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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0006556,
umls-concept:C0017262,
umls-concept:C0030685,
umls-concept:C0085080,
umls-concept:C0185117,
umls-concept:C0205263,
umls-concept:C0391871,
umls-concept:C0596235,
umls-concept:C0680255,
umls-concept:C1153410,
umls-concept:C1283071,
umls-concept:C1419779,
umls-concept:C1963578,
umls-concept:C2911684
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pubmed:issue |
4
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pubmed:dateCreated |
1993-3-4
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pubmed:abstractText |
We constructed an expression plasmid (pMAMCRR51) that carried the entire protein-coding sequence of the rabbit cardiac ryanodine receptor cDNA, linked to the dexamethasone-inducible mouse mammary tumor virus promoter and Escherichia coli xanthine-guanine phosphoribosyltransferase (gpt). Chinese hamster ovary (CHO) cells were transfected with pMAMCRR51 and mycophenolic acid-resistant cells showing caffeine-induced intracellular Ca2+ transients were selected. Immunoprecipitation with a monoclonal antibody against the canine cardiac ryanodine receptor revealed that the cell clones thus selected exhibited Ca(2+)-dependent [3H]ryanodine binding activity, which was stimulated by 5 mM ATP or 1 M KCl. The apparent dissociation constant (Kd) for [3H]ryanodine was 6.6 nM in 1 M KCl, which was similar to the Kd obtained with cardiac microsomes. Immunoprecipitation also demonstrated that these cell clones expressed a protein indistinguishable in M(r) from the ryanodine receptor in canine cardiac microsomes. The ryanodine binding activity expressed in CHO cells increased significantly after dexamethasone induction. In saponin-skinned CHO cells transfected with pMAMCRR51, micromolar Ca2+ or millimolar caffeine evoked rapid Ca2+ release from the intracellular Ca2+ stores. In skinned control CHO cells, we did not observe such Ca2+ release activity. These results clearly demonstrate that the cardiac ryanodine receptor is stably expressed in internal membranes of CHO cells and functions as Ca(2+)-induced Ca2+ release channels.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Caffeine,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/Dexamethasone,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cholinergic,
http://linkedlifedata.com/resource/pubmed/chemical/Ryanodine Receptor Calcium Release...,
http://linkedlifedata.com/resource/pubmed/chemical/Saponins
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0021-924X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
112
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
508-13
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pubmed:dateRevised |
2007-12-19
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pubmed:meshHeading |
pubmed-meshheading:1337083-Animals,
pubmed-meshheading:1337083-CHO Cells,
pubmed-meshheading:1337083-Caffeine,
pubmed-meshheading:1337083-Calcium,
pubmed-meshheading:1337083-Calcium Channels,
pubmed-meshheading:1337083-Cricetinae,
pubmed-meshheading:1337083-DNA,
pubmed-meshheading:1337083-Dexamethasone,
pubmed-meshheading:1337083-Extracellular Space,
pubmed-meshheading:1337083-Intracellular Membranes,
pubmed-meshheading:1337083-Myocardium,
pubmed-meshheading:1337083-Plasmids,
pubmed-meshheading:1337083-Rabbits,
pubmed-meshheading:1337083-Receptors, Cholinergic,
pubmed-meshheading:1337083-Ryanodine Receptor Calcium Release Channel,
pubmed-meshheading:1337083-Saponins,
pubmed-meshheading:1337083-Transfection
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pubmed:year |
1992
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pubmed:articleTitle |
Expression of Ca(2+)-induced Ca2+ release channel activity from cardiac ryanodine receptor cDNA in Chinese hamster ovary cells.
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pubmed:affiliation |
Department of Molecular Physiology, National Cardiovascular Center Research Institute, Osaka.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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