激活C-C化学受体5型,通过依赖ERK的途径刺激脂肪细胞的分化
Luen-Kui Chen1, Chien-Wei Chen2, Shao-Yun Wu1
1Institute of Physiology, College of Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.
International journal of medical sciences
|September 17, 2025
概括
通过RANTES激活CCR5,通过依赖ERK的途径促进脂肪细胞分化和肥胖. 阻止CCR5可以抑制这些效应,强调其在肥胖发展中的作用.
科学领域:
- 代谢和内分泌学
- 免疫学和炎症 免疫学和炎症
背景情况:
- 肥胖与慢性炎症有关,肥胖个体的内脏脂肪组织中RANTES和CCR5mRNA升高.
- 在肥胖病原体中CCR5激活的特定作用仍然不完全理解.
研究的目的:
- 为了研究CCR5激活对脂肪生成的影响.
- 阐明CCR5在肥胖中的作用背后的调控机制.
主要方法:
- 使用了来自野生类型 (WT) 和CCR5淘汰 (CCR5-/-) 鼠的3T3-F442A预脂细胞和初级预脂细胞.
- 用RANTES,CCR5抑制剂 (maraviroc) 和ERK抑制剂 (PD98059) 来评估脂肪细胞的分化.
- 食WT和CCR5-/-小鼠正常或高脂肪饮食以评估体内对肥胖的影响.
主要成果:
- 在分化脂肪细胞中,RANTES治疗增加了甘油三积累和脂肪基因表达 (PPARγ,C/EBPα,aP2).
- CCR5抑制和ERK通路阻塞减弱了RANTES诱导的脂肪细胞分化.
- 在高脂肪饮食中的WT小鼠表现出增加的RANTES,脂肪CCR5表达和肥胖,与CCR5-/-小鼠不同.
结论:
- 通过RANTES激活CCR5,通过依赖ERK的机制增强脂肪细胞的分化.
- CCR5在高脂肪饮食引起的肥胖发展中发挥着重要作用.
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