Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- α:
-
Extracellular volume fraction
- ADC:
-
Apparent diffusion coefficient
- ADCw:
-
Apparent diffusion coefficient of water
- AMPA:
-
α-Amino-3-hydroxy-5-metyl-isoxazol-4-propionic acid
- CNS:
-
Central nervous system
- CSPG:
-
Chondroitin-sulphate proteoglycan
- D:
-
Diffusion coefficient
- dpw:
-
Day post wounding
- DW-MRI:
-
Diffusion-weighted magnetic resonance imaging
- EAE:
-
Experimental autoimmune encephalomyelitis
- ECM:
-
Extracellular matrix
- ECS:
-
Extracellular space
- GABA:
-
γ-Aminobutyric acid
- GFAP:
-
Glial fibrillary acidic protein
- IOS:
-
Intrinsic optical signals
- ISM:
-
Ion-selective microelectrode
- k':
-
Nonspecific cellular uptake
- [K+]e:
-
Extracellular concentration of potassium ions
- λ :
-
Tortuosity
- NMDA:
-
N-methyl-d-aspartate
- pHe:
-
Extracellular pH
- pHi:
-
Intracellular pH
- RVD:
-
Regulatory volume decrease
- TEA:
-
Tetraethylammonium
- TMA:
-
Tetramethylammonium
- TN:
-
Tenascin
- WHO:
-
World Health Organization
References
Agnati LF, Zoli M, Stromberg I, Fuxe K (1995) Intercellular communication in the brain: Wiring versus volume transmission. Neurosci 69:711–726
Alberts B, Bray D, Lewis J, Raff M, Roberts K, Watson JD (1994) Molecular Biology of the Cell. Garland Science New York
Andrew RD, Jarvis CR, Obeidat AS (1999) Potential sources of intrinsic optical signals imaged in live brain slices. Methods Enzymol 18:185–196
Araque A, Parpura V, Sanzgiri RP, Haydon PG (1999) Tripartite synapses: Glia, the unacknowledged partner. Trends Neurosci 22:208–215
Astion ML, Chvatal A, Orkand RK (1989) Na+./H+ exchange in glial cells of Necturus optic nerve Neurosci Lett 107:167–172
Astion ML, Chvatal A, Orkand RK (1991) Further studies of electrogenic Na+. /HCO3 − cotransport in glial cells of Necturus optic nerve: regulation of pHi Glia 4:461–468
Berger T, Schnitzer J, Kettenmann H (1991) Developmental changes in the membrane current pattern, K+. buffer capacity, and morphology of glial cells in the corpus callosum slice J Neurosci 11:3008–3024
Bonfanti L, Poulain DA, Theodosis DT (1993) Radial glia-like cells in the supraoptic nucleus of the adult rat. J Neuroendocrinol 5:1–5
Camby I, Belot N, Lefranc F, Sadeghi N, de Launoit Y, Kaltner H, Musette S, Darro F, Danguy A, Salmon I, Gabius HJ, Kiss R (2002) Galectin-1 modulates human glioblastoma cell migration into the brain through modifications to the actin cytoskeleton and levels of expression of small GTPases. J Neuropathol Exp Neurol 61:585–596
Cardin V, Lezama R, Torres-Marquez ME, Pasantes-Morales H (2003) Potentiation of the osmosensitive taurine release and cell volume regulation by cytosolic Ca2+. rise in cultured cerebellar astrocytes Glia 44:119–128
Celio MR, Spreafico R, De Biasi S, Vitellaro-Zuccarello L (1998) Perineuronal nets: past and present. Trends Neurosci 21:510–515
Chesler M (1987) pH regulation in the vertebrate central nervous system: microelectrode studies in the brain stem of the lamprey. Can J Physiol Pharmacol 65:986–993
Chvatal A, Pastor A, Mauch M, Sykova E, Kettenmann H (1995) Distinct populations of identified glial cells in the developing rat spinal cord slice: ion channel properties and cell morphology. Eur J Neurosci 7:129–142
Chvatal A, Berger T, Vorisek I, Orkand RK, Kettenmann H, Sykova E (1997) Changes in glial K+ currents with decreased extracellular volume in developing rat white matter. J Neurosci Res 49:98–106
Chvatal A, Anderova M, Ziak D, Sykova E (1999) Glial depolarization evokes a larger potassium accumulation around oligodendrocytes than around astrocytes in gray matter of rat spinal cord slices. J Neurosci Res 56:493–505
Chvatal A, Anderova M, Sykova E (2004) Analysis of K+. accumulation reveals privileged extracellular region in the vicinity of glial cells in situ J Neurosci Res 78:668–682
Chvatal A, Anderova M, Hock M, Prajerova I, Neprasova H, Chvatal V, Kirchhoff F, Sykova E (2007) Three-dimensional confocal morphometry reveals structural changes in astrocyte morphology in situ. J Neurosci Res 85:260–271
Coles JA, Orkand RK (1983) Modification of potassium movement through the retina of the drone (Apis mellifera male) by glial uptake. J Physiol 340:157–174
Cserr HF, DePasquale M, Nicholson C, Patlak CS, Pettigrew KD, Rice ME (1991) Extracellular volume decreases while cell volume is maintained by ion uptake in rat brain during acute hypernatremia. J Physiol 442:277–295
Deitmer JW, Schlue WR (1987) The regulation of intracellular pH by identified glial cells and neurones in the central nervous system of the leech. J Physiol 388:261–283
Dityatev A, Schachner M (2003) Extracellular matrix molecules and synaptic plasticity. Nat Rev Neurosci 4:456–468
Fuxe K, Agnati LF (1991) Volume Transmission in the Brain: Novel Mechanisms for Neural Transmission. Raven PressNew York
Gold R, Linington C, Lassmann H (2006) Understanding pathogenesis and therapy of multiple sclerosis via animal models: 70 years of merits and culprits in experimental autoimmune encephalomyelitis research. Brain 129:1953–1971
Gullans SR, Verbalis JG (1993) Control of brain volume during hyperosmolar and hypoosmolar conditions. Annu Rev Med 44:289–301
Hardingham TE, Fosang AJ (1992) Proteoglycans: many forms and many functions. Faseb J 6:861–870
Harvey AR, Kendall CL, Sykova E (1997) The status and organization of astrocytes, oligodendroglia and microglia in grafts of fetal rat cerebral cortex. Neurosci Lett 228:58–62
Hatten ME, Liem RK, Shelanski ML, Mason CA (1991) Astroglia in CNS injury. Glia 4:233–243
Hatton GI (1997) Function-related plasticity in hypothalamus. Annu Rev Neurosci 20:375–397
Haydon PG (2001) GLIA: listening and talking to the synapse. Nat Rev Neurosci 2:185–193
Hayen W, Goebeler M, Kumar S, Riessen R, Nehls V (1999) Hyaluronan stimulates tumor cell migration by modulating the fibrin fiber architecture. J Cell Sci 112 (Pt 13):2241–2251
Heinemann U, Lux HD (1977) Ceiling of stimulus induced rises in extracellular potassium concentration in the cerebral cortex of cat. Brain Res 120:231–249
Herkenham M (1987) Mismatches between neurotransmitter and receptor localizations in brain: observations and implications. Neuroscience 23:1–38
Hirrlinger J, Hulsmann S, Kirchhoff F (2004) Astroglial processes show spontaneous motility at active synaptic terminals in situ. Eur J Neurosci 20:2235–2239
Jendelova P, Sykova E (1991) Role of glia in K+. and pH homeostasis in the neonatal rat spinal cord Glia 4:56–63
Kempski O, Staub F, Jansen M, Baethmann A (1990) Molecular mechanisms of glial cell swelling in acidosis. Adv Neurol 52:39–45
Kettenmann H, Orkand RK, Schachner M (1983) Coupling among identified cells in mammalian nervous system cultures. J Neurosci 3:506–516
Kilb W, Dierkes PW, Sykova E, Vargova L, Luhmann HJ (2006) Hypoosmolar conditions reduce extracellular volume fraction and enhance epileptiform activity in the CA3 region of the immature rat hippocampus. J Neurosci Res 84:119–129
Kimelberg HK (1991) Swelling and volume control in brain astroglial cells. In: Giles Raa, ed), pp Advances in Comparative and Environmental PhysiologySpringerBerlin: 81–117.
Kimelberg HK, Goderie SK, Higman S, Pang S, Waniewski RA (1990) Swelling-induced release of glutamate, aspartate, and taurine from astrocyte cultures. J Neurosci 10:1583–1591
Kimelberg HK, Sankar P, O’Connor ER, Jalonen T, Goderie SK (1992) Functional consequences of astrocytic swelling. Prog Brain Res 94:57–68
Kiss JP, Vizi ES (2001) Nitric oxide: a novel link between synaptic and nonsynaptic transmission. Trends Neurosci 24:211–215
Kleene R, Schachner M (2004) Glycans and neural cell interactions. Nat Rev Neurosci 5:195–208
Kriz N, Sykova E, Ujec E, Vyklicky L (1974) Changes of extracellular potassium concentration induced by neuronal activity in the sinal cord of the cat. J Physiol 238:1–15
Lehmenkuhler A, Sykova E, Svoboda J, Zilles K, Nicholson C (1993) Extracellular space parameters in the rat neocortex and subcortical white matter during postnatal development determined by diffusion analysis. Neuroscience 55:339–351
MacVicar BA (1984) Voltage-dependent calcium channels in glial cells. Science 226:1345–1347
MacVicar BA, Hochman D (1991) Imaging of synaptically evoked intrinsic optical signals in hippocampal slices. J Neurosci 11:1458–1469
Mamata H, Mamata Y, Westin CF, Shenton ME, Kikinis R, Jolesz FA, Maier SE (2002) High-resolution line scan diffusion tensor MR imaging of white matter fiber tract anatomy. AJNR Am J Neuroradiol 23:67–75
Margolis RK, Margolis RU (1993) Nervous tissue proteoglycans. Experientia 49:429–446
Matsuoka Y, Hossmann KA (1982) Cortical impedance and extracellular volume changes following middle cerebral artery occlusion in cats. J Cereb Blood Flow Metab 2:466–474
Mazel T, Simonova Z, Sykova E (1998) Diffusion heterogeneity and anisotropy in rat hippocampus. Neuroreport 9:1299–1304
Meech RW, Thomas RC (1987) Voltage-dependent intracellular pH in Helix aspersa neurones. J Physiol 390:433–452
Mongin AA, Orlov SN (2001) Mechanisms of cell volume regulation and possible nature of the cell volume sensor. Pathophysiology 8:77–88
Neprasova H, Anderova M, Petrik D, Vargova L, Kubinova S, Chvatal A, Sykova E (2007) High extracellular K(+) evokes changes in voltage-dependent K(+) and Na (+) currents and volume regulation in astrocytes. Pflugers Arch 453:839–849
Nicholson C, Phillips JM (1981) Ion diffusion modified by tortuosity and volume fraction in the extracellular microenvironment of the rat cerebellum. J Physiol (Lond) 321:225–257
Nicholson C, Tao L (1993a) Hindered diffusion of high molecular weight compounds in brain extracellular microenvironment measured with integrative optical imaging. Biophys J 65:2277–2290
Nicholson C, Tao L (1993b) Hindered diffusion of high molecular weight compounds in brain extracellular microenvironment measured with integrative optical imaging. Biophys J 65:2277–2290
Nicholson C, Sykova E (1998) Extracellular space structure revealed by diffusion analysis. Trends Neurosci 21:207–215
Norton WT, Aquino DA, Hozumi I, Chiu FC, Brosnan CF (1992) Quantitative aspects of reactive gliosis: a review. Neurochem Res 17:877–885
Oliet SH, Piet R, Poulain DA (2001) Control of glutamate clearance and synaptic efficacy by glial coverage of neurons. Science 292:923–926
Orkand RK, Nicholls JG, Kuffler SW (1966) Effect of nerve impulses on the membrane potential of glial cells in the central nervous system of amphibia. J Neurophysiol 29:788–806
Pasantes Morales H, Schousboe A (1988) Volume regulation in astrocytes: a role for taurine as an osmoeffector. J Neurosci Res 20:503–509
Pasantes-Morales H, Franco R, Torres-Marquez ME, Hernandez-Fonseca K, Ortega A (2000) Amino acid osmolytes in regulatory volume decrease and isovolumetric regulation in brain cells: contribution and mechanisms. Cell Physiol Biochem 10:361–370
Pierpaoli C, Jezzard P, Basser PJ, Barnett A, Di Chiro G (1996) Diffusion tensor MR imaging of the human brain. Radiology 201:637–648
Piet R, Vargova L, Sykova E, Poulain DA, Oliet SH (2004) Physiological contribution of the astrocytic environment of neurons to intersynaptic crosstalk. Proc Natl Acad Sci U S A 101:2151–2155
Prokopova S, Vargova L, Sykova E (1997) Heterogeneous and anisotropic diffusion in the developing rat spinal cord. Neuroreport 8:3527–3532
Prokopova-Kubinova S, Vargova L, Tao L, Ulbrich K, Subr V, Sykova E, Nicholson C (2001) Poly[N. -(2-hydroxypropyl)methacrylamide] polymers diffuse in brain extracellular space with same tortuosity as small molecules Biophys J 80:542–548
Reum T, Olshausen F, Mazel T, Vorisek I, Morgenstern R, Sykova E (2002) Diffusion parameters in the striatum of rats with 6-hydroxydopamine-induced lesions and with fetal mesencephalic grafts. J Neurosci Res 70:680–693
Rice ME, Okada YC, Nicholson C (1993) Anisotropic and heterogeneous diffusion in the turtle cerebellum: Implications for volume transmission. J Neurophysiol 70:2035–2044
Roitbak T, Sykova E (1999) Diffusion barriers evoked in the rat cortex by reactive astrogliosis. Glia 28:40–48
Sykova E (1992) Ionic and Volume Changes in the Microenvironment of Nerve and Receptor Cells. SpringerBerlin
Siesjo BK, von Hanwehr R, Nergelius G, Nevander G, Ingvar M (1985) Extra- and intracellular pH in the brain during seizures and in the recovery period following the arrest of seizure activity. J Cereb Blood Flow Metab 5:47–57
Simonova Z, Svoboda J, Orkand P, Bernard CC, Lassmann H, Sykova E (1996) Changes of extracellular space volume and tortuosity in the spinal cord of Lewis rats with experimental autoimmune encephalomyelitis. Physiol Res 45:11–22
Sims TJ, Gilmore SA (1992) Glial response to dorsal root lesion in the irradiated spinal cord. Glia 6:96–107
Sontheimer H, Kettenmann H (1988) Heterogeneity of potassium currents in cultured oligodendrocytes. Glia 1:415–420
Sontheimer H, Trotter J, Schachner M, Kettenmann H (1989) Channel expression correlates with differentiation stage during the development of oligodendrocytes from their precursor cells in culture. Neuron 2:1135–1145
Svoboda J, Sykova E (1991) Extracellular space volume changes in the rat spinal cord produced by nerve stimulation and peripheral injury. Brain Res 560:216–224
Sykova E (1997) Extracellular space in the CNS: its regulation, volume and geometry in normal and pathological neuronal function. Neuroscientist 3:28–41
Sykova E (2001) Glial diffusion barriers during aging and pathological states. Prog Brain Res 132:339–363
Sykova E (2003) Diffusion parameters of the extracellular space. Israel J Chem 43:55–69
Sykova E (2004a) Extrasynaptic volume transmission and diffusion parameters of the extracellular space. Neuroscience 129:861–876
Sykova E (2004b) Diffusion properties of the brain in health and disease. Neurochem Int 45:453–466
Sykova E, Svoboda J (1990) Extracellular alkaline-acid-alkaline transients in the rat spinal cord evoked by peripheral stimulation. Brain Res 512:181–189
Sykova E, Svoboda J, Simonova Z, Lehmenkuhler A, Lassmann H (1996) X-irradiation-induced changes in the diffusion parameters of the developing rat brain. Neuroscience 70:597–612
Sykova E, Mazel T, Simonova Z (1998) Diffusion constraints and neuron-glia interaction during aging. Exp Gerontol 33:837–851
Sykova E, Vargova L, Prokopova S, Simonova Z (1999a) Glial swelling and astrogliosis produce diffusion barriers in the rat spinal cord. Glia 25:56–70
Sykova E, Roitbak T, Mazel T, Simonova Z, Harvey AR (1999b) Astrocytes, oligodendroglia, extracellular space volume and geometry in rat fetal brain grafts. Neuroscience 91:783–798
Sykova E, Mazel T, Hasenohrl RU, Harvey AR, Simonova Z, Mulders WH, Huston JP (2002) Learning deficits in aged rats related to decrease in extracellular volume and loss of diffusion anisotropy in hippocampus. Hippocampus 12:269–279
Sykova E, Vargova L, Kubinova S, Jendelova P, Chvatal A (2003) The relantionship between changes in intrinsic optical signals and cell swelling in rat spinal cord slices. NeuroImage 18:214–230
Sykova E, Vorisek I, Mazel T, Antonova T, Schachner M (2005a) Reduced extracellular space in the brain of tenascin-R- and HNK-1-sulphotransferase deficient mice. Eur J Neurosci 22:1873–1880
Sykova E, Vorisek I, Antonova T, Mazel T, Meyer-Luehmann M, Jucker M, Hajek M, Ort M, Bures J (2005b) Changes in extracellular space size and geometry in APP23 transgenic mice: a model of Alzheimer's disease. Proc Natl Acad Sci U S A 102:479–484
Thomas RC (1977) The role of bicarbonate, chloride and sodium ions in the regulation of intracellular pH in snail neurones. J Physiol (Lond) 273:317–338
Tao L, Masri D, Hrabetova S, Nicholson C (2002) Light scattering in rat neocortical slices differs during spreading depression and ischemia. Brain Res 952:290–300
Theodosis DT, Poulain DA (1993) Activity-dependent neuronal-glial and synaptic plasticity in the adult mammalian hypothalamus. Neuroscience 57:501–535
Thorne RG, Nicholson C (2006) In vivo diffusion analysis with quantum dots and dextrans predicts the width of brain extracellular space. Proc Natl Acad Sci U S A 103:5567–5572
Thorne RG, Hrabetova S, Nicholson C (2004) Diffusion of epidermal growth factor in rat brain extracellular space measured by integrative optical imaging. J Neurophysiol 92:3471–3481
Villegas GM, Fernandez J (1966) Permeability to thorium dioxide of the intercellular spaces of the frog cerebral hemisphere. Exp Neurol 15:18–36
Van der Toorn A, Sykova E, Dijkhuizen RM, Vorisek I, Vargova L, Skobisova E, Van Lookeren Campagne M, Reese T, Nicolay K (1996) Dynamic changes in water ADC, energy metabolism, extracellular space volume, and tortuosity in neonatal rat brain during global ischemia. Magn Reson Med 36:52–60
Van Harreveld A, Dafny N, Khattab FI (1971) Effects of calcium on electrical resistance and the extracellular space of cerebral cortex. Exp Neurol 31:358–367
Vargova L, Jendelova P, Chvatal A, Sykova E (2001a) Glutamate, NMDA, and AMPA induced changes in extracellular space volume and tortuosity in the rat spinal cord. J Cereb Blood Flow Metab 21:1077–1089
Vargova L, Chvatal A, Anderova M, Kubinova S, Ziak D, Sykova E (2001b) Effect of osmotic stress on potassium accumulation around glial cells and extracellular space volume in rat spinal cord slices. J Neurosci Res 65:129–138
Vargova L, Homola A, Zamecnik J, Tichy M, Benes V, Sykova E (2003) Diffusion parameters of the extracellular space in human gliomas. Glia 42:77–88
Vizi ES (1980) Nonsynaptic modulation of transmitter release: Pharmacological implication. Trends Pharmacol Sci 1:172–175
Vizi ES (1984) Non-synaptic Interaction Between Neurones: Modulation of Neurochemical Transmission. WileyChichester/New York
Vizi ES (2000) Role of high-affinity receptors and membrane transporters in nonsynaptic communication and drug action in the central nervous system. Pharmacol Rev 52
Vizi ES (2003) Non-synaptic interaction between neurons in the brain, an analog system: far from Cajal-Sherringtons’s galaxy. Bull Mem Acad R Med Belg 158:373–379
Vizi ES, Kiss JP, Lendvai B (2004) Nonsynaptic communication in the central nervous system. Neurochem Int 45:443–451
Vorisek I, Sykova E (1997a) Evolution of anisotropic diffusion in the developing rat corpus callosum. J Neurophysiol 78:912–919
Vorisek I, Sykova E (1997b) Ischemia-induced changes in the extracellular space diffusion parameters, K+., and pH in the developing rat cortex and corpus callosum J Cereb Blood Flow Metab 17:191–203
Vorisek I, Hajek M, Tintera J, Nicolay K, Sykova E (2002a) Water ADC, extracellular space volume, and tortuosity in the rat cortex after traumatic injury. Magn Reson Med 48:994–1003
Vorisek I, Hajek M, Tintera J, Nicolay K, Sykova E (2002b) Water ADC, extracellular space volume, and tortuosity in the rat cortex after traumatic injury. Magn Reson Med 48:994–1003
Walz W, Hertz L (1983) Intracellular ion changes of astrocytes in response to extracellular potassium. J Neurosci Res 10:411–423
Walz W, Hinks EC (1986) A transmembrane sodium cycle in astrocytes. Brain Res 368:226–232
Wieshmann UC, Clark CA, Symms MR, Barker GJ, Birnie KD, Shorvon SD (1999) Water diffusion in the human hippocampus in epilepsy. Magn Reson Imaging 17:29–36
Zamecnik J, Vargova L, Homola A, Kodet R, Sykova E (2004) Extracellular matrix glycoproteins and diffusion barriers in human astrocytic tumours. Neuropathol Appl Neurobiol 30:338–350
Zhang H, Kelly G, Zerillo C, Jaworski DM, Hockfield S (1998) Expression of a cleaved brain-specific extracellular matrix protein mediates glioma cell invasion In vivo. J Neurosci 18:2370–2376
Zoli M, Jansson A, Sykova E, Agnati LF, Fuxe K (1999) Intercellular communication in the central nervous system. The emergence of the volume transmission concept and its relevance for neuropsychopharmacology. Trends Pharmacol Sci 20:142–150
Acknowledgments
The authors acknowledge the support of grants AV0Z50390512 from the Academy of Sciences of the Czech Republic and LC554 from the Ministry of Education, Youth and Sports of the Czech Republic.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2009 Springer Science+Business Media, LLC
About this chapter
Cite this chapter
Vargova, L., Sykova, E. (2009). Astrocytes in Control of the Biophysical Properties of Extracellular Space. In: Haydon, P., Parpura, V. (eds) Astrocytes in (Patho)Physiology of the Nervous System. Springer, Boston, MA. https://doi.org/10.1007/978-0-387-79492-1_9
Download citation
DOI: https://doi.org/10.1007/978-0-387-79492-1_9
Published:
Publisher Name: Springer, Boston, MA
Print ISBN: 978-0-387-79491-4
Online ISBN: 978-0-387-79492-1
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)