TY - JOUR
T1 - Aging is associated with an altered macrophage response during human skeletal muscle regeneration
AU - Ahmadi, Mohadeseh
AU - Karlsen, Anders
AU - Mehling, Jack
AU - Soendenbroe, Casper
AU - Mackey, Abigail L.
AU - Hyldahl, Robert D.
PY - 2022
Y1 - 2022
N2 - 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.
AB - 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.
U2 - 10.1016/j.exger.2022.111974
DO - 10.1016/j.exger.2022.111974
M3 - Journal article
C2 - 36228835
JO - Experimental Gerontology
JF - Experimental Gerontology
SN - 0531-5565
M1 - 111974
ER -