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Sci Rep ; 13(1): 13716, 2023 08 22.
Artículo en Inglés | MEDLINE | ID: mdl-37607956

RESUMEN

The enhanced availability of functional fibroblasts from precious tissue samples requires an ideal cell-culture system. Therefore, this study was designed to investigate the performance of caprine adult fibroblast cells (cadFibroblast) when cultivated in different culture media. The cadFibroblast cell lines from adult Barbari (Capra hircus) bucks were established and the effect of different media viz. DMEM/F-12 [with low-glucose (5.5 mM; DL) and high-glucose (30 mM; DH)], α-MEM [with low-glucose (5.5 mM; ML) and with high-glucose (30 mM; MH)], and fibroblast growth medium (FGM) were evaluated. Cells were then compared for growth characteristics and in-vitro dynamics through cellular morphology, proliferation, population-doubling time, double-immunocytochemistry, colony-forming units, wound healing, transwell migration, and differential expression of fibroblast-specific markers (FSP-1 and vimentin). The results of immunocytochemistry, transwell migration/invasion, and wound healing assays showed the superiority of DH over DL and other media tested. Whereas, similar effects of glucose supplementation and expression of FSP-1 were not observed in α-MEM. Transwell migration was significantly (p < 0.05) lower in FGM compared with other media tested. Overall, our results illustrate the media-dependent deviation in in-vitro dynamics and culture characteristics of cadFibroblasts that may be useful to develop strategies to cultivate these cells efficiently for research and downstream applications.


Asunto(s)
Medios de Cultivo , Dermis , Fibroblastos , Cabras , Técnicas de Cultivo de Célula , Fibroblastos/citología , Fibroblastos/efectos de los fármacos , Fibroblastos/microbiología , Medios de Cultivo/química , Medios de Cultivo/farmacología , Técnicas In Vitro , Dermis/citología , Animales , Línea Celular , Masculino , Glucosa/metabolismo , Perfilación de la Expresión Génica , Cicatrización de Heridas , Ensayos de Migración Celular , Biomarcadores
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