
Regulatory T cells produce the analgesic peptide enkephalin, which modulates basal somatic sensitivity in mice.


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CD4+CD25+Foxp3+ regulatory T cells (Treg) have been implicated in pain modulation in various inflammatory conditions. However, whether Treg cells hamper pain at steady state and by which mechanism is still unclear. From a meta-analysis of the transcriptomes of murine Treg and conventional T cells (Tconv), we observe that the proenkephalin gene ( Penk ), encoding the precursor of analgesic opioid peptides, ranks among the top 25 genes most enriched in Treg cells. We then present various evidence suggesting that Penk is regulated in part by members of the TNF receptor family and the transcription factor Batf. Using mice in which the promoter activity of Penk can be tracked with a fluorescent reporter, we also show that Penk expression is mostly detected in Treg and activated Tconv in non-inflammatory conditions in the colon and skin. Functionally, Treg cells proficient or deficient for Penk suppress equally well the proliferation of effector T cells in vitro and autoimmune colitis in vivo . In contrast, inducible ablation of Penk in Treg leads to heat hyperalgesia in both male and female mice. Overall, our results indicate that Treg might play a key role at modulating basal somatic sensitivity in mice through the production of analgesic opioid peptides.

### Competing Interest Statement

The authors have declared no competing interest.

Enkephalin-mediated modulation of basal somatic sensitivity by regulatory T cells in mice

enkephalin-production-by-regulatory-t-cells-modulates-basal-somatic-sensitivity-in-mice


Enkephalin Production by Regulatory T Cells Modulates Basal Somatic Sensitivity in Mice
