黄斑变性
视网膜
全基因组关联研究
电池类型
转录组
生物
计算生物学
视网膜
穆勒胶质细胞
基因
细胞
遗传学
神经科学
基因表达
医学
单核苷酸多态性
基因型
眼科
干细胞
祖细胞
生物化学
作者
Madhvi Menon,Shahin Mohammadi,José Dávila-Velderrain,Brittany A. Goods,Tanina D. Cadwell,Yu Xing,Anat Stemmer‐Rachamimov,Alex K. Shalek,J. Christopher Love,Manolis Kellis,Brian P. Hafler
标识
DOI:10.1038/s41467-019-12780-8
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI