Aging is associated with an altered macrophage response during human skeletal muscle regeneration

Exp Gerontol. 2022 Nov:169:111974. doi: 10.1016/j.exger.2022.111974. Epub 2022 Oct 11.

Abstract

Skeletal muscle injury in aged rodents is characterized by an asynchronous infiltration of pro- and anti-inflammatory macrophage waves, leading to improper and incomplete regeneration. It is unclear whether this aberration also occurs in aged human muscle. In this study, we quantified the macrophage responses in a human model of muscle damage and regeneration induced by electrical stimulation in 7 young and 21 older adults. At baseline, total resident macrophage (CD68+/DAPI+) content was not different between young and old subjects, but pro-inflammatory (CD206-/CD68+/DAPI+) macrophage content was lower in the old. Following damage, muscle Infiltration of CD206-/CD68+/DAPI+ macrophages was lower in old relative to young subjects. Further, only the increase in CD206-/CD68+ macrophages correlated with the change in muscle satellite cell content. Our data show that older individuals have a compromised macrophage response during muscle regeneration, pointing to an altered inflammatory response as a potential mechanism for reduced muscle regenerative efficacy in aged humans.

Keywords: Aging; Immunosenescence; Inflammation; Muscle damage; Muscle regeneration; Satellite cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aging
  • Humans
  • Macrophages* / physiology
  • Muscle, Skeletal* / physiology
  • Regeneration
  • Wound Healing