Department of Cellular Neurophysiology, Institute of Physiology, Czech Academy of Sciences, Videnska 1083, 142 20, Prague 4, Czech Republic.
Department of Physiology, Faculty of Science, Charles University, Prague, Czech Republic.
J Physiol Sci. 2024 Oct 3;74(1):50. doi: 10.1186/s12576-024-00942-3.
Our understanding of how the mammalian somatosensory system detects noxious cold is still limited. While the role of TRPM8 in signaling mild non-noxious coolness is reasonably understood, the molecular identity of channels transducing painful cold stimuli remains unresolved. TRPC5 was originally described to contribute to moderate cold responses of dorsal root ganglia neurons in vitro, but mice lacking TRPC5 exhibited no change in behavioral responses to cold temperature. The question of why a channel endowed with the ability to be activated by cooling contributes to the cold response only under certain conditions is currently being intensively studied. It seems increasingly likely that the physiological detection of cold temperatures involves multiple different channels and mechanisms that modulate the threshold and intensity of perception. In this review, we aim to outline how TRPC5 may contribute to these mechanisms and what molecular features are important for its role as a cold sensor.
我们对于哺乳动物躯体感觉系统如何感知有害冷刺激的理解仍然有限。虽然 TRPM8 在信号传递温和非有害凉爽刺激方面的作用已经得到了合理的理解,但传递疼痛冷刺激的通道的分子身份仍未得到解决。TRPC5 最初被描述为有助于体外背根神经节神经元对中等寒冷刺激的反应,但缺乏 TRPC5 的小鼠在对冷温度的行为反应上没有变化。目前正在深入研究一个赋予被冷却激活能力的通道为什么只在某些条件下有助于冷反应的问题。似乎越来越有可能的是,冷温度的生理检测涉及多种不同的通道和机制,这些通道和机制调节感知的阈值和强度。在这篇综述中,我们旨在概述 TRPC5 如何有助于这些机制,以及对其作为冷传感器的作用而言,哪些分子特征是重要的。