Increase of intracellular Ca2+ by P2X and P2Y receptor-subtypes in cultured cortical astroglia of the rat

Abstract Astrocytes express purinergic receptors that are involved in glial–neuronal cell communication. Experiments were conducted to characterize the expression of functional P2X/P2Y nucleotide receptors in glial cells of mixed cortical cell cultures of the rat. The vast majority of these cells wa...

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Veröffentlicht in:Neuroscience 2009-06, Vol.160 (4), p.767-783
Hauptverfasser: Fischer, W, Appelt, K, Grohmann, M, Franke, H, Nörenberg, W, Illes, P
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container_issue 4
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container_title Neuroscience
container_volume 160
creator Fischer, W
Appelt, K
Grohmann, M
Franke, H
Nörenberg, W
Illes, P
description Abstract Astrocytes express purinergic receptors that are involved in glial–neuronal cell communication. Experiments were conducted to characterize the expression of functional P2X/P2Y nucleotide receptors in glial cells of mixed cortical cell cultures of the rat. The vast majority of these cells was immunopositive for glial fibrillary acidic protein (GFAP) and was considered therefore astrocyte-like; for the sake of simplicity they were termed “astroglia” throughout. Astroglia expressed predominantly P2X4,6,7 as well as P2Y1,2 receptor-subtypes. Less intensive immunostaining was also found for P2X5 and P2Y4,6,13,14 receptors. Pressure application of ATP and a range of agonists selective for certain P2X or P2Y receptor-subtypes caused a concentration-dependent increase of intracellular Ca2+ ([Ca2+ ]i ). Of the agonists tested, only the P2X1,3 receptor-selective α,β-methylene ATP was ineffective. Experiments with Ca2+ -free solution and cyclopiazonic acid, an inhibitor of the endoplasmic Ca2+ -ATPase, indicated that the [Ca2+ ]i response to most nucleotides, except for ATP and 2′,3′- O -(benzoyl-4-benzoyl)-ATP, was due primarily to the release of Ca2+ from intracellular stores. A Gprotein–mediated release of Ca2+ is the typical signaling mechanism of various P2Y receptor-subtypes, whose presence was confirmed also by cross-desensitization experiments and by using selective antagonists. Thus, our results provide direct evidence that astroglia in mixed cortical cell cultures express functional P2Y (P2Y1,2,6,14 and probably also P2Y4 ) receptors. Several unidentified P2X receptors, including P2X7 , may also be present, although they appear to only moderately participate in the regulation of [Ca2+ ]i . The rise of [Ca2+ ]i is due in this case to the transmembrane flux of Ca2+ via the P2X receptor-channel. In conclusion, P2Y rather than P2X receptor-subtypes are involved in modulating [Ca2+ ]i of cultured astroglia and thereby may play an important role in cell-to-cell signaling.
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Experiments were conducted to characterize the expression of functional P2X/P2Y nucleotide receptors in glial cells of mixed cortical cell cultures of the rat. The vast majority of these cells was immunopositive for glial fibrillary acidic protein (GFAP) and was considered therefore astrocyte-like; for the sake of simplicity they were termed “astroglia” throughout. Astroglia expressed predominantly P2X4,6,7 as well as P2Y1,2 receptor-subtypes. Less intensive immunostaining was also found for P2X5 and P2Y4,6,13,14 receptors. Pressure application of ATP and a range of agonists selective for certain P2X or P2Y receptor-subtypes caused a concentration-dependent increase of intracellular Ca2+ ([Ca2+ ]i ). Of the agonists tested, only the P2X1,3 receptor-selective α,β-methylene ATP was ineffective. Experiments with Ca2+ -free solution and cyclopiazonic acid, an inhibitor of the endoplasmic Ca2+ -ATPase, indicated that the [Ca2+ ]i response to most nucleotides, except for ATP and 2′,3′- O -(benzoyl-4-benzoyl)-ATP, was due primarily to the release of Ca2+ from intracellular stores. A Gprotein–mediated release of Ca2+ is the typical signaling mechanism of various P2Y receptor-subtypes, whose presence was confirmed also by cross-desensitization experiments and by using selective antagonists. Thus, our results provide direct evidence that astroglia in mixed cortical cell cultures express functional P2Y (P2Y1,2,6,14 and probably also P2Y4 ) receptors. Several unidentified P2X receptors, including P2X7 , may also be present, although they appear to only moderately participate in the regulation of [Ca2+ ]i . The rise of [Ca2+ ]i is due in this case to the transmembrane flux of Ca2+ via the P2X receptor-channel. 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Experiments were conducted to characterize the expression of functional P2X/P2Y nucleotide receptors in glial cells of mixed cortical cell cultures of the rat. The vast majority of these cells was immunopositive for glial fibrillary acidic protein (GFAP) and was considered therefore astrocyte-like; for the sake of simplicity they were termed “astroglia” throughout. Astroglia expressed predominantly P2X4,6,7 as well as P2Y1,2 receptor-subtypes. Less intensive immunostaining was also found for P2X5 and P2Y4,6,13,14 receptors. Pressure application of ATP and a range of agonists selective for certain P2X or P2Y receptor-subtypes caused a concentration-dependent increase of intracellular Ca2+ ([Ca2+ ]i ). Of the agonists tested, only the P2X1,3 receptor-selective α,β-methylene ATP was ineffective. Experiments with Ca2+ -free solution and cyclopiazonic acid, an inhibitor of the endoplasmic Ca2+ -ATPase, indicated that the [Ca2+ ]i response to most nucleotides, except for ATP and 2′,3′- O -(benzoyl-4-benzoyl)-ATP, was due primarily to the release of Ca2+ from intracellular stores. A Gprotein–mediated release of Ca2+ is the typical signaling mechanism of various P2Y receptor-subtypes, whose presence was confirmed also by cross-desensitization experiments and by using selective antagonists. Thus, our results provide direct evidence that astroglia in mixed cortical cell cultures express functional P2Y (P2Y1,2,6,14 and probably also P2Y4 ) receptors. Several unidentified P2X receptors, including P2X7 , may also be present, although they appear to only moderately participate in the regulation of [Ca2+ ]i . The rise of [Ca2+ ]i is due in this case to the transmembrane flux of Ca2+ via the P2X receptor-channel. 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Psychology</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>Immunohistochemistry</subject><subject>Intracellular Fluid - drug effects</subject><subject>Intracellular Fluid - metabolism</subject><subject>Neurology</subject><subject>Nucleotides - metabolism</subject><subject>Nucleotides - pharmacology</subject><subject>Purinergic P2 Receptor Agonists</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, G-Protein-Coupled - drug effects</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>Receptors, Purinergic P2 - metabolism</subject><subject>Receptors, Purinergic P2X</subject><subject>Receptors, Purinergic P2Y12</subject><subject>Signal Transduction - drug effects</subject><subject>Signal Transduction - physiology</subject><subject>Up-Regulation - physiology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkVur1DAQgIMonvXoX5Ag6It0ndyaxgdBFi8HDiiooE8hTaeatduuuQj7703ZRQ0DQ-CbGeYbQp4w2DJg7Yv9dsYSl-QDzh63HMBsgddo75AN67RotJLyLtmAgLaRivMr8iClPdSnpLhPrpjhnWFKbki4mX1El5AuIw1zjs7jNJXJRbpz_DntT_Qj_0rdPNT8jUb0eMxLbFLp8-mIqdZQX6ZcIg7ULzEH7ybqUo7L9ym4tWv-gTS6_JDcG92U8NElX5Mvb9983r1vbj-8u9m9vm28MF1uBumdFrodx04aLQfQrRoFGsON5rr3KOpHQw9q9KIbgElQ3Ctgfa-w7iuuybNz32NcfhVM2R5CWpdyMy4l2VazGqyr4Msz6KvLFHG0xxgOLp4sA7uKtnv7v2i7irbAa6xTHl-mlP6Aw7_Si9kKPL0ALlUlY3SzD-kvx5kUrN6jcq_OHFYnvwNG66cwrxZ_4gnTfilxrross6lOtp_Wm64nBQPABefiD_3knzs</recordid><startdate>20090602</startdate><enddate>20090602</enddate><creator>Fischer, W</creator><creator>Appelt, K</creator><creator>Grohmann, M</creator><creator>Franke, H</creator><creator>Nörenberg, W</creator><creator>Illes, P</creator><general>Elsevier</general><scope>IQODW</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></search><sort><creationdate>20090602</creationdate><title>Increase of intracellular Ca2+ by P2X and P2Y receptor-subtypes in cultured cortical astroglia of the rat</title><author>Fischer, W ; Appelt, K ; Grohmann, M ; Franke, H ; Nörenberg, W ; Illes, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-d4ca7376ff84974d0765f3e9929727bce33e970b05fc38d014052c501bb5e3063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adenosine Triphosphate - analogs &amp; derivatives</topic><topic>Adenosine Triphosphate - pharmacology</topic><topic>Animals</topic><topic>Astrocytes - metabolism</topic><topic>Astrocytes - ultrastructure</topic><topic>Biological and medical sciences</topic><topic>Calcium - metabolism</topic><topic>Calcium Signaling - drug effects</topic><topic>Calcium Signaling - physiology</topic><topic>Calcium-Transporting ATPases - antagonists &amp; inhibitors</topic><topic>Calcium-Transporting ATPases - metabolism</topic><topic>Cells, Cultured</topic><topic>Cerebral Cortex - cytology</topic><topic>Cerebral Cortex - metabolism</topic><topic>Coculture Techniques</topic><topic>Dose-Response Relationship, Drug</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glial Fibrillary Acidic Protein - metabolism</topic><topic>Immunohistochemistry</topic><topic>Intracellular Fluid - drug effects</topic><topic>Intracellular Fluid - metabolism</topic><topic>Neurology</topic><topic>Nucleotides - metabolism</topic><topic>Nucleotides - pharmacology</topic><topic>Purinergic P2 Receptor Agonists</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, G-Protein-Coupled - drug effects</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>Receptors, Purinergic P2 - metabolism</topic><topic>Receptors, Purinergic P2X</topic><topic>Receptors, Purinergic P2Y12</topic><topic>Signal Transduction - drug effects</topic><topic>Signal Transduction - physiology</topic><topic>Up-Regulation - physiology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fischer, W</creatorcontrib><creatorcontrib>Appelt, K</creatorcontrib><creatorcontrib>Grohmann, M</creatorcontrib><creatorcontrib>Franke, H</creatorcontrib><creatorcontrib>Nörenberg, W</creatorcontrib><creatorcontrib>Illes, P</creatorcontrib><collection>Pascal-Francis</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><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fischer, W</au><au>Appelt, K</au><au>Grohmann, M</au><au>Franke, H</au><au>Nörenberg, W</au><au>Illes, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increase of intracellular Ca2+ by P2X and P2Y receptor-subtypes in cultured cortical astroglia of the rat</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2009-06-02</date><risdate>2009</risdate><volume>160</volume><issue>4</issue><spage>767</spage><epage>783</epage><pages>767-783</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Abstract Astrocytes express purinergic receptors that are involved in glial–neuronal cell communication. Experiments were conducted to characterize the expression of functional P2X/P2Y nucleotide receptors in glial cells of mixed cortical cell cultures of the rat. The vast majority of these cells was immunopositive for glial fibrillary acidic protein (GFAP) and was considered therefore astrocyte-like; for the sake of simplicity they were termed “astroglia” throughout. Astroglia expressed predominantly P2X4,6,7 as well as P2Y1,2 receptor-subtypes. Less intensive immunostaining was also found for P2X5 and P2Y4,6,13,14 receptors. Pressure application of ATP and a range of agonists selective for certain P2X or P2Y receptor-subtypes caused a concentration-dependent increase of intracellular Ca2+ ([Ca2+ ]i ). Of the agonists tested, only the P2X1,3 receptor-selective α,β-methylene ATP was ineffective. Experiments with Ca2+ -free solution and cyclopiazonic acid, an inhibitor of the endoplasmic Ca2+ -ATPase, indicated that the [Ca2+ ]i response to most nucleotides, except for ATP and 2′,3′- O -(benzoyl-4-benzoyl)-ATP, was due primarily to the release of Ca2+ from intracellular stores. A Gprotein–mediated release of Ca2+ is the typical signaling mechanism of various P2Y receptor-subtypes, whose presence was confirmed also by cross-desensitization experiments and by using selective antagonists. Thus, our results provide direct evidence that astroglia in mixed cortical cell cultures express functional P2Y (P2Y1,2,6,14 and probably also P2Y4 ) receptors. Several unidentified P2X receptors, including P2X7 , may also be present, although they appear to only moderately participate in the regulation of [Ca2+ ]i . The rise of [Ca2+ ]i is due in this case to the transmembrane flux of Ca2+ via the P2X receptor-channel. In conclusion, P2Y rather than P2X receptor-subtypes are involved in modulating [Ca2+ ]i of cultured astroglia and thereby may play an important role in cell-to-cell signaling.</abstract><cop>Amsterdam</cop><pub>Elsevier</pub><pmid>19289154</pmid><doi>10.1016/j.neuroscience.2009.02.026</doi><tpages>17</tpages></addata></record>
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subjects Adenosine Triphosphate - analogs & derivatives
Adenosine Triphosphate - pharmacology
Animals
Astrocytes - metabolism
Astrocytes - ultrastructure
Biological and medical sciences
Calcium - metabolism
Calcium Signaling - drug effects
Calcium Signaling - physiology
Calcium-Transporting ATPases - antagonists & inhibitors
Calcium-Transporting ATPases - metabolism
Cells, Cultured
Cerebral Cortex - cytology
Cerebral Cortex - metabolism
Coculture Techniques
Dose-Response Relationship, Drug
Enzyme Inhibitors - pharmacology
Fundamental and applied biological sciences. Psychology
Glial Fibrillary Acidic Protein - metabolism
Immunohistochemistry
Intracellular Fluid - drug effects
Intracellular Fluid - metabolism
Neurology
Nucleotides - metabolism
Nucleotides - pharmacology
Purinergic P2 Receptor Agonists
Rats
Rats, Wistar
Receptors, G-Protein-Coupled - drug effects
Receptors, G-Protein-Coupled - metabolism
Receptors, Purinergic P2 - metabolism
Receptors, Purinergic P2X
Receptors, Purinergic P2Y12
Signal Transduction - drug effects
Signal Transduction - physiology
Up-Regulation - physiology
Vertebrates: nervous system and sense organs
title Increase of intracellular Ca2+ by P2X and P2Y receptor-subtypes in cultured cortical astroglia of the rat
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