Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/34241

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dc.contributor.authorLamas, Nuno Jorgepor
dc.contributor.authorSerra, Sofia Cristinapor
dc.contributor.authorSalgado, A. J.por
dc.contributor.authorSousa, Nunopor
dc.date.accessioned2015-03-06T13:14:08Z-
dc.date.available2015-03-06T13:14:08Z-
dc.date.issued2015-01-07-
dc.identifier.issn1178-6957por
dc.identifier.urihttps://hdl.handle.net/1822/34241-
dc.description.abstractY-27632 is a well-known inhibitor of the Rho-associated coiled kinase (ROCK) and has been shown to significantly improve the culture of a variety of multipotent stem cell types. However, the effects of Y-27632 on the expansion of adult human adipose-derived stem cell (hADSC) cultures remain to be established. Here, we aimed to characterize the effects of Y-27632 on the culture of hADSCs. Adult hADSCs were isolated from subjects submitted to elective plastic surgery procedures and cultivated in vitro under optimized conditions. Our results show that the continuous supplementation of hADSC cultures with Y-27632 led to decreased numbers of cells and decreased global metabolic viability of hADSC cultures when compared with control conditions. This effect appeared to be dependent on the continuous presence of the drug and was shown to be concentration-dependent and significant for 10 muM and 20 muM of Y-27632. Moreover, the Y-27632-induced decrease in hADSC numbers was not linked to a block in global cell proliferation, as cell numbers consistently increased from the moment of plating until passaging. In addition, Y-27632 was not able to increase the number of hADSCs present in culture 24 hours after passaging. Taken together, our results suggest that, in contrast to other stem cell types, Y-27632 supplementation is not a suitable strategy to enhance hADSC culture expansion.por
dc.description.sponsorshipWe thank Jeffrey M Gimble (Center for Stem Cell Research and Regenerative Medicine, Tulane University and LaCell LLC, New Orleans, LA, USA) for kindly isolating, characterizing, and sharing the cellular lines of hADSCs used in the present study and for critical input on the manuscript. We also would very much like to thank Laurent Roybon (Stem Cell Laboratory for CNS Disease Modeling, Department of Experimental Medical Science, Lund University, Lund, Sweden) for the utilization of Metamorph NX software for automated cell quantification. We are grateful to Miguel Carvalho, Ana Pires, Eduardo Gomes, Fabio Teixeira and Nuno Silva for technical assistance. This work was supported by the Portuguese Foundation for Science and Technology (predoctoral fellowship to NJL [SFRH/BD/33421/2008]; FCT Investigator Program to AJS) and the Luso-American Development Foundation.por
dc.language.isoengpor
dc.publisherDove Press Ltdpor
dc.rightsopenAccesspor
dc.subjectHuman mesenchymal stem cellspor
dc.subjectHuman multipotent stromal cells (hMSCs)por
dc.subjectROCK inhibitorpor
dc.subjectMTS assaypor
dc.titleFailure of Y-27632 to improve the culture of adult human adipose-derived stem cellspor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttp://www.dovepress.compor
sdum.publicationstatuspublishedpor
oaire.citationStartPage15por
oaire.citationEndPage26por
oaire.citationTitleStem cells and cloning : advances and applicationspor
oaire.citationVolume8por
dc.date.updated2015-03-02T16:30:25Z-
dc.identifier.doi10.2147/SCCAA.S66597por
dc.subject.wosScience & Technologypor
sdum.journalStem Cells and Cloning: Advances and Applicationspor
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

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