| Literature DB >> 32447718 |
Gian Luca Vita1, M'hammed Aguennouz2,3, Maria Sframeli1, Francesca Sanarica4, Paola Mantuano4, Rosaria Oteri5, Francesca Polito5, Norma Licata5, Sara Romeo5, Maria Grazia Distefano5, Matteo La Rosa5, Carmen Bonanno5, Giulia Nicocia5, Giuseppe Vita1,5, Annamaria De Luca4, Sonia Messina1,5.
Abstract
In Duchenne muscular dystrophy (DMD), telomere shortening has been postulated to contribute to the failure of regenerative activity promoting the premature senescence of satellite cells. The aim of the present study was to investigate the telomere length and the expression of telomeric repeat-binding factor-1 (TRF1), poly (ADP-ribose) polymerase-1 (PARP1) and mouse telomerase reverse transcriptase (MTERT) in gastrocnemius, tibialis anterior and diaphragm muscles of the murine model of DMD, the mdx mouse and whether a chronic protocol of forced exercise impacts on them. Our results confirmed a telomere shortening in mdx muscles, more evident in the diaphragm, in which exercise induced a greater shortening than in wild-type mice. Moreover, we showed for the first time in mdx an increased TRF1 and PARP1 expression and an augmented activity of MTERT, further enhanced by exercise. These results reinforce the hypothesis that a deregulation of mechanisms involved in telomere length occurs and may pave the way for the test of compounds targeting proteins modulating telomere maintenance as a novel strategy to treat dystrophinopathies.Entities:
Keywords: Exercise; Mdx; PARP1; TERT; TRF1; Telomere length
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Year: 2020 PMID: 32447718 DOI: 10.1007/s11010-020-03761-3
Source DB: PubMed Journal: Mol Cell Biochem ISSN: 0300-8177 Impact factor: 3.396