The effect of collagen coating on titanium with nanotopography on in vitro osteogenesis.
Daniel G CostaEmanuela P FerrazRodrigo P F AbunaPaulo T de OliveiraMarco MorraMarcio M BelotiAdalberto Luiz RosaPublished in: Journal of biomedical materials research. Part A (2017)
Several studies have shown the positive effects of Ti either with nanotopography or coated with collagen on osteoblast differentiation. Thus, we hypothesized that the association of nanotopography with collagen may increase the in vitro osteogenesis on Ti surface. Ti discs with nanotopography with or without collagen coating were characterized by scanning electron microscopy and atomic force microscopy. Rat calvaria-derived osteoblastic cells were cultured on both Ti surfaces for up to 14 days and the following parameters were evaluated: cell proliferation, alkaline phosphatase (ALP) activity, extracellular matrix mineralization, protein expression of bone sialoprotein (BSP) and osteopontin (OPN), and gene expression of collagen type 1a (Coll1a), runt-related transcription factor 2 (Runx2), osterix (OSX), osteocalcin (OC), Ki67, Survivin, and Bcl2-associated X protein (BAX). Surface characterization evidenced that collagen coating did not alter the nanotopography. Collagen coating increased cell proliferation, ALP activity, extracellular matrix mineralization, and Coll1a, OSX, OC, and BAX gene expression. Also, OPN and BSP proteins were strongly detected in cultures grown on both Ti surfaces. In conclusion, our results showed that the combination of nanotopography with collagen coating stimulates the early, intermediate, and final events of the in vitro osteogenesis and may be considered a potential approach to promote osseointegration of Ti implants. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 2783-2788, 2017.
Keyphrases
- extracellular matrix
- gene expression
- transcription factor
- cell proliferation
- wound healing
- induced apoptosis
- atomic force microscopy
- electron microscopy
- escherichia coli
- oxidative stress
- small molecule
- radiation therapy
- risk assessment
- high resolution
- soft tissue
- cystic fibrosis
- staphylococcus aureus
- bone regeneration
- endothelial cells
- binding protein
- pi k akt
- cell cycle arrest
- dna binding
- bone loss
- locally advanced