Ultra-processed foods sourced 7-ketositosterol aggravates colitis through gut dysbiosis induced-PDLIM3 activation

  • Gut Microbes. 2025 Dec 31;17(1):2587980. doi: 10.1080/19490976.2025.2587980.
Jing Yan  1  2 Xiaoqi Pang  1 Qi Chen  1 Jingjing Wang  1  3 Zimin Wang  1 Kailin Jiao  2 Yujie Dai  4 Ting Xia  5 Ge Jin  1 Weilong Zhong  1 Nan Wang  2 Bangmao Wang  1 Jin Zheng  2 Xin Xu  1 Hailong Cao  1
Affiliations
  • 1. Department of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, National Key Clinical Specialty, Tianjin Institute of Digestive Diseases, Tianjin Key Laboratory of Digestive Diseases, Tianjin, China.
  • 2. Department of Nutrition, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
  • 3. Department of Nutrition, the Third Central Hospital of Tianjin, Tianjin, China.
  • 4. Department of Nutrition, the First Affiliated Hospital, Air Force Medical University, Xi'an, China.
  • 5. State Key Laboratory of Food Nutrition and Safety, Key Laboratory of Industrial Fermentation Microbiology, College of Biotechnology, Tianjin University of Science and Technology, Tianjin, China.
Abstract

Excessive ultra-processed foods (UPFs) consumption has been reported to increase the risk of inflammatory bowel disease (IBD). However, the specific mechanisms involved remain unclear. As an important ingredient of UPFs, 7-ketositosterol (KS) is synthesized mainly from high-temperature heated oils. We found that KS intake is higher in IBD patients and is related to disease activity. KS exacerbates colitis in a gut microbiota-dependent manner in mice, altering the gut microbiota composition and increasing the abundance of potential pathogenic bacteria, especially Staphylococcus lentus (SL). Moreover, SL aggravates DSS-induced colitis. Mechanically, KS upregulates the expression of PDZ and LIM domain 3 (PDLIM3). SL-derived lysin motif peptidoglycan-binding domain-containing protein (LPDP) interacts with PDLIM3 and activates the p38MAPK/NF-κB signaling pathway. Furthermore, tubuloside B, which is selected by high-throughput screening, blocks the interaction of PDLIM3 and LPDP, and ameliorates SL-aggravated colitis. Our study reveals that KS exposure promotes colitis via the gut microbiota and PDLIM3 interaction, providing evidence of IBD pathogenesis and a potential therapeutic strategy for IBD treatment.

Keywords
7-ketositosterol; PDLIM3; Ultra-processed foods; colitis; gut microbiota; protein interaction.
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