Source:http://linkedlifedata.com/resource/pubmed/id/20201888
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2010-3-5
|
pubmed:abstractText |
Because previous findings showed that in human embryonic stem cell-derived cardiomyocytes (hESC-CM) the machinery for Ca2+-induced release of calcium is immature, we tested the hypothesis that hESC-CM contain functional 1,4,5-inositol triphosphate (IP3)-operated intracellular Ca2+ ([Ca2+]i) stores. We investigated the effects of angiotensin II (AT-II) and endothelin 1 (ET-1), which activate the 1,4,5-IP3 pathway, on [Ca2+]i transients and contractions in hESC-CM. Our major findings were that in hESC-CM, both AT-II (10(-9)-10(-7) M) and ET-1 (10(-9)-10(-7) M) exert inotropic and lusitropic effects. The involvement of 1,4,5-IP3-dependent intracellular Ca2+ release in AT-I-induced effects was supported by these findings: the effects of AT-II were blocked by 2-aminoethoxyphenyl borate (2-APB, a 1,4,5-IP3 receptor blocker) and U73122 (a phosopholipase C blocker); and hESC-CM express AT-II type 1 and IP3 type I and II receptors as determined by fluorescence immunostaining. In conclusion, hESC-CM exhibit functional AT-II and ET-1 signaling pathways, as well as 1,4,5-IP3-operated releasable Ca2+ stores.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
1749-6632
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
1188
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
68-77
|
pubmed:meshHeading |
pubmed-meshheading:20201888-Angiotensin II,
pubmed-meshheading:20201888-Animals,
pubmed-meshheading:20201888-Calcium,
pubmed-meshheading:20201888-Cell Differentiation,
pubmed-meshheading:20201888-Cell Line,
pubmed-meshheading:20201888-Embryonic Stem Cells,
pubmed-meshheading:20201888-Endothelin-1,
pubmed-meshheading:20201888-Humans,
pubmed-meshheading:20201888-Mice,
pubmed-meshheading:20201888-Mice, Inbred ICR,
pubmed-meshheading:20201888-Myocytes, Cardiac,
pubmed-meshheading:20201888-Signal Transduction
|
pubmed:year |
2010
|
pubmed:articleTitle |
Human embryonic stem cell-derived cardiomyocytes can mobilize 1,4,5-inositol trisphosphate-operated [Ca2+]i stores: the functionality of angiotensin-II/endothelin-1 signaling pathways.
|
pubmed:affiliation |
Ruth and Bruce Rappaport Faculty of Medicine, The Rappaport Family Institute for Research in the Medical Sciences, TechnionIsrael Institute of Technology, Haifa, Israel.
|
pubmed:publicationType |
Journal Article
|