A subset of mouse colonic goblet cells expresses the bitter taste receptor Tas2r131
The concept that gut nutrient sensing involves taste receptors has been fueled by recent reports associating the expression of taste receptors and taste-associated signaling molecules in the gut and in gut-derived cell lines with physiological responses induced by known taste stimuli. However, for b...
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description | The concept that gut nutrient sensing involves taste receptors has been fueled by recent reports associating the expression of taste receptors and taste-associated signaling molecules in the gut and in gut-derived cell lines with physiological responses induced by known taste stimuli. However, for bitter taste receptors (Tas2rs), direct evidence for their functional role in gut physiology is scarce and their cellular expression pattern remained unknown. We therefore investigated Tas2r expression in mice. RT-PCR experiments assessed the presence of mRNA for Tas2rs and taste signaling molecules in the gut. A gene-targeted mouse strain was established to visualize and identify cell types expressing the bitter receptor Tas2r131. Messenger RNA for various Tas2rs and taste signaling molecules were detected by RT-PCR in the gut. Using our knock-in mouse strain we demonstrate that a subset of colonic goblet cells express Tas2r131. Cells that express this receptor are absent in the upper gut and do not correspond to enteroendocrine and brush cells. Expression in colonic goblet cells is consistent with a role of Tas2rs in defense mechanisms against potentially harmful xenobiotics. |
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However, for bitter taste receptors (Tas2rs), direct evidence for their functional role in gut physiology is scarce and their cellular expression pattern remained unknown. We therefore investigated Tas2r expression in mice. RT-PCR experiments assessed the presence of mRNA for Tas2rs and taste signaling molecules in the gut. A gene-targeted mouse strain was established to visualize and identify cell types expressing the bitter receptor Tas2r131. Messenger RNA for various Tas2rs and taste signaling molecules were detected by RT-PCR in the gut. Using our knock-in mouse strain we demonstrate that a subset of colonic goblet cells express Tas2r131. Cells that express this receptor are absent in the upper gut and do not correspond to enteroendocrine and brush cells. Expression in colonic goblet cells is consistent with a role of Tas2rs in defense mechanisms against potentially harmful xenobiotics.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0082820</identifier><identifier>PMID: 24367558</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animal experimentation ; Animals ; Bitter taste ; Cell lines ; Cells, Cultured ; Colon - cytology ; Gastrointestinal surgery ; Gene expression ; Goblet cells ; Goblet Cells - metabolism ; Immunohistochemistry ; In Situ Hybridization ; Integrases - genetics ; Integrases - metabolism ; Mice ; Mice, Inbred C57BL ; mRNA ; Nutrition ; Physiological aspects ; Physiological responses ; Physiology ; Polymerase chain reaction ; Receptors ; Receptors, G-Protein-Coupled - genetics ; Receptors, G-Protein-Coupled - metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Ribonucleic acid ; RNA ; Rodents ; Signaling ; Studies ; Taste ; Taste receptors ; Taste stimuli ; Toxicology ; Xenobiotics</subject><ispartof>PloS one, 2013-12, Vol.8 (12), p.e82820</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Prandi et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Prandi et al 2013 Prandi et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c809t-b3449a5df1ea69763873c170bd4f0ecece3fb140bea3bf442000ff12a9cd255f3</citedby><cites>FETCH-LOGICAL-c809t-b3449a5df1ea69763873c170bd4f0ecece3fb140bea3bf442000ff12a9cd255f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867391/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867391/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24367558$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Glendinning, John I.</contributor><creatorcontrib>Prandi, Simone</creatorcontrib><creatorcontrib>Bromke, Marta</creatorcontrib><creatorcontrib>Hübner, Sandra</creatorcontrib><creatorcontrib>Voigt, Anja</creatorcontrib><creatorcontrib>Boehm, Ulrich</creatorcontrib><creatorcontrib>Meyerhof, Wolfgang</creatorcontrib><creatorcontrib>Behrens, Maik</creatorcontrib><title>A subset of mouse colonic goblet cells expresses the bitter taste receptor Tas2r131</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The concept that gut nutrient sensing involves taste receptors has been fueled by recent reports associating the expression of taste receptors and taste-associated signaling molecules in the gut and in gut-derived cell lines with physiological responses induced by known taste stimuli. However, for bitter taste receptors (Tas2rs), direct evidence for their functional role in gut physiology is scarce and their cellular expression pattern remained unknown. We therefore investigated Tas2r expression in mice. RT-PCR experiments assessed the presence of mRNA for Tas2rs and taste signaling molecules in the gut. A gene-targeted mouse strain was established to visualize and identify cell types expressing the bitter receptor Tas2r131. Messenger RNA for various Tas2rs and taste signaling molecules were detected by RT-PCR in the gut. Using our knock-in mouse strain we demonstrate that a subset of colonic goblet cells express Tas2r131. Cells that express this receptor are absent in the upper gut and do not correspond to enteroendocrine and brush cells. Expression in colonic goblet cells is consistent with a role of Tas2rs in defense mechanisms against potentially harmful xenobiotics.</description><subject>Animal experimentation</subject><subject>Animals</subject><subject>Bitter taste</subject><subject>Cell lines</subject><subject>Cells, Cultured</subject><subject>Colon - cytology</subject><subject>Gastrointestinal surgery</subject><subject>Gene expression</subject><subject>Goblet cells</subject><subject>Goblet Cells - metabolism</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>Integrases - genetics</subject><subject>Integrases - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>mRNA</subject><subject>Nutrition</subject><subject>Physiological aspects</subject><subject>Physiological responses</subject><subject>Physiology</subject><subject>Polymerase chain reaction</subject><subject>Receptors</subject><subject>Receptors, G-Protein-Coupled - genetics</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Rodents</subject><subject>Signaling</subject><subject>Studies</subject><subject>Taste</subject><subject>Taste receptors</subject><subject>Taste stimuli</subject><subject>Toxicology</subject><subject>Xenobiotics</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl2L1DAUhoso7rr6D0QLguDFjPlq2twIw-LHwMKCu3ob0vSkkyHTjEkq678343SXKShILhJOnvOew8tbFC8xWmJa4_dbP4ZBueXeD7BEqCENQY-KcywoWXCC6OOT91nxLMYtQhVtOH9anBFGeV1VzXlxsyrj2EZIpTflzo8RSu2dH6wue9-6XNfgXCzhbh8gRohl2kDZ2pQglEnFBGUADfvkQ3mrIgmY4ufFE6NchBfTfVF8-_Tx9vLL4ur68_pydbXQDRJp0VLGhKo6g0FxUXPa1FTjGrUdMyhraqCmxQy1oGhrGCMIIWMwUUJ3pKoMvSheH3X3zkc5-RElZlxQxDihmVgfic6rrdwHu1Phl_TKyj8FH3qpQrLagVQAXS0UEaozjANvkWCG1xihTtSgD9M-TNPGdgedhiEF5Wai85_BbmTvf8rseU0FzgJvJoHgf4wQ0z9Wnqhe5a3sYHwW0zsbtVyxuiFEVE2VqeVfqHw62FmdE2Fsrs8a3s0aMpPgLvVqjFGub77-P3v9fc6-PWE3oFzaRO_GZP0Q5yA7gjr4GAOYB-cwkodA37shD4GWU6Bz26tT1x-a7hNMfwOmpvEU</recordid><startdate>20131218</startdate><enddate>20131218</enddate><creator>Prandi, Simone</creator><creator>Bromke, Marta</creator><creator>Hübner, Sandra</creator><creator>Voigt, Anja</creator><creator>Boehm, Ulrich</creator><creator>Meyerhof, Wolfgang</creator><creator>Behrens, Maik</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20131218</creationdate><title>A subset of mouse colonic goblet cells expresses the bitter taste receptor Tas2r131</title><author>Prandi, Simone ; Bromke, Marta ; Hübner, Sandra ; Voigt, Anja ; Boehm, Ulrich ; Meyerhof, Wolfgang ; Behrens, Maik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c809t-b3449a5df1ea69763873c170bd4f0ecece3fb140bea3bf442000ff12a9cd255f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animal experimentation</topic><topic>Animals</topic><topic>Bitter taste</topic><topic>Cell lines</topic><topic>Cells, Cultured</topic><topic>Colon - cytology</topic><topic>Gastrointestinal surgery</topic><topic>Gene expression</topic><topic>Goblet cells</topic><topic>Goblet Cells - metabolism</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization</topic><topic>Integrases - genetics</topic><topic>Integrases - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>mRNA</topic><topic>Nutrition</topic><topic>Physiological aspects</topic><topic>Physiological responses</topic><topic>Physiology</topic><topic>Polymerase chain reaction</topic><topic>Receptors</topic><topic>Receptors, G-Protein-Coupled - genetics</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Rodents</topic><topic>Signaling</topic><topic>Studies</topic><topic>Taste</topic><topic>Taste receptors</topic><topic>Taste stimuli</topic><topic>Toxicology</topic><topic>Xenobiotics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prandi, Simone</creatorcontrib><creatorcontrib>Bromke, Marta</creatorcontrib><creatorcontrib>Hübner, Sandra</creatorcontrib><creatorcontrib>Voigt, Anja</creatorcontrib><creatorcontrib>Boehm, Ulrich</creatorcontrib><creatorcontrib>Meyerhof, Wolfgang</creatorcontrib><creatorcontrib>Behrens, Maik</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</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>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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However, for bitter taste receptors (Tas2rs), direct evidence for their functional role in gut physiology is scarce and their cellular expression pattern remained unknown. We therefore investigated Tas2r expression in mice. RT-PCR experiments assessed the presence of mRNA for Tas2rs and taste signaling molecules in the gut. A gene-targeted mouse strain was established to visualize and identify cell types expressing the bitter receptor Tas2r131. Messenger RNA for various Tas2rs and taste signaling molecules were detected by RT-PCR in the gut. Using our knock-in mouse strain we demonstrate that a subset of colonic goblet cells express Tas2r131. Cells that express this receptor are absent in the upper gut and do not correspond to enteroendocrine and brush cells. Expression in colonic goblet cells is consistent with a role of Tas2rs in defense mechanisms against potentially harmful xenobiotics.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24367558</pmid><doi>10.1371/journal.pone.0082820</doi><tpages>e82820</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal experimentation Animals Bitter taste Cell lines Cells, Cultured Colon - cytology Gastrointestinal surgery Gene expression Goblet cells Goblet Cells - metabolism Immunohistochemistry In Situ Hybridization Integrases - genetics Integrases - metabolism Mice Mice, Inbred C57BL mRNA Nutrition Physiological aspects Physiological responses Physiology Polymerase chain reaction Receptors Receptors, G-Protein-Coupled - genetics Receptors, G-Protein-Coupled - metabolism Reverse Transcriptase Polymerase Chain Reaction Ribonucleic acid RNA Rodents Signaling Studies Taste Taste receptors Taste stimuli Toxicology Xenobiotics |
title | A subset of mouse colonic goblet cells expresses the bitter taste receptor Tas2r131 |
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