青光眼
神经科学
视网膜
生物
视网膜神经节细胞
视网膜波
神经节
视网膜
巨大视网膜神经节细胞
解剖
生物化学
作者
Kushal Nimkar,Nicole Tsai,Mengya Zhao,Yujuan Yi,Matthew R Lum,Tavita Garrett,Yixiao Wang,Kenichi Toma,Franklin Caval-Holme,Nikhil Reddy,Aliza T. Ehrlich,Arnold R. Kriegstein,Michael Tri H.,Yang Hu,Benjamin Sivyer,Karthik Shekhar,Xin Duan
出处
期刊:Neuron
[Cell Press]
日期:2025-08-21
卷期号:113 (20): 3390-3407.e8
被引量:8
标识
DOI:10.1016/j.neuron.2025.07.025
摘要
Recent transcriptomic studies have categorized mouse retinal ganglion cells (RGCs) into 45 types; however, little is known about their spatial distributions on the two-dimensional retinal surface and how their local microenvironments impact their functions. Here, we optimized a workflow combining imaging-based spatial transcriptomics (multiplexed-error robust fluorescent in situ hybridization [MERFISH]) and immunostaining on retinal flatmounts. We computationally registered the somata distributions of all RGCs and found that 34/45 molecularly defined types exhibited non-uniform distributions. We analyzed local neighborhoods for each cell and identified seven RGC types enriched in the perivascular niche, including direction-selective RGC (DSGC) and intrinsically photosensitive RGC (ipRGC) types. We further examined an experimental glaucoma model and found that surviving RGCs are enriched in the perivascular niche. Perivascular DSGCs and M1 ipRGCs were especially resilient, suggesting that proximity to vasculatures confers mTOR-independent, cell-extrinsic neuroprotection. Together, our work provides a comprehensive spatial atlas of RGC types and links their microenvironment to differential vulnerability in neurodegeneration.
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