Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/37047
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorSABOGAL-GUAQUETA, Angelica Maria
dc.contributor.authorMARMOLEJO-GARZA, Alejandro
dc.contributor.authorPADUA, Vitor Passos de
dc.contributor.authorEGGEN, Bart
dc.contributor.authorBODDEKE, Erik
dc.contributor.authorDOLGA, Amalia M.
dc.date.accessioned2020-08-20T13:26:14Z-
dc.date.available2020-08-20T13:26:14Z-
dc.date.issued2020
dc.identifier.citationPROGRESS IN NEUROBIOLOGY, v.190, article ID 101805, 17p, 2020
dc.identifier.issn0301-0082
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/37047-
dc.description.abstractMicroglia are the main innate immune cells of the central nervous system (CNS). Unlike neurons and glial cells, which derive from ectoderm, microglia migrate early during embryo development from the yolk-sac, a mesodermal-derived structure. Microglia regulate synaptic pruning during development and induce or modulate inflammation during aging and chronic diseases. Microglia are sensitive to brain injuries and threats, altering their phenotype and function to adopt a so-called immune-activated state in response to any perceived threat to the CNS integrity. Here, we present a short overview on the role of microglia in human neurodegenerative diseases and provide an update on the current model systems to study microglia, including cell lines, iPSC-derived microglia with an emphasis in their transcriptomic profile and integration into 3D brain organoids. We present various strategies to model and study their role in neurodegeneration providing a relevant platform for the development of novel and more effective therapies.eng
dc.description.sponsorshipAbel Tasman program
dc.description.sponsorshipAlzheimer Nederland grant [WE.03-2018-04]
dc.description.sponsorshipStichtingParkinsonFonds (SPF)
dc.description.sponsorshipRosalind Franklin Fellowship
dc.description.sponsorshipEuropean UnionEuropean Union (EU)
dc.description.sponsorshipUniversity of Groningen
dc.description.sponsorshipColcienciasDepartamento Administrativo de Ciencia, Tecnologia e Innovacion Colciencias
dc.language.isoeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDeng
dc.relation.ispartofProgress in Neurobiology
dc.rightsopenAccesseng
dc.subjectMicrogliaeng
dc.subjectiPSCeng
dc.subjectNeurodegenerative diseaseseng
dc.subjectOrganoidseng
dc.subjectTranscriptomicseng
dc.subject.othercentral-nervous-systemeng
dc.subject.otheralzheimers-diseaseeng
dc.subject.otherparkinsons-diseaseeng
dc.subject.otherbrain-developmenteng
dc.subject.othermouse modeleng
dc.subject.othermitochondrial dysfunctioneng
dc.subject.othergene-expressioneng
dc.subject.othertau pathologyeng
dc.subject.otheractivationeng
dc.subject.otherdifferentiationeng
dc.titleMicroglia alterations in neurodegenerative diseases and their modeling with human induced pluripotent stem cell and other platformseng
dc.typearticleeng
dc.rights.holderCopyright PERGAMON-ELSEVIER SCIENCE LTDeng
dc.identifier.doi10.1016/j.pneurobio.2020.101805
dc.identifier.pmid32335273
dc.subject.wosNeuroscienceseng
dc.type.categoryrevieweng
dc.type.versionpublishedVersioneng
hcfmusp.author.externalSABOGAL-GUAQUETA, Angelica Maria:Univ Groningen, Groningen Res Inst Pharm Behav & Cognit Neurosci, Dept Mol Pharmacol, Fac Sci & Engn, Groningen, Netherlands; Univ Groningen, Univ Med Ctr Groningen, Mol Neurobiol Sect, Dept Biomed Sci Cells & Syst,Fac Med Sci, Groningen, Netherlands; Univ Antioquia, Neurosci Grp Antioquia, Cellular & Mol Neurobiol Area, SIU,Sch Med, Medellin, Colombia
hcfmusp.author.externalMARMOLEJO-GARZA, Alejandro:Univ Groningen, Groningen Res Inst Pharm Behav & Cognit Neurosci, Dept Mol Pharmacol, Fac Sci & Engn, Groningen, Netherlands; Univ Groningen, Univ Med Ctr Groningen, Mol Neurobiol Sect, Dept Biomed Sci Cells & Syst,Fac Med Sci, Groningen, Netherlands
hcfmusp.author.externalEGGEN, Bart:Univ Groningen, Univ Med Ctr Groningen, Mol Neurobiol Sect, Dept Biomed Sci Cells & Syst,Fac Med Sci, Groningen, Netherlands
hcfmusp.author.externalBODDEKE, Erik:Univ Groningen, Univ Med Ctr Groningen, Mol Neurobiol Sect, Dept Biomed Sci Cells & Syst,Fac Med Sci, Groningen, Netherlands
hcfmusp.author.externalDOLGA, Amalia M.:Univ Groningen, Groningen Res Inst Pharm Behav & Cognit Neurosci, Dept Mol Pharmacol, Fac Sci & Engn, Groningen, Netherlands
hcfmusp.description.articlenumber101805
hcfmusp.description.volume190
hcfmusp.origemWOS
hcfmusp.origem.idWOS:000539458700003
hcfmusp.origem.id2-s2.0-85086286111
hcfmusp.publisher.cityOXFORDeng
hcfmusp.publisher.countryENGLANDeng
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