Nutrient-derived signals regulate eosinophil adaptation to the small intestine.

eosinophils inflammation retinoic acid small intestine

Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
30 Jan 2024
Historique:
medline: 25 1 2024
pubmed: 25 1 2024
entrez: 25 1 2024
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 38271336
doi: 10.1073/pnas.2316446121
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2316446121

Subventions

Organisme : Howard Hughes Medical Institute (HHMI)
ID : N/A
Organisme : HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID)
ID : AI144152-01

Déclaration de conflit d'intérêts

Competing interests statement:The authors declare no competing interest.

Auteurs

Vassily I Kutyavin (V)

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

Lisa L Korn (LL)

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

Ruslan Medzhitov (R)

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

Classifications MeSH