Source:http://linkedlifedata.com/resource/pubmed/id/15306542
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2004-11-4
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pubmed:abstractText |
Ca(2+) sparks are highly localized Ca(2+) transients caused by Ca(2+) release from sarcoplasmic reticulum through ryanodine receptors (RyR). In smooth muscle, Ca(2+) sparks activate nearby large-conductance, Ca(2+)-sensitive K(+) (BK) channels to generate spontaneous transient outward currents (STOC). The properties of individual sites that give rise to Ca(2+) sparks have not been examined systematically. We have characterized individual sites in amphibian gastric smooth muscle cells with simultaneous high-speed imaging of Ca(2+) sparks using wide-field digital microscopy and patch-clamp recording of STOC in whole cell mode. We used a signal mass approach to measure the total Ca(2+) released at a site and to estimate the Ca(2+) current flowing through RyR [I(Ca(spark))]. The variance between spark sites was significantly greater than the intrasite variance for the following parameters: Ca(2+) signal mass, I(Ca(spark)), STOC amplitude, and 5-ms isochronic STOC amplitude. Sites that failed to generate STOC did so consistently, while those at the remaining sites generated STOC without failure, allowing the sites to be divided into STOC-generating and STOC-less sites. We also determined the average number of spark sites, which was 42/cell at a minimum and more likely on the order of at least 400/cell. We conclude that 1) spark sites differ in the number of RyR, BK channels, and coupling ratio of RyR-BK channels, and 2) there are numerous Ca(2+) spark-generating sites in smooth muscle cells. The implications of these findings for the organization of the spark microdomain are explored.
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pubmed:grant | |
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 |
Dec
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pubmed:issn |
0363-6143
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
287
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
C1577-88
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:15306542-Animals,
pubmed-meshheading:15306542-Bufo marinus,
pubmed-meshheading:15306542-Calcium,
pubmed-meshheading:15306542-Calcium Signaling,
pubmed-meshheading:15306542-Cytoplasm,
pubmed-meshheading:15306542-Large-Conductance Calcium-Activated Potassium Channels,
pubmed-meshheading:15306542-Microscopy, Fluorescence,
pubmed-meshheading:15306542-Myocytes, Smooth Muscle,
pubmed-meshheading:15306542-Patch-Clamp Techniques,
pubmed-meshheading:15306542-Potassium Channels, Calcium-Activated,
pubmed-meshheading:15306542-Ryanodine Receptor Calcium Release Channel,
pubmed-meshheading:15306542-Sarcoplasmic Reticulum
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pubmed:year |
2004
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pubmed:articleTitle |
Ca(2+) spark sites in smooth muscle cells are numerous and differ in number of ryanodine receptors, large-conductance K(+) channels, and coupling ratio between them.
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pubmed:affiliation |
Department of Physiology, University of Massachusetts Medical Center, 55 Lake Ave. North, Worcester, MA 01655, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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