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Single-cell transcriptomic atlas of the human retina identifies cell types associated with age-related macular degeneration

机译:人视网膜的单细胞转录组织地图鉴定与年龄相关性黄斑变性相关的细胞类型

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Genome-wide association studies (GWAS) have identified genetic variants associated with age-related macular degeneration (AMD), one of the leading causes of blindness in the elderly. However, it has been challenging to identify the cell types associated with AMD given the genetic complexity of the disease. Here we perform massively parallel single-cell RNA sequencing (scRNA-seq) of human retinas using two independent platforms, and report the first single-cell transcriptomic atlas of the human retina. Using a multi-resolution network-based analysis, we identify all major retinal cell types, and their corresponding gene expression signatures. Heterogeneity is observed within macroglia, suggesting that human retinal glia are more diverse than previously thought. Finally, GWAS-based enrichment analysis identifies glia, vascular cells, and cone photoreceptors to be associated with the risk of AMD. These data provide a detailed analysis of the human retina, and show how scRNA-seq can provide insight into cell types involved in complex, inflammatory genetic diseases.
机译:基因组 - 宽协会研究(GWAs)已鉴定与年龄相关的黄斑变性(AMD)相关的遗传变异,是老年人失明的主要原因之一。然而,鉴定鉴于疾病的遗传复杂性鉴定与AMD相关的细胞类型一直挑战。在这里,我们使用两个独立平台对人视网膜进行大规模平行的单细胞RNA测序(ScRNA-SEQ),并报告人视网膜的第一个单细胞转录组图。使用基于多分辨率的网络的分析,我们识别所有主要视网膜细胞类型,以及它们相应的基因表达签名。在宏观lia中观察到异质性,表明人类视网膜峡谷比以前认为更多样化。最后,基于GWAS的富集分析鉴定了胶质植物,血管细胞和锥形光感受器与AMD的风险相关。这些数据提供了对人视网膜的详细分析,并展示了Scrna-SEQ如何能够深入了解复杂的炎症性遗传疾病所涉及的细胞类型。

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