肠道微生物群,新编程细胞死亡和巨细胞极化之间的交叉通话机制
1School of Rehabilitation Medicine, Henan University of Traditional Chinese Medicine, Zhengzhou 450046, China.
Pharmacological research
|January 9, 2026
概括
肠道微生物群失调促进细胞死亡途径,如热和铁,以及M1巨细胞两极分化,导致器官功能障碍. 了解这种联系是治疗疾病的关键.
科学领域:
- 微生物学 微生物学
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
背景情况:
- 新兴的编程细胞死亡 (PCD) 途径 (pyroptosis,ferroptosis,necroptosis,cuproptosis,disulfidptosis) 和巨细胞极化都与组织损伤和器官功能障碍有关.
- 这些PCD路径和巨细胞两极分化与肠道微生物群的恒常性密切相关.
研究的目的:
- 系统地审查肠道微生物群及其代谢物对新型PCD途径和巨细胞两极分化的影响.
- 阐明肠道微生物群在调节这些细胞死亡机制和巨细胞表型中的作用.
主要方法:
- 文献综述侧重于肠道微生物群,编程细胞死亡和巨细胞两极分化之间的相互作用.
- 综合目前关于代谢物改变及其对炎症信号通路的影响的研究.
主要成果:
- 肠道失生导致有害代谢物产生和炎症,激活PCD通路和M1巨细胞两极分化.
- 改变肠道微生物群的组成会影响宿主的新陈代谢,免疫力和生理平衡,加剧疾病的发病.
结论:
- 了解PCD中的肠道微生物群的动态调节和巨细胞两极分化对于疾病的发病是至关重要的.
- 本综述为开发针对肠道微生物群治疗相关疾病的治疗策略提供了理论基础.
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