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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/482
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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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1846082886496681984 |
score |
13.22299 |