Targeted Ablation of Fn14 Receptor Improves Exercise Capacity and Inhibits Neurogenic Muscle Atrophy

Authors

Meiricris Tomaz da Silva
Aniket S Joshi
Tatiana E Koike
Anirban Roy
Kavya Mathukumalli
Danesh H Sopariwala
Vihang A Narkar
Ashok Kumar

Publication Date

12-1-2022

Journal

The FASEB Journal

Abstract

Skeletal muscle atrophy is a prevalent complication in multiple chronic diseases and disuse conditions. Fibroblast growth factor-inducible 14 (Fn14) is a member of the TNF receptor superfamily and a bona fide receptor of the TWEAK cytokine. Accumulating evidence suggests that Fn14 levels are increased in catabolic conditions as well as during exercise. However, the role of Fn14 in the regulation of skeletal muscle mass and function remains poorly understood. In this study, through the generation of novel skeletal muscle-specific Fn14-knockout mice, we have investigated the muscle role of Fn14 in the regulation of exercise capacity and denervation-induced muscle atrophy. Our results demonstrate that there was no difference in skeletal muscle mass between control and muscle-specific Fn14-knockout mice. Nevertheless, the deletion of Fn14 in skeletal muscle significantly improved exercise capacity and resistance to fatigue. This effect of Fn14 deletion is associated with an increased proportion of oxidative myofibers and higher capillaries number per myofiber in skeletal muscle. Furthermore, our results demonstrate that targeted deletion of Fn14 inhibits denervation-induced muscle atrophy in adult mice. Deletion of Fn14 reduced the expression of components of the ubiquitin-proteasome system and non-canonical NF-kappa B signaling in denervated skeletal muscle, as well as increased the phosphorylation of Akt kinase and FoxO3a transcription factor. Collectively, our results demonstrate that targeted inhibition of Fn14 improves exercise tolerance and inhibits denervation-induced muscle atrophy in adult mice.

Keywords

Mice, Animals, TWEAK Receptor, Exercise Tolerance, Tumor Necrosis Factors, Muscular Atrophy, Mice, Knockout

Comments

Data Availability Statement

PMID: 36412933