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Article: Expression and regulation of Ang-2 in murine ovaries during sexual maturation and development of corpus luteum.

TitleExpression and regulation of Ang-2 in murine ovaries during sexual maturation and development of corpus luteum.
Authors
Issue Date2012
Citation
Molekuliarnaia biologiia, 2012, v. 46, n. 6, p. 900-906 How to Cite?
AbstractThe aim of this study was to examine the expression and regulation of angiopoietin-2 (Ang-2) in murine ovaries during sexual maturation, gonadotropin treatment and luteal development by in situ hybridization and RT-PCR. By in situ hybridization Ang-2 mRNA was mainly localized in granulosa cells, thecal cells and corpus luteum, otherwise in oocytes. Moreover, Ang-2 mRNA was highly expressed in corpus luteum and granulosa cells of atretic follicles. According to RT-PCR data, Ang-2 mRNA was lowly expressed on day 10 after birth, then expression levels gradually increased and reached their highest values on day 25 after birth. In the superovulated model of immature mice, Ang-2 expression was strongly induced by equine chorionic gonadotropin (eCG) 48 h post the eCG injection, and was high from 0.5 to 13 h after hCG treatment. In situ hybridization showed that Ang-2 mRNA was highly expressed in corpus luteum from day 2 to 9 post the hCG injection, then the expression levels gradually declined on days 11 and 13 after hCG treatment. According to RT-PCR data, the levels of Ang-2 mRNA expression showed a decline after the hCG injection, with a nadir on day 3, followed by an increase, reaching the highest level on day 9 post-hCG injection. Then again Ang-2 expression gradually declined from day 11 to 15 after hCG injection. These results suggest that Ang-2 may be involved in follicular development, atresia, ovulation, and corpus luteum formation and regression.
Persistent Identifierhttp://hdl.handle.net/10722/334309
ISSN
2023 SCImago Journal Rankings: 0.153

 

DC FieldValueLanguage
dc.contributor.authorGuo, B.-
dc.contributor.authorZhang, X. M.-
dc.contributor.authorLi, S. J.-
dc.contributor.authorTian, X. C.-
dc.contributor.authorWang, S. T.-
dc.contributor.authorLi, D. D.-
dc.contributor.authorLiu, D. F.-
dc.contributor.authorYue, Z. P.-
dc.date.accessioned2023-10-20T06:47:13Z-
dc.date.available2023-10-20T06:47:13Z-
dc.date.issued2012-
dc.identifier.citationMolekuliarnaia biologiia, 2012, v. 46, n. 6, p. 900-906-
dc.identifier.issn0026-8984-
dc.identifier.urihttp://hdl.handle.net/10722/334309-
dc.description.abstractThe aim of this study was to examine the expression and regulation of angiopoietin-2 (Ang-2) in murine ovaries during sexual maturation, gonadotropin treatment and luteal development by in situ hybridization and RT-PCR. By in situ hybridization Ang-2 mRNA was mainly localized in granulosa cells, thecal cells and corpus luteum, otherwise in oocytes. Moreover, Ang-2 mRNA was highly expressed in corpus luteum and granulosa cells of atretic follicles. According to RT-PCR data, Ang-2 mRNA was lowly expressed on day 10 after birth, then expression levels gradually increased and reached their highest values on day 25 after birth. In the superovulated model of immature mice, Ang-2 expression was strongly induced by equine chorionic gonadotropin (eCG) 48 h post the eCG injection, and was high from 0.5 to 13 h after hCG treatment. In situ hybridization showed that Ang-2 mRNA was highly expressed in corpus luteum from day 2 to 9 post the hCG injection, then the expression levels gradually declined on days 11 and 13 after hCG treatment. According to RT-PCR data, the levels of Ang-2 mRNA expression showed a decline after the hCG injection, with a nadir on day 3, followed by an increase, reaching the highest level on day 9 post-hCG injection. Then again Ang-2 expression gradually declined from day 11 to 15 after hCG injection. These results suggest that Ang-2 may be involved in follicular development, atresia, ovulation, and corpus luteum formation and regression.-
dc.languageeng-
dc.relation.ispartofMolekuliarnaia biologiia-
dc.titleExpression and regulation of Ang-2 in murine ovaries during sexual maturation and development of corpus luteum.-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.pmid23350236-
dc.identifier.scopuseid_2-s2.0-84873736364-
dc.identifier.volume46-
dc.identifier.issue6-
dc.identifier.spage900-
dc.identifier.epage906-

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