The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T reg Cell Homeostasis

Author:

Smith Patrick M.1,Howitt Michael R.1,Panikov Nicolai1,Michaud Monia1,Gallini Carey Ann1,Bohlooly-Y Mohammad2,Glickman Jonathan N.34,Garrett Wendy S.1567

Affiliation:

1. Departments of Immunology and Infectious Diseases and Genetics and Complex Diseases, Harvard School of Public Health, Boston, MA, USA.

2. AstraZeneca, RAD-Transgenic, Mölndal, Sweden.

3. Department of Pathology, Harvard Medical School, Boston, MA, USA.

4. Miraca Life Sciences, Newton, MA, USA.

5. Department of Medicine, Harvard Medical School, Boston, MA, USA.

6. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

7. Broad Institute of Harvard and MIT, Cambridge, MA, USA.

Abstract

Protecting the Guts Regulatory T cells (T regs ) in the gut are important sentinels in maintaining the peace between our gut and its trillions of resident bacteria and have been shown to be regulated by specific strains of bacteria in mouse models. Smith et al. (p. 569 , published online 4 July; see the Perspective by Bollrath and Powrie ) asked whether metabolite(s) generated by resident bacterial species may regulate T regs in the gut. Indeed, short-chain fatty acids (SCFAs), bacterial fermentation products of dietary fibers produced by a range of bacteria, restored colonic T reg numbers in mice devoid of a gut microbiota and increased T reg numbers in colonized mice. The effects of SCFAs on T regs were mediated through GPCR43, a receptor for SCFAs, which is expressed on colonic T regs . Mice fed SCFAs were protected against experimentally induced colitis in a manner that was dependent on GPR43-expressing T regs .

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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