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Stimulation of bone formation by monocyte-activator functionalized graphene oxide: In vivo

  • Valentina Bordoni
    ,
  • Giacomo Reina
    ,
  • ,
  • Giulia Furesi
    ,
  • Stefanie Thiele
    ,
  • Chiara Gardin
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

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.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 19408-19421 (14 pages)

Journal (Volume, Issue Number)

Nanoscale (Volume 11, Issue 41)

Publication milestones

  • Published - 11/07/2019

Publication status

Published - 11/07/2019

ISSN

2040-3364

Publication IDs

  • Scopus: 85074117655
  • PubMed: 31386739

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Funding Details

This work was partly supported by the Centre National de la Recherche Scientique (CNRS), the Agence Nationale de la Recherche (ANR) through the LabEx project Chemistry of Complex Systems (ANR-10-LABX-0026_CSC), and the International Center for Frontier Research in Chemistry (icFRC). The authors gratefully acknowledge financial support from ANR (ANR-15-GRFL-0001-05), MIUR JTC Graphene 2015 (G-IMMUNOMICS project), European Union HORIZON 2020 research and innovation programme under MSCA RISE 2016 project Carbo-Immap grant no. 734381. LGD thanks the Italian MIUR (PRIN call 2015, project: 2015TWP83Z). LGD is grateful to Prof. Lorenz Hofbauer for the assistance and the great support. The authors wish to thank Cathy Royer and Valérie Demais for help with TEM analyses at the “Plateforme Imagerie in vitro” at the Center of Neurochemistry (INCI, Strasbourg, France).
FundersFunding numbers
Labex
-
Centre National de la Recherche Scientique
-
H2020
-
ANR‐10‐LABX‐0026_CSC
-
MIUR
-
MSCA
734381
Centre International de Recherche aux Frontières de la Chimie
ANR-15-GRFL-0001-05
ANR
ANR-15-GRFL-0001