Department of Pharmacology, University of Heidelberg, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany.
Department of Pharmacology, University of Heidelberg, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany; Department of Functional Neuroanatomy, Institute for Anatomy and Cell Biology, University of Heidelberg, Im Neuenheimer Feld 307, 69120 Heidelberg, Germany.
Neuron. 2021 Oct 20;109(20):3283-3297.e11. doi: 10.1016/j.neuron.2021.10.001.
Deep brain temperature detection by hypothalamic warm-sensitive neurons (WSNs) has been proposed to provide feedback information relevant for thermoregulation. WSNs increase their action potential firing rates upon warming, a property that has been presumed to rely on the composition of thermosensitive ion channels within WSNs. Here, we describe a synaptic mechanism that regulates temperature sensitivity of preoptic WSNs and body temperature. Experimentally induced warming of the mouse hypothalamic preoptic area in vivo triggers body cooling. TRPM2 ion channels facilitate this homeostatic response and, at the cellular level, enhance temperature responses of WSNs, thereby linking WSN function with thermoregulation for the first time. Rather than acting within WSNs, we-unexpectedly-find TRPM2 to temperature-dependently increase synaptic drive onto WSNs by disinhibition. Our data emphasize a network-based interoceptive paradigm that likely plays a key role in encoding body temperature and that may facilitate integration of diverse inputs into thermoregulatory pathways.
下丘脑热敏神经元(WSNs)的深部脑温度检测被提议提供与体温调节相关的反馈信息。WSNs 在升温时会增加其动作电位的发放频率,这种特性被认为依赖于 WSN 内热敏离子通道的组成。在这里,我们描述了一种调节视前区 WSNs 和体温温度敏感性的突触机制。在体内实验性诱导小鼠下丘脑视前区升温会触发身体降温。TRPM2 离子通道促进这种体内平衡反应,并且在细胞水平上增强 WSNs 的温度反应,从而首次将 WSN 功能与体温调节联系起来。出乎意料的是,我们发现 TRPM2 不是在 WSN 内发挥作用,而是通过去抑制作用来温度依赖性地增加对 WSN 的突触驱动。我们的数据强调了一种基于网络的内脏感知范式,它可能在编码体温方面发挥关键作用,并可能促进将各种输入整合到体温调节途径中。