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<dc:title xml:lang="fr">Brisures de symétrie et directionnalité dans les systèmes vivants</dc:title>
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<dc:subject xml:lang="fr">Physique cellulaire</dc:subject>
<dc:subject xml:lang="fr">Biologie quantitative</dc:subject>
<dc:subject xml:lang="fr">GTPase Rho</dc:subject>
<dc:subject xml:lang="fr">Cytosquelette</dc:subject>
<dc:subject xml:lang="fr">Adhésions focales</dc:subject>
<dc:subject xml:lang="fr">Migration dirigée</dc:subject>
<dc:subject xml:lang="fr">Ratchetaxis</dc:subject>
<dc:subject xml:lang="fr">Brisure de symétrie</dc:subject>
<dc:subject xml:lang="fr">Mouvements collectifs</dc:subject>
<dc:subject xml:lang="fr">Cohérence</dc:subject>
<dc:subject xml:lang="fr">Polarité cellulaire</dc:subject>
<dc:subject xml:lang="fr">Micro-fabrication</dc:subject>
<dc:subject xml:lang="fr">Simulation numérique</dc:subject>
<dc:subject xml:lang="en">Cell physics</dc:subject>
<dc:subject xml:lang="en">Quantitative biology</dc:subject>
<dc:subject xml:lang="en">Rho GTPase</dc:subject>
<dc:subject xml:lang="en">Cytoskeleton</dc:subject>
<dc:subject xml:lang="en">Focal adhesions</dc:subject>
<dc:subject xml:lang="en">Directed migration</dc:subject>
<dc:subject xml:lang="en">Ratchetaxis</dc:subject>
<dc:subject xml:lang="en">Broken symmetry</dc:subject>
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<tef:elementdEntree autoriteExterne="031122043" autoriteSource="Sudoc">Cellules -- Adhésivité</tef:elementdEntree>
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<dcterms:abstract xml:lang="fr">La manière dont les cellules suivent un mouvement dirigé sur de longues distances constitue une question fondamentale en Biologie. Ces migrations, individuelles ou collectives, émergent spontanément. Dans ce travail de thèse aux Interfaces entre la Physique et la Biologie, nous avons étudié les brisures de symétrie pour des cellules individuelles et pour un ensemble cellulaire. Nous montrons que des cellules migrant au sein d’environnements dont la symétrie a été brisée localement adoptent un mouvement directionnel. Ce type de phénomène, appelé ratchetaxis, est dicté par la dynamique des adhésions focales sur les aires accessibles à la cellule. En 3D, la compression du noyau cellulaire et l’organisation du cytosquelette sont les principaux déterminants. Nous avons enfin étudié le comportement d’un ensemble de cellules sur des anneaux. Dans ce contexte, la symétrie de l’environnement n’est pas brisée, mais les cellules adoptent un mouvement directionnel, cohérent, impliquant l’ensemble de la cohorte. Nous montrons que cette cohérence est le résultat d’interactions entre polarités voisines, effets de bord imposés par les câbles d’acto-myosine, activité Rho.</dcterms:abstract>
<dcterms:abstract xml:lang="en">Directed cell migration is fundamental in Biology. These motions – at the single cell level or at the multicellular scale – can emerge spontaneously. In this work at the Interface between Physics and Biology, we studied directed motion at these two different scales. We show that single cells migrate directionally when placed into micro-environments with local broken symmetries. This motion, coined ratchetaxis, is driven by the dynamics of focal adhesions. In 3D, nucleus compression and cytoskeleton organization are involved in setting cell direction. We next studied the behaviour of a collection of cells on rings patterns. In this context, the micro-environment is isotropic. However, cells spontaneously undergo a directed coherent motion which involves the cellular cohort. We show that the onset of coherence is driven by simple interaction rules between single cell polarities, acto-myosin cables at boundaries and RhoA activity.</dcterms:abstract>
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