Detyrosinated Microtubules Modulate Mechanotransduction in Heart and Skeletal Muscle
ABSTRACT: In striated muscle, X-ROS is the mechanotransduction pathway by which mechanical stress transduced by the microtubule network elicits reactive oxygen species. X-ROS tunes Ca2+ signalling in healthy muscle, but in diseases such as Duchenne muscular dystrophy (DMD), microtubule alterations d...
- Autores:
-
Colorado Becerra, Natalia Yiset
Raiteri, Roberto
Kerr P., Jaclyn
Robison, Patrick
Shi, Guoli
Bogush, Alexey
Kempema, Aaron
Hexum, Joseph
Harki, Daniel
Martin, Stuart
Prosser, Benjamin
Ward, Christopher
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2015
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/36449
- Acceso en línea:
- https://hdl.handle.net/10495/36449
- Palabra clave:
- Fenómenos Biomecánicos
Biomechanical Phenomena
Calcio
Calcium
Ratones Endogámicos C57BL
Mice, Inbred C57BL
Microscopía de Fuerza Atómica
Microscopy, Atomic Force
Fibras Musculares Esqueléticas
Muscle Fibers, Skeletal
Miocitos cardíacos
Myocytes, Cardiac
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/2.5/co/
| Summary: | ABSTRACT: In striated muscle, X-ROS is the mechanotransduction pathway by which mechanical stress transduced by the microtubule network elicits reactive oxygen species. X-ROS tunes Ca2+ signalling in healthy muscle, but in diseases such as Duchenne muscular dystrophy (DMD), microtubule alterations drive elevated X-ROS, disrupting Ca2+ homeostasis and impairing function. Here we show that detyrosination, a post-translational modification of α-tubulin, influences X-ROS signalling, contraction speed and cytoskeletal mechanics. In the mdx mouse model of DMD, the pharmacological reduction of detyrosination in vitro ablates aberrant X-ROS and Ca2+ signalling, and in vivo it protects against hallmarks of DMD, including workload-induced arrhythmias and contraction-induced injury in skeletal muscle. We conclude that detyrosinated microtubules increase cytoskeletal stiffness and mechanotransduction in striated muscle and that targeting this post-translational modification may have broad therapeutic potential in muscular dystrophies. |
|---|
