Evidence that RXFP4 is located in enterochromaffin cells and can regulate production and release of serotonin.


Journal

Bioscience reports
ISSN: 1573-4935
Titre abrégé: Biosci Rep
Pays: England
ID NLM: 8102797

Informations de publication

Date de publication:
26 04 2023
Historique:
received: 17 09 2022
revised: 26 02 2023
accepted: 22 03 2023
medline: 11 4 2023
pubmed: 23 3 2023
entrez: 22 3 2023
Statut: ppublish

Résumé

RXFP4 is a G protein-coupled receptor (GPCR) in the relaxin family. It has recently been recognised that this receptor and its cognate ligand INSL5 may have a role in the regulation of food intake, gut motility, and other functions relevant to metabolic health and disease. Recent data from reporter-mice showed co-location of Rxfp4 and serotonin (5-HT) in the lower gut. We used human single-cell RNA sequence data (scRNASeq) to show that RXFP4 is in a subset of gut enterochromaffin cells that produce 5-HT in humans. We also used RNAScope to show co-location of Rxfp4 mRNA and 5-HT in mouse colon, confirming prior findings. To understand whether RXFP4 might regulate serotonin production, we developed a cell model using Colo320, a human gut-derived immortalised cell line that produces and releases serotonin. Overexpression of RXFP4 in these cells resulted in a constitutive decrease in cAMP levels in both the basal state and in cells treated with forskolin. Treatment of cells with two RXFP4 agonists, INSL5 derived peptide INSL5-A13 and small molecule compound-4, further reduced cAMP levels. This was paralleled by a reduction in expression of mRNA for TPH1, the enzyme controlling the rate limiting step in the production of serotonin. Overexpression of RXFP4 also attenuated the cAMP-induced release of serotonin from Colo320 cells. Together this demonstrates that serotonin producing enterochromaffin cells are the major site of RXFP4 expression in the gut and that RXFP4 can have inhibitory functional impacts on cAMP production as well as TPH1 expression and serotonin release.

Identifiants

pubmed: 36947541
pii: 232789
doi: 10.1042/BSR20221956
pmc: PMC10086114
pii:
doi:

Substances chimiques

Insulin 0
Receptors, G-Protein-Coupled 0
Receptors, Peptide 0
RNA, Messenger 0
RXFP4 protein, human 0
RXFP4 protein, mouse 0
Serotonin 333DO1RDJY

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023 The Author(s).

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Auteurs

Shalinda J A Fernando (SJA)

Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Maurice Wilkins Centre for Molecular Biodiscovery, New Zealand.

Qian Wang (Q)

Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Maurice Wilkins Centre for Molecular Biodiscovery, New Zealand.

Debbie L Hay (DL)

Maurice Wilkins Centre for Molecular Biodiscovery, New Zealand.
Department of Pharmacology and Toxicology, University of Otago, Dunedin, New Zealand.

Ross A D Bathgate (RAD)

Florey Institute of Neuroscience and Mental Health and Department of Biochemistry and Pharmacology, University of Melbourne, Parkville, Victoria, Australia.

Peter R Shepherd (PR)

Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Maurice Wilkins Centre for Molecular Biodiscovery, New Zealand.

Kate L Lee (KL)

Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Maurice Wilkins Centre for Molecular Biodiscovery, New Zealand.

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Classifications MeSH