压电1
紫杉醇
角质形成细胞
刺激
医学
机械敏感通道
药理学
表皮(动物学)
神经病理性疼痛
化疗
化学
内分泌学
内科学
离子通道
体外
受体
解剖
生物化学
作者
Alexander R. Mikesell,Elena Isaeva,Marie L. Schulte,Anthony D. Menzel,Anvitha Sriram,Megan M. Prahl,Seung Min Shin,Katelyn E. Sadler,Hongwei Yu,Cheryl L. Stucky
标识
DOI:10.1126/scitranslmed.adn5629
摘要
Recent work demonstrates that epidermal keratinocytes are critical for normal touch sensation. However, it is unknown whether keratinocytes contribute to touch-evoked pain and hypersensitivity after tissue injury. Here, we used a mouse model of paclitaxel treatment to determine the extent to which keratinocyte activity contributes to the severe neuropathic pain that accompanies chemotherapy. We found that keratinocyte inhibition by either optogenetic or chemogenetic methods largely alleviated paclitaxel-induced mechanical hypersensitivity across acute and persistent time points from 2 days through 3 weeks. Furthermore, we found that paclitaxel exposure sensitized mouse and human keratinocytes to mechanical stimulation and enhanced currents of PIEZO1, a mechanosensitive channel highly expressed in keratinocytes. Deletion of PIEZO1 from keratinocytes alleviated paclitaxel-induced mechanical hypersensitivity in mice. These findings suggest that nonneuronal cutaneous cells contribute substantially to neuropathic pain and pave the way for the development of new pain relief strategies that target epidermal keratinocytes and PIEZO1.
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