在体外,单细胞/巨细胞调节血管化
Yin Tintut1, Jignesh Patel, Mary Territo
1Department of Medicine, UCLA School of Medicine, Los Angeles, California, USA.
Circulation
|February 6, 2002
概括
单细胞/巨细胞 (M/Ms) 在体外显著增强血管化. 这通过直接的细胞接触和释放诸如瘤死因子-alpha.
科学领域:
- 血管生物学 血管生物学
- 细胞生物学 细胞生物学
- 动脉样硬化研究 动脉样硬化研究
背景情况:
- 血管化是动脉样硬化和慢性炎症的常见并发症.
- 它涉及单细胞的透和巨细胞在动脉壁中的积累.
研究的目的:
- 研究单细胞/巨细胞 (M/Ms) 在调节血管化中的作用.
- 阐明M/Ms影响化的机制.
主要方法:
- 与人类外周血液单细胞一起培养化血管细胞 (CVCs) 5天.
- 评估性酸酶 (ALP) 活性和矩阵矿化.
- 使用条件介质和跨井共同培养来区分细胞与细胞接触和可溶性因子效应.
- 使用ELISA检测细胞因子分泌和中和抗体以阻止特定因素.
主要成果:
- 同培养具有单细胞的CVC显著增加了ALP活性和矩阵矿化.
- 单细胞数量的增加相应地增加了ALP活动和矿物化.
- 通过氧化LDL或脂多糖酸盐激活M/Ms进一步增加了化.
- 细胞与细胞接触和可溶性因子 (如瘤亡因子-α) 被确定为关键机制.
结论:
- 单细胞/巨细胞 (M/Ms) 在体外增强血管化.
- 其中涉及两个主要机制:直接的细胞相互作用和可溶性因子的分泌,特别是瘤亡因子-alpha.
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