Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/60690
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dc.contributor.authorTam, K.en
dc.contributor.authorRussell, D.en
dc.contributor.authorPeet, D.en
dc.contributor.authorBracken, C.en
dc.contributor.authorRodgers, R.en
dc.contributor.authorThompson, J.en
dc.contributor.authorKind, K.en
dc.date.issued2010en
dc.identifier.citationMolecular and Cellular Endocrinology, 2010; 327(1-2):47-55en
dc.identifier.issn0303-7207en
dc.identifier.issn1872-8057en
dc.identifier.urihttp://hdl.handle.net/2440/60690-
dc.description.abstractHypoxia inducible factors (HIFs) are transcription factors that mediate physiological responses to hypoxia. Hypoxia is established as the major inducer of HIFs, but stimuli such as transition metals and hormones also induce HIF target genes. Whilst the ovarian granulosa cell layer is known to be avascular and the follicle is vascularised via the thecal cell layer, little is known about the role of hypoxia or HIFs in regulating ovarian function. In this study, we hypothesized that hypoxia as well as non-hypoxic stimuli cooperate in promoting follicle differentiation and luteinization via HIF activity and resultant gene regulation. We quantitatively measured the HIF1alpha protein response to hCG in ovarian granulosa cell cultures and in vivo and developed a transgenic (HRE(4)-SV40-EGFP) HIF reporter mouse line. We observed a time-dependent increase of HIF1alpha protein levels in granulosa cells post-hCG in vivo, maximal around time of ovulation. hCG alone was unable to promote HIF1alpha protein accumulation in cultured granulosa cells, but increased protein abundance was observed when combined with a hypoxic stimulus. HRE-EGFP ovaries showed no follicular EGFP in stages prior to antrum formation. However, HIF regulated EGFP was maximally induced in granulosa cells around the time of ovulation and readily observed in corpora lutea. There was also an increase in HIF regulated EGFP activity in the corpora lutea from functional to regressing stages. Taken together, these observations establish the notion that HIFs play a role during follicular differentiation and luteinization.en
dc.description.statementofresponsibilityKimberley K.Y. Tam, Darryl L. Russell, Daniel J. Peet, Cameron P. Bracken, Raymond J. Rodgers, Jeremy G. Thompson, and Karen L. Kinden
dc.language.isoenen
dc.publisherElsevier Sci Ireland Ltden
dc.rightsCopyright © 2010 Elsevier Ireland Ltd. All rights reserved.en
dc.subjectFollicle; Ovulation; Human chorionic gonadotropin; Hypoxia inducible factoren
dc.titleHormonally regulated follicle differentiation and luteinization in the mouse is associated with hypoxia inducible factor activityen
dc.typeJournal articleen
dc.identifier.rmid0020100519en
dc.identifier.doi10.1016/j.mce.2010.06.008en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/453556en
dc.identifier.pubid33495-
pubs.library.collectionMolecular and Biomedical Science publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidRussell, D. [0000-0002-4930-7658]en
dc.identifier.orcidPeet, D. [0000-0002-6085-8936]en
dc.identifier.orcidRodgers, R. [0000-0002-2139-2969]en
dc.identifier.orcidThompson, J. [0000-0003-4941-7731]en
Appears in Collections:Molecular and Biomedical Science publications

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