MOTS-c is an Exercise-Induced Mitochondrial-Encoded Regulator of Age-Dependent Physical Decline and Muscle Homeostasis

• Published in: bioRxiv
• Main Authors: Reynolds, Joseph C, Lai, Rochelle W, Jonathan St Woodhead, Joly, James H, Mitchell, Cameron J, Cameron-Smith, David, Lu, Ryan, Cohen, Pinchas, Graham, Nicholas Alexander, Benayoun, Bérénice Anath, Merry, Troy L, Lee, Changhan
• Format: Paper
• Language: English
• Published: Cold Spring Harbor Cold Spring Harbor Laboratory Press 16.08.2020
• Subjects: Aging; Amino acids; Bioenergetics; Cellular stress response; Chronic illnesses; Gene expression; Genomes; Glucose metabolism; Homeostasis; HSF1 protein; Life span; Metabolism; Mitochondria; Musculoskeletal system; Myoblasts; Organelles; Peptides; Physiology; Protein turnover; Risk factors; siRNA; Skeletal muscle; Therapeutic applications
• DOI: 10.1101/2019.12.22.886432

Healthy aging can be promoted by enhancing metabolic fitness and physical capacity (1, 2). Mitochondria are chief metabolic organelles with strong implications in aging (3-8). In addition to their prominent role in bioenergetics, mitochondria also coordinate broad physiological functions by communicating to other cellular compartments or distal cells using multiple factors (9, 10), including peptides that are encoded within their own independent genome (11, 12). However, it is unknown if aging is actively regulated by factors encoded in the mitochondrial genome. MOTS-c is a mitochondrial-encoded peptide that regulates metabolic homeostasis (13, 14), in part, by translocating to the nucleus to regulate adaptive nuclear gene expression in response to cellular stress (15-17). Here, we report that MOTS-c is an exercise-induced mitochondrial-encoded peptide that significantly enhanced physical performance when administered to young (2 mo.), middle- aged (12 mo.), and old (22 mo.) mice. In humans, we found that endogenous MOTS-c levels significantly increased in response to exercise in skeletal muscle (11.9-fold) and in circulation (1.5-fold). Systemic MOTS-c treatment in mice significantly enhanced the performance on a treadmill of all age groups (~2-fold). MOTS-c regulated (i) nuclear genes, including those related to metabolism and protein homeostasis, (ii) glucose and amino acid metabolism in skeletal muscle, and (iii) myoblast adaptation to metabolic stress. Late-life (23.5 mo.) initiated intermittent MOTS- c treatment (3x/week) improved physical capacity and trended towards increasing lifespan. Our data indicate that aging is regulated by genes that are encoded not only in the nuclear genome (18, 19), but also in the mitochondrial genome. Considering that aging is the major risk factor for multiple chronic diseases (20, 21), our study provides new grounds for further investigation into mitochondrial-encoded regulators of healthy lifespan. Competing Interest Statement The authors have declared no competing interest. Footnotes * https://github.com/BenayounLaboratory/MOTSc_Exercise