TRPM2型
瞬时受体电位通道
TRPM8型
离子通道
TRPV1型
体感系统
人口
化学
电生理学
感觉系统
神经科学
生物物理学
生物
医学
生物化学
受体
环境卫生
作者
Chun‐Hsiang Tan,Peter A. McNaughton
出处
期刊:Nature
[Springer Nature]
日期:2016-08-01
卷期号:536 (7617): 460-463
被引量:294
摘要
Thermally activated ion channels are known to detect the entire thermal range from extreme heat (TRPV2), painful heat (TRPV1, TRPM3 and ANO1), non-painful warmth (TRPV3 and TRPV4) and non-painful coolness (TRPM8) through to painful cold (TRPA1). Genetic deletion of each of these ion channels, however, has only modest effects on thermal behaviour in mice, with the exception of TRPM8, the deletion of which has marked effects on the perception of moderate coolness in the range 10-25 °C. The molecular mechanism responsible for detecting non-painful warmth, in particular, is unresolved. Here we used calcium imaging to identify a population of thermally sensitive somatosensory neurons which do not express any of the known thermally activated TRP channels. We then used a combination of calcium imaging, electrophysiology and RNA sequencing to show that the ion channel generating heat sensitivity in these neurons is TRPM2. Autonomic neurons, usually thought of as exclusively motor, also express TRPM2 and respond directly to heat. Mice in which TRPM2 had been genetically deleted showed a striking deficit in their sensation of non-noxious warm temperatures, consistent with the idea that TRPM2 initiates a 'warm' signal which drives cool-seeking behaviour.
科研通智能强力驱动
Strongly Powered by AbleSci AI