表观遗传学
生物
组蛋白
炎症性肠病
染色质
免疫系统
巨噬细胞
染色质重塑
遗传学
细胞生物学
免疫学
转录组
炎症
基因表达调控
癌症研究
基因表达
先天免疫系统
结肠炎
神经发生的表观遗传调控
微生物群
人类遗传学
DNA甲基化
疾病
促炎细胞因子
信号转导
组蛋白甲基转移酶
基因
作者
Zhaoran Sun,Fanyi Meng,Chunjian Piao,Yuqiao Fu,Yingying Zhao,Liangyu Xing,Yunzhi Liu,Fengqin Jia,Liyu Li,Jin Li,Hailong Cao,Xudong Wu
标识
DOI:10.1093/procel/pwag069
摘要
Inflammatory gene programs must be precisely controlled to maintain immune homeostasis, yet the chromatin mechanisms enforcing transcriptional shutdown remain unclear. Here we show that the histone variant H2A.Z is evicted from pro-inflammatory loci upon acute macrophage activation and re-deposited during resolution. Myeloid-specific H2a.z deletion in mice causes unrestrained inflammatory transcription, arrested macrophage maturation, exacerbates colitis and dysbiosis, depleting butyrate-producing bacteria. Consistently, gut short-chain fatty acids, particularly butyrate, promote H2A.Z deposition through histone acylation, and butyrate's anti-inflammatory effects require H2A.Z. Strikingly, human inflammatory bowel disease (IBD)-associated risk variants are linked to reduced expression of GAS41 and TIP60, which form a reader-writer module that senses acylation mark to direct H2A.Z deposition. Diminished GAS41/TIP60 expression in patient tissues correlates with IBD progression and poor response to anti-TNF therapy. Thus, H2A.Z deposition functions as an acylation-dependent epigenetic checkpoint that couples macrophage differentiation to inflammatory resolution, integrating host genetics and microbial metabolites to calibrate immune responses.
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