References
Allam SL, Ghaderi VS, Bouteiller JMC, Legendre A, Nicolas A, Greget R, Bischoff S, Baudry M, Berger TW (2012) A computational model to investigate astrocytic glutamate uptake influence on synaptic transmission and neuronal spiking. Front Comput Neurosci 6:70
Allaman I, Belanger M, Magistretti PJ (2011) Astrocyte–neuron metabolic relationships: for better and for worse. Trends Neurosci 34(2):76–87
Allen NJ (2013) Role of glia in developmental synapse formation. Curr Opin Neurobiol 23(6):1027–1033
Alvarellos-González A, Pazos A, Porto-Pazos AB (2012) Computational models of neuron-astrocyte interactions lead to improved efficacy in the performance of neural networks. Comput Math Methods Med 2012:476,324
Amzica F, Massimini M, Manfridi A (2002) Spatial buffering during slow and paroxysmal sleep oscillations in cortical networks of glial cells in vivo. J Neurosci 22(3):1042–1053
Anderson WD, Makadia HK, Greenhalgh AD, Schwaber JS, David S, Vadigepalli R (2015) Computational modeling of cytokine signaling in microglia. Mol BioSyst 11(12):3332–3346
Arancibia-Carcamo IL, Ford MC, Cossell L, Ishida K, Tohyama K, Attwell D (2017) Node of Ranvier length as a potential regulator of myelinated axon conduction speed. elife 6:e23,329
Araque A, Parpura V, Sanzgiri RP, Haydon PG (1998) Glutamate-dependent astrocyte modulation of synaptic transmission between cultured hippocampal neurons. Eur J Neurosci 10:2129–2142
Araque A, Carmignoto G, Haydon PG, Oliet SHR, Robitaille R, Volterra A (2014) Gliotransmitters travel in time and space. Neuron 81(4):728–739
Attwell D, Buchan AM, Charpak S, Lauritzen M, MacVicar BA, Newman EA (2010) Glial and neuronal control of brain blood flow. Nature 468(7321):232–243
Bains JS, Oliet SHR (2007) Glia: they make your memories stick! Trends Neurosci 30(8):417–424
Barbour B (2001) An evaluation of synapse independence. J Neurosci 21(20):7969–7984
Bazargani N, Attwell D (2016) Astrocyte calcium signaling: The third wave. Nat Neurosci 19(2):182–189
Bazhenov M, Timofeev I, Steriade M, Sejnowski TJ (2004) Potassium model for slow (2–3 Hz) in vivo neocortical paroxysmal oscillations. J Neurophysiol 92(2):1116–1132
Beattie E, Stellwagen D, Morishita W, Bresnahan J, Ha B, Von Zastrow M, Beattie M, Malenka R (2002) Control of synaptic strength by glial TNFα. Science 295(5563):2282–2285
Bezzi P, Domercq M, Brambilla L, Galli R, Schols D, De Clercq E, Vescovi A, Bagetta G, Kollias G, Meldolesi J, Volterra A (2001) CXCR4-activated astrocyte glutamate release via TNFα: amplification by microglia triggers neurotoxicity. Nat Neurosci 4(7):702–710
Bienenstock E, Cooper L, Munro P (1982) Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex. J Neurosci 2(1):32–48
Bindocci E, Savtchouk I, Liaudet N, Becker D, Carriero G, Volterra A (2017) Three-dimensional Ca2+ imaging advances understanding of astrocyte biology. Science 356:6339
Brawek B, Garaschuk O (2017) Monitoring in vivo function of cortical microglia. Cell Calcium 64:109–117
Brawek B, Liang Y, Savitska D, Li K, Fomin-Thunemann N, Kovalchuk Y, Zirdum E, Jakobsson J, Garaschuk O (2017) A new approach for ratiometric in vivo calcium imaging of microglia. Sci Rep 7(1):6030
Brea J, Senn W, Pfister JP (2013) Matching recall and storage in sequence learning with spiking neural networks. J Neurosci 33(23):9565–9575
Breslin K, Wade JJ, Wong-Lin K, Harkin J, Flanagan B, Van Zalinge H, Hall S, Walker M, Verkhratsky A, McDaid L (2018) Potassium and sodium microdomains in thin astroglial processes: a computational model study. PLoS Comput Biol 14(5):e1006,151
Bullock T, Horridge GA (1965) Structure and function in the nervous systems of invertebrates. Freeman, San Francisco
Bushong EA, Martone ME, Jones YZ, Ellisman MH (2002) Protoplasmic astrocyte in CA1 stratum radiatum occupy separate anatomical domains. J Neurosci 22(1):183–192
Butt AM (2013) Structure and function of oligodendrocytes. In: Neuroglia. Oxford University Press, Oxford, pp 62–73
Carr CE, Konishi M (1990) A circuit for detection of interaural time differences in the brain stem of the barn owl. J Neurosci 10(10):3227–3246
Carr CE, Soares D (2002) Evolutionary convergence and shared computational principles in the auditory system. Brain Behav Evol 59(5–6):294–311
Carr CE, Soares D, Parameshwaran S, Perney T (2001) Evolution and development of time coding systems. Curr Opin Neurobiol 11(6):727–733
Castro MA, Beltrán FA, Brauchi S, Concha II (2009) A metabolic switch in brain: glucose and lactate metabolism modulation by ascorbic acid. J Neurochem 110(2):423–440
Chao CC, Hu S, Sheng WS, Peterson PK (1995) Tumor necrosis factor-alpha production by human fetal microglial cells: regulation by other cytokines. Dev Neurosci 17(2):97–105
Chao TI, Rickmann M, Wolff JR (2002) The synapse-astrocyte boundary: an anatomical basis for an integrative role of glia in synaptic transmission. In: Volterra A, Magistretti PJ, Haydon PG (eds) The tripartite synapse: glia in synaptic transmission. Oxford University Press, New York, chap 1, pp 3–23
Chen N, Sugihara H, Sharma J, Perea G, Petravicz J, Le C, Sur M (2012) Nucleus basalis enabled stimulus specific plasticity in the visual cortex is mediated by astrocytes. Proc Natl Acad Sci U S A 109(41):E2832–E2841
Chever O, Djukic B, McCarthy KD, Amzica F (2010) Implication of Kir4.1 channel in excess potassium clearance: an in vivo study on anesthetized glial-conditional Kir4.1 knock-out mice. J Neurosci 30(47):15,769–15,777
Chvátal A, Anděrová M, Kirchhoff F (2007) Three-dimensional confocal morphometry–a new approach for studying dynamic changes in cell morphology in brain slices. J Anat 210(6):671–683
Clarke LE, Barres BA (2013) Emerging roles of astrocytes in neural circuit development. Nat Rev Neurosci 14(5):311–321
Clements JD (1996) Transmitter timecourse in the synaptic cleft: its role in central synaptic function. Trends Neurosci 19(5):163–171
Covelo A, Araque A (2018) Neuronal activity determines distinct gliotransmitter release from a single astrocyte. elife 7:e32,237
Cui Y, Yang Y, Ni Z, Dong Y, Cai G, Foncelle A, Ma S, Sang K, Tang S, Li Y, Berry H, Shengzi W, Hailan H (2018) Astroglial Kir4.1 in the lateral habenula drives neuronal bursts in depression. Nature 554(7692):323
D’Ambrosio R, Gordon DS, Winn HR (2002) Differential role of KIR channel and Na+/K+-pump in the regulation of extracellular K+ in rat hippocampus. J Neurophysiol 87(1):87–102
Danbolt NC (2001) Glutamate uptake. Prog Neurobiol 65:1–105
Danbolt NC, Lehre KP, Dehnes Y, Ullensvang K (2002) Transporters for synaptic transmitter on the glial cell plasma membrane. In: Volterra A, Magistretti PJ, Haydon PG (eds) The tripartite synapse: glia in synaptic transmission. Oxford University Press, New York, chap 1, pp 47–61
De Pittà M (2019) Gliotransmitter exocytosis and its consequences on synaptic transmission. In: De Pittà M, Berry H (eds) Computational glioscience. Springer, Cham, Switzerland, chap 10, pp 245–287
De Pittà M, Berry H (2019a) Computational glioscience. Springer, Cham, Switzerland
De Pittà M, Berry H (2019b) A neuron–glial perspective for computational neuroscience. In: De Pittà M, Berry H (eds) Computational glioscience. Springer, Cham, Switzerland, chap 1, pp 3–35
De Pittà M, Brunel N (2016) Modulation of synaptic plasticity by glutamatergic gliotransmission: a modeling study. Neural Plast 2016:7607924
De Pittà M, Volman V, Berry H, Ben-Jacob E (2011) A tale of two stories: astrocyte regulation of synaptic depression and facilitation. PLoS Comput Biol 7(12):e1002,293
De Pittà M, Brunel N, Volterra A (2015) Astrocytes: orchestrating synaptic plasticity? Neuroscience 323:43–61
Debanne D, Campanac E, Bialowas A, Carlier E, Alcaraz G (2011) Axon physiology. Physiol Rev 91(2):555–602
Deitmer JW, Rose CR (1996) pH regulation and proton signalling by glial cells. Prog Neurobiol 48(2):73–103
Di Castro M, Chuquet J, Liaudet N, Bhaukaurally K, Santello M, Bouvier D, Tiret P, Volterra A (2011) Local Ca2+ detection and modulation of synaptic release by astrocytes. Nat Neurosci 14:1276–1284
Diamond JS (2005) Deriving the glutamate clearance time course from transporter currents in CA1 hippocampal astrocytes: transmitter uptake gets faster during development. J Neurosci 25(11):2906–2916
Dringen R (2000) Metabolism and functions of glutathione in brain. Prog Neurobiol 62(6):649–671
Durkee CA, Covelo A, Lines J, Kofuji P, Aguilar J, Araque A (2019) Gi/o protein-coupled receptors inhibit neurons but activate astrocytes and stimulate gliotransmission. Glia 67(6):1076–1093
Ermentrout GB, Terman DH (2010) Mathematical foundations of neuroscience. Springer, New York
Eroglu C, Barres BA (2010) Regulation of synaptic connectivity by glia. Nature 468(7321):223–231
Fellin T, Pascual O, Gobbo S, Pozzan T, Haydon PG, Carmignoto G (2004) Neuronal synchrony mediated by astrocytic glutamate through activation of extrasynaptic NMDA receptors. Neuron 43:729–743
Fields RD (2008) White matter in learning, cognition and psychiatric disorders. Trends Neurosci 31(7):361–370
Fields RD, Woo DH, Basser PJ (2015) Glial regulation of the neuronal connectome through local and long-distant communication. Neuron 86(2):374–386
FitzHugh R (1962) Computation of impulse initiation and saltatory conduction in a myelinated nerve fiber. Biophys J 2(1):11–21
Flanagan B, McDaid L, Wade J, Wong-Lin K, Harkin J (2018) A computational study of astrocytic glutamate influence on post-synaptic neuronal excitability. PLoS Comput Biol 14(4):e1006040
Florence CM, Baillie LD, Mulligan SJ (2012) Dynamic volume changes in astrocytes are an intrinsic phenomenon mediated by bicarbonate ion flux. PLoS One 7(11):e51,124
Ford MC, Alexandrova O, Cossell L, Stange-Marten A, Sinclair J, Kopp-Scheinpflug C, Pecka M, Attwell D, Grothe B (2015) Tuning of Ranvier node and internode properties in myelinated axons to adjust action potential timing. Nat Commun 6:8073
Fourcaud-Trocmé N, Hansel D, van Vreeswijk C, Brunel N (2003) How spike generation mechanisms determine the neuronal response to fluctuating inputs. J Neurosci 23(37):11,628–11,640
Franze K, Grosche J, Skatchkov SN, Schinkinger S, Foja C, Schild D, Uckermann O, Travis K, Reichenbach A, Guck J (2007) Müller cells are living optical fibers in the vertebrate retina. Proc Natl Acad Sci 104(20):8287–8292
Funahashi S, Bruce CJ, Goldman-Rakic PS (1989) Mnemonic coding of visual space in the monkey’s dorsolateral prefrontal cortex. J Neurophysiol 61(2):331–349
Garnier A, Vidal A, Benali H (2016) A theoretical study on the role of astrocytic activity in neuronal hyperexcitability by a novel neuron-glia mass model. J Math Neurosci 6(1):10
Gerstner W, Kistler WM (2002) Mathematical formulations of Hebbian learning. Biol Cybern 87(5–6):404–415
Goldman L, Albus JS (1968) Computation of impulse conduction in myelinated fibers; theoretical basis of the velocity-diameter relation. Biophys J 8(5):596–607
Goldman-Rakic PS (1995) Cellular basis of working memory. Neuron 14(3):477–485
Gordon G, Baimoukhametova D, Hewitt S, Rajapaksha W, Fisher T, Bains J (2005) Norepinephrine triggers release of glial ATP to increase postsynaptic efficacy. Nat Neurosci 8(8):1078–1086
Gordon GRJ, Choi HB, Rungta RL, Ellis-Davies GCR, MacVicar BA (2008) Brain metabolism dictates the polarity of astrocyte control over arterioles. Nature 456(7223):745
Götz M (2013) Radial glial cells. In: Neuroglia. Oxford University Press, Oxford, pp 50–61
Haber M, Zhou L, Murai KK (2006) Cooperative astrocyte and dendritic spine dynamics at hippocampal excitatory synapses. J Neurosci 26(35):8881–8891
Halassa MM, Fellin T, Takano H, Dong JH, Haydon PG (2007) Synaptic islands defined by the territory of a single astrocyte. J Neurosci 27(24):6473–6477
Halter JA, Clark JW Jr (1991) A distributed-parameter model of the myelinated nerve fiber. J Theor Biol 148(3):345–382
Hama K, Arii T, Katayama E, Martone M, Ellisman MH (2004) Tri-dimensional morphometric analysis of astrocytic processes with high voltage electron microscopy of thick Golgi preparations. J Neurocytol 33:277–285
Han X, Chen M, Wang F, Windrem M, Wang S, Shanz S, Xu Q, Oberheim NA, Bekar L, Betstadt S, Silva AJ, Takano T, Goldman SA, Nedergaard M (2013) Forebrain engraftment by human glial progenitor cells enhances synaptic plasticity and learning in adult mice. Cell Stem Cell 12(3):342–353
Hartline DK (2011) The evolutionary origins of glia. Glia 59(9):1215–1236
Henneberger C, Papouin T, Oliet SHR, Rusakov DA (2010) Long-term potentiation depends on release of D-serine from astrocytes. Nature 463:232–237
Herculano-Houzel S (2014) The glia/neuron ratio: how it varies uniformly across brain structures and species and what that means for brain physiology and evolution. Glia 62(9):1377–1391
Hirase H, Qian L, Barthó P, Buzsáki G (2004) Calcium dynamics of cortical astrocytic networks in vivo. PLoS Biol 2(4):0494–0496
Hua JY, Smith SJ (2004) Neural activity and the dynamics of central nervous system development. Nat Neurosci 7(4):327
Huang YH, Bergles DE (2004) Glutamate transporters bring competition to the synapse. Curr Opin Neurobiol 14(3):346–352
Hughes EG, Orthmann-Murphy JL, Langseth AJ, Bergles DE (2018) Myelin remodeling through experience-dependent oligodendrogenesis in the adult somatosensory cortex. Nat Neurosci 21:696–706
Jadhav AP, Roesch K, Cepko CL (2009) Development and neurogenic potential of müller glial cells in the vertebrate retina. Prog Retin Eye Res 28(4):249–262
James G, Butt AM (2001) P2X and P2Y purinoreceptors mediate ATP-evoked calcium signalling in optic nerve glia in situ. Cell Calcium 30(4):251–259
Kakegawa W, Miyoshi Y, Hamase K, Matsuda S, Matsuda K, Kohda K, Emi K, Motohashi J, Konno R, Zaitsu K, Yuzaki M (2011) D-serine regulates cerebellar LTD and motor coordination through the δ2 glutamate receptor. Nat Neurosci 14(5):603–611
Kaneko M, Stellwagen D, Malenka RC, Stryker MP (2008) Tumor necrosis factor-alpha mediates one component of competitive, experience-dependent plasticity in developing visual cortex. Neuron 58:673–680
Kaschube M, Schnabel M, Löwel S, Coppola DM, White LE, Wolf F (2010) Universality in the evolution of orientation columns in the visual cortex. Science 330(6007):1113–1116
Kasthuri N, Hayworth K, Berger DR, Schalek RL, Conchello JA, Knowles-Barley S, Lee D, Vázquez-Reina A, Kaynig V, Jones TR, Roberts M, Lyskowski JM, Tapia HS, Seung JC, Roncal WG, Vogelstein JT, Burns R, Sussman DL, Priebe CE, Pfister H, Lichtman JW (2015) Saturated reconstruction of a volume of neocortex. Cell 162(3):648–661
Kettenmann H, Ransom BR (2013) Neuroglia, 3rd edn. Oxford University Press, Oxford
Kettenmann H, Kirchhoff F, Verkhratsky A (2013) Microglia: new roles for the synaptic stripper. Neuron 77(1):10–18
Kimura F, Itami C (2009) Myelination and isochronicity in neural networks. Front Neuroanat 3:12
Kinney GA, Spain WJ (2002) Synaptically evoked GABA transporter currents in neocortical glia. J Neurophysiol 88(6):2899–2908
Kinney JP, Spacek J, Bartol TM, Bajaj CL, Harris KM, Sejnowski TJ (2013) Extracellular sheets and tunnels modulate glutamate diffusion in hippocampal neuropil. J Comp Neurol 521(2):448–464
Kirov SA, Sorra KE, Harris KM (1999) Slices have more synapses than perfusion-fixed hippocampus from both young and mature rats. J Neurosci 19(8):2876–2886
Kisvárday ZF, Toth E, Rausch M, Eysel UT (1997) Orientation-specific relationship between populations of excitatory and inhibitory lateral connections in the visual cortex of the cat. Cereb Cortex 7(7):605–618
Kofuji P, Newman EA (2004) Potassium buffering in the central nervous system. Neuroscience 129(4):1043–1054
Kuga N, Sasaki T, Takahara Y, Matsuki N, Ikegaya Y (2011) Large-scale calcium waves traveling through astrocytic networks in vivo. J Neurosci 31(7):2607–2614
Labin AM, Ribak EN (2010) Retinal glial cells enhance human vision acuity. Phys Rev Lett 104(15):158,102
Labin AM, Safuri SK, Ribak EN, Perlman I (2014) Müller cells separate between wavelengths to improve day vision with minimal effect upon night vision. Nat Commun 5:4319
Laming PR, Kimelberg H, Robinson S, Salm A, Hawrylak N, Müller C, Roots B, Ng K (2000) Neuronal-glial interactions and behaviour. Neurosci Biobehav Rev 24:295–340
Langer J, Stephan J, Theis M, Rose CR (2012) Gap junctions mediate intercellular spread of sodium between hippocampal astrocytes in situ. Glia 60(2):239–252
Larsen BR, Assentoft M, Cotrina ML, Hua SZ, Nedergaard M, Kaila K, Voipio J, MacAulay N (2014) Contributions of the Na+/K+-ATPase, NKCC1, and Kir4.1 to hippocampal K+ clearance and volume responses. Glia 62(4):608–622
Larter R, Craig MG (2005) Glutamate-induced glutamate release: a proposed mechanism for calcium bursting in astrocytes. Chaos 15:047,511
Lawson LJ, Perry VH, Dri P, Gordon S (1990) Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain. Neuroscience 39(1):151–170
Le Meur K, Mendizabal-Zubiaga J, Grandes P, Audinat E (2012) GABA release by hippocampal astrocytes. Front Comput Neurosci 6:59
Lewitus GM, Pribiag H, Duseja R, St-Hilaire M, Stellwagen D (2014) An adaptive role of TNFα in the regulation of striatal synapses. J Neurosci 34(18):6146–6155
López-Hidalgo M, Hoover WB, Schummers J (2016) Spatial organization of astrocytes in ferret visual cortex. J Comp Neurol 524(17):3561–3576
Markram H, Lübke J, Frotscher M, Roth A, Sakmann B (1997) Physiology and anatomy of synaptic connections between thick tufted pyramidal neurones in the developing rat neocortex. J Physiol 500(2):409–440
Masland RH (2001) The fundamental plan of the retina. Nat Neurosci 4(9):877
Mathiisen TM, Lehre KP, Danbolt NC, Ottersen OP (2010) The perivascular astroglial sheath provides a complete covering of the brain microvessels: an electron microscopic 3D reconstruction. Glia 58(9):1094–1103
Matsuzaki M, Ellis-Davies G, Nemoto T, Miyashita Y, Iino M, Kasai H (2001) Dendritic spine geometry is critical for AMPA receptor expression in hippocampal CA1 pyramidal neurons. Nat Neurosci 4(11):1086–1092
Matyash V, Kettenmann H (2010) Heterogeneity in astrocyte morphology and physiology. Brain Res Rev 63(1–2):2–10
May JM (2012) Vitamin C transport and its role in the central nervous system. In: Stanger O (ed) Water soluble vitamins. Springer, Dordrecht, pp 85–103
McAlpine D, Grothe B (2003) Sound localization and delay lines–do mammals fit the model? Trends Neurosci 26(7):347–350
McCormick DA, Shu Y, Hasenstaub A, Sanchez-Vives M, Badoual M, Bal T (2003) Persistent cortical activity: mechanisms of generation and effects on neuronal excitability. Cereb Cortex 13(11):1219–1231
Medvedev N, Popov V, Henneberger C, Kraev I, Rusakov DA, Stewart MG (2014) Glia selectively approach synapses on thin dendritic spines. Philos Trans R Soc B 369(1654):20140,047
Mesejo P, Ibánez O, Fernández-Blanco E, Cedrón F, Pazos A, Porto-Pazos AB (2015) Artificial neuron–glia networks learning approach based on cooperative coevolution. Int J Neural Syst 25(04):1550,012
Molofsky AV, Kelley KW, Tsai HH, Redmond SA, Chang SM, Madireddy L, Chan JR, Baranzini SE, Ullian EM, Rowitch DH (2014) Astrocyte-encoded positional cues maintain sensorimotor circuit integrity. Nature 509(7499):189
Moore JW, Joyner RW, Brill MH, Waxman SD, Najar-Joa M (1978) Simulations of conduction in uniform myelinated fibers. Relative sensitivity to changes in nodal and internodal parameters. Biophys J 21(2):147–160
Mulligan S, MacVicar B (2004) Calcium transients in astrocyte endfeet cause cerebrovascular constrictions. Nature 431(7005):195–199
Navarrete M, Perea G, de Sevilla D, Gómez-Gonzalo M, Núñez A, Martín E, Araque A (2012) Astrocytes mediate in vivo cholinergic-induced synaptic plasticity. PLoS Biol 10(2):e1001,259
Navarrete M, Díez A, Araque A (2014) Astrocytes in endocannabinoid signalling. Philos Trans R Soc B 369(1654):20130,599
Nave KA (2010) Myelination and support of axonal integrity by glia. Nature 468(7321):244
Nimmerjahn A, Kirchhoff F, Kerr JND, Helmchen F (2004) Sulforhodamine 101 as a specific marker of astroglia in the neocortex in vivo. Nat Methods 1:31–37
Nimmerjahn A, Kirchhoff F, Helmchen F (2005) Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo. Science 308(5726):1314–1318
Oberheim NA, Takano T, Han X, He W, Lin JHC, Wang F, Xu Q, Wyatt JD, Pilcher W, Ojemann JG, Ransom BR, Goldman SA, Nedergaard M (2009) Uniquely hominid features of adult human astrocytes. J Neurosci 29(10):3276–3287
O’Connor DH, Wittenberg GM, Wang SSH (2005) Graded bidirectional synaptic plasticity is composed of switch-like unitary events. Proc Natl Acad Sci 102(27):9679–9684
Ogata K, Kosaka T (2002) Structural and quantitative analysis of astrocytes in the mouse hippocampus. Neuroscience 113(1):221–233
Ohki K, Chung S, Ch’ng YH, Kara P, Reid RC (2005) Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex. Nature 433(7026):597
Otsu Y, Couchman K, Lyons DG, Collot M, Agarwal A, Mallet JM, Pfrieger FW, Bergles DE, Charpak S (2015) Calcium dynamics in astrocyte processes during neurovascular coupling. Nat Neurosci 18(2):210
Øyehaug L, Østby I, Lloyd CM, Omholt SW, Einevoll GT (2012) Dependence of spontaneous neuronal firing and depolarisation block on astroglial membrane transport mechanisms. J Comput Neurosci 32(1):147–165
Panatier A, Theodosis DT, Mothet JP, Touquet B, Pollegioni L, Poulain DA, Oliet SH (2006) Glia-derived d-serine controls NMDA receptor activity and synaptic memory. Cell 125:775–784
Pascual O, Ben Achour S, Rostaing P, Triller A, Bessis A (2011) Microglia activation triggers astrocyte-mediated modulation of excitatory neurotransmission. Proc Natl Acad Sci:1–9
Pelvig DP, Pakkenberg H, Stark AK, Pakkenberg B (2008) Neocortical glial cell numbers in human brains. Neurobiol Aging 29(11):1754–1762
Perea G, Araque A (2007) Astrocytes potentiate transmitter release at single hippocampal synapses. Science 317:1083–1086
Perea G, Yang A, Boyden ES, Sur M (2014) Optogenetic astrocyte activation modulates response selectivity of visual cortex neurons in vivo. Nat Commun 5:ncomms4262
Perez-Alvarez A, Navarrete M, Covelo A, Martin ED, Araque A (2014) Structural and functional plasticity of astrocyte processes and dendritic spine interactions. J Neurosci 34(38):12,738–12,744
Philips RT, Sur M, Chakravarthy VS (2017) The influence of astrocytes on the width of orientation hypercolumns in visual cortex: a computational perspective. PLoS Comput Biol 13(10):e1005,785
Porto-Pazos AB, Veiguela N, Mesejo P, Navarrete M, Alvarellos A, Ibáñez O, Pazos A, Araque A (2011) Artificial astrocytes improve neural network performance. PLoS One 6(4):e19,109
Pósfai B, Cserép C, Orsolits B, Dénes Á (2019) New insights into microglia–neuron interactions: a neuron’s perspective. Neuroscience 405:103–117
Pribiag H, Stellwagen D (2013) TNF-α downregulates inhibitory neurotransmission through protein phosphatase 1-dependent trafficking of GABAA receptors. J Neurosci 33(40):15,879–15,893
Ransom CB, Ransom BR, Sontheimer H (2000) Activity-dependent extracellular K+ accumulation in rat optic nerve: the role of glial and axonal Na+ pumps. J Physiol 522(3):427–442
Reichenbach A, Robinson SR (1995) Phylogenetic constraints on retinal organisation and development. Prog Retin Eye Res 15(1):139–171
Reichenbach A, Wolburg H (2013) Astrocytes and ependymal glia. In: Neuroglia. Oxford University Press, Oxford, pp 35–49
Reichenbach A, Derouiche A, Kirchhoff F (2010) Morphology and dynamics of perisynaptic glia. Brain Res Rev 63(1):11–25
Richardson AG, McIntyre CC, Grill WM (2000) Modelling the effects of electric fields on nerve fibres: influence of the myelin sheath. Med Biol Eng Comput 38(4):438–446
Rothman DL, Behar KL, Hyder F, Shulman RG (2003) In vivo NMR studies of the glutamate neurotransmitter flux and neuroenergetics: implications for brain function. Annu Rev Physiol 65(1):401–427
Rothstein JD, Dykes-Hoberg M, Pardo CA, Bristol LA, Jin L, Kuncl RW, Kanai Y, Hediger MA, Wang Y, Schielke JP, , Welty DF (1996) Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate. Neuron 16(3):675–686
Roxin A, Montbrió E (2011) How effective delays shape oscillatory dynamics in neuronal networks. Physica D: Nonlinear Phenomena 240(3):323–345
Roxin A, Brunel N, Hansel D (2005) Role of delays in shaping spatiotemporal dynamics of neuronal activity in large networks. Phys Rev Lett 94(23):238,103
Rusakov DA (2015) Disentangling calcium-driven astrocyte physiology. Nat Rev Neurosci 16:226–233
Sahlender DA, Savtchouk I, Volterra A (2014) What do we know about gliotransmitter release from astrocytes? Philos Trans R Soc B 369:20130,592
Sanchez-Vives MV, McCormick DA (2000) Cellular and network mechanisms of rhythmic recurrent activity in neocortex. Nat Neurosci 3(10):1027
Santello M, Volterra A (2012) TNFα in synaptic function: switching gears. Trends Neurosci 35(10):638–647
Santello M, Bezzi P, Volterra A (2011) TNFα controls glutamatergic gliotransmission in the hippocampal dentate gyrus. Neuron 69:988–1001
Sasaki T, Matsuki N, Ikegaya Y (2011) Action-potential modulation during axonal conduction. Science 331(6017):599–601
Savin C, Triesch J, Meyer-Hermann M (2009) Epileptogenesis due to glia-mediated synaptic scaling. J R Soc Interface 6(37):655–668
Savtchenko LP, Rusakov DA (2014) Regulation of rhythm genesis by volume-limited, astroglia-like signals in neural networks. Phil Trans Royal Soc B: Biological Sciences 369(1654):20130,614
Savtchouk I, Volterra A (2018) Gliotransmission: beyond black-and-white. J Neurosci 38(1):14–25
Scemes E, Giaume C (2006) Astrocyte calcium waves: What they are and what they do. Glia 54:716–725
Schummers J, Yu H, Sur M (2008) Tuned responses of astrocytes and their influence on hemodynamic signals in the visual cortex. Sci STKE 320(5883):1638
Seidl AH, Rubel EW, Harris DM (2010) Mechanisms for adjusting interaural time differences to achieve binaural coincidence detection. J Neurosci 30(1):70–80
Seifert G, Steinhäuser C (2017) Heterogeneity and function of hippocampal macroglia. Cell Tissue Res 373:1–18
Seung HS, Lee DD, Reis BY, Tank DW (2000) The autapse: a simple illustration of short-term analog memory storage by tuned synaptic feedback. J Comput Neurosci 9(2):171–185
Sibson NR, Dhankhar A, Mason GF, Behar KL, Rothman DL, Shulman RG (1997) In vivo 13C NMR measurements of cerebral glutamine synthesis as evidence for glutamate–glutamine cycling. Proc Natl Acad Sci 94(6):2699–2704
Somjen GG, Kager H, Wadman WJ (2008) Computer simulations of neuron-glia interactions mediated by ion flux. J Comput Neurosci 25(2):349–365
Stassart R, Goebbels S, Nave KA (2013) Factors controlling myelin formation. In: Neuroglia. Oxford University Press, Oxford, pp 555–572
Steinmetz CC, Turrigiano GG (2010) Tumor necrosis factor-α signaling maintains the ability of cortical synapses to express synaptic scaling. J Neurosci 30(44):14,685–14,690
Stellwagen D, Malenka RC (2006) Synaptic scaling mediated by glial TNF-α. Nature 440(7087):1054–1059
Stellwagen D, Beattie EC, Seo JY, Malenka RC (2005) Differential regulation of AMPA receptor and GABA receptor trafficking by tumor necrosis factor-α. J Neurosci 25(12):3219–3228
Stevens JLR, Law JS, Antolík J, Bednar JA (2013) Mechanisms for stable, robust, and adaptive development of orientation maps in the primary visual cortex. J Neurosci 33(40):15,747–15,766
Stobart JL, Ferrari KD, Barrett MJP, Glück C, Stobart MJ, Zuend M, Weber B (2018) Cortical circuit activity evokes rapid astrocyte calcium signals on a similar timescale to neurons. Neuron 98:726–735
Takata N, Mishima T, Hisatsune C, Nagai T, Ebisui E, Mikoshiba K, Hirase H (2011) Astrocyte calcium signaling transforms cholinergic modulation to cortical plasticity in vivo. J Neurosci 31(49):18,155–18,165
Tang F, Lane S, Korsak A, Paton JFR, Gourine AV, Kasparov S, Teschemacher AG (2014) Lactate-mediated glia-neuronal signalling in the mammalian brain. Nat Commun 5:3284
Tomassy GS, Berger DR, Chen H, Kasthuri N, Hayworth KJ, Vercelli A, Seung HS, Lichtman JW, Arlotta P (2014) Distinct profiles of myelin distribution along single axons of pyramidal neurons in the neocortex. Science 344(6181):319–324
Tomassy GS, Dershowitz LB, Arlotta P (2016) Diversity matters: A revised guide to myelination. Trends Cell Biol 26(2):135–147
Toyoizumi T, Kaneko M, Stryker MP, Miller KD (2014) Modeling the dynamic interaction of Hebbian and homeostatic plasticity. Neuron 84(2):497–510
Tuchin V (2000) Tissue optics. SPIE Press, Bellingham
Ullah G, Cressman JR Jr, Barreto E, Schiff SJ (2009) The influence of sodium and potassium dynamics on excitability, seizures, and the stability of persistent states: II. Network and glial dynamics. J Comput Neurosci 26(2):171–183
Ullén F (2009) Is activity regulation of late myelination a plastic mechanism in the human nervous system? Neuron Glia Biol 5(1–2):29–34
Ventura R, Harris KM (1999) Three-dimensional relationships between hippocampal synapses and astrocytes. J Neurosci 19(16):6897–6906
Verkhratsky A, Nedergaard M (2016) The homeostatic astroglia emerges from evolutionary specialization of neural cells. Philos Trans R Soc B 371(1700):20150,428
Volman V, Ben-Jacob E, Levine H (2007) The astrocyte as a gatekeeper of synaptic information transfer. Neural Comput 19:303–326
Volman V, Bazhenov M, Sejnowski TJ (2013) Divide and conquer: Functional segregation of synaptic inputs by astrocytic microdomains could alleviate paroxysmal activity following brain trauma. PLoS Comput Biol 9(1):e1002,856
Volterra A, Liaudet N, Savtchouk I (2014) Astrocyte Ca2+ signalling: an unexpected complexity. Nat Rev Neurosci 15:327–334
Wade JJ, McDaid LJ, Harkin J, Crunelli V, Kelso JAS (2011) Bidirectional coupling between astrocytes and neurons mediates learning and dynamic coordination in the brain: a multiple modeling approach. PLoS One 6(12):e29,445
Wang F, Smith NA, Xu Q, Fujita T, Baba A, Matsuda T, Takano T, Bekar L, Nedergaard M (2012a) Astrocytes modulate neural network activity by Ca2+-dependent uptake of extracellular K+. Sci Signal 5(218):ra26
Wang F, Xu Q, Wang W, Takano T, Nedergaard M (2012b) Bergmann glia modulate cerebellar purkinje cell bistability via Ca2+-dependent K+ uptake. Proc Natl Acad Sci U S A 109(20):7911–7916
Wang X, Lou N, Xu Q, Tian GF, Peng WG, Han X, Kang J, Takano T, Nedergaard M (2006) Astrocytic Ca2+ signaling evoked by sensory stimulation in vivo. Nat Neurosci 9(6):816–823
Waxman SG (1980) Determinants of conduction velocity in myelinated nerve fibers. Muscle Nerve 3(2):141–150
Wiesel TN (1982) Postnatal development of the visual cortex and the influence of environment. Nature 299(5884):583
Winship I, Plaa N, Murphy T (2007) Rapid astrocyte calcium signals correlate with neuronal activity and onset of the hemodynamic response in vivo. J Neurosci 27(23):6268–6272
Wu Y, Dissing-Olesen L, MacVicar BA, Stevens B (2015) Microglia: dynamic mediators of synapse development and plasticity. Trends Immunol 36(10):605–613
Xiang J, Ennis SR, Abdelkarim GE, Fujisawa M, Kawai N, Keep RF (2003) Glutamine transport at the blood–brain and blood–cerebrospinal fluid barriers. Neurochem Int 43(4–5):279–288
Yamazaki Y, Hozumi Y, Kaneko K, Sugihara T, Fujii S, Goto K, Kato H (2007) Modulatory effects of oligodendrocytes on the conduction velocity of action potentials along axons in the alveus of the rat hippocampal CA1 region. Neuron Glia Biol 3(4):325–334
Yang Y, Ge W, Chen Y, Zhang Z, Shen W, Wu C, Poo M, Duan S (2003) Contribution of astrocytes to hippocampal long-term potentiation through release of D-serine. Proc Natl Acad Sci U S A 100(25):15,194–15,199
Zalc B, Colman DR (2000) Origins of vertebrate success. Science 288(5464):271–271
Zenke F, Gerstner W, Ganguli S (2017) The temporal paradox of Hebbian learning and homeostatic plasticity. Curr Opin Neurobiol 43:166–176
Zhang Z, Gong N, Wang W, Xu L, Xu T (2008) Bell-shaped D-serine actions on hippocampal long-term depression and spatial memory retrieval. Cereb Cortex 18(10):2391–2401
Zonta M, Angulo MC, Gobbo S, Rosengarten B, Hossmann KA, Pozzan T, Carmignoto G (2003) Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation. Nat Neurosci 6:43–40
Acknowledgments
Writing of this chapter was made possible by the generous support of the Junior Leader Fellowship Program by “la Caixa” Banking Foundation (LCF/BQ/LI18/11630006), as well as by the support of the Basque Government through the BERC 2018–2012 program, and by the Spanish Ministry of Science, Innovation and Universities: BCAM Severo Ochoa Accreditation SEV-2017-0718.
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De Pittà, M. (2020). Neuron-Glial Interactions. In: Jaeger, D., Jung, R. (eds) Encyclopedia of Computational Neuroscience. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-7320-6_100691-1
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