TY - JOUR
T1 - Electroless palladium-coated polymer scaffolds for electrical stimulation of osteoblast-like Saos-2 cells
AU - Careta, Oriol
AU - Salicio-Paz, Asier
AU - Pellicer, Eva
AU - Ibáñez, Elena
AU - Fornell, Jordina
AU - García-Lecina, Eva
AU - Sort, Jordi
AU - Nogués, Carme
N1 - Funding Information:
Funding: This research was funded by the Generalitat de Catalunya grant numbers 2017-SGR-292 and 2017-SGR-503, by the Spanish Ministerio de Economía y Competitividad (MINECO) grant numbers MAT2017-86357-C3-1-R (co-financed by the Fondo Europeo de Desarrollo Regional, FEDER), MAT2017-86357-C3-2-R and MAT2017-86357-C3-3-R and by the Spanish Ministerio de Ciencia e Innovación (MICINN) grant number CER-20191003.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/1/2
Y1 - 2021/1/2
N2 - Three-dimensional porous scaffolds offer some advantages over conventional treatments for bone tissue engineering. Amongst all non-bioresorbable scaffolds, biocompatible metallic scaffolds are preferred over ceramic and polymeric scaffolds, as they can be used as electrodes with different electric field intensities (or voltages) for electric stimulation (ES). In the present work we have used a palladium-coated polymeric scaffold, generated by electroless deposition, as a bipolar electrode to electrically stimulate human osteoblast-like Saos-2 cells. Cells grown on palladium-coated polyurethane foams under ES presented higher proliferation than cells grown on foams without ES for up to 14 days. In addition, cells grown in both conditions were well adhered, with a flat appearance and a typical actin cytoskeleton distribution. However, after 28 days in culture, cells without ES were filling the entire structure, while cells under ES appeared rounded and not well adhered, a sign of cell death onset. Regarding osteoblast differentiation, ES seems to enhance the expression of early expressed genes. The results suggest that palladium-coated polyurethane foams may be good candidates for osteoblast scaffolds and demonstrate that ES enhances osteoblast proliferation up to 14 days and upregulate expression genes related to extracellular matrix formation.
AB - Three-dimensional porous scaffolds offer some advantages over conventional treatments for bone tissue engineering. Amongst all non-bioresorbable scaffolds, biocompatible metallic scaffolds are preferred over ceramic and polymeric scaffolds, as they can be used as electrodes with different electric field intensities (or voltages) for electric stimulation (ES). In the present work we have used a palladium-coated polymeric scaffold, generated by electroless deposition, as a bipolar electrode to electrically stimulate human osteoblast-like Saos-2 cells. Cells grown on palladium-coated polyurethane foams under ES presented higher proliferation than cells grown on foams without ES for up to 14 days. In addition, cells grown in both conditions were well adhered, with a flat appearance and a typical actin cytoskeleton distribution. However, after 28 days in culture, cells without ES were filling the entire structure, while cells under ES appeared rounded and not well adhered, a sign of cell death onset. Regarding osteoblast differentiation, ES seems to enhance the expression of early expressed genes. The results suggest that palladium-coated polyurethane foams may be good candidates for osteoblast scaffolds and demonstrate that ES enhances osteoblast proliferation up to 14 days and upregulate expression genes related to extracellular matrix formation.
KW - Differentiation
KW - Electrical stimulation
KW - Gene expression
KW - Osteoblast
KW - Pd-coated polyurethane scaffold
KW - electrical stimulation
KW - differentiation
KW - osteoblast
KW - gene expression
UR - http://www.scopus.com/inward/record.url?scp=85099140313&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/f4e9e7a0-a01b-31e9-b78c-3befd2d809fb/
U2 - https://doi.org/10.3390/ijms22020528
DO - https://doi.org/10.3390/ijms22020528
M3 - Artículo
C2 - 33430266
AN - SCOPUS:85099140313
SN - 1661-6596
VL - 22
SP - 1
EP - 16
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 2
M1 - 528
ER -