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FYCO1 Regulates Cardiomyocyte Autophagy and Prevents Heart Failure Due to Pressure Overload In Vivo

Autophagy is a cellular degradation process that has been implicated in diverse disease processes. The authors provide evidence that FYCO1, a component of the autophagic machinery, is essential for adaptation to cardiac stress. Although the absence of FYCO1 does not affect basal autophagy in isolate...

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Detalles Bibliográficos
Autores principales: Kuhn, Christian, Menke, Maja, Senger, Frauke, Mack, Claudia, Dierck, Franziska, Hille, Susanne, Schmidt, Inga, Brunke, Gabriele, Bünger, Pia, Schmiedel, Nesrin, Will, Rainer, Sossalla, Samuel, Frank, Derk, Eschenhagen, Thomas, Carrier, Lucie, Lüllmann-Rauch, Renate, Rangrez, Ashraf Yusuf, Frey, Norbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093479/
https://www.ncbi.nlm.nih.gov/pubmed/33997522
http://dx.doi.org/10.1016/j.jacbts.2021.01.001
Descripción
Sumario:Autophagy is a cellular degradation process that has been implicated in diverse disease processes. The authors provide evidence that FYCO1, a component of the autophagic machinery, is essential for adaptation to cardiac stress. Although the absence of FYCO1 does not affect basal autophagy in isolated cardiomyocytes, it abolishes induction of autophagy after glucose deprivation. Likewise, Fyco1-deficient mice subjected to starvation or pressure overload are unable to respond with induction of autophagy and develop impaired cardiac function. FYCO1 overexpression leads to induction of autophagy in isolated cardiomyocytes and transgenic mouse hearts, thereby rescuing cardiac dysfunction in response to biomechanical stress.