Interactions between Purkinje neurones and Bergmann glia (original) (raw)

• Araque A, Carmignoto G, Haydon PG. Dynamic signaling between astrocytes and neurons. Annu Rev Physiol. 2001; 63:795–813.
  PubMed CAS Google Scholar
• Verkhratsky A, Orkand RK, Kettenmann H. Glial calcium: homeostasis and signaling function. Physiol Rev. 1998;78: 99–141.
  PubMed CAS Google Scholar
• Carmignoto G. Reciprocal communication systems between astrocytes and neurones. Prog Neurobiol. 2000;62:561–81.
  PubMed CAS Google Scholar
• Ullian EM, Sapperstein SK, Christopherson KS, Barres BA. Control of synapse number by glia. Science. 2001;291: 657–61.
  PubMed CAS Google Scholar
• Fellin T, Pascual O, Gobbo S, Pozzan T, Haydon PG, Carmignoto G. Neuronal synchrony mediated by astrocytic glutamate through activation of extrasynaptic NMDA receptors. Neuron. 2004;43:729–43.
  PubMed CAS Google Scholar
• Zonta M, Angulo MC, Gobbo S, Rosengarten B, Hossmann KA, Pozzan T, et al. Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation. Nat Neurosci. 2003;6:43–50.
  PubMed CAS Google Scholar
• Kang J, Jiang L, Goldman SA, Nedergaard M. Astrocytemediated potentiation of inhibitory synaptic transmission. Nat Neurosci. 1998;1:683–92.
  PubMed CAS Google Scholar
• Smit AB, Syed NI, Schaap D, van Minnen J, Klumperman J, Kits KS, et al. A glia-derived acetylcholine-binding protein that modulates synaptic transmission. Nature. 2001;411: 261–8.
  PubMed CAS Google Scholar
• Palay SL, Chan-Palay V. Cerebellar Cortex. Cytology and Organization. Berlin: Springer-Verlag, 1974.
  Google Scholar
• Grosche J, Kettenmann H, Reichenbach A. Bergmann glial cells form distinct morphological structures to interact with cerebellar neurons. J Neurosci Res. 2002;68:138–49.
  PubMed CAS Google Scholar
• Newman E, Reichenbach A. The Muller cell: a functional element of the retina. Trends Neurosci. 1996;19:307–12.
  PubMed CAS Google Scholar
• Kettenmann H, Ransom B. Neuroglia. New York: Oxford University Press, 1995.
  Google Scholar
• Rakic P. Neuron-glia relationship during granule cell migration in developing cerebellar cortex. A Golgi and electronmicroscopic study in_Macacus rhesus_. J Comp Neurol. 1971;141:283–312.
  PubMed CAS Google Scholar
• Yamada K, Fukaya M, Shibata T, Kurihara H, Tanaka K, Inoue Y, et al. Dynamic transformation of Bergmann glial fibers proceeds in correlation with dendritic outgrowth and synapse formation of cerebellar Purkinje cells. J Comp Neurol. 2000;418:106–20.
  PubMed CAS Google Scholar
• Lordkipanidze T, Dunaevsky A. Purkinje cell dendrites grow in alignment with Bergmann glia. Glia. 2005;51:229–34.
  PubMed Google Scholar
• Eiraku M, Tohgo A, Ono K, Kaneko M, Fujishima K, Hirano T, et al. DNER acts as a neuron-specific Notch ligand during Bergmann glial development. Nat Neurosci. 2005;8:873–80.
  PubMed CAS Google Scholar
• Muller T, Fritschy JM, Grosche J, Pratt GD, Mohler H, Kettenmann H. Developmental regulation of voltage-gated K+ channel and GABAA receptor expression in Bergmann glial cells. J Neurosci. 1994;14:2503–14.
  PubMed CAS Google Scholar
• Muller T, Moller T, Berger T, Schnitzer J, Kettenmann H. Calcium entry through kainate receptors and resulting potassium-channel blockade in Bergmann glial cells. Science. 1992;256:1563–6.
  PubMed CAS Google Scholar
• Clark BA, Barbour B. Currents evoked in Bergmann glial cells by parallel fibre stimulation in rat cerebellar slices. J Physiol. 1997;502(Pt 2):335–50.
  PubMed CAS Google Scholar
• Bergles DE, Dzubay JA, Jahr CE. Glutamate transporter currents in bergmann glial cells follow the time course of extrasynaptic glutamate. Proc Natl Acad Sci USA. 1997; 94:14821–5.
  PubMed CAS Google Scholar
• Bellamy TC, Ogden D. Short-term plasticity of Bergmann glial cell extrasynaptic currents during parallel fibre stimulation in rat cerebellum. Glia. 2005;52:325–35.
  PubMed Google Scholar
• Riquelme R, Miralles CP, De Blas AL. Bergmann glia GABA(A) receptors concentrate on the glial processes that wrap inhibitory synapses. J Neurosci. 2002;22:10720–30.
  PubMed CAS Google Scholar
• Muller T, Moller T, Neuhaus J, Kettenmann H. Electrical coupling among Bergmann glial cells and its modulation by glutamate receptor activation. Glia. 1996;17:274–84.
  PubMed CAS Google Scholar
• Yamada K, Watanabe M. Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells. Anat Sci Int. 2002;77:94–108.
  PubMed Google Scholar
• Muller T, Kettenmann H. Physiology of Bergmann glial cells. Int Rev Neurobiol. 1995;38:341–59.
  Article PubMed CAS Google Scholar
• Sotelo C. Cellular and genetic regulation of the development of the cerebellar system. Prog Neurobiol. 2004;72:295–339.
  PubMed CAS Google Scholar
• Xu-Friedman MA, Harris KM, Regehr WG. Three-dimensional comparison of ultrastructural characteristics at depressing and facilitating synapses onto cerebellar Purkinje cells. J Neurosci. 2001;21:6666–72.
  PubMed CAS Google Scholar
• Grosche J, Matyash V, Moller T, Verkhratsky A, Reichenbach A, Kettenmann H. Microdomains for neuron-glia interaction: parallel fiber signaling to Bergmann glial cells. Nat Neurosci. 1999;2:139–43.
  PubMed CAS Google Scholar
• Rothstein JD, Martin L, Levey AI, Dykes-Hoberg M, Jin L, Wu D, et al. Localization of neuronal and glial glutamate transporters. Neuron. 1994;13:713–25.
  PubMed CAS Google Scholar
• Wadiche JI, Kavanaugh MP. Macroscopic and microscopic properties of a cloned glutamate transporter/chloride channel. J Neurosci. 1998;18:7650–61.
  PubMed CAS Google Scholar
• Klockner U, Storck T, Conradt M, Stoffel W. Electrogenic L-glutamate uptake in_Xenopus laevis_ oocytes expressing a cloned rat brain L-glutamate/L-aspartate transporter (GLAST-1). J Biol Chem. 1993;268:14594–6.
  PubMed CAS Google Scholar
• Otis TS, Kavanaugh MP. Isolation of current components and partial reaction cycles in the glial glutamate transporter EAAT2. J Neurosci. 2000;20:2749–57.
  PubMed CAS Google Scholar
• Auger C, Attwell D. Fast removal of synaptic glutamate by postsynaptic transporters. Neuron. 2000;28:547–58.
  PubMed CAS Google Scholar
• Sonders MS, Amara SG. Channels in transporters. Curr Opin Neurobiol. 1996;6:294–302.
  PubMed CAS Google Scholar
• Hertz L, Zielke HR. Astrocytic control of glutamatergic activity: astrocytes as stars of the show. Trends Neurosci. 2004;27:735–43.
  PubMed CAS Google Scholar
• Takahashi M, Sarantis M, Attwell D. Postsynaptic glutamate uptake in rat cerebellar Purkinje cells. J Physiol. 1996;497(Pt 2):523–30.
  PubMed CAS Google Scholar
• Otis TS, Wu YC, Trussell LO. Delayed clearance of transmitter and the role of glutamate transporters at synapses with multiple release sites. J Neurosci. 1996;16:1634–44.
  PubMed CAS Google Scholar
• Brasnjo G, Otis TS. Neuronal glutamate transporters control activation of postsynaptic metabotropic glutamate receptors and influence cerebellar long-term depression. Neuron. 2001;31:607–16.
  PubMed CAS Google Scholar
• Reichelt W, Knopfel T. Glutamate uptake controls expression of a slow postsynaptic current mediated by mGluRs in cerebellar Purkinje cells. J Neurophysiol. 2002;87:1974–80.
  PubMed CAS Google Scholar
• Barbour B. An evaluation of synapse independence. J Neurosci. 2001;21:7969–84.
  PubMed CAS Google Scholar
• Meldrum B, Garthwaite J. Excitatory amino acid neurotoxicity and neurodegenerative disease. Trends Pharmacol Sci. 1990;11:379–87.
  PubMed CAS Google Scholar
• Voutsinos-Porche B, Bonvento G, Tanaka K, Steiner P, Welker E, Chatton JY, et al. Glial glutamate transporters mediate a functional metabolic crosstalk between neurons and astrocytes in the mouse developing cortex. Neuron. 2003;37:275–86.
  PubMed CAS Google Scholar
• Rothstein JD, Dykes-Hoberg M, Pardo CA, Bristol LA, Jin L, Kuncl RW, et al. Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate. Neuron. 1996;16:675–86.
  PubMed CAS Google Scholar
• Watase K, Hashimoto K, Kano M, Yamada K, Watanabe M, Inoue Y, et al. Motor discoordination and increased susceptibility to cerebellar injury in GLAST mutant mice. Eur J Neurosci. 1998;10:976–88.
  PubMed CAS Google Scholar
• Marcaggi P, Billups D, Attwell D. The role of glial glutamate transporters in maintaining the independent operation of juvenile mouse cerebellar parallel fibre synapses. J Physiol. 2003;552:89–107.
  PubMed CAS Google Scholar
• Takayasu Y, Iino M, Kakegawa W, Maeno H, Watase K, Wada K, et al. Differential roles of glial and neuronal glutamate transporters in Purkinje cell synapses. J Neurosci. 2005;25:8788–93.
  PubMed CAS Google Scholar
• Brockhaus J, Deitmer JW. Long-lasting modulation of synaptic input to Purkinje neurons by Bergmann glia stimulation in rat brain slices. J Physiol. 2002;545: 581–93.
  PubMed CAS Google Scholar
• Danbolt NC. Glutamate uptake. Prog Neurobiol. 2001;65:1–105.
  PubMed CAS Google Scholar
• Bordey A, Sontheimer H. Modulation of glutamatergic transmission by bergmann glial cells in rat cerebellum in situ. J Neurophysiol. 2003;89:979–88.
  PubMed CAS Google Scholar
• Huang H, Bordey A. Glial glutamate transporters limit spillover activation of presynaptic NMDA receptors and influence synaptic inhibition of Purkinje neurons. J Neurosci. 2004;24:5659–69.
  PubMed CAS Google Scholar
• Burnashev N, Khodorova A, Jonas P, Helm PJ, Wisden W, Monyer H, et al. Calcium-permeable AMPA-kainate receptors in fusiform cerebellar glial cells. Science. 1992; 256:1566–70.
  PubMed CAS Google Scholar
• Hollmann M, Hartley M, Heinemann S. Ca2+ permeability of KA-AMPA-gated glutamate receptor channels depends on subunit composition. Science. 1991;252:851–3.
  PubMed CAS Google Scholar
• Burnashev N, Monyer H, Seeburg PH, Sakmann B. Divalent ion permeability of AMPA receptor channels is dominated by the edited form of a single subunit. Neuron. 1992;8:189–98.
  PubMed CAS Google Scholar
• Koh DS, Burnashev N, Jonas P. Block of native Ca(2+)permeable AMPA receptors in rat brain by intracellular polyamines generates double rectification. J Physiol. 1995; 486(Pt 2):305–12.
  PubMed CAS Google Scholar
• Matsui K, Jahr CE. Ectopic release of synaptic vesicles. Neuron. 2003;40:1173–83.
  PubMed CAS Google Scholar
• Iino M, Goto K, Kakegawa W, Okado H, Sudo M, Ishiuchi S, et al. Glia-synapse interaction through Ca2+permeable AMPA receptors in Bergmann glia. Science. 2001;292:926–9.
  PubMed CAS Google Scholar
• Strata P, Rossi F. Plasticity of the olivocerebellar pathway. Trends Neurosci. 1998;21:407–13.
  PubMed CAS Google Scholar
• Millan A, Arias-Montano JA, Mendez JA, Hernandez-Kelly LC, Ortega A. Alpha-amino-3-hydroxy-5-methyl-4isoxazolepropionic acid receptors signaling complexes in Bergmann glia. J Neurosci Res. 2004;78:56–63.
  PubMed CAS Google Scholar
• Mendez JA, Lopez-Bayghen E, Rojas F, Hernandez ME, Ortega A. Glutamate regulates Oct-2 DNA-binding activity through alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate receptors in cultured chick Bergmann glia cells. J Neurochem. 2004;88:835–43.
  Article PubMed CAS Google Scholar
• Lopez-Bayghen E, Espinoza-Rojo M, Ortega A. Glutamate down-regulates GLAST expression through AMPA receptors in Bergmann glial cells. Brain Res Mol Brain Res. 2003;115:1–9.
  PubMed CAS Google Scholar
• Aguirre A, Lopez-Bayghen E, Ortega A. Glutamate-dependent transcriptional regulation of the chkbp gene: signaling mechanisms. J Neurosci Res. 2002;70:117–27.
  PubMed CAS Google Scholar
• Millan A, Aguilar P, Mendez JA, Arias-Montano JA, Ortega A. Glutamate activates PP125(FAK) through AMPA/kainate receptors in Bergmann glia. J Neurosci Res. 2001;66:723–9.
  PubMed CAS Google Scholar
• Lopez-Bayghen E, Ortega A. Glutamate-dependent transcriptional regulation of GLAST: role of PKC. J Neurochem. 2004;91:200–9.
  PubMed CAS Google Scholar
• Matsui K, Jahr CE, Rubio ME. High-concentration rapid transients of glutamate mediate neural-glial communication via ectopic release. J Neurosci. 2005;25:7538–47.
  PubMed CAS Google Scholar
• Matsui K, Jahr CE. Differential control of synaptic and ectopic vesicular release of glutamate. J Neurosci. 2004;24: 8932–9.
  PubMed CAS Google Scholar
• Sugihara I, Wu H, Shinoda Y. Morphology of single olivocerebellar axons labeled with biotinylated dextran amine in the rat. J Comp Neurol. 1999;414:131–48.
  PubMed CAS Google Scholar
• Hamori J, Szentagothai J. Lack of evidence of synaptic contacts by climbing fibre collaterals to basket and stellate cells in developing rat cerebellar cortex. Brain Res. 1980;186:454–7.
  PubMed CAS Google Scholar
• Lin SC, Huck JH, Roberts JD, Macklin WB, Somogyi P, Bergles DE. Climbing fiber innervation of NG2-expressing glia in the mammalian cerebellum. Neuron. 2005;46: 773–85.
  PubMed CAS Google Scholar
• Bergles DE, Roberts JD, Somogyi P, Jahr CE. Glutamatergic synapses on oligodendrocyte precursor cells in the hippocampus. Nature. 2000;405:187–91.
  PubMed CAS Google Scholar
• Jabs R, Pivneva T, Huttmann K, Wyczynski A, Nolte C, Kettenmann H, et al. Synaptic transmission onto hippocampal glial cells with hGFAP promoter activity. J Cell Sci. 2005;118:3791–803.
  PubMed CAS Google Scholar
• Bellamy TC, Ogden D. Long-term depression of neuron to glial signalling in rat cerebellar cortex. Eur J Neurosci. 2006;23:581–6.
  PubMed Google Scholar
• Dittman JS, Kreitzer AC, Regehr WG. Interplay between facilitation, depression, and residual calcium at three presynaptic terminals. J Neurosci. 2000;20:1374–85.
  PubMed CAS Google Scholar
• Zucker RS, Regehr WG. Short-term synaptic plasticity. Annu Rev Physiol. 2002;64:355–405.
  PubMed CAS Google Scholar
• Harrison J, Jahr CE. Receptor occupancy limits synaptic depression at climbing fiber synapses. J Neurosci. 2003;23: 377–83.
  PubMed CAS Google Scholar
• Clements JD. Transmitter timecourse in the synaptic cleft: its role in central synaptic function. Trends Neurosci. 1996;19:163–71.
  PubMed CAS Google Scholar
• Coesmans M, Weber JT, De Zeeuw CI, Hansel C. Bidirectional parallel fiber plasticity in the cerebellum under climbing fiber control. Neuron. 2004;44:691–700.
  PubMed CAS Google Scholar
• Foster KA, Crowley JJ, Regehr WG. The influence of multivesicular release and postsynaptic receptor saturation on transmission at granule cell to Purkinje cell synapses. J Neurosci. 2005;25:11655–65.
  PubMed CAS Google Scholar
• Takahashi M, Kovalchuk Y, Attwell D. Preand postsynaptic determinants of EPSC waveform at cerebellar climbing fiber and parallel fiber to Purkinje cell synapses. J Neurosci. 1995;15:5693–702.
  PubMed CAS Google Scholar
• Neale SA, Garthwaite J, Batchelor AM. Metabotropic glutamate receptor subtypes modulating neurotransmission at parallel fibre-Purkinje cell synapses in rat cerebellum. Neuropharmacology. 2001;41:42–9.
  PubMed CAS Google Scholar
• Maejima T, Hashimoto K, Yoshida T, Aiba A, Kano M. Presynaptic inhibition caused by retrograde signal from metabotropic glutamate to cannabinoid receptors. Neuron. 2001;31:463–75.
  PubMed CAS Google Scholar
• Kirischuk S, Tuschick S, Verkhratsky A, Kettenmann H. Calcium signalling in mouse Bergmann glial cells mediated by alpha 1-adrenoreceptors and H1 histamine receptors. Eur J Neurosci. 1996;8:1198–208.
  PubMed CAS Google Scholar
• Kirischuk S, Kirchhoff F, Matyash V, Kettenmann H, Verkhratsky A. Glutamate-triggered calcium signalling in mouse bergmann glial cells in situ: role of inositol-1,4,5trisphosphate-mediated intracellular calcium release. Neuroscience. 1999;92:1051–9.
  PubMed CAS Google Scholar
• Tuschick S, Kirischuk S, Kirchhoff F, Liefeldt L, Paul M, Verkhratsky A, et al. Bergmann glial cells in situ express endothelinB receptors linked to cytoplasmic calcium signals. Cell Calcium. 1997;21:409–19.
  PubMed CAS Google Scholar
• Southam E, Morris R, Garthwaite J. Sources and targets of nitric oxide in rat cerebellum. Neurosci Lett. 1992;137: 241–4.
  PubMed CAS Google Scholar
• Kirischuk S, Moller T, Voitenko N, Kettenmann H, Verkhratsky A. ATP-induced cytoplasmic calcium mobilization in Bergmann glial cells. J Neurosci. 1995;15:7861–71.
  PubMed CAS Google Scholar
• Matyash V, Filippov V, Mohrhagen K, Kettenmann H. Nitric oxide signals parallel fiber activity to Bergmann glial cells in the mouse cerebellar slice. Mol Cell Neurosci. 2001;18:664–70.
  PubMed CAS Google Scholar
• Kulik A, Haentzsch A, Luckermann M, Reichelt W, Ballanyi K. Neuron-glia signaling via alpha(1) adrenoceptor-mediated Ca(2+) release in Bergmann glial cells in situ. J Neurosci. 1999;19:8401–8.
  PubMed CAS Google Scholar
• Pakhotin P, Verkhratsky A. Electrical synapses between Bergmann glial cells and Purkinje neurones in rat cerebellar slices. Mol Cell Neurosci. 2005;28:79–84.
  PubMed Google Scholar
• Hounsgaard J, Nicholson C. Potassium accumulation around individual purkinje cells in cerebellar slices from the guinea-pig. J Physiol. 1983;340:359–88.
  PubMed CAS Google Scholar
• Haydon PG. GLIA: listening and talking to the synapse. Nat Rev Neurosci. 2001;2:185–93.
  PubMed CAS Google Scholar
• Bezzi P, Gundersen V, Galbete JL, Seifert G, Steinhauser C, Pilati E, et al. Astrocytes contain a vesicular compartment that is competent for regulated exocytosis of glutamate. Nat Neurosci. 2004;7:613–20.
  PubMed CAS Google Scholar
• Parpura V, Haydon PG. Physiological astrocytic calcium levels stimulate glutamate release to modulate adjacent neurons. Proc Natl Acad Sci USA. 2000;97:8629–34.
  PubMed CAS Google Scholar
• Kreft M, Stenovec M, Rupnik M, Grilc S, Krzan M, Potokar M, et al. Properties of Ca(2+)-dependent exocytosis in cultured astrocytes. Glia. 2004;46:437–45.
  PubMed Google Scholar
• Parri HR, Gould TM, Crunelli V. Spontaneous astrocytic Ca2+ oscillations in situ drive NMDAR-mediated neuronal excitation. Nat Neurosci. 2001;4:803–12.
  PubMed CAS Google Scholar
• Glitsch M, Marty A. Presynaptic effects of NMDA in cerebellar Purkinje cells and interneurons. J Neurosci. 1999;19:511–9.
  PubMed CAS Google Scholar
• Casado M, Dieudonne S, Ascher P. Presynaptic N-methylD-aspartate receptors at the parallel fiber-Purkinje cell synapse. Proc Natl Acad Sci USA. 2000;97:11593–7.
  PubMed CAS Google Scholar
• Casado M, Isope P, Ascher P. Involvement of presynaptic N-methyl-D-aspartate receptors in cerebellar long-term depression. Neuron. 2002;33:123–30.
  PubMed CAS Google Scholar
• Newman EA. Glial cell inhibition of neurons by release of ATP. J Neurosci. 2003;23:1659–66.
  PubMed CAS Google Scholar
• Brockhaus J, Dressel D, Herold S, Deitmer JW. Purinergic modulation of synaptic input to Purkinje neurons in rat cerebellar brain slices. Eur J Neurosci. 2004;19:2221–30.
  PubMed Google Scholar
• Casel D, Brockhaus J, Deitmer JW. Enhancement of spontaneous synaptic activity in rat Purkinje neurones by ATP during development. J Physiol. 2005;568:111–22.
  PubMed CAS Google Scholar
• Lopez E, Lee-Rivera I, Lopez-Colome AM. Characteristics and regulation of glycine transport in Bergmann glia. Neurochem Res. 2005;30:1567–77.
  PubMed CAS Google Scholar
• Miller RF. D-Serine as a glial modulator of nerve cells. Glia. 2004;47:275–83.
  PubMed Google Scholar
• Kim PM, Aizawa H, Kim PS, Huang AS, Wickramasinghe SR, Kashani AH, et al. Serine racemase: activation by glutamate neurotransmission via glutamate receptor interacting protein and mediation of neuronal migration. Proc Natl Acad Sci USA. 2005;102:2105–10.
  PubMed CAS Google Scholar
• Barakat L, Wang D, Bordey A. Carrier-mediated uptake and release of taurine from Bergmann glia in rat cerebellar slices. J Physiol. 2002;541:753–67.
  PubMed CAS Google Scholar
• Lafarga M, Berciano MT, Suarez I, Viadero CF, Andres MA, Berciano J. Cytology and organization of reactive astroglia in human cerebellar cortex with severe loss of granule cells: a study on the ataxic form of Creutzfeldt-Jakob disease. Neuroscience. 1991;40:337–52.
  PubMed CAS Google Scholar
• Pekny M, Nilsson M. Astrocyte activation and reactive gliosis. Glia. 2005;50:427–34.
  PubMed Google Scholar