| Literature DB >> 26942423 |
Ya Hui Hung1, Mark Walterfang1,2, Leonid Churilov3,4, Lisa Bray1, Laura H Jacobson5, Kevin J Barnham5,6,7, Nigel C Jones8, Terence J O'Brien8, Dennis Velakoulis2, Ashley I Bush9.
Abstract
Autosomal recessive inheritance of NPC1 with loss-of-function mutations underlies Niemann-Pick disease, type C1 (NP-C1), a lysosomal storage disorder with progressive neurodegeneration. It is uncertain from limited biochemical studies and patient case reports whether NPC1 haploinsufficiency can cause a partial NP-C1 phenotype in carriers. In the present study, we examined this possibility in heterozygotes of a natural loss-of-function mutant Npc1 mouse model. We found partial motor dysfunction and increased anxiety-like behavior in Npc1 (+/-) mice by 9 weeks of age. Relative to Npc1 (+/+) mice, Npc1 (+/-) mice failed to show neurodevelopmental improvements in motor coordination and balance on an accelerating Rotarod. In the open-field test, Npc1 (+/-) mice showed an intermediate phenotype in spontaneous locomotor activity compared with Npc1 (+/+) and Npc1 (-/-) mice, as well as decreased center tendency. Together with increased stride length under anxiogenic conditions on the DigiGait treadmill, these findings are consistent with heightened anxiety. Our findings indicate that pathogenic NPC1 allele carriers, who represent about 0.66 % of humans, could be vulnerable to motor and anxiety disorders.Entities:
Keywords: Carrier; Heterozygote disease; NPC1; Neurological; Niemann–Pick disease type C; haploinsufficiency
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Year: 2016 PMID: 26942423 PMCID: PMC4965399 DOI: 10.1007/s13311-016-0427-5
Source DB: PubMed Journal: Neurotherapeutics ISSN: 1878-7479 Impact factor: 7.620