Myeloid AEG-1/MTDH drives inflammation and hepatocellular dysfunction in diet-induced steatohepatitis
Astrocyte elevated gene-1 (AEG-1)/metadherin plays an important role in regulating lipid metabolism and inflammation in hepatocytes and promotes metabolic dysfunction-associated steatohepatitis (MASH). Myeloid cells, such as macrophages, play a key role in regulating inflammation. Here, we investigated the role of AEG-1 in myeloid cells in regulating high fat)/high sugar diet (HF/HSD)-induced MASH. Littermates of myeloid cell-specific AEG-1 knockout mice (AEG-1<sup>ΔMAC</sup>) and AEG-1 floxed mice (AEG-1<sup>fl/fl</sup>) were fed either a control diet or an HF/HSD for 20 weeks. Both male and female AEG-1<sup>ΔMAC</sup> mice were significantly protected from MASH development compared with AEG-1<sup>fl/fl</sup> mice. In control diet-fed mice, spatial transcriptomics analysis revealed inhibition of hepatic steatosis and development of hepatocellular carcinoma and activation of fatty acid β-oxidation in the periportal and pericentral hepatocytes of AEG-1<sup>ΔMAC</sup> livers. Single-cell RNA-Seq, performed in HF/HSD-fed mice, identified a significant decrease in the total number of Kupffer cells in AEG-1<sup>ΔMAC</sup>versus AEG-1<sup>fl/fl</sup> livers. A marked inhibition of inflammation and fibrosis in Kupffer cells and stellate cells, increased fatty acid β-oxidation in stellate and endothelial cells, and inhibition of proliferation and invasion in the hepatocytes, especially in pericentral hepatocytes, were observed in AEG-1<sup>ΔMAC</sup> liver versus AEG-1<sup>fl/fl</sup> liver. Mesenteric fat weight, adipocyte size, and inflammation were significantly decreased in HF/HSD-fed AEG-1<sup>ΔMAC</sup> mice compared with AEG-1<sup>fl/fl</sup> mice. Inhibition of inflammation is a key feature in AEG-1<sup>ΔMAC</sup> mice. AEG-1 in myeloid cells regulate gene expression in hepatocytes and other nonparenchymal cells, thereby playing an important role in regulating MASH.
Authors
- Mark A. Subler
- J. Liu
- Rachel G. Mendoza
- Jolene J. Windle (ORCID: https://orcid.org/0000-0001-6690-385X)
- Suchismita Raha (ORCID: https://orcid.org/0000-0002-0185-2948)
- Rebecca Martin (ORCID: https://orcid.org/0000-0001-9948-5463)
- Devanand Sarkar (ORCID: https://orcid.org/0000-0003-0973-2323)
- Ali Gawi Ermi (ORCID: https://orcid.org/0000-0002-5973-8347)
- Saranya Chidambaranathan Reghupaty
- Paul B. Fisher
- Devon Farrar
- Eva Davis
- Xufeng Qu
Institutions
- Virginia Commonwealth University (US)
- Stanford University (US)
Publication Details
- Journal
- Journal of Biological Chemistry
- Published
- 2025-12-24
- DOI
- https://doi.org/10.1016/j.jbc.2025.111101
- Primary Topic
- Cancer Mechanisms and Therapy
- Type
- article
- Field-Weighted Citation Impact
- 0.00