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Author Notes:

B.D. Boyan, Tel.: +1 404 385 4108; fax: +1 404 894 2291. barbara.boyan@bme.gatech.edu

Subjects:

Research Funding:

This project was supported by a grant from the National Institute of Arthritis, Musculoskeletal, and Skin Diseases at the National Institutes of Health (USPHS Grant AR052102).

Titanium disks were provided by Institut Straumann AG (Basel, Switzerland) as a gift.

Keywords:

  • Science & Technology
  • Technology
  • Engineering, Biomedical
  • Materials Science, Biomaterials
  • Engineering
  • Materials Science
  • Cell signaling
  • Titanium surface roughness
  • Osteoblast differentiation
  • Gene expression
  • Regulatory factors
  • RECEPTOR TYROSINE KINASE
  • C3H10T1/2 MESENCHYMAL CELLS
  • STEM-CELLS
  • BONE-FORMATION
  • MICRON-SCALE
  • ROR2
  • CATENIN
  • PROTEIN
  • DIFFERENTIATION
  • PATHWAY

Role of non-canonical Wnt signaling in osteoblast maturation on microstructured titanium surfaces

Tools:

Journal Title:

Acta Biomaterialia

Volume:

Volume 7, Number 6

Publisher:

, Pages 2740-2750

Type of Work:

Article | Post-print: After Peer Review

Abstract:

The Wnt signaling pathway inhibitor Dickkopf-2 (Dkk2) regulates osteoblast differentiation on microstructured titanium (Ti) surfaces, suggesting involvement of Wnt signaling in this process. To test this, human osteoblast-like MG63 cells were cultured on tissue culture polystyrene or Ti (smooth PT (Ra = 0.2 μm), sand-blasted and acid-etched SLA (Ra = 3.22 μm), modSLA (hydrophilic SLA)). Expression of Wnt pathway receptors, activators and inhibitors was measured by qPCR. Non-canonical pathway ligands, receptors and intracellular signaling molecules, as well as bone morphogenetic proteins BMP2 and BMP4, were upregulated on SLA and modSLA, whereas canonical pathway members were downregulated. To confirm that non-canonical signaling was involved, cells were cultured daily with exogenous Wnt3a (canonical pathway) or Wnt5a (non-canonical pathway). Alternatively, cells were cultured with antibodies to Wnt3a or Wnt5a to validate that Wnt proteins secreted by the cells were mediating cell responses to the surface. Wnt5a, but not Wnt3a, increased MG63 cell differentiation and BMP2 and BMP4 proteins, suggesting Wnt5a promotes osteogenic differentiation through production of BMPs. Effects of exogenous and endogenous Wnt5a were synergistic with surface microstructure, suggesting the response also depends on cell maturation state. These results indicate a major role for the non-canonical, calcium-dependent Wnt pathway in differentiation of osteoblasts on microstructured titanium surfaces during implant osseointegration.

Copyright information:

Copyright © 2011 Published by Elsevier Ltd.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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