Reynolds Regina H, Botía Juan, Nalls Mike A, Hardy John, Gagliano Taliun Sarah A, Ryten Mina
1Department of Neurodegenerative Disease, University College London (UCL) Institute of Neurology, London, UK.
2Departamento de Ingeniería de la Información y las Comunicaciones, Universidad de Murcia, Murcia, Spain.
NPJ Parkinsons Dis. 2019 Apr 17;5:6. doi: 10.1038/s41531-019-0076-6. eCollection 2019.
Parkinson's disease (PD), with its characteristic loss of nigrostriatal dopaminergic neurons and deposition of α-synuclein in neurons, is often considered a neuronal disorder. However, in recent years substantial evidence has emerged to implicate glial cell types, such as astrocytes and microglia. In this study, we used stratified LD score regression and expression-weighted cell-type enrichment together with several brain-related and cell-type-specific genomic annotations to connect human genomic PD findings to specific brain cell types. We found that PD heritability attributable to common variation does not enrich in global and regional brain annotations or brain-related cell-type-specific annotations. Likewise, we found no enrichment of PD susceptibility genes in brain-related cell types. In contrast, we demonstrated a significant enrichment of PD heritability in a curated lysosomal gene set highly expressed in astrocytic, microglial, and oligodendrocyte subtypes, and in LoF-intolerant genes, which were found highly expressed in almost all tested cellular subtypes. Our results suggest that PD risk loci do not lie in specific cell types or individual brain regions, but rather in global cellular processes detectable across several cell types.
帕金森病(PD)以黑质纹状体多巴胺能神经元的特征性丧失和神经元中α-突触核蛋白的沉积为特点,通常被认为是一种神经元疾病。然而,近年来出现了大量证据表明胶质细胞类型,如星形胶质细胞和小胶质细胞也与之相关。在本研究中,我们使用分层LD评分回归和表达加权细胞类型富集,以及几种与脑相关和细胞类型特异性的基因组注释,将人类基因组帕金森病研究结果与特定脑细胞类型联系起来。我们发现,由常见变异导致的帕金森病遗传力在全脑和区域脑注释或与脑相关的细胞类型特异性注释中并未富集。同样,我们在与脑相关的细胞类型中未发现帕金森病易感基因的富集。相反,我们证明帕金森病遗传力在一组精心挑选的溶酶体基因集中显著富集,这些基因在星形胶质细胞、小胶质细胞和少突胶质细胞亚型中高度表达,并且在功能丧失不耐受基因中也显著富集,这些基因在几乎所有测试的细胞亚型中都高度表达。我们的结果表明,帕金森病风险位点并不存在于特定细胞类型或单个脑区,而是存在于可在多种细胞类型中检测到的全局细胞过程中。