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EMBO Mol Med. 2018 Mar;10(3). pii: e8166. doi: 10.15252/emmm.201708166.

Inhibition of Drp1/Fis1 interaction slows progression of amyotrophic lateral sclerosis.

Author information

1
Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA.
2
Behavioral and Functional Neuroscience Laboratory, Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA, USA.
3
Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
4
Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA mochly@stanford.edu.

Abstract

Bioenergetic failure and oxidative stress are common pathological hallmarks of amyotrophic lateral sclerosis (ALS), but whether these could be targeted effectively for novel therapeutic intervention needs to be determined. One of the reported contributors to ALS pathology is mitochondrial dysfunction associated with excessive mitochondrial fission and fragmentation, which is predominantly mediated by Drp1 hyperactivation. Here, we determined whether inhibition of excessive fission by inhibiting Drp1/Fis1 interaction affects disease progression. We observed mitochondrial excessive fragmentation and dysfunction in several familial forms of ALS patient-derived fibroblasts as well as in cultured motor neurons expressing SOD1 mutant. In both cell models, inhibition of Drp1/Fis1 interaction by a selective peptide inhibitor, P110, led to a significant reduction in reactive oxygen species levels, and to improvement in mitochondrial structure and functions. Sustained treatment of mice expressing G93A SOD1 mutation with P110, beginning at the onset of disease symptoms at day 90, produced an improvement in motor performance and survival, suggesting that Drp1 hyperactivation may be an attractive target in the treatment of ALS patients.

KEYWORDS:

Protein–Protein interactions; amyotrophic lateral sclerosis; dynamin‐related protein 1; fission 1; mitochondrial dysfunction

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