Source:http://linkedlifedata.com/resource/pubmed/id/17525153
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
30
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pubmed:dateCreated |
2007-7-23
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pubmed:abstractText |
Indirect evidence suggests that the Müller/glial cell water channel aquaporin-4 (AQP4) modulates K(+) channel function of the closely associated Kir4.1 protein. We used patch clamp to compare Kir4.1 K(+) channel function in freshly isolated Müller cells from retinas of wild-type (+/+) and AQP4 knock-out (-/-) mice. Immunocytochemistry showed a comparable Kir4.1 protein expression pattern in Müller cells from +/+ and -/- retinas, with greatest expression at their end feet. Osmotic water permeability was >4-fold reduced in -/- than in +/+ Müller cells. Resting membrane potential did not differ significantly in +/+ versus -/- Müller cells (-64 +/- 1 versus -64 +/- 1 mV, S.E., n = 24). Whole-cell K(+) currents recorded with a micropipette inserted into the cell soma were Ba(2+)-sensitive and showed no significant differences in magnitude in +/+ versus -/- Müller cells (1.3 +/- 0.1 versus 1.2 +/- 0.1 nA at -160 mV) or in inwardly rectifying current-voltage relationships. Spatially resolved K(+) currents generated by pulsed K(+) injections along Müller cell bodies were also comparable in +/+ versus -/- Müller cells. Single-channel cell-attached patch clamp showed comparable unitary conductance, current-voltage data, and open probability in +/+ versus -/- Müller cells. Thus, contrary to the generally accepted view, our results provide direct evidence against functionally significant AQP4 modulation of Müller cell Kir4.1 K(+) channel function.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/DK35124,
http://linkedlifedata.com/resource/pubmed/grant/DK72517,
http://linkedlifedata.com/resource/pubmed/grant/EB00415,
http://linkedlifedata.com/resource/pubmed/grant/EY13574,
http://linkedlifedata.com/resource/pubmed/grant/HL59198,
http://linkedlifedata.com/resource/pubmed/grant/HL73856
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
27
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pubmed:volume |
282
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
21866-72
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pubmed:dateRevised |
2007-12-3
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pubmed:meshHeading |
pubmed-meshheading:17525153-Animals,
pubmed-meshheading:17525153-Aquaporin 4,
pubmed-meshheading:17525153-Electrophysiology,
pubmed-meshheading:17525153-Eye Enucleation,
pubmed-meshheading:17525153-Immunohistochemistry,
pubmed-meshheading:17525153-Mice,
pubmed-meshheading:17525153-Mice, Knockout,
pubmed-meshheading:17525153-Patch-Clamp Techniques,
pubmed-meshheading:17525153-Permeability,
pubmed-meshheading:17525153-Retina
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pubmed:year |
2007
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pubmed:articleTitle |
Evidence against functional interaction between aquaporin-4 water channels and Kir4.1 potassium channels in retinal Müller cells.
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pubmed:affiliation |
Department of Medicine, Cardiovascular Research Institute, University of California, San Francisco, CA 94143-0521, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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