A5) define a presynaptic component of human startle disease. Nat Genet 38:801–806

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Rousseau F, Aubrey KR, Supplisson S (2008) The glycine transporter GlyT2 controls the dynamics of synaptic vesicle refilling in inhibitory spinal cord neurons. J Neurosci 28:9755–9768

    Article  CAS  PubMed  Google Scholar 

  • Schnell SA, Staines WA, Wessendorf MW (1999) Reduction of lipofuscin-like autofluorescence in fluorescently labeled tissue. J Histochem Cytochem 47:719–730

    Article  CAS  PubMed  Google Scholar 

  • Su TZ, Lunney E, Cambell G, Oxender DL (1995) Transport of gabapentin, a gamma-amino acid drug, by system L alpha amino acid transporters: a comparative study in astrocytes, synaptosomes and CHO cells. J Neurochem 64:2125–2131

    Article  CAS  PubMed  Google Scholar 

  • Supplisson S, Bergman C (1997) Control of NMDA receptor activation by a glycine transporter co-expressed in xenopus oocytes. J Neurosci 17:4580–4590

    CAS  PubMed  Google Scholar 

  • Tunnicliff G (2003) Membrane glycine transport proteins. J Biomed Sci 10:30–36

    Article  CAS  PubMed  Google Scholar 

  • Vargas-Medrano J, Castrejon-Tellez V, Plenge F, Ramirez I, Miranda M (2011) PKCβ-dependent phosphorylation of the glycine transporter 1. Neurochem Int 59(8):1123–1132

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Vaz SH, Jørgensen TN, Cristóvão-Ferreira S, Duflot S, Ribeiro JA, Gether U, Sebastião AM (2011) Brain-derived neurotrophic factor (BDNF) enhances GABA transport by modulating the trafficking of GABA transporter-1 (GAT-1) from the plasma membrane of rat cortical astrocytes. J Biol Chem 286(47):40464–40476

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Weiss MD, Derazi S, Kilberg MS, Anderson KJ (2001) Ontogeny and localization of the neutral amino acid transporter ASCT1 in rat brain. Brain Res Dev Brain Res 130:183–190

    Article  CAS  PubMed  Google Scholar 

  • Wu ZL, O’Kane TM, Connors TJ, Marina MJ, Schaffhauser H (2008) The phosphatidylinositol 3- kinase inhibitor LY 294002 inhibits GlyT1-mediated glycine uptake. Brain Res 1227:42–51

    Article  CAS  PubMed  Google Scholar 

  • Yee BK, Balic E, Singer P, Schwerdel C, Grampp T, Gabernet L, Knuesel I, Benke D, Feldon J, Mohler H, Boison D (2006) Disruption of glycine transporter 1 restricted to forebrain neuron is associated with a procognitive and antipsychotic phenotypic profile. J Neurosci 26(12):3169–3181

    Article  CAS  PubMed  Google Scholar 

  • Zafra F, Aragón C, Olivares L, Danbolt NC, Giménez C, Storm-Mathisen J (1995) Glycine transporters are differentially expressed among CNS cells. J Neurosci 15:3952–3969

    CAS  PubMed  Google Scholar 

Download references

Acknowledgments

The authors thank Dr. Manuel Miranda-Arango (Texas) for kindly supplying the antibodies against GlyT1 and GlyT2. This work was supported by Fundação para a Ciência e a Tecnologia (FCT), Portugal. Rita I Aroeira is in receipt of a fellowship (SFRH/BD/62831/2009) from FCT. The authors declare that this research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Cláudia A. Valente.

Electronic supplementary material

Below is the link to the electronic supplementary material.

429_2013_537_MOESM1_ESM.ppt

Supplementary material 1 Online Resource 1 melting curves of GlyT1, GlyT2 and β-actin transcripts analyzed by qPCR. Y axis represents the first derivate of raw fluorescence and X axis corresponds to an increase in temperature. Each curve has a single melting peak, which indicates that a single PCR product is being amplified. (PPT 126 kb)

429_2013_537_MOESM2_ESM.ppt

Supplementary material 2 Online Resource 2 transport progression curves using two concentrations of glycine, 50 µM to study GlyT1 (a) and 1,500 µM to study GlyT2 (b). Incubation time ranging from 30 to 240 s was tested. Arrows point to the incubation time used in the subsequent experiments. (PPT 176 kb)

429_2013_537_MOESM3_ESM.ppt

Supplementary material 3 Online Resource 3 concentration-dependent uptake of glycine in rat cultured cortical astrocytes by GlyT inhibitors. GlyT1-specific inhibitor Org 24598 (a), GlyT2-blockers ALX 1393 (b) and amoxapine (c) were used in several concentrations. Note the differences in X axis scale between graphs. Y axis represents [3H]glycine uptake as percentage of the control value (absence of inhibitors) in the same experiment. Arrows point to the concentration of inhibitor used in the subsequent experiments to isolate GlyT1 and GlyT2 specific transport. (PPT 134 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Aroeira, R.I., Sebastião, A.M. & Valente, C.A. GlyT1 and GlyT2 in brain astrocytes: expression, distribution and function. Brain Struct Funct 219, 817–830 (2014). https://doi.org/10.1007/s00429-013-0537-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00429-013-0537-3

Keywords

Navigation