Neurofilament accumulation disrupts autophagy in giant axonal neuropathy

Neurofilament accumulation is associated with many neurodegenerative diseases, but it is the primary pathology in giant axonal neuropathy (GAN). This childhood-onset autosomal recessive disease is caused by loss-of-function mutations in gigaxonin, the E3 adaptor protein that enables neurofilament degradation. Using a combination of genetic and RNA interference approaches, we found that dorsal root ganglia from mice lacking gigaxonin have impaired autophagy and lysosomal degradation through 2 mechanisms. First, neurofilament accumulations interfere with the distribution of autophagic organelles, impairing their maturation and fusion with lysosomes. Second, the accumulations attract the chaperone 14-3-3, which is responsible for the proper localization of the key autophagy regulator transcription factor EB (TFEB). We propose that this dual disruption of autophagy contributes to the pathogenesis of other neurodegenerative diseases involving neurofilament accumulations.

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Publication Details

Journal
JCI Insight
Published
2025-03-09
DOI
https://doi.org/10.1172/jci.insight.177999
Citations
2
Primary Topic
Hereditary Neurological Disorders
Type
article
Field-Weighted Citation Impact
1.82

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article

Neurofilament accumulation disrupts autophagy in giant axonal neuropathy

Natasha T. Snider, Chiranjit Panja, Jean‐Michel Paumier, Jeffrey N. Savas et al.
2 citations
JCI Insight
Hereditary Neurological Disorders
1.82
article

Neurofilament accumulation disrupts autophagy in giant axonal neuropathy

Natasha T. Snider, Chiranjit Panja, Jean‐Michel Paumier, Jeffrey N. Savas, James P. Zewe, Shikha Prasad, Eitan Israeli, Melissa R. Pergande, Puneet Opal, Meghana Venkatesan
article en
2 citations

Abstract

Neurofilament accumulation is associated with many neurodegenerative diseases, but it is the primary pathology in giant axonal neuropathy (GAN). This childhood-onset autosomal recessive disease is caused by loss-of-function mutations in gigaxonin, the E3 adaptor protein that enables neurofilament degradation. Using a combination of genetic and RNA interference approaches, we found that dorsal root ganglia from mice lacking gigaxonin have impaired autophagy and lysosomal degradation through 2 mechanisms. First, neurofilament accumulations interfere with the distribution of autophagic organelles, impairing their maturation and fusion with lysosomes. Second, the accumulations attract the chaperone 14-3-3, which is responsible for the proper localization of the key autophagy regulator transcription factor EB (TFEB). We propose that this dual disruption of autophagy contributes to the pathogenesis of other neurodegenerative diseases involving neurofilament accumulations.

JCI InsightVol. 10(5)
Northwestern University (US), University of North Carolina at Chapel Hill (US)
Muscular Dystrophy Association, Northwestern University, National Institutes of Health, Feinberg School of Medicine, Robert H. Lurie Comprehensive Cancer Center, National Cancer Institute, National Institute of Neurological Disorders and Stroke, National Center for Advancing Translational Sciences
Zero hunger
Openalex Percentile: Top 17%
Hereditary Neurological Disorders
1.82
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