Literature DB >> 2853139

Electrical coupling between astrocytes and between oligodendrocytes studied in mammalian cell cultures.

H Kettenmann1, B R Ransom.   

Abstract

The characteristics of electrical coupling between astrocytes and between oligodendrocytes were analyzed in cell cultures derived from rodent central nervous system. Experiments were carried out by impaling one member of a glial pair with separate voltage recording and current passing electrodes (cell 1) and the other cell, a measured distance from the first, with a voltage-recording electrode (cell 2). Astrocyte pairs within 300 microns of one another were always coupled. The coupling ratio was determined for 23 astrocytic pairs various distances apart, and decreased with distance in a roughly exponential manner. The average coupling ratio of astrocytes within 100 microns of each other was 0.44 +/- 0.32. Oligodendrocytes were less strongly coupled to each other than astrocytes. Even cells immediately adjacent to one another were often uncoupled. Among coupled oligodendrocytes within 100 microns of each other, the average coupling ratio was 0.11 +/- 0.1. Current passage between pairs of astrocytes and pairs of oligodendrocytes was nonrectifying. Application of 0.5 mM BaCl2 or 44.6 mM CsCl (substituted for NaCl) depolarized and increased the input resistance of astrocytes and oligodendrocytes. These ions also increased the coupling ratio in astrocyte pairs and oligodendrocyte pairs; this effect was rapid in onset and completely reversible. Ba++ and Cs+ appear to block resting K+ conductance in glia and probably increase the coupling ratio by increasing the effective length constant of the glial membrane without any direct effect on junctional resistance. In three cases, oligodendrocyte pairs that appear uncoupled in normal solution exhibited coupling in the presence of BaCl2 or CsCl. This suggests that oligodendrocytes may be widely coupled by junctions that provide only weak electrical interaction; such junctions might be important for the exchange of small metabolically active molecules. The strong electrical coupling among astrocytes, in concert with their K+-selective membrane conductance, would provide for an electrical syncytium well designed to transport K+ away from areas of focal extracellular accumulation (i.e., the spatial buffer mechanism), and these cells, more than oligodendrocytes, may provide this function.

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Year:  1988        PMID: 2853139     DOI: 10.1002/glia.440010108

Source DB:  PubMed          Journal:  Glia        ISSN: 0894-1491            Impact factor:   7.452


  36 in total

1.  Gap-junctional coupling between neurons and astrocytes in primary central nervous system cultures.

Authors:  M M Fróes; A H Correia; J Garcia-Abreu; D C Spray; A C Campos de Carvalho; M V Neto
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-22       Impact factor: 11.205

2.  Functional coupling between neurons and glia.

Authors:  V Alvarez-Maubecin; F Garcia-Hernandez; J T Williams; E J Van Bockstaele
Journal:  J Neurosci       Date:  2000-06-01       Impact factor: 6.167

3.  Electrical coupling between glial cells in the rat retina.

Authors:  P W Ceelen; A Lockridge; E A Newman
Journal:  Glia       Date:  2001-07       Impact factor: 7.452

4.  Specificity of cell-cell coupling in rat optic nerve astrocytes in vitro.

Authors:  H Sontheimer; J E Minturn; J A Black; S G Waxman; B R Ransom
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

5.  Chronic encephalopathies induced by mercury or lead: aspects of underlying cellular and molecular mechanisms.

Authors:  L Rönnbäck; E Hansson
Journal:  Br J Ind Med       Date:  1992-04

6.  Adrenergic regulation of intercellular communications between cultured striatal astrocytes from the mouse.

Authors:  C Giaume; P Marin; J Cordier; J Glowinski; J Premont
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-01       Impact factor: 11.205

7.  Two populations of glial cells from fish optic nerve/tract with distinct electrophysiological properties.

Authors:  D Hoppe; M Bastmeyer; G von Blankenfeld; H Kettenmann; C A Stuermer
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

Review 8.  Gap junctions couple astrocytes and oligodendrocytes.

Authors:  Jennifer L Orthmann-Murphy; Charles K Abrams; Steven S Scherer
Journal:  J Mol Neurosci       Date:  2008-05       Impact factor: 3.444

9.  Differential expression of three gap junction proteins in developing and mature brain tissues.

Authors:  R Dermietzel; O Traub; T K Hwang; E Beyer; M V Bennett; D C Spray; K Willecke
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

Review 10.  Modulation of brain hemichannels and gap junction channels by pro-inflammatory agents and their possible role in neurodegeneration.

Authors:  Juan A Orellana; Pablo J Sáez; Kenji F Shoji; Kurt A Schalper; Nicolás Palacios-Prado; Victoria Velarde; Christian Giaume; Michael V L Bennett; Juan C Sáez
Journal:  Antioxid Redox Signal       Date:  2009-02       Impact factor: 8.401

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