Artículos de revistas
Estradiol exerts antiapoptotic effects in skeletal myoblasts via mitochondrial PTP and MnSOD.
Fecha
2013-03Registro en:
la Colla, Anabela Belén; Vasconsuelo, Andrea Anahi; Boland, Ricardo Leopoldo; Estradiol exerts antiapoptotic effects in skeletal myoblasts via mitochondrial PTP and MnSOD.; BioScientifica; Journal of Endocrinology; 216; 3; 3-2013; 331-341
0022-0795
Autor
la Colla, Anabela Belén
Vasconsuelo, Andrea Anahi
Boland, Ricardo Leopoldo
Resumen
17beta-Estradiol (E2) protects several non-reproductive tissues from apoptosis, including skeletal muscle. We have shown that E2 at physiological concentrations prevented apoptosis induced by H2O2 in C2C12 skeletal myoblasts. As we also demonstrated the presence of estrogen receptors in mitochondria, the present work was focused on the effects of E2 on this organelle. Specifically, we evaluated the actions of E2 on the mitochondrial permeability transition pore (MPTP) by the calcein-acetoxymethylester/cobalt method using fluorescence microscopy and flow cytometry. Pretreatment with E2 prevented MPTP opening induced by H2O2, which preceded loss of mitochondrial membrane potential. In addition, it was observed that H2O2 induced translocation of Bax to mitochondria; however, in the presence of the steroid this effect was abrogated suggesting that members of the Bcl-2 family may be regulated by E2 to exert an antiapoptotic effect. Moreover, E2 increased mitochondrial manganese superoxide dismutase protein expression and activity, as part of a mechanism activated by E2 that improved mitochondrial performance. Our results suggest a role of E2 in the regulation of apoptosis with a clear action at the mitochondrial level in C2C12 skeletal myoblast cells.