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Cyclooxygenase‐2 is acutely induced by CCAAT/enhancer‐binding protein β to produce prostaglandin E 2 and F 2α following gonadotropin stimulation in Leydig cells
Cyclooxygenase 2 (COX‐2) is an inducible rate‐limiting enzyme for prostanoid production. Because COX‐2 represents one of the inducible genes in mouse mesenchymal stem cells upon differentiation into Leydig cells, we investigated COX‐2 expression and production of prostaglandin (PG) in Leydig cells....
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Published in: | Molecular reproduction and development 2019-07, Vol.86 (7), p.786-797 |
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creator | Yazawa, Takashi Imamichi, Yoshitaka Yuhki, Koh‐ichi Uwada, Junsuke Mikami, Daisuke Shimada, Masayuki Miyamoto, Kaoru Kitano, Takeshi Takahashi, Satoru Sekiguchi, Toshio Suzuki, Nobuo Rafiqul Islam Khan, Md Ushikubi, Fumitaka Umezawa, Akihiro Taniguchi, Takanobu |
description | Cyclooxygenase 2 (COX‐2) is an inducible rate‐limiting enzyme for prostanoid production. Because COX‐2 represents one of the inducible genes in mouse mesenchymal stem cells upon differentiation into Leydig cells, we investigated COX‐2 expression and production of prostaglandin (PG) in Leydig cells. Although COX‐2 was undetectable in mouse testis, it was transiently induced in Leydig cells by human chorionic gonadotropin (hCG) administration. Consistent with the finding that Leydig cells expressed aldo‐keto reductase 1B7 (PGF synthase) and PGE synthase 2, induction of COX‐2 by hCG caused a marked increase in testicular PGF
2α and PGE
2 levels. Using mouse Leydig cell tumor‐derived MA‐10 cells as a model, it was indicated by reporter assays and electron mobility shift assays that transcription of the COX‐2 gene was activated by CCAAT/enhancer‐binding protein β (C/EBPβ) with cAMP‐stimulation. C/EBPβ expression was induced by cAMP‐stimulation, whereas expression of C/EBP homolog protein (CHOP) was robustly downregulated. Transfection of CHOP expression plasmid inhibited cAMP‐induced COX‐2 promoter activity. In addition, CHOP reduced constitutive COX‐2 expression in other mouse Leydig cell tumor‐derived TM3 cells. These results indicate that COX‐2 is induced in Leydig cells by activation of C/EBPβ via reduction of CHOP expression upon gonadotropin‐stimulation to produce PGF
2α and PGE
2.
In testis, cyclooxygenase 2 is transiently induced by human chorionic gonadotropin in Leydig cells. Testicular concentrations of PGF2ɑ and PGE2 are markedly increased at this time. |
doi_str_mv | 10.1002/mrd.23163 |
format | article |
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2α and PGE
2 levels. Using mouse Leydig cell tumor‐derived MA‐10 cells as a model, it was indicated by reporter assays and electron mobility shift assays that transcription of the COX‐2 gene was activated by CCAAT/enhancer‐binding protein β (C/EBPβ) with cAMP‐stimulation. C/EBPβ expression was induced by cAMP‐stimulation, whereas expression of C/EBP homolog protein (CHOP) was robustly downregulated. Transfection of CHOP expression plasmid inhibited cAMP‐induced COX‐2 promoter activity. In addition, CHOP reduced constitutive COX‐2 expression in other mouse Leydig cell tumor‐derived TM3 cells. These results indicate that COX‐2 is induced in Leydig cells by activation of C/EBPβ via reduction of CHOP expression upon gonadotropin‐stimulation to produce PGF
2α and PGE
2.
In testis, cyclooxygenase 2 is transiently induced by human chorionic gonadotropin in Leydig cells. Testicular concentrations of PGF2ɑ and PGE2 are markedly increased at this time.</description><identifier>ISSN: 1040-452X</identifier><identifier>EISSN: 1098-2795</identifier><identifier>DOI: 10.1002/mrd.23163</identifier><identifier>PMID: 31087493</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; C/EBPβ ; CCAAT-Enhancer-Binding Protein-beta - metabolism ; Cell Line, Tumor ; CHOP ; Chorionic Gonadotropin - pharmacology ; COX‐2 ; Cyclic AMP - metabolism ; Cyclooxygenase 2 - genetics ; Cyclooxygenase 2 - metabolism ; Dinoprostone - metabolism ; Leydig cells ; Leydig Cells - metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Promoter Regions, Genetic ; Reproductive Control Agents - pharmacology ; Signal Transduction - drug effects ; transcription ; Transcription Factor CHOP - genetics ; Transcription Factor CHOP - metabolism ; Transcription, Genetic ; Transfection</subject><ispartof>Molecular reproduction and development, 2019-07, Vol.86 (7), p.786-797</ispartof><rights>2019 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2403-b50b949ed4429d6d2c65209d137b96b018f27ea0866e7cc2f2d8a339d2860b9b3</citedby><cites>FETCH-LOGICAL-c2403-b50b949ed4429d6d2c65209d137b96b018f27ea0866e7cc2f2d8a339d2860b9b3</cites><orcidid>0000-0003-4526-6585</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31087493$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yazawa, Takashi</creatorcontrib><creatorcontrib>Imamichi, Yoshitaka</creatorcontrib><creatorcontrib>Yuhki, Koh‐ichi</creatorcontrib><creatorcontrib>Uwada, Junsuke</creatorcontrib><creatorcontrib>Mikami, Daisuke</creatorcontrib><creatorcontrib>Shimada, Masayuki</creatorcontrib><creatorcontrib>Miyamoto, Kaoru</creatorcontrib><creatorcontrib>Kitano, Takeshi</creatorcontrib><creatorcontrib>Takahashi, Satoru</creatorcontrib><creatorcontrib>Sekiguchi, Toshio</creatorcontrib><creatorcontrib>Suzuki, Nobuo</creatorcontrib><creatorcontrib>Rafiqul Islam Khan, Md</creatorcontrib><creatorcontrib>Ushikubi, Fumitaka</creatorcontrib><creatorcontrib>Umezawa, Akihiro</creatorcontrib><creatorcontrib>Taniguchi, Takanobu</creatorcontrib><title>Cyclooxygenase‐2 is acutely induced by CCAAT/enhancer‐binding protein β to produce prostaglandin E 2 and F 2α following gonadotropin stimulation in Leydig cells</title><title>Molecular reproduction and development</title><addtitle>Mol Reprod Dev</addtitle><description>Cyclooxygenase 2 (COX‐2) is an inducible rate‐limiting enzyme for prostanoid production. Because COX‐2 represents one of the inducible genes in mouse mesenchymal stem cells upon differentiation into Leydig cells, we investigated COX‐2 expression and production of prostaglandin (PG) in Leydig cells. Although COX‐2 was undetectable in mouse testis, it was transiently induced in Leydig cells by human chorionic gonadotropin (hCG) administration. Consistent with the finding that Leydig cells expressed aldo‐keto reductase 1B7 (PGF synthase) and PGE synthase 2, induction of COX‐2 by hCG caused a marked increase in testicular PGF
2α and PGE
2 levels. Using mouse Leydig cell tumor‐derived MA‐10 cells as a model, it was indicated by reporter assays and electron mobility shift assays that transcription of the COX‐2 gene was activated by CCAAT/enhancer‐binding protein β (C/EBPβ) with cAMP‐stimulation. C/EBPβ expression was induced by cAMP‐stimulation, whereas expression of C/EBP homolog protein (CHOP) was robustly downregulated. Transfection of CHOP expression plasmid inhibited cAMP‐induced COX‐2 promoter activity. In addition, CHOP reduced constitutive COX‐2 expression in other mouse Leydig cell tumor‐derived TM3 cells. These results indicate that COX‐2 is induced in Leydig cells by activation of C/EBPβ via reduction of CHOP expression upon gonadotropin‐stimulation to produce PGF
2α and PGE
2.
In testis, cyclooxygenase 2 is transiently induced by human chorionic gonadotropin in Leydig cells. Testicular concentrations of PGF2ɑ and PGE2 are markedly increased at this time.</description><subject>Animals</subject><subject>C/EBPβ</subject><subject>CCAAT-Enhancer-Binding Protein-beta - metabolism</subject><subject>Cell Line, Tumor</subject><subject>CHOP</subject><subject>Chorionic Gonadotropin - pharmacology</subject><subject>COX‐2</subject><subject>Cyclic AMP - metabolism</subject><subject>Cyclooxygenase 2 - genetics</subject><subject>Cyclooxygenase 2 - metabolism</subject><subject>Dinoprostone - metabolism</subject><subject>Leydig cells</subject><subject>Leydig Cells - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Promoter Regions, Genetic</subject><subject>Reproductive Control Agents - pharmacology</subject><subject>Signal Transduction - drug effects</subject><subject>transcription</subject><subject>Transcription Factor CHOP - genetics</subject><subject>Transcription Factor CHOP - metabolism</subject><subject>Transcription, Genetic</subject><subject>Transfection</subject><issn>1040-452X</issn><issn>1098-2795</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kE1OwzAQhS0EoqWw4ALIWxZpHTt_XlahBaQiJFQkdpFjO8HIjas4VcmOI3AK9nCQHoKT4BBgx2pmNN97M3oAnPpo7COEJ6tajDHxI7IHhj6iiYdjGu53fYC8IMQPA3Bk7RNCiNIEHYIB8VESB5QMwVvacm3Mc1vKiln5-fKKobKQ8U0jdQtVJTZcCpi3ME2n0-VEVo-s4rJ2YO6WqirhujaNVBXcfcDGdFMn6aptWKlZB8EZxNB1cA7x7h0WRmuz7bSlqZgwTW3WDrKNWm00a5Sp3GG4kK1QJeRSa3sMDgqmrTz5qSNwP58t0ytvcXt5nU4XHscBIl4eopwGVIogwFREAvMoxIgKn8Q5jXLkJwWOJUNJFMmYc1xgkTBCqMBJ5JQ5GYHz3pe7920ti2xdqxWr28xHWZd15rLOvrN27FnPrjf5Soo_8jdcB0x6YKu0bP93ym7uLnrLL3o7jlU</recordid><startdate>201907</startdate><enddate>201907</enddate><creator>Yazawa, Takashi</creator><creator>Imamichi, Yoshitaka</creator><creator>Yuhki, Koh‐ichi</creator><creator>Uwada, Junsuke</creator><creator>Mikami, Daisuke</creator><creator>Shimada, Masayuki</creator><creator>Miyamoto, Kaoru</creator><creator>Kitano, Takeshi</creator><creator>Takahashi, Satoru</creator><creator>Sekiguchi, Toshio</creator><creator>Suzuki, Nobuo</creator><creator>Rafiqul Islam Khan, Md</creator><creator>Ushikubi, Fumitaka</creator><creator>Umezawa, Akihiro</creator><creator>Taniguchi, Takanobu</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-4526-6585</orcidid></search><sort><creationdate>201907</creationdate><title>Cyclooxygenase‐2 is acutely induced by CCAAT/enhancer‐binding protein β to produce prostaglandin E 2 and F 2α following gonadotropin stimulation in Leydig cells</title><author>Yazawa, Takashi ; Imamichi, Yoshitaka ; Yuhki, Koh‐ichi ; Uwada, Junsuke ; Mikami, Daisuke ; Shimada, Masayuki ; Miyamoto, Kaoru ; Kitano, Takeshi ; Takahashi, Satoru ; Sekiguchi, Toshio ; Suzuki, Nobuo ; Rafiqul Islam Khan, Md ; Ushikubi, Fumitaka ; Umezawa, Akihiro ; Taniguchi, Takanobu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2403-b50b949ed4429d6d2c65209d137b96b018f27ea0866e7cc2f2d8a339d2860b9b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>C/EBPβ</topic><topic>CCAAT-Enhancer-Binding Protein-beta - metabolism</topic><topic>Cell Line, Tumor</topic><topic>CHOP</topic><topic>Chorionic Gonadotropin - pharmacology</topic><topic>COX‐2</topic><topic>Cyclic AMP - metabolism</topic><topic>Cyclooxygenase 2 - genetics</topic><topic>Cyclooxygenase 2 - metabolism</topic><topic>Dinoprostone - metabolism</topic><topic>Leydig cells</topic><topic>Leydig Cells - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Promoter Regions, Genetic</topic><topic>Reproductive Control Agents - pharmacology</topic><topic>Signal Transduction - drug effects</topic><topic>transcription</topic><topic>Transcription Factor CHOP - genetics</topic><topic>Transcription Factor CHOP - metabolism</topic><topic>Transcription, Genetic</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yazawa, Takashi</creatorcontrib><creatorcontrib>Imamichi, Yoshitaka</creatorcontrib><creatorcontrib>Yuhki, Koh‐ichi</creatorcontrib><creatorcontrib>Uwada, Junsuke</creatorcontrib><creatorcontrib>Mikami, Daisuke</creatorcontrib><creatorcontrib>Shimada, Masayuki</creatorcontrib><creatorcontrib>Miyamoto, Kaoru</creatorcontrib><creatorcontrib>Kitano, Takeshi</creatorcontrib><creatorcontrib>Takahashi, Satoru</creatorcontrib><creatorcontrib>Sekiguchi, Toshio</creatorcontrib><creatorcontrib>Suzuki, Nobuo</creatorcontrib><creatorcontrib>Rafiqul Islam Khan, Md</creatorcontrib><creatorcontrib>Ushikubi, Fumitaka</creatorcontrib><creatorcontrib>Umezawa, Akihiro</creatorcontrib><creatorcontrib>Taniguchi, Takanobu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Molecular reproduction and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yazawa, Takashi</au><au>Imamichi, Yoshitaka</au><au>Yuhki, Koh‐ichi</au><au>Uwada, Junsuke</au><au>Mikami, Daisuke</au><au>Shimada, Masayuki</au><au>Miyamoto, Kaoru</au><au>Kitano, Takeshi</au><au>Takahashi, Satoru</au><au>Sekiguchi, Toshio</au><au>Suzuki, Nobuo</au><au>Rafiqul Islam Khan, Md</au><au>Ushikubi, Fumitaka</au><au>Umezawa, Akihiro</au><au>Taniguchi, Takanobu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cyclooxygenase‐2 is acutely induced by CCAAT/enhancer‐binding protein β to produce prostaglandin E 2 and F 2α following gonadotropin stimulation in Leydig cells</atitle><jtitle>Molecular reproduction and development</jtitle><addtitle>Mol Reprod Dev</addtitle><date>2019-07</date><risdate>2019</risdate><volume>86</volume><issue>7</issue><spage>786</spage><epage>797</epage><pages>786-797</pages><issn>1040-452X</issn><eissn>1098-2795</eissn><abstract>Cyclooxygenase 2 (COX‐2) is an inducible rate‐limiting enzyme for prostanoid production. Because COX‐2 represents one of the inducible genes in mouse mesenchymal stem cells upon differentiation into Leydig cells, we investigated COX‐2 expression and production of prostaglandin (PG) in Leydig cells. Although COX‐2 was undetectable in mouse testis, it was transiently induced in Leydig cells by human chorionic gonadotropin (hCG) administration. Consistent with the finding that Leydig cells expressed aldo‐keto reductase 1B7 (PGF synthase) and PGE synthase 2, induction of COX‐2 by hCG caused a marked increase in testicular PGF
2α and PGE
2 levels. Using mouse Leydig cell tumor‐derived MA‐10 cells as a model, it was indicated by reporter assays and electron mobility shift assays that transcription of the COX‐2 gene was activated by CCAAT/enhancer‐binding protein β (C/EBPβ) with cAMP‐stimulation. C/EBPβ expression was induced by cAMP‐stimulation, whereas expression of C/EBP homolog protein (CHOP) was robustly downregulated. Transfection of CHOP expression plasmid inhibited cAMP‐induced COX‐2 promoter activity. In addition, CHOP reduced constitutive COX‐2 expression in other mouse Leydig cell tumor‐derived TM3 cells. These results indicate that COX‐2 is induced in Leydig cells by activation of C/EBPβ via reduction of CHOP expression upon gonadotropin‐stimulation to produce PGF
2α and PGE
2.
In testis, cyclooxygenase 2 is transiently induced by human chorionic gonadotropin in Leydig cells. Testicular concentrations of PGF2ɑ and PGE2 are markedly increased at this time.</abstract><cop>United States</cop><pmid>31087493</pmid><doi>10.1002/mrd.23163</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-4526-6585</orcidid></addata></record> |
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subjects | Animals C/EBPβ CCAAT-Enhancer-Binding Protein-beta - metabolism Cell Line, Tumor CHOP Chorionic Gonadotropin - pharmacology COX‐2 Cyclic AMP - metabolism Cyclooxygenase 2 - genetics Cyclooxygenase 2 - metabolism Dinoprostone - metabolism Leydig cells Leydig Cells - metabolism Male Mice Mice, Inbred C57BL Promoter Regions, Genetic Reproductive Control Agents - pharmacology Signal Transduction - drug effects transcription Transcription Factor CHOP - genetics Transcription Factor CHOP - metabolism Transcription, Genetic Transfection |
title | Cyclooxygenase‐2 is acutely induced by CCAAT/enhancer‐binding protein β to produce prostaglandin E 2 and F 2α following gonadotropin stimulation in Leydig cells |
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