周围白细胞微RNA中的8-oxoguanine修饰通过重塑基因调节网络来促进与年龄相关的炎症
Ming-Ming Han1, Qian Liu2, Lan Yang3
1The Key Laboratory of Geriatrics, Beijing Institute of Geriatrics, Beijing Hospital, National Center of Gerontology, National Health Commission, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, China; Graduate School of Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.
Free radical biology & medicine
|April 27, 2025
概括
反应性氧物种 (ROS) 会对微RNA造成氧化损伤,改变基因调节并促进与年龄相关的炎症. 这项研究揭示了氧化微RNA如何在衰老过程中促进炎症途径.
科学领域:
- 分子生物学分子生物学
- 衰老研究研究 衰老研究
- 免疫学 免疫学 免疫学
背景情况:
- 反应性氧物种 (ROS) 与细胞衰老和炎症有关.
- 将ROS与这些过程联系在一起的精确分子机制仍然不清楚.
研究的目的:
- 阐明ROS对与年龄相关的炎症有所贡献的分子机制.
- 为了研究氧化修饰在老化过程中微RNA功能中的作用.
主要方法:
- 核酸池检测系统的核酸池检测系统
- 氧化型微RNA测序的测序方法
- 细胞因子芯片检测技术
主要成果:
- 增加的8-oxo-guanosine三酸盐 (8-oxo-GTP) 水平与年龄,氧化微RNA和炎症因素相关.
- 在微RNA种子区域 (miR-98-5p,miR-8085) 中瓜的氧化损害了标结合 (ICAM1,CXCL16) 并增加了它们的表达.
- 氧化微RNA可以通过非正规的基因不匹配来准新基因.
结论:
- 由ROS诱导的微RNA氧化重塑了基因调节网络.
- 氧化微RNA激活炎症通路,导致与年龄相关的炎症.
- 这为老化和炎症的分子基础提供了新的见解.
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