Efficient co‐cultivation of human fibroblast cells (HFCs) and adipose‐derived stem cells (ADSs) on gelatin/PLCL nanofiber

In this study, we investigated whether the nanofibers produced by natural‐synthetic polymers can probably promote the proliferation of co‐cultured adipose‐derived stem cells/human fibroblast cells (ADSs/HFCs) and synthesis of collagen. Nanofiber was fabricated by blending gelatin and poly (L‐lactide co‐ɛ‐caprolactone) (PLCL) polymer nanofiber (Gel/PLCL). Cell morphology and the interaction between cells and Gel/PLCL nanofiber were evaluated by FESEM and fluorescent microscopy. MTS assay and quantitative real‐time polymerase chain reaction were applied to assess the proliferation of co‐cultured ADSs/HFCs and the collagen type I and III synthesis, respectively. The concentrations of two cytokines including fibroblast growth factor‐basic and transforming growth factor‐β1 were also measured in culture medium of co‐cultured ADSs/HDCs using enzyme‐linked immunosorbent assay assay. Actually, nanofibers exhibited proper structural properties in terms of stability in cell proliferation and toxicity analysis processes. Gel/PLCL nanofiber promoted the growth and the adhesion of HFCs. Our results showed in contact co‐culture of ADSs/HFCs on the Gel/PLCL nanofiber increased cellular adhesion and proliferation synergistically compared to non‐coated plate. Also, synthesis of collagen and cytokines secretion of co‐cultured ADSs/HFCs on Gel/PLCL scaffolds is significantly higher than non‐coated plates. To conclude, the results suggest that Gel/PLCL nanofiber can imitate physiological characteristics in vivo and enhance the efficacy of co‐cultured ADSs/HFCs in wound healing process.Inspec keywords: biomedical materials, enzymes, adhesion, fluorescence, polymer fibres, tissue engineering, wounds, nanofibres, cellular biophysics, molecular biophysics, gelatin, biochemistry, nanomedicine, field emission scanning electron microscopy, nanofabricationOther keywords: cell morphology, cell proliferation, efficient cocultivation, HFCs, ADSs, gelatin‐PLCL nanofiber, natural‐synthetic polymers, cocultured adipose‐derived stem cells‐human fibroblast cells, FESEM, fluorescent microscopy, MTS assay, quantitative real‐time polymerase chain reaction, collagen type I synthesis, collagen type III synthesis, cytokines, transforming growth factor‐β1, fibroblast growth factor‐basic growth factor‐β1, culture medium, enzyme‐linked immunosorbent assay assay, structural properties, toxicity analysis, cellular adhesion, physiological characteristics in vivo, wound healing