单细胞特征对循环内皮前代细胞新血管化能力的相关性
Carmen Urbich1, Christopher Heeschen, Alexandra Aicher
1Molecular Cardiology, Department of Internal Medicine IV, University of Frankfurt, Germany.
Circulation
|October 29, 2003
概括
来自周围血液的内皮原生细胞 (EPC) 改善了缺血后的新血管化. 单细胞和非单细胞EPC都表现出类似的治疗潜力,突出了它们在再生医学中的价值.
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:
- 循环内皮原生细胞 (EPC) 增强神经血管化后缺血.
- 目前,EPC的确切来源和特征尚不清楚.
- 研究单细胞起源在EPC功能中的作用至关重要.
研究的目的:
- 为了确定EPC表型和新血管化能力是否取决于单细胞起源.
- 为了比较来自CD14+和CD14-细胞的EPCs的治疗潜力.
- 为了评估ex vivo扩展EPCs与新分离的细胞的疗效.
主要方法:
- 从外围血液单核细胞中分离单细胞CD14+细胞.
- 用血管内皮生长因子在内皮介质中培养细胞.
- 评估内皮细胞标记物表达和殖民地形成单位.
- 将EPC移植到后肢缺血小鼠中,以评估新血管化.
主要成果:
- CD14+和CD14-衍生的EPC表现出类似的内皮标记体表达和克隆扩张能力.
- 从两个来源移植的EPC显著改善了缺血性后肢的新血管化.
- 活体扩张是必不可少的;新鲜分离的CD14+细胞没有改善新血管化.
- 不同化的巨细胞或树突细胞在促进新血管化方面不如EPC有效.
结论:
- EPCs可以从非单细胞的CD14-外周血液细胞产生.
- 在后肢缺血症后,EPC具有独特的功能活性,可以改善后肢缺血后的新血管化.
- 新血管化的治疗潜力不仅限于单细胞起源的EPC.
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