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Carbonyl cyanide m-chlorophenylhydrazone induced calcium signaling and activation of plasma membrane H⁺-ATPase in the yeast Saccharomyces cerevisiae
The plasma membrane H⁺-ATPase from Saccharomyces cerevisiae is an enzyme that plays a very important role in the yeast physiology. The addition of protonophores, such as 2,4-dinitrophenol (DNP) and carbonyl cyanide m-chlorophenylhydrazone (CCCP), also triggers a clear in vivo activation of this enzy...
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Published in: | FEMS yeast research 2008-06, Vol.8 (4), p.622-630 |
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creator | Pereira, Michele B.P Tisi, Renata Fietto, Luciano G Cardoso, Anamaria S França, Mônica M Carvalho, Fernanda M Trópia, Maria José M Martegani, Enzo Castro, Ieso M Brandão, Rogelio L |
description | The plasma membrane H⁺-ATPase from Saccharomyces cerevisiae is an enzyme that plays a very important role in the yeast physiology. The addition of protonophores, such as 2,4-dinitrophenol (DNP) and carbonyl cyanide m-chlorophenylhydrazone (CCCP), also triggers a clear in vivo activation of this enzyme. Here, we demonstrate that CCCP-induced activation of the plasma membrane H⁺-ATPase shares some similarities with the sugar-induced activation of the enzyme. Phospholipase C and protein kinase C activities are essential for this activation process while Gpa2p, a G protein involved in the glucose-induced activation of the ATPase, is not required. CCCP also induces a phospholipase C-dependent increase in intracellular calcium. Moreover, we show that the availability of extracellular calcium is required for CCCP stimulation of H⁺-ATPase, suggesting a possible connection between calcium signaling and activation of ATPase. |
doi_str_mv | 10.1111/j.1567-1364.2008.00380.x |
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The addition of protonophores, such as 2,4-dinitrophenol (DNP) and carbonyl cyanide m-chlorophenylhydrazone (CCCP), also triggers a clear in vivo activation of this enzyme. Here, we demonstrate that CCCP-induced activation of the plasma membrane H⁺-ATPase shares some similarities with the sugar-induced activation of the enzyme. Phospholipase C and protein kinase C activities are essential for this activation process while Gpa2p, a G protein involved in the glucose-induced activation of the ATPase, is not required. CCCP also induces a phospholipase C-dependent increase in intracellular calcium. Moreover, we show that the availability of extracellular calcium is required for CCCP stimulation of H⁺-ATPase, suggesting a possible connection between calcium signaling and activation of ATPase.</description><identifier>ISSN: 1567-1356</identifier><identifier>EISSN: 1567-1364</identifier><identifier>DOI: 10.1111/j.1567-1364.2008.00380.x</identifier><identifier>PMID: 18399987</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>2,4-Dinitrophenol ; Calcium (extracellular) ; Calcium (intracellular) ; Calcium - analysis ; Calcium Signaling - drug effects ; Calcium signalling ; Carbonyl compounds ; Carbonyl Cyanide m-Chlorophenyl Hydrazone - analogs & derivatives ; Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology ; Cell Membrane - enzymology ; Cyanides ; Cytosol - chemistry ; depolarizing compounds ; Enzymes ; GTP-Binding Protein alpha Subunits - metabolism ; H+-transporting ATPase ; Hydrogen ; Ionophores - pharmacology ; Kinases ; Phospholipase C ; Plasma membrane H+‐ATPase ; Protein kinase C ; Protein Kinase C - metabolism ; Proton-Translocating ATPases - metabolism ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - chemistry ; Saccharomyces cerevisiae - metabolism ; Saccharomyces cerevisiae Proteins - metabolism ; Type C Phospholipases - metabolism ; Yeast</subject><ispartof>FEMS yeast research, 2008-06, Vol.8 (4), p.622-630</ispartof><rights>2008 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved 2008</rights><rights>2008 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. 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The addition of protonophores, such as 2,4-dinitrophenol (DNP) and carbonyl cyanide m-chlorophenylhydrazone (CCCP), also triggers a clear in vivo activation of this enzyme. Here, we demonstrate that CCCP-induced activation of the plasma membrane H⁺-ATPase shares some similarities with the sugar-induced activation of the enzyme. Phospholipase C and protein kinase C activities are essential for this activation process while Gpa2p, a G protein involved in the glucose-induced activation of the ATPase, is not required. CCCP also induces a phospholipase C-dependent increase in intracellular calcium. Moreover, we show that the availability of extracellular calcium is required for CCCP stimulation of H⁺-ATPase, suggesting a possible connection between calcium signaling and activation of ATPase.</description><subject>2,4-Dinitrophenol</subject><subject>Calcium (extracellular)</subject><subject>Calcium (intracellular)</subject><subject>Calcium - analysis</subject><subject>Calcium Signaling - drug effects</subject><subject>Calcium signalling</subject><subject>Carbonyl compounds</subject><subject>Carbonyl Cyanide m-Chlorophenyl Hydrazone - analogs & derivatives</subject><subject>Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology</subject><subject>Cell Membrane - enzymology</subject><subject>Cyanides</subject><subject>Cytosol - chemistry</subject><subject>depolarizing compounds</subject><subject>Enzymes</subject><subject>GTP-Binding Protein alpha Subunits - metabolism</subject><subject>H+-transporting ATPase</subject><subject>Hydrogen</subject><subject>Ionophores - pharmacology</subject><subject>Kinases</subject><subject>Phospholipase C</subject><subject>Plasma membrane H+‐ATPase</subject><subject>Protein kinase C</subject><subject>Protein Kinase C - metabolism</subject><subject>Proton-Translocating ATPases - metabolism</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - chemistry</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Saccharomyces cerevisiae Proteins - metabolism</subject><subject>Type C Phospholipases - metabolism</subject><subject>Yeast</subject><issn>1567-1356</issn><issn>1567-1364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kc2K1TAUx4sozoe-ggYEd61J0-YD3AwXZ0YYUJyZhatwmqa3ubRNTdpx6s6X8GF8HJ_E1DuOoJhNDjm_3yGcf5IggjMSz6tdRkrGU0JZkeUYiwxjKnB2-yA5vG88vK9LdpAchbDDmPAIP04OiKBSSsEPk28b8JUblg7pBQZbG9Snuu2cd2Nr4nO71B6-uMEgO9SzNjXS0Gk79yjY7QCdHbYIhhqBnuwNTNYNyDVo7CD0gHrTVx6ie_7j6_f05Oo9hHUOmlqDFgNhQpegdQve9Ys2AWnjzY0NFsyT5FEDXTBP7-7j5Pr0zdXmPL14d_Z2c3KR6oJRnLKagaQN07rBTFZlY0xFJMGNkJVkJteSlaXQouAFq3nsayhLInBZ8gYkE_Q4ebmfO3r3aTZhUr0N2nRd_LWbg-KY5zmXPIIv_gJ3bvZxAUHllJaE5VyQSD27o-aqN7Uave3BL-r3viPweg98tp1Z_vSxWnNVO7VGptb41Jqr-pWrulWnHz_EIup0r7t5_I-c_iNH6_neasAp2Hob1PVljgmNkGSEFvQnhPWxWQ</recordid><startdate>200806</startdate><enddate>200806</enddate><creator>Pereira, Michele B.P</creator><creator>Tisi, Renata</creator><creator>Fietto, Luciano G</creator><creator>Cardoso, Anamaria S</creator><creator>França, Mônica M</creator><creator>Carvalho, Fernanda M</creator><creator>Trópia, Maria José M</creator><creator>Martegani, Enzo</creator><creator>Castro, Ieso M</creator><creator>Brandão, Rogelio L</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Oxford University Press</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200806</creationdate><title>Carbonyl cyanide m-chlorophenylhydrazone induced calcium signaling and activation of plasma membrane H⁺-ATPase in the yeast Saccharomyces cerevisiae</title><author>Pereira, Michele B.P ; Tisi, Renata ; Fietto, Luciano G ; Cardoso, Anamaria S ; França, Mônica M ; Carvalho, Fernanda M ; Trópia, Maria José M ; Martegani, Enzo ; Castro, Ieso M ; Brandão, Rogelio L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4630-6d6a93f6ccf069b5feeb1910f89b96e2c96558c84746d7b5fca55180557fa9683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>2,4-Dinitrophenol</topic><topic>Calcium (extracellular)</topic><topic>Calcium (intracellular)</topic><topic>Calcium - analysis</topic><topic>Calcium Signaling - drug effects</topic><topic>Calcium signalling</topic><topic>Carbonyl compounds</topic><topic>Carbonyl Cyanide m-Chlorophenyl Hydrazone - analogs & derivatives</topic><topic>Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology</topic><topic>Cell Membrane - enzymology</topic><topic>Cyanides</topic><topic>Cytosol - chemistry</topic><topic>depolarizing compounds</topic><topic>Enzymes</topic><topic>GTP-Binding Protein alpha Subunits - metabolism</topic><topic>H+-transporting ATPase</topic><topic>Hydrogen</topic><topic>Ionophores - pharmacology</topic><topic>Kinases</topic><topic>Phospholipase C</topic><topic>Plasma membrane H+‐ATPase</topic><topic>Protein kinase C</topic><topic>Protein Kinase C - metabolism</topic><topic>Proton-Translocating ATPases - metabolism</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - chemistry</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Saccharomyces cerevisiae Proteins - 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The addition of protonophores, such as 2,4-dinitrophenol (DNP) and carbonyl cyanide m-chlorophenylhydrazone (CCCP), also triggers a clear in vivo activation of this enzyme. Here, we demonstrate that CCCP-induced activation of the plasma membrane H⁺-ATPase shares some similarities with the sugar-induced activation of the enzyme. Phospholipase C and protein kinase C activities are essential for this activation process while Gpa2p, a G protein involved in the glucose-induced activation of the ATPase, is not required. CCCP also induces a phospholipase C-dependent increase in intracellular calcium. 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subjects | 2,4-Dinitrophenol Calcium (extracellular) Calcium (intracellular) Calcium - analysis Calcium Signaling - drug effects Calcium signalling Carbonyl compounds Carbonyl Cyanide m-Chlorophenyl Hydrazone - analogs & derivatives Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology Cell Membrane - enzymology Cyanides Cytosol - chemistry depolarizing compounds Enzymes GTP-Binding Protein alpha Subunits - metabolism H+-transporting ATPase Hydrogen Ionophores - pharmacology Kinases Phospholipase C Plasma membrane H+‐ATPase Protein kinase C Protein Kinase C - metabolism Proton-Translocating ATPases - metabolism Saccharomyces cerevisiae Saccharomyces cerevisiae - chemistry Saccharomyces cerevisiae - metabolism Saccharomyces cerevisiae Proteins - metabolism Type C Phospholipases - metabolism Yeast |
title | Carbonyl cyanide m-chlorophenylhydrazone induced calcium signaling and activation of plasma membrane H⁺-ATPase in the yeast Saccharomyces cerevisiae |
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