表观遗传学
重编程
细胞生物学
组蛋白
巨噬细胞
生物
乙酰化
线粒体
冷应激
新陈代谢
生物化学
基因
体外
作者
Jingjing Lu,Shoupeng Fu,Jie Dai,Jianwen Hu,Shize Li,Hong Ji,Zhiquan Wang,Jiahong Yu,Jiming Bao,Bin Xu,Jingru Guo,Huanmin Yang
标识
DOI:10.1631/jzus.b2101091
摘要
The negative effects of low temperature can readily induce a variety of diseases. We sought to understand the reasons why cold stress induces disease by studying the mechanisms of fine-tuning in macrophages following cold exposure. We found that cold stress triggers increased macrophage activation accompanied by metabolic reprogramming of aerobic glycolysis. The discovery, by genome-wide RNA sequencing, of defective mitochondria in mice macrophages following cold exposure indicated that mitochondrial defects may contribute to this process. In addition, changes in metabolism drive the differentiation of macrophages by affecting histone modifications. Finally, we showed that histone acetylation and lactylation are modulators of macrophage differentiation following cold exposure. Collectively, metabolism-related epigenetic modifications are essential for the differentiation of macrophages in cold-stressed mice, and the regulation of metabolism may be crucial for alleviating the harm induced by cold stress.
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