Co-localization of microsomal prostaglandin E synthase-1 with cyclooxygenase-1 in layer II of murine placental syncytiotrophoblasts

Mai Inagaki, Tomohiro Nishimura, Shin ichi Akanuma, Takeo Nakanishi, Masanori Tachikawa, Ikumi Tamai, Ken ichi Hosoya, Emi Nakashima, Masatoshi Tomi

Research output: Contribution to journalArticle

Abstract

The placenta is an organ that secretes prostaglandin (PG) E2 into the fetal-placental circulation to regulate both vascular tone and remodeling of the fetal ductus arteriosus. Placental PGE2 synthesis might be mediated by microsomal PGE synthase-1 (mPGES-1), in addition to cyclooxygenase (COX) isoforms. Thus, the purpose of this study is to clarify the temporal and spatial expression patterns of mPGES-1, together with COX-1 and COX-2, in murine placenta. We found that mPGES-1 and COX-1 protein levels continuously increased in the placental labyrinth from gestational day (GD) 13.5 to GD19.5, becoming higher than in the decidua or the junctional zone by GD17.5. The PGE2 level at GD17.5 was also highest in the labyrinth. Immunofluorescence stainings for mPGES-1 and COX-1 in the labyrinth at GD17.5 overlapped and were located on the fetal side of the signals for connexin 26, which forms gap junctions between maternal-facing (SynT-I) and fetal-facing (SynT-II) syncytiotrophoblast layers, and on the maternal side of the signals for glucose transporter 1 on the basal plasma membrane of SynT-II. On the other hand, the signals for COX-2 did not overlap with those for mPGES-1. These results indicate that COX-1 and mPGES-1 are co-localized in murine placental SynT-II, facing the fetal-placental circulation. Therefore, SynT-II could contribute to placental synthesis of PGE2 for release into the fetal-placental circulation.

Original languageEnglish
Pages (from-to)174-182
Number of pages9
JournalPlacenta
Volume53
DOIs
Publication statusPublished - 2017 May 1

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Cyclooxygenase 1
Trophoblasts
Prostaglandins E
Placental Circulation
Dinoprostone
Inner Ear
Cyclooxygenase 2
Placenta
Mothers
Ductus Arteriosus
Decidua
Facilitative Glucose Transport Proteins
Gap Junctions
Prostaglandin-Endoperoxide Synthases
Fluorescent Antibody Technique
Prostaglandin-E Synthases
Protein Isoforms
Cell Membrane
Staining and Labeling
Proteins

Keywords

  • Cyclooxygenase
  • Placenta
  • Prostaglandin E synthase
  • Prostaglandin E
  • Syncytiotrophoblasts

ASJC Scopus subject areas

  • Reproductive Medicine
  • Obstetrics and Gynaecology
  • Developmental Biology

Cite this

Co-localization of microsomal prostaglandin E synthase-1 with cyclooxygenase-1 in layer II of murine placental syncytiotrophoblasts. / Inagaki, Mai; Nishimura, Tomohiro; Akanuma, Shin ichi; Nakanishi, Takeo; Tachikawa, Masanori; Tamai, Ikumi; Hosoya, Ken ichi; Nakashima, Emi; Tomi, Masatoshi.

In: Placenta, Vol. 53, 01.05.2017, p. 174-182.

Research output: Contribution to journalArticle

Inagaki, Mai ; Nishimura, Tomohiro ; Akanuma, Shin ichi ; Nakanishi, Takeo ; Tachikawa, Masanori ; Tamai, Ikumi ; Hosoya, Ken ichi ; Nakashima, Emi ; Tomi, Masatoshi. / Co-localization of microsomal prostaglandin E synthase-1 with cyclooxygenase-1 in layer II of murine placental syncytiotrophoblasts. In: Placenta. 2017 ; Vol. 53. pp. 174-182.
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T1 - Co-localization of microsomal prostaglandin E synthase-1 with cyclooxygenase-1 in layer II of murine placental syncytiotrophoblasts

AU - Inagaki, Mai

AU - Nishimura, Tomohiro

AU - Akanuma, Shin ichi

AU - Nakanishi, Takeo

AU - Tachikawa, Masanori

AU - Tamai, Ikumi

AU - Hosoya, Ken ichi

AU - Nakashima, Emi

AU - Tomi, Masatoshi

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N2 - The placenta is an organ that secretes prostaglandin (PG) E2 into the fetal-placental circulation to regulate both vascular tone and remodeling of the fetal ductus arteriosus. Placental PGE2 synthesis might be mediated by microsomal PGE synthase-1 (mPGES-1), in addition to cyclooxygenase (COX) isoforms. Thus, the purpose of this study is to clarify the temporal and spatial expression patterns of mPGES-1, together with COX-1 and COX-2, in murine placenta. We found that mPGES-1 and COX-1 protein levels continuously increased in the placental labyrinth from gestational day (GD) 13.5 to GD19.5, becoming higher than in the decidua or the junctional zone by GD17.5. The PGE2 level at GD17.5 was also highest in the labyrinth. Immunofluorescence stainings for mPGES-1 and COX-1 in the labyrinth at GD17.5 overlapped and were located on the fetal side of the signals for connexin 26, which forms gap junctions between maternal-facing (SynT-I) and fetal-facing (SynT-II) syncytiotrophoblast layers, and on the maternal side of the signals for glucose transporter 1 on the basal plasma membrane of SynT-II. On the other hand, the signals for COX-2 did not overlap with those for mPGES-1. These results indicate that COX-1 and mPGES-1 are co-localized in murine placental SynT-II, facing the fetal-placental circulation. Therefore, SynT-II could contribute to placental synthesis of PGE2 for release into the fetal-placental circulation.

AB - The placenta is an organ that secretes prostaglandin (PG) E2 into the fetal-placental circulation to regulate both vascular tone and remodeling of the fetal ductus arteriosus. Placental PGE2 synthesis might be mediated by microsomal PGE synthase-1 (mPGES-1), in addition to cyclooxygenase (COX) isoforms. Thus, the purpose of this study is to clarify the temporal and spatial expression patterns of mPGES-1, together with COX-1 and COX-2, in murine placenta. We found that mPGES-1 and COX-1 protein levels continuously increased in the placental labyrinth from gestational day (GD) 13.5 to GD19.5, becoming higher than in the decidua or the junctional zone by GD17.5. The PGE2 level at GD17.5 was also highest in the labyrinth. Immunofluorescence stainings for mPGES-1 and COX-1 in the labyrinth at GD17.5 overlapped and were located on the fetal side of the signals for connexin 26, which forms gap junctions between maternal-facing (SynT-I) and fetal-facing (SynT-II) syncytiotrophoblast layers, and on the maternal side of the signals for glucose transporter 1 on the basal plasma membrane of SynT-II. On the other hand, the signals for COX-2 did not overlap with those for mPGES-1. These results indicate that COX-1 and mPGES-1 are co-localized in murine placental SynT-II, facing the fetal-placental circulation. Therefore, SynT-II could contribute to placental synthesis of PGE2 for release into the fetal-placental circulation.

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