Aging increases susceptibility to liver fibrosis through enhanced NAT10-mediated ac4C modification of TGFβ1 mRNA
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 agin...
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BMC
2025-08-01
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| Series: | Genome Medicine |
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| Online Access: | https://doi.org/10.1186/s13073-025-01520-x |
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| _version_ | 1849234999582130176 |
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| author | Xuyun Peng Panlong Li Ying Zhang Qi Zhang Weicheng Liang |
| author_facet | Xuyun Peng Panlong Li Ying Zhang Qi Zhang Weicheng Liang |
| author_sort | Xuyun Peng |
| collection | DOAJ |
| description | 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. |
| format | Article |
| id | doaj-art-4dd2eb35c99f4e269119729f77c4818b |
| institution | Kabale University |
| issn | 1756-994X |
| language | English |
| publishDate | 2025-08-01 |
| publisher | BMC |
| record_format | Article |
| series | Genome Medicine |
| spelling | doaj-art-4dd2eb35c99f4e269119729f77c4818b2025-08-20T04:02:56ZengBMCGenome Medicine1756-994X2025-08-0117111810.1186/s13073-025-01520-xAging increases susceptibility to liver fibrosis through enhanced NAT10-mediated ac4C modification of TGFβ1 mRNAXuyun Peng0Panlong Li1Ying Zhang2Qi Zhang3Weicheng Liang4Biotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen UniversityBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen UniversityAffiliated Cancer Hospital of Guangzhou Medical UniversityBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen UniversityBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen UniversityAbstract 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.https://doi.org/10.1186/s13073-025-01520-xLiver fibrosisAgingRNA modificationTGFβ/SMAD signaling pathwayNAT10 |
| spellingShingle | Xuyun Peng Panlong Li Ying Zhang Qi Zhang Weicheng Liang Aging increases susceptibility to liver fibrosis through enhanced NAT10-mediated ac4C modification of TGFβ1 mRNA Genome Medicine Liver fibrosis Aging RNA modification TGFβ/SMAD signaling pathway NAT10 |
| title | Aging increases susceptibility to liver fibrosis through enhanced NAT10-mediated ac4C modification of TGFβ1 mRNA |
| title_full | Aging increases susceptibility to liver fibrosis through enhanced NAT10-mediated ac4C modification of TGFβ1 mRNA |
| title_fullStr | Aging increases susceptibility to liver fibrosis through enhanced NAT10-mediated ac4C modification of TGFβ1 mRNA |
| title_full_unstemmed | Aging increases susceptibility to liver fibrosis through enhanced NAT10-mediated ac4C modification of TGFβ1 mRNA |
| title_short | Aging increases susceptibility to liver fibrosis through enhanced NAT10-mediated ac4C modification of TGFβ1 mRNA |
| title_sort | aging increases susceptibility to liver fibrosis through enhanced nat10 mediated ac4c modification of tgfβ1 mrna |
| topic | Liver fibrosis Aging RNA modification TGFβ/SMAD signaling pathway NAT10 |
| url | https://doi.org/10.1186/s13073-025-01520-x |
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