Literature DB >> 2416364

Is the potassium channel distribution in glial cells optimal for spatial buffering of potassium?

H Brew, D Attwell.   

Abstract

Glial cells in the nervous system are believed to reduce changes of extracellular potassium concentration ([K+]o), caused by neural activity, by carrying out spatial buffering of potassium. In the case of retinal glial cells (Müller cells), light-evoked increases of [K+]o within the retina are reduced by K ions flowing through the Müller cell to the vitreous fluid of the eye. We have calculated the optimal way to distribute the potassium conductance of the Müller cell to maximize spatial buffering to the vitreous fluid. The best distribution is with half the potassium conductance in the outer part of the cell, where K+ enters, and half the conductance in the vitreal endfoot, where K+ leaves the cell. This calculated distribution is very different from the actual distribution measured by Newman (1984, Nature [Lond.], 309: 155-157), where only 6% of the Müller cell conductance is in the outer cell and 94% is in the endfoot. The experimentally observed distribution gives less than a quarter of the spatial buffering that would be produced by the optimal distribution. The possible advantages of this arrangement are discussed.

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Year:  1985        PMID: 2416364      PMCID: PMC1329410          DOI: 10.1016/S0006-3495(85)83843-1

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  16 in total

1.  Photoreceptor coupling in retina of the toad, Bufo marinus. I. Anatomy.

Authors:  G H Gold; J E Dowling
Journal:  J Neurophysiol       Date:  1979-01       Impact factor: 2.714

2.  Current source-density analysis of the b-wave of frog retina.

Authors:  E A Newman
Journal:  J Neurophysiol       Date:  1980-05       Impact factor: 2.714

3.  Generation of b-wave currents in the skate retina.

Authors:  R P Kline; H Ripps; J E Dowling
Journal:  Proc Natl Acad Sci U S A       Date:  1978-11       Impact factor: 11.205

4.  Regional specialization of retinal glial cell membrane.

Authors:  E A Newman
Journal:  Nature       Date:  1984 May 10-16       Impact factor: 49.962

5.  Field potential induced by injection of potassium ion into the frog retina: a test of current interpretations of the electroretinographic (ERG) b-wave.

Authors:  M Fujimoto; T Tomita
Journal:  Brain Res       Date:  1981-01-05       Impact factor: 3.252

6.  Analysis of potassium dynamics in mammalian brain tissue.

Authors:  A R Gardner-Medwin
Journal:  J Physiol       Date:  1983-02       Impact factor: 5.182

7.  Light-evoked changes in [K+]0 in retina of intact cat eye.

Authors:  R H Steinberg; B Oakley; G Niemeyer
Journal:  J Neurophysiol       Date:  1980-11       Impact factor: 2.714

8.  Effect of nerve impulses on the membrane potential of glial cells in the central nervous system of amphibia.

Authors:  R K Orkand; J G Nicholls; S W Kuffler
Journal:  J Neurophysiol       Date:  1966-07       Impact factor: 2.714

9.  Neuronal-type Na+ and K+ channels in rabbit cultured Schwann cells.

Authors:  S Y Chiu; P Schrager; J M Ritchie
Journal:  Nature       Date:  1984 Sep 13-19       Impact factor: 49.962

10.  Effects of the rod receptor potential upon retinal extracellular potassium concentration.

Authors:  B Oakley; D G Flaming; K T Brown
Journal:  J Gen Physiol       Date:  1979-12       Impact factor: 4.086

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  2 in total

1.  Spatial buffering of potassium ions in brain extracellular space.

Authors:  K C Chen; C Nicholson
Journal:  Biophys J       Date:  2000-06       Impact factor: 4.033

2.  Electrophysiological properties of ependymal cells (radial glia) in dorsal cortex of the turtle, Pseudemys scripta.

Authors:  B W Connors; B R Ransom
Journal:  J Physiol       Date:  1987-04       Impact factor: 5.182

  2 in total

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