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背根神经节的单细胞转录组分析:概述

Single-cell transcriptomic profiling of dorsal root ganglion: an overview.

作者信息

Xie Keyu, Cheng Xu, Zhu Tao, Zhang Donghang

机构信息

Department of Anesthesiology, West China Hospital, Sichuan University, Chengdu, China.

Department of Anesthesiology, Chengdu Second People's Hospital, Chengdu, China.

出版信息

Front Neuroanat. 2023 Jun 19;17:1162049. doi: 10.3389/fnana.2023.1162049. eCollection 2023.

DOI:10.3389/fnana.2023.1162049
PMID:37405309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10315536/
Abstract

The somatosensory neurons in the dorsal root ganglion (DRG) are responsible to detect peripheral physical and noxious stimuli, and then transmit these inputs into the central nervous system. DRG neurons are composed of various subpopulations, which are suggested to respond to different stimuli, such as mechanical, thermal, and cold perception. For a long time, DRG neurons were classified based on anatomical criteria. Recently, single-cell (scRNA-seq) and single-nucleus RNA-sequencing (snRNA-seq) has advanced our understanding of the composition and functional heterogeneity of both human and rodent DRG neurons at single-cell resolution. In this review, we summarized the current literature regarding single-cell transcriptomic profiling of DRG to provide an integral understanding in the molecular transcriptomes, cell types, and functional annotations of DRG neurons in humans and rodents.

摘要

背根神经节(DRG)中的躯体感觉神经元负责检测外周的物理和有害刺激,然后将这些输入传递到中枢神经系统。DRG神经元由各种亚群组成,这些亚群被认为对不同的刺激有反应,如机械、热和冷觉。长期以来,DRG神经元是根据解剖学标准进行分类的。最近,单细胞(scRNA-seq)和单细胞核RNA测序(snRNA-seq)使我们在单细胞分辨率水平上对人和啮齿动物DRG神经元的组成和功能异质性有了更深入的了解。在这篇综述中,我们总结了当前关于DRG单细胞转录组分析的文献,以便全面了解人和啮齿动物DRG神经元的分子转录组、细胞类型和功能注释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34b5/10315536/6af0555dc424/fnana-17-1162049-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34b5/10315536/3d89bf9a98a0/fnana-17-1162049-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34b5/10315536/6af0555dc424/fnana-17-1162049-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34b5/10315536/3d89bf9a98a0/fnana-17-1162049-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34b5/10315536/6af0555dc424/fnana-17-1162049-g002.jpg

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本文引用的文献

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Cellular complexity of the peripheral nervous system: Insights from single-cell resolution.外周神经系统的细胞复杂性:单细胞分辨率下的见解
Front Neurosci. 2023 Mar 14;17:1098612. doi: 10.3389/fnins.2023.1098612. eCollection 2023.
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Single-Soma Deep RNA sequencing of Human DRG Neurons Reveals Novel Molecular and Cellular Mechanisms Underlying Somatosensation.人背根神经节神经元的单神经元深度RNA测序揭示了躯体感觉背后新的分子和细胞机制。
bioRxiv. 2023 Sep 28:2023.03.17.533207. doi: 10.1101/2023.03.17.533207.
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Cross-species transcriptomic atlas of dorsal root ganglia reveals species-specific programs for sensory function.
岩藻多糖通过肠-血-背根神经节轴减少中性粒细胞胞外陷阱积累并减轻化疗引起的周围神经病变。
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Anoctamin-1 is a core component of a mechanosensory anion channel complex in C. elegans.无翅型肌球蛋白1是秀丽隐杆线虫机械感觉阴离子通道复合体的核心组成部分。
Nat Commun. 2025 Feb 16;16(1):1680. doi: 10.1038/s41467-025-56938-z.
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Single-cell profiling of cellular changes in the somatic peripheral nerves following nerve injury.神经损伤后躯体周围神经细胞变化的单细胞分析
Front Pharmacol. 2024 Oct 2;15:1448253. doi: 10.3389/fphar.2024.1448253. eCollection 2024.
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Interplay of Nav1.8 and Nav1.7 channels drives neuronal hyperexcitability in neuropathic pain.Nav1.8 和 Nav1.7 通道的相互作用导致神经性疼痛中的神经元过度兴奋。
J Gen Physiol. 2024 Nov 4;156(11). doi: 10.1085/jgp.202413596. Epub 2024 Oct 8.
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A novel Na1.8-FLPo driver mouse for intersectional genetics to uncover the functional significance of primary sensory neuron diversity.一种用于交叉遗传学的新型Na1.8-FLPo驱动小鼠,以揭示初级感觉神经元多样性的功能意义。
iScience. 2024 Mar 5;27(4):109396. doi: 10.1016/j.isci.2024.109396. eCollection 2024 Apr 19.
背根神经节跨物种转录组图谱揭示了感觉功能的物种特异性程序。
Nat Commun. 2023 Jan 23;14(1):366. doi: 10.1038/s41467-023-36014-0.
4
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Elife. 2022 Oct 20;11:e76063. doi: 10.7554/eLife.76063.
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Transcriptomic analysis of human sensory neurons in painful diabetic neuropathy reveals inflammation and neuronal loss.痛性糖尿病周围神经病患者感觉神经元的转录组分析显示炎症和神经元丢失。
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