Literature DB >> 11676192

Potassium channels of glial cells: distribution and function.

Y Horio1.   

Abstract

Firing of neurons changes the extracellular concentration of K+ ions ([K+]o). Glial cells have the ability to maintain [K+]o at a constant level. This function has been called "K+-spatial buffering". K+ channels are believed to be involved in K+-spatial buffering. Kir4.1 in retinal glial cells and Kir2.1, Kir2.3 and Kv1.5 in Schwann cells have been identified. All of these K+ channels show polarized distribution, which enables the channels to transport K+ ions to appropriate regions such as blood vessels and the vitreous body. These channels have a consensus C-terminal sequence that can bind a protein containing PDZ (PSD-95/dlg/ZO1) domains, which may regulate the distribution of the channels. Kir4.1 is predominantly expressed in membranes adjacent to basement membranes. Laminin, a component of basement membranes, is necessary for the surface expression of Kir4.1 in cultured retinal glial cells, suggesting that an extracellular signal regulates the function of glial cells. In some cases, K+ buffering has been considered to couple tightly with water flux. Actually the aquaporin-4 water channel has been found to colocalize with Kir4.1 in retinal glial cells. Recent studies of K+ channels have elucidated the mechanisms of old well-known phenomena and present new unknown roles of glial cells.

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Year:  2001        PMID: 11676192     DOI: 10.1254/jjp.87.1

Source DB:  PubMed          Journal:  Jpn J Pharmacol        ISSN: 0021-5198


  7 in total

1.  Human Mesenchymal Stem Cells from Adipose Tissue Differentiated into Neuronal or Glial Phenotype Express Different Aquaporins.

Authors:  Rosanna Avola; Adriana Carol Eleonora Graziano; Giovanna Pannuzzo; Venera Cardile
Journal:  Mol Neurobiol       Date:  2016-12-05       Impact factor: 5.590

2.  Selective inhibition of the K(ir)2 family of inward rectifier potassium channels by a small molecule probe: the discovery, SAR, and pharmacological characterization of ML133.

Authors:  Hao-Ran Wang; Meng Wu; Haibo Yu; Shunyou Long; Amy Stevens; Darren W Engers; Henry Sackin; J Scott Daniels; Eric S Dawson; Corey R Hopkins; Craig W Lindsley; Min Li; Owen B McManus
Journal:  ACS Chem Biol       Date:  2011-06-13       Impact factor: 5.100

3.  Kir4.1 expression by astrocytes and oligodendrocytes in CNS white matter: a developmental study in the rat optic nerve.

Authors:  Amanpreet S Kalsi; Kirsty Greenwood; Graham Wilkin; Arthur M Butt
Journal:  J Anat       Date:  2004-06       Impact factor: 2.610

4.  Silencing the Kir4.1 potassium channel subunit in satellite glial cells of the rat trigeminal ganglion results in pain-like behavior in the absence of nerve injury.

Authors:  Jean-Philippe Vit; Peter T Ohara; Aditi Bhargava; Kanwar Kelley; Luc Jasmin
Journal:  J Neurosci       Date:  2008-04-16       Impact factor: 6.167

Review 5.  Aquaporins in development -- a review.

Authors:  Huishu Liu; E Marelyn Wintour
Journal:  Reprod Biol Endocrinol       Date:  2005-05-11       Impact factor: 5.211

6.  Expression of Kir4.1 and Kir5.1 inwardly rectifying potassium channels in oligodendrocytes, the myelinating cells of the CNS.

Authors:  C Brasko; V Hawkins; I Chacon De La Rocha; A M Butt
Journal:  Brain Struct Funct       Date:  2016-02-15       Impact factor: 3.270

7.  Genetically encoded fluorescent indicators for imaging intracellular potassium ion concentration.

Authors:  Yi Shen; Sheng-Yi Wu; Vladimir Rancic; Abhi Aggarwal; Yong Qian; Shin-Ichiro Miyashita; Klaus Ballanyi; Robert E Campbell; Min Dong
Journal:  Commun Biol       Date:  2019-01-14
  7 in total

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