Intracrine FFA4 signaling controls lipolysis at lipid droplets

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Abstract
G-protein-coupled receptors (GPCRs) can signal from intracellular compartments but the occurrence and relevance of this phenomenon for metabolite-sensing GPCRs is largely unknown. Here, we investigate free fatty acid receptor 4 (FFA4), a metabolite-sensing GPCR activated by medium-chain and long-chain fatty acids. Using live-cell imaging, bioluminescence resonance energy transfer, super-resolution microscopy and cell fractionation, we show that FFA4 localizes to intracellular membranes, particularly endoplasmic reticulum subdomains surrounding lipid droplets, in both immortalized adipocytes and mouse adipose tissue. Upon lipolysis, locally released fatty acids appear to rapidly activate this intracellular FFA4 pool, leading to G i /o protein signaling and preferential reduction of cyclic adenosine monophosphate levels near lipid droplets. These mechanisms are required for efficient FFA4-mediated lipolysis regulation, as shown using tethered mini-Gα i/o proteins to locally inhibit G i/o signaling. These findings reveal an unexpected ‘intracrine’ GPCR signaling modality involved in the local regulation of cell metabolism, with biological and pharmacological implications.
Funding Information
  • Wellcome Trust (212313/Z/18/Z)
  • RCUK | Medical Research Council (MR/Z505973/1)
  • Gouvernement du Canada | Canadian Institutes of Health Research (PJT-183758)
  • Cancer Research UK (C17422/A25154)
  • Cancer Research UK (SEBSTF-2021\100002)
  • RCUK | Biotechnology and Biological Sciences Research Council (BB/R001480/1)

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