Journal
NATURE
Volume 504, Issue 7480, Pages 451-+Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/nature12726
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Funding
- Damon Runyon Cancer Research Foundation [DRG-2143-13]
- Ludwig Center at Memorial Sloan Kettering Cancer Center
- US National Institutes of Health (NIH) [T32 A1007621, R37 AI034206]
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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(1). 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(2-6), 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(1,7). 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.
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