Molecular, biochemical and behavioural evidence for a novel oxytocin receptor and serotonin 2C receptor heterocomplex

• Published in: Neuropharmacology Vol. 183; p. 108394
• Main Authors: Chruścicka, Barbara, Cowan, Caitlin S.M., Wallace Fitzsimons, Shauna E., Borroto-Escuela, Dasiel O., Druelle, Clémentine M., Stamou, Panagiota, Bergmann, Cristian A., Dinan, Timothy G., Slattery, David A., Fuxe, Kjell, Cryan, John F., Schellekens, Harriët
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01-02-2021
• Subjects: 5-HTR2C; GPCR crosstalk; Heteroreceptor complexes; Hypoactivity; Medicin och hälsovetenskap; OTR; Heteroreceptor complexes; OTR; 5-HTR2C; Hypoactivity; GPCR crosstalk; 5-HTR(2C)
• ISSN: 0028-3908; 1873-7064; 1873-7064
• DOI: 10.1016/j.neuropharm.2020.108394

The complexity of oxytocin-mediated functions is strongly associated with its modulatory effects on other neurotransmission systems, including the serotonin (5-hydroxytryptamine, 5-HT) system. Signalling between oxytocin (OT) and 5-HT has been demonstrated during neurodevelopment and in the regulation of specific emotion-based behaviours. It is suggested that crosstalk between neurotransmitters is driven by interaction between their specific receptors, particularly the oxytocin receptor (OTR) and the 5-hydroxytryptamine 2C receptor (5-HTR2C), but evidence for this and the downstream signalling consequences that follow are lacking. Considering the overlapping central expression profiles and shared involvement of OTR and 5-HTR2C in certain endocrine functions and behaviours, including eating behaviour, social interaction and locomotor activity, we investigated the existence of functionally active OTR/5-HTR2C heterocomplexes. Here, we demonstrate evidence for a potential physical interaction between OTR and 5-HTR2Cin vitro in a cellular expression system using flow cytometry-based FRET (fcFRET). We could recapitulate this finding under endogenous expression levels of both receptors via in silico analysis of single cell transcriptomic data and ex vivo proximity ligation assay (PLA). Next, we show that co-expression of the OTR/5-HTR2C pair resulted in a significant depletion of OTR-mediated Gαq-signalling and significant changes in receptor trafficking. Of note, attenuation of OTR-mediated downstream signalling was restored following pharmacological blockade of the 5-HTR2C. Finally, we demonstrated a functional relevance of this novel heterocomplex, in vivo, as 5-HTR2C antagonism increased OT-mediated hypoactivity in mice. Overall, we provide compelling evidence for the formation of functionally active OTR/5-HTR2C heterocomplexes, adding another level of complexity to OTR and 5-HTR2C signalling functionality.
This article is part of the special issue on Neuropeptides.
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•Novel OTR/5-HTR2C heteroreceptor complex identified in vitro in cellular expression system and ex vivo in rodent brain.•Depletion of OTR-mediated Gαq signalling upon OTR/5-HTR2C co-expression in cells.•Restoration of OTR-mediated downstream signalling following 5-HTR2C antagonism in cells co-expressing both receptors.•5-HTR2C antagonism augments OT-mediated hypoactivity of mice in vivo.