老化骨髓巨细胞通过细胞外囊介导诱导膜衰老驱动系统衰老和与年龄相关的功能障碍
Jing Hou1, Kai-Xuan Chen1, Chen He1
1Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
Nature aging
|September 12, 2024
概括
生理上老化的骨髓单细胞/巨细胞 (BMM) 通过细胞外囊泡 (EV) 传播衰老,导致与年龄相关的功能障碍. 费诺纤维酸治疗恢复了平衡,并可能延长健康的寿命.
科学领域:
- 细胞衰老 细胞衰老
- 生物老龄化生物学
- 免疫学 免疫学 免疫学
背景情况:
- 细胞衰老的积累驱动着衰老和与年龄有关的疾病.
- 负责衰老传播的特定细胞类型尚不清楚.
研究的目的:
- 识别在衰老中传播衰老的细胞类型.
- 研究衰老传播的机制.
- 评估与年龄有关的功能障碍的治疗干预措施.
主要方法:
- 对老化骨髓单细胞/巨细胞 (BMM) 和它们的细胞外囊泡 (EV) 的分析.
- 在老年小鼠体内研究.
- 在EVs中的微RNA分析.
- 这是一项对7986名人类参与者的队列研究.
主要成果:
- 老年BMM通过EV传播衰老到多种组织,在小鼠中引起与年龄有关的功能障碍.
- 氧酶增殖器激活受体α (PPARα) 被确定为老年BMM-EV中的一个关键标.
- 费诺纤维酸治疗恢复了老年小鼠的组织平衡.
- 在人类中,芬纤维酸的使用与慢性疾病风险降低和预期寿命增加相关.
结论:
- 骨髓单细胞/巨细胞是衰老传播和与年龄有关的功能障碍的关键驱动因素.
- PPARα信号传递是与年龄相关的功能障碍的关键调解者.
- 费诺纤维酸盐显示出延长健康寿命和减轻与年龄有关的疾病的治疗潜力.
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