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dc.contributor.authorCastaño, Julio
dc.contributor.authorMenéndez, Pablo
dc.contributor.authorBruzos Cidón, Cristina ORCID
dc.contributor.authorStraccia, Marco
dc.contributor.authorSousa, Amaia
dc.contributor.authorZabaleta, Lorea
dc.contributor.authorVázquez, Nerea
dc.contributor.authorZubiarrain, Amaia
dc.contributor.authorSonntag, Kai-Christian
dc.contributor.authorUgedo Urruela, Luisa
dc.contributor.authorCarvajal Vergara, Xonia
dc.contributor.authorCanals, Josep Maria
dc.contributor.authorTorrecilla Sesma, María ORCID
dc.contributor.authorSánchez-Pernaute, Rosario
dc.contributor.authorGiorgetti, Alessandra
dc.date.accessioned2015-10-05T15:33:14Z
dc.date.available2015-10-05T15:33:14Z
dc.date.issued2014-12-09
dc.identifier.citationStem Cell Reports 3 (6) : 1118-1131 (2014)es
dc.identifier.issn2213-6711
dc.identifier.urihttp://hdl.handle.net/10810/15770
dc.description.abstractNeurons obtained directly from human somatic cells hold great promise for disease modeling and drug screening. Available protocols rely on overexpression of transcription factors using integrative vectors and are often slow, complex, and inefficient. We report a fast and efficient approach for generating induced neural cells (iNCs) directly from human hematopoietic cells using Sendai virus. Upon SOX2 and c-MYC expression, CD133-positive cord blood cells rapidly adopt a neuroepithelial morphology and exhibit high expansion capacity. Under defined neurogenic culture conditions, they express mature neuronal markers and fire spontaneous action potentials that can be modulated with neurotransmitters. SOX2 and c-MYC are also sufficient to convert peripheral blood mononuclear cells into iNCs. However, the conversion process is less efficient and resulting iNCs have limited expansion capacity and electrophysiological activity upon differentiation. Our study demonstrates rapid and efficient generation of iNCs from hematopoietic cells while underscoring the impact of target cells on conversion efficiency.es
dc.description.sponsorshipFunding for this project was provided by the Basque Government, Department of Industry (SAIOTEK PE12IB003), and Kutxa Obra Social to A.G.; the Basque Government, Department of Education (EC2011-47) and Kutxa Obra Social to R.S.-P.; Obra Social "La Caixa-Fundacio Josep Carreras,'' ISCII/ERANET (P112/03112) to P.M.; the Ministerio de Economia y Competitividad (SAF201237417) to J.M.C., Spain; Instituto de Salud Carlos III, Ministerio de Economia y Competitividad (RETICS [RD12/0019/0002; Red de Terapia Celular]) to J.M.C.; and Generalitat de Catalunya (2009SGR-00326); The University of the Basque Country (UFI 11/32) and the Spanish Government; The Ministerio de Economia y Competitividad (FIS PI12/00613) to C.B.-C., L.U., and M.T.; and in part from the National Institute of Neurological Disorders and Stroke R21 NS067335 to K.C.-S.C.B.-C. was supported by a UPV/EHU fellowship. We would like to thank Drs. Kausalia Vijayaragavan and Marc Bosse for helpful discussion and Angelica Horillo and Clara Bueno for technical assistance. Some antibodies were obtained from the Developmental Studies Hybridoma Bank (DSHB) developed under the auspices of the National Institute of Child Health and Human Development and maintained by the Department of Biology, University of Iowa.es
dc.language.isoenges
dc.publisherCell Presses
dc.relationinfo:eu-repo/grantAgreement/MINECO/SAF2012-37417
dc.relationinfo:eu-repo/grantAgreement/MINECO/RD12/0019/0002
dc.relationinfo:eu-repo/grantAgreement/MINECO/FIS-PI12-00613
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectpluripotent stem-cellses
dc.subjectadult human fibroblastses
dc.subjectinduced neuronal cellses
dc.subjectfuntional-neuronses
dc.subjectcord bloodes
dc.subjectin-vivoes
dc.subjectdopaminergic-neuronses
dc.subjectmouse fibroblastses
dc.subjectprogenitor cellses
dc.subjectdefiner factorses
dc.titleFast and Efficient Neural Conversion of Human Hematopoietic Cellses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder2014 The Authorses
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S2213671114003300es
dc.identifier.doi10.1016/j.stemcr.2014.10.008
dc.departamentoesFarmacologíaes_ES
dc.departamentoeuFarmakologiaes_ES


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