Ca2+-sensing receptor-TRP channel-mediated Ca2+ signaling: Functional diversity and pharmacological complexity
The Ca2+-sensing receptor (CaSR) is a G-protein-coupled receptor activated by elevated concentrations of extracellular Ca2+, and was initially known for its regulation of parathyroid hormone (PTH) release. Ubiquitous expression of CaSR in different tissues and organs was later noted and CaSR partici...
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Veröffentlicht in: | European journal of pharmacology 2024-08, Vol.977, p.176717, Article 176717 |
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description | The Ca2+-sensing receptor (CaSR) is a G-protein-coupled receptor activated by elevated concentrations of extracellular Ca2+, and was initially known for its regulation of parathyroid hormone (PTH) release. Ubiquitous expression of CaSR in different tissues and organs was later noted and CaSR participation in various physiological functions was demonstrated. Accumulating evidence has suggested that CaSR functionally interacts with transient receptor potential (TRP) channels, which are mostly non-selective cation channels involved in sensing temperature, pain and stress. This review describes the interactions of CaSR with TRP channels in diverse cell types to trigger a variety of biological responses. CaSR has been known to interact with different types of G proteins. Possible involvements of G proteins, other signaling and scaffolding protein intermediates in CaSR-TRP interaction are discussed. In addition, an attempt will be made to extend the current understanding of biased agonism of CaSR. |
doi_str_mv | 10.1016/j.ejphar.2024.176717 |
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Ubiquitous expression of CaSR in different tissues and organs was later noted and CaSR participation in various physiological functions was demonstrated. Accumulating evidence has suggested that CaSR functionally interacts with transient receptor potential (TRP) channels, which are mostly non-selective cation channels involved in sensing temperature, pain and stress. This review describes the interactions of CaSR with TRP channels in diverse cell types to trigger a variety of biological responses. CaSR has been known to interact with different types of G proteins. Possible involvements of G proteins, other signaling and scaffolding protein intermediates in CaSR-TRP interaction are discussed. 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Ubiquitous expression of CaSR in different tissues and organs was later noted and CaSR participation in various physiological functions was demonstrated. Accumulating evidence has suggested that CaSR functionally interacts with transient receptor potential (TRP) channels, which are mostly non-selective cation channels involved in sensing temperature, pain and stress. This review describes the interactions of CaSR with TRP channels in diverse cell types to trigger a variety of biological responses. CaSR has been known to interact with different types of G proteins. Possible involvements of G proteins, other signaling and scaffolding protein intermediates in CaSR-TRP interaction are discussed. In addition, an attempt will be made to extend the current understanding of biased agonism of CaSR.</description><subject>Biased agonism</subject><subject>Ca2+-sensing receptors</subject><subject>G protein</subject><subject>TRP channels</subject><subject>β-arrestin</subject><issn>0014-2999</issn><issn>1879-0712</issn><issn>1879-0712</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LJDEQhsPiwo6u_8BDHwXpsSpmkm4Pggx-geCyuOcQk-oxQ3fSJj2y_nsztGdPRfF-UPUwdoKwREB5vl3Sdnw1acmBiyUqqVD9YAtsVFuDQn7AFgAoat627S92mPMWAFYtXy1YWBt-VmcK2YdNlcjSOMVUP__9U9lXEwL19UDOm4lctbdW2W-C6Yv5srrdBTv5WNbK-XdK2U8flQmu2t8yGBv7uPG2qDYOY0__i_yb_exMn-n4ax6xf7c3z-v7-vHp7mF9_Vhbjs1UC45AaK2VDTYoJbbgVthxYRQI5xx0UgglG_6iSHCwJEznmk4SOnixqrk4Yqdz75ji247ypAefLfW9CRR3WV-AlKrFVoliFbPVpphzok6PyQ8mfWgEvcert3rGq_d49Yy3xK7mGJU33j0lna2nYAusQnHSLvrvCz4BSZeGFA</recordid><startdate>20240815</startdate><enddate>20240815</enddate><creator>Wu, King-Chuen</creator><creator>Leong, Iat-Lon</creator><creator>Leung, Yuk-Man</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0626-1768</orcidid></search><sort><creationdate>20240815</creationdate><title>Ca2+-sensing receptor-TRP channel-mediated Ca2+ signaling: Functional diversity and pharmacological complexity</title><author>Wu, King-Chuen ; Leong, Iat-Lon ; Leung, Yuk-Man</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c218t-4210e1ccc6818166190d51f24a704ddd0f6447682b7e420ce4afd8f6e1d0bc783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Biased agonism</topic><topic>Ca2+-sensing receptors</topic><topic>G protein</topic><topic>TRP channels</topic><topic>β-arrestin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, King-Chuen</creatorcontrib><creatorcontrib>Leong, Iat-Lon</creatorcontrib><creatorcontrib>Leung, Yuk-Man</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, King-Chuen</au><au>Leong, Iat-Lon</au><au>Leung, Yuk-Man</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ca2+-sensing receptor-TRP channel-mediated Ca2+ signaling: Functional diversity and pharmacological complexity</atitle><jtitle>European journal of pharmacology</jtitle><date>2024-08-15</date><risdate>2024</risdate><volume>977</volume><spage>176717</spage><pages>176717-</pages><artnum>176717</artnum><issn>0014-2999</issn><issn>1879-0712</issn><eissn>1879-0712</eissn><abstract>The Ca2+-sensing receptor (CaSR) is a G-protein-coupled receptor activated by elevated concentrations of extracellular Ca2+, and was initially known for its regulation of parathyroid hormone (PTH) release. Ubiquitous expression of CaSR in different tissues and organs was later noted and CaSR participation in various physiological functions was demonstrated. Accumulating evidence has suggested that CaSR functionally interacts with transient receptor potential (TRP) channels, which are mostly non-selective cation channels involved in sensing temperature, pain and stress. This review describes the interactions of CaSR with TRP channels in diverse cell types to trigger a variety of biological responses. CaSR has been known to interact with different types of G proteins. Possible involvements of G proteins, other signaling and scaffolding protein intermediates in CaSR-TRP interaction are discussed. In addition, an attempt will be made to extend the current understanding of biased agonism of CaSR.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.ejphar.2024.176717</doi><orcidid>https://orcid.org/0000-0002-0626-1768</orcidid></addata></record> |
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subjects | Biased agonism Ca2+-sensing receptors G protein TRP channels β-arrestin |
title | Ca2+-sensing receptor-TRP channel-mediated Ca2+ signaling: Functional diversity and pharmacological complexity |
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