dc.creatorDANOVIZ, Maria Elena
dc.creatorBASSANEZE, Vinicius
dc.creatorNAKAMUTA, Juliana Sanajotti
dc.creatorSANTOS-JUNIOR, Gabriel Ribeiro dos
dc.creatorSAINT-CLAIR, Danilo
dc.creatorBAJGELMAN, Marcio Chaim
dc.creatorFAE, Kellen Cristhina
dc.creatorKALIL, Jorge
dc.creatorMIYAKAWA, Ayumi Aurea
dc.creatorKRIEGER, Jose Eduardo
dc.date.accessioned2012-04-18T21:37:19Z
dc.date.accessioned2018-07-04T14:35:14Z
dc.date.available2012-04-18T21:37:19Z
dc.date.available2018-07-04T14:35:14Z
dc.date.created2012-04-18T21:37:19Z
dc.date.issued2011
dc.identifierSTEM CELLS AND DEVELOPMENT, v.20, n.4, p.661-670, 2011
dc.identifier1547-3287
dc.identifierhttp://producao.usp.br/handle/BDPI/15241
dc.identifier10.1089/scd.2010.0231
dc.identifierhttp://dx.doi.org/10.1089/scd.2010.0231
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1612081
dc.description.abstractAdipose tissue-derived stem cells (ASCs) are among the more attractive adult stem cell options for potential therapeutic applications. Here, we studied and compared the basic biological characteristics of ASCs isolated from humans (hASCs) and mice (mASCs) and maintained in identical culture conditions, which must be examined prior to considering further potential clinical applications. hASCs and mASCs were compared for immunophenotype, differentiation potential, cell growth characteristics, senescence, nuclear morphology, and DNA content. Although both strains of ASCs displayed a similar immunophenotype, the percentage of CD73(+) cells was markedly lower and CD31(+) was higher in mASC than in hASC cultures. The mean population doubling time was 98.08 +/- 6.15 h for hASCs and 52.58 +/- 3.74 h for mASCs. The frequency of nuclear aberrations was noticeably lower in hASCs than in mASCs regardless of the passage number. Moreover, as the cells went through several in vitro passages, mASCs showed changes in DNA content and cell cycle kinetics (frequency of hypodiploid, G0/G1, G2/M, and hyperdiploid cells), whereas all of these parameters remained constant in hASCs. Collectively, these results suggest that mASCs display higher proliferative capacity and are more unstable than hASCs in long-term cultures. These results underscore the need to consider specificities among model systems that may influence outcomes when designing potential human applications.
dc.languageeng
dc.publisherMARY ANN LIEBERT INC
dc.relationStem Cells and Development
dc.rightsCopyright MARY ANN LIEBERT INC
dc.rightsclosedAccess
dc.titleAdipose Tissue-Derived Stem Cells from Humans and Mice Differ in Proliferative Capacity and Genome Stability in Long-Term Cultures
dc.typeArtículos de revistas


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