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dc.contributor.authorMuntión Olave, Sandra
dc.contributor.authorPreciado Pérez, Silvia 
dc.contributor.authorSánchez Luis, Elena
dc.contributor.authorCorchete Sánchez, Luis Antonio
dc.contributor.authorDíez-Campelo, María
dc.contributor.authorOsugui, Lika
dc.contributor.authorMartí Chillón, Gerardo Javier
dc.contributor.authorVidriales Vicente, María Belén 
dc.contributor.authorNavarro Bailón, Almudena 
dc.contributor.authorRivas Sanz, Javier de las
dc.contributor.authorSánchez Guijo Martín, Fermín 
dc.date.accessioned2025-01-08T13:21:23Z
dc.date.available2025-01-08T13:21:23Z
dc.date.issued2022-12
dc.identifier.citationMuntión S, Preciado S, Sánchez-Luis E, Corchete L, Díez-Campelo M, Osugui L, Martí-Chillón GJ, Vidriales MB, Navarro-Bailón A, De Las Rivas J, Sánchez-Guijo F. Eltrombopag increases the hematopoietic supporting ability of mesenchymal stem/stromal cells. Ther Adv Hematol. 2022 Dec 26;13:20406207221142137. doi: 10.1177/20406207221142137. PMID: 36601635; PMCID: PMC9806379.es_ES
dc.identifier.issn2040-6207
dc.identifier.urihttp://hdl.handle.net/10366/161402
dc.description.abstract[EN]Background: Eltrombopag (EP) is a small molecule that acts directly on hematopoietic stem cells (HSCs) and megakaryocytes to stimulate the hematopoietic process. Mesenchymal stem/ stromal cells (MSCs) are key hematopoietic niche regulators. Objectives: We aimed to determine whether EP has any effect on MSC function and properties (especially on their hematopoietic-supporting ability) and if so, what changes (e.g. genomewide transcriptomic alterations) are induced in MSC after EP treatment. Design/Methods: MSCs were isolated from 12 healthy donors and treated with 15 μM and 50 μM of EP for 24 h. The toxicity of the drug on MSCs and their differentiation ability were analyzed, as well as the transcriptomic profile, reactive oxygen species (ROS) and DNA damage and the changes induced in the clonogenic capacity of HSCs. Results: The results show that EP also modifies MSC functions, decreasing their adipogenic differentiation, increasing the expression of genes involved in hypoxia and other pathways related to oxygen homeostasis, and enhancing their ability to support hematopoiesis in vitro. Conclusion: Our findings support the use of EP in cases where hematopoiesis is defective, despite its well-known direct effects on hematopoietic cells. Our findings suggest that further studies on the effects of EP on MSCs from patients with aplastic anemia are warranted.es_ES
dc.description.sponsorshipNovartis Pharmaceuticals Instituto de Salud Carlos III (ISCIII) Ministerio de Ciencia e Innovaciónes_ES
dc.language.isoenges_ES
dc.publisherSage Journalses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAplasia, Eltrombopag, Hematopoiesis, Mesenchymal stem cells, MSCes_ES
dc.subjectAplasiaes_ES
dc.subjectEltrombopages_ES
dc.subjectHematopoiesises_ES
dc.subjectMesenchymal stem cellses_ES
dc.subject.meshReceptors, Thrombopoietin *
dc.subject.meshAnemia, Aplastic *
dc.subject.meshMesenchymal Stromal Cells *
dc.subject.meshHematopoiesis *
dc.titleEltrombopag increases the hematopoietic supporting ability of mesenchymal stem/stromal cellses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1177/20406207221142137es_ES
dc.subject.unesco3205.04 Hematologíaes_ES
dc.identifier.doi10.1177/20406207221142137
dc.relation.projectIDRD16/0011/0015es_ES
dc.relation.projectIDRD21/0017/0006es_ES
dc.relation.projectIDFPU18/03533es_ES
dc.relation.projectIDPFIS/19/00272es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn2040-6215
dc.journal.titleTherapeutic Advances in Hematologyes_ES
dc.volume.number13es_ES
dc.page.initial1es_ES
dc.page.final13es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decshematopoyesis *
dc.subject.decsreceptores de trombopoyetina *
dc.subject.decscélulas del estroma mesenquimatoso *
dc.subject.decsanemia aplásica *


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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