Single-Cell RNA Sequencing in Parkinson's Disease

被引:20
|
作者
Ma, Shi-Xun [1 ]
Lim, Su Bin [2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Baltimore, MD 21205 USA
[2] Ajou Univ, Sch Med, Dept Biochem & Mol Biol, Suwon 16499, South Korea
关键词
Parkinson's disease; single-cell RNA sequencing; bioinformatics; GENOME-WIDE ASSOCIATION; PLURIPOTENT STEM-CELLS; ALPHA-SYNUCLEIN; DOPAMINE NEURONS; ANIMAL-MODELS; POSTMORTEM INTERVAL; ECONOMIC BURDEN; GENE; EXPRESSION; LRRK2;
D O I
10.3390/biomedicines9040368
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Single-cell and single-nucleus RNA sequencing (sc/snRNA-seq) technologies have enhanced the understanding of the molecular pathogenesis of neurodegenerative disorders, including Parkinson's disease (PD). Nonetheless, their application in PD has been limited due mainly to the technical challenges resulting from the scarcity of postmortem brain tissue and low quality associated with RNA degradation. Despite such challenges, recent advances in animals and human in vitro models that recapitulate features of PD along with sequencing assays have fueled studies aiming to obtain an unbiased and global view of cellular composition and phenotype of PD at the single-cell resolution. Here, we reviewed recent sc/snRNA-seq efforts that have successfully characterized diverse cell-type populations and identified cell type-specific disease associations in PD. We also examined how these studies have employed computational and analytical tools to analyze and interpret the rich information derived from sc/snRNA-seq. Finally, we highlighted important limitations and emerging technologies for addressing key technical challenges currently limiting the integration of new findings into clinical practice.
引用
收藏
页数:21
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