Evidence that RXFP4 is located in enterochromaffin cells and can regulate production and release of serotonin
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-...
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description | 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. |
doi_str_mv | 10.1042/BSR20221956 |
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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.</description><identifier>ISSN: 0144-8463</identifier><identifier>EISSN: 1573-4935</identifier><identifier>DOI: 10.1042/BSR20221956</identifier><identifier>PMID: 36947541</identifier><language>eng</language><publisher>England: Portland Press Ltd The Biochemical Society</publisher><subject>Animals ; Antibodies ; Constipation ; Cyclic AMP ; Datasets ; Endocrinology ; Enterochromaffin Cells - metabolism ; Food intake ; Forskolin ; G protein-coupled receptors ; Gastric motility ; Gastrointestinal, Renal & Hepatic Systems ; Gene expression ; Humans ; Insulin ; Insulin - metabolism ; Insulin-like growth factors ; Laboratory animals ; Ligands ; Mice ; Motility ; mRNA ; Nucleotide sequence ; Peptides ; Receptors ; Receptors, G-Protein-Coupled - genetics ; Receptors, G-Protein-Coupled - metabolism ; Receptors, Peptide - chemistry ; Receptors, Peptide - genetics ; Receptors, Peptide - metabolism ; Relaxin ; RNA, Messenger - genetics ; Serotonin ; Serotonin - metabolism</subject><ispartof>Bioscience reports, 2023-04, Vol.43 (4), p.1</ispartof><rights>2023 The Author(s).</rights><rights>2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright Portland Press Ltd The Biochemical Society Apr 2023</rights><rights>2023 The Author(s). 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-c8fbd2742426868d15a5f43bc566e26525cf058d8b2994ff1a839ea11573f3bd3</citedby><cites>FETCH-LOGICAL-c438t-c8fbd2742426868d15a5f43bc566e26525cf058d8b2994ff1a839ea11573f3bd3</cites><orcidid>0000-0001-6848-4767 ; 0000-0001-9742-5811</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086114/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2924007088?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,12724,12753,21367,21371,27901,27902,33429,33430,33721,33722,34311,34312,36242,36243,43592,43781,44049,44380,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36947541$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fernando, Shalinda J A</creatorcontrib><creatorcontrib>Wang, Qian</creatorcontrib><creatorcontrib>Hay, Debbie L</creatorcontrib><creatorcontrib>Bathgate, Ross A D</creatorcontrib><creatorcontrib>Shepherd, Peter R</creatorcontrib><creatorcontrib>Lee, Kate L</creatorcontrib><title>Evidence that RXFP4 is located in enterochromaffin cells and can regulate production and release of serotonin</title><title>Bioscience reports</title><addtitle>Biosci Rep</addtitle><description>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.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Constipation</subject><subject>Cyclic AMP</subject><subject>Datasets</subject><subject>Endocrinology</subject><subject>Enterochromaffin Cells - metabolism</subject><subject>Food intake</subject><subject>Forskolin</subject><subject>G protein-coupled receptors</subject><subject>Gastric motility</subject><subject>Gastrointestinal, Renal & Hepatic Systems</subject><subject>Gene expression</subject><subject>Humans</subject><subject>Insulin</subject><subject>Insulin - metabolism</subject><subject>Insulin-like growth factors</subject><subject>Laboratory animals</subject><subject>Ligands</subject><subject>Mice</subject><subject>Motility</subject><subject>mRNA</subject><subject>Nucleotide sequence</subject><subject>Peptides</subject><subject>Receptors</subject><subject>Receptors, G-Protein-Coupled - genetics</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>Receptors, Peptide - chemistry</subject><subject>Receptors, Peptide - genetics</subject><subject>Receptors, Peptide - metabolism</subject><subject>Relaxin</subject><subject>RNA, Messenger - genetics</subject><subject>Serotonin</subject><subject>Serotonin - metabolism</subject><issn>0144-8463</issn><issn>1573-4935</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kU1rFTEYhYMo9ra6ci8BN0IZffM5yUq0tCoUlKrgLmTy0TtlJrkmMwX_vbm2lurCVSDnySEPB6FnBF4R4PT1uy8XFCglWsgHaENEzzqumXiINkA47xSX7AAd1noFAC3gj9EBk5r3gpMNmk-vRx-SC3jZ2gVffD_7zPFY8ZSdXYLHY8IhLaFkty15tjG2CxemqWKbPHY24RIu16mxeFeyX90y5vQ7K2EKtgacI67t_ZLTmJ6gR9FONTy9PY_Qt7PTrycfuvNP7z-evD3vHGdq6ZyKg6c9p5xKJZUnworI2eCElIFKQYWLIJRXA9Wax0isYjpYsnePbPDsCL256d2twxy8awrFTmZXxtmWnybb0fydpHFrLvO1IQBKEsJbw8vbhpJ_rKEuZh7rXtymkNdqaK90T6gGaOiLf9CrvJbU_AwDzhgBCeJ_FNWUA_SgVKOObyhXcq0lxLs_EzD7tc29tRv9_L7mHftnXvYL526kWg</recordid><startdate>20230426</startdate><enddate>20230426</enddate><creator>Fernando, Shalinda J A</creator><creator>Wang, Qian</creator><creator>Hay, Debbie L</creator><creator>Bathgate, Ross A D</creator><creator>Shepherd, Peter R</creator><creator>Lee, Kate L</creator><general>Portland Press Ltd The Biochemical Society</general><general>Portland Press Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6848-4767</orcidid><orcidid>https://orcid.org/0000-0001-9742-5811</orcidid></search><sort><creationdate>20230426</creationdate><title>Evidence that RXFP4 is located in enterochromaffin cells and can regulate production and release of serotonin</title><author>Fernando, Shalinda J A ; Wang, Qian ; Hay, Debbie L ; Bathgate, Ross A D ; Shepherd, Peter R ; Lee, Kate L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-c8fbd2742426868d15a5f43bc566e26525cf058d8b2994ff1a839ea11573f3bd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Constipation</topic><topic>Cyclic AMP</topic><topic>Datasets</topic><topic>Endocrinology</topic><topic>Enterochromaffin Cells - metabolism</topic><topic>Food intake</topic><topic>Forskolin</topic><topic>G protein-coupled receptors</topic><topic>Gastric motility</topic><topic>Gastrointestinal, Renal & Hepatic Systems</topic><topic>Gene expression</topic><topic>Humans</topic><topic>Insulin</topic><topic>Insulin - metabolism</topic><topic>Insulin-like growth factors</topic><topic>Laboratory animals</topic><topic>Ligands</topic><topic>Mice</topic><topic>Motility</topic><topic>mRNA</topic><topic>Nucleotide sequence</topic><topic>Peptides</topic><topic>Receptors</topic><topic>Receptors, G-Protein-Coupled - genetics</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>Receptors, Peptide - chemistry</topic><topic>Receptors, Peptide - genetics</topic><topic>Receptors, Peptide - metabolism</topic><topic>Relaxin</topic><topic>RNA, Messenger - genetics</topic><topic>Serotonin</topic><topic>Serotonin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fernando, Shalinda J A</creatorcontrib><creatorcontrib>Wang, Qian</creatorcontrib><creatorcontrib>Hay, Debbie L</creatorcontrib><creatorcontrib>Bathgate, Ross A D</creatorcontrib><creatorcontrib>Shepherd, Peter R</creatorcontrib><creatorcontrib>Lee, Kate L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Bioscience reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fernando, Shalinda J A</au><au>Wang, Qian</au><au>Hay, Debbie L</au><au>Bathgate, Ross A D</au><au>Shepherd, Peter R</au><au>Lee, Kate L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence that RXFP4 is located in enterochromaffin cells and can regulate production and release of serotonin</atitle><jtitle>Bioscience reports</jtitle><addtitle>Biosci Rep</addtitle><date>2023-04-26</date><risdate>2023</risdate><volume>43</volume><issue>4</issue><spage>1</spage><pages>1-</pages><issn>0144-8463</issn><eissn>1573-4935</eissn><abstract>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.</abstract><cop>England</cop><pub>Portland Press Ltd The Biochemical Society</pub><pmid>36947541</pmid><doi>10.1042/BSR20221956</doi><orcidid>https://orcid.org/0000-0001-6848-4767</orcidid><orcidid>https://orcid.org/0000-0001-9742-5811</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibodies Constipation Cyclic AMP Datasets Endocrinology Enterochromaffin Cells - metabolism Food intake Forskolin G protein-coupled receptors Gastric motility Gastrointestinal, Renal & Hepatic Systems Gene expression Humans Insulin Insulin - metabolism Insulin-like growth factors Laboratory animals Ligands Mice Motility mRNA Nucleotide sequence Peptides Receptors Receptors, G-Protein-Coupled - genetics Receptors, G-Protein-Coupled - metabolism Receptors, Peptide - chemistry Receptors, Peptide - genetics Receptors, Peptide - metabolism Relaxin RNA, Messenger - genetics Serotonin Serotonin - metabolism |
title | Evidence that RXFP4 is located in enterochromaffin cells and can regulate production and release of serotonin |
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