Nano hydroxyapatite-blasted titanium surface creates a biointerface able to govern Src-dependent osteoblast metabolism as prerequisite to ECM remodeling

• Published in: Colloids and surfaces, B, Biointerfaces Vol. 163; pp. 321 - 328
• Main Authors: Fernandes, Célio J.C., Bezerra, Fábio, Ferreira, Marcel R., Andrade, Amanda F.C., Pinto, Thais Silva, Zambuzzi, Willian F.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.03.2018
• Subjects: Adhesion; Biointerfaces; Biotechnology; Hydroxyapatite; Implants; Nanotechnology; Osteoblast; Signal transduction; Biotechnology; Signal transduction; Biointerfaces; Implants; Osteoblast; Hydroxyapatite; Adhesion; Nanotechnology
• ISSN: 0927-7765; 1873-4367
• DOI: 10.1016/j.colsurfb.2017.12.049

[Display omitted] •Pre-osteoblast/titanium biointerface requires a dynamic genes reprogramming.•Titanium-modified surfaces differentially orchestrate ECM remodeling-related genes.•Src and ECM remodeling-related genes are hallmarks osteogenic phenotype. Over the last several years, we have focused on the importance of intracellular signaling pathways in dynamically governing the biointerface between pre-osteoblast and surface of biomaterial. Thus, this study investigates the molecular hallmarks involved in the pre-osteoblast relationship with different topography considering Machined (Mc), Dual Acid-Etching (DAE), and nano hydroxyapatite-blasted (nHA) groups. There was substantial differences in topography of titanium surface, considering Atomic Force Microscopy and water contact angle (Mc = 81.41 ± 0.01; DAE = 97.18 ± 0.01; nHA = 40.95 ± 0.02). Later, to investigate their topography differences on biological responses, pre-osteoblast was seeded on the different surfaces and biological samples were collected after 24 h (to consider adhesion signaling) and 10 days (to consider differentiation signaling). Preliminary results evidenced significant differences in morphological changes of pre-osteoblasts mainly resulting from the interaction with the DAE and nHA, distinguishing cellular adaptation. These results pushed us to analyze activation of specific genes by exploring qPCR technology. In sequence, we showed that Src performs crucial roles during cell adhesion and later differentiation of the pre-osteoblast in relationship with titanium-based biomaterials, as our results confirmed strong feedback of the Src activity on the integrin-based pathway, because integrin-ß1 (∼5-fold changes), FAK (∼12-fold changes), and Src (∼3.5-fold changes) were significantly up-expressed when Src was chemically inhibited by PP1 (5 μM). Moreover, ECM-related genes were rigorously reprogrammed in response to the different surfaces, resulting on Matrix Metalloproteinase (MMP) activities concomitant to a significant decrease of MMP inhibitors. In parallel, we showed PP1-based Src inhibition promotes a significant increase of MMP activity. Taking all our results into account, we showed for the first time nano hydroxyapatite-blasted titanium surface creates a biointerface able to govern Src-dependent osteoblast metabolism as pre-requisite to ECM remodeling