Lysosomes to the rescue: Anterograde axonal lysosome transport and neuronal proteostasis
- PMID: 34004149
- DOI: 10.1016/j.devcel.2021.04.024
Lysosomes to the rescue: Anterograde axonal lysosome transport and neuronal proteostasis
Abstract
Niemann-Pick is a lysosomal storage disease caused by loss of the lysosomal cholesterol exporter NPC1 and leads to axon degeneration. Roney et al. report that immature autophagosomes accumulate in axons because cholesterol-laden lysosomes in the soma are not transported to the axon for autophagosome fusion and maturation because they aberrantly sequester non-functioning kinesin-1.
Copyright © 2021 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of interests The authors declare no competing interests.
Comment on
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Lipid-mediated motor-adaptor sequestration impairs axonal lysosome delivery leading to autophagic stress and dystrophy in Niemann-Pick type C.Dev Cell. 2021 May 17;56(10):1452-1468.e8. doi: 10.1016/j.devcel.2021.03.032. Epub 2021 Apr 19. Dev Cell. 2021. PMID: 33878344 Free PMC article.
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