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A thermogenic fat-epithelium cell axis regulates intestinal disease tolerance
Author(s) -
Kevin Man,
Christopher Bowman,
Kristi. Braverman,
Veronica Escalante,
Yuan Tian,
Jordan E. Bisanz,
Kirthana Ganeshan,
Biao Wang,
Andrew D. Patterson,
James R. Bayrer,
Peter J. Turnbaugh,
Ajay Chawla
Publication year - 2020
Publication title -
proceedings of the national academy of sciences
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.2012003117
Subject(s) - colitis , disease , intestinal epithelium , biology , inflammation , immune system , immune tolerance , inflammatory bowel disease , immunology , intestinal mucosa , epithelium , medicine , pathology , genetics
Disease tolerance, the capacity of tissues to withstand damage caused by a stimulus without a decline in host fitness, varies across tissues, environmental conditions, and physiologic states. While disease tolerance is a known strategy of host defense, its role in noninfectious diseases has been understudied. Here, we provide evidence that a thermogenic fat-epithelial cell axis regulates intestinal disease tolerance during experimental colitis. We find that intestinal disease tolerance is a metabolically expensive trait, whose expression is restricted to thermoneutral mice and is not transferable by the microbiota. Instead, disease tolerance is dependent on the adrenergic state of thermogenic adipocytes, which indirectly regulate tolerogenic responses in intestinal epithelial cells. Our work has identified an unexpected mechanism that controls intestinal disease tolerance with implications for colitogenic diseases.

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