Hypothalamic opsin 3 suppresses MC4R signaling and potentiates Kir7.1 to promote food consumption

Proc Natl Acad Sci U S A. 2025 Feb 25;122(8):e2403891122. doi: 10.1073/pnas.2403891122. Epub 2025 Feb 14.

Abstract

Mammalian opsin 3 (OPN3) is a member of the opsin family of G-protein-coupled receptors with ambiguous light sensitivity. OPN3 was first identified in the brain (and named encephalopsin) and subsequently found to be expressed in other tissues. In adipocytes, OPN3 is necessary for light responses that modulate lipolysis and glucose uptake, while OPN3 in human skin melanocytes regulates pigmentation in a light-independent manner. Despite its initial discovery in the brain, OPN3 functional mechanisms in the brain remain elusive. Here, we investigated the molecular mechanism of OPN3 function in the paraventricular nucleus (PVN) of the hypothalamus. We show that Opn3 is coexpressed with the melanocortin 4 receptor (Mc4r) in a population of PVN neurons, where it negatively regulates MC4R-mediated cAMP signaling in a specific and Gαi/o-dependent manner. Under baseline conditions, OPN3 via Gαi/o potentiates the activity of the inward rectifying Kir7.1 channel, previously shown to be closed in response to agonist-mediated activation of MC4R in a Gαs-independent manner. In mice, we found that Opn3 in Mc4r-expressing neurons regulates food consumption. Our results reveal the first mechanistic insight into OPN3 function in the hypothalamus, uncovering a unique mechanism by which OPN3 functions to potentiate Kir7.1 activity and negatively regulate MC4R-mediated cAMP signaling, thereby promoting food intake.

Keywords: G-protein coupled receptor (GPCR); Opsin 3 (OPN3); cAMP signaling; melanocortin 4 receptor (MC4R).

MeSH terms

  • Animals
  • Cyclic AMP / metabolism
  • Eating* / physiology
  • G Protein-Coupled Inwardly-Rectifying Potassium Channels* / metabolism
  • Humans
  • Hypothalamus* / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neurons / metabolism
  • Paraventricular Hypothalamic Nucleus / metabolism
  • Potassium Channels, Inwardly Rectifying* / metabolism
  • Receptor, Melanocortin, Type 4* / genetics
  • Receptor, Melanocortin, Type 4* / metabolism
  • Rod Opsins* / genetics
  • Rod Opsins* / metabolism
  • Signal Transduction

Substances

  • Receptor, Melanocortin, Type 4
  • Kir7.1 channel
  • Rod Opsins
  • MC4R protein, mouse
  • Cyclic AMP
  • Potassium Channels, Inwardly Rectifying
  • G Protein-Coupled Inwardly-Rectifying Potassium Channels