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A central role for cAMP/EPAC/RAP/PI3K/AKT/CREB signaling in LH-induced follicular Pgr expression at medaka ovulation

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Biol. Reprod. 105-2_413–426.pdf9.05 MBPDFView/Open
Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/86439

Title: A central role for cAMP/EPAC/RAP/PI3K/AKT/CREB signaling in LH-induced follicular Pgr expression at medaka ovulation
Authors: Ogiwara, Katsueki Browse this author →KAKEN DB
Hoyagi, Miyuki Browse this author
Takahashi, Takayuki Browse this author
Keywords: teleost
medaka
LH
ovulation
PGR
EPAC/RAP/PI3K/AKT/CREB signaling
Issue Date: Aug-2021
Publisher: Oxford University Press
Journal Title: Biology of reproduction
Volume: 105
Issue: 2
Start Page: 413
End Page: 426
Publisher DOI: 10.1093/biolre/ioab077
Abstract: Nuclear progestin receptor (PGR) is a ligand-activated transcription factor that has been identified as a pivotal mediator of many processes associated with ovarian and uterine function, and aberrant control of PGR activity causes infertility and disease including cancer. The essential role of PGR in vertebrate ovulation is well recognized, but the mechanisms by which PGR is rapidly and transiently induced in preovulatory follicles after the ovulatory LH surge are not known in lower vertebrates. To address this issue, we utilized the small freshwater teleost medaka Oryzias latipes, which serves as a good model system for studying vertebrate ovulation. In the in vitro ovulation system using preovulatory follicles dissected from the fish ovaries, we found that inhibitors of EPAC (brefeldin A), RAP (GGTI298), PI3K (Wortmannin), AKT (AKT inhibitor IV), and CREB (KG-501) inhibited LH-induced follicle ovulation, while the PKA inhibitor H-89 had no effect on follicle ovulation. The inhibitors capable of inhibiting follicle ovulation also inhibited follicular expression of Pgr and matrix metalloproteinase-15 (Mmp15), the latter of which was previously shown to not only be a downstream effector of Pgr but also a proteolytic enzyme indispensable for follicle rupture in medaka ovulation. Further detailed analysis revealed for the first time that the cAMP/EPAC/RAP/PI3K/AKT/CREB signaling pathway mediates the LH signal to induce Pgr expression in preovulatory follicles. Our data also showed that phosphorylated Creb1 is a transcription factor essential for pgr expression and that Creb1 phosphorylated by Akt1, rather than PKA, may be preferably used to induce pgr expression. Summary sentence EPAC/RAP/PI3K/AKT/CREB signaling mediates LH-induced cAMP signaling to induce medaka Pgr expression in ovulating follicles.
Rights: This is a pre-copyedited, author-produced version of an article accepted for publication in Biology of reproduction following peer review. The version of record Biology of Reproduction, Volume 105, Issue 2, August 2021, Pages 413–426 is available online at: https://doi.org/10.1093/biolre/ioab077.
Type: article (author version)
URI: http://hdl.handle.net/2115/86439
Appears in Collections:理学院・理学研究院 (Graduate School of Science / Faculty of Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 荻原 克益

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