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外周神经末梢伤害性 TRP 通道功能的光学评估。

Optical Assessment of Nociceptive TRP Channel Function at the Peripheral Nerve Terminal.

机构信息

Instituto de Neurociencias, Universidad Miguel Hernández-CSIC, 03550 San Juan de Alicante, Spain.

Department of Medical Neurobiology, Institute for Medical Research Israel-Canada, Hadassah School of Medicine, The Hebrew University, Jerusalem 91123, Israel.

出版信息

Int J Mol Sci. 2021 Jan 6;22(2):481. doi: 10.3390/ijms22020481.

DOI:10.3390/ijms22020481
PMID:33418928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7825137/
Abstract

Free nerve endings are key structures in sensory transduction of noxious stimuli. In spite of this, little is known about their functional organization. Transient receptor potential (TRP) channels have emerged as key molecular identities in the sensory transduction of pain-producing stimuli, yet the vast majority of our knowledge about sensory TRP channel function is limited to data obtained from in vitro models which do not necessarily reflect physiological conditions. In recent years, the development of novel optical methods such as genetically encoded calcium indicators and photo-modulation of ion channel activity by pharmacological tools has provided an invaluable opportunity to directly assess nociceptive TRP channel function at the nerve terminal.

摘要

游离神经末梢是伤害性刺激感觉转导的关键结构。尽管如此,对于它们的功能组织,我们知之甚少。瞬时受体电位 (TRP) 通道已成为产生疼痛刺激感觉转导的关键分子特征,但我们对感觉 TRP 通道功能的绝大多数了解仅限于从体外模型获得的数据,这些数据不一定反映生理状况。近年来,新型光学方法的发展,如基因编码的钙指示剂和药理学工具对离子通道活性的光调节,为直接评估神经末梢的伤害性 TRP 通道功能提供了宝贵的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e2d/7825137/0de58e09e3fb/ijms-22-00481-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e2d/7825137/05b0c8185bc6/ijms-22-00481-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e2d/7825137/228b7a5cad7f/ijms-22-00481-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e2d/7825137/0de58e09e3fb/ijms-22-00481-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e2d/7825137/05b0c8185bc6/ijms-22-00481-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e2d/7825137/228b7a5cad7f/ijms-22-00481-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e2d/7825137/0de58e09e3fb/ijms-22-00481-g003.jpg

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1
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J Neurosci. 2020 Dec 2;40(49):9346-9363. doi: 10.1523/JNEUROSCI.1546-20.2020. Epub 2020 Oct 28.
2
Piezo2 Mediates Low-Threshold Mechanically Evoked Pain in the Cornea.Piezo2 介导热敏机械刺激诱导的角膜疼痛。
J Neurosci. 2020 Nov 18;40(47):8976-8993. doi: 10.1523/JNEUROSCI.0247-20.2020. Epub 2020 Oct 14.
3
TRPswitch-A Step-Function Chemo-optogenetic Ligand for the Vertebrate TRPA1 Channel.
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Pain Rep. 2021 Dec 8;6(4):e968. doi: 10.1097/PR9.0000000000000968. eCollection 2021 Nov-Dec.
4
The Calcium Channel α2δ1 Subunit: Interactional Targets in Primary Sensory Neurons and Role in Neuropathic Pain.钙通道α2δ1亚基:初级感觉神经元中的相互作用靶点及在神经性疼痛中的作用
Front Cell Neurosci. 2021 Sep 30;15:699731. doi: 10.3389/fncel.2021.699731. eCollection 2021.
TRPswitch-A:一种用于脊椎动物 TRPA1 通道的阶跃功能化学遗传学配体。
J Am Chem Soc. 2020 Oct 14;142(41):17457-17468. doi: 10.1021/jacs.0c06811. Epub 2020 Oct 5.
4
Upregulation of TRPM3 in nociceptors innervating inflamed tissue.伤害感受神经元中 TRPM3 的上调。
Elife. 2020 Sep 3;9:e61103. doi: 10.7554/eLife.61103.
5
Heat detection by the TRPM2 ion channel.TRPM2离子通道对热的检测
Nature. 2020 Aug;584(7820):E5-E12. doi: 10.1038/s41586-020-2510-7. Epub 2020 Aug 12.
6
Reply to: Heat detection by the TRPM2 ion channel.回复:TRPM2离子通道对热的检测
Nature. 2020 Aug;584(7820):E13-E15. doi: 10.1038/s41586-020-2511-6.
7
The Sensory Coding of Warm Perception.温暖感知的感觉编码。
Neuron. 2020 Jun 3;106(5):830-841.e3. doi: 10.1016/j.neuron.2020.02.035. Epub 2020 Mar 23.
8
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9
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Cells. 2019 Dec 24;9(1):57. doi: 10.3390/cells9010057.
10
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Nat Commun. 2019 Dec 12;10(1):5678. doi: 10.1038/s41467-019-13536-0.