PPARalpha激动剂抑制了人体单细胞和巨细胞中的组织因子表达
B P Neve1, D Corseaux, G Chinetti
1Département d'Athérosclérose, U.325 INSERM, Institut Pasteur de Lille, and the Faculté de Pharmacie, Université de Lille II, France.
Circulation
|February 24, 2001
概括
像纤维化物一样,氧酶增殖器激活受体α (PPARα) 激动剂会降低单细胞和巨细胞中的组织因子 (TF) 基因表达. 这表明PPARα激活可以控制动脉样硬化斑块的血栓性.
科学领域:
- 心血管生物学 心血管生物学
- 分子医学是分子医学.
- 血栓形成研究研究
背景情况:
- 单细胞组织因子 (TF) 表达有助于血管损伤中的血栓发生.
- 内毒素通过AP-1和NF-kappaB诱导TF表达,这些通路是由氧酶增殖器激活受体-α (PPARα) 调节的.
研究的目的:
- 研究纤维酸和其他PPARα激动剂对单细胞TF表达的作用.
主要方法:
- 在THP-1细胞和原发性人类单细胞/巨细胞中评估PPARα表达.
- 测量TF mRNA和激活后的活性与脂多糖或白蛋白-1β在存在PPARα激动剂 (纤维酸,WY14643,GW2331) 的刺激.
主要成果:
- PPARα蛋白在THP-1细胞中表达,类似于人类初级单细胞.
- PPARα激动剂显著抑制了TF mRNA上调和TF活性诱导的脂多糖或白蛋白-1β在细胞系和原始细胞.
结论:
- PPARα激活导致TF基因的下调.
- PPARα通过调节单细胞和巨细胞中的TF表达,在控制动脉样硬化斑块血栓发生性方面发挥着新的作用.
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