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...

Full description

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/
Description
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.