Ferrandiz-Huertas Clotilde, Mathivanan Sakthikumar, Wolf Christoph Jakob, Devesa Isabel, Ferrer-Montiel Antonio
Instituto de Biología Molecular y Celular, Universidad Miguel Hernández, Alicante 03202, Spain.
Membranes (Basel). 2014 Aug 19;4(3):525-64. doi: 10.3390/membranes4030525.
ThermoTRP channels (thermoTRPs) define a subfamily of the transient receptor potential (TRP) channels that are activated by changes in the environmental temperature, from noxious cold to injurious heat. Acting as integrators of several stimuli and signalling pathways, dysfunction of these channels contributes to several pathological states. The surface expression of thermoTRPs is controlled by both, the constitutive and regulated vesicular trafficking. Modulation of receptor surface density during pathological processes is nowadays considered as an interesting therapeutic approach for management of diseases, such as chronic pain, in which an increased trafficking is associated with the pathological state. This review will focus on the recent advances trafficking of the thermoTRP channels, TRPV1, TRPV2, TRPV4, TRPM3, TRPM8 and TRPA1, into/from the plasma membrane. Particularly, regulated membrane insertion of thermoTRPs channels contributes to a fine tuning of final channel activity, and indeed, it has resulted in the development of novel therapeutic approaches with successful clinical results such as disruption of SNARE-dependent exocytosis by botulinum toxin or botulinomimetic peptides.
热瞬态受体电位通道(thermoTRPs)是瞬态受体电位(TRP)通道的一个亚家族,可被环境温度变化激活,范围从有害寒冷到致伤热。这些通道作为多种刺激和信号通路的整合者,其功能障碍会导致多种病理状态。thermoTRPs的表面表达受组成型和调节型囊泡运输的共同控制。在病理过程中调节受体表面密度如今被认为是治疗慢性疼痛等疾病的一种有趣的治疗方法,在这些疾病中,运输增加与病理状态相关。本综述将聚焦于热瞬态受体电位通道TRPV1、TRPV2、TRPV4、TRPM3、TRPM8和TRPA1进出质膜的运输的最新进展。特别是,热瞬态受体电位通道的调节性膜插入有助于对最终通道活性进行微调,实际上,这已促成了具有成功临床结果的新型治疗方法的开发,如肉毒杆菌毒素或类肉毒杆菌肽破坏SNARE依赖性胞吐作用。