Age-associated NF-κB signaling in myofibers alters the satellite cell niche and re-strains muscle stem cell function
Year: 2016
Type: article
Abstract: Skeletal muscle is a highly regenerative tissue, but muscle repair potential is increasingly compromised with advancing age. In this study, we demonstrate that increased NF-κB activity in aged muscle fibers contributes to diminished myogenic potential of their associated satellite cells. We further examine the impact of genetic modulation of NF-κB signaling in muscle satellite cells or myofibers on recovery after damage. These studies reveal that NF-κB activity in differentiated myofibers is sufficient to drive dysfunction of muscle regenerative cells via cell-non-autonomous mechanisms. Inhibition of NF-κB, or its downstream target Phospholipase A2, in myofibers rescued muscle regenerative potential in aged muscle. Moreover, systemic administration of sodium salicylate, an FDA-approved NF-κB inhibitor, decreased inflammatory gene expression and improved repair in aged muscle. Together, these studies identify a unique NF-κB regulated, non-cell autonomous mechanism by which stem cell function is linked to lipid signaling and homeostasis, and provide important new targets to stimulate muscle repair in aged individuals.
Source: Aging
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Awards: G2076095595, Reversing age-related dysfunction of skeletal muscle stem cells, Reversing age-related dysfunction of skeletal muscle stem cells, G5659566681, Boston OAIC: A Translational Approach to Function Promoting Therapies, Training Grant in Diabetes and Metabolism, Diabetes Research Center
OpenAlex ID: W2552976270
