Visualising functional 5-HT 3 receptors containing A and C subunits at or near the cell surface
Five different subunits of the human serotonin 3 (5-hydroxytrptamine 3; 5-HT ) receptor exist and these are present in both central and peripheral systems. Different subunits alter the efficacy of 5-HT receptor antagonists used to treat diarrhoea predominant-irritable bowel syndrome, chemotherapy in...
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Veröffentlicht in: | Biomedicine & pharmacotherapy 2020-12, Vol.132, p.110860 |
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creator | Abad, Isaiah P L Fam, Ray L Nguyen, Dan-Thanh Nowell, Cameron J Trinh, Phuc N H Manallack, David T Freihat, Lubna A Chakrabarti, Jay Jamil, Aamani Exintaris, Betty Yaakob, Nor S Irving, Helen R |
description | Five different subunits of the human serotonin 3 (5-hydroxytrptamine 3; 5-HT
) receptor exist and these are present in both central and peripheral systems. Different subunits alter the efficacy of 5-HT
receptor antagonists used to treat diarrhoea predominant-irritable bowel syndrome, chemotherapy induced nausea and vomiting and depression. Cell surface arrangement of 5-HT
receptor complexes and the contribution of C, D and E subunits to receptor function is poorly understood. Here, we examine interactions of A and C subunits using 5-HT
receptor subunits containing fluorescent protein inserts between the 3rd and 4th transmembrane spanning region. HEK293T cells that do not normally express 5-HT
receptor subunits, were transiently transfected with A or C or both subunits. Patch clamp experiments show that cells transfected with either fluorescent protein tagged A or A and C subunits generate whole cell currents in response to 5-HT. These findings correlate with the apparent distribution of fluorescent protein tagged A and C subunits at or near cell surfaces detected using TIRF microscopy. In co-transfected cells, the A and C subunits are associated forming AC heteromer complexes at or near the cell surface and a proportion can also form A or C homomers. In conclusion, it is likely that both A homomers and AC heteromers contribute to whole cell currents in response to 5-HT with minimal contribution from C homomers. |
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) receptor exist and these are present in both central and peripheral systems. Different subunits alter the efficacy of 5-HT
receptor antagonists used to treat diarrhoea predominant-irritable bowel syndrome, chemotherapy induced nausea and vomiting and depression. Cell surface arrangement of 5-HT
receptor complexes and the contribution of C, D and E subunits to receptor function is poorly understood. Here, we examine interactions of A and C subunits using 5-HT
receptor subunits containing fluorescent protein inserts between the 3rd and 4th transmembrane spanning region. HEK293T cells that do not normally express 5-HT
receptor subunits, were transiently transfected with A or C or both subunits. Patch clamp experiments show that cells transfected with either fluorescent protein tagged A or A and C subunits generate whole cell currents in response to 5-HT. These findings correlate with the apparent distribution of fluorescent protein tagged A and C subunits at or near cell surfaces detected using TIRF microscopy. In co-transfected cells, the A and C subunits are associated forming AC heteromer complexes at or near the cell surface and a proportion can also form A or C homomers. In conclusion, it is likely that both A homomers and AC heteromers contribute to whole cell currents in response to 5-HT with minimal contribution from C homomers.</description><identifier>EISSN: 1950-6007</identifier><identifier>PMID: 33059258</identifier><language>eng</language><publisher>France</publisher><subject>HEK293 Cells ; Humans ; Patch-Clamp Techniques ; Receptors, Serotonin, 5-HT3 - chemistry ; Receptors, Serotonin, 5-HT3 - drug effects ; Receptors, Serotonin, 5-HT3 - metabolism ; Serotonin 5-HT3 Receptor Antagonists - pharmacology ; Transfection</subject><ispartof>Biomedicine & pharmacotherapy, 2020-12, Vol.132, p.110860</ispartof><rights>Copyright © 2020 The Authors. Published by Elsevier Masson SAS.. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33059258$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abad, Isaiah P L</creatorcontrib><creatorcontrib>Fam, Ray L</creatorcontrib><creatorcontrib>Nguyen, Dan-Thanh</creatorcontrib><creatorcontrib>Nowell, Cameron J</creatorcontrib><creatorcontrib>Trinh, Phuc N H</creatorcontrib><creatorcontrib>Manallack, David T</creatorcontrib><creatorcontrib>Freihat, Lubna A</creatorcontrib><creatorcontrib>Chakrabarti, Jay</creatorcontrib><creatorcontrib>Jamil, Aamani</creatorcontrib><creatorcontrib>Exintaris, Betty</creatorcontrib><creatorcontrib>Yaakob, Nor S</creatorcontrib><creatorcontrib>Irving, Helen R</creatorcontrib><title>Visualising functional 5-HT 3 receptors containing A and C subunits at or near the cell surface</title><title>Biomedicine & pharmacotherapy</title><addtitle>Biomed Pharmacother</addtitle><description>Five different subunits of the human serotonin 3 (5-hydroxytrptamine 3; 5-HT
) receptor exist and these are present in both central and peripheral systems. Different subunits alter the efficacy of 5-HT
receptor antagonists used to treat diarrhoea predominant-irritable bowel syndrome, chemotherapy induced nausea and vomiting and depression. Cell surface arrangement of 5-HT
receptor complexes and the contribution of C, D and E subunits to receptor function is poorly understood. Here, we examine interactions of A and C subunits using 5-HT
receptor subunits containing fluorescent protein inserts between the 3rd and 4th transmembrane spanning region. HEK293T cells that do not normally express 5-HT
receptor subunits, were transiently transfected with A or C or both subunits. Patch clamp experiments show that cells transfected with either fluorescent protein tagged A or A and C subunits generate whole cell currents in response to 5-HT. These findings correlate with the apparent distribution of fluorescent protein tagged A and C subunits at or near cell surfaces detected using TIRF microscopy. In co-transfected cells, the A and C subunits are associated forming AC heteromer complexes at or near the cell surface and a proportion can also form A or C homomers. In conclusion, it is likely that both A homomers and AC heteromers contribute to whole cell currents in response to 5-HT with minimal contribution from C homomers.</description><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Patch-Clamp Techniques</subject><subject>Receptors, Serotonin, 5-HT3 - chemistry</subject><subject>Receptors, Serotonin, 5-HT3 - drug effects</subject><subject>Receptors, Serotonin, 5-HT3 - metabolism</subject><subject>Serotonin 5-HT3 Receptor Antagonists - pharmacology</subject><subject>Transfection</subject><issn>1950-6007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFjksKwjAUAIMgtn6uIO8ChWhIbZdSFA9Q3JbXNNVImpa8ZOHtVdC1q1nMLGbG0l0peZZzfkjYkujBOZe5KBYsEYLLci-LlDVXQxGtIeNu0EenghkdWpDZpQYBXis9hdETqNEFNO6THQFdBxVQbKMzgQADjB6cRg_hrkFpa9_S96j0ms17tKQ3X67Y9nyqq0s2xXbQXTN5M6B_Nr8j8Td4AU6nQMc</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Abad, Isaiah P L</creator><creator>Fam, Ray L</creator><creator>Nguyen, Dan-Thanh</creator><creator>Nowell, Cameron J</creator><creator>Trinh, Phuc N H</creator><creator>Manallack, David T</creator><creator>Freihat, Lubna A</creator><creator>Chakrabarti, Jay</creator><creator>Jamil, Aamani</creator><creator>Exintaris, Betty</creator><creator>Yaakob, Nor S</creator><creator>Irving, Helen R</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>202012</creationdate><title>Visualising functional 5-HT 3 receptors containing A and C subunits at or near the cell surface</title><author>Abad, Isaiah P L ; Fam, Ray L ; Nguyen, Dan-Thanh ; Nowell, Cameron J ; Trinh, Phuc N H ; Manallack, David T ; Freihat, Lubna A ; Chakrabarti, Jay ; Jamil, Aamani ; Exintaris, Betty ; Yaakob, Nor S ; Irving, Helen R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_330592583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>HEK293 Cells</topic><topic>Humans</topic><topic>Patch-Clamp Techniques</topic><topic>Receptors, Serotonin, 5-HT3 - chemistry</topic><topic>Receptors, Serotonin, 5-HT3 - drug effects</topic><topic>Receptors, Serotonin, 5-HT3 - metabolism</topic><topic>Serotonin 5-HT3 Receptor Antagonists - pharmacology</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abad, Isaiah P L</creatorcontrib><creatorcontrib>Fam, Ray L</creatorcontrib><creatorcontrib>Nguyen, Dan-Thanh</creatorcontrib><creatorcontrib>Nowell, Cameron J</creatorcontrib><creatorcontrib>Trinh, Phuc N H</creatorcontrib><creatorcontrib>Manallack, David T</creatorcontrib><creatorcontrib>Freihat, Lubna A</creatorcontrib><creatorcontrib>Chakrabarti, Jay</creatorcontrib><creatorcontrib>Jamil, Aamani</creatorcontrib><creatorcontrib>Exintaris, Betty</creatorcontrib><creatorcontrib>Yaakob, Nor S</creatorcontrib><creatorcontrib>Irving, Helen R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Biomedicine & pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abad, Isaiah P L</au><au>Fam, Ray L</au><au>Nguyen, Dan-Thanh</au><au>Nowell, Cameron J</au><au>Trinh, Phuc N H</au><au>Manallack, David T</au><au>Freihat, Lubna A</au><au>Chakrabarti, Jay</au><au>Jamil, Aamani</au><au>Exintaris, Betty</au><au>Yaakob, Nor S</au><au>Irving, Helen R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Visualising functional 5-HT 3 receptors containing A and C subunits at or near the cell surface</atitle><jtitle>Biomedicine & pharmacotherapy</jtitle><addtitle>Biomed Pharmacother</addtitle><date>2020-12</date><risdate>2020</risdate><volume>132</volume><spage>110860</spage><pages>110860-</pages><eissn>1950-6007</eissn><abstract>Five different subunits of the human serotonin 3 (5-hydroxytrptamine 3; 5-HT
) receptor exist and these are present in both central and peripheral systems. Different subunits alter the efficacy of 5-HT
receptor antagonists used to treat diarrhoea predominant-irritable bowel syndrome, chemotherapy induced nausea and vomiting and depression. Cell surface arrangement of 5-HT
receptor complexes and the contribution of C, D and E subunits to receptor function is poorly understood. Here, we examine interactions of A and C subunits using 5-HT
receptor subunits containing fluorescent protein inserts between the 3rd and 4th transmembrane spanning region. HEK293T cells that do not normally express 5-HT
receptor subunits, were transiently transfected with A or C or both subunits. Patch clamp experiments show that cells transfected with either fluorescent protein tagged A or A and C subunits generate whole cell currents in response to 5-HT. These findings correlate with the apparent distribution of fluorescent protein tagged A and C subunits at or near cell surfaces detected using TIRF microscopy. In co-transfected cells, the A and C subunits are associated forming AC heteromer complexes at or near the cell surface and a proportion can also form A or C homomers. In conclusion, it is likely that both A homomers and AC heteromers contribute to whole cell currents in response to 5-HT with minimal contribution from C homomers.</abstract><cop>France</cop><pmid>33059258</pmid></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete; EZB-FREE-00999 freely available EZB journals |
subjects | HEK293 Cells Humans Patch-Clamp Techniques Receptors, Serotonin, 5-HT3 - chemistry Receptors, Serotonin, 5-HT3 - drug effects Receptors, Serotonin, 5-HT3 - metabolism Serotonin 5-HT3 Receptor Antagonists - pharmacology Transfection |
title | Visualising functional 5-HT 3 receptors containing A and C subunits at or near the cell surface |
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