Positive Allosteric Modulation of the Calcium-sensing Receptor by Physiological Concentrations of Glucose
The calcium-sensing receptor (CaSR) is activated by various cations, cationic compounds, and amino acids. In the present study we investigated the effect of glucose on CaSR in HEK293 cells stably expressing human CaSR (HEK-CaSR cells). When glucose concentration in the buffer was raised from 3 to 25...
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description | The calcium-sensing receptor (CaSR) is activated by various cations, cationic compounds, and amino acids. In the present study we investigated the effect of glucose on CaSR in HEK293 cells stably expressing human CaSR (HEK-CaSR cells). When glucose concentration in the buffer was raised from 3 to 25 mm, a rapid elevation of cytoplasmic Ca2+ concentration ([Ca2+]c) was observed. This elevation was immediate and transient and was followed by a sustained decrease in [Ca2+]c. The effect of glucose was detected at a concentration of 4 mm and reached its maximum at 5 mm. 3-O-Methylglucose, a non-metabolizable analogue of glucose, reproduced the effect of glucose. Sucrose also induced an elevation of [Ca2+]c in HEK-CaSR cells. Similarly, sucralose was nearly as effective as glucose in inducing elevation of [Ca2+]c. Glucose was not able to increase [Ca2+]c in the absence of extracellular Ca2+. The effect of glucose on [Ca2+]c was inhibited by NPS-2143, an allosteric inhibitor of CaSR. In addition, NPS-2143 also inhibited the [Ca2+]c responses to sucralose and sucrose. Glucose as well as sucralose decreased cytoplasmic cAMP concentration in HEK-CaSR cells. The reduction of cAMP induced by glucose was blocked by pertussis toxin. Likewise, sucralose reduced [cAMP]c. Finally, glucose increased [Ca2+]c in PT-r parathyroid cells and in Madin-Darby canine kidney cells, both of which express endogenous CaSR. These results indicate that glucose acts as a positive allosteric modulator of CaSR. |
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In the present study we investigated the effect of glucose on CaSR in HEK293 cells stably expressing human CaSR (HEK-CaSR cells). When glucose concentration in the buffer was raised from 3 to 25 mm, a rapid elevation of cytoplasmic Ca2+ concentration ([Ca2+]c) was observed. This elevation was immediate and transient and was followed by a sustained decrease in [Ca2+]c. The effect of glucose was detected at a concentration of 4 mm and reached its maximum at 5 mm. 3-O-Methylglucose, a non-metabolizable analogue of glucose, reproduced the effect of glucose. Sucrose also induced an elevation of [Ca2+]c in HEK-CaSR cells. Similarly, sucralose was nearly as effective as glucose in inducing elevation of [Ca2+]c. Glucose was not able to increase [Ca2+]c in the absence of extracellular Ca2+. The effect of glucose on [Ca2+]c was inhibited by NPS-2143, an allosteric inhibitor of CaSR. In addition, NPS-2143 also inhibited the [Ca2+]c responses to sucralose and sucrose. Glucose as well as sucralose decreased cytoplasmic cAMP concentration in HEK-CaSR cells. The reduction of cAMP induced by glucose was blocked by pertussis toxin. Likewise, sucralose reduced [cAMP]c. Finally, glucose increased [Ca2+]c in PT-r parathyroid cells and in Madin-Darby canine kidney cells, both of which express endogenous CaSR. These results indicate that glucose acts as a positive allosteric modulator of CaSR.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M116.729863</identifier><identifier>PMID: 27613866</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Allosteric Regulation ; beta cell (B-cell) ; calcium ; Calcium - metabolism ; calcium-sensing receptor ; cyclic AMP (cAMP) ; Cytoplasm - chemistry ; Cytoplasm - genetics ; Cytoplasm - metabolism ; G protein-coupled receptor (GPCR) ; glucose ; Glucose - analysis ; Glucose - metabolism ; HEK293 Cells ; Humans ; Receptors, Calcium-Sensing - chemistry ; Receptors, Calcium-Sensing - genetics ; Receptors, Calcium-Sensing - metabolism ; Signal Transduction ; sweet taste receptor</subject><ispartof>The Journal of biological chemistry, 2016-10, Vol.291 (44), p.23126-23135</ispartof><rights>2016 © 2016 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology</rights><rights>2016 by The American Society for Biochemistry and Molecular Biology, Inc.</rights><rights>2016 by The American Society for Biochemistry and Molecular Biology, Inc. 2016 The American Society for Biochemistry and Molecular Biology, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c623t-f7ca9f5b1164f23434ab01cd4a8f4c4a333fc5e56d0ed43c067261b7896873f93</citedby><cites>FETCH-LOGICAL-c623t-f7ca9f5b1164f23434ab01cd4a8f4c4a333fc5e56d0ed43c067261b7896873f93</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/PMC5087731/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087731/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27613866$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Medina, Johan</creatorcontrib><creatorcontrib>Nakagawa, Yuko</creatorcontrib><creatorcontrib>Nagasawa, Masahiro</creatorcontrib><creatorcontrib>Fernandez, Anny</creatorcontrib><creatorcontrib>Sakaguchi, Kazushige</creatorcontrib><creatorcontrib>Kitaguchi, Tetsuya</creatorcontrib><creatorcontrib>Kojima, Itaru</creatorcontrib><title>Positive Allosteric Modulation of the Calcium-sensing Receptor by Physiological Concentrations of Glucose</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>The calcium-sensing receptor (CaSR) is activated by various cations, cationic compounds, and amino acids. In the present study we investigated the effect of glucose on CaSR in HEK293 cells stably expressing human CaSR (HEK-CaSR cells). When glucose concentration in the buffer was raised from 3 to 25 mm, a rapid elevation of cytoplasmic Ca2+ concentration ([Ca2+]c) was observed. This elevation was immediate and transient and was followed by a sustained decrease in [Ca2+]c. The effect of glucose was detected at a concentration of 4 mm and reached its maximum at 5 mm. 3-O-Methylglucose, a non-metabolizable analogue of glucose, reproduced the effect of glucose. Sucrose also induced an elevation of [Ca2+]c in HEK-CaSR cells. Similarly, sucralose was nearly as effective as glucose in inducing elevation of [Ca2+]c. Glucose was not able to increase [Ca2+]c in the absence of extracellular Ca2+. The effect of glucose on [Ca2+]c was inhibited by NPS-2143, an allosteric inhibitor of CaSR. In addition, NPS-2143 also inhibited the [Ca2+]c responses to sucralose and sucrose. Glucose as well as sucralose decreased cytoplasmic cAMP concentration in HEK-CaSR cells. The reduction of cAMP induced by glucose was blocked by pertussis toxin. Likewise, sucralose reduced [cAMP]c. Finally, glucose increased [Ca2+]c in PT-r parathyroid cells and in Madin-Darby canine kidney cells, both of which express endogenous CaSR. These results indicate that glucose acts as a positive allosteric modulator of CaSR.</description><subject>Allosteric Regulation</subject><subject>beta cell (B-cell)</subject><subject>calcium</subject><subject>Calcium - metabolism</subject><subject>calcium-sensing receptor</subject><subject>cyclic AMP (cAMP)</subject><subject>Cytoplasm - chemistry</subject><subject>Cytoplasm - genetics</subject><subject>Cytoplasm - metabolism</subject><subject>G protein-coupled receptor (GPCR)</subject><subject>glucose</subject><subject>Glucose - analysis</subject><subject>Glucose - metabolism</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Receptors, Calcium-Sensing - chemistry</subject><subject>Receptors, Calcium-Sensing - genetics</subject><subject>Receptors, Calcium-Sensing - metabolism</subject><subject>Signal Transduction</subject><subject>sweet taste receptor</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtr3DAUhUVpaCZp190VLbvxRC_L8qYQhjQNJDSEBLoTsnw1o6CxppI9MP--mjoN7aLa3IXOOffxIfSRkiUljbh47uzyjlK5bFirJH-DFpQoXvGa_niLFoQwWrWsVqfoLOdnUp5o6Tt0yhpJuZJygfx9zH70e8CXIcQ8QvIW38V-Cmb0ccDR4XEDeGWC9dO2yjBkP6zxA1jYjTHh7oDvN4fsY4hrb03AqzhYGMb0256P_usw2ZjhPTpxJmT48FLP0dPXq8fVt-r2-_XN6vK2spLxsXKNNa2ru7KUcIwLLkxHqO2FUU5YYTjnztZQy55AL7glsmGSdo1qpWq4a_k5-jLn7qZuC_08TNC75LcmHXQ0Xv_7M_iNXse9rolqGk5LwOeXgBR_TpBHvfXZQghmgDhlTRWvpSKMiSK9mKU2xZwTuNc2lOgjIF0A6SMgPQMqjk9_T_eq_0OkCNpZAOVGew9JZ-uh3LT3Ceyo--j_G_4LfIWicw</recordid><startdate>20161028</startdate><enddate>20161028</enddate><creator>Medina, Johan</creator><creator>Nakagawa, Yuko</creator><creator>Nagasawa, Masahiro</creator><creator>Fernandez, Anny</creator><creator>Sakaguchi, Kazushige</creator><creator>Kitaguchi, Tetsuya</creator><creator>Kojima, Itaru</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20161028</creationdate><title>Positive Allosteric Modulation of the Calcium-sensing Receptor by Physiological Concentrations of Glucose</title><author>Medina, Johan ; Nakagawa, Yuko ; Nagasawa, Masahiro ; Fernandez, Anny ; Sakaguchi, Kazushige ; Kitaguchi, Tetsuya ; Kojima, Itaru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c623t-f7ca9f5b1164f23434ab01cd4a8f4c4a333fc5e56d0ed43c067261b7896873f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Allosteric Regulation</topic><topic>beta cell (B-cell)</topic><topic>calcium</topic><topic>Calcium - metabolism</topic><topic>calcium-sensing receptor</topic><topic>cyclic AMP (cAMP)</topic><topic>Cytoplasm - chemistry</topic><topic>Cytoplasm - genetics</topic><topic>Cytoplasm - metabolism</topic><topic>G protein-coupled receptor (GPCR)</topic><topic>glucose</topic><topic>Glucose - analysis</topic><topic>Glucose - metabolism</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>Receptors, Calcium-Sensing - chemistry</topic><topic>Receptors, Calcium-Sensing - genetics</topic><topic>Receptors, Calcium-Sensing - metabolism</topic><topic>Signal Transduction</topic><topic>sweet taste receptor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Medina, Johan</creatorcontrib><creatorcontrib>Nakagawa, Yuko</creatorcontrib><creatorcontrib>Nagasawa, Masahiro</creatorcontrib><creatorcontrib>Fernandez, Anny</creatorcontrib><creatorcontrib>Sakaguchi, Kazushige</creatorcontrib><creatorcontrib>Kitaguchi, Tetsuya</creatorcontrib><creatorcontrib>Kojima, Itaru</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Medina, Johan</au><au>Nakagawa, Yuko</au><au>Nagasawa, Masahiro</au><au>Fernandez, Anny</au><au>Sakaguchi, Kazushige</au><au>Kitaguchi, Tetsuya</au><au>Kojima, Itaru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Positive Allosteric Modulation of the Calcium-sensing Receptor by Physiological Concentrations of Glucose</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2016-10-28</date><risdate>2016</risdate><volume>291</volume><issue>44</issue><spage>23126</spage><epage>23135</epage><pages>23126-23135</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>The calcium-sensing receptor (CaSR) is activated by various cations, cationic compounds, and amino acids. In the present study we investigated the effect of glucose on CaSR in HEK293 cells stably expressing human CaSR (HEK-CaSR cells). When glucose concentration in the buffer was raised from 3 to 25 mm, a rapid elevation of cytoplasmic Ca2+ concentration ([Ca2+]c) was observed. This elevation was immediate and transient and was followed by a sustained decrease in [Ca2+]c. The effect of glucose was detected at a concentration of 4 mm and reached its maximum at 5 mm. 3-O-Methylglucose, a non-metabolizable analogue of glucose, reproduced the effect of glucose. Sucrose also induced an elevation of [Ca2+]c in HEK-CaSR cells. Similarly, sucralose was nearly as effective as glucose in inducing elevation of [Ca2+]c. Glucose was not able to increase [Ca2+]c in the absence of extracellular Ca2+. The effect of glucose on [Ca2+]c was inhibited by NPS-2143, an allosteric inhibitor of CaSR. In addition, NPS-2143 also inhibited the [Ca2+]c responses to sucralose and sucrose. Glucose as well as sucralose decreased cytoplasmic cAMP concentration in HEK-CaSR cells. The reduction of cAMP induced by glucose was blocked by pertussis toxin. Likewise, sucralose reduced [cAMP]c. Finally, glucose increased [Ca2+]c in PT-r parathyroid cells and in Madin-Darby canine kidney cells, both of which express endogenous CaSR. These results indicate that glucose acts as a positive allosteric modulator of CaSR.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27613866</pmid><doi>10.1074/jbc.M116.729863</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Allosteric Regulation beta cell (B-cell) calcium Calcium - metabolism calcium-sensing receptor cyclic AMP (cAMP) Cytoplasm - chemistry Cytoplasm - genetics Cytoplasm - metabolism G protein-coupled receptor (GPCR) glucose Glucose - analysis Glucose - metabolism HEK293 Cells Humans Receptors, Calcium-Sensing - chemistry Receptors, Calcium-Sensing - genetics Receptors, Calcium-Sensing - metabolism Signal Transduction sweet taste receptor |
title | Positive Allosteric Modulation of the Calcium-sensing Receptor by Physiological Concentrations of Glucose |
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