Cargando…
Sarcospan reduces dystrophic pathology: stabilization of the utrophin–glycoprotein complex
Mutations in the dystrophin gene cause Duchenne muscular dystrophy and result in the loss of dystrophin and the entire dystrophin–glycoprotein complex (DGC) from the sarcolemma. We show that sarcospan (SSPN), a unique tetraspanin-like component of the DGC, ameliorates muscular dystrophy in dystrophi...
Autores principales: | Peter, Angela K., Marshall, Jamie L., Crosbie, Rachelle H. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2575773/ https://www.ncbi.nlm.nih.gov/pubmed/18981229 http://dx.doi.org/10.1083/jcb.200808027 |
Ejemplares similares
-
Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration
por: Marshall, Jamie L., et al.
Publicado: (2012) -
Sarcospan: a small protein with large potential for Duchenne muscular dystrophy
por: Marshall, Jamie L, et al.
Publicado: (2013) -
Myogenic Akt signaling upregulates the utrophin–glycoprotein complex and promotes sarcolemma stability in muscular dystrophy
por: Peter, Angela K., et al.
Publicado: (2009) -
Membrane Targeting and Stabilization of Sarcospan Is Mediated by the Sarcoglycan Subcomplex
por: Crosbie, Rachelle H., et al.
Publicado: (1999) -
Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle
por: Kennedy, Tahnee L., et al.
Publicado: (2017)