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Article: Differential expression and regulation of Cryab in mouse uterus during preimplantation period

TitleDifferential expression and regulation of Cryab in mouse uterus during preimplantation period
Authors
Issue Date2013
Citation
Reproduction, 2013, v. 145, n. 6, p. 577-585 How to Cite?
AbstractThe aim of this study was to examine the expression and regulation of the crystallin, alpha B (Cryab) gene in mouse uterus during the peri-implantation period by in situ hybridization and real-time PCR. There was no detectable Cryab mRNA signal on days 1-4 of pregnancy. On day 5 of pregnancy when embryo implanted, a high level of Cryab mRNA signal was found in the subluminal stroma surrounding the implanting blastocyst. On days 6-8, Cryab mRNA was strongly expressed in the primary decidua. By real-time PCR, a high level of Cryab expression was detected on days 7 and 8 of pregnancy, although Cryab expression was seen from days 1 to 8. Under in vivo and in vitro artificial decidualization, Cryab expression was significantly elevated. Compared with the progesterone-primed delayed implantation uterus, a high level of Cryab mRNA expression was observed in estrogen-activated implantation uterus. In the uterine stromal cells, cAMP, estrogen, and progesterone could induce the expression of Cryab gene. In the ovariectomized mouse uterus, estrogen could also induce the expression of Cryab while progesterone inhibited its expression. Our data suggest that Cryab may play an important role during mouse embryo implantation and decidualization and that estrogen and progesterone can regulate the expression of Cryab gene. © 2013 Society for Reproduction and Fertility.
Persistent Identifierhttp://hdl.handle.net/10722/334319
ISSN
2023 Impact Factor: 3.7
2023 SCImago Journal Rankings: 1.131
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorTian, Xue Chao-
dc.contributor.authorWang, Qu Yuan-
dc.contributor.authorLi, Dang Dang-
dc.contributor.authorWang, Shou Tang-
dc.contributor.authorYang, Zhan Qing-
dc.contributor.authorGuo, Bin-
dc.contributor.authorYue, Zhan Peng-
dc.date.accessioned2023-10-20T06:47:17Z-
dc.date.available2023-10-20T06:47:17Z-
dc.date.issued2013-
dc.identifier.citationReproduction, 2013, v. 145, n. 6, p. 577-585-
dc.identifier.issn1470-1626-
dc.identifier.urihttp://hdl.handle.net/10722/334319-
dc.description.abstractThe aim of this study was to examine the expression and regulation of the crystallin, alpha B (Cryab) gene in mouse uterus during the peri-implantation period by in situ hybridization and real-time PCR. There was no detectable Cryab mRNA signal on days 1-4 of pregnancy. On day 5 of pregnancy when embryo implanted, a high level of Cryab mRNA signal was found in the subluminal stroma surrounding the implanting blastocyst. On days 6-8, Cryab mRNA was strongly expressed in the primary decidua. By real-time PCR, a high level of Cryab expression was detected on days 7 and 8 of pregnancy, although Cryab expression was seen from days 1 to 8. Under in vivo and in vitro artificial decidualization, Cryab expression was significantly elevated. Compared with the progesterone-primed delayed implantation uterus, a high level of Cryab mRNA expression was observed in estrogen-activated implantation uterus. In the uterine stromal cells, cAMP, estrogen, and progesterone could induce the expression of Cryab gene. In the ovariectomized mouse uterus, estrogen could also induce the expression of Cryab while progesterone inhibited its expression. Our data suggest that Cryab may play an important role during mouse embryo implantation and decidualization and that estrogen and progesterone can regulate the expression of Cryab gene. © 2013 Society for Reproduction and Fertility.-
dc.languageeng-
dc.relation.ispartofReproduction-
dc.titleDifferential expression and regulation of Cryab in mouse uterus during preimplantation period-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1530/REP-13-0042-
dc.identifier.pmid23579188-
dc.identifier.scopuseid_2-s2.0-84877967627-
dc.identifier.volume145-
dc.identifier.issue6-
dc.identifier.spage577-
dc.identifier.epage585-
dc.identifier.eissn1741-7899-
dc.identifier.isiWOS:000320370800006-

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