Nutrient-derived signals regulate eosinophil adaptation to the small intestine

Author:

I. Kutyavin Vassily1ORCID,Korn Lisa L.12,Medzhitov Ruslan13ORCID

Affiliation:

1. Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06510

2. Department of Medicine (Rheumatology), Yale University School of Medicine, New Haven, CT 06510

3. HHMI, Yale University School of Medicine, New Haven, CT 06510

Abstract

Eosinophils are well recognized as effector cells of type 2 immunity, yet they also accumulate in many tissues under homeostatic conditions. However, the processes that govern homeostatic eosinophil accumulation and tissue-specific adaptation, and their functional significance, remain poorly defined. Here, we investigated how eosinophils adapt to the small intestine (SI) microenvironment and the local signals that regulate this process. We observed that eosinophils gradually migrate along the crypt–villus axis, giving rise to a villus-resident subpopulation with a distinct transcriptional signature. Retinoic acid signaling was specifically required for maintenance of this subpopulation, while IL-5 was largely dispensable outside of its canonical role in eosinophil production. Surprisingly, we found that a high-protein diet suppressed the accumulation of villus-resident eosinophils. Purified amino acids were sufficient for this effect, which was a consequence of accelerated eosinophil turnover within the tissue microenvironment and was not due to altered development in the bone marrow. Our study provides insight into the process of eosinophil adaptation to the SI, highlighting its reliance on nutrient-derived signals.

Funder

Howard Hughes Medical Institute

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

Proceedings of the National Academy of Sciences

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