Publication:
Advances in Alzheimer’s Disease Research: Human Cerebral Organoids

dc.contributor.authorMateos-Martínez, Patricia
dc.contributor.authorGonzález-Sastre, Rosa
dc.contributor.authorCoronel Lopez, Raquel
dc.contributor.authorRosca, Andreea
dc.contributor.authorMartín Benito, Sabela
dc.contributor.authorBernabeu-Zornoza, Adela
dc.contributor.authorLópez-Alonso, Victoria
dc.contributor.authorListe-Noya, Isabel
dc.contributor.funderMinisterio de Ciencia e Innovación (España)es_ES
dc.contributor.funderInstituto de Salud Carlos IIIes_ES
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (España)es_ES
dc.date.accessioned2024-01-18T08:46:40Z
dc.date.available2024-01-18T08:46:40Z
dc.date.issued2023
dc.description.abstractAlzheimer’s disease (AD) is the main neurodegenerative disorder in old age, causing memory impairment and dependency. The histopathology of AD is characterized by the presence of amyloid plaques and neurofibrillary tangles formed by Aβ peptide and hyperphosphorylated Tau, respectively. There is still no cure or effective treatment for AD. This could be due, in part, to the lack of suitable research models since animal models do not recapitulate the full physiological complexity of the human brain. With the development of induced pluripotent stem cells (iPSCs), these limitations could be overcome. Even so, the bi-dimensional (2D) culture models still do not allow to recapitulate all types of brain cells and do not show a three-dimensional (3D) arrangement. Since obtaining 3D cultures called organoids, a new opportunity arises to overcome the limitations of previous models. Human Cerebral Organoids (hCOs) represent a pioneering model, in which part of the complexity of the human brain is present. For this reason, they are fast becoming a very remarkable model for the study of the evolution of the molecular and cellular pathology of AD. This review provides a brief overview of AD research, focusing on the most recent advances achieved through the development of stem cell and cerebral organoid technologyes_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThe authors would like to thank to financing entities: i. State R+D+i Program Oriented to the Challenges of Society. Ministry of Science and Innovation (PID2021-126715OB-I00). ii. Strategic Action in Intramural Health (PI22/00055). iii. Ministry of Science and Innovation and Universities, within the program “R&D Projects «Retos Investigación» (RTI2018-101663-B-100).es_ES
dc.format.number1es_ES
dc.format.pageAJBSR.MS.ID.002421es_ES
dc.format.volume18es_ES
dc.identifier.citationAm J Biomed Sci & Res. 2023 18(1): AJBSR.MS.ID.002421.es_ES
dc.identifier.doi10.34297/AJBSR.2023.18.002421es_ES
dc.identifier.e-issn2642-1747es_ES
dc.identifier.journalAmerican Journal of Biomedical Science & Researches_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/17225
dc.language.isoenges_ES
dc.publisherBiomedgrides_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PID2021-126715OB-I00es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/RTI2018-101663-B-100es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/PI22/00055es_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.scitotenv.2023.169475es_ES
dc.repisalud.centroISCIII::Unidad Funcional de Investigación de Enfermedades Crónicas (UFIEC)es_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectAlzheimer diseasees_ES
dc.subjectPluripotent stem cellses_ES
dc.subjectOrganoidses_ES
dc.subjectCerebral organoidses_ES
dc.subject3D modelses_ES
dc.titleAdvances in Alzheimer’s Disease Research: Human Cerebral Organoidses_ES
dc.typereview articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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