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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0006675,
umls-concept:C0010453,
umls-concept:C0032102,
umls-concept:C0035031,
umls-concept:C0036536,
umls-concept:C0036537,
umls-concept:C0178719,
umls-concept:C0205112,
umls-concept:C0237401,
umls-concept:C0300926,
umls-concept:C0312853,
umls-concept:C0332120,
umls-concept:C0936012,
umls-concept:C1135969,
umls-concept:C1555029
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pubmed:issue |
9
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pubmed:dateCreated |
1993-1-25
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pubmed:abstractText |
Ca2+ redistribution from an intracellular site(s) is a key biochemical event associated with relaxin (RLX) secretion by large luteal cells (LLCs) of porcine origin. However, the functional significance of internal stores of Ca2+ to basal rates of RLX secretion is not well understood. In addition, the identity of the intracellular storage site(s) for Ca2+ within LLCs is not known, nor is it clear if all RLX-releasing LLCs are equally dependent on this pool. In the present study, release of RLX from 24 h cultured luteal cells derived from early pregnant swine was monitored by a reverse hemolytic plaque assay (RHPA). Incubation of cultures in the presence of graded concentrations of thapsigargin (1 nM-1 microM), a plant sesquiterpene lactone that inhibits endoplasmic reticulum Ca(2+)-ATPase and thereby increases cytosolic Ca2+ concentrations, resulted in a dose-related increase in basal RLX secretion. The stimulatory effect of thapsigargin on RLX production was not abrogated by culture in Ca(2+)-free medium. Suppression of Ca2+ release from the endoplasmic reticulum of LLCs, achieved by incubating monolayers in medium containing dantrolene (1-100 microM), resulted in dose-related inhibition of basal RLX release. Taken together, these results suggest that the endoplasmic reticulum serves as a major storage site for Ca2+ redistribution within LLCs and, furthermore, that mobilization from this site is functionally coupled to basal secretion of RLX.
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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/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Dantrolene,
http://linkedlifedata.com/resource/pubmed/chemical/Relaxin,
http://linkedlifedata.com/resource/pubmed/chemical/Terpenes,
http://linkedlifedata.com/resource/pubmed/chemical/Thapsigargin
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0143-4160
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
571-80
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1468119-Animals,
pubmed-meshheading:1468119-Calcium,
pubmed-meshheading:1468119-Cell Compartmentation,
pubmed-meshheading:1468119-Cells, Cultured,
pubmed-meshheading:1468119-Corpus Luteum,
pubmed-meshheading:1468119-Dantrolene,
pubmed-meshheading:1468119-Endoplasmic Reticulum,
pubmed-meshheading:1468119-Female,
pubmed-meshheading:1468119-Hemolytic Plaque Technique,
pubmed-meshheading:1468119-Intracellular Fluid,
pubmed-meshheading:1468119-Pregnancy,
pubmed-meshheading:1468119-Relaxin,
pubmed-meshheading:1468119-Secretory Rate,
pubmed-meshheading:1468119-Stimulation, Chemical,
pubmed-meshheading:1468119-Swine,
pubmed-meshheading:1468119-Terpenes,
pubmed-meshheading:1468119-Thapsigargin
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pubmed:year |
1992
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pubmed:articleTitle |
Evidence that basal secretion of relaxin by individual cultured large luteal cells is influenced by mobilization of intracellular calcium: analysis by a reverse hemolytic plaque assay.
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pubmed:affiliation |
Department of Veterinary Physiology and Pharmacology, College of Veterinary Medicine, Iowa State University, Ames.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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