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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c2403-b50b949ed4429d6d2c65209d137b96b018f27ea0866e7cc2f2d8a339d2860b9b3
cites cdi_FETCH-LOGICAL-c2403-b50b949ed4429d6d2c65209d137b96b018f27ea0866e7cc2f2d8a339d2860b9b3
container_end_page 797
container_issue 7
container_start_page 786
container_title Molecular reproduction and development
container_volume 86
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
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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. 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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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identifier ISSN: 1040-452X
ispartof Molecular reproduction and development, 2019-07, Vol.86 (7), p.786-797
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1098-2795
language eng
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source Wiley-Blackwell Read & Publish Collection
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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