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不同分子亚型的脊髓和三叉神经投射神经元亚群对疼痛和痒觉的处理。

Pain and itch processing by subpopulations of molecularly diverse spinal and trigeminal projection neurons.

机构信息

Department of Anatomy, University of California, San Francisco, CA 94158.

Department of Anatomy, University of California, San Francisco, CA 94158

出版信息

Proc Natl Acad Sci U S A. 2021 Jul 13;118(28). doi: 10.1073/pnas.2105732118.

DOI:10.1073/pnas.2105732118
PMID:34234018
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8285968/
Abstract

A remarkable molecular and functional heterogeneity of the primary sensory neurons and dorsal horn interneurons transmits pain- and or itch-relevant information, but the molecular signature of the projection neurons that convey the messages to the brain is unclear. Here, using retro-TRAP (translating ribosome affinity purification) and RNA sequencing, we reveal extensive molecular diversity of spino- and trigeminoparabrachial projection neurons. Among the many genes identified, we highlight distinct subsets of -, -, -, and -expressing projection neurons. By combining in situ hybridization of retrogradely labeled neurons with Fos-based assays, we also demonstrate significant functional heterogeneity, including both convergence and segregation of pain- and itch-provoking inputs into molecularly diverse subsets of NK1R- and non-NK1R-expressing projection neurons.

摘要

初级感觉神经元和背角中间神经元的显著分子和功能异质性传递疼痛和/或瘙痒相关信息,但将这些信息传递到大脑的投射神经元的分子特征尚不清楚。在这里,我们使用 retro-TRAP(翻译核糖体亲和纯化)和 RNA 测序,揭示了脊髓和三叉神经-臂旁投射神经元的广泛分子多样性。在鉴定的许多基因中,我们突出了表达 - 、 - 、 - 和 - 的投射神经元的不同亚群。通过将逆行标记神经元的原位杂交与基于 Fos 的测定相结合,我们还证明了显著的功能异质性,包括疼痛和瘙痒刺激输入在 NK1R 和非 NK1R 表达投射神经元的分子多样性亚群中的会聚和分离。

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Proc Natl Acad Sci U S A. 2021 Jul 13;118(28). doi: 10.1073/pnas.2105732118.
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本文引用的文献

1
Phox2a Defines a Developmental Origin of the Anterolateral System in Mice and Humans.Phox2a 定义了小鼠和人类前外侧系统的发育起源。
Cell Rep. 2020 Nov 24;33(8):108425. doi: 10.1016/j.celrep.2020.108425.
2
Parallel ascending spinal pathways for affective touch and pain.情感触摸和疼痛的并行上升的脊髓通路。
Nature. 2020 Nov;587(7833):258-263. doi: 10.1038/s41586-020-2860-1. Epub 2020 Oct 28.
3
Spinal cord projection neurons: a superficial, and also deep, analysis.脊髓投射神经元:一项浅层及深层分析。
Curr Opin Physiol. 2019 Oct;11:109-115. doi: 10.1016/j.cophys.2019.10.002. Epub 2019 Oct 10.
4
Selective-cold output through a distinct subset of lamina I spinoparabrachial neurons.通过一小部分 I 层脊髓丘脑神经元实现选择性冷输出。
Pain. 2020 Jan;161(1):185-194. doi: 10.1097/j.pain.0000000000001710.
5
An Atlas of Vagal Sensory Neurons and Their Molecular Specialization.迷走感觉神经元及其分子特化图谱。
Cell Rep. 2019 May 21;27(8):2508-2523.e4. doi: 10.1016/j.celrep.2019.04.096.
6
Expression of cholecystokinin by neurons in mouse spinal dorsal horn.小鼠脊髓背角神经元中胆囊收缩素的表达
J Comp Neurol. 2019 Aug 1;527(11):1857-1871. doi: 10.1002/cne.24657. Epub 2019 Feb 20.
7
A Mast-Cell-Specific Receptor Mediates Neurogenic Inflammation and Pain.一种肥大细胞特异性受体介导神经原性炎症和疼痛。
Neuron. 2019 Feb 6;101(3):412-420.e3. doi: 10.1016/j.neuron.2019.01.012. Epub 2019 Jan 24.
8
Identifying the pathways required for coping behaviours associated with sustained pain.识别与持续疼痛相关的应对行为所需的途径。
Nature. 2019 Jan;565(7737):86-90. doi: 10.1038/s41586-018-0793-8. Epub 2018 Dec 10.
9
NPTX2 is a key component in the regulation of anxiety.NPTX2 是调节焦虑的关键组成部分。
Neuropsychopharmacology. 2018 Aug;43(9):1943-1953. doi: 10.1038/s41386-018-0091-z. Epub 2018 May 11.
10
Sensory Afferents Use Different Coding Strategies for Heat and Cold.感觉传入纤维使用不同的编码策略来编码热和冷。
Cell Rep. 2018 May 15;23(7):2001-2013. doi: 10.1016/j.celrep.2018.04.065.