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dc.contributor.advisorBenedito, Rui 
dc.contributor.authorPontes-Quero, Samuel 
dc.date.accessioned2019-06-05T11:21:29Z
dc.date.available2019-06-05T11:21:29Z
dc.date.issued2018-07-13
dc.identifier.urihttp://hdl.handle.net/20.500.12105/7737
dc.description.abstractThe formation of new blood vessels by angiogenesis requires the precise coordination of endothelial cell differentiation, proliferation, migration and maturation to ensure that a proper vasculature is formed to satisfy the metabolic needs of the surrounding tissue. The Notch signaling pathway is a critical regulator of endothelial cell biology, participating in different processes of blood vessel formation from tipTcell specification to arterioTvenous differentiation and blood vessel stabilization. Inhibition of this pathway during angiogenesis has been associated with increased proliferation of endothelial cells. However, this seemingly antiproliferative effect of Notch activation does not adjust well to the current tipT stalk cell model of molecular control of angiogenesis, in which proliferative stalk cells are defined as having higher Notch activity. In this work we have tried to resolve this apparent paradox by characterizing in detail the effects of Notch on endothelial cell proliferation In vivo. We have used different pharmacological and classical genetic approaches in combination with newly developed mosaic genetic tools to evaluate, with high spatioTtemporal resolution, endothelial cell cycle dynamics. We have found that physiological Notch activation is required for maintaining endothelial cell proliferation by repressing excessive activation of proTproliferative molecular mechanism. Inhibition of Notch activity induces and hyperproliferative response that is partially dependent on ERK activation. This response is, however, not sustained in time and leads to proliferative arrest, partially mediated by ERK overactivation and p21 upregulation. This cellTcycle arrest is associated with an increase in the expression of genes characteristic of sprouting tip cells. Thus, Notch can control a mechanism to differentiate between a proliferative and migratory cellular response. Comparative trancriptomics revealed new putative NotchTrepressed genes that promote cell cycle progression like Myc and Odc1. Functional analysis of these genes showed their absolute requirement for normal endothelial cell proliferation.es_ES
dc.language.isoenges_ES
dc.publisherUniversidad Autónoma de Madrides_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.titleRegulation of enfothelial cell cycle dynamics by Notch during angiogenesises_ES
dc.typeTesis doctorales_ES
dc.rights.licenseAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.identifier.doi10.4321/repisalud.7737
dc.contributor.funderMinisterio de Economía, Industria y Competitividad (España)es_ES
dc.contributor.funderEuropean Commissiones_ES
dc.contributor.funderEuropean Research Counciles_ES
dc.contributor.funderFundación ProCNICes_ES
dc.contributor.funderFundación La Caixaes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Genética Molecular de la Angiogénesises_ES
dc.repisalud.institucionCNICes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SAF2013-44329-Pes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SEV-2015-0505es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SAF2013-42359-ERCes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RYC-2013-13209es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/638028es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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Atribución-NoComercial-CompartirIgual 4.0 Internacional
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