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dc.contributor.authorMuñoz, Pilar
dc.contributor.authorBenabdellah, Karim
dc.contributor.authorCobo, Marien
dc.contributor.authorGutiérrez Guerrero, Alejandra
dc.contributor.authorSánchez Hernández, Sabina
dc.contributor.authorGarcía Pérez, Angélica
dc.contributor.authorAnderson, Per Olof 
dc.contributor.authorCarrillo Gálvez, Ana Belén 
dc.contributor.authorToscano, Miguel G
dc.contributor.authorMartín Molina, Francisco 
dc.date.accessioned2025-01-16T08:14:32Z
dc.date.available2025-01-16T08:14:32Z
dc.date.issued2016-11
dc.identifier.urihttps://hdl.handle.net/10481/99312
dc.description.abstractConditional transgene expression in human stem cells has been difficult to achieve due to the low efficiency of existing delivery methods, the strong silencing of the transgenes and the toxicity of the regulators. Most of the existing technologies are based on stem cells clones expressing appropriate levels of tTA or rtTA transactivators (based on the TetR-VP16 chimeras). In the present study, we aim the generation of Tet-On all-in-one lentiviral vectors (LVs) that tightly regulate transgene expression in human stem cells using the original TetR repressor. By using appropriate promoter combinations and shielding the LVs with the Is2 insulator, we have constructed the Lent-On-Plus Tet-On system that achieved efficient transgene regulation in human multipotent and pluripotent stem cells. The generation of inducible stem cell lines with the Lent-ON-Plus LVs did not require selection or cloning, and transgene regulation was maintained after long-term cultured and upon differentiation toward different lineages. To our knowledge, Lent-On-Plus is the first all-in-one vector system that tightly regulates transgene expression in bulk populations of human pluripotent stem cells and its progeny.es_ES
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs 3.0 Licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es_ES
dc.titleLent-On-Plus lentiviral vectors for conditional expression in human stem cellses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES


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