人类动脉样硬化中的内皮细胞衰老:端粒在内皮功能障碍中的作用
Tohru Minamino1, Hideaki Miyauchi, Toshihiko Yoshida
1Department of Cardiovascular Science and Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Circulation
|April 3, 2002
概括
细胞衰老,以端粒缩短为特征,存在于人类动脉样硬化病变中. 血管内皮细胞中的这种衰老有助于动脉样硬化和相关的血管疾病的发展.
科学领域:
- 心血管研究研究心血管研究
- 细胞生物学 细胞生物学
- 衰老研究研究 衰老研究
背景情况:
- 细胞衰老与衰老和血管疾病有关.
- 端粒和端粒酶在血管细胞衰老中起作用.
- 在体内,端粒缩短表明它在动脉样硬化中起着作用.
研究的目的:
- 为了研究人类动脉样硬化病变中衰老的血管细胞的存在.
- 要确定内皮细胞衰老是否有助于动脉生成.
主要方法:
- 在人类冠状动脉和内部乳腺动脉中检查了与衰老相关的β-galactosidase活性.
- 使用免疫组织化学来识别β-galactosidase阳性细胞.
- 人类大动脉内皮细胞 (HAEC) 的诱导衰老,以评估功能变化.
- 研究了端粒酶引入对衰老HAECs的影响.
主要成果:
- 在冠状动脉的动脉样性病变中观察到强烈的β-galactosidase染色.
- 鉴定出β-银酸酶阳性细胞是血管内皮细胞.
- 衰老的HAECs显示ICAM-1表达增加和eNOS活动减少.
- 端粒酶的引入延长了HAEC的寿命,并抑制了与衰老相关的功能变化.
结论:
- 衰老的血管内皮细胞存在于人类动脉样硬化病变中.
- 由端粒缩短引起的内皮细胞衰老可能会导致动脉生成.
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