Rezvanian, P.; Álvarez-López, A.; Tabraue-Rubio, R.; Daza, R.; Colchero, L.; Elices, M.; Guinea, G.V.; González-Nieto, D.; Pérez-Rigueiro, J. Modulation of Cell Response through the Covalent Binding of Fibronectin to Titanium Substrates. J. Funct. Biomater.2023, 14, 342.
Rezvanian, P.; Álvarez-López, A.; Tabraue-Rubio, R.; Daza, R.; Colchero, L.; Elices, M.; Guinea, G.V.; González-Nieto, D.; Pérez-Rigueiro, J. Modulation of Cell Response through the Covalent Binding of Fibronectin to Titanium Substrates. J. Funct. Biomater. 2023, 14, 342.
Rezvanian, P.; Álvarez-López, A.; Tabraue-Rubio, R.; Daza, R.; Colchero, L.; Elices, M.; Guinea, G.V.; González-Nieto, D.; Pérez-Rigueiro, J. Modulation of Cell Response through the Covalent Binding of Fibronectin to Titanium Substrates. J. Funct. Biomater.2023, 14, 342.
Rezvanian, P.; Álvarez-López, A.; Tabraue-Rubio, R.; Daza, R.; Colchero, L.; Elices, M.; Guinea, G.V.; González-Nieto, D.; Pérez-Rigueiro, J. Modulation of Cell Response through the Covalent Binding of Fibronectin to Titanium Substrates. J. Funct. Biomater. 2023, 14, 342.
Abstract
Titanium (Ti-6Al-4V) substrates were functionalized through the covalent binding of fibronectin, and the effect of the presence of this extracellular matrix protein on the surface of the material was assessed employing mesenchymal stem cell (MSC) cultures. The functionalization process com-prised the usage of the activation vapor silanization (AVS) technique to deposit a thin film with a high surface density of amine groups on the material, followed by the covalent binding of fi-bronectin to the amine groups using the N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hy-drochloride / N-hydroxysuccinimide (EDC/NHS) crosslinking chemistry. The biological effect of the fibronectin on murine MSCs was assessed in vitro. It was found that functionalized samples not only showed enhanced initial cell adhesion compared with bare titanium, but also a three-fold increase in the cell area, reaching values comparable to those found on the polystyrene controls. These results represent a clear indication of the potential of modulating the response of the or-ganism to an implant through the covalent binding of extracellular matrix proteins on the pros-thesis.
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.