Viana Félix
Instituto de Neurociencias de Alicante, Universidad Miguel Hernández-CSIC, Alicante, Spain.
J Physiol. 2016 Aug 1;594(15):4151-69. doi: 10.1113/JP270935.
TRPA1 is a non-selective cation channel expressed in mammalian peripheral pain receptors, with a major role in chemonociception. TRPA1 has also been implicated in noxious cold and mechanical pain sensation. TRPA1 has an ancient origin and plays important functions in lower organisms, including thermotaxis, mechanotransduction and modulation of lifespan. Here we highlight the role of TRPA1 as a multipurpose sensor of harmful signals, including toxic bacterial products and UV light, and as a sensor of stress and tissue damage. Sensing roles span beyond the peripheral nervous system to include major barrier tissues: gut, skin and lung. Tissue injury, environmental irritants and microbial pathogens are danger signals that can threaten the health of organisms. These signals lead to the coordinated activation of the nociceptive and the innate immune system to provide a homeostatic response trying to re-establish physiological conditions including tissue repair. Activation of TRPA1 participates in protective neuroimmune interactions at multiple levels, sensing ROS and bacterial products and triggering the release of neuropeptides. However, an exaggerated response to danger signals is maladaptive and can lead to the development of chronic inflammatory conditions.
瞬时受体电位锚蛋白1(TRPA1)是一种在哺乳动物外周痛觉感受器中表达的非选择性阳离子通道,在化学性痛觉感受中起主要作用。TRPA1也与有害冷觉和机械性痛觉感受有关。TRPA1起源古老,在包括趋温性、机械转导和寿命调节等较低等生物中发挥重要功能。在此,我们强调TRPA1作为有害信号(包括有毒细菌产物和紫外线)的多功能传感器以及作为应激和组织损伤传感器的作用。其传感作用不仅限于外周神经系统,还包括主要的屏障组织:肠道、皮肤和肺。组织损伤、环境刺激物和微生物病原体都是可能威胁生物体健康的危险信号。这些信号导致伤害性感受系统和固有免疫系统的协同激活,以提供一种试图重新建立包括组织修复在内的生理状态的稳态反应。TRPA1的激活在多个层面参与保护性神经免疫相互作用,感知活性氧和细菌产物并触发神经肽的释放。然而,对危险信号的过度反应是适应不良的,可能导致慢性炎症性疾病的发展。