Oral administration of helminth fluid modulates distinct tuft cell and immune‐metabolic cues linked to reduced body fat

Author:

Andersen Daniel1,Moll Janne Marie1,Arora Pankaj1,Danneskiold‐Samsøe Niels Banhos2,Sonne Si Brask2ORCID,Workman Christopher Thomas1,Williams Andrew Richard3ORCID,Kristiansen Karsten2ORCID,Brix Susanne1ORCID

Affiliation:

1. Department of Biotechnology and Biomedicine Technical University of Denmark Kongens Lyngby Denmark

2. Laboratory of Genomics and Molecular Biomedicine, Department of Biology University of Copenhagen Copenhagen Denmark

3. Department of Veterinary and Animal Sciences University of Copenhagen Frederiksberg Denmark

Abstract

AbstractIntestinal tuft cells have been shown to induce type 2 immune responses during viable parasite infections, but whether oral supplementation with a parasitic exudate is able to promote type 2 immune responses that have been shown to positively regulate obesogenic metabolic processes is yet unresolved. High‐fat fed mice were gavaged with pseudocoelomic fluid (PCF) derived from the helminth Ascaris suum or saline thrice a week during weeks 5–9, followed by examination of intestinal tuft cell activity, immune, and metabolic parameters. Helminth PCF upregulated expression of distinct genes in small intestinal tuft cells, including genes involved in regulation of RUNX1 and organic cation transporters. Helminth PCF also enhanced levels of innate lymphoid cells in the ileum, and eosinophils in epididymal white adipose tissue (eWAT). Network analyses revealed two distinct immunometabolic cues affected by oral helminth PCF in high‐fat fed mice: one coupling the small intestinal tuft cell responses to the fat‐to‐lean mass ratio and a second coupling eosinophils in eWAT to general regulation of body fat mass. Our findings point to specific mechanisms by which oral supplementation with helminth PCF may translate into systems‐wide effects linking to reduced body and fat mass gain in mice during high‐fat feeding.

Funder

Novo Nordisk Fonden

Publisher

Wiley

Subject

Immunology,Parasitology

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