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dc.contributor.authorMartín Piedra, Miguel Angel
dc.contributor.authorGarzón, Ingrid
dc.contributor.authorOliveira, Ana Celeste
dc.contributor.authorAlfonso-Rodriguez, Camilo
dc.contributor.authorCarriel, Victor
dc.contributor.authorScionti, Giuseppe
dc.contributor.authorAlaminos, Miguel
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament de Ciència dels Materials i Enginyeria Metal·lúrgica
dc.date.accessioned2016-04-11T10:45:42Z
dc.date.available2016-04-11T10:45:42Z
dc.date.issued2014-02
dc.identifier.citationMartín-Piedra, M.A., Garzón, I., Oliveira, A., Alfonso, C.A., Carriel, V., Scionti, G., Alaminos, M. Cell viability and proliferation capability of long-term human dental pulp stem cell cultures. "Cytotherapy", Febrer 2014, vol. 16, núm. 2, p. 266-277.
dc.identifier.issn1465-3249
dc.identifier.urihttp://hdl.handle.net/2117/85469
dc.description.abstractackground aims Evaluation of cell viability is one of the most important steps of the quality control process for therapeutic use of cells. The aim of this study was to evaluate the long-term cell viability profile of human dental pulp stem cell (hDPSC) subcultures (beyond 10 passages) to determine which of these passages are suitable for clinical use and to identify the cell death processes that may occur in the last passages. Methods Four different cell viability assays were combined to determine the average cell viability levels at each cell passage: trypan blue exclusion test, water-soluble tetrazolium 1 (WST-1), LIVE/DEAD Viability/Cytotoxicity Kit and electron probe x-ray microanalysis (EPXMA). Apoptosis was assessed by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay and caspase 4 and BCL7C Western blotting, and cell proliferation was analyzed by WST-1 and proliferating cell nuclear antigen protein detection. Results hDPSCs showed high average cell viability levels from passages 11–14, with adequate cytoplasmic and mitochondrial functionality at these subcultures. A non-significant trend to decreased cell proliferation was found from passages 16–20. EPXMA and TUNEL analyses suggested that a pre-apoptotic process could be activated from passages 15–20 (P < 0.001), with a correlation with caspase 4 and BCL7C expression. Conclusions hDPSCs corresponding to passages 11–14 show adequate cell function, proliferation and viability. These cells could be considered as potentially useful for clinical applications.
dc.format.extent12 p.
dc.language.isoeng
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectÀrees temàtiques de la UPC::Enginyeria dels materials
dc.subject.lcshTissue engineering
dc.subject.otherCell viability
dc.subject.otherdental pulp
dc.subject.otherelectron-probe x-ray microanalysis
dc.subject.othermesenchymal stromal cells
dc.titleCell viability and proliferation capability of long-term human dental pulp stem cell cultures
dc.typeArticle
dc.subject.lemacEnginyeria de teixits
dc.identifier.doi10.1016/j.jcyt.2013.10.016
dc.description.peerreviewedPeer Reviewed
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S1465324913007743
dc.rights.accessOpen Access
drac.iddocument17546496
dc.description.versionPostprint (author's final draft)
upcommons.citation.authorMartín-Piedra, M.A.; Garzón, I.; Oliveira, A.; Alfonso, C.A.; Carriel, V.; Scionti, G.; Alaminos, M.
upcommons.citation.publishedtrue
upcommons.citation.publicationNameCytotherapy
upcommons.citation.volume16
upcommons.citation.number2
upcommons.citation.startingPage266
upcommons.citation.endingPage277


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