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Electrical properties of oligodendrocytes in culture

  • Excitable Tissues and Central Nervous
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Abstract

The electrical properties of immunocytologically identified oligondendrocytes from embryonic mouse spinal cord maintained in culture for 3 to 6 weeks were studied by passing current and recording potential changes with two separate intracellular electrodes. The average input resistance was 3.3 M Ω and ranged from 0.7 to 16 M Ω (n=35). The input resistance increased by 19% with depolarization and decreased by 9% with hyperpolarization of 25 mV. The membrane time constant determined from the slope of the late exponential tail was 3.45±2.5 ms SD (n=15). The specific membrane resistance of three cells was determined by a simplified square pulse analysis combined with measurement of membrane area. Membrane area was estimated from photomicrographs of cells injected with Lucifer Yellow CH and stained with the cell surface-reactive antibody 04 and from electron micrographs. An average specific membrane resistance of 1.3×103 Ωcm2 and specific capacitance of 1.7 μF/cm2 were calculated. Increasing [K+]o depolarized the cells and decreased the input resistance and the time constant.

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References

  • Barrett JN, Crill WE (1974) Specific membrane properties of cat motoneurones. J Physiol 239:301–324

    Google Scholar 

  • Barry PH, Hope AB (1969) Electro-osmosis in membranes: effects of unstirred layers and transport numbers. I. Theory. Biophys J 9:700–728

    Google Scholar 

  • Berg G, Schachner M (1981) Immunoelectron microscopic identification of 0-antigen-bearing oligodendroglial cells in vitro. Cell Tiss Res 219:313–325

    Google Scholar 

  • Berg G, Schachner M (1982) Immunoelectron microscopic characterization of galactocerebroside and nervous system antigen-1 (NS-1) positive oligodendrocytes in culture. Neurosc Lett 28:75–80

    Google Scholar 

  • Bunge RP (1968) Glial cells and the central myelin sheath. Physiol Rev 48:197–251

    Google Scholar 

  • Bunge MB, Williams AK, Wood PM, Vitto J, Jeffrey JJ (1980) Comparison of nerve cell and nerve cell plus Schwann cell cultures, with particular emphasis on basal lamina and collagen formation. J Cell Biol 84:184–202

    Google Scholar 

  • Camerer H (1978) The measurement of the electrical capacity and synaptic charge transfer of neurons. Neurosc Lett, Suppl 1:75

    Google Scholar 

  • Camerer H (1980) Die elektrotonische Spannungsausbreitung im Soma, Dendritenbaum und Axon von Nervenzellen. Doctoral Thesis, University of Tübingen (FRG)

    Google Scholar 

  • Coles JA, Orkand RK (1983) Modification of potassium movement through the retina of the drone (Apis mellifera ⧄) by glial uptake. J Physiol (Lond) 340:157–174

    Google Scholar 

  • Dietzel I, Heinemann U, Hofmeier G, Lux HD (1980) Transient changes in the size of the extracellular space in the sensorimotor cortex of cats in relation to stimulus induced changes in potassium concentration. Exp Brain Res 40:432–439

    Google Scholar 

  • Eisenberg RS, Johnson EA (1970) Three-dimensional field problems in physiology. Prog Biophys mol Biol 20:1–65

    Google Scholar 

  • Gardner-Medwin AR, Coles JA, Tsacopoulos M (1981) Clearance of extracellular potassium: evidence for spatial buffering by glial cells in the retina of the drone. Brain Res 209:452–457

    Google Scholar 

  • Gardner-Medwin AR (1983) Analysis of potassium dynamics in brain tissue. J Physiol (Lond) 335:393–426

    Google Scholar 

  • Glötzner FL (1973) Membrane properties of neuroglia in epileptogenic gliosis. Brain Res 55:159–1171

    Google Scholar 

  • Goldman DE (1943) Potential, impedance and rectification in membranes. J Gen Physiol 27:37–60

    Google Scholar 

  • Gonatas NK, Hirayama M, Stieber A, Silberberg DH (1982) The ultrastructure of isolated rat oligodendroglial cell cultures. J Neurocytol 11:997–1008

    Google Scholar 

  • Hild W, Tasaki I (1962) Morphological and physiological properties of neurons and glial cells in tissue culture. J Neurophysiol 25:277–304

    Google Scholar 

  • Hille B (1977) Excitation and conduction. In: Kandel ER (ed) Cellular biology of neurons, vol I, sect I. Williams & Wilkins, Baltimore

    Google Scholar 

  • Hodgkin AL, Katz B (1949) The effect of sodium ions on the electrical activity of the giant axon on the squid. J Physiol (Lond) 108:37–77

    Google Scholar 

  • Kettenmann H, Sonnhof U, Schachner M (1983a) Exclusive potassium dependence of the membrane potential in cultured mouse oligodendrocytes. J Neurosci 3:500–505

    Google Scholar 

  • Kettenmann H, Orkand RK, Schachner M (1983b) Coupling among identified cells in mammalian nervous system cultures. J Neurosci 3:506–516

    Google Scholar 

  • Kettenmann H, Orkand RK, Lux HD (1984) Some properties of potassium channels in cultured oligodendrocytes. Pflügers Arch 400:215–221

    Google Scholar 

  • Kimelberg HK, Bowman C, Biddlecome, S, Bourke RS (1979) Cation transport and membrane potential properties of primary astroglial cultures from neonatal rat brains. Brain Res 177:533–550

    Google Scholar 

  • Kimelberg HK, Hirata H, Bowman C, Mazurkiewicz J (1982) Effects of K+, Na+ and Cl on membrane potentials and I–V curves of primary astrocyte cultures. Soc Neurosci Abstr 8

  • Lux HD, Schubert P, Kreutzberg GW (1970) Direct matching of morphological and electrophysiological data in cat spinal motoneurons. In: Andersen P, Jansen JKS (eds) Excitatory synaptic mechanisms, Proc. of the Fifth International Meeting of Neurobiologists. Universitetsforlaget, Oslo

    Google Scholar 

  • Mori S, Leblond CP (1970) Electron microscopic identification of three classes of oligodendrocytes and a preliminary study of their proliferative activity in the capus callosum of young rats. J Comp Neurol 139:1–30

    Google Scholar 

  • Orkand RK, Orkand PM, Tang C-M (1981) Membrane properties of neuroglia in the optic nerve of necturus. J Exp Biol 95: 49–59

    Google Scholar 

  • Privat A (1975) Postnatal gliogenesis in the mammalian brain. Int Rev Cytol 40:281–323

    Google Scholar 

  • Rall W (1959) Branching dendritic trees and motoneuron membrane resistivity. Exp Neurol 1:491–527

    Google Scholar 

  • Rall W (1969) Time constants and electrotonic length of membrane cylinders and neurons. Biophys J 9:1483–1508

    Google Scholar 

  • Rall W (1977) Core conductor theory and cable properties of neurons. In: Kandel ER (ed) Cellular biology of neurons. Williams & Wilkins, Baltimore, pp 39–97

    Google Scholar 

  • Raine CS, Poduslo SE Norton WT (1971) The ultrastructure of purified preparations of neurons and glial cells. Brain Res 27:11–29

    Google Scholar 

  • Ransom BR, Goldring S (1973) Slow depolarization in cells presumed to be glia in the cerebral cortex of the cat. J Neurophysiol 36:869–878

    Google Scholar 

  • Somjen GG (1970) Evoked sustained focal potential of neurons and of unresponsive cells of the spinal cord. J Neurophysiol 33:562–582

    Google Scholar 

  • Somjen GG (1975) Electrophysiology of neuroglia. Annu Rev Physiol 37:163–190

    Google Scholar 

  • Sommer I, Schachner M (1981) Monoclonal antibodies (01 to 04) to oligodendrocyte cell surfaces: an immunocytological study in the central nervous system. Dev Biol 83:311–323

    Google Scholar 

  • Sonnhof U, Richter DW, Taugner R (1977) Electrotonic coupling between frog spinal motoneurons. An electrophysiological and morphological study. Brain Res 138:197–215

    Google Scholar 

  • Sonnhof U, Förderer R, Schneider W, Kettenmann H (1982) Cell puncturing with a step motor driven manipulator with simultaneous measurement of displacement. Pflügers Arch 392: 295–300

    Google Scholar 

  • Trachtenberg MC, Kornblith PL, Häuptli J (1972) Biophysical properties of cultured human glial cells. Brain Res 38:279–298

    Google Scholar 

  • Trachtenberg MC, Pollen DA (1970) Neuroglia: biophysical properties and physiologic function. Science 167:1248–1252

    Google Scholar 

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Kettenmann, H., Sonnhof, U., Camerer, H. et al. Electrical properties of oligodendrocytes in culture. Pflugers Arch. 401, 324–332 (1984). https://doi.org/10.1007/BF00584331

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  • DOI: https://doi.org/10.1007/BF00584331

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