| Literature DB >> 32879486 |
Kevin X Zhang1,2,3,4, Shane D'Souza1,2,3, Brian A Upton1,2,3,4, Stace Kernodle5, Shruti Vemaraju1,2, Gowri Nayak1,2, Kevin D Gaitonde1,2,3,4, Amanda L Holt6, Courtney D Linne1,2,3,4, April N Smith1,2, Nathan T Petts7, Matthew Batie7, Rajib Mukherjee8, Durgesh Tiwari9, Ethan D Buhr10, Russell N Van Gelder10,11,12, Christina Gross9,13, Alison Sweeney6, Joan Sanchez-Gurmaches8,13,14, Randy J Seeley5,15, Richard A Lang16,17,18,19.
Abstract
The opsin family of G-protein-coupled receptors are used as light detectors in animals. Opsin 5 (also known as neuropsin or OPN5) is a highly conserved opsin that is sensitive to visible violet light1,2. In mice, OPN5 is a known photoreceptor in the retina3 and skin4 but is also expressed in the hypothalamic preoptic area (POA)5. Here we describe a light-sensing pathway in which POA neurons that express Opn5 regulate thermogenesis in brown adipose tissue (BAT). We show that Opn5 is expressed in glutamatergic warm-sensing POA neurons that receive synaptic input from several thermoregulatory nuclei. We further show that Opn5 POA neurons project to BAT and decrease its activity under chemogenetic stimulation. Opn5-null mice show overactive BAT, increased body temperature, and exaggerated thermogenesis when cold-challenged. Moreover, violet photostimulation during cold exposure acutely suppresses BAT temperature in wild-type mice but not in Opn5-null mice. Direct measurements of intracellular cAMP ex vivo show that Opn5 POA neurons increase cAMP when stimulated with violet light. This analysis thus identifies a violet light-sensitive deep brain photoreceptor that normally suppresses BAT thermogenesis.Entities:
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Year: 2020 PMID: 32879486 PMCID: PMC8130195 DOI: 10.1038/s41586-020-2683-0
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962