Quantifying forms and functions of intestinal bile acid pools in mice

Koichi Sudo, Amber Delmas-Eliason, Shannon Soucy,Kaitlyn E. Barrack,Jiabao Liu, Akshaya Balasubramanian, Chengyi Jenny Shu,Michael J. James,Courtney L. Hegner, Henry D. Dionne,Alex Rodriguez-Palacios,Henry M. Krause,George A. O’Toole,Saul J. Karpen,Paul A. Dawson,Daniel Schultz,Mark S. Sundrud

bioRxiv the preprint server for biology(2024)

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Abstract
Bile acids (BAs) are gastrointestinal metabolites that serve dual functions in lipid absorption and cell signaling. BAs circulate actively between the liver and distal small intestine ( i.e ., ileum), yet the dynamics through which complex BA pools are absorbed in the ileum and interact with intestinal cells in vivo remain ill-defined. Through multi-site sampling of nearly 100 BA species in individual wild type mice, as well as mice lacking the ileal BA transporter, Asbt/ Slc10a2 , we calculate the ileal BA pool in fasting C57BL/6J mice to be ∼0.3 μmoles/g. Asbt-mediated transport accounts for ∼80% of this pool and amplifies size, whereas passive absorption explains the remaining ∼20%, and generates diversity. Accordingly, ileal BA pools in mice lacking Asbt are ∼5-fold smaller than in wild type controls, enriched in secondary BA species normally found in the colon, and elicit unique transcriptional responses in cultured ileal explants. This work quantitatively defines ileal BA pools in mice and reveals how BA dysmetabolism can impinge on intestinal physiology. ### Competing Interest Statement C.J.S. and M.J.J. were employees of Synlogic Therapeutics during this study. M.S.S. was a consultant to Synlogic, Inc., and a member of the immunology advisory board at Sage Therapeutics. The remaining authors declare no competing interests.
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