ATP柠檬酸裂解酶
效应器
乙酰化
重编程
组蛋白
细胞生物学
生物
基因表达
组蛋白H3
柠檬酸合酶
生物化学
化学
基因
酶
作者
Niamh C. Williams,Luke O'neill
标识
DOI:10.1016/j.it.2019.12.009
摘要
Metabolic reprogramming in macrophages supports effector functions and differs depending on the activating stimulus. Lauterbach et al. now show that early metabolic alterations in macrophages driven by LPS signaling serve to increase the acetyl-CoA pool via citrate metabolism by the ATP-citrate lyase (ACLY), leading to histone acetylation and regulation of TLR-driven gene expression.
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