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<dc:title xml:lang="fr">Formation des sites d'exocytose dans les cellules chromaffines : importance fonctionnelle, régulation et externalisation de l'Annexine A2</dc:title>
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<dc:subject xml:lang="fr">Annexine A2</dc:subject>
<dc:subject xml:lang="fr">Exocytose</dc:subject>
<dc:subject xml:lang="fr">Microdomaines lipidiques</dc:subject>
<dc:subject xml:lang="fr">Actine</dc:subject>
<dc:subject xml:lang="fr">Phosphorylation</dc:subject>
<dc:subject xml:lang="fr">Externalisation</dc:subject>
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<tef:elementdEntree autoriteExterne="130112879" autoriteSource="Sudoc">Microdomaines membranaires</tef:elementdEntree>
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<dcterms:abstract xml:lang="fr">L’exocytose est un mécanisme biologique fondamental qui permet la libération du contenu des granules de sécrétion dans le milieu extracellulaire. C’est un processus finement régulé par le calcium qui nécessite entre autre, la réorganisation de la membrane plasmique et la formation de domaines lipidiques. Dans les cellules chromaffines, l’annexine A2, protéine capable de lier les phospholipides et l’actine de manière calcium-dépendante, est responsable de la formation et de la stabilisation de ces plateformes lipidiques. Le résultat majeur de ma thèse concerne l’organisation tridimensionnelle et le rôle de l’actine au niveau des sites d’exocytose. Sachant que la phosphorylation de la tyrosine 23 de l’annexine A2 affecte sa liaison à l’actine et aux membranes, deux acteurs majeurs de l’exocytose, j’ai mis en évidence l’importance fonctionnelle de cette phosphorylation. Une autre conséquence de cette phosphorylation est le passage de l’annexine A2 de la face interne à la face externe de la membrane plasmique. Le mécanisme de sortie et le rôle de l’annexine A2 extracellulaire dans les cellules chromaffines ont également été étudiés.</dcterms:abstract>
<dcterms:abstract xml:lang="en">Exocytosis is a fundamental biological mechanism which allows liberation of the contents of secretory granules into the extracellular medium. This calcium-regulated process requires the formation of lipid domains for the structural and spatial organisation of exocytotic sites. In the chromaffin cell, annexine A2, a calcium-, actin- and lipid-binding protein participates in the formation and stabilization of lipid microdomains. The major advance resulting from my thesis is the elucidation of the three-dimensional organization and the role of actin at the exocytotic site. Phosphorylation of the tyrosine 23 is known to affect the binding of annexin A2 to actin filaments and plasma membrane, two major actors of the exocytotic process and my results highlight the functional importance of this phosphorylation on exocytosis. Furthermore, tyrosine 23 phosphorylation also triggers a translocation of annexin A2 to the external face of the plasma membrane. The role and functional signification of this externalization was also examined.</dcterms:abstract>
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