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Cytotherapy ; 13(1): 114-28, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-20230224

RESUMO

BACKGROUND AIMS: Ex vivo generation of megakaryocytes (MK) from hematopoietic stem cells (HSC) is important for both basic research, to understand the mechanism of platelet biogenesis, and clinical infusions, for rapid platelet recovery in thrombocytopenic patients. We investigated the role of two nutraceuticals, docosahexanoic acid (DHA) and arachidonic acid (AA), in the in vitro generation of MK. METHODS: Umbilical cord blood (UCB)-derived CD34+cells were cultured with stem cell factor (SCF) and thrombopoietin (TPO) in the presence (test) or absence (control) of the two additives. On day 10, MK and platelets generated were quantitated by morphologic, phenotypic and functional assays. RESULTS: The cell yield of MK and platelet numbers were significantly higher in test compared with control cells. Phenotypic analyzes and gene expression profiles confirmed these findings. Functional properties, such as colony-forming unit (CFU)-MK formation, chemotaxis and platelet activation, were found to be enhanced in cells cultured with nutraceuticals. The engraftment potential of ex vivo-expanded cells was studied in NOD/SCID mice. Mice that received MK cultured in the presence of DHA/AA engrafted better. There was a reduction in apoptosis and total reactive oxygen species (ROS) levels in the CD41(+) compartment of the test compared with control sets. The data suggest that these compounds probably exert their beneficial effect by modulating apoptotic and redox pathways. CONCLUSIONS: Use of nutraceuticals like DHA and AA may prove to be a useful strategy for efficient generation of MK and platelets from cord blood cells, for future use in clinics and basic research.


Assuntos
Antígenos CD34/metabolismo , Ácido Araquidônico/farmacologia , Meios de Cultura/química , Citocinas/farmacologia , Ácidos Docosa-Hexaenoicos/farmacologia , Sangue Fetal/citologia , Megacariócitos/citologia , Animais , Apoptose/efeitos dos fármacos , Plaquetas/citologia , Plaquetas/efeitos dos fármacos , Diferenciação Celular/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Quimiotaxia/efeitos dos fármacos , Ensaio de Unidades Formadoras de Colônias , Suplementos Nutricionais , Humanos , Megacariócitos/transplante , Camundongos , Camundongos SCID , Fenótipo , Ativação Plaquetária/efeitos dos fármacos , Ploidias , Espécies Reativas de Oxigênio/metabolismo , Fatores de Transcrição/metabolismo
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