血管内皮中的孕激素受体触发了生理性子宫透性植入前
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
概括
孕激素受体 (PR) 控制胚胎植入的生理血管透性,独立于VEGF. PR通过NR4A1基因调节血管泄漏,这对生殖成功至关重要.
科学领域:
- 生殖生物学 生殖生物学
- 血管生物学 血管生物学
- 内分泌学 在内分泌学.
背景情况:
- 血管透性与炎症和诸如VEGF.这样的因素有关.
- 生理血管透性对于胚胎植入至关重要.
研究的目的:
- 研究孕激素受体 (PR) 在胚胎植入期间调节生理血管透性的作用.
- 确定PR控制血管透性的分子机制.
主要方法:
- 利用了全球性和内皮细胞特异性PR删除小鼠模型.
- 在内皮细胞中进行全基因组转录分析和ChIP测序.
- 研究了NR4A1 (Nur77/TR3) 在PR介导的血管透性中的作用.
主要成果:
- 孕激素受体 (PR) 直接控制子宫血管透性用于植入,独立于VEGF.
- 内皮细胞中的PR缺失阻断了生理血管透性;错误表达导致子宫外泄漏.
- PR诱导一个依赖NR4A1的转录程序,抑制结点蛋白,调节血管屏障功能.
结论:
- 孕激素受体 (PR) 是生理血管透性的关键调节器,对于胚胎植入至关重要.
- 在繁殖过程中,PR-NR4A1通路调节静脉特异性血管屏障调节.
- 针对这种途径可能会提供有关生殖和血管疾病的见解.
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