Human Pluripotent Stem Cell-Derived Neural Cells as a Relevant Platform for Drug Screening in Alzheimer’s Disease.

dc.centroFacultad de Cienciases_ES
dc.contributor.authorGarcía-León, Juan Antonio
dc.contributor.authorCáceres Palomo, Laura
dc.contributor.authorSánchez-Mejías, Elisabeth
dc.contributor.authorMejías-Ortega, Marina
dc.contributor.authorNúñez-Díaz, Cristina
dc.contributor.authorFernández-Valenzuela, Juan José
dc.contributor.authorSánchez-Varo, Raquel María
dc.contributor.authorDávila-Cansino, José Carlos
dc.contributor.authorVitorica Ferrández, Javier
dc.contributor.authorGutiérrez-Pérez, Antonia
dc.date.accessioned2024-07-03T06:50:57Z
dc.date.available2024-07-03T06:50:57Z
dc.date.issued2020-09-18
dc.departamentoBiología Celular, Genética y Fisiología
dc.description.abstractExtracellular amyloid-beta deposition and intraneuronal Tau-laden neurofibrillary tangles are prime features of Alzheimer’s disease (AD). The pathology of AD is very complex and still not fully understood, since different neural cell types are involved in the disease. Although neuronal function is clearly deteriorated in AD patients, recently, an increasing number of evidences have pointed towards glial cell dysfunction as one of the main causative phenomena implicated in AD pathogenesis. The complex disease pathology together with the lack of reliable disease models have precluded the development of effective therapies able to counteract disease progression. The discovery and implementation of human pluripotent stem cell technology represents an important opportunity in this field, as this system allows the generation of patient-derived cells to be used for disease modeling and therapeutic target identification and as a platform to be employed in drug discovery programs. In this review, we discuss the current studies using human pluripotent stem cells focused on AD, providing convincing evidences that this system is an excellent opportunity to advance in the comprehension of AD pathology, which will be translated to the development of the still missing effective therapies.es_ES
dc.description.sponsorshipInstituto de Salud Carlos III (ISCiii) de España, cofinanciado por fondos FEDER de la Union Europea ref. PI18/01557 (AG), ref. PI18/01556 (JV). CIBERNED (ref. CB06/05/1116 para AG; ref. CB06/05/0094 para JV). Junta de Andalucia, Consejería de Economía y Conocimiento ref. UMA18-FEDERJA-211 (AG), PY18-RT-2233 (AG) and US-1262734 (JV) co-financiado por Programa Operativo FEDER 2014-2020 y Consejeria de Salud ref. PI-0276-2018 (JAGL). Ayuda a proyectos de Jóvenes Investigadores de la Universidad de Málaga ref. PPIT.UMA.B1.2017/26 (RSV). JJFV - beca FPU del Ministerio Español de Ciencia, Innovación y Universidades. RSV y MMO - contrato postdoctoral y predoctoral de la Universidad de Málaga, respectivamente.es_ES
dc.identifier.citationGarcia-Leon JA, Caceres-Palomo L, Sanchez-Mejias E, Mejias-Ortega M, Nuñez-Diaz C, Fernandez-Valenzuela JJ, Sanchez-Varo R, Davila JC, Vitorica J, Gutierrez A. Human Pluripotent Stem Cell-Derived Neural Cells as a Relevant Platform for Drug Screening in Alzheimer's Disease. Int J Mol Sci. 2020 Sep 18;21(18):6867. doi: 10.3390/ijms21186867. PMID: 32962164; PMCID: PMC7558359.es_ES
dc.identifier.doi10.3390/ijms21186867
dc.identifier.urihttps://hdl.handle.net/10630/31849
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectAlzheimer, Enfermedad dees_ES
dc.subjectCélulas madre - Investigaciónes_ES
dc.subjectOligodendrogliaes_ES
dc.subject.otherAlzheimer’s diseasees_ES
dc.subject.otherMicrogliaes_ES
dc.subject.otherAstrocyteses_ES
dc.subject.other3D cultureses_ES
dc.subject.otherHuman induced pluripotent stem cells (hiPSCs)es_ES
dc.subject.otherDisease modelinges_ES
dc.subject.otherOligodendrocyteses_ES
dc.subject.otherBrain organoidses_ES
dc.titleHuman Pluripotent Stem Cell-Derived Neural Cells as a Relevant Platform for Drug Screening in Alzheimer’s Disease.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery576d499e-904a-4f51-887e-13395c761574

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