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Two modes of exocytosis from synaptosomes are differentially regulated by protein phosphatase types 2A and 2B
The inhibitors okadaic acid (OA), fostriecin (FOS) and cyclosporin A (CsA), were used to investigate the roles of protein phosphatases in regulating exocytosis in rat brain synaptosomes by measuring glutamate release and the release of the styryl dye FM 2‐10. Depolarization was induced by 30 mm KCl,...
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Published in: | Journal of neurochemistry 2003-06, Vol.85 (5), p.1190-1199 |
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description | The inhibitors okadaic acid (OA), fostriecin (FOS) and cyclosporin A (CsA), were used to investigate the roles of protein phosphatases in regulating exocytosis in rat brain synaptosomes by measuring glutamate release and the release of the styryl dye FM 2‐10. Depolarization was induced by 30 mm KCl, or 0.3 mm or 1 mm 4‐aminopyridine (4AP). OA and FOS produced a similar partial inhibition of KCl‐ and 0.3 mm 4AP‐ evoked exocytosis in both assays, but had little effect upon exocytosis evoked by 1 mm 4AP. In contrast, CsA had no effect upon KCl‐ and 0.3 mm 4AP‐evoked exocytosis, but significantly enhanced glutamate release but not FM 2‐10 dye release evoked by 1 mm 4AP. None of the phosphatase inhibitors changed calcium signals from FURA‐2‐loaded synaptosomes either before or after depolarization. Pretreatment with 100 nm phorbol 12‐myristate 13‐acetate abolished the inhibitory effect of OA on exocytosis induced by 0.3 mm 4AP. Taken together, these results show that exocytosis from synaptosomes has a phosphatase‐sensitive and phosphatase‐insensitive component, and that there are two modes of phosphatase‐sensitive exocytosis that can be elicited by different depolarization conditions. Moreover, these two modes are differentially sensitive to phosphatase 2A and 2B. |
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P. ; Sim, Alistair T. R.</creator><creatorcontrib>Baldwin, Monique L. ; Rostas, John A. P. ; Sim, Alistair T. R.</creatorcontrib><description>The inhibitors okadaic acid (OA), fostriecin (FOS) and cyclosporin A (CsA), were used to investigate the roles of protein phosphatases in regulating exocytosis in rat brain synaptosomes by measuring glutamate release and the release of the styryl dye FM 2‐10. Depolarization was induced by 30 mm KCl, or 0.3 mm or 1 mm 4‐aminopyridine (4AP). OA and FOS produced a similar partial inhibition of KCl‐ and 0.3 mm 4AP‐ evoked exocytosis in both assays, but had little effect upon exocytosis evoked by 1 mm 4AP. In contrast, CsA had no effect upon KCl‐ and 0.3 mm 4AP‐evoked exocytosis, but significantly enhanced glutamate release but not FM 2‐10 dye release evoked by 1 mm 4AP. None of the phosphatase inhibitors changed calcium signals from FURA‐2‐loaded synaptosomes either before or after depolarization. Pretreatment with 100 nm phorbol 12‐myristate 13‐acetate abolished the inhibitory effect of OA on exocytosis induced by 0.3 mm 4AP. Taken together, these results show that exocytosis from synaptosomes has a phosphatase‐sensitive and phosphatase‐insensitive component, and that there are two modes of phosphatase‐sensitive exocytosis that can be elicited by different depolarization conditions. Moreover, these two modes are differentially sensitive to phosphatase 2A and 2B.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1046/j.1471-4159.2003.01779.x</identifier><identifier>PMID: 12753078</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Biological and medical sciences ; Brain Chemistry ; Calcineurin - chemistry ; Calcineurin - metabolism ; Calcineurin Inhibitors ; Calcium - analysis ; Calcium - metabolism ; Cell physiology ; Cyclosporine - pharmacology ; Enzyme Inhibitors - pharmacology ; exocytosis ; Exocytosis - drug effects ; Exocytosis - physiology ; Fluorescent Dyes - chemistry ; FM 2‐10 ; Fundamental and applied biological sciences. Psychology ; glutamate ; Glutamic Acid - metabolism ; kiss‐and‐run ; Molecular and cellular biology ; Phosphoprotein Phosphatases - antagonists & inhibitors ; Phosphoprotein Phosphatases - chemistry ; Phosphoprotein Phosphatases - metabolism ; protein phosphatase ; Protein Phosphatase 2 ; Rats ; Secretion. Exocytosis ; synaptic vesicle ; Synaptosomes - chemistry ; Synaptosomes - drug effects ; Synaptosomes - enzymology</subject><ispartof>Journal of neurochemistry, 2003-06, Vol.85 (5), p.1190-1199</ispartof><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4929-75805fbfefcb189f9c456546f6e492202dcb7f6f265e445607c83265f0e1339c3</citedby><cites>FETCH-LOGICAL-c4929-75805fbfefcb189f9c456546f6e492202dcb7f6f265e445607c83265f0e1339c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14792649$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12753078$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baldwin, Monique L.</creatorcontrib><creatorcontrib>Rostas, John A. P.</creatorcontrib><creatorcontrib>Sim, Alistair T. R.</creatorcontrib><title>Two modes of exocytosis from synaptosomes are differentially regulated by protein phosphatase types 2A and 2B</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>The inhibitors okadaic acid (OA), fostriecin (FOS) and cyclosporin A (CsA), were used to investigate the roles of protein phosphatases in regulating exocytosis in rat brain synaptosomes by measuring glutamate release and the release of the styryl dye FM 2‐10. Depolarization was induced by 30 mm KCl, or 0.3 mm or 1 mm 4‐aminopyridine (4AP). OA and FOS produced a similar partial inhibition of KCl‐ and 0.3 mm 4AP‐ evoked exocytosis in both assays, but had little effect upon exocytosis evoked by 1 mm 4AP. In contrast, CsA had no effect upon KCl‐ and 0.3 mm 4AP‐evoked exocytosis, but significantly enhanced glutamate release but not FM 2‐10 dye release evoked by 1 mm 4AP. None of the phosphatase inhibitors changed calcium signals from FURA‐2‐loaded synaptosomes either before or after depolarization. Pretreatment with 100 nm phorbol 12‐myristate 13‐acetate abolished the inhibitory effect of OA on exocytosis induced by 0.3 mm 4AP. Taken together, these results show that exocytosis from synaptosomes has a phosphatase‐sensitive and phosphatase‐insensitive component, and that there are two modes of phosphatase‐sensitive exocytosis that can be elicited by different depolarization conditions. Moreover, these two modes are differentially sensitive to phosphatase 2A and 2B.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain Chemistry</subject><subject>Calcineurin - chemistry</subject><subject>Calcineurin - metabolism</subject><subject>Calcineurin Inhibitors</subject><subject>Calcium - analysis</subject><subject>Calcium - metabolism</subject><subject>Cell physiology</subject><subject>Cyclosporine - pharmacology</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>exocytosis</subject><subject>Exocytosis - drug effects</subject><subject>Exocytosis - physiology</subject><subject>Fluorescent Dyes - chemistry</subject><subject>FM 2‐10</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>glutamate</subject><subject>Glutamic Acid - metabolism</subject><subject>kiss‐and‐run</subject><subject>Molecular and cellular biology</subject><subject>Phosphoprotein Phosphatases - antagonists & inhibitors</subject><subject>Phosphoprotein Phosphatases - chemistry</subject><subject>Phosphoprotein Phosphatases - metabolism</subject><subject>protein phosphatase</subject><subject>Protein Phosphatase 2</subject><subject>Rats</subject><subject>Secretion. Exocytosis</subject><subject>synaptic vesicle</subject><subject>Synaptosomes - chemistry</subject><subject>Synaptosomes - drug effects</subject><subject>Synaptosomes - enzymology</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqNkU9v1DAQxS0EokvhKyBf4Jbgf7HjA4eyAlpUtZdythxnTLNK4mBn1c23r9Nd0SM9eUbvN56neQhhSkpKhPyyK6lQtBC00iUjhJeEKqXLwyu0-Se8RhtCGCs4EewMvUtpRwiVQtK36IwyVXGi6g0a7h4CHkILCQeP4RDcMofUJexjGHBaRjvlPgxZtxFw23kPEca5s32_4Ah_9r2docXNgqcYZuhGPN2HNN3b2SbA8zLlSXaB7dhi9u09euNtn-DD6T1Hv398v9teFte3P6-2F9eFE5rpQlU1qXzjwbuG1tprJypZCeklZJ0R1rpGeemZrEBkiShX89x4ApRz7fg5-nz8N3v6u4c0m6FLDvrejhD2ySjOakaE_i-YtwteVyKD9RF0MaQUwZspdoONi6HErJmYnVlPb9bTmzUT85SJOeTRj6cd-2aA9nnwFEIGPp0Am5ztfbSj69IzJ5Rm8sns1yP30PWwvNiA-XWzXSv-CFnmp_g</recordid><startdate>200306</startdate><enddate>200306</enddate><creator>Baldwin, Monique L.</creator><creator>Rostas, John A. P.</creator><creator>Sim, Alistair T. R.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</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>200306</creationdate><title>Two modes of exocytosis from synaptosomes are differentially regulated by protein phosphatase types 2A and 2B</title><author>Baldwin, Monique L. ; Rostas, John A. P. ; Sim, Alistair T. R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4929-75805fbfefcb189f9c456546f6e492202dcb7f6f265e445607c83265f0e1339c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain Chemistry</topic><topic>Calcineurin - chemistry</topic><topic>Calcineurin - metabolism</topic><topic>Calcineurin Inhibitors</topic><topic>Calcium - analysis</topic><topic>Calcium - metabolism</topic><topic>Cell physiology</topic><topic>Cyclosporine - pharmacology</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>exocytosis</topic><topic>Exocytosis - drug effects</topic><topic>Exocytosis - physiology</topic><topic>Fluorescent Dyes - chemistry</topic><topic>FM 2‐10</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>glutamate</topic><topic>Glutamic Acid - metabolism</topic><topic>kiss‐and‐run</topic><topic>Molecular and cellular biology</topic><topic>Phosphoprotein Phosphatases - antagonists & inhibitors</topic><topic>Phosphoprotein Phosphatases - chemistry</topic><topic>Phosphoprotein Phosphatases - metabolism</topic><topic>protein phosphatase</topic><topic>Protein Phosphatase 2</topic><topic>Rats</topic><topic>Secretion. Exocytosis</topic><topic>synaptic vesicle</topic><topic>Synaptosomes - chemistry</topic><topic>Synaptosomes - drug effects</topic><topic>Synaptosomes - enzymology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baldwin, Monique L.</creatorcontrib><creatorcontrib>Rostas, John A. P.</creatorcontrib><creatorcontrib>Sim, Alistair T. R.</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>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baldwin, Monique L.</au><au>Rostas, John A. P.</au><au>Sim, Alistair T. R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two modes of exocytosis from synaptosomes are differentially regulated by protein phosphatase types 2A and 2B</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2003-06</date><risdate>2003</risdate><volume>85</volume><issue>5</issue><spage>1190</spage><epage>1199</epage><pages>1190-1199</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>The inhibitors okadaic acid (OA), fostriecin (FOS) and cyclosporin A (CsA), were used to investigate the roles of protein phosphatases in regulating exocytosis in rat brain synaptosomes by measuring glutamate release and the release of the styryl dye FM 2‐10. Depolarization was induced by 30 mm KCl, or 0.3 mm or 1 mm 4‐aminopyridine (4AP). OA and FOS produced a similar partial inhibition of KCl‐ and 0.3 mm 4AP‐ evoked exocytosis in both assays, but had little effect upon exocytosis evoked by 1 mm 4AP. In contrast, CsA had no effect upon KCl‐ and 0.3 mm 4AP‐evoked exocytosis, but significantly enhanced glutamate release but not FM 2‐10 dye release evoked by 1 mm 4AP. None of the phosphatase inhibitors changed calcium signals from FURA‐2‐loaded synaptosomes either before or after depolarization. Pretreatment with 100 nm phorbol 12‐myristate 13‐acetate abolished the inhibitory effect of OA on exocytosis induced by 0.3 mm 4AP. Taken together, these results show that exocytosis from synaptosomes has a phosphatase‐sensitive and phosphatase‐insensitive component, and that there are two modes of phosphatase‐sensitive exocytosis that can be elicited by different depolarization conditions. Moreover, these two modes are differentially sensitive to phosphatase 2A and 2B.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>12753078</pmid><doi>10.1046/j.1471-4159.2003.01779.x</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Brain Chemistry Calcineurin - chemistry Calcineurin - metabolism Calcineurin Inhibitors Calcium - analysis Calcium - metabolism Cell physiology Cyclosporine - pharmacology Enzyme Inhibitors - pharmacology exocytosis Exocytosis - drug effects Exocytosis - physiology Fluorescent Dyes - chemistry FM 2‐10 Fundamental and applied biological sciences. Psychology glutamate Glutamic Acid - metabolism kiss‐and‐run Molecular and cellular biology Phosphoprotein Phosphatases - antagonists & inhibitors Phosphoprotein Phosphatases - chemistry Phosphoprotein Phosphatases - metabolism protein phosphatase Protein Phosphatase 2 Rats Secretion. Exocytosis synaptic vesicle Synaptosomes - chemistry Synaptosomes - drug effects Synaptosomes - enzymology |
title | Two modes of exocytosis from synaptosomes are differentially regulated by protein phosphatase types 2A and 2B |
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