Literature DB >> 11169792

Identification of an inward rectifier potassium channel gene expressed in mouse cortical astrocytes.

L Li1, V Head, L C Timpe.   

Abstract

These experiments identify an inward rectifier K+ (Kir) channel expressed in mouse cortical and white matter astrocytes at the molecular level. Messenger RNA for one of the known Kir channel genes, Kir4.1, is present at much higher levels in cortical astrocytes in primary culture than the other known Kir family members. In culture, the level of Kir4.1 mRNA is lower in proliferating cells and in cells cultured for 16 h under hypoxic conditions, compared to confluent cells. Partial differentiation of the astrocytes with dibutyryl cAMP or by coculture with neurons has no effect on the Kir4.1 mRNA level. In situ hybridization experiments show that Kir4.1 mRNA is broadly distributed in the adult brain, including the neocortex, the stratum pyrimadale of the hippocampus, and the piriform cortex. Immunostaining confirms that the Kir4.1 protein is expressed by cultured astrocytes and also by cocultured cortical neurons. Astrocytes and neurons display a patchy pattern of immunostaining, raising the possibility that the channels sort themselves in clusters in the plasma membrane. Stellate cells in the neocortex and white matter are immunoreactive for Kir4.1, and double immunofluorescence experiments show colocalization of Kir4.1 and glial acidic fibrillary protein (GFAP) on stellate cells in the white matter. The cloned mouse Kir4.1 cDNA, when expressed heterologously in HEK cells, gives rise to inactivating Kir channels similar to those recorded from cultured astrocytes. These results indicate that the Kir4.1 gene product forms a Kir channel, or is a subunit of the channel, in mouse cortical astrocytes both in culture and in vivo.

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Year:  2001        PMID: 11169792     DOI: 10.1002/1098-1136(20010101)33:1<57::aid-glia1006>3.0.co;2-0

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


  24 in total

Review 1.  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 2.  Potassium buffering in the central nervous system.

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

3.  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

Review 4.  Functional implications for Kir4.1 channels in glial biology: from K+ buffering to cell differentiation.

Authors:  Michelle L Olsen; Harald Sontheimer
Journal:  J Neurochem       Date:  2008-08-08       Impact factor: 5.372

Review 5.  Role of membrane potential in the regulation of cell proliferation and differentiation.

Authors:  Sarah Sundelacruz; Michael Levin; David L Kaplan
Journal:  Stem Cell Rev Rep       Date:  2009-06-27       Impact factor: 5.739

Review 6.  Gap junctions in inherited human disorders of the central nervous system.

Authors:  Charles K Abrams; Steven S Scherer
Journal:  Biochim Biophys Acta       Date:  2011-08-16

7.  Correlating Gene-specific DNA Methylation Changes with Expression and Transcriptional Activity of Astrocytic KCNJ10 (Kir4.1).

Authors:  Sinifunanya E Nwaobi; Michelle L Olsen
Journal:  J Vis Exp       Date:  2015-09-26       Impact factor: 1.355

8.  Role of Kir4.1 channels in growth control of glia.

Authors:  Haruki Higashimori; Harald Sontheimer
Journal:  Glia       Date:  2007-12       Impact factor: 7.452

9.  Immunocytochemical studies of aquaporin 4, Kir4.1, and α1-syntrophin in the astrocyte endfeet of mouse brain capillaries.

Authors:  Hisatsugu Masaki; Yoshihiro Wakayama; Hajime Hara; Takahiro Jimi; Akihiko Unaki; Shoji Iijima; Hiroaki Oniki; Kiyoko Nakano; Koji Kishimoto; Yoshiko Hirayama
Journal:  Acta Histochem Cytochem       Date:  2010-07-21       Impact factor: 1.938

10.  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

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