Fibroblast growth factor 2 regulates cumulus differentiation under the control of the oocyte
Purpose We first assessed regulation of FGF2 expression in cumulus cells by FSH and oocyte-secreted factors during in vitro maturation (IVM). Then, we tested the hypothesis that FGF2 regulates meiotic progression, cumulus expansion, and apoptosis in cumulus-oocyte complexes (COC) undergoing IVM. Met...
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Veröffentlicht in: | Journal of assisted reproduction and genetics 2019-05, Vol.36 (5), p.905-913 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Purpose
We first assessed regulation of
FGF2
expression in cumulus cells by FSH and oocyte-secreted factors during in vitro maturation (IVM). Then, we tested the hypothesis that FGF2 regulates meiotic progression, cumulus expansion, and apoptosis in cumulus-oocyte complexes (COC) undergoing IVM.
Methods
In vitro maturation of bovine COC was utilized as a model to assess regulation of
FGF2
expression by FSH and oocyte-secreted factors (via microsurgical removal of the oocyte), as well as effects of graded doses of FGF2 on meiotic progression, degree of cumulus expansion, dissociation of cumulus cells, and cumulus cells apoptosis. Expression of genes regulating functional endpoints altered by FGF2 treatment was assessed in cumulus cells by real-time PCR. Cultures were replicated 4–5 times and effects of treatments were tested by ANOVA.
Results
FGF2
mRNA expression was increased by FSH and oocyte-secreted factors during IVM. Addition of FGF2 to the IVM medium advanced meiosis resumption, decreased the ease with which cumulus cells were dissociated, and inhibited cumulus cells apoptosis. Decreased cumulus dissociation was accompanied by decreased expression of
TNFAIP6.
Conclusions
This is the first study showing that
FGF2
expression is regulated by the oocyte in cumulus cells. Moreover, we report novel effects of FGF2 on cumulus cell survival and extracellular matrix (ECM) quality during IVM that may favor acquisition of developmental competence and suggest physiological roles during the final steps of COC differentiation. |
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ISSN: | 1058-0468 1573-7330 |
DOI: | 10.1007/s10815-019-01436-7 |