Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization

Autores
Buschiazzo, Jorgelina; Ialy Radio, Come; Auer, Jana; Wolf, Jean Philippe; Serres, Catherine; Lefèvre, Brigitte; Ziyyat, Ahmed
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Drastic membrane reorganization occurs when mammalian sperm binds to and fuses with the oocyte membrane. Two oocyte protein families are essential for fertilization, tetraspanins and glycosylphosphatidylinositol-anchored proteins. The firsts are associated to tetraspanin-enriched microdomains and the seconds to lipid rafts. Here we report membrane raft involvement in mouse fertilization assessed by cholesterol modulation using methyl-β-cyclodextrin. Cholesterol removal induced: (1) a decrease of the fertilization rate and index; and (2) a delay in the extrusion of the second polar body. Cholesterol repletion recovered the fertilization ability of cholesterol-depleted oocytes, indicating reversibility of these effects. In vivo time-lapse analyses using fluorescent cholesterol permitted to identify the time-point at which the probe is mainly located at the plasma membrane enabling the estimation of the extent of the cholesterol depletion. We confirmed that the mouse oocyte is rich in rafts according to the presence of the raft marker lipid, ganglioside GM1 on the membrane of living oocytes and we identified the coexistence of two types of microdomains, planar rafts and caveolae-like structures, by terms of two differential rafts markers, flotillin-2 and caveolin-1, respectively. Moreover, this is the first report that shows characteristic caveolae-like invaginations in the mouse oocyte identified by electron microscopy. Raft disruption by cholesterol depletion disturbed the subcellular localization of the signal molecule c-Src and the inhibition of Src kinase proteins prevented second polar body extrusion, consistent with a role of Src-related kinases in fertilization via signaling complexes. Our data highlight the functional importance of intact membrane rafts for mouse fertilization and its dependence on cholesterol.
Fil: Buschiazzo, Jorgelina. Universite Paris Descartes; Francia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina
Fil: Ialy Radio, Come. Universite Paris Descartes; Francia
Fil: Auer, Jana. Universite Paris Descartes; Francia
Fil: Wolf, Jean Philippe. Universite Paris Descartes; Francia
Fil: Serres, Catherine. Universite Paris Descartes; Francia
Fil: Lefèvre, Brigitte. Universite Paris Descartes; Francia
Fil: Ziyyat, Ahmed. Universite Paris Descartes; Francia
Materia
CHOLESTEROL
RAFTS
FERTILIZATION
MOUSE OOCYTE
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/482

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oai_identifier_str oai:ri.conicet.gov.ar:11336/482
network_acronym_str CONICETDig
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network_name_str CONICET Digital (CONICET)
spelling Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse FertilizationBuschiazzo, JorgelinaIaly Radio, ComeAuer, JanaWolf, Jean PhilippeSerres, CatherineLefèvre, BrigitteZiyyat, AhmedCHOLESTEROLRAFTSFERTILIZATIONMOUSE OOCYTEhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Drastic membrane reorganization occurs when mammalian sperm binds to and fuses with the oocyte membrane. Two oocyte protein families are essential for fertilization, tetraspanins and glycosylphosphatidylinositol-anchored proteins. The firsts are associated to tetraspanin-enriched microdomains and the seconds to lipid rafts. Here we report membrane raft involvement in mouse fertilization assessed by cholesterol modulation using methyl-β-cyclodextrin. Cholesterol removal induced: (1) a decrease of the fertilization rate and index; and (2) a delay in the extrusion of the second polar body. Cholesterol repletion recovered the fertilization ability of cholesterol-depleted oocytes, indicating reversibility of these effects. In vivo time-lapse analyses using fluorescent cholesterol permitted to identify the time-point at which the probe is mainly located at the plasma membrane enabling the estimation of the extent of the cholesterol depletion. We confirmed that the mouse oocyte is rich in rafts according to the presence of the raft marker lipid, ganglioside GM1 on the membrane of living oocytes and we identified the coexistence of two types of microdomains, planar rafts and caveolae-like structures, by terms of two differential rafts markers, flotillin-2 and caveolin-1, respectively. Moreover, this is the first report that shows characteristic caveolae-like invaginations in the mouse oocyte identified by electron microscopy. Raft disruption by cholesterol depletion disturbed the subcellular localization of the signal molecule c-Src and the inhibition of Src kinase proteins prevented second polar body extrusion, consistent with a role of Src-related kinases in fertilization via signaling complexes. Our data highlight the functional importance of intact membrane rafts for mouse fertilization and its dependence on cholesterol.Fil: Buschiazzo, Jorgelina. Universite Paris Descartes; Francia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaFil: Ialy Radio, Come. Universite Paris Descartes; FranciaFil: Auer, Jana. Universite Paris Descartes; FranciaFil: Wolf, Jean Philippe. Universite Paris Descartes; FranciaFil: Serres, Catherine. Universite Paris Descartes; FranciaFil: Lefèvre, Brigitte. Universite Paris Descartes; FranciaFil: Ziyyat, Ahmed. Universite Paris Descartes; FranciaPublic Library of Science2013-04-25info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/482Buschiazzo, Jorgelina; Ialy Radio, Come; Auer, Jana; Wolf, Jean Philippe; Serres, Catherine; et al.; Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization; Public Library of Science; Plos One; 8; 4; 25-4-2013; 1-13; e629191932-6203CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0062919info:eu-repo/semantics/altIdentifier/url/http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0062919info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:39:50Zoai:ri.conicet.gov.ar:11336/482instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 14:39:50.304CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization
title Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization
spellingShingle Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization
Buschiazzo, Jorgelina
CHOLESTEROL
RAFTS
FERTILIZATION
MOUSE OOCYTE
title_short Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization
title_full Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization
title_fullStr Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization
title_full_unstemmed Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization
title_sort Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization
dc.creator.none.fl_str_mv Buschiazzo, Jorgelina
Ialy Radio, Come
Auer, Jana
Wolf, Jean Philippe
Serres, Catherine
Lefèvre, Brigitte
Ziyyat, Ahmed
author Buschiazzo, Jorgelina
author_facet Buschiazzo, Jorgelina
Ialy Radio, Come
Auer, Jana
Wolf, Jean Philippe
Serres, Catherine
Lefèvre, Brigitte
Ziyyat, Ahmed
author_role author
author2 Ialy Radio, Come
Auer, Jana
Wolf, Jean Philippe
Serres, Catherine
Lefèvre, Brigitte
Ziyyat, Ahmed
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv CHOLESTEROL
RAFTS
FERTILIZATION
MOUSE OOCYTE
topic CHOLESTEROL
RAFTS
FERTILIZATION
MOUSE OOCYTE
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Drastic membrane reorganization occurs when mammalian sperm binds to and fuses with the oocyte membrane. Two oocyte protein families are essential for fertilization, tetraspanins and glycosylphosphatidylinositol-anchored proteins. The firsts are associated to tetraspanin-enriched microdomains and the seconds to lipid rafts. Here we report membrane raft involvement in mouse fertilization assessed by cholesterol modulation using methyl-β-cyclodextrin. Cholesterol removal induced: (1) a decrease of the fertilization rate and index; and (2) a delay in the extrusion of the second polar body. Cholesterol repletion recovered the fertilization ability of cholesterol-depleted oocytes, indicating reversibility of these effects. In vivo time-lapse analyses using fluorescent cholesterol permitted to identify the time-point at which the probe is mainly located at the plasma membrane enabling the estimation of the extent of the cholesterol depletion. We confirmed that the mouse oocyte is rich in rafts according to the presence of the raft marker lipid, ganglioside GM1 on the membrane of living oocytes and we identified the coexistence of two types of microdomains, planar rafts and caveolae-like structures, by terms of two differential rafts markers, flotillin-2 and caveolin-1, respectively. Moreover, this is the first report that shows characteristic caveolae-like invaginations in the mouse oocyte identified by electron microscopy. Raft disruption by cholesterol depletion disturbed the subcellular localization of the signal molecule c-Src and the inhibition of Src kinase proteins prevented second polar body extrusion, consistent with a role of Src-related kinases in fertilization via signaling complexes. Our data highlight the functional importance of intact membrane rafts for mouse fertilization and its dependence on cholesterol.
Fil: Buschiazzo, Jorgelina. Universite Paris Descartes; Francia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina
Fil: Ialy Radio, Come. Universite Paris Descartes; Francia
Fil: Auer, Jana. Universite Paris Descartes; Francia
Fil: Wolf, Jean Philippe. Universite Paris Descartes; Francia
Fil: Serres, Catherine. Universite Paris Descartes; Francia
Fil: Lefèvre, Brigitte. Universite Paris Descartes; Francia
Fil: Ziyyat, Ahmed. Universite Paris Descartes; Francia
description Drastic membrane reorganization occurs when mammalian sperm binds to and fuses with the oocyte membrane. Two oocyte protein families are essential for fertilization, tetraspanins and glycosylphosphatidylinositol-anchored proteins. The firsts are associated to tetraspanin-enriched microdomains and the seconds to lipid rafts. Here we report membrane raft involvement in mouse fertilization assessed by cholesterol modulation using methyl-β-cyclodextrin. Cholesterol removal induced: (1) a decrease of the fertilization rate and index; and (2) a delay in the extrusion of the second polar body. Cholesterol repletion recovered the fertilization ability of cholesterol-depleted oocytes, indicating reversibility of these effects. In vivo time-lapse analyses using fluorescent cholesterol permitted to identify the time-point at which the probe is mainly located at the plasma membrane enabling the estimation of the extent of the cholesterol depletion. We confirmed that the mouse oocyte is rich in rafts according to the presence of the raft marker lipid, ganglioside GM1 on the membrane of living oocytes and we identified the coexistence of two types of microdomains, planar rafts and caveolae-like structures, by terms of two differential rafts markers, flotillin-2 and caveolin-1, respectively. Moreover, this is the first report that shows characteristic caveolae-like invaginations in the mouse oocyte identified by electron microscopy. Raft disruption by cholesterol depletion disturbed the subcellular localization of the signal molecule c-Src and the inhibition of Src kinase proteins prevented second polar body extrusion, consistent with a role of Src-related kinases in fertilization via signaling complexes. Our data highlight the functional importance of intact membrane rafts for mouse fertilization and its dependence on cholesterol.
publishDate 2013
dc.date.none.fl_str_mv 2013-04-25
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/482
Buschiazzo, Jorgelina; Ialy Radio, Come; Auer, Jana; Wolf, Jean Philippe; Serres, Catherine; et al.; Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization; Public Library of Science; Plos One; 8; 4; 25-4-2013; 1-13; e62919
1932-6203
CONICET Digital
CONICET
url http://hdl.handle.net/11336/482
identifier_str_mv Buschiazzo, Jorgelina; Ialy Radio, Come; Auer, Jana; Wolf, Jean Philippe; Serres, Catherine; et al.; Cholesterol Depletion Disorganizes Oocyte Membrane Rafts Altering Mouse Fertilization; Public Library of Science; Plos One; 8; 4; 25-4-2013; 1-13; e62919
1932-6203
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0062919
info:eu-repo/semantics/altIdentifier/url/http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0062919
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Public Library of Science
publisher.none.fl_str_mv Public Library of Science
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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