血管透性和血管扩张的增加对于干细胞治疗的益血管效应至关重要
Dong You1, Ludovic Waeckel, Téni G Ebrahimian
1Cardiovascular Research Center, INSERM U689, Hopital Lariboisière, 41 boulevard de la chapelle, 75475 Paris Cedex 10, France.
Circulation
|July 19, 2006
概括
亲血管原生细胞通过氧化信号增强缺血组织中的血液流动和血管透性. 这种机制对于它们在治疗缺血性疾病中的治疗潜力至关重要.
科学领域:
- 再生医学是一种再生医学.
- 血管生物学 血管生物学
- 细胞疗法细胞疗法
背景情况:
- 使用骨髓衍生单核细胞 (BMC) 或内皮细胞 (EPC) 的亲血管细胞疗法正在研究缺血性疾病.
- BMC 和 EPC 的治疗益处背后的精确机制尚未完全理解.
研究的目的:
- 阐明BMC和原生细胞在缺血条件下发挥其益血管性作用的机制.
主要方法:
- 研究了BMCs和CD34+衍生原生细胞与缺血性大腿动脉的相互作用.
- 通过依赖内皮氧化合成酶 (eNOS) 的途径,分析的氧化 (NO) 释放.
- 在后肢缺血症的小鼠模型中评估了NO对血管扩张,血管透性和细胞透的影响.
主要成果:
- 骨干细胞和原生细胞利用SDF-1和CXCR4信号与缺血血管相互作用.
- BMCs通过依赖eNOS的途径释放NO,导致血管扩张和增加血管透性.
- 在缺血性后肢中,NO介导的血管扩张和超透性对于BMC透和益血管性活性至关重要.
结论:
- 亲血管细胞疗法的有效性可能来自于调节现有的血管功能,而不仅仅来自内皮细胞分化.
- 涉及NO信号的细胞相互作用对原始细胞透和缺血的治疗作用至关重要.
- 这项研究提出了益血管细胞疗法的新机制,强调血管调节而不是直接的细胞替代.
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