Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, United States; Department of Neuroscience, Yale University School of Medicine, New Haven, United States; Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, United States
Yury A Nikolaev
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, United States
Dana K Merriman
Department of Biology, University of Wisconsin-Oshkosh, Oshkosh, United States
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, United States; Department of Neuroscience, Yale University School of Medicine, New Haven, United States; Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, New Haven, United States
Most mammals maintain their body temperature around 37°C, whereas in hibernators it can approach 0°C without triggering a thermogenic response. The remarkable plasticity of the thermoregulatory system allowed mammals to thrive in variable environmental conditions and occupy a wide range of geographical habitats, but the molecular basis of thermoregulation remains poorly understood. Here we leverage the thermoregulatory differences between mice and hibernating thirteen-lined ground squirrels (Ictidomys tridecemlineatus) to investigate the mechanism of cold sensitivity in the preoptic area (POA) of the hypothalamus, a critical thermoregulatory region. We report that, in comparison to squirrels, mice have a larger proportion of cold-sensitive neurons in the POA. We further show that mouse cold-sensitive neurons express the cyclic nucleotide-gated ion channel CNGA3, and that mouse, but not squirrel, CNGA3 is potentiated by cold. Our data reveal CNGA3 as a hypothalamic cold sensor and a molecular marker to interrogate the neuronal circuitry underlying thermoregulation.