Serotonin (5-HT7) Receptor-Stimulated Activation of cAMP-PKA Pathway in Bovine Corneal Epithelial and Endothelial Cells
Background: 5-Hydroxytryptamine (5-HT; serotonin) is a major neurotransmitter, and its receptors are found throughout the whole body. The 5-HT7 receptor subtype was detected in human corneal epithelial and endothelial cells and found to be functionally active in a corneal epithelial cell line. The a...
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Veröffentlicht in: | Ophthalmic research 2012-01, Vol.48 (1), p.22-27 |
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description | Background: 5-Hydroxytryptamine (5-HT; serotonin) is a major neurotransmitter, and its receptors are found throughout the whole body. The 5-HT7 receptor subtype was detected in human corneal epithelial and endothelial cells and found to be functionally active in a corneal epithelial cell line. The aim of the present study was to demonstrate that native bovine corneal epithelial and endothelial cells express a functional 5-HT7 receptor positively coupled to adenylyl cyclase and protein kinase A (PKA) formation. Methods: 5-HT7 receptors were studied using polyclonal antibodies. cAMP concentration after 5-HT7 receptor stimulation with 5-carboxamidotryptamine (5-CT, a 5-HT7 agonist) was tested by enzyme immunoassay, PKA activity was estimated by kinase consumption of ATP. Results: Immunocytochemistry and immunofluorescence revealed the presence of 5-HT7 receptors in corneal epithelial and endothelial cells. Stimulation of corneal 5-HT7 receptors with 5-CT revealed a dose-dependent increase in intracellular cAMP concentration in corneal epithelium (0.01–0.34 pmol/ml) and endothelium (0.01–0.19 pmol/ml) between 10 –10 and 10 –7 mg/ml 5-CT (p = 0.001) with maximal stimulation from 10 –7 to 10 –3 mg/ml 5-CT (0.30 ± 0.03 and 0.18 ± 0.01 pmol/ml, respectively). Incubation with 10 –6 mg/ml SB269970 (a selective 5-HT7 antagonist) blocked 5-CT-induced cAMP increase in corneal epithelial (0.03 pmol/ml) and endothelial cells (0.02 pmol/ml; p = 0.001). Stimulation of corneal 5-HT7 receptors with 5-CT revealed a dose-dependent increase in PKA activity between 10 –10 and 10 –8 mg/ml 5-CT in corneal epithelium and endothelium (99%; p = 0.013 and p = 0.017, respectively) with maximal stimulation from 10 –8 to 10 –4 mg/ml (>99%) 5-CT. Conclusions: Our data demonstrate that native corneal epithelial and endothelial cells express a functional 5-HT7 receptor positively coupled to adenylyl cyclase and PKA formation. However, at the present time, the physiological role of 5-HT receptors and the cAMP-PKA pathway in the cornea remains a matter of speculation. |
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The 5-HT7 receptor subtype was detected in human corneal epithelial and endothelial cells and found to be functionally active in a corneal epithelial cell line. The aim of the present study was to demonstrate that native bovine corneal epithelial and endothelial cells express a functional 5-HT7 receptor positively coupled to adenylyl cyclase and protein kinase A (PKA) formation. Methods: 5-HT7 receptors were studied using polyclonal antibodies. cAMP concentration after 5-HT7 receptor stimulation with 5-carboxamidotryptamine (5-CT, a 5-HT7 agonist) was tested by enzyme immunoassay, PKA activity was estimated by kinase consumption of ATP. Results: Immunocytochemistry and immunofluorescence revealed the presence of 5-HT7 receptors in corneal epithelial and endothelial cells. Stimulation of corneal 5-HT7 receptors with 5-CT revealed a dose-dependent increase in intracellular cAMP concentration in corneal epithelium (0.01–0.34 pmol/ml) and endothelium (0.01–0.19 pmol/ml) between 10 –10 and 10 –7 mg/ml 5-CT (p = 0.001) with maximal stimulation from 10 –7 to 10 –3 mg/ml 5-CT (0.30 ± 0.03 and 0.18 ± 0.01 pmol/ml, respectively). Incubation with 10 –6 mg/ml SB269970 (a selective 5-HT7 antagonist) blocked 5-CT-induced cAMP increase in corneal epithelial (0.03 pmol/ml) and endothelial cells (0.02 pmol/ml; p = 0.001). Stimulation of corneal 5-HT7 receptors with 5-CT revealed a dose-dependent increase in PKA activity between 10 –10 and 10 –8 mg/ml 5-CT in corneal epithelium and endothelium (<1 to >99%; p = 0.013 and p = 0.017, respectively) with maximal stimulation from 10 –8 to 10 –4 mg/ml (>99%) 5-CT. Conclusions: Our data demonstrate that native corneal epithelial and endothelial cells express a functional 5-HT7 receptor positively coupled to adenylyl cyclase and PKA formation. However, at the present time, the physiological role of 5-HT receptors and the cAMP-PKA pathway in the cornea remains a matter of speculation.</description><identifier>ISSN: 0030-3747</identifier><identifier>EISSN: 1423-0259</identifier><identifier>DOI: 10.1159/000334912</identifier><identifier>PMID: 22222787</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Adenylyl Cyclases - metabolism ; Animals ; Cattle ; Cyclic AMP - metabolism ; Cyclic AMP-Dependent Protein Kinases - metabolism ; Dose-Response Relationship, Drug ; Endothelium, Corneal - enzymology ; Enzyme Activation ; Epithelium, Corneal - enzymology ; Fluorescent Antibody Technique, Indirect ; Immunohistochemistry ; Original Paper ; Phenols - pharmacology ; Receptors, Serotonin - metabolism ; Serotonin - analogs & derivatives ; Serotonin - pharmacology ; Serotonin Antagonists - pharmacology ; Serotonin Receptor Agonists - pharmacology ; Sulfonamides - pharmacology</subject><ispartof>Ophthalmic research, 2012-01, Vol.48 (1), p.22-27</ispartof><rights>2012 S. Karger AG, Basel</rights><rights>Copyright © 2012 S. Karger AG, Basel.</rights><rights>Copyright (c) 2012 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c334t-bf1589b28689b03fd01b4a51a269806ce6214550b2c9371e962f69b8f6d7ff253</citedby><cites>FETCH-LOGICAL-c334t-bf1589b28689b03fd01b4a51a269806ce6214550b2c9371e962f69b8f6d7ff253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2422,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22222787$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grueb, Matthias</creatorcontrib><creatorcontrib>Rohrbach, Jens Martin</creatorcontrib><creatorcontrib>Schlote, Torsten</creatorcontrib><creatorcontrib>Mielke, Joerg</creatorcontrib><title>Serotonin (5-HT7) Receptor-Stimulated Activation of cAMP-PKA Pathway in Bovine Corneal Epithelial and Endothelial Cells</title><title>Ophthalmic research</title><addtitle>Ophthalmic Res</addtitle><description>Background: 5-Hydroxytryptamine (5-HT; serotonin) is a major neurotransmitter, and its receptors are found throughout the whole body. The 5-HT7 receptor subtype was detected in human corneal epithelial and endothelial cells and found to be functionally active in a corneal epithelial cell line. The aim of the present study was to demonstrate that native bovine corneal epithelial and endothelial cells express a functional 5-HT7 receptor positively coupled to adenylyl cyclase and protein kinase A (PKA) formation. Methods: 5-HT7 receptors were studied using polyclonal antibodies. cAMP concentration after 5-HT7 receptor stimulation with 5-carboxamidotryptamine (5-CT, a 5-HT7 agonist) was tested by enzyme immunoassay, PKA activity was estimated by kinase consumption of ATP. Results: Immunocytochemistry and immunofluorescence revealed the presence of 5-HT7 receptors in corneal epithelial and endothelial cells. Stimulation of corneal 5-HT7 receptors with 5-CT revealed a dose-dependent increase in intracellular cAMP concentration in corneal epithelium (0.01–0.34 pmol/ml) and endothelium (0.01–0.19 pmol/ml) between 10 –10 and 10 –7 mg/ml 5-CT (p = 0.001) with maximal stimulation from 10 –7 to 10 –3 mg/ml 5-CT (0.30 ± 0.03 and 0.18 ± 0.01 pmol/ml, respectively). Incubation with 10 –6 mg/ml SB269970 (a selective 5-HT7 antagonist) blocked 5-CT-induced cAMP increase in corneal epithelial (0.03 pmol/ml) and endothelial cells (0.02 pmol/ml; p = 0.001). Stimulation of corneal 5-HT7 receptors with 5-CT revealed a dose-dependent increase in PKA activity between 10 –10 and 10 –8 mg/ml 5-CT in corneal epithelium and endothelium (<1 to >99%; p = 0.013 and p = 0.017, respectively) with maximal stimulation from 10 –8 to 10 –4 mg/ml (>99%) 5-CT. Conclusions: Our data demonstrate that native corneal epithelial and endothelial cells express a functional 5-HT7 receptor positively coupled to adenylyl cyclase and PKA formation. However, at the present time, the physiological role of 5-HT receptors and the cAMP-PKA pathway in the cornea remains a matter of speculation.</description><subject>Adenylyl Cyclases - metabolism</subject><subject>Animals</subject><subject>Cattle</subject><subject>Cyclic AMP - metabolism</subject><subject>Cyclic AMP-Dependent Protein Kinases - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Endothelium, Corneal - enzymology</subject><subject>Enzyme Activation</subject><subject>Epithelium, Corneal - enzymology</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Immunohistochemistry</subject><subject>Original Paper</subject><subject>Phenols - pharmacology</subject><subject>Receptors, Serotonin - metabolism</subject><subject>Serotonin - analogs & derivatives</subject><subject>Serotonin - pharmacology</subject><subject>Serotonin Antagonists - pharmacology</subject><subject>Serotonin Receptor Agonists - pharmacology</subject><subject>Sulfonamides - pharmacology</subject><issn>0030-3747</issn><issn>1423-0259</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpd0TlPwzAUAGALgWgpDOwIWWKBIeAjceKxVOUQICqOOXISmxpSu9hOEf8eVz0GPPjS956e_QA4xugS44xfIYQoTTkmO6CPU0ITRDK-C_rxGiU0T_MeOPD-E6GIOdoHPbIceZH3wc-rdDZYow08z5K7t_wCvshazoN1yWvQs64VQTZwWAe9EEFbA62C9fBpkkwehnAiwvRH_MIYfW0X2kg4ss5I0cLxXIepbHXcCtPAsWns5jySbesPwZ4SrZdH63UA3m_Gb6O75PH59n40fEzq-KKQVApnBa9IweKMqGoQrlKRYUEYLxCrJSM4zTJUkZrTHEvOiGK8KhRrcqVIRgfgfJV37ux3J30oZ9rXsQJhpO18iRHBhCGWF5Ge_aOftnMmVrdUlKe4wDSqi5WqnfXeSVXOnZ4J9xtRuexGue1GtKfrjF01k81Wbr4_gpMV-BLuQ7otWMf_Adl6ioI</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Grueb, Matthias</creator><creator>Rohrbach, Jens Martin</creator><creator>Schlote, Torsten</creator><creator>Mielke, Joerg</creator><general>S. 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metabolism</topic><topic>Animals</topic><topic>Cattle</topic><topic>Cyclic AMP - metabolism</topic><topic>Cyclic AMP-Dependent Protein Kinases - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Endothelium, Corneal - enzymology</topic><topic>Enzyme Activation</topic><topic>Epithelium, Corneal - enzymology</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Immunohistochemistry</topic><topic>Original Paper</topic><topic>Phenols - pharmacology</topic><topic>Receptors, Serotonin - metabolism</topic><topic>Serotonin - analogs & derivatives</topic><topic>Serotonin - pharmacology</topic><topic>Serotonin Antagonists - pharmacology</topic><topic>Serotonin Receptor Agonists - pharmacology</topic><topic>Sulfonamides - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grueb, Matthias</creatorcontrib><creatorcontrib>Rohrbach, Jens Martin</creatorcontrib><creatorcontrib>Schlote, Torsten</creatorcontrib><creatorcontrib>Mielke, Joerg</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>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</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>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Ophthalmic research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grueb, Matthias</au><au>Rohrbach, Jens Martin</au><au>Schlote, Torsten</au><au>Mielke, Joerg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serotonin (5-HT7) Receptor-Stimulated Activation of cAMP-PKA Pathway in Bovine Corneal Epithelial and Endothelial Cells</atitle><jtitle>Ophthalmic research</jtitle><addtitle>Ophthalmic Res</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>48</volume><issue>1</issue><spage>22</spage><epage>27</epage><pages>22-27</pages><issn>0030-3747</issn><eissn>1423-0259</eissn><abstract>Background: 5-Hydroxytryptamine (5-HT; serotonin) is a major neurotransmitter, and its receptors are found throughout the whole body. The 5-HT7 receptor subtype was detected in human corneal epithelial and endothelial cells and found to be functionally active in a corneal epithelial cell line. The aim of the present study was to demonstrate that native bovine corneal epithelial and endothelial cells express a functional 5-HT7 receptor positively coupled to adenylyl cyclase and protein kinase A (PKA) formation. Methods: 5-HT7 receptors were studied using polyclonal antibodies. cAMP concentration after 5-HT7 receptor stimulation with 5-carboxamidotryptamine (5-CT, a 5-HT7 agonist) was tested by enzyme immunoassay, PKA activity was estimated by kinase consumption of ATP. Results: Immunocytochemistry and immunofluorescence revealed the presence of 5-HT7 receptors in corneal epithelial and endothelial cells. Stimulation of corneal 5-HT7 receptors with 5-CT revealed a dose-dependent increase in intracellular cAMP concentration in corneal epithelium (0.01–0.34 pmol/ml) and endothelium (0.01–0.19 pmol/ml) between 10 –10 and 10 –7 mg/ml 5-CT (p = 0.001) with maximal stimulation from 10 –7 to 10 –3 mg/ml 5-CT (0.30 ± 0.03 and 0.18 ± 0.01 pmol/ml, respectively). Incubation with 10 –6 mg/ml SB269970 (a selective 5-HT7 antagonist) blocked 5-CT-induced cAMP increase in corneal epithelial (0.03 pmol/ml) and endothelial cells (0.02 pmol/ml; p = 0.001). Stimulation of corneal 5-HT7 receptors with 5-CT revealed a dose-dependent increase in PKA activity between 10 –10 and 10 –8 mg/ml 5-CT in corneal epithelium and endothelium (<1 to >99%; p = 0.013 and p = 0.017, respectively) with maximal stimulation from 10 –8 to 10 –4 mg/ml (>99%) 5-CT. Conclusions: Our data demonstrate that native corneal epithelial and endothelial cells express a functional 5-HT7 receptor positively coupled to adenylyl cyclase and PKA formation. However, at the present time, the physiological role of 5-HT receptors and the cAMP-PKA pathway in the cornea remains a matter of speculation.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>22222787</pmid><doi>10.1159/000334912</doi><tpages>6</tpages></addata></record> |
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subjects | Adenylyl Cyclases - metabolism Animals Cattle Cyclic AMP - metabolism Cyclic AMP-Dependent Protein Kinases - metabolism Dose-Response Relationship, Drug Endothelium, Corneal - enzymology Enzyme Activation Epithelium, Corneal - enzymology Fluorescent Antibody Technique, Indirect Immunohistochemistry Original Paper Phenols - pharmacology Receptors, Serotonin - metabolism Serotonin - analogs & derivatives Serotonin - pharmacology Serotonin Antagonists - pharmacology Serotonin Receptor Agonists - pharmacology Sulfonamides - pharmacology |
title | Serotonin (5-HT7) Receptor-Stimulated Activation of cAMP-PKA Pathway in Bovine Corneal Epithelial and Endothelial Cells |
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