Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation Journal Article
| Authors: | Arpaia, N.; Campbell, C.; Fan, X.; Dikiy, S.; Van Der Veeken, J.; Deroos, P.; Liu, H.; Cross, J. R.; Pfeffer, K.; Coffer, P. J.; Rudensky, A. Y. |
| Article Title: | Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation |
| Abstract: | Intestinal microbes provide multicellular hosts with nutrients and confer resistance to infection. The delicate balance between pro- and anti-inflammatory mechanisms, essential for gut immune homeostasis, is affected by the composition of the commensal microbial community. Regulatory T cells (T reg cells) expressing transcription factor Foxp3 have a key role in limiting inflammatory responses in the intestine. Although specific members of the commensal microbial community have been found to potentiate the generation of anti-inflammatory T reg or pro-inflammatory T helper 17 (T H 17) cells, the molecular cues driving this process remain elusive. Considering the vital metabolic function afforded by commensal microorganisms, we reasoned that their metabolic by-products are sensed by cells of the immune system and affect the balance between pro- and anti-inflammatory cells. We tested this hypothesis by exploring the effect of microbial metabolites on the generation of anti-inflammatory T reg cells. We found that in mice a short-chain fatty acid (SCFA), butyrate, produced by commensal microorganisms during starch fermentation, facilitated extrathymic generation of T reg cells. A boost in T reg -cell numbers after provision of butyrate was due to potentiation of extrathymic differentiation of T reg cells, as the observed phenomenon was dependent on intronic enhancer CNS1 (conserved non-coding sequence 1), essential for extrathymic but dispensable for thymic T reg -cell differentiation. In addition to butyrate, de novo T reg -cell generation in the periphery was potentiated by propionate, another SCFA of microbial origin capable of histone deacetylase (HDAC) inhibition, but not acetate, which lacks this HDAC-inhibitory activity. Our results suggest that bacterial metabolites mediate communication between the commensal microbiota and the immune system, affecting the balance between pro- and anti-inflammatory mechanisms. © 2013 Macmillan Publishers Limited. All rights reserved. |
| Journal Title: | Nature |
| Volume: | 504 |
| Issue: | 7480 |
| ISSN: | 0028-0836 |
| Publisher: | Nature Publishing Group |
| Date Published: | 2013-12-19 |
| Start Page: | 451 |
| End Page: | 455 |
| Language: | English |
| DOI: | 10.1038/nature12726 |
| PROVIDER: | scopus |
| PMCID: | PMC3869884 |
| PUBMED: | 24226773 |
| DOI/URL: | |
| Notes: | Export Date: 2 January 2014 -- CODEN: NATUA -- Source: Scopus |
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
Related MSK Work