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本文引用的文献

1
Gbx2 Identifies Two Amacrine Cell Subtypes with Distinct Molecular, Morphological, and Physiological Properties.Gbx2 鉴定出两种具有不同分子、形态和生理特性的无长突细胞亚型。
Cell Rep. 2020 Nov 17;33(7):108382. doi: 10.1016/j.celrep.2020.108382.
2
Cell atlas of aqueous humor outflow pathways in eyes of humans and four model species provides insight into glaucoma pathogenesis.人眼和四种模式物种房水流出通路的细胞图谱为青光眼发病机制提供了新见解。
Proc Natl Acad Sci U S A. 2020 May 12;117(19):10339-10349. doi: 10.1073/pnas.2001250117. Epub 2020 Apr 27.
3
Binary Fate Choice between Closely Related Interneuronal Types Is Determined by a Fezf1-Dependent Postmitotic Transcriptional Switch.两种密切相关的中间神经元类型之间的二元命运选择是由 Fezf1 依赖性的出生后转录开关决定的。
Neuron. 2020 Feb 5;105(3):464-474.e6. doi: 10.1016/j.neuron.2019.11.002. Epub 2019 Dec 4.
4
Single-Cell Profiles of Retinal Ganglion Cells Differing in Resilience to Injury Reveal Neuroprotective Genes.单细胞分析揭示了对损伤具有不同抵抗力的视网膜神经节细胞的特征,并发现了神经保护基因。
Neuron. 2019 Dec 18;104(6):1039-1055.e12. doi: 10.1016/j.neuron.2019.11.006. Epub 2019 Nov 26.
5
MEIS transcription factors in development and disease.MEIS 转录因子在发育和疾病中的作用。
Development. 2019 Aug 15;146(16):dev174706. doi: 10.1242/dev.174706.
6
DoubletFinder: Doublet Detection in Single-Cell RNA Sequencing Data Using Artificial Nearest Neighbors.DoubletFinder:基于人工最近邻算法检测单细胞 RNA 测序数据中的双细胞。
Cell Syst. 2019 Apr 24;8(4):329-337.e4. doi: 10.1016/j.cels.2019.03.003. Epub 2019 Apr 3.
7
Molecular Classification and Comparative Taxonomics of Foveal and Peripheral Cells in Primate Retina.灵长类动物视网膜中央凹和周边细胞的分子分类和比较分类学。
Cell. 2019 Feb 21;176(5):1222-1237.e22. doi: 10.1016/j.cell.2019.01.004. Epub 2019 Jan 31.
8
Expression and Roles of the Immunoglobulin Superfamily Recognition Molecule Sidekick1 in Mouse Retina.免疫球蛋白超家族识别分子Sidekick1在小鼠视网膜中的表达及作用
Front Mol Neurosci. 2019 Jan 9;11:485. doi: 10.3389/fnmol.2018.00485. eCollection 2018.
9
A Self-Regulating Gap Junction Network of Amacrine Cells Controls Nitric Oxide Release in the Retina.一种自我调节的无长突细胞缝隙连接网络控制视网膜中的一氧化氮释放。
Neuron. 2018 Dec 5;100(5):1149-1162.e5. doi: 10.1016/j.neuron.2018.09.047. Epub 2018 Oct 25.
10
Mapping Transgene Insertion Sites Reveals Complex Interactions Between Mouse Transgenes and Neighboring Endogenous Genes.绘制转基因插入位点揭示小鼠转基因与邻近内源基因之间的复杂相互作用。
Front Mol Neurosci. 2018 Oct 23;11:385. doi: 10.3389/fnmol.2018.00385. eCollection 2018.

鼠视网膜细胞图谱:六十多种无长突细胞类型的分子鉴定

Mouse Retinal Cell Atlas: Molecular Identification of over Sixty Amacrine Cell Types.

机构信息

Center for Brain Science and Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138.

Klarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142.

出版信息

J Neurosci. 2020 Jul 1;40(27):5177-5195. doi: 10.1523/JNEUROSCI.0471-20.2020. Epub 2020 May 26.

DOI:10.1523/JNEUROSCI.0471-20.2020
PMID:32457074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7329304/
Abstract

Amacrine cells (ACs) are a diverse class of interneurons that modulate input from photoreceptors to retinal ganglion cells (RGCs), rendering each RGC type selectively sensitive to particular visual features, which are then relayed to the brain. While many AC types have been identified morphologically and physiologically, they have not been comprehensively classified or molecularly characterized. We used high-throughput single-cell RNA sequencing to profile >32,000 ACs from mice of both sexes and applied computational methods to identify 63 AC types. We identified molecular markers for each type and used them to characterize the morphology of multiple types. We show that they include nearly all previously known AC types as well as many that had not been described. Consistent with previous studies, most of the AC types expressed markers for the canonical inhibitory neurotransmitters GABA or glycine, but several expressed neither or both. In addition, many expressed one or more neuropeptides, and two expressed glutamatergic markers. We also explored transcriptomic relationships among AC types and identified transcription factors expressed by individual or multiple closely related types. Noteworthy among these were and , expressed by most GABAergic and most glycinergic types, respectively. Together, these results provide a foundation for developmental and functional studies of ACs, as well as means for genetically accessing them. Along with previous molecular, physiological, and morphologic analyses, they establish the existence of at least 130 neuronal types and nearly 140 cell types in the mouse retina. The mouse retina is a leading model for analyzing the development, structure, function, and pathology of neural circuits. A complete molecular atlas of retinal cell types provides an important foundation for these studies. We used high-throughput single-cell RNA sequencing to characterize the most heterogeneous class of retinal interneurons, amacrine cells, identifying 63 distinct types. The atlas includes types identified previously as well as many novel types. We provide evidence for the use of multiple neurotransmitters and neuropeptides, and identify transcription factors expressed by groups of closely related types. Combining these results with those obtained previously, we proposed that the mouse retina contains ∼130 neuronal types and is therefore comparable in complexity to other regions of the brain.

摘要

无