4.7 Article

Gut Microbiota-Produced Tryptamine Activates an Epithelial G-Protein-Coupled Receptor to Increase Colonic Secretion

Journal

CELL HOST & MICROBE
Volume 23, Issue 6, Pages 775-+

Publisher

CELL PRESS
DOI: 10.1016/j.chom.2018.05.004

Keywords

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Funding

  1. NIH [DK100638, DK111850, DK114007]
  2. NIDDK [K23 103911]
  3. Integrated Physiology Core of the Hopkins Conte Digestive Disease Basic and Translational Research Core Center [P30 DK-089502]
  4. Global Probiotic Council
  5. Center for Individualized Medicine, Mayo Clinic, Rochester, MN
  6. VA merit review funds
  7. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P30DK089502, P30DK041301, R03DK111850, K23DK103911, K08DK100638, R01DK114007] Funding Source: NIH RePORTER

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Tryptamine, a tryptophan-derived monoamine similar to 5-hydroxytryptamine (5-HT), is produced by gut bacteria and is abundant in human and rodent feces. However, the physiologic effect of tryptamine in the gastrointestinal (GI) tract remains unknown. Here, we show that the biological effects of tryptamine are mediated through the 5-HT4 receptor (5-HT4R), a G-protein-coupled receptor (GPCR) uniquely expressed in the colonic epithelium. Tryptamine increases both ionic flux across the colonic epithelium and fluid secretion in colonoids from germ-free (GF) and humanized (ex-GF colonized with human stool) mice, consistent with increased intestinal secretion. The secretory effect of tryptamine is dependent on 5-HT4R activation and is blocked by 5-HT4R antagonist and absent in 5-HT4R-/- mice. GF mice colonized by Bacteroides thetaiotaomicron engineered to produce tryptamine exhibit accelerated GI transit. Our study demonstrates an aspect of host physiology under control of a bacterial metabolite that can be exploited as a therapeutic modality.

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