Skip to main content
Log in

Astrocytic processes compensate for the apparent lack of GABA transporters in the axon terminals of cerebellar Purkinje cells

  • Original Articles
  • Published:
Anatomy and Embryology Aims and scope Submit manuscript

Abstract

The aim of the present study was to evaluate the expression of two high affinity GABA transporters (GAT-1 and GAT-3) in the rat cerebellum using immunocytochemistry and affinity purified antibodies. GAT-1 immunoreactivity was prominent in punctate structures and axons in all layers of the cerebellar cortex, and was especially prominent around the somata of Purkinje cells. In contrast, the deep cerebellar nuclei showed few if any GAT-1 immunoreactive puncta. Weak GAT-3 immunoreactive processes were present in the cerebellar cortex, whereas GAT-3 immunostaining was prominent around the somata of neurons in the deep cerebellar nuclei. Electron microscopic preparations of the cerebellar cortex demonstrated that GAT-1 immunoreactive axon terminals formed symmetric synapses with somata, axon initial segments and dendrites of Purkinje cells and the dendrites of granule cells. Astrocytic processes in the cerebellar cortex were also immunolabeled for GAT-1. However, Purkinje cell axon terminals that formed symmetric synapses with neurons in the deep cerebellar nuclei lacked GAT-1 immunoreactivity. Instead, weak GAT 1 and strong GAT-3 immunoreactivities were expressed by astrocytic processes that enveloped the Purkinje cell axon terminals. In addition, GAT-3-immunoreactivity appeared in astrocytic processes in the cerebellar cortex. These observations demonstrate that GAT-1 is localized to axon terminals of three of the four neuronal types that were previously established as being GABAergic, i.e. basket, stellate and Golgi cells. GAT-1 and GAT-3 are expressed by astrocytes. The failure to identify a GABA transporter in Purkinje cells is consistent with previous data that indicated that Purkinje cells lacked terminal uptake mechanisms for GABA. The individual glial envelopment of Purkinje cell axon terminals in the deep cerebellar nuclei and the dense immunostaining of GAT-3, and to a lesser extent GAT-1, expressed by astrocytic processes provide a compensatory mechanism for the removal of GABA from the synaptic cleft of synapses formed by Purkinje cell axon terminals.

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.

Similar content being viewed by others

References

  • Borden LA, Smith KE, Hartig PR, Branchek TA, Weinshank RL (1992) Molecular heterogeneity of the γ-aminobutyric acid (GABA) transport system. J Biol Chem 267:21908–21104

    Google Scholar 

  • Brecha NC, Weigmann C (1993) Identification of cell types expressing GABA transport mRNA in the rat retina. Invest Ophthalmol Vis Sci 34:1380

    Google Scholar 

  • Brecha NC, Weigmann C (1994) Expression of GAT-1, a high affinity gamma-aminobutyric acid plasma membrane transporter in the rat retina. J Comp Neurol 345:602–611

    Google Scholar 

  • Chan-Palay V (1977) Cerebellar dentate nucleus, organization, cytology, and transmitters. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Clark JA, Deutch AY, Gallipoli AZ, Amara SG (1992) Functional expression and CNS distribution of a β-alanine-sensitive neuronal GABA transporter. Neuron 9:337–348

    Google Scholar 

  • During MJ, Ryder KM, Spencer DD (1995) Hippocampal GABA transporter function in temporal-lobe epilepsy. Nature 376:174–177

    Article  CAS  PubMed  Google Scholar 

  • Durkin MM, Smith KE, Borden LA, Weinshank RL, Branchek TA, Gustafson EL (1995) Localization of messenger RNAs encoding three GABA transporters in rat brain: an in situ hybridization study. Mol Brain Res 33:7–21

    Google Scholar 

  • Eccles JC, Ito M, Szentágothai J (1967) The cerebellum as a neuronal machine. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Greif KF, Erlander MG, Tillakaratne NJK, Tobin AJ (1991) Postnatal expression of glutamate decarboxylases in developing rat cerebellum. Neurochem Res 16:235–242

    Google Scholar 

  • Guastella J, Nelson N, Nelson H, Czyzyk L, Keynan S, Miedel MC, Davidson N, Lester HA, Kanner BI (1990) Cloning and expression of a rat brain GABA transporter. Science 249:1303–1306

    Google Scholar 

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

    Google Scholar 

  • Hökfelt T, Ljungdahl Å (1970) Cellular localization of labeled gamma-aminobutyric acid (3H-GABA) in rat cerebellar cortex: an autoradiographic study. Brain Res 22:391–396

    Google Scholar 

  • Hökfelt T, Ljungdahl Å (1972) Autoradiographic identification of cerebral and cerebellar cortical neurones accumulating labeled gamma-aminobutyric acid (3H-GABA). Exp Brain Res 14:354–362

    Google Scholar 

  • Ikegaki N, Saito N, Hashima M, Tanaka C (1994) Production of specific antibodies against GABA transporter subtypes (GAT1, GAT2, GAT3) and their application to immunocytochemistry. Mol Brain Res 26:47–54

    Google Scholar 

  • Johnson J, Chen TK, Rickman D, Evans C, Brecha NC (1996) Multiple γ-aminobutyric acid plasma membrane transporters (GAT-1, GAT-2, GAT-3) in the rat retina. J Comp Neurol (in press)

  • Kelly JS, Dick F (1976) Differential labeling of glial cells and GABA-inhibitory interneurons and nerve terminals following the microinjection of [β-3H]alanine, [3H]DABA and [3H]GABA into single folia of the cerebellum. Cold Spring Harb Symp Quant Biol 40:93–106

    Google Scholar 

  • Levi G, Raiteri M (1993) Carrier-mediated release of neurotrans-mitters. Trends Neurosci 16:415–418

    Google Scholar 

  • Liu QR, Lopez-Corcuera B, Mandiyan S, Nelson H, Nelson N (1993) Molecular characterization of four pharmacologically distinct γ-aminobutyric acid transporters in mouse brain. J Biol Chem 268:2106–2112

    Google Scholar 

  • Lopez-Corcuera B, Liu QR, Mandiyan S, Nelson H, Nelson N (1992) Expression of a mouse brain cDNA encoding a novel γ-aminobutyric acid transporter. J Biol Chem 267:17491–17493

    Google Scholar 

  • McLaughlin BJ, Wood JG, Saito K, Barber R, Vaughn JE, Roberts E, Wu J-Y (1974) The fine structural localization of glutamate decarboxylase in synaptic terminals of rodent cerebellum. Brain Res 76:377–391

    Google Scholar 

  • Minelli A, Brecha NC, Karschin C, DeBiasi S, Conti F (1995) GAT-1, a high-affinity GABA plasma membrane transporter, is localized to neurons and astroglia in the cerebral cortex. J Neurosci 15:7734–7746.

    Google Scholar 

  • Oertel WH, Schmechel DE, Mugnaini E, Tappaz ML, Kopin IJ (1981) Immunocytochemical localization of glutamate decarboxylase in rat cerebellum with a new antiserum. Neuroscience 6:2715–2735

    Google Scholar 

  • Ottersen OP, Davanger S, Storm-Mathisen J (1987) Glycine-like immunoreactivity in the cerebellum of rat and Senegalese baboon, Papio papio: a comparison with the distribution of GABA-like immunoreactivity and with (3H)glycine and (3H)GABA uptake. Exp Brain Res 66:211–221

    Google Scholar 

  • Palay SL, Chan-Palay V (1974) Cerebellar cortex, cytology and organization. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Peters A, Palay SL, Webster H de F (1991) The fine structure of the nervous system. Oxford University Press, Oxford New York

    Google Scholar 

  • Pin J-P, Bockaert J (1989) Two distinct mechanisms, differentially affected by excitatory amino acids, trigger GABA release from fetal mouse striatal neurons in primary culture. J Neurosci 9:648–656

    CAS  PubMed  Google Scholar 

  • Radian R, Ottersen OP, Storm-Mathisen J, Castel M, Kanner BI (1990) Immunocytochemical localization of the GABA transporter in rat brain. J Neurosci 10:1319–1330

    Google Scholar 

  • Rattray M, Priestley JV (1993) Differential expression of GABA transporter-1 messenger RNA in subpopulations of GABA neurons. Neurosci Lett 156:163–166

    Google Scholar 

  • Ribak CE, Vaughn JE, Saito K, Barber R, Roberts E (1976) Immunocytochemical localization of glutamate decarboxylase in rat substantia nigra. Brain Res 116:287–298

    Google Scholar 

  • Ribak CE, Vaughn JE, Saito K (1978) Immunocytochemical localization of glutamic acid decarboxylase in neuronal somata following colchicine inhibition of axonal transport. Brain Res 140:315–332

    Google Scholar 

  • Ribak CE, Tong WMY, Brecha NC (1996) The GABA plasma membrane transporters, GAT-1 and GAT-3, display different distributions in the rat hippocampus. J Comp Neurol 367:595–606

    Article  CAS  PubMed  Google Scholar 

  • Saito K, Barber R, Wu JY, Matsuda T, Roberts E, Vaughn JE (1974) Immunohistochemical localization of glutamate decarboxylase in rat cerebellum. Proc Natl Acad Sci USA 71:269–273

    Google Scholar 

  • Schon F, Iversen LL (1972) Selective accumulation of [3H]-GABA by stellate cells in rat cerebellar cortex in vivo. Brain Res 42:503–507

    Google Scholar 

  • Seguela P, Geffard M, Buijs RM, Moal ML (1984) Antibodies against γ-aminobutyric acid: Specificity studies and immunocytochemical results. Proc Natl Acad Sci USA 81:3888–3892

    Google Scholar 

  • Swan M, Najlerahim A, Watson REB, Bennett JP (1994) Distribution of mRNA for the GABA transporter GAT-1 in the rat brain: evidence that GABA uptake is not limited to presynaptic neurons. J Anat 185:315–323

    Google Scholar 

  • Tolbert DL, Bantli H (1980) Uptake and transport of 3H-GABA (γ-aminobutyric acid) injected into the cat dentate nucleus. Exp Neurol 70:525–538

    Google Scholar 

  • Walberg F, Holländer H, Grofová I (1976) An autoradiographic identification of Purkinje axon terminals in the cat. J Neurocytol 5:157–169

    Google Scholar 

  • Wiklund L, Künzle H, Cuenod M (1983) Failure to demonstrate retrograde labeling of cerebellar Purkinje cells after injection of (3H)GABA in Deiters' nucleus. Neurosci Lett 38:23–28

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Charles E. Ribak.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ribak, C.E., Tong, W.M.Y. & Brecha, N.C. Astrocytic processes compensate for the apparent lack of GABA transporters in the axon terminals of cerebellar Purkinje cells. Anat Embryol 194, 379–390 (1996). https://doi.org/10.1007/BF00198540

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00198540

Key words

Navigation