Wilson Sarah R, Bautista Diana M
Members of the transient receptor potential (TRP) family have emerged as key players in itch transduction in the periphery. TRP family members are tetrameric cation selective channels that are expressed in diverse species, from flies to humans. The founding member of the TRP channel superfamily is TRP, a transduction channel required for light-evoked excitation of photoreceptors. In phototransduction, activation of the phospholipase C (PLC) pathway leads to the opening of TRP and its homolog TRP-L; flies lacking these channels display no light-evoked transduction currents and are blind. Over 27 members have since been identified in a variety of cell types and tissues (Figure 16.1). TRP channels are divided into seven subgroups based on protein homology rather than function: TRPC, TRPV, TRPM, TRPA, TRPN, TRPP, and TRPML. Generally, TRP channels function as polymodal cellular sensors involved in a wide variety of cellular processes. Many TRPs have been found to participate in sensory transduction pathways, including thermosensation, mechanosensation, taste, perception of pungent compounds, pheromone sensing, and osmolarity regulation. A number of excellent reviews describe the vast roles of TRP channels which will not be discussed. Here, we discuss the role of four TRP channels that have been proposed to play a role in itch transduction: TRPV1, TRPA1, TRPM8, and TRPV3. Historically, these four channels have been implicated in the transduction of noxious thermal, chemical, and/or mechanical stimuli, and more recent studies have implicated these channels in the transduction of itch.
瞬时受体电位(TRP)家族成员已成为外周瘙痒传导的关键参与者。TRP家族成员是四聚体阳离子选择性通道,在从果蝇到人类的多种物种中都有表达。TRP通道超家族的创始成员是TRP,它是光感受器光诱发兴奋所需的转导通道。在光转导过程中,磷脂酶C(PLC)途径的激活导致TRP及其同源物TRP-L的开放;缺乏这些通道的果蝇没有光诱发的转导电流,并且是失明的。此后,在多种细胞类型和组织中已鉴定出超过27个成员(图16.1)。TRP通道根据蛋白质同源性而非功能分为七个亚组:TRPC、TRPV、TRPM、TRPA、TRPN、TRPP和TRPML。一般来说,TRP通道作为多模式细胞传感器参与多种细胞过程。已发现许多TRP参与感觉转导途径,包括热感觉、机械感觉、味觉、刺激性化合物的感知、信息素感知和渗透压调节。许多优秀的综述描述了TRP通道的广泛作用,在此不再讨论。在这里,我们讨论已被提出在瘙痒传导中起作用的四个TRP通道的作用:TRPV1、TRPA1、TRPM8和TRPV3。从历史上看,这四个通道与有害热、化学和/或机械刺激的转导有关,最近的研究表明这些通道也参与瘙痒的转导。