Literature DB >> 2785716

Spatial buffering of light-evoked potassium increases by retinal Müller (glial) cells.

C J Karwoski1, H K Lu, E A Newman.   

Abstract

Activity-dependent variations in extracellular potassium concentration in the central nervous system may be regulated, in part, by potassium spatial buffering currents in glial cells. The role of spatial buffering in the retina was assessed by measuring light-evoked potassium changes in amphibian eyecups. The amplitude of potassium increases in the vitreous humor was reduced to approximately 10 percent by 50 micromolar barium, while potassium increases in the inner plexiform layer were largely unchanged. The decrease in the vitreal potassium response was accurately simulated with a numerical model of potassium current flow through Müller cells, the principal glial cells of the retina. Barium also substantially increased the input resistance of Müller cells and blocked the Müller cell-generated M-wave, indicating that barium blocks the potassium channels of Müller cells. Thus, after a light-evoked potassium increase within the retina, there is a substantial transfer of potassium from the retina to the vitreous humor by potassium current flow through Müller cells.

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Year:  1989        PMID: 2785716      PMCID: PMC2562506          DOI: 10.1126/science.2785716

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  20 in total

1.  Effects of bicarbonate on glial cell membrane potential in Necturus optic nerve.

Authors:  M L Astion; J A Coles; R K Orkand
Journal:  Neurosci Lett       Date:  1987-04-23       Impact factor: 3.046

2.  Passive ionic properties of frog retinal pigment epithelium.

Authors:  S S Miller; R H Steinberg
Journal:  J Membr Biol       Date:  1977-09-15       Impact factor: 1.843

3.  Distribution of potassium conductance in mammalian Müller (glial) cells: a comparative study.

Authors:  E A Newman
Journal:  J Neurosci       Date:  1987-08       Impact factor: 6.167

Review 4.  Diversity and ubiquity of K channels.

Authors:  B Rudy
Journal:  Neuroscience       Date:  1988-06       Impact factor: 3.590

5.  Generation of the e-wave of the electroretinogram in the frog retina.

Authors:  C J Karwoski; E A Newman
Journal:  Vision Res       Date:  1988       Impact factor: 1.886

6.  Model of potassium dynamics in the central nervous system.

Authors:  L L Odette; E A Newman
Journal:  Glia       Date:  1988       Impact factor: 7.452

7.  Changes in [K+]0 induced by transretinal currents in frog retina.

Authors:  C J Karwoski
Journal:  Physiol Bohemoslov       Date:  1988

8.  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

9.  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

10.  Neurons, potassium, and glia in proximal retina of Necturus.

Authors:  C J Karwoski; L M Proenza
Journal:  J Gen Physiol       Date:  1980-02       Impact factor: 4.086

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  46 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.  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

3.  Regulation of inwardly rectifying K+ channels in retinal pigment epithelial cells by intracellular pH.

Authors:  Yukun Yuan; Masahiko Shimura; Bret A Hughes
Journal:  J Physiol       Date:  2003-03-28       Impact factor: 5.182

Review 4.  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 5.  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

6.  K(+)-evoked Müller cell depolarization generates b-wave of electroretinogram in toad retina.

Authors:  R Wen; B Oakley
Journal:  Proc Natl Acad Sci U S A       Date:  1990-03       Impact factor: 11.205

7.  Implication of Kir4.1 channel in excess potassium clearance: an in vivo study on anesthetized glial-conditional Kir4.1 knock-out mice.

Authors:  Oana Chever; Biljana Djukic; Ken D McCarthy; Florin Amzica
Journal:  J Neurosci       Date:  2010-11-24       Impact factor: 6.167

Review 8.  Potassium buffering in the central nervous system.

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

Review 9.  Müller cells and diabetic retinopathy.

Authors:  Brandon A Coughlin; Derrick J Feenstra; Susanne Mohr
Journal:  Vision Res       Date:  2017-09-05       Impact factor: 1.886

10.  Delayed K+ clearance associated with aquaporin-4 mislocalization: phenotypic defects in brains of alpha-syntrophin-null mice.

Authors:  Mahmood Amiry-Moghaddam; Anne Williamson; Maria Palomba; Tore Eid; Nihal C de Lanerolle; Erlend A Nagelhus; Marvin E Adams; Stanley C Froehner; Peter Agre; Ole P Ottersen
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-03       Impact factor: 11.205

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