Histone deacetylase 6 inhibition promotes microtubule acetylation and facilitates autophagosome–lysosome fusion in dystrophin‐deficient <i>mdx</i> mice

Our data highlight that autophagy is differentially regulated by redox and acetylation in mdx mice. By improving autophagy through promoting tubulin acetylation, Tubastatin A decreases the dystrophic phenotype and improves muscle function, suggesting a great potential for clinical translation and treating dystrophic patients.

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Publication Details

Journal
Acta Physiologica
Published
2024-10-18
DOI
https://doi.org/10.1111/apha.14243
Citations
7
Primary Topic
Histone Deacetylase Inhibitors Research
Type
article
Field-Weighted Citation Impact
1.64

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article

Histone deacetylase 6 inhibition promotes microtubule acetylation and facilitates autophagosome–lysosome fusion in dystrophin‐deficient mdx mice

George G. Rodney, Akanksha Agrawal, Erin L. Clayton, Benjamin A. Clayton et al.
7 citations
Acta Physiologica
Histone Deacetylase Inhibitors Research
1.64
article

Histone deacetylase 6 inhibition promotes microtubule acetylation and facilitates autophagosome–lysosome fusion in dystrophin‐deficient mdx mice

George G. Rodney, Akanksha Agrawal, Erin L. Clayton, Benjamin A. Clayton, Courtney L. Cavazos
article en
7 citations

Abstract

Our data highlight that autophagy is differentially regulated by redox and acetylation in mdx mice. By improving autophagy through promoting tubulin acetylation, Tubastatin A decreases the dystrophic phenotype and improves muscle function, suggesting a great potential for clinical translation and treating dystrophic patients.

Acta PhysiologicaVol. 241(1)
Baylor College of Medicine (US)
National Institutes of Health
Good health and well-being
Openalex Percentile: Top 16%
Histone Deacetylase Inhibitors Research
1.64
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