Literature DB >> 6717594

Regional specialization of retinal glial cell membrane.

E A Newman.   

Abstract

Neural activity generates increases in extracellular K+ concentration, [K+]0, which must be regulated in order to maintain normal brain function. Glial cells are thought to play an important part in this regulation through the process of K+ spatial buffering: K+-mediated current flow through glial cells redistributes extracellular K+ following localized [K+]0 increases. As is the case in other glia, the retinal Müller cell is permeable almost exclusively to K+ . Recent experiments have suggested that this K+ conductance may not be distributed uniformly over the cell surface. In the present study, two novel techniques have been used to assess the Müller cell K+ conductance distribution. The results demonstrate that 94% of all membrane conductance lies in the endfoot process of the cell. This strikingly asymmetric distribution has important consequences for theories concerning K+ buffering and should help to explain the generation of the electroretinogram.

Mesh:

Substances:

Year:  1984        PMID: 6717594      PMCID: PMC2693194          DOI: 10.1038/309155a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  13 in total

1.  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

2.  B-wave currents in the frog retina.

Authors:  E A Newman
Journal:  Vision Res       Date:  1979       Impact factor: 1.886

3.  Contribution to steady potential shifts of slow depolarization in cells presumed to be glia.

Authors:  V F Castellucci; S Goldring
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1970-02

4.  Neuroglia: biophysical properties and physiologic function.

Authors:  M C Trachtenberg; D A Pollen
Journal:  Science       Date:  1970-02-27       Impact factor: 47.728

5.  Intracellular responses of the Müller (glial) cells of mudpuppy retina: their relation to b-wave of the electroretinogram.

Authors:  R F Miller; J E Dowling
Journal:  J Neurophysiol       Date:  1970-05       Impact factor: 2.714

6.  Relationship between Müller cell responses, a local transretinal potential, and potassium flux.

Authors:  C J Karowski; L M Proenza
Journal:  J Neurophysiol       Date:  1977-03       Impact factor: 2.714

7.  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

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.  The contribution by glial cells to surface recordings from the optic nerve of an amphibian.

Authors:  M W Cohen
Journal:  J Physiol       Date:  1970-10       Impact factor: 5.182

10.  A voltage-clamp study of the light response in solitary rods of the tiger salamander.

Authors:  C R Bader; P R Macleish; E A Schwartz
Journal:  J Physiol       Date:  1979-11       Impact factor: 5.182

View more
  66 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

Review 2.  Molecular substrates of potassium spatial buffering in glial cells.

Authors:  Paulo Kofuji; Nathan C Connors
Journal:  Mol Neurobiol       Date:  2003-10       Impact factor: 5.590

Review 3.  Glial K⁺ clearance and cell swelling: key roles for cotransporters and pumps.

Authors:  Nanna Macaulay; Thomas Zeuthen
Journal:  Neurochem Res       Date:  2012-02-26       Impact factor: 3.996

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

Review 5.  Potassium channels and neurovascular coupling.

Authors:  Kathryn M Dunn; Mark T Nelson
Journal:  Circ J       Date:  2010-03-16       Impact factor: 2.993

Review 6.  Potassium buffering in the central nervous system.

Authors:  P Kofuji; E A Newman
Journal:  Neuroscience       Date:  2004       Impact factor: 3.590

7.  Functional expression of Kir4.1 channels in spinal cord astrocytes.

Authors:  M L Olsen; H Higashimori; S L Campbell; J J Hablitz; H Sontheimer
Journal:  Glia       Date:  2006-04-01       Impact factor: 7.452

8.  Targeted deletion of β1-syntrophin causes a loss of Kir 4.1 from Müller cell endfeet in mouse retina.

Authors:  Shreyas B Rao; Shirin Katoozi; Nadia Skauli; Stanley C Froehner; Ole Petter Ottersen; Marvin E Adams; Mahmood Amiry-Moghaddam
Journal:  Glia       Date:  2019-02-25       Impact factor: 7.452

9.  Secondary paracentral retinal holes following internal limiting membrane removal.

Authors:  P Steven; H Laqua; D Wong; H Hoerauf
Journal:  Br J Ophthalmol       Date:  2006-03       Impact factor: 4.638

10.  Computer simulations of neuron-glia interactions mediated by ion flux.

Authors:  G G Somjen; H Kager; W J Wadman
Journal:  J Comput Neurosci       Date:  2008-02-23       Impact factor: 1.621

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.