Cerebellar Long Noncoding RNA Expression Profile in a Niemann-Pick C Disease Mouse Model

Niemann-Pick type C (NP-C) disease is a neurodegenerative lysosomal storage disorder primarily caused by mutations in NPC1. However, its pathogenesis remains poorly understood. While mounting evidence has demonstrated the involvement of long noncoding RNAs (lncRNAs) in the pathogenesis of neurodegenerative disorders, the lncRNA expression profile in NP-C has not been determined. Here, we used RNA-seq analysis to determine lncRNA and mRNA expression profiles of the cerebella of NPC1(-/-) mice. We found that 272 lncRNAs and 856 mRNAs were significantly dysregulated in NPC1(-/-) mice relative to controls (>= 2.0-fold, p < 0.05). Quantitative real-time PCR (qRT-PCR) was utilized to validate the expression of selected lncRNAs and mRNAs. Next, a lncRNA-mRNA coexpression network was employed to examine the potential roles of the differentially expressed (DE) lncRNAs. Functional analysis revealed that mRNAs coexpressed with lncRNAs are mainly linked to immune system-related processes and neuroinflammation. Moreover, knockdown of the lncRNA H19 ameliorated changes in ROS levels and cell viability and suppressed the lipopolysaccharide (LPS)-induced inflammatory response in vitro. Our findings indicate that dysregulated lncRNA expression patterns are associated with NP-C pathogenesis and offer insight into the development of novel therapeutics based on lncRNAs.

Automated summary

This study revealed dysregulated lncRNA expression patterns in NP-C disease, potentially playing a crucial role in its pathogenesis. RNA-seq analysis showed that mRNAs coexpressed with lncRNAs are mainly associated with immune system-related processes and neuroinflammation. Knockdown of specific lncRNAs could improve intracellular ROS levels and cell viability, as well as suppress inflammatory responses in vitro.