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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1998-12-29
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pubmed:abstractText |
We established and characterized a novel experimental model of in vitro decidualization in normal human endometrial stromal cells. In a comparison of decidualization induction, 8-Br-cAMP showed the strongest ability to induce decidualization in stromal cells among four inducers examined: progesterone, medroxyprogesterone acetate, prostaglandin E2, and 8-Br-cAMP. The effects of 8-Br-cAMP were enhanced by prostaglandin E2 but not altered by medroxyprogesterone acetate. Both progesterone and medroxyprogesterone acetate activity was so weak that it took more than 2 weeks to induce in vitro decidualization. These results suggest that there are two independent decidualization signals in the in vitro decidualization, a cAMP-mediated signaling pathway and a progesterone receptor-mediated signaling pathway, and that cAMP-inducers are major factors in decidualization in vivo. Differential expressions of three membrane aminopeptidases on the stromal cells during the decidualization are also discussed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0030-6096
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
44
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
105-15
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9834623-Cells, Cultured,
pubmed-meshheading:9834623-Decidua,
pubmed-meshheading:9834623-Endometrium,
pubmed-meshheading:9834623-Female,
pubmed-meshheading:9834623-Humans,
pubmed-meshheading:9834623-Pregnancy,
pubmed-meshheading:9834623-Reference Values,
pubmed-meshheading:9834623-Stromal Cells
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pubmed:year |
1998
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pubmed:articleTitle |
Establishment and characterization of in vitro decidualization in normal human endometrial stromal cells.
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pubmed:affiliation |
Department of Obstetrics, Osaka City University Medical School, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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