血管内皮のプロゲステロン受容体は,生理学的子宮の浸透性を誘発する
Lauren M Goddard1, Thomas J Murphy2, Tönis Org1
1Department of Molecular, Cell, and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Cell
|February 4, 2014
まとめ
プロゲステロン受容体 (PR) は,VEGFから独立して,胚の埋め込みのための生理学的血管透過性を制御します. PRは,生殖の成功に不可欠なNR4A1遺伝子を介して血管の漏れを調節します.
科学分野:
- 生殖生物学 生殖生物学
- 血管生物学 血管生物学とは
- エンドクリノロジー エンドクリノロジー
背景:
- 血管の浸透性は炎症とVEGF.のような要因に関連しています.
- 生理学的血管透過性は,胚の移植に不可欠である.
研究 の 目的:
- 胚の植入時に生理学的血管透過性を調節するプロゲステロン受容体 (PR) の役割を調査する.
- PRが血管透過性を制御する分子メカニズムを特定する.
主な方法:
- 全球性および内皮特異性PR消去マウスモデルを使用した.
- ゲノム全体の転写プロファイリングと内皮細胞におけるChIP配列決定を行いました.
- PR媒介による血管透過性におけるNR4A1 (Nur77/TR3) の役割を調査した.
主要な成果:
- プロゲステロン受容体 (PR) は,VEGFから独立して,移植のための子宮血管の透過性を直接制御します.
- 内皮細胞におけるPRの消去は,生理学的血管透過性を阻害し,誤った発現は子宮外漏れを引き起こします.
- PRはNR4A1依存の転写プログラムを誘導し,交差点タンパク質を抑制し,血管バリア機能を調節します.
結論:
- プロゲステロン受容体 (PR) は,胚の植え付けに不可欠な生理学的血管浸透性の主要な調節体です.
- PR-NR4A1経路は,生殖中の静脈特異的血管壁の調節を媒介する.
- この経路をターゲットにすると,生殖器系および血管疾患の洞察が得られます.
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