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通过雌激素介导的内皮氧化合成酶与热冲击蛋白90的关联需要依赖诺单酸盐的蛋白质激酶
Eberhard Schulz1, Elad Anter, Ming-Hui Zou
1Evans Memorial Department of Medicine, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Mass 02118, USA.
Circulation
|June 22, 2005
概括
雌激醇在内皮细胞中激活AMP激活蛋白激酶 (AMPK),这对于氧化合成酶 (eNOS) 激活至关重要. 这一途径涉及热冲击蛋白90 (HSP90) 并影响NO的生物活性.
科学领域:
- 内分泌学 在内分泌学.
- 分子生物学分子生物学
- 心血管研究研究心血管研究
背景情况:
- 雌激醇通过各种信号通路激活内皮氧化合成酶 (eNOS).
- AMP激活蛋白激酶 (AMPK) 对于细胞适应至关重要,并与其他激素的eNOS激活有关.
研究的目的:
- 为了研究雌激醇是否在内皮细胞中激活AMPK.
- 确定AMPK在雌激醇诱导的eNOS激活中的作用.
主要方法:
- 猪大动脉内皮细胞被用雌激醇治疗.
- 通过酸化AMPK和乙-CoA核糖酶来评估AMPK的激活.
- 使用了主导负AMPK的腺病毒介导表达和对alpha1-AMPK-null小鼠的研究.
主要成果:
- 雌激素时间和度依赖激活AMPK,独立于AMP水平和ERalpha,但需要雌激素代谢产物.
- 雌激醇增加了eNOS催化活性,这种效应被主导负AMPK逆转.
- 抑制AMPK降低了eNOS与HSP90的相互作用,并在小鼠血管中降低了雌二醇诱导的NO生产.
结论:
- AMPK激活对于雌激醇诱导的eNOS激活至关重要.
- AMPK促进了eNOS与HSP90的相互作用,调节了内皮细胞NO的生物活性.
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