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Peer-reviewedCC BYInternational Journal of Biological Sciences

A context-dependent METTL1-m7G-SLC7A11 axis links metabolic stress to epithelial fate in ulcerative colitis

  1. 1Center for Clinical Sciences, Japan Institute for Health Security, Tokyo, Japan
  2. 2Department of General Surgery, The Second Xiangya Hospital of Central South University, 410011 Changsha, China

Abstract

, inhibition of the METTL1/m7G/SLC7A11 axis exacerbates chronic DSS-induced colitis but alleviates acute DSS-induced colitis, revealing a switch from adaptive to maladaptive signaling with escalating metabolic stress. Collectively, these findings establish the METTL1-m7G-SLC7A11 axis as a metabolic rheostat that integrates inflammatory cues and nutrient availability to determine epithelial cell fate in UC, highlighting the importance of stage- and context-specific therapeutic strategies.

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BibTeX
@article{yang2026contextdependent,
  title = {{A context-dependent METTL1-m7G-SLC7A11 axis links metabolic stress to epithelial fate in ulcerative colitis}},
  author = {Lichao Yang and Qi Sun and Zhixian Jiang and Baojia Yao and Caimei Yang and Ganglei Liu and Lianwen Yuan},
  journal = {International Journal of Biological Sciences},
  year = {2026},
  month = may,
  doi = {10.7150/ijbs.133562},
  url = {https://doi.org/10.7150/ijbs.133562},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - A context-dependent METTL1-m7G-SLC7A11 axis links metabolic stress to epithelial fate in ulcerative colitis
AU  - Lichao Yang
AU  - Qi Sun
AU  - Zhixian Jiang
AU  - Baojia Yao
AU  - Caimei Yang
AU  - Ganglei Liu
AU  - Lianwen Yuan
PY  - 2026
DA  - 2026/05/11
JO  - International Journal of Biological Sciences
DO  - 10.7150/ijbs.133562
UR  - https://doi.org/10.7150/ijbs.133562
AB  - , inhibition of the METTL1/m7G/SLC7A11 axis exacerbates chronic DSS-induced colitis but alleviates acute DSS-induced colitis, revealing a switch from adaptive to maladaptive signaling with escalating metabolic stress. Collectively, these findings establish the METTL1-m7G-SLC7A11 axis as a metabolic rheostat that integrates inflammatory cues and nutrient availability to determine epithelial cell fate in UC, highlighting the importance of stage- and context-specific therapeutic strategies.
SN  - 1449-2288
ER  -