Geriatric muscle stem cells switch reversible quiescence into senescence
By Pedro Sousa‐Victor, Susana Gutarra, Laura Garcia-Prat, J. Rodríguez-Ubreva, L. Ortet, Vanessa Ruiz-Bonilla, M. Jardí, Esteban Ballestar, S. González, A. Serrano and 2 more. Nature, 2014
896 citations recorded by the source corpus.
Subfields: Aging, Molecular Biology, Physiology
View Paper: https://www.semanticscholar.org/paper/5594037b999265d08c8d741425e80cf0f2fdd027
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Citations in the corpus
- In Vivo Amelioration of Age-Associated Hallmarks by Partial Reprogramming (2016, neutral): “…aging and as a consequence of environmental and cell-intrinsic factors, there is a decrease in the number and functionality of satellite cells that switch from a quiescent to a pre-senescence state that hampers their regenerative capacity (Garcı´a-Prat et al., 2016; Sousa-Victor et al., 2014).”
- Satellite Cells and Skeletal Muscle Regeneration (2015, neutral): “Loss of reversible quiescence in aged satellite cells is accompanied by derepression of the CKI Cdkn2a (285).”
- Mitochondrial Dysfunction Induces Senescence with a Distinct Secretory Phenotype (2015, background): “The permanent growth arrest can deplete progenitor or stem cell pools, thereby compromising tissue repair and regeneration (Kuilman et al., 2010; Sousa-Victor et al., 2014; Velarde et al., 2015).”
- Senescence and aging: Causes, consequences, and therapeutic avenues (2018, background): “However, with age, they become senescent, up-regulating p16INK4a (Sousa-Victor et al., 2014).”