Journal
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 23, Issue 9, Pages -Publisher
MDPI
DOI: 10.3390/ijms23095082
Keywords
Niemann-Pick disease; type C; N-linked glycosylation; MGAT5; LAMP1; disease severity score; Purkinje neuron
Funding
- intramural research programs of the Eunice Kennedy Shriver National Institute of Child Health and Human Development
- National Human Genome Research Institute
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Complex asparagine-linked glycosylation plays a critical role in cellular functions. The deficiency of MGAT5, a key enzyme involved in this process, leads to increased severity of NPC1 disease in mice. The reduction in asparagine-linked glycosylation is associated with the progression of NPC1 disease.
Complex asparagine-linked glycosylation plays key roles in cellular functions, including cellular signaling, protein stability, and immune response. Previously, we characterized the appearance of a complex asparagine-linked glycosylated form of lysosome-associated membrane protein 1 (LAMP1) in the cerebellum of Npc1(-/-) mice. This LAMP1 form was found on activated microglia, and its appearance correlated both spatially and temporally with cerebellar Purkinje neuron loss. To test the importance of complex asparagine-linked glycosylation in NPC1 pathology, we generated NPC1 knock-out mice deficient in MGAT5, a key Golgi-resident glycosyl transferase involved in complex asparagine-linked glycosylation. Our results show that Mgat5(-/-):Npc1(-/-) mice were smaller than Mgat5(+/+):Npc1(-/-) mice, and exhibited earlier NPC1 disease onset and reduced lifespan. Western blot and lectin binding analyses of cerebellar extracts confirmed the reduction in complex asparagine-linked glycosylation, and the absence of the hyper-glycosylated LAMP1 previously observed. Western blot analysis of cerebellar extracts demonstrated reduced calbindin staining in Mgat5(-/-):Npc1(-/-) mice compared to Mgat5(+/+):Npc1(-/-) mutant mice, and immunofluorescent staining of cerebellar sections indicated decreased levels of Purkinje neurons and increased astrogliosis in Mgat5(-/-):Npc1(-/-) mice. Our results suggest that reduced asparagine-linked glycosylation increases NPC1 disease severity in mice, and leads to the hypothesis that mutations in genes involved in asparagine-linked glycosylation may contribute to disease severity progression in individuals with NPC1. To examine this with respect to MGAT5, we analyzed 111 NPC1 patients for two MGAT5 SNPs associated with multiple sclerosis; however, we did not identify an association with NPC1 phenotypic severity.
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