在人类动脉样硬化的不同阶段表达巨细胞迁移抑制因子
Anke Burger-Kentischer1, Heike Goebel, Rüdiger Seiler
1Laboratory of Biochemistry, Institute for Interfacial Engineering, University of Stuttgart, Stuttgart, Germany.
Circulation
|April 3, 2002
概括
巨细胞迁移抑制因子 (MIF) 在动脉样硬化上升调节,在所有病变细胞中发现,并与Jab1相互作用. 氧化LDL会增加内皮细胞中的MIF表达,这表明它在斑块发育中的作用.
科学领域:
- 心血管生物学 心血管生物学
- 免疫学 免疫学 免疫学
- 病理学 病理学 病理学
背景情况:
- 动脉样硬化是一种慢性炎症性动脉疾病.
- 巨细胞迁移抑制因子 (MIF) 是一种关键的炎症性细胞因子,与疾病进展有关.
研究的目的:
- 研究人类动脉样硬化病变中的MIF和Jab1表达.
- 确定MIF在早期动脉动脉生成中的作用及其通过氧化LDL的调节.
主要方法:
- 免疫组织化学和共免疫沉分析MIF和Jab1.
- 在培养的人类带血管内皮细胞和巨细胞中研究了MIF表达.
主要成果:
- MIF和Jab1存在于动脉样硬化病变中的所有细胞类型中.
- 随着动脉样硬化的进展,MIF表达增加,并且局部产生.
- 在体内MIF和Jab1形成复合体;氧化LDL在内皮细胞中调节MIF.
结论:
- 在所有动脉样硬化病变中,MIF是丰富的,可能导致早期斑块发育和晚期疾病.
- MIF-Jab1复合体可能调节动脉样硬化病变的演变.
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