Roessingh Sanne, Wolfgang Werner, Stanewsky Ralf
Department of Cell and Developmental Biology, University College London, London, UK School of Biological and Chemical Sciences, Queen Mary College, London, UK.
School of Biological and Chemical Sciences, Queen Mary College, London, UK.
J Biol Rhythms. 2015 Dec;30(6):492-505. doi: 10.1177/0748730415605633. Epub 2015 Oct 12.
To maintain synchrony with the environment, circadian clocks use a wide range of cycling sensory cues that provide input to the clock (zeitgebers), including environmental temperature cycles (TCs). There is some knowledge about which clock neuronal groups are important for temperature synchronization, but we currently lack knowledge on the temperature receptors and their signaling pathways that feed temperature information to the (neuronal) clock. Since TRPA1 is a well-known thermosensor that functions in a range of temperature-related behaviors, and it is potentially expressed in clock neurons, we set out to test the putative role of TRPA1 in temperature synchronization of the circadian clock. We found that flies lacking TRPA1 are still able to synchronize their behavioral activity to TCs comparable to wild-type flies, both in 16°C : 25°C and 20°C : 29°C TCs. In addition, we found that flies lacking TRPA1 show higher activity levels during the middle of the warm phase of 20°C : 29°C TCs, and we show that this TRPA1-mediated repression of locomotor activity during the "siesta" is caused by a lack of sleep. Based on these data, we conclude that the TRPA1 channel is not required for temperature synchronization in this broad temperature range but instead is required to repress activity during the warm part of the day.
为了与环境保持同步,生物钟利用多种周期性的感官线索(授时因子)向生物钟提供输入,包括环境温度循环(TCs)。我们对哪些时钟神经元群体对于温度同步很重要已有一定了解,但目前我们尚不清楚将温度信息传递给(神经元)生物钟的温度感受器及其信号通路。由于瞬时受体电位锚蛋白1(TRPA1)是一种知名的热敏感受器,在一系列与温度相关的行为中发挥作用,并且它可能在时钟神经元中表达,我们着手测试TRPA1在生物钟温度同步中的假定作用。我们发现,缺乏TRPA1的果蝇在16°C : 25°C和20°C : 29°C的温度循环条件下,仍能使其行为活动与温度循环同步,与野生型果蝇相当。此外,我们发现缺乏TRPA1的果蝇在20°C : 29°C温度循环的温暖阶段中期表现出更高的活动水平,并且我们表明,这种在“午睡”期间由TRPA1介导的运动活动抑制是由睡眠不足引起的。基于这些数据,我们得出结论,在这个较宽的温度范围内,温度同步不需要TRPA1通道,相反,它是在白天温暖时段抑制活动所必需的。