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The Effects of Muscle Cell Aging on Myogenesis.
Moustogiannis, Athanasios; Philippou, Anastassios; Taso, Orjona; Zevolis, Evangelos; Pappa, Maria; Chatzigeorgiou, Antonios; Koutsilieris, Michael.
Afiliación
  • Moustogiannis A; Department of Physiology, Medical School, National and Kapodistrian University of Athens, 75 MicrasAsias, 115 27 Goudi-Athens, Greece.
  • Philippou A; Department of Physiology, Medical School, National and Kapodistrian University of Athens, 75 MicrasAsias, 115 27 Goudi-Athens, Greece.
  • Taso O; Department of Physiology, Medical School, National and Kapodistrian University of Athens, 75 MicrasAsias, 115 27 Goudi-Athens, Greece.
  • Zevolis E; Department of Physiology, Medical School, National and Kapodistrian University of Athens, 75 MicrasAsias, 115 27 Goudi-Athens, Greece.
  • Pappa M; First Department of Propaedeutic Internal Medicine, Joint Rheumatology Program, National and Kapodistrian University of Athens, 75 MicrasAsias, 115 27 Goudi-Athens, Greece.
  • Chatzigeorgiou A; Department of Physiology, Medical School, National and Kapodistrian University of Athens, 75 MicrasAsias, 115 27 Goudi-Athens, Greece.
  • Koutsilieris M; Department of Physiology, Medical School, National and Kapodistrian University of Athens, 75 MicrasAsias, 115 27 Goudi-Athens, Greece.
Int J Mol Sci ; 22(7)2021 Apr 02.
Article en En | MEDLINE | ID: mdl-33918414
ABSTRACT
The process of myogenesis gradually deteriorates as the skeletal muscle ages, contributing to muscle mass loss. The aim of this study is to investigate the effect of senescence/aging on skeletal myogenesis, in vitro. A model of multiple cell divisions of C2C12 myoblasts was used to replicate cell senescence. Control and aged myoblasts were investigated during myogenesis, i.e., at days 0, 2, and 6of differentiation. SA-ß-gal activity and comet assay were used as markers of aging and DNA damage. Flow cytometry was performed to characterize potential differences in cell cycle between control and aged cells. Alterations in the mRNA and/or protein expression of myogenic regulatory factors (MRFs), IGF-1 isoforms, apoptotic, atrophy, inflammatory, metabolic and aging-related factors were evaluated. Compared with the control cells, aged myoblasts exhibited G0/G1 cell cycle arrest, DNA damage, increased SA-ß-gal activity, and increased expression of aging-related factors p16 and p21 during differentiation. Moreover, aged myoblasts showed a reduction in the expression of MRFs and metabolic/anabolic factors, along with an increased expression of apoptotic, atrophy and inflammatory factors. A diminished differentiation capacity characterized the aged myoblasts which, in combination with the induction of apoptotic and atrophy factors, indicated a disrupted myogenic lineage in the senescent muscle cells.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Senescencia Celular / Desarrollo de Músculos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Grecia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Senescencia Celular / Desarrollo de Músculos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Grecia