Properties of human glial cells associated with epileptic seizure foci

Epilepsy Research

Volumn 32, Issue 1-2, 1998, Pages 286-303

  Bordey, Angélique ^a   Sontheimer, Harald ^a  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

Biopsies; Glial cells; Immunohistochemical cell identification; Intractable mesio temporal lobe epilepsy; Morphological reconstruction

Indexed keywords

GLIAL FIBRILLARY ACIDIC PROTEIN; INTERMEDIATE FILAMENT PROTEIN; SODIUM CHANNEL;

ADULT; ANIMAL CELL; ASTROCYTE; CELL STRUCTURE; CONFERENCE PAPER; CONTROLLED STUDY; EPILEPSY; FEMALE; GLIA CELL; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; NONHUMAN; PATCH CLAMP; POTASSIUM CONDUCTANCE; POTASSIUM CURRENT; PRIORITY JOURNAL; RAT; SODIUM CONDUCTANCE; TEMPORAL LOBE EPILEPSY;

ADULT; ANIMALS; ASTROCYTES; EPILEPSIES, PARTIAL; EPILEPSY, TEMPORAL LOBE; FEMALE; GLIAL FIBRILLARY ACIDIC PROTEIN; HIPPOCAMPUS; HUMANS; MEMBRANE POTENTIALS; MIDDLE AGED; NEUROGLIA; POTASSIUM CHANNELS; RATS; REFERENCE VALUES; SODIUM CHANNELS; TEMPORAL LOBE;

EID: 0032169291     PISSN: 09201211     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0920-1211(98)00059-X     Document Type: Conference Paper

References (51)

1. Ballanyi K., Grafe P., TenBruggencate G. Ion activities and potassium uptake mechanisms of glial cells in guinea-pig olfactory cortex slices. J. Physiol. (London). 382:1987;159-174.
2. Barres B.A., Koroshetz W.J., Swartz K.J., Chun L.L.Y., Corey D.P. Ion channel expression by white matter glia: The O2A glial progenitor cell. Neuron. 4:1990;507-524.
3. Beach T.G., Woodhurst W.B., MacDonald D.B., Jones M.W. Reactive microglia in hippocampal sclerosis associated with human temporal lobe epilepsy. Neurosci. Lett. 191:1995;27-30.
4. Bordey A., Sontheimer H. Postnatal development of ionic currents in rat hippocampal astrocytes in situ. J. Neurophysiol. 78:1997;461-477.
5. Castiglioni A.J., Peterson S.L., Sanabria E.L., Tiffany-Castiglioni E. Structural changes in astrocytes induced by seizures in a model of temporal lobe epilepsy. J. Neurosci. Res. 26:1990;334-341.
6. + channels in human astrocytes. Soc. Neurosci. Abstr. 20(Suppl. Parts 1&2):1994;1113.
7. During M.J., Spencer D.D. Extracellular hippocampal glutamate and spontaneous seizure in the conscious human brain. Lancet. 341:1993;1607-1610.
8. Edwards F.A., Konnerth A., Sakmann B., Takahashi T. A thin slice preparation for patch clamp recordings from neurones of the mammalian central nervous system. Pflügers Arch. 414:1989;600-612.
9. Eng L.F., Ghirnikar R.S. GFAP and astrogliosis (Review). Brain Pathol. 4:1994;229-237.
10. Eng L.F., Yu A.C., Lee Y.L. Astrocytic response to injury (Review). Prog. Brain Res. 94:1992;353-365.
11. Gardner-Medwin A.R., Coles J.A., Tsacopoulos M. Clearance of extracellular potassium: evidence for spatial buffering by glial cells in the retina of the drone. Brain Res. 209:1981;452-457.
12. Glotzner F.L. Membrane properties of neuroglia in epileptogenic gliosis. Brain Res. 55:1973;159-171.
13. +)-ATPase to focal epilepsy: a brief review (Review; 10 Refs.). Epilepsy Res. 12:1992;141-149.
14. 2+ changes during epileptiform discharges in the immature rat neocortex. Dev. Brain Res. 36:1987.
15. Hablitz, J.J., Heinemann, U., 1994. Alterations in the microenvironment during spreading depression associated with epileptiform activity in the immature neocortex. Brain Res. 243-252.
16. Hashimoto I., Manaka S., Sano K. The role of extracellular potassium in early epilepsy. Neurol. Res. 1:1979;39-49.
17. Heinemann U., Dietzel I. Extracellular potassium concentration in chronic alumina cream foci of cats. J. Neurophysiol. 52:1984;421-434.
18. Heinemann U., Konnerth A., Pumain R., Wadman W.J. Extracellular calcium and potassium concentration changes in chronic epileptic brain tissue (Review; 195 Refs.). Adv. Neurol. 44:1986;641-661.
19. Hoppe D., Chvatal A., Kettenmann H., Orkand R.K., Ransom B.R. Characteristics of activity-dependent potassium accumulation in mammalian peripheral nerve in vitro. Brain Res. 552:1991;106-112.
20. Hoppe D., Chvatal A., Kettenmann H., Orkand R.K., Ransom B.R. Characteristics of activity-dependent potassium accumulation in mammalian peripheral nerve in vitro. Brain Res. 552:1991;106-112.
21. Jacobs K.M., Gutnick M.J., Prince D.A. Hyperexcitability in a model of cortical maldevelopment. Cerebral Cortex. 6:1996;514-523.
22. + uptake in glia prevents long-term depression maintenance and causes epileptiform activity. J. Neurosci. 17:1997;2813-2824.
23. Kettenmann, H., Orkand, R.K., Schachner, M., 1985. Ion measurements in physiology and medicine. In: Kessler, M. et al. (Eds.), Potassium Uptake Mechanisms of Cultured Oligodendrocytes Studied with Ion-sensitive Electrodes. Springer-Verlag, Berlin, Heidelberg, pp. 195-198.
24. Kettenmann H., Sykova E., Orkand R.K., Schachner M. Glial potassium uptake following depletion by intracellular ionophoresis. Pflügers Arch. 410:1987;1-6.
25. Kimelberg, H.K., Jalonen, T., Walz, W., 1993. Regulation of the brain microenvironment: Transmitters and ions. In: Murphy, S. (Ed.), Astrocytes, Pharmacology and Function. Academic Press, San Diego, CA, pp. 193-228.
26. Kuffler S.W., Nicholls J.G., Orkand R.K. Physiological properties of glial cells in the central nervous system of amphibia. J. Neurophysiol. 29:1966;768-787.
27. Lewis D.V., Mutsaga N., Schuete W.H., Van Buren J., Mutsuga N., Schuette W.H. Potassium clearance and reactive gliosis in the alumina gel lesion. Epilepsia. 18:1977;499-506.
28. Lux H.D. The kinetics of extracellular potassium: Relation to epileptogenesis. Epilepsia. 15:1974;375-393.
29. Meldrum B.S. The role of glutamate in epilepsy and other cns disorders (Review; 128 Refs.). Neurology. 44(Suppl. 8):1994;S14-23.
30. Miller H.P., Levey A.I., Rothstein J.D., Tzingounis A.V., Conn P.J. Alterations in glutamate transporter protein levels in kindling-induced epilepsy. J. Neurochem. 68:1997;1564-1570.
31. Nee MacFarlane S., Sontheimer H. Electrophysiological changes that accompany reactive gliosis in vitro. J. Neurosci. 17:1997;7316-7329.
32. Newman E.A. Inward-rectifying potassium channels in retinal glial (Müller) cells. J. Neurosci. 13:1993;3333-3345.
33. Niquet J., Ben-Ari Y., Represa A. Glial reaction after seizure induced hippocampal lesion: Immunohistochemical characterization of proliferating glial cells. J. Neurocytol. 23:1994;641-656.
34. Niquet J., Jorquera I., Ben A.Y., Represa A. NCAM immunoreactivity on mossy fibers and reactive astrocytes in the hippocampus of epileptic rats. Brain Res. 626:1993;106-116.
35. Orkand R.K., Nicholls J.G., Kuffler S.W. Effect of nerve impulses on the membrane potential of glial cells in the central nervous system of amphibia. J. Neurophysiol. 29:1966;788-806.
36. Patt S., Labrakakis C., Bernstein M., Weydt P., Cervos-Navarro J., Nisch G., Kettenmann H. Neuron-like physiological properties of cells from human oligodendroglial tumors. Neuroscience. 71:1996;601-611.
37. Pollen D.A., Trachtenberg M.C. Neuroglia: Gliosis and focal epilepsy. Science. 167:1970;1252-1253.
38. Prince D.A., Neher E., Lux H.-D. Measurement of extracellular potassium activity in cat cortex. Brain Res. 50:1973;489-495.
39. Ransom B. Pathophysiology of epilepsy. Neurol. Neurosurg. 1:1979;2-7.
40. + currents in rat spinal cord astrocytes. J. Neurophysiol. 73:1995;333-345.
41. Ransom C.B., Sontheimer H., Janigro D. Astrocytic inwardly rectifying potassium currents are dependent on external sodium ions. J. Neurophysiol. 76:1996;626-630.
42. Reier, P.J., 1986. Gliosis following CNS injury: The anatomy of astrocytic scars and their influences on axonal elongation. In: Vernadakis, S.F.A. (Eds.), Astrocytes, Cell Biology and Pathology of Astrocytes. Academic Press, Orlando, FL, pp. 263-324.
43. Rothstein J.D., Dykes-Hoberg M., Pardo C.A., Bristol L.A., Jin L., Kuncl R.W., Kanai Y., Hediger M.A., Wang Y.F., Schielke J.P., Welty D.F. Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate. Neuron. 16:1996;675-686.
44. Roy M.-L., Sontheimer H. β-Adrenergic modulation of glial inwardly rectifying potassium channels. J. Neurochem. 64:1995;1576-1584.
45. Sontheimer H. Glial neuronal interactions: a physiological perspective. Neuroscientist. 1:1995;328-337.
46. + channels. J. Neurophysiol. 68:1992;985-1000.
47. Tang C.-M., Cohen M.W., Orkand R.K. Electrogenic pumps in axons and neuroglia and extracellular potassium homeostasis. Brain Res. 194:1980;283-286.
48. Thio C.L., Waxman S.G., Sontheimer H. Ion channels in spinal cord astrocytes in vitro: III. Modulation of channel expression by co-culture with neurons and neuron-conditioned medium. J. Neurophysiol. 69:1993;819-831.
49. Thomas R.J. Excitatory amino acids in health and disease (Review). J. Am. Geriatr. Soc. 43:1995;1279-1289.
50. Tiffany-Castiglioni, E., Castiglioni, A.J. Jr., 1986. Astrocytes in epilepsy. In: Vernadakis, S.F.A. (Eds.), Astrocytes, Cell Biology and Pathology of Astrocytes. Academic Press, Orlando, FL, pp. 401-424.
51. Walz W. Role of glial cells in the regulation of the brain microenvironment. Prog. Neurobiol. 33:1989;309-333.