长期高脂肪饮食影响骨髓微环境在老化时单细胞分辨率
Yidan Pang1,2, Siyuan Zhu3, Peng Ding1,2
1Department of Orthopaedics Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai China.
MedComm
|July 22, 2025
概括
在老年小鼠中长期高脂肪饮食 (HFD) 消费将骨髓从骨形成转移到脂肪生产. 这导致免疫细胞功能障碍和全身炎症,表明骨髓作为治疗点.
科学领域:
- 生物医学科学 生物医学科学
- 衰老研究研究 衰老研究
- 代谢性疾病 代谢性疾病
背景情况:
- 由于高脂肪饮食 (HFD) 而导致的肥胖和衰老是慢性疾病的重要风险因素.
- 了解长期HFD对衰老 (LHA) 的影响对于开发干预措施至关重要.
研究的目的:
- 研究LHA对骨髓微环境和固体器官的影响.
- 确定将LHA与病理和炎症联系起来的分子机制.
主要方法:
- 建立一个长期的HFD到老化 (LHA) 的小鼠模型.
- 骨髓细胞的单细胞转录组学分析.
- 对基因表达的分析,包括巨细胞中的Chil3和Fabp4.
主要成果:
- 在骨髓中,LHA诱导骨质生成转变为脂肪生成.
- LHA改变了免疫细胞群和它们的代谢适应.
- 在骨髓巨细胞中观察到Chil3和Fabp4的上调.
- 确定了骨髓和大脑之间的潜在交叉轴 (Ptn-Sdc3,Cxcl12-Cxcr4).
结论:
- 骨髓微环境是LHA诱导病理的中心枢纽.
- 脂肪性重编程和髓状细胞功能障碍驱动LHA中的炎症.
- 准骨髓为肥胖加速衰老提供了治疗潜力.
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