Dissecting the role of heterochromatic conformation in age-related sarcopenia and frailty (DSB.AD006.212)
Area tematica
Area progettuale
Biologia Molecolare/Cellulare (DSB.AD006)Struttura responsabile del progetto di ricerca
Istituto di Biochimica e Biologia Cellulare (IBBC)
Responsabile di progetto
CLAUDIA BEARZI
Telefono: 0690091307
E-mail: fabio.mammano@cnr.it
Abstract
Frailty syndrome in the elderly is a condition in which the individual is in a vulnerable state with increased risk of adverse health outcomes and/or death when exposed to a stressor. Although they are 2 separate conditions, sarcopenia is believed to be an important component of frailty. There is now agreement that the definition of sarcopenia, originally referred solely to the loss of skeletal muscle mass with age, should incorporate also the loss of muscle function concept. Fat infiltration is one of the parameters to be considered when evaluating sarcopenia. Recently cutting-edge studies highlighted the role of epigenetic mechanisms in muscle senescence and sarcopenia. In particular Polycomb group (PcG) of proteins, key regulators of cell identity, are directly involved in muscular homeostasis and senescence. We have demonstrated that PcG function and PcG dependent heterochromatin conformation depend on the integrity of the nuclear lamin. We believe that the heterochromatin alterations observed during physiological and pathological senescence are dependent on the natural Lamin A/C destabilization and a subsequent Lamin/PcG axis dysfunction. In the muscle this could lead to impai
Data inizio attività
01/04/2018
Parole chiave
frailty syndrome, sarcopenia, muscular aging
Ultimo aggiornamento: 27/09/2024