The Effects of Titanium Dioxide Nanoparticles on Osteoblasts Mineralization: A Comparison between 2D and 3D Cell Culture Models.
Gabriela de Souza CastroWanderson de SouzaThais Suelen Mello LimaDanielle Cabral BonfimJacques WerckmannBraulio Soares ArchanjoJosé Mauro GranjeiroAna Rosa Lopes Pereira RibeiroSara G PiperniPublished in: Nanomaterials (Basel, Switzerland) (2023)
Although several studies assess the biological effects of micro and titanium dioxide nanoparticles (TiO 2 NPs), the literature shows controversial results regarding their effect on bone cell behavior. Studies on the effects of nanoparticles on mammalian cells on two-dimensional (2D) cell cultures display several disadvantages, such as changes in cell morphology, function, and metabolism and fewer cell-cell contacts. This highlights the need to explore the effects of TiO 2 NPs in more complex 3D environments, to better mimic the bone microenvironment. This study aims to compare the differentiation and mineralized matrix production of human osteoblasts SAOS-2 in a monolayer or 3D models after exposure to different concentrations of TiO 2 NPs. Nanoparticles were characterized, and their internalization and effects on the SAOS-2 monolayer and 3D spheroid cells were evaluated with morphological analysis. The mineralization of human osteoblasts upon exposure to TiO 2 NPs was evaluated by alizarin red staining, demonstrating a dose-dependent increase in mineralized matrix in human primary osteoblasts and SAOS-2 both in the monolayer and 3D models. Furthermore, our results reveal that, after high exposure to TiO 2 NPs, the dose-dependent increase in the bone mineralized matrix in the 3D cells model is higher than in the 2D culture, showing a promising model to test the effect on bone osteointegration.
Keyphrases
- single cell
- endothelial cells
- cell therapy
- bone mineral density
- bone regeneration
- quantum dots
- stem cells
- induced apoptosis
- systematic review
- soft tissue
- gene expression
- signaling pathway
- mesenchymal stem cells
- cell cycle arrest
- endoplasmic reticulum stress
- postmenopausal women
- cell proliferation
- visible light
- bone loss
- oxidative stress
- walled carbon nanotubes
- case control