红细胞生成
生物
组蛋白乙酰转移酶
组蛋白
肠道菌群
组蛋白脱乙酰基酶
表观遗传学
无效红细胞生成
贫血
黄脲酸
免疫学
红细胞生成性原卟啉症
喹啉酸
细胞生物学
癌症研究
染色质
内分泌学
丁酸钠
组蛋白乙酰转移酶
苯乙酸
组蛋白脱乙酰酶抑制剂
组蛋白脱乙酰基酶2
染色质重塑
内科学
基因沉默
造血
组蛋白H3
作者
Yifei Xie,Xiangrui Qiao,Hao Wu,Yiming Hua,Bolin Li,Ning Ding,Jinglong Pang,Mingmin Zhang,Wen Xi,Kai Deng,Yu Xu,Peining Liu,Xue Shi,Lele Cheng,Xiaozhen Zhuo,Ting Li,Zuyi Yuan,Yue Wu
出处
期刊:Blood
[Elsevier BV]
日期:2026-07-10
标识
DOI:10.1182/blood.2026033155
摘要
Anemia, the most prevalent hematologic disorder in older adults, imposes a significant burden of cardiovascular events, cognitive decline, and mortality. However, the mechanisms underlying aging-related anemia, especially epigenetic dysregulation in hematopoietic stem and progenitor cells (HSPCs), remain incompletely understood. Although the gut microbiota is critical for hematopoiesis, its specific contribution to aging-related erythropoiesis impairment remains unclear. Here, we reveal that aging markedly activates phenylalanine metabolism and elevates plasma phenylacetic acid (PAA) levels in both humans and mice. We identify Odoribacter splanchnicus (O.splanchnicus) as a key gut symbiont whose abundance is significantly increased in aged mice and which directly drives PAA production from phenylalanine via the oxoacid:ferredoxin oxidoreductase (OFOR) superfamily encoded by porA,nifJ, and iorA/iorB. Rifaximin treatment selectively reduces O.splanchnicus and plasma PAA, thereby alleviating aging-related anemia. Mechanistically, PAA promotes a novel post-translational modification (PTMs) termed histone lysine phenylacetylation (Kpa) through the acetyltransferases HBO1. Elevated histone Kpa increases chromatin accessibility at the GATA2 promoter, disrupts the GATA switch, and blocks erythroid differentiation of HSPCs. In vivo, supplementation with sodium phenylacetate (NaPA) exacerbates anemia in microbiota-depleted mice, whereas the HBO1 inhibitor WM-3835 restores erythropoiesis by reversing histone Kpa and normalizing the GATA switch. Furthermore, dietary phenylalanine restriction lowers circulating PAA and effectively ameliorates aging-related anemia in both naturally aged mice and O.splanchnicus-colonized mice. These findings provide the first evidence that gut microbiota-derived PAA plays a critical role in the development of aging-related erythropoiesis impairment and offer multiple translatable strategies for treating this condition.
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