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MrgprC11 sensory neurons mediate glabrous skin itch.MrgprC11 感觉神经元介导无毛皮肤瘙痒。
Proc Natl Acad Sci U S A. 2021 Apr 13;118(15). doi: 10.1073/pnas.2022874118.
2
Enhanced excitability of MRGPRA3- and MRGPRD-positive nociceptors in a model of inflammatory itch and pain.MRGPRA3 和 MRGPRD 阳性伤害感受器在炎症性瘙痒和疼痛模型中的兴奋性增强。
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3
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6
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Molecular Signature of Pruriceptive MrgprA3 Neurons.瘙痒性 MrgprA3 神经元的分子特征。
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Divergent sensory pathways of sneezing and coughing.打喷嚏和咳嗽的感觉通路分歧。
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The nociceptive activity of peripheral sensory neurons is modulated by the neuronal membrane proteasome.外周感觉神经元的伤害感受活性受神经元膜蛋白酶体的调节。
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Sensing of protease activity as a triggering mechanism of Th2 cell immunity and allergic disease.将蛋白酶活性感知作为Th2细胞免疫和过敏性疾病的触发机制。
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10
Neuroimmune interactions in atopic and allergic contact dermatitis.特应性皮炎和过敏性接触性皮炎中的神经免疫相互作用。
J Allergy Clin Immunol. 2023 May;151(5):1169-1177. doi: 10.1016/j.jaci.2023.03.013.

本文引用的文献

1
Visualizing the Itch-Sensing Skin Arbors.可视化瘙痒感知皮肤树突。
J Invest Dermatol. 2021 May;141(5):1308-1316. doi: 10.1016/j.jid.2020.08.030. Epub 2020 Oct 20.
2
Differential Coding of Itch and Pain by a Subpopulation of Primary Afferent Neurons.初级传入神经元亚群对瘙痒和疼痛的差异编码。
Neuron. 2020 Jun 17;106(6):940-951.e4. doi: 10.1016/j.neuron.2020.03.021. Epub 2020 Apr 15.
3
The emergence of transcriptional identity in somatosensory neurons.躯体感觉神经元中转录身份的出现。
Nature. 2020 Jan;577(7790):392-398. doi: 10.1038/s41586-019-1900-1. Epub 2020 Jan 8.
4
Development of a Mouse Pain Scale Using Sub-second Behavioral Mapping and Statistical Modeling.利用亚秒级行为映射和统计建模开发小鼠疼痛量表。
Cell Rep. 2019 Aug 6;28(6):1623-1634.e4. doi: 10.1016/j.celrep.2019.07.017.
5
Deep Sequencing of Somatosensory Neurons Reveals Molecular Determinants of Intrinsic Physiological Properties.对感觉神经元进行深度测序揭示了内在生理特性的分子决定因素。
Neuron. 2019 Aug 21;103(4):598-616.e7. doi: 10.1016/j.neuron.2019.05.039. Epub 2019 Jun 24.
6
MRGPRX4 is a G protein-coupled receptor activated by bile acids that may contribute to cholestatic pruritus.MRGPRX4 是一种 G 蛋白偶联受体,可被胆汁酸激活,可能与胆汁淤积性瘙痒有关。
Proc Natl Acad Sci U S A. 2019 May 21;116(21):10525-10530. doi: 10.1073/pnas.1903316116. Epub 2019 May 8.
7
Nppb Neurons Are Sensors of Mast Cell-Induced Itch.Nppb 神经元是肥大细胞诱导瘙痒的传感器。
Cell Rep. 2019 Mar 26;26(13):3561-3573.e4. doi: 10.1016/j.celrep.2019.02.089.
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
The role of the histamine H receptor in atopic dermatitis and psoriasis.组胺 H 受体在特应性皮炎和银屑病中的作用。
Br J Pharmacol. 2020 Feb;177(3):490-502. doi: 10.1111/bph.14550. Epub 2019 Jan 2.
10
The Role of Histamine and Histamine Receptors in Mast Cell-Mediated Allergy and Inflammation: The Hunt for New Therapeutic Targets.组胺和组胺受体在肥大细胞介导的过敏和炎症中的作用:寻找新的治疗靶点。
Front Immunol. 2018 Aug 13;9:1873. doi: 10.3389/fimmu.2018.01873. eCollection 2018.

MrgprC11 感觉神经元介导无毛皮肤瘙痒。

MrgprC11 sensory neurons mediate glabrous skin itch.

机构信息

School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA 30332.

School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA 30332

出版信息

Proc Natl Acad Sci U S A. 2021 Apr 13;118(15). doi: 10.1073/pnas.2022874118.

DOI:10.1073/pnas.2022874118
PMID:33876765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8053975/
Abstract

Itch arising from glabrous skin (palms and soles) has attracted limited attention within the field due to the lack of methodology. This is despite glabrous itch arising from many medical conditions such as plantar and palmar psoriasis, dyshidrosis, and cholestasis. Therefore, we developed a mouse glabrous skin behavioral assay to investigate the contribution of three previously identified pruriceptive neurons in glabrous skin itch. Our results show that MrgprA3 and MrgprD neurons, although key mediators for hairy skin itch, do not play important roles in glabrous skin itch, demonstrating a mechanistic difference in itch sensation between hairy and glabrous skin. We found that MrgprC11 neurons are the major mediators for glabrous skin itch. Activation of MrgprC11 neurons induced glabrous skin itch, while ablation of MrgprC11 neurons reduced both acute and chronic glabrous skin itch. Our study provides insights into the mechanisms of itch and opens up new avenues for future glabrous skin itch research.

摘要

无毛皮肤(手掌和脚底)引起的瘙痒由于缺乏方法而在该领域受到的关注有限。尽管许多医学病症都会引起无毛瘙痒,例如足底和手掌银屑病、汗疱疹和胆汁淤积,但这种情况还是存在。因此,我们开发了一种小鼠无毛皮肤行为检测方法,以研究先前鉴定的三种瘙痒神经元在无毛皮肤瘙痒中的作用。我们的结果表明,MrgprA3 和 MrgprD 神经元虽然是毛发皮肤瘙痒的主要介质,但在无毛皮肤瘙痒中不起重要作用,这表明毛发皮肤和无毛皮肤的瘙痒感觉在机制上存在差异。我们发现 MrgprC11 神经元是无毛皮肤瘙痒的主要介质。MrgprC11 神经元的激活会引起无毛皮肤瘙痒,而 MrgprC11 神经元的消融会减少急性和慢性无毛皮肤瘙痒。我们的研究为瘙痒机制提供了新的见解,并为未来的无毛皮肤瘙痒研究开辟了新的途径。