Adenosine triphosphate-evoked currents in cultured dorsal root ganglion neurons obtained from rat embryos: desensitization kinetics and modulation of glutamate release
Sensory neurons express purinergic P2X receptors on their central and peripheral terminals as well as their cell bodies. ATP activation of these receptors drives action potential firing and glutamate release with potentially important consequences for sensory function. Here we show ATP-gated current...
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Veröffentlicht in: | Neuroscience 2000-01, Vol.101 (4), p.1117-1126 |
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description | Sensory neurons express purinergic P2X receptors on their central and peripheral terminals as well as their cell bodies. ATP activation of these receptors drives action potential firing and glutamate release with potentially important consequences for sensory function. Here we show ATP-gated currents activated in cultured embryonic dorsal root ganglion neurons have heterogeneity of time-courses comparable to those observed in different subpopulations of acutely dissociated adult dorsal root ganglion neurons. The distribution of time-courses across the population of cultured neurons is strongly influenced by culture conditions. Heterogeneity in ATP current kinetics occurs even though immunocytochemical staining reveals a relatively homogeneous and widespread expression of the P2X2 and P2X3 subunits. We show that the time-courses of ATP-gated currents recorded at the cell bodies are mirrored by the time-courses of transmitter release from the dorsal root ganglion nerve terminals, indicating similar P2X receptor properties on the soma and their associated terminals.
Our results illustrate a functional heterogeneity of P2X receptor-mediated currents that is strongly influenced by external factors. This heterogeneity in current kinetics may have implications for neuronal function as it constrains the time-course of ATP-mediated modulation of neurotransmitter release at sensory nerve terminals. |
doi_str_mv | 10.1016/S0306-4522(00)00373-0 |
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Our results illustrate a functional heterogeneity of P2X receptor-mediated currents that is strongly influenced by external factors. This heterogeneity in current kinetics may have implications for neuronal function as it constrains the time-course of ATP-mediated modulation of neurotransmitter release at sensory nerve terminals.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/S0306-4522(00)00373-0</identifier><identifier>PMID: 11113360</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Adenosine Triphosphate - pharmacology ; Animals ; Biological and medical sciences ; Cells, Cultured ; Central nervous system ; Drug Resistance ; Electric Conductivity ; Electrophysiology ; Embryo, Mammalian ; Fundamental and applied biological sciences. Psychology ; Ganglia, Spinal - cytology ; Ganglia, Spinal - drug effects ; Ganglia, Spinal - physiology ; Glutamic Acid - metabolism ; Immunohistochemistry ; Kinetics ; mEPSCs ; modulation of neurotransmitter release ; Neurons - drug effects ; Neurons - physiology ; P2X-receptors ; Rats ; Receptors, Purinergic P2 - metabolism ; Receptors, Purinergic P2X2 ; Receptors, Purinergic P2X3 ; sensory neurons ; Time Factors ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 2000-01, Vol.101 (4), p.1117-1126</ispartof><rights>2000 IBRO</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c533t-f11bbe148af615ce3f57859203c6459114b507e097907fd6fbf5f45f8d0aadb53</citedby><cites>FETCH-LOGICAL-c533t-f11bbe148af615ce3f57859203c6459114b507e097907fd6fbf5f45f8d0aadb53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0306-4522(00)00373-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=843641$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11113360$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Labrakakis, C</creatorcontrib><creatorcontrib>Gerstner, E</creatorcontrib><creatorcontrib>MacDermott, A.B</creatorcontrib><title>Adenosine triphosphate-evoked currents in cultured dorsal root ganglion neurons obtained from rat embryos: desensitization kinetics and modulation of glutamate release</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Sensory neurons express purinergic P2X receptors on their central and peripheral terminals as well as their cell bodies. ATP activation of these receptors drives action potential firing and glutamate release with potentially important consequences for sensory function. Here we show ATP-gated currents activated in cultured embryonic dorsal root ganglion neurons have heterogeneity of time-courses comparable to those observed in different subpopulations of acutely dissociated adult dorsal root ganglion neurons. The distribution of time-courses across the population of cultured neurons is strongly influenced by culture conditions. Heterogeneity in ATP current kinetics occurs even though immunocytochemical staining reveals a relatively homogeneous and widespread expression of the P2X2 and P2X3 subunits. We show that the time-courses of ATP-gated currents recorded at the cell bodies are mirrored by the time-courses of transmitter release from the dorsal root ganglion nerve terminals, indicating similar P2X receptor properties on the soma and their associated terminals.
Our results illustrate a functional heterogeneity of P2X receptor-mediated currents that is strongly influenced by external factors. This heterogeneity in current kinetics may have implications for neuronal function as it constrains the time-course of ATP-mediated modulation of neurotransmitter release at sensory nerve terminals.</description><subject>Adenosine Triphosphate - pharmacology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>Central nervous system</subject><subject>Drug Resistance</subject><subject>Electric Conductivity</subject><subject>Electrophysiology</subject><subject>Embryo, Mammalian</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ganglia, Spinal - cytology</subject><subject>Ganglia, Spinal - drug effects</subject><subject>Ganglia, Spinal - physiology</subject><subject>Glutamic Acid - metabolism</subject><subject>Immunohistochemistry</subject><subject>Kinetics</subject><subject>mEPSCs</subject><subject>modulation of neurotransmitter release</subject><subject>Neurons - drug effects</subject><subject>Neurons - physiology</subject><subject>P2X-receptors</subject><subject>Rats</subject><subject>Receptors, Purinergic P2 - metabolism</subject><subject>Receptors, Purinergic P2X2</subject><subject>Receptors, Purinergic P2X3</subject><subject>sensory neurons</subject><subject>Time Factors</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc-KFDEQxoMo7jr6CEpAED20ViZJd48XWRb_wYIH9RzSSWU2bjoZk_TC-kK-ppmdYT1uXaoofl9VUR8hzxm8ZcD6d9-BQ98JuV6_BngDwAfewQNyysZWDFKIh-T0DjkhT0r5BS2k4I_JCWvBeQ-n5O-ZxZiKj0hr9rvLVHaXumKH1-kKLTVLzhhroT62OtQlt6ZNuehAc0qVbnXcBp8ijbjkFAtNU9VtmqUup5lmXSnOU75J5T21WDAWX_0fXfeSq8ZVbwrV0dI52SUc-snRbViqntshNGNAXfApeeR0KPjsmFfk56ePP86_dBffPn89P7vojOS8do6xaUImRu16Jg1yJ4dRbtbATS_khjExSRgQNsMGBmd7NznphHSjBa3tJPmKvDrM3eX0e8FS1eyLwRB0xLQUNazFAFwM94JsZP0I7csrIg-gyamUjE7tsp91vlEM1N5KdWul2vukANStlQqa7sVxwTLNaP-rjt414OUR0MXo4LKOxpc7bhS8F6xRHw4Utq9de8yqGI_RoPUZTVU2-XsO-QcQ678c</recordid><startdate>20000101</startdate><enddate>20000101</enddate><creator>Labrakakis, C</creator><creator>Gerstner, E</creator><creator>MacDermott, A.B</creator><general>Elsevier Ltd</general><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>7TK</scope><scope>7X8</scope></search><sort><creationdate>20000101</creationdate><title>Adenosine triphosphate-evoked currents in cultured dorsal root ganglion neurons obtained from rat embryos: desensitization kinetics and modulation of glutamate release</title><author>Labrakakis, C ; Gerstner, E ; MacDermott, A.B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c533t-f11bbe148af615ce3f57859203c6459114b507e097907fd6fbf5f45f8d0aadb53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adenosine Triphosphate - pharmacology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Central nervous system</topic><topic>Drug Resistance</topic><topic>Electric Conductivity</topic><topic>Electrophysiology</topic><topic>Embryo, Mammalian</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ganglia, Spinal - cytology</topic><topic>Ganglia, Spinal - drug effects</topic><topic>Ganglia, Spinal - physiology</topic><topic>Glutamic Acid - metabolism</topic><topic>Immunohistochemistry</topic><topic>Kinetics</topic><topic>mEPSCs</topic><topic>modulation of neurotransmitter release</topic><topic>Neurons - drug effects</topic><topic>Neurons - physiology</topic><topic>P2X-receptors</topic><topic>Rats</topic><topic>Receptors, Purinergic P2 - metabolism</topic><topic>Receptors, Purinergic P2X2</topic><topic>Receptors, Purinergic P2X3</topic><topic>sensory neurons</topic><topic>Time Factors</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Labrakakis, C</creatorcontrib><creatorcontrib>Gerstner, E</creatorcontrib><creatorcontrib>MacDermott, A.B</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Labrakakis, C</au><au>Gerstner, E</au><au>MacDermott, A.B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adenosine triphosphate-evoked currents in cultured dorsal root ganglion neurons obtained from rat embryos: desensitization kinetics and modulation of glutamate release</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2000-01-01</date><risdate>2000</risdate><volume>101</volume><issue>4</issue><spage>1117</spage><epage>1126</epage><pages>1117-1126</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Sensory neurons express purinergic P2X receptors on their central and peripheral terminals as well as their cell bodies. ATP activation of these receptors drives action potential firing and glutamate release with potentially important consequences for sensory function. Here we show ATP-gated currents activated in cultured embryonic dorsal root ganglion neurons have heterogeneity of time-courses comparable to those observed in different subpopulations of acutely dissociated adult dorsal root ganglion neurons. The distribution of time-courses across the population of cultured neurons is strongly influenced by culture conditions. Heterogeneity in ATP current kinetics occurs even though immunocytochemical staining reveals a relatively homogeneous and widespread expression of the P2X2 and P2X3 subunits. We show that the time-courses of ATP-gated currents recorded at the cell bodies are mirrored by the time-courses of transmitter release from the dorsal root ganglion nerve terminals, indicating similar P2X receptor properties on the soma and their associated terminals.
Our results illustrate a functional heterogeneity of P2X receptor-mediated currents that is strongly influenced by external factors. This heterogeneity in current kinetics may have implications for neuronal function as it constrains the time-course of ATP-mediated modulation of neurotransmitter release at sensory nerve terminals.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>11113360</pmid><doi>10.1016/S0306-4522(00)00373-0</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Triphosphate - pharmacology Animals Biological and medical sciences Cells, Cultured Central nervous system Drug Resistance Electric Conductivity Electrophysiology Embryo, Mammalian Fundamental and applied biological sciences. Psychology Ganglia, Spinal - cytology Ganglia, Spinal - drug effects Ganglia, Spinal - physiology Glutamic Acid - metabolism Immunohistochemistry Kinetics mEPSCs modulation of neurotransmitter release Neurons - drug effects Neurons - physiology P2X-receptors Rats Receptors, Purinergic P2 - metabolism Receptors, Purinergic P2X2 Receptors, Purinergic P2X3 sensory neurons Time Factors Vertebrates: nervous system and sense organs |
title | Adenosine triphosphate-evoked currents in cultured dorsal root ganglion neurons obtained from rat embryos: desensitization kinetics and modulation of glutamate release |
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