Stimulation of bone formation by monocyte-activator functionalized graphene oxide in vivo.
Valentina BordoniGiacomo ReinaMarco OrecchioniGiulia FuresiStefanie ThieleChiara GardinBarbara ZavanGianaurelio CunibertiAlberto BiancoMartina RaunerLucia Gemma DeloguPublished in: Nanoscale (2019)
Nanosystems are able to enhance bone regeneration, a complex process requiring the mutual interplay between immune and skeletal cells. Activated monocytes can communicate pro-osteogenic signals to mesenchymal stem cells and promote osteogenesis. Thus, the activation of monocytes is a promising strategy to improve bone regeneration. Nanomaterials specifically selected to provoke immune-mediated bone formation are still missing. As a proof of concept, we apply here the intrinsic immune-characteristics of graphene oxide (GO) with the well-recognized osteoinductive capacity of calcium phosphate (CaP) in a biocompatible nanomaterial called maGO-CaP (monocytes activator GO complexed with CaP). In the presence of monocytes, the alkaline phosphatase activity and the expression of osteogenic markers increased. Studying the mechanisms of action, we detected an up-regulation of Wnt and BMP signaling, two key osteogenic pathways. The role of the immune activation was evidenced by the over-production of oncostatin M, a pro-osteogenic factor produced by monocytes. Finally, we tested the pro-osteogenic effects of maGO-CaP in vivo. maGO-CaP injected into the tibia of mice enhanced local bone mass and the bone formation rate. Our study suggests that maGO-CaP can activate monocytes to enhance osteogenesis ex vivo and in vivo.
Keyphrases
- bone regeneration
- mesenchymal stem cells
- dendritic cells
- peripheral blood
- bone marrow
- umbilical cord
- poor prognosis
- cell therapy
- stem cells
- cell proliferation
- anti inflammatory
- metabolic syndrome
- induced apoptosis
- immune response
- endothelial cells
- nuclear factor
- adipose tissue
- drug delivery
- signaling pathway
- drug release
- long non coding rna
- binding protein
- endoplasmic reticulum stress
- toll like receptor
- bone loss
- pi k akt