YAP signaling in preovulatory granulosa cells is critical for the functioning of the EGF network during ovulation

Failure to ovulate is a major cause of infertility. The critical pathway that induces ovulation involves the EGF and MAPK phosphorylation, but studies in rodents have suggested that the Hippo activator, YAP, is also involved. It is unknown whether YAP-dependent transcriptional activity is important...

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Veröffentlicht in:Molecular and cellular endocrinology 2022-02, Vol.541, p.111524-111524, Article 111524
Hauptverfasser: Dos Santos, Esdras Corrêa, Lalonde-Larue, Ariane, Antoniazzi, Alfredo Quites, Barreta, Marcos Henrique, Price, Christopher A., Dias Gonçalves, Paulo Bayard, Portela, Valério Marques, Zamberlam, Gustavo
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container_title Molecular and cellular endocrinology
container_volume 541
creator Dos Santos, Esdras Corrêa
Lalonde-Larue, Ariane
Antoniazzi, Alfredo Quites
Barreta, Marcos Henrique
Price, Christopher A.
Dias Gonçalves, Paulo Bayard
Portela, Valério Marques
Zamberlam, Gustavo
description Failure to ovulate is a major cause of infertility. The critical pathway that induces ovulation involves the EGF and MAPK phosphorylation, but studies in rodents have suggested that the Hippo activator, YAP, is also involved. It is unknown whether YAP-dependent transcriptional activity is important for the LH- or EGF-induced ovulatory cascade in monovulatory species such as the cow. Using a well-defined preovulatory GC culture system, we employed pharmacological inhibitors to demonstrate that YAP signaling is critical for expression of EGFR and downstream target genes EREG, EGR1 and TNFAIP6. Most importantly, by using an ultrasound guided follicle injection system, we also showed that the classic Hippo signaling inhibitor Verteporfin inhibits GnRH-induced ovulation in vivo in cattle. In conclusion, YAP transcriptional activity is critical for EGF-like cascade induced by LH to promote ovulation in a monovulatory species. •YAP and TEAD 1-4 are expressed in bovine preovulatory granulosa cells.•Classic LH-induced preovulatory genes are affected by YAP signaling disruption.•Verteporfin and P17 affect EGF receptor expression in preovulatory granulosa cells.•EGFR-downstream signaling depends, at least partly, on YAP-TEAD interaction.•In vivo intrafollicular administration of Verteporfin decreases ovulation in cattle.
doi_str_mv 10.1016/j.mce.2021.111524
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The critical pathway that induces ovulation involves the EGF and MAPK phosphorylation, but studies in rodents have suggested that the Hippo activator, YAP, is also involved. It is unknown whether YAP-dependent transcriptional activity is important for the LH- or EGF-induced ovulatory cascade in monovulatory species such as the cow. Using a well-defined preovulatory GC culture system, we employed pharmacological inhibitors to demonstrate that YAP signaling is critical for expression of EGFR and downstream target genes EREG, EGR1 and TNFAIP6. Most importantly, by using an ultrasound guided follicle injection system, we also showed that the classic Hippo signaling inhibitor Verteporfin inhibits GnRH-induced ovulation in vivo in cattle. 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The critical pathway that induces ovulation involves the EGF and MAPK phosphorylation, but studies in rodents have suggested that the Hippo activator, YAP, is also involved. It is unknown whether YAP-dependent transcriptional activity is important for the LH- or EGF-induced ovulatory cascade in monovulatory species such as the cow. Using a well-defined preovulatory GC culture system, we employed pharmacological inhibitors to demonstrate that YAP signaling is critical for expression of EGFR and downstream target genes EREG, EGR1 and TNFAIP6. Most importantly, by using an ultrasound guided follicle injection system, we also showed that the classic Hippo signaling inhibitor Verteporfin inhibits GnRH-induced ovulation in vivo in cattle. 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Lalonde-Larue, Ariane ; Antoniazzi, Alfredo Quites ; Barreta, Marcos Henrique ; Price, Christopher A. ; Dias Gonçalves, Paulo Bayard ; Portela, Valério Marques ; Zamberlam, Gustavo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-3dd5593ed336daca43a0bf133dc571d1b22a3951707823379be163048ec66d9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Cattle</topic><topic>Cells, Cultured</topic><topic>Cow</topic><topic>EGF receptor</topic><topic>Epidermal Growth Factor - metabolism</topic><topic>Female</topic><topic>Granulosa Cells - drug effects</topic><topic>Granulosa Cells - metabolism</topic><topic>Granulosa Cells - physiology</topic><topic>Hippo</topic><topic>Luteinizing Hormone - pharmacology</topic><topic>Ovarian Follicle - drug effects</topic><topic>Ovarian Follicle - metabolism</topic><topic>Ovary</topic><topic>Ovulation - drug effects</topic><topic>Ovulation - physiology</topic><topic>Peptide 17</topic><topic>Signal Transduction - drug effects</topic><topic>Signal Transduction - physiology</topic><topic>Verteporfin</topic><topic>YAP-Signaling Proteins - genetics</topic><topic>YAP-Signaling Proteins - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dos Santos, Esdras Corrêa</creatorcontrib><creatorcontrib>Lalonde-Larue, Ariane</creatorcontrib><creatorcontrib>Antoniazzi, Alfredo Quites</creatorcontrib><creatorcontrib>Barreta, Marcos Henrique</creatorcontrib><creatorcontrib>Price, Christopher A.</creatorcontrib><creatorcontrib>Dias Gonçalves, Paulo Bayard</creatorcontrib><creatorcontrib>Portela, Valério Marques</creatorcontrib><creatorcontrib>Zamberlam, Gustavo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular and cellular endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dos Santos, Esdras Corrêa</au><au>Lalonde-Larue, Ariane</au><au>Antoniazzi, Alfredo Quites</au><au>Barreta, Marcos Henrique</au><au>Price, Christopher A.</au><au>Dias Gonçalves, Paulo Bayard</au><au>Portela, Valério Marques</au><au>Zamberlam, Gustavo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>YAP signaling in preovulatory granulosa cells is critical for the functioning of the EGF network during ovulation</atitle><jtitle>Molecular and cellular endocrinology</jtitle><addtitle>Mol Cell Endocrinol</addtitle><date>2022-02-05</date><risdate>2022</risdate><volume>541</volume><spage>111524</spage><epage>111524</epage><pages>111524-111524</pages><artnum>111524</artnum><issn>0303-7207</issn><eissn>1872-8057</eissn><abstract>Failure to ovulate is a major cause of infertility. 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subjects Animals
Cattle
Cells, Cultured
Cow
EGF receptor
Epidermal Growth Factor - metabolism
Female
Granulosa Cells - drug effects
Granulosa Cells - metabolism
Granulosa Cells - physiology
Hippo
Luteinizing Hormone - pharmacology
Ovarian Follicle - drug effects
Ovarian Follicle - metabolism
Ovary
Ovulation - drug effects
Ovulation - physiology
Peptide 17
Signal Transduction - drug effects
Signal Transduction - physiology
Verteporfin
YAP-Signaling Proteins - genetics
YAP-Signaling Proteins - physiology
title YAP signaling in preovulatory granulosa cells is critical for the functioning of the EGF network during ovulation
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