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Mapacalcine protects mouse neurons against hypoxia by blocking cell calcium overload
Stroke is one of a major cause of death and adult disability. Despite intense researches, treatment for stroke remains reduced to fibrinolysis, a technique useful for less than 10% of patients. Finding molecules able to treat or at least to decrease the deleterious consequences of stroke is an urgen...
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Published in: | PloS one 2013-07, Vol.8 (7), p.e66194-e66194 |
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creator | Moha Ou Maati, Hamid Widmann, Catherine Sedjelmaci, Djamila Gallois, Djamila Sedjelmaci Bernard Gallois, Bernard Heurteaux, Catherine Borsotto, Marc Hugues, Michel |
description | Stroke is one of a major cause of death and adult disability. Despite intense researches, treatment for stroke remains reduced to fibrinolysis, a technique useful for less than 10% of patients. Finding molecules able to treat or at least to decrease the deleterious consequences of stroke is an urgent need. Here, we showed that mapacalcine, a homodimeric peptide purified from the marine sponge Cliona vastifica, is able to protect mouse cortical neurons against hypoxia. We have also identified a subtype of L-type calcium channel as a target for mapacalcine and we showed that the channel has to be open for mapacalcine binding. The two main L-type subunits at the brain level are CaV1.3 and CaV1.2 subunits but mapacalcine was unable to block these calcium channels.Mapacalcine did not interfere with N-, P/Q- and R-type calcium channels. The protective effect was studied by measuring internal calcium level variation triggered by Oxygen Glucose Deprivation protocol, which mimics stroke, or glutamate stimulation. We showed that NMDA/AMPA receptors are not involved in the mapacalcine protection. The protective effect was confirmed by measuring the cell survival rate after Oxygen Glucose Deprivation condition. Our data indicate that mapacalcine is a promising molecule for stroke treatment. |
doi_str_mv | 10.1371/journal.pone.0066194 |
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Despite intense researches, treatment for stroke remains reduced to fibrinolysis, a technique useful for less than 10% of patients. Finding molecules able to treat or at least to decrease the deleterious consequences of stroke is an urgent need. Here, we showed that mapacalcine, a homodimeric peptide purified from the marine sponge Cliona vastifica, is able to protect mouse cortical neurons against hypoxia. We have also identified a subtype of L-type calcium channel as a target for mapacalcine and we showed that the channel has to be open for mapacalcine binding. The two main L-type subunits at the brain level are CaV1.3 and CaV1.2 subunits but mapacalcine was unable to block these calcium channels.Mapacalcine did not interfere with N-, P/Q- and R-type calcium channels. The protective effect was studied by measuring internal calcium level variation triggered by Oxygen Glucose Deprivation protocol, which mimics stroke, or glutamate stimulation. We showed that NMDA/AMPA receptors are not involved in the mapacalcine protection. The protective effect was confirmed by measuring the cell survival rate after Oxygen Glucose Deprivation condition. Our data indicate that mapacalcine is a promising molecule for stroke treatment.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0066194</identifier><identifier>PMID: 23843951</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Apoptosis ; Biology ; Blocking ; Brain ; Brain research ; Calcium ; Calcium - metabolism ; Calcium Channel Blockers - isolation & purification ; Calcium Channel Blockers - pharmacology ; Calcium channels ; Calcium channels (L-type) ; Calcium channels (R-type) ; Calcium channels (voltage-gated) ; Calcium Channels, L-Type - metabolism ; Cell Hypoxia ; Cell survival ; Cerebral Cortex - cytology ; Cerebral Cortex - drug effects ; Cerebral Cortex - metabolism ; Channels ; Deprivation ; Drug therapy ; Embryo, Mammalian ; Experiments ; Fibrinolysis ; Genetic aspects ; Glucose ; Glucose - deficiency ; Glutamic acid receptors (ionotropic) ; HEK293 Cells ; Humans ; Hypoxia ; Ischemia ; Laboratory animals ; Male ; Medical prognosis ; Medicine ; Membrane Potentials - drug effects ; Membrane Potentials - physiology ; Mice ; N-Methyl-D-aspartic acid receptors ; Nervous system ; Neurons ; Neurons - cytology ; Neurons - drug effects ; Neurons - metabolism ; Oxygen ; Oxygen - metabolism ; Oxygen - pharmacology ; Pain ; Patch-Clamp Techniques ; Peptides ; Physiological aspects ; Porifera - chemistry ; Primary Cell Culture ; Protection and preservation ; Proteins - isolation & purification ; Proteins - pharmacology ; Receptors ; Receptors, AMPA - metabolism ; Receptors, N-Methyl-D-Aspartate - metabolism ; Rodents ; Stroke ; α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid ; α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors</subject><ispartof>PloS one, 2013-07, Vol.8 (7), p.e66194-e66194</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Moha ou Maati et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Moha ou Maati et al 2013 Moha ou Maati et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-a041d5aa9f7348564f8d96100769e7ffff1a673b418efe7147a3ca75cd73ac103</citedby><cites>FETCH-LOGICAL-c692t-a041d5aa9f7348564f8d96100769e7ffff1a673b418efe7147a3ca75cd73ac103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1426970580/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1426970580?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23843951$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Woodhall, Gavin</contributor><creatorcontrib>Moha Ou Maati, Hamid</creatorcontrib><creatorcontrib>Widmann, Catherine</creatorcontrib><creatorcontrib>Sedjelmaci, Djamila</creatorcontrib><creatorcontrib>Gallois, Djamila Sedjelmaci Bernard</creatorcontrib><creatorcontrib>Gallois, Bernard</creatorcontrib><creatorcontrib>Heurteaux, Catherine</creatorcontrib><creatorcontrib>Borsotto, Marc</creatorcontrib><creatorcontrib>Hugues, Michel</creatorcontrib><title>Mapacalcine protects mouse neurons against hypoxia by blocking cell calcium overload</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Stroke is one of a major cause of death and adult disability. Despite intense researches, treatment for stroke remains reduced to fibrinolysis, a technique useful for less than 10% of patients. Finding molecules able to treat or at least to decrease the deleterious consequences of stroke is an urgent need. Here, we showed that mapacalcine, a homodimeric peptide purified from the marine sponge Cliona vastifica, is able to protect mouse cortical neurons against hypoxia. We have also identified a subtype of L-type calcium channel as a target for mapacalcine and we showed that the channel has to be open for mapacalcine binding. The two main L-type subunits at the brain level are CaV1.3 and CaV1.2 subunits but mapacalcine was unable to block these calcium channels.Mapacalcine did not interfere with N-, P/Q- and R-type calcium channels. The protective effect was studied by measuring internal calcium level variation triggered by Oxygen Glucose Deprivation protocol, which mimics stroke, or glutamate stimulation. We showed that NMDA/AMPA receptors are not involved in the mapacalcine protection. The protective effect was confirmed by measuring the cell survival rate after Oxygen Glucose Deprivation condition. 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deficiency</subject><subject>Glutamic acid receptors (ionotropic)</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Hypoxia</subject><subject>Ischemia</subject><subject>Laboratory animals</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Membrane Potentials - drug effects</subject><subject>Membrane Potentials - physiology</subject><subject>Mice</subject><subject>N-Methyl-D-aspartic acid receptors</subject><subject>Nervous system</subject><subject>Neurons</subject><subject>Neurons - cytology</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Oxygen</subject><subject>Oxygen - metabolism</subject><subject>Oxygen - pharmacology</subject><subject>Pain</subject><subject>Patch-Clamp Techniques</subject><subject>Peptides</subject><subject>Physiological aspects</subject><subject>Porifera - chemistry</subject><subject>Primary Cell Culture</subject><subject>Protection and preservation</subject><subject>Proteins - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moha Ou Maati, Hamid</au><au>Widmann, Catherine</au><au>Sedjelmaci, Djamila</au><au>Gallois, Djamila Sedjelmaci Bernard</au><au>Gallois, Bernard</au><au>Heurteaux, Catherine</au><au>Borsotto, Marc</au><au>Hugues, Michel</au><au>Woodhall, Gavin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mapacalcine protects mouse neurons against hypoxia by blocking cell calcium overload</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-07-02</date><risdate>2013</risdate><volume>8</volume><issue>7</issue><spage>e66194</spage><epage>e66194</epage><pages>e66194-e66194</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Stroke is one of a major cause of death and adult disability. Despite intense researches, treatment for stroke remains reduced to fibrinolysis, a technique useful for less than 10% of patients. Finding molecules able to treat or at least to decrease the deleterious consequences of stroke is an urgent need. Here, we showed that mapacalcine, a homodimeric peptide purified from the marine sponge Cliona vastifica, is able to protect mouse cortical neurons against hypoxia. We have also identified a subtype of L-type calcium channel as a target for mapacalcine and we showed that the channel has to be open for mapacalcine binding. The two main L-type subunits at the brain level are CaV1.3 and CaV1.2 subunits but mapacalcine was unable to block these calcium channels.Mapacalcine did not interfere with N-, P/Q- and R-type calcium channels. The protective effect was studied by measuring internal calcium level variation triggered by Oxygen Glucose Deprivation protocol, which mimics stroke, or glutamate stimulation. We showed that NMDA/AMPA receptors are not involved in the mapacalcine protection. The protective effect was confirmed by measuring the cell survival rate after Oxygen Glucose Deprivation condition. Our data indicate that mapacalcine is a promising molecule for stroke treatment.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23843951</pmid><doi>10.1371/journal.pone.0066194</doi><tpages>e66194</tpages><oa>free_for_read</oa></addata></record> |
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recordid | cdi_plos_journals_1426970580 |
source | Publicly Available Content Database; PubMed Central |
subjects | Animals Apoptosis Biology Blocking Brain Brain research Calcium Calcium - metabolism Calcium Channel Blockers - isolation & purification Calcium Channel Blockers - pharmacology Calcium channels Calcium channels (L-type) Calcium channels (R-type) Calcium channels (voltage-gated) Calcium Channels, L-Type - metabolism Cell Hypoxia Cell survival Cerebral Cortex - cytology Cerebral Cortex - drug effects Cerebral Cortex - metabolism Channels Deprivation Drug therapy Embryo, Mammalian Experiments Fibrinolysis Genetic aspects Glucose Glucose - deficiency Glutamic acid receptors (ionotropic) HEK293 Cells Humans Hypoxia Ischemia Laboratory animals Male Medical prognosis Medicine Membrane Potentials - drug effects Membrane Potentials - physiology Mice N-Methyl-D-aspartic acid receptors Nervous system Neurons Neurons - cytology Neurons - drug effects Neurons - metabolism Oxygen Oxygen - metabolism Oxygen - pharmacology Pain Patch-Clamp Techniques Peptides Physiological aspects Porifera - chemistry Primary Cell Culture Protection and preservation Proteins - isolation & purification Proteins - pharmacology Receptors Receptors, AMPA - metabolism Receptors, N-Methyl-D-Aspartate - metabolism Rodents Stroke α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors |
title | Mapacalcine protects mouse neurons against hypoxia by blocking cell calcium overload |
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