内输蛋白
外围设备
神经科学
感觉系统
核运输
慢性疼痛
核心
医学
生物
内科学
细胞核
作者
Letizia Marvaldi,Nicolas Panayotis,Stefanie Alber,Shachar Y. Dagan,Nataliya Okladnikov,Indrek Koppel,Agostina Di Pizio,Didi‐Andreas Song,Y. Tzur,Marco Terenzio,Ida Rishal,Dalia Gordon,Franziska Rother,Enno Hartmann,Michael Bäder,Mike Fainzilber
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2020-08-14
卷期号:369 (6505): 842-846
被引量:70
标识
DOI:10.1126/science.aaz5875
摘要
How is neuropathic pain regulated in peripheral sensory neurons? Importins are key regulators of nucleocytoplasmic transport. In this study, we found that importin α3 (also known as karyopherin subunit alpha 4) can control pain responsiveness in peripheral sensory neurons in mice. Importin α3 knockout or sensory neuron-specific knockdown in mice reduced responsiveness to diverse noxious stimuli and increased tolerance to neuropathic pain. Importin α3-bound c-Fos and importin α3-deficient neurons were impaired in c-Fos nuclear import. Knockdown or dominant-negative inhibition of c-Fos or c-Jun in sensory neurons reduced neuropathic pain. In silico screens identified drugs that mimic importin α3 deficiency. These drugs attenuated neuropathic pain and reduced c-Fos nuclear localization. Thus, perturbing c-Fos nuclear import by importin α3 in peripheral neurons can promote analgesia.
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