Induced pluripotent stem cells' self-renewal and pluripotency is maintained by a bovine granulosa cell line-conditioned medium

Induced pluripotent stem cells (iPSCs) are a promising type of stem cells, comparable to embryonic stem cells (ESCs) in terms of self-renew and pluripotency, generated by reprogramming somatic cells. These cells are an attractive approach to supply patient-specific pluripotent cells, for producing i...

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Autor principal: Solari, C.
Otros Autores: Losino, N., Luzzani, C., Waisman, A., Bluguermann, C., Questa, M., Sevlever, G., Miriuka, S., Barañao, L., Guberman, A.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2011
Acceso en línea:Registro en Scopus
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245 1 0 |a Induced pluripotent stem cells' self-renewal and pluripotency is maintained by a bovine granulosa cell line-conditioned medium 
260 |c 2011 
270 1 0 |m Guberman, A.; Laboratorio de Regulación de la Expresión Génica en el Crecimiento, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires, Intendente Guiraldes 2160, Ciudad Univ., Pab. 2, 4to piso, QB-71W, Buenos Aires, Argentina; email: algub@qb.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a Induced pluripotent stem cells (iPSCs) are a promising type of stem cells, comparable to embryonic stem cells (ESCs) in terms of self-renew and pluripotency, generated by reprogramming somatic cells. These cells are an attractive approach to supply patient-specific pluripotent cells, for producing in vitro models of disease, drug discovery, toxicology and potentially treating degenerative disease circumventing immune rejection. In spite of the great advance since iPSCs' establishment, their obtention and propagation is an increasing area of great interest.In a recent work, we have shown that the conditioned medium from a bovine granulosa cell line (BGC-CM) is able to preserve the basic properties of mESCs. Therefore, based on our previous results and the reported resemblance between iPSCs and ESCs, we hypothesized that BGC-CM could provide a favorable context to culturing iPSCs. In this work, we have reprogrammed mouse embryonic fibroblasts obtaining iPSC lines, and showed that they can be propagated in BGC-CM while maintaining self-renewal and pluripotency, evidenced by expression of specific gene markers and capability of in vitro and in vivo differentiation to cell types from the three germ layers. We believe that these findings may provide a novel context to propagate iPSCs to study the molecular mechanisms involved in self-renewal and pluripotency. © 2011 Elsevier Inc.  |l eng 
536 |a Detalles de la financiación: Universidad de Buenos Aires, X849 
536 |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica, PID 115-PAE 37075 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: U.S. Children's Bureau 
536 |a Detalles de la financiación: The authors wish to thank Dr. Fernando Pitossi and Dr. Gustavo Mostoslavsky for providing the five-plasmid transfection system utilized in this work, to Francisco Guaimas for his help with confocal microscopy and to Estefanía Rojas, Naomi Arakaki, and Daniela Pérez Sirkin for teratoma processing and analysis. This work was supported by grants (to A.S.G.) from the University of Buenos Aires (X849), Agencia Nacional de Promoción Científica y Tecnológica (ANPCyT) (PID 115-PAE 37075) and by Biosidus S.A. CS, CL and MQ are fellows from CONICET, NL is supported by a fellowship Grant from University of Buenos Aires and CB by a fellowship Grant from ANPCyT . 
593 |a Laboratorio de Regulación de la Expresión Génica en el Crecimiento, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina 
593 |a Laboratorio de Biología del Desarrollo Celular, FLENI, Buenos Aires, Argentina 
593 |a Departamento de Fisiología y Biología Molecular y Celular, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina 
690 1 0 |a BGC 
690 1 0 |a BGC-CM 
690 1 0 |a CM 
690 1 0 |a CONDITIONED MEDIUM 
690 1 0 |a CULTURE CONDITIONS 
690 1 0 |a ESC 
690 1 0 |a GC 
690 1 0 |a INDUCED PLURIPOTENT STEM CELL 
690 1 0 |a IPSC 
690 1 0 |a LIF 
690 1 0 |a MEF 
690 1 0 |a MESC 
690 1 0 |a PLURIPOTENCY 
690 1 0 |a SELF-RENEWAL 
690 1 0 |a SM 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ARTICLE 
690 1 0 |a CELL DIFFERENTIATION 
690 1 0 |a CELL TYPE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a FIBROBLAST 
690 1 0 |a GENE EXPRESSION 
690 1 0 |a GRANULOSA CELL 
690 1 0 |a IMMUNOFLUORESCENCE 
690 1 0 |a IN VITRO STUDY 
690 1 0 |a IN VIVO STUDY 
690 1 0 |a LENTIVIRINAE 
690 1 0 |a MARKER GENE 
690 1 0 |a MOUSE 
690 1 0 |a NONHUMAN 
690 1 0 |a PLURIPOTENT STEM CELL 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a ANIMALS 
690 1 0 |a CATTLE 
690 1 0 |a CELL CULTURE TECHNIQUES 
690 1 0 |a CELL LINE 
690 1 0 |a CULTURE MEDIA, CONDITIONED 
690 1 0 |a FEMALE 
690 1 0 |a GRANULOSA CELLS 
690 1 0 |a INDUCED PLURIPOTENT STEM CELLS 
690 1 0 |a MICE 
690 1 0 |a OCTAMER TRANSCRIPTION FACTOR-3 
690 1 0 |a REGENERATION 
690 1 0 |a BOVINAE 
700 1 |a Losino, N. 
700 1 |a Luzzani, C. 
700 1 |a Waisman, A. 
700 1 |a Bluguermann, C. 
700 1 |a Questa, M. 
700 1 |a Sevlever, G. 
700 1 |a Miriuka, S. 
700 1 |a Barañao, L. 
700 1 |a Guberman, A. 
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