γδ T cells regulate the intestinal response to nutrient sensing

Author:

Sullivan Zuri A.1ORCID,Khoury-Hanold William1ORCID,Lim Jaechul1ORCID,Smillie Chris2,Biton Moshe2ORCID,Reis Bernardo S.3,Zwick Rachel K.4ORCID,Pope Scott D.15ORCID,Israni-Winger Kavita1ORCID,Parsa Roham3,Philip Naomi H.1ORCID,Rashed Saleh1,Palm Noah1ORCID,Wang Andrew16ORCID,Mucida Daniel3ORCID,Regev Aviv278ORCID,Medzhitov Ruslan15ORCID

Affiliation:

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

2. Klarman Cell Observatory, Broad Institute, Cambridge, MA, USA.

3. Laboratory of Mucosal Immunology, The Rockefeller University, New York, NY, USA.

4. Program in Craniofacial Biology and Department of Orofacial Sciences, University of California, San Francisco, CA, USA.

5. Howard Hughes Medical Institute, New Haven, CT, USA.

6. Division of Rheumatology, Department of Medicine, Yale University School of Medicine, New Haven, CT, USA.

7. The David H. Koch Institute for Integrative Cancer Research at MIT, Department of Biology, Massachusetts Institute of Technology (MIT), Cambridge, MA, USA.

8. Howard Hughes Medical Institute, Cambridge, MA, USA.

Abstract

γδ T cells link immunity to nutrition Gamma delta (γδ) T cells are immune cells best known for host barrier defenses in epithelial tissues. Sullivan et al. discovered a previously unrecognized role for γδ T cells in sensing nutrient uptake in the small intestine (see the Perspective by Talbot and Littman). The researchers analyzed mice fed a high-carbohydrate versus a high-protein diet and observed remodeling of the small intestinal epithelium in response to dietary carbohydrates. Nutrient availability triggered an epithelial–immune cell circuit that was required for digestion and absorption of carbohydrates. Intestinal γδ T cells regulated the expression of a carbohydrate transcriptional program by limiting interleukin-22 production from type 3 innate lymphoid cells. These findings may also provide insights into how γδ T cells modulate metabolic disease. Science , this issue p. eaba8310 ; see also p. 1202

Funder

Howard Hughes Medical Institute

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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