Glycan degradation promotes macroautophagy
Baudot, Alice D. and Wang, Victoria M.-Y. and Leach, Josh D. and O’Prey, Jim and Long, Jaclyn S. and Paulus-Hock, Viola and Lilla, Sergio and Thomson, David M. and Greenhorn, John and Ghaffar, Farah and Nixon, Colin and Helfrich, Miep H. and Strathdee, Douglas and Pratt, Judith and Marchesi, Francesco and Zanivan, Sara and Ryan, Kevin M. (2022) Glycan degradation promotes macroautophagy. Proceedings of the National Academy of Sciences, 119 (26). e2111506119. ISSN 0027-8424 (https://doi.org/10.1073/pnas.2111506119)
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Abstract
Macroautophagy promotes cellular homeostasis by delivering cytoplasmic constituents to lysosomes for degradation [Mizushima, Nat. Cell Biol. 20, 521–527 (2018)]. However, while most studies have focused on the mechanisms of protein degradation during this process, we report here that macroautophagy also depends on glycan degradation via the glycosidase, α- l -fucosidase 1 (FUCA1), which removes fucose from glycans. We show that cells lacking FUCA1 accumulate lysosomal glycans, which is associated with impaired autophagic flux. Moreover, in a mouse model of fucosidosis—a disease characterized by inactivating mutations in FUCA1 [Stepien et al. , Genes (Basel) 11, E1383 (2020)]—glycan and autophagosome/autolysosome accumulation accompanies tissue destruction. Mechanistically, using lectin capture and mass spectrometry, we identified several lysosomal enzymes with altered fucosylation in FUCA1-null cells. Moreover, we show that the activity of some of these enzymes in the absence of FUCA1 can no longer be induced upon autophagy stimulation, causing retardation of autophagic flux, which involves impaired autophagosome–lysosome fusion. These findings therefore show that dysregulated glycan degradation leads to defective autophagy, which is likely a contributing factor in the etiology of fucosidosis.
ORCID iDs
Baudot, Alice D., Wang, Victoria M.-Y., Leach, Josh D., O’Prey, Jim, Long, Jaclyn S., Paulus-Hock, Viola, Lilla, Sergio, Thomson, David M. ORCID: https://orcid.org/0000-0002-0356-3525, Greenhorn, John, Ghaffar, Farah, Nixon, Colin, Helfrich, Miep H., Strathdee, Douglas, Pratt, Judith, Marchesi, Francesco, Zanivan, Sara and Ryan, Kevin M.;-
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Item type: Article ID code: 81389 Dates: DateEvent28 June 2022Published22 June 2022Published Online22 April 2022AcceptedSubjects: Medicine > Therapeutics. Pharmacology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 07 Jul 2022 11:02 Last modified: 11 Nov 2024 13:33 URI: https://strathprints.strath.ac.uk/id/eprint/81389