Saito et al. [167] |
In vivo |
Cells extracted-mouse molar |
To clarify the expression of GM-CSF and OPN in the process of reparative dentin formation by allogenic tooth transplantation using in situ hybridization for OPN and immunohistochemistry for GM-CSF and OPN |
The secretion of GM-CSF and OPN by immunocompetent cells such as macrophages and dendritic cells plays a role in the maturation of dendritic cells and the differentiation of odontoblasts, respectively, in the regenerated pulp tissue following tooth transplantation |
Addison et al. [164] |
In vitro |
MC3T3-E1 osteoblast |
To examine the role of OPN acidic serine- and aspartate-rich motif and its interaction with PHEX enzyme |
OPN acidic serine- and aspartate-rich motif inhibits mineralization by binding to hydroxyapatite in a phosphorylation-dependent manner |
Grimm et al. [166] |
In vivo; healthy men |
|
To investigate the changes in biochemical parameters of bone turnover following human endotoxemia, an experimental model of self-limiting systemic infection and inflammation |
The early human response to systemic endotoxemia boosts OPN levels and modifies bone biomarkers, indicating a decrease in the lytic activity of osteoclasts, accompanied by an increase in the activity of immature osteoblasts |
Wu et al. [165] |
In vitro |
Human fetal-osteoblast (hFOB 1.19) |
To explore the osteoblastic cellular response to physicochemical characteristics of fluoridated hydroxyapatite |
Sintered fluoridated- calcined hydroxyapatite composites could enhance OPN and COL I gene expression after 6-day culture (Pp < 0.05). Otherwise, sintered hydroxy fluorapatites composites inhibited the expression. Sintered fluoridated-calcined hydroxyapatite composites with both OH and OH···F bands were bioactive bone graft materials |
Li et al. [159] |
In vitro |
Osteoblast |
To identify whether haploinsufficiency of Nf1 (Nf1±) osteoblasts and their precursors secrete cytokines that have a central role |
OPN, a matrix protein found in mineralized tissues and pivotal in modulating osteoclast functions, was present in increased concentrations in Nf1± osteoblasts. Addition of OPN neutralizing antibody to Nf1± osteoblast conditioned media diminished the gain in bioactivity on osteoclast functions, including osteoclast migration and bone resorption |
Bernards et al. [170, 171] |
In vitro |
MC3T3-E1 cell |
To compare the cell binding ability of adsorbed BSP and OPN specifically bound to hydroxyapatite |
There is a preference for cell binding to HA with adsorbed BSP as compared to OPN, but not to a statistically significant level |
Bernards et al. [170, 171] |
In vitro |
MC3T3-E1 cell |
To examine and compare the orientation of BSP under similar circumstances with OPN |
OPN is more important than BSP for osteoblast adhesion to the collagen matrix |
Ono et al. [160] |
In vivo; parathyroid hormone receptor (PPR) transgenic mice |
|
To examine the effects of deficiency of the bone matrix protein osteopontin (OPN) on the systemic effects of PTH specifically within osteoblastic cell lineages |
Local feedback regulation by the bone matrix protein OPN also plays a significant role in the regulation of PTH actions |
Zirngibl et al. [161] |
In vitro |
Rat osteosarcoma ROS17/2.8 cells, non-osteoblastic (HeLa) cell lines |
To investigate whether the transcriptional regulation by ERRalpha of the gene for OPN |
OPN is an ERRalpha target gene whose promoter is regulated by ERRalpha in a cell context-dependent manner and that a predicted silencing mutation in AF2 or a more flexible helix 12 increases ERRalpha transcriptional activity, effects with implications for ERRalpha as a therapeutic target in bone |
Addison et al. [173] |
In vitro |
MC3T3-E1 osteoblast |
To investigate the effect of inorganic pyrophosphate on osteoblast function and matrix mineralization |
Inorganic pyrophosphate prevents mineralization in MC3T3-E1 osteoblast cultures by at least three different mechanisms that include direct binding to growing crystals, induction of OPN expression, and inhibition of tissue-nonspecific alkaline phosphatase activity |
Ishijima et al. [158] |
In vitro |
Bone marrow cells obtained from hind limb bones of OPN−/− mice |
To obtain further insight into the role of OPN in mediating mechanical stress effect on bone |
OPN has an important role in the effects of unloading-induced alterations of differentiation of bone marrow into osteoblasts and osteoclasts |
Kato et al. [163] |
In vivo; wild-type mice |
|
To test whether deficiency of OPN, a secreted phosphorylated protein, could modulate the effects of prostaglandin E receptor agonist |
OPN deficiency enhanced the direct anabolic action of prostaglandin E receptor agonist locally injected onto the parietal bone in inducing new bone formation |
Liu et al. [92, 162] |
In vitro |
Osteoblast MC3T3-E1 |
To attempt to control the orientation/conformation of bone OPN via its specific interactions with type I collagen |
The specific binding of OPN to collagen I may naturally orient OPN, thus influencing osteoblast adhesion |
Osathanon et al. [80] |
In vitro |
Human osteoblast-like cells (SaOS-2) |
To compare the early response of human osteoblast-like cells (SaOS-2) on commercially pure titanium (cpTi) and titanium-6-aluminium-7-niobium (Ti-6Al-7Nb) |
Ti-6Al-7Nb possess a good potential to support SaOS-2 cells on spreading and fibronectin and OPN synthesis, therefore, this material may be one of a candidate material used in implant dentistry |