ACSS2-KAT5 complex-driven histone crotonylation orchestrates a pro-inflammatory program to promote the transition from MASLD to MASH

作者：Xiao Wen, Keyan Wu, M Wang, Zihan Ma, T Wang, J J Zhang, Bei Wang, S X Chen, Yi-Xiang Wang, S X Chen, Yang Fa, Liu Ch, Xianyang Chen, Lu Deng, Yafan Cheng, Qing Miao, Baofa Sun, Xiongzhong Ruan, K Li, Yajun Duan, Wenquan Hu · 发表于：Nature Communications · 年份：2026 · DOI：10.1038/s41467-026-75819-7 · 研究领域：Liver Disease Diagnosis and Treatment、Lipid metabolism and disorders、Peroxisome Proliferator-Activated Receptors

Inflammation is a pivotal driver of the progression from metabolic dysfunction-associated steatotic liver disease (MASLD) to metabolic dysfunction-associated steatohepatitis (MASH), an aggressive form associated with substantial liver-related mortality. However, the molecular mechanisms underlying the initiation and persistence of liver inflammation remain poorly defined. Here, we demonstrated a previously unrecognized role for hepatic acetyl-CoA synthetase short-chain family member 2 (ACSS2) in MASH, showing that ACSS2 upregulation in patients exacerbates MASH progression by functioning as an epigenetic regulator, independent of its canonical lipogenic role. Mechanistically, ACSS2, in complex with lysine acetyltransferase 5 (KAT5), upregulates allograft inflammatory factor-1 (AIF1) transcription via histone crotonylation, thereby inducing liver inflammation and subsequently resulting in the aberrant accumulation of senescent hepatocytes, which further enhances proinflammatory cytokine production. This ultimately initiates a vicious cycle of chronic inflammation, which directly promotes the progression from simple steatosis to MASH. Thus, our work reveals a mechanistically defined and pivotal role for ACSS2 in promoting the MASLD-to-MASH transition, highlighting its potential as a compelling therapeutic target. Acetyl-CoA synthetase 2 (ACSS2) is known to regulate lipid metabolism. Here the authors identified ACSS2 drives MASH through nuclear translocation and complexes wiht K...