6533b852fe1ef96bd12ab5ba
RESEARCH PRODUCT
αB-crystallin activation in cardiac muscle by acute exercise mirrors the sHSP kinetic in oxidative skeletal muscle fibers: animal and cellular study
Neri MercatelliDaniela CaporossiAmbra AntonioniFilippo MacalusoValentina Di FeliceRosario BaroneIvan Dimaurosubject
MyogenesisCardiac muscleOxidative phosphorylationBiologymedicine.disease_causeBiochemistryCell biologymedicine.anatomical_structureBiochemistryPhysiology (medical)Heat shock proteinmedicineAerobic exerciseMyofibrilC2C12Oxidative stressdescription
Alpha-B-Crystallin (CRYAB), a Small Heat Shock Protein sensitive to oxidative stress, is implicated in various biological processes in many tissues. In cardiac muscle, CRYAB exerts a cardio protective role in ischemia-induced damage preventing apoptosis and necrosis. We aimed to study αB-crystallin’ response in mouse cardiac tissue (H), at different time of recovery from an acute aerobic exercise (1 hour), correlating its modulation with oxidative stress level. We found that a single bout exercise lead to a specific short-term increase of phospho-αB-crystallin level (pCRYAB), without changes of its total expression. Further, the level of 4-hydroxynonenal, a marker of lipidic peroxidation, has shown a similar trend of pCRYAB enhancement. This may indicate that CRYAB in cardiac muscle is activated and it has a putative role in oxidative stress during exercise. These results are supported by our previous data obtained in mouse skeletal tissues (i.e. gastrocnemius, soleus) and in H₂O₂-treated C2C12 myotubes. In particular, we observed not only a fiber-dependent response of pCRYAB, but also its translocation into myofibrillar compartment. Experiments are in progress to further investigate on CRYAB role during exercise and its interactions with cytoskeletal structures.
year | journal | country | edition | language |
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2017-07-01 | Free Radical Biology and Medicine |