视网膜
生物
糖尿病性视网膜病变
视网膜
糖尿病
2型糖尿病
电池类型
视网膜病变
全基因组关联研究
细胞
遗传学
神经科学
基因
内分泌学
单核苷酸多态性
植物
基因型
作者
Kai Chen,Yinhao Wang,Youyuan Huang,Xinxin Liu,Xiaodong Tian,Yinmo Yang,Aimei Dong
出处
期刊:Genomics
[Elsevier]
日期:2023-06-04
卷期号:115 (4): 110644-110644
被引量:6
标识
DOI:10.1016/j.ygeno.2023.110644
摘要
Single-cell RNA sequencing (scRNA-seq) analysis have provided an unprecedented resolution for the studies on diabetic retinopathy (DR). However, the early changes in the retina in diabetes remain unclear. A total of 8 human and mouse scRNA-seq datasets, containing 276,402 cells were analyzed individually to comprehensively delineate the retinal cell atlas. The neural retinas were isolated from the type 2 diabetes (T2D) and control mice, and scRNA-seq analysis was conducted to evaluate the early effects of diabetes on the retina. Bipolar cell (BC) heterogeneity were identified. We found some stable BCs across multiple datasets, and explored their biological functions. A new RBC subtype (Car8_RBC) in the mouse retina was validated using the multi-color immunohistochemistry. AC149090.1 was significantly upregulated in the rod cells, ON cone BCs (CBCs), OFF CBCs, and RBCs in T2D mice. Additionally, the interneurons, especially BCs, were the most vulnerable cells to diabetes by integrating scRNA-seq and genome-wide association studies (GWAS) analyses. In conclusion, this study delineated a cross-species retinal cell atlas and uncovered the early pathological alterations in the retina of T2D mice.
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