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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
Main Authors: Baldwin, Monique L., Rostas, John A. P., Sim, Alistair T. R.
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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. 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Psychology ; glutamate ; Glutamic Acid - metabolism ; kiss‐and‐run ; Molecular and cellular biology ; Phosphoprotein Phosphatases - antagonists &amp; inhibitors ; Phosphoprotein Phosphatases - chemistry ; Phosphoprotein Phosphatases - metabolism ; protein phosphatase ; Protein Phosphatase 2 ; Rats ; Secretion. 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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 &amp; 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. 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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 &amp; 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. 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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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source Wiley; Free Full-Text Journals in Chemistry
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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