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Pax7+ Satellite Cells in Human Skeletal Muscle After Exercise: A Systematic Review and Meta-analysis

Journal

SPORTS MEDICINE
Volume 53, Issue 2, Pages 457-480

Publisher

ADIS INT LTD
DOI: 10.1007/s40279-022-01767-z

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This study provides a quantitative estimate of the changes in Pax7(+) muscle stem cells and circulating CD34(+) bone marrow stem cells in humans following acute exercise. The results show that Pax7(+) cells in skeletal muscle increase significantly after resistance exercise, while circulating CD34(+) cells also increase after both resistance exercise and aerobic exercise but quickly return to baseline levels.
Background Skeletal muscle has extraordinary regenerative capabilities against challenge, mainly owing to its resident muscle stem cells, commonly identified by Pax7(+), which expediently donate nuclei to the regenerating multinucleated myofibers. This local reserve of stem cells in damaged muscle tissues is replenished by undifferentiated bone marrow stem cells (CD34(+)) permeating into the surrounding vascular system. Objective The purpose of the study was to provide a quantitative estimate for the changes in Pax7(+) muscle stem cells (satellite cells) in humans following an acute bout of exercise until 96 h, in temporal relation to circulating CD34(+) bone marrow stem cells. A subgroup analysis of age was also performed. Methods Four databases (Web of Science, PubMed, Scopus, and BASE) were used for the literature search until February 2022. Pax7(+) cells in human skeletal muscle were the primary outcome. Circulating CD34(+) cells were the secondary outcome. The standardized mean difference (SMD) was calculated using a random-effects meta-analysis. Subgroup analyses were conducted to examine the influence of age, training status, type of exercise, and follow-up time after exercise. Results The final search identified 20 studies for Pax7(+) cells comprising a total of 370 participants between the average age of 21 and 74 years and 26 studies for circulating CD34(+) bone marrow stem cells comprising 494 participants between the average age of 21 and 67 years. Only one study assessed Pax7(+) cells immediately after aerobic exercise and showed a 32% reduction in exercising muscle followed by a fast repletion to pre-exercise level within 3 h. A large effect on increasing Pax7(+) cell content in skeletal muscles was observed 24 h after resistance exercise (SMD = 0.89, p < 0.001). Pax7(+) cells increased to 50% above pre-exercise level 24-72 h after resistance exercise. For a subgroup analysis of age, a large effect (SMD = 0.81, p < 0.001) was observed on increasing Pax7(+) cells in exercised muscle among adults aged> 50 years, whereas adults at younger age presented a medium effect (SMD = 0.64, p < 0.001). Both resistance exercise and aerobic exercise showed a medium overall effect in increasing circulating CD34(+) cells (SMD = 0.53, p < 0.001), which declined quickly to the pre-exercise baseline level after exercise within 6 h. Conclusions An immediate depletion of Pax7(+) cells in exercising skeletal muscle concurrent with a transient release of CD34(+) cells suggest a replenishment of the local stem cell reserve from bone marrow. A protracted Pax7(+) cell expansion in the muscle can be observed during 24-72 h after resistance exercise. This result provides a scientific basis for exercise recommendations on weekly cycles allowing for adequate recovery time. Exercise-induced Pax7(+) cell expansion in muscle remains significant at higher age, despite a lower stem cell reserve after age 50 years. More studies are required to confirm whether Pax7(+) cell increment can occur after aerobic exercise.

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