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Cholinergic agonists increase intracellular Ca2+ in cultured human microglia
Microglia are resident phagocytic cells in the central nervous system (CNS), and can be activated in response to various stimuli including neurotransmitters. Using fura-2 imaging, we investigated the effects of carbachol (CCh), a cholinergic agonist, on [Ca2+]i in cultured human microglia. Treatment...
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Published in: | Neuroscience letters 1998-10, Vol.255 (1), p.33-36 |
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container_title | Neuroscience letters |
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creator | ZHANG, L MCLARNON, J. G GOGHARI, V YONG BEOM LEE KIM, S. U KRIEGER, C |
description | Microglia are resident phagocytic cells in the central nervous system (CNS), and can be activated in response to various stimuli including neurotransmitters. Using fura-2 imaging, we investigated the effects of carbachol (CCh), a cholinergic agonist, on [Ca2+]i in cultured human microglia. Treatment of microglia with CCh (100 microM) produced a transient increase in [Ca2+]i, which was atropine-sensitive and was associated with release from intracellular Ca2+ stores. Successive applications of CCh showed a change in the amplitude of the [Ca2+]i signal consistent with desensitization. These results show that human microglia express functional muscarinic receptors and respond to cholinergic agonists. The rapid change of [Ca2+]i in microglia may serve as a second messenger to trigger downstream cascades which contribute to signalling pathways in CNS pathology. |
doi_str_mv | 10.1016/S0304-3940(98)00706-X |
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G ; GOGHARI, V ; YONG BEOM LEE ; KIM, S. U ; KRIEGER, C</creator><creatorcontrib>ZHANG, L ; MCLARNON, J. G ; GOGHARI, V ; YONG BEOM LEE ; KIM, S. U ; KRIEGER, C</creatorcontrib><description>Microglia are resident phagocytic cells in the central nervous system (CNS), and can be activated in response to various stimuli including neurotransmitters. Using fura-2 imaging, we investigated the effects of carbachol (CCh), a cholinergic agonist, on [Ca2+]i in cultured human microglia. Treatment of microglia with CCh (100 microM) produced a transient increase in [Ca2+]i, which was atropine-sensitive and was associated with release from intracellular Ca2+ stores. Successive applications of CCh showed a change in the amplitude of the [Ca2+]i signal consistent with desensitization. These results show that human microglia express functional muscarinic receptors and respond to cholinergic agonists. The rapid change of [Ca2+]i in microglia may serve as a second messenger to trigger downstream cascades which contribute to signalling pathways in CNS pathology.</description><identifier>ISSN: 0304-3940</identifier><identifier>EISSN: 1872-7972</identifier><identifier>DOI: 10.1016/S0304-3940(98)00706-X</identifier><identifier>PMID: 9839720</identifier><identifier>CODEN: NELED5</identifier><language>eng</language><publisher>Shannon: Elsevier</publisher><subject>Atropine - pharmacology ; Biological and medical sciences ; Calcium - metabolism ; Carbachol - administration & dosage ; Carbachol - pharmacology ; Cells, Cultured ; Cholinergic Agonists - administration & dosage ; Cholinergic Agonists - pharmacology ; Drug Administration Schedule ; Drug Combinations ; Fetus ; Fundamental and applied biological sciences. Psychology ; Humans ; Intracellular Membranes - metabolism ; Isolated neuron and nerve. Neuroglia ; Microglia - drug effects ; Microglia - metabolism ; Muscarinic Antagonists - pharmacology ; Osmolar Concentration ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience letters, 1998-10, Vol.255 (1), p.33-36</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c317t-bcac234b5225aed84f01e22bfdaeefdcebbb0ba92bbe3a6fee48d64a639643463</citedby><cites>FETCH-LOGICAL-c317t-bcac234b5225aed84f01e22bfdaeefdcebbb0ba92bbe3a6fee48d64a639643463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2435984$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9839720$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ZHANG, L</creatorcontrib><creatorcontrib>MCLARNON, J. G</creatorcontrib><creatorcontrib>GOGHARI, V</creatorcontrib><creatorcontrib>YONG BEOM LEE</creatorcontrib><creatorcontrib>KIM, S. U</creatorcontrib><creatorcontrib>KRIEGER, C</creatorcontrib><title>Cholinergic agonists increase intracellular Ca2+ in cultured human microglia</title><title>Neuroscience letters</title><addtitle>Neurosci Lett</addtitle><description>Microglia are resident phagocytic cells in the central nervous system (CNS), and can be activated in response to various stimuli including neurotransmitters. Using fura-2 imaging, we investigated the effects of carbachol (CCh), a cholinergic agonist, on [Ca2+]i in cultured human microglia. Treatment of microglia with CCh (100 microM) produced a transient increase in [Ca2+]i, which was atropine-sensitive and was associated with release from intracellular Ca2+ stores. Successive applications of CCh showed a change in the amplitude of the [Ca2+]i signal consistent with desensitization. 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Neuroglia</subject><subject>Microglia - drug effects</subject><subject>Microglia - metabolism</subject><subject>Muscarinic Antagonists - pharmacology</subject><subject>Osmolar Concentration</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0304-3940</issn><issn>1872-7972</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNo9kEtLxDAQx4Mo67r6ERZ6EFGkOk3S11GKL1jwoMLewiSd7kb6WJP24Le3-2BPGTK_mfnzY2wewUMEUfL4CQJkKHIJt3l2B5BCEi5P2DTKUh6mecpP2fSInLML738AII5iOWGTPBMjAVO2KNZdbVtyK2sCXHWt9b0PbGscoaex6B0aquuhRhcUyO_Hr8AMdT84KoP10GAbNNa4blVbvGRnFdaerg7vjH2_PH8Vb-Hi4_W9eFqERkRpH2qDhgupY85jpDKTFUTEua5KJKpKQ1pr0JhzrUlgUhHJrEwkJiJPpJCJmLGb_d6N634H8r1qrN-mxJa6wasUIMukSEcw3oNjQO8dVWrjbIPuT0WgthbVzqLaKlJ5pnYW1XKcmx8ODLqh8jh10Db2rw999AbrymFrrD9iXIo4HwP8A9n6fCg</recordid><startdate>19981009</startdate><enddate>19981009</enddate><creator>ZHANG, L</creator><creator>MCLARNON, J. 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U ; KRIEGER, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c317t-bcac234b5225aed84f01e22bfdaeefdcebbb0ba92bbe3a6fee48d64a639643463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Atropine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Calcium - metabolism</topic><topic>Carbachol - administration & dosage</topic><topic>Carbachol - pharmacology</topic><topic>Cells, Cultured</topic><topic>Cholinergic Agonists - administration & dosage</topic><topic>Cholinergic Agonists - pharmacology</topic><topic>Drug Administration Schedule</topic><topic>Drug Combinations</topic><topic>Fetus</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Intracellular Membranes - metabolism</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>Microglia - drug effects</topic><topic>Microglia - metabolism</topic><topic>Muscarinic Antagonists - pharmacology</topic><topic>Osmolar Concentration</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ZHANG, L</creatorcontrib><creatorcontrib>MCLARNON, J. G</creatorcontrib><creatorcontrib>GOGHARI, V</creatorcontrib><creatorcontrib>YONG BEOM LEE</creatorcontrib><creatorcontrib>KIM, S. 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U</au><au>KRIEGER, C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cholinergic agonists increase intracellular Ca2+ in cultured human microglia</atitle><jtitle>Neuroscience letters</jtitle><addtitle>Neurosci Lett</addtitle><date>1998-10-09</date><risdate>1998</risdate><volume>255</volume><issue>1</issue><spage>33</spage><epage>36</epage><pages>33-36</pages><issn>0304-3940</issn><eissn>1872-7972</eissn><coden>NELED5</coden><abstract>Microglia are resident phagocytic cells in the central nervous system (CNS), and can be activated in response to various stimuli including neurotransmitters. Using fura-2 imaging, we investigated the effects of carbachol (CCh), a cholinergic agonist, on [Ca2+]i in cultured human microglia. Treatment of microglia with CCh (100 microM) produced a transient increase in [Ca2+]i, which was atropine-sensitive and was associated with release from intracellular Ca2+ stores. Successive applications of CCh showed a change in the amplitude of the [Ca2+]i signal consistent with desensitization. These results show that human microglia express functional muscarinic receptors and respond to cholinergic agonists. The rapid change of [Ca2+]i in microglia may serve as a second messenger to trigger downstream cascades which contribute to signalling pathways in CNS pathology.</abstract><cop>Shannon</cop><pub>Elsevier</pub><pmid>9839720</pmid><doi>10.1016/S0304-3940(98)00706-X</doi><tpages>4</tpages></addata></record> |
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subjects | Atropine - pharmacology Biological and medical sciences Calcium - metabolism Carbachol - administration & dosage Carbachol - pharmacology Cells, Cultured Cholinergic Agonists - administration & dosage Cholinergic Agonists - pharmacology Drug Administration Schedule Drug Combinations Fetus Fundamental and applied biological sciences. Psychology Humans Intracellular Membranes - metabolism Isolated neuron and nerve. Neuroglia Microglia - drug effects Microglia - metabolism Muscarinic Antagonists - pharmacology Osmolar Concentration Vertebrates: nervous system and sense organs |
title | Cholinergic agonists increase intracellular Ca2+ in cultured human microglia |
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