Interleukin-13 drives metabolic conditioning of muscle to endurance exercise

Author:

Knudsen Nelson H.1ORCID,Stanya Kristopher J.1ORCID,Hyde Alexander L.1,Chalom Mayer M.1ORCID,Alexander Ryan K.1ORCID,Liou Yae-Huei1ORCID,Starost Kyle A.1ORCID,Gangl Matthew R.1,Jacobi David1ORCID,Liu Sihao1,Sopariwala Danesh H.2,Fonseca-Pereira Diogo3ORCID,Li Jun4ORCID,Hu Frank B.45,Garrett Wendy S.13ORCID,Narkar Vihang A.2ORCID,Ortlund Eric A.6ORCID,Kim Jonathan H.67,Paton Chad M.8ORCID,Cooper Jamie A.8,Lee Chih-Hao1ORCID

Affiliation:

1. Department of Molecular Metabolism, Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA.

2. Metabolic and Degenerative Diseases, Institute of Molecular Medicine, University of Texas McGovern Medical School, Houston, TX 77030, USA.

3. Department of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA.

4. Department of Nutrition and Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA.

5. Channing Division of Network Medicine, Department of Medicine, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA 02115, USA.

6. Emory University School of Medicine, Atlanta, GA 30322, USA.

7. Emory Clinical Cardiovascular Research Institute, Atlanta, GA 30322, USA.

8. Department of Foods and Nutrition, University of Georgia, Athens, GA 30602, USA.

Abstract

IL-13 hits the gym Interleukin-13 (IL-13) is a cytokine secreted by T cells, innate lymphoid cells (ILC2s), and granulocytes. It acts as a central mediator in allergy and antihelminth defense with various effects. Knudsen et al. report a distinct role for IL-13 in exercise and metabolism (see the Perspective by Correia and Ruas). Mice subjected to endurance training showed increases in circulating IL-13, which correlated with ILC2 expansion in the muscles. By contrast, exercise-induced increases in muscle fatty acid utilization and mitochondrial biogenesis were erased when mice lacked IL-13. Activation of signaling pathways downstream of the muscle IL-13 receptor was key to this effect. Intramuscular injection of adenoviral IL-13 could recapitulate exercise-induced metabolic reprogramming. This signaling pathway may have evolved to combat the metabolic stresses of parasite infection. Science , this issue p. eaat3987 ; see also p. 470

Funder

National Institutes of Health

American Heart Association

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference34 articles.

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