Source:http://linkedlifedata.com/resource/pubmed/id/11502574
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2001-8-14
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pubmed:abstractText |
The quantitative effects of Ca(2+) signaling on gap junctional coupling in lens epithelial cells have been determined using either the spread of Mn(2+) that is imaged by its ability to quench the fluorescence of fura 2 or the spread of the fluorescent dye Alexa Fluor 594. Gap junctional coupling was unaffected by a mechanically stimulated cell-to-cell Ca(2+) wave. Furthermore, when cytosolic Ca(2+) concentration (Ca) increased after the addition of the agonist ATP, coupling was unaffected during the period that Ca was maximal. However, coupling decreased transiently approximately 5-10 min after agonist addition when Ca returned to resting levels, indicating that this transient decrease in coupling was unlikely due to a direct action of Ca on gap junctions. An increase in Ca mediated by the ionophore ionomycin that was sustained for several minutes resulted in a more rapid and sustained decrease in coupling (IC(50) ~300 nM Ca(2+), Hill coefficient of 4), indicating that an increase in Ca alone could regulate gap junctions. Thus Ca increases that occurred during agonist stimulation and cell-to-cell Ca(2+) waves were too transient to mediate a sustained uncoupling of lens epithelial cells.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Fluorescent Dyes,
http://linkedlifedata.com/resource/pubmed/chemical/Fura-2,
http://linkedlifedata.com/resource/pubmed/chemical/Ionomycin,
http://linkedlifedata.com/resource/pubmed/chemical/Manganese
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0363-6143
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
281
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
C972-81
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11502574-Adenosine Triphosphate,
pubmed-meshheading:11502574-Animals,
pubmed-meshheading:11502574-Calcium,
pubmed-meshheading:11502574-Calcium Signaling,
pubmed-meshheading:11502574-Cells, Cultured,
pubmed-meshheading:11502574-Fluorescent Dyes,
pubmed-meshheading:11502574-Fura-2,
pubmed-meshheading:11502574-Gap Junctions,
pubmed-meshheading:11502574-Ionomycin,
pubmed-meshheading:11502574-Kinetics,
pubmed-meshheading:11502574-Lens, Crystalline,
pubmed-meshheading:11502574-Manganese,
pubmed-meshheading:11502574-Pigment Epithelium of Eye,
pubmed-meshheading:11502574-Sheep,
pubmed-meshheading:11502574-Time Factors
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pubmed:year |
2001
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pubmed:articleTitle |
Ca(2+) regulation of gap junctional coupling in lens epithelial cells.
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pubmed:affiliation |
Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, Minnesota 55455, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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