Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/40008
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dc.contributor.authorGilchrist, R.en
dc.contributor.authorRitter, L.en
dc.contributor.authorMyllymaa, S.en
dc.contributor.authorKaivo-Oja, N.en
dc.contributor.authorAmato, F.en
dc.contributor.authorRitvos, O.en
dc.contributor.authorMottershead, D.en
dc.date.issued2004en
dc.identifier.citationhttp://abstracts.co.allenpress.com/pweb/ssr2004/document/?ID=38518, 2004 / pp.223en
dc.identifier.issn0006-3363en
dc.identifier.urihttp://hdl.handle.net/2440/40008-
dc.descriptionAbstract onlyen
dc.description.abstractOocytes regulate follicle growth and development by secreting paracrine growth factors that act on granulosa cells (GC). We have recently determined that growth differentiation factor-9 (GDF-9) accounts for ∼50% of the total mitogenic activity of oocytes, the remaining portion is as yet uncharacterized. This study was conducted to identify the receptor/signalling system utilized by oocytes to promote GC proliferation. We used an established oocyte-secreted mitogen bioassay, where denuded oocytes are co-cultured with primed-mouse mural GC. In this system, oocytes, GDF-9, TGF-b1 and activin-A all promoted GC DNA synthesis in a dose-dependent manner, but bone-morphogenic protein-6 (BMP-6) and BMP-7 did not. The type-II receptor for GDF-9 is BMPRII and using real-time RT-PCR, cumulus cells (CC) and mural GC were found to express equivalent levels of BMPRII mRNA. We tested the capacity of the receptor ectodomain (ECD) to neutralize oocyte-stimulated mural GC proliferation. The BMPRII ECD antagonised both oocyte and GDF-9 bioactivity in a dose-dependent manner, completely abolishing activity of both mitogens at 1 ug/ml. The BMPRII ECD did not antagonize TGF-b and partially antagonized activin-A bioactivity, demonstrating its specificity. The TGFbR-II ECD, ActR-II ECD and ActR-IIB ECD all failed to neutralize oocyte- or GDF-9-stimulated GC DNA synthesis, whereas they did antagonize the activity of their respective ligands. The BMPRII ECD also completely antagonized oocyte-stimulated CC DNA synthesis. Using this oocyte-factor bioassay with mural GC transfected with Smad luciferase reporter constructs, we found that oocytes, GDF-9 and TGF-b (but not BMP-6) activated the Smad2/3 pathway. Consistent with this, oocytes and GDF-9 led to phosphorylation of GC Smad2 molecules as detected by Western blot. Conversely the Smad1/5/8 pathway was activated by BMP-6, but not by GDF-9, TGF-b nor surprisingly by oocytes. This study provides evidence that BMPRII is a key receptor for transmitting the paracrine actions of oocytes in GC. However, oocyte-secreted factors do not activate the BMP intracellular signalling pathway but rather the TGF-b/activin intracellular pathway. Thus oocytes utilize an unusual interaction of the two TGF-b superfamily receptor/signalling systems that are generally considered distinct.en
dc.description.urihttp://abstracts.co.allenpress.com/pweb/ssr2004/document/?ID=38518en
dc.language.isoenen
dc.publisherAllen Press Incen
dc.titleMouse oocyte-secreted factors and gdf-9 stimulate granulosa cell proliferation via bmpr-ii and activate the smad2/3 pathwayen
dc.typeConference paperen
dc.identifier.rmid0020072104en
dc.contributor.conferenceThe Society for the Study of Reproduction Annual Meeting (01 Aug 2004 - 04 Aug 2004 : Vancouver, BC, Canada)en
dc.publisher.placeonlineen
dc.identifier.pubid47912-
pubs.library.collectionObstetrics and Gynaecology publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidRitter, L. [0000-0001-5942-851X]en
Appears in Collections:Obstetrics and Gynaecology publications

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