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  3. Aging increases susceptibility to liver fibrosis through enhanced NAT10-mediated ac4C modification of TGFβ1 mRNA

Aging increases susceptibility to liver fibrosis through enhanced NAT10-mediated ac4C modification of TGFβ1 mRNA

  • Genome Med. 2025 Aug 15;17(1):90. doi: 10.1186/s13073-025-01520-x.
Xuyun Peng 1 2,  Panlong Li 1 2,  Ying Zhang 3,  Qi Zhang 4 5,  Weicheng Liang 6 7 8
Affiliations

Affiliations

  • 1 Biotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China.
  • 2 Cell-Gene Therapy Translational Medicine Research Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China.
  • 3 Affiliated Cancer Hospital of Guangzhou Medical University, Guangzhou, People's Republic of China.
  • 4 Biotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China. zhangq27@mail.sysu.edu.cn.
  • 5 Cell-Gene Therapy Translational Medicine Research Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China. zhangq27@mail.sysu.edu.cn.
  • 6 Biotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China. liangweicheng11@gmail.com.
  • 7 Cell-Gene Therapy Translational Medicine Research Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China. liangweicheng11@gmail.com.
  • 8 Vaccine Research Institute, The Third Affiliated Hospital of Sun Yat-Sen University, Sun Yat-Sen University, Guangzhou, People's Republic of China. liangweicheng11@gmail.com.
PMID: 40817062 DOI: 10.1186/s13073-025-01520-x
Abstract

Background: The epidemiological observational studies unveiled that aging is one of the risk factors for liver fibrosis, and the hepatic tissues in the elderly harbor more fibrotic lesions when compared to those in young people. Previous investigations found that TGFβ1 was elevated with aging and promoted liver fibrosis. However, the underlying mechanisms of aging and liver fibrosis remain largely unknown.

Methods: CCl4-induced liver fibrosis animal models were used in this study. The impact of NAT10 on liver fibrosis and cellular senescence was analyzed by using NAT10 overexpression or knockout hepatic stellate cell lines. The distribution of ac4C RNA modification was monitored by the acRIP-seq. The RNA-protein interaction was examined by the RNA immunoprecipitation.

Results: We demonstrated that the middle-aged mice were more susceptible to the CCl4-induced liver fibrosis when compared to the young mice. Then, we found that RNA ac4C-modifying enzyme NAT10 was transcriptionally activated by TGFβ1/SMAD2/3 axis and highly expressed in the aging liver as well as liver fibrosis mouse model. Suppression of NAT10 by its inhibitor Remodelin or specific shRNA attenuated senescence and activation of hepatic stellate cells. Subsequent studies found that NAT10 directly triggered the ac4C RNA modification of TGFβ1 mRNA by physically interacting with the RNA-binding protein PTBP1, enhancing the stabilization of TGFβ1 mRNA and subsequent activation of TGFβ/SMAD signaling pathway. Animal studies demonstrated that inhibition of NAT10 by Remodelin significantly alleviated liver fibrosis and cellular senescence.

Conclusions: Our study identified a previously unknown mechanism of how TGFβ1 drives cellular senescence and liver fibrosis through NAT10-mediated ac4C mRNA modification.

Keywords

Aging; Liver fibrosis; NAT10; RNA modification; TGFβ/SMAD signaling pathway.

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