Influence of sexual dimorphism on satellite cell regulation and inflammatory response during skeletal muscle regeneration

Abstract

After injury, skeletal muscle regenerates thanks to the key role of satellite cells (SC). The regeneration process is supported and coordinated by other cell types among which immune cells. Among the mechanisms involved in skeletal muscle regeneration, a sexual dimorphism, involving sex hormones and more particularly estrogens, has been suggested. However, the role of sexual dimorphism on skeletal muscle regeneration is not fully understood, likely to the use of various experimental settings in both animals and human. This review aims at addressing how sex and estrogens regulate both the SC and the inflammatory response during skeletal muscle regeneration by considering the different experimental designs used in both animal models (i.e., ovarian hormone deficiency, estrogen replacement or supplementation, treatments with estrogen receptors agonists/antagonists and models knockout for estrogen receptors) and human (hormone therapy replacement, pre vs. postmenopausal, menstrual cycle variation…).

Impaired skeletal muscle regeneration induced by Cre recombinase activation in skeletal muscle stem cells

“…Estrogens and estrogen-like compounds are known modulators of skeletal muscle regeneration, as reviewed before e.g., 10,11 . We therefore asked if Tx treatment per se could cause alterations in skeletal muscle regeneration.…”