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Oligodendrocyte loss during the disease course in a canine model of the lysosomal storage disease fucosidosis
journal contributionposted on 2023-05-21, 03:17 authored by Jessica FletcherJessica Fletcher, Kondagari, GS, Vite, CH, Williamson, P, Taylor, RM
Hypomyelination is a poorly understood feature of many neurodegenerative lysosomal storage diseases, including fucosidosis in children and animals. To gain insight into hypomyelination in fucosidosis, we investigated lysosomal storage, oligodendrocyte death, and axonal and neuron loss in CNS tissues of fucosidosis-affected dogs aged 3 weeks to 42 months using immunohistochemistry, electron microscopy, and gene expression assays. Vacuole accumulation in fucosidosis oligodendrocytes commenced by 5 weeks of age; all oligodendrocytes were affected by 16 weeks. Despite progressive vacuolation, mature oligodendrocyte loss by apoptosis (caspase-6 positive) in the corpus callosum and cerebellar white matter stabilized by 16 weeks, with no further subsequent loss. Axonal neurofilament loss progressed only in late disease, suggesting that disturbed axon-oligodendrocyte interactions are unlikely to be the primary cause of hypomyelination. A 67% decline in the number of Purkinje cell layer oligodendrocytes coincided with a 67% increase in the number of caspase-6-positive Purkinje cells at 16 weeks, suggesting that early oligodendrocyte loss contributes to Purkinje cell apoptosis. Fucosidosis hypomyelination appeared to follow normal spatiotemporal patterns of myelination, with greater loss of oligodendrocytes and larger downregulation of CNP, MAL, and PLP1 genes at 16 weeks in the cerebellum versus the frontal cortex. These studies suggest that survival of oligodendrocytes in fucosidosis is limited during active myelination, although the mechanisms remain unknown.
Publication titleJournal of Neuropathology and Experimental Neurology
Department/SchoolMenzies Institute for Medical Research
PublisherAmer Assn Neuropathologists Inc
Place of publication1041 New Hampshire St, Lawrence, USA, Ks, 66044
Rights statementCopyright © 2014 by the American Association of Neuropathologists, Inc. Unauthorized reproduction of this article is prohibited.