内皮原生细胞被招募到解决静脉瘤的过程中
B Modarai1, K G Burnand, B Sawyer
1Academic Department of Surgery, Cardiovascular Division, King's College, London, United Kingdom.
Circulation
|May 11, 2005
概括
在分辨过程中,表达Tie2的骨髓细胞被招募到瘤中,但没有形成新的血管. 这些细胞具有巨细胞标记物,可能会协调血栓再通道化.
科学领域:
- 血液学 血液学 血液学
- 血管生物学 血管生物学
- 再生医学是一种再生医学.
背景情况:
- 血栓再通道对于在凝块形成后恢复血液流动至关重要.
- 细胞的起源和在血栓分辨中的作用仍然不完全理解.
- 研究骨髓衍生细胞为血管修复机制提供了洞察力.
研究的目的:
- 为了确定骨髓衍生的内皮细胞在血栓再通道化中的参与.
- 确定在解决瘤中招募的骨髓细胞的表型和功能.
主要方法:
- 利用带有Tie2促进体的绿色光蛋白 (GFP) 转基因小鼠追踪骨髓衍生细胞.
- 在小鼠中诱导了血栓,并在7天和14天分析了细胞招募和表型.
- 使用流动细胞计量 (CD34+/VEGFR2+) 量化循环内皮细胞,用于血栓携带动物和对照动物.
主要成果:
- 在瘤发作7至14天之间,GFP表达骨髓细胞显著增加了3倍.
- 招募的GFP表达细胞表现出巨细胞标记物 (Mac-3,CD68) 和VEGFR2,但没有排列新的血管.
- 在动物中检测到高水平的循环CD34+/VEGFR2+细胞被诱导血栓.
结论:
- 骨髓衍生的Tie2表达细胞在分辨过程中被招募到瘤中.
- 这些细胞具有巨细胞表型,不会在血栓内促进新血管化.
- 来自骨髓的塑料干细胞群可能会协调血栓再化.
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