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Estradiol deficiency reduces the satellite cell pool by impairing cell cycle progression
The size of the satellite cell pool is reduced in estradiol (E(2))-deficient female mice and humans. Here, we use a combination of in vivo and in vitro approaches to identify mechanisms, whereby E(2) deficiency impairs satellite cell maintenance. By measuring satellite cell numbers in mice at severa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Physiological Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169829/ https://www.ncbi.nlm.nih.gov/pubmed/35442828 http://dx.doi.org/10.1152/ajpcell.00429.2021 |
Sumario: | The size of the satellite cell pool is reduced in estradiol (E(2))-deficient female mice and humans. Here, we use a combination of in vivo and in vitro approaches to identify mechanisms, whereby E(2) deficiency impairs satellite cell maintenance. By measuring satellite cell numbers in mice at several early time points postovariectomy (Ovx), we determine that satellite cell numbers decline by 33% between 10 and 14 days post-Ovx in tibialis anterior and gastrocnemius muscles. At 14 days post-Ovx, we demonstrate that satellite cells have a reduced propensity to transition from G(0)/G(1) to S and G(2)/M phases, compared with cells from ovary-intact mice, associated with changes in two key satellite cell cycle regulators, ccna2 and p16(INK4a). Further, freshly isolated satellite cells treated with E(2) in vitro have 62% greater cell proliferation and require less time to complete the first division. Using clonal and differentiation assays, we measured 69% larger satellite cell colonies and enhanced satellite cell-derived myoblast differentiation with E(2) treatment compared with vehicle-treated cells. Together, these results identify a novel mechanism for preservation of the satellite cell pool by E(2) via promotion of satellite cell cycling. |
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