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Anchoring cortical granules in the cortex ensures trafficking to the plasma membrane for post-fertilization exocytosis

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dc.contributor.author Vogt, Edgar-John
dc.contributor.author Tokuhiro, Keizo
dc.contributor.author Guo, Min
dc.contributor.author Dale, Ryan
dc.contributor.author Yang, Guanghui
dc.contributor.author Jiménez-Movilla, María
dc.contributor.author Shroff, Hari
dc.contributor.author Dean, Jurrien
dc.date.accessioned 2026-02-12T12:19:39Z
dc.date.available 2026-02-12T12:19:39Z
dc.date.issued 2019-05-22
dc.identifier.citation Vogt EJ, Tokuhiro K, Guo M, Dale R, Yang G, Shin SW, et al. Anchoring cortical granules in the cortex ensures trafficking to the plasma membrane for post-fertilization exocytosis. Nat Commun. 22 de mayo de 2019;10(1):2271.
dc.identifier.issn 2041-1723
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/24447
dc.description.abstract Following fertilization, cortical granules exocytose ovastacin, a metalloendopeptidase that cleaves ZP2 in the zona pellucida surrounding mouse eggs to prevent additional sperm binding. Using high- and super-resolution imaging with ovastacin(mCherry) as a fluorescent marker, we characterize cortical granule dynamics at single granule resolution in transgenic mouse eggs. Newly-developed imaging protocols provide an unprecedented view of vesicular dynamics near the plasma membrane in mouse eggs. We discover that cortical granule anchoring in the cortex is dependent on maternal MATER and document that myosin IIA is required for biphasic trafficking to the plasma membrane. We observe local clearance of cortical actin during exocytosis and determine that pharmacologic or genetic disruption of trafficking to the plasma membrane impairs secretion of cortical granules and results in polyspermy. Thus, the regulation of cortical granule dynamics at the cortex-plasma membrane interface is critical for exocytosis and the post-fertilization block to sperm binding that ensures monospermic fertilization.
dc.language.iso eng
dc.publisher NATURE PUBLISHING GROUP
dc.rights Attribution 4.0 International
dc.rights.uri http://creativecommons.org/licenses/by/4.0 *
dc.subject.mesh Animals
dc.subject.mesh Antigens/metabolism
dc.subject.mesh Cell Membrane/metabolism
dc.subject.mesh Cytoplasmic Granules/metabolism
dc.subject.mesh Egg Proteins/metabolism
dc.subject.mesh Exocytosis/physiology
dc.subject.mesh Female
dc.subject.mesh Intravital Microscopy
dc.subject.mesh Luminescent Proteins/chemistry/genetics
dc.subject.mesh Male
dc.subject.mesh Metalloproteases/chemistry/genetics/metabolism
dc.subject.mesh Mice
dc.subject.mesh Mice, Transgenic
dc.subject.mesh Microscopy, Fluorescence
dc.subject.mesh Sperm-Ovum Interactions/physiology
dc.subject.mesh Zona Pellucida/metabolism
dc.subject.mesh Zona Pellucida Glycoproteins/metabolism
dc.subject.mesh Red Fluorescent Protein
dc.title Anchoring cortical granules in the cortex ensures trafficking to the plasma membrane for post-fertilization exocytosis
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 31118423
dc.relation.publisherversion https://www.nature.com/articles/s41467-019-10171-7
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1038/s41467-019-10171-7
dc.journal.title Nature Communications


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