Hydroxyapatite coating affects the Wnt signaling pathway during peri-implant healing in vivo

Acta Biomater. 2014 Mar;10(3):1451-62. doi: 10.1016/j.actbio.2013.12.012. Epub 2013 Dec 14.

Abstract

Owing to its bio- and osteoconductivity, hydroxyapatite (HA) is a widely used implant material, but its osteogenic properties are only partly evaluated in vitro and in vivo. The present study focused on bone healing adjacent to HA-coated titanium (Ti) implants, with or without incorporated lithium ions (Li(+)). Special attention was given to the Wnt signaling pathway. The implants were inserted into rat tibia for 7 or 28 days and analyzed ex vivo, mainly by histomorphometry and quantitative real-time polymerase chain reaction (qPCR). HA-coated implants showed, irrespective of Li(+) content, bone-implant contact (BIC) and removal torque values significantly higher than those of reference Ti. Further, the expression of OCN, CTSK, COL1A1, LRP5/6 and WISP1 was significantly higher in implant-adherent cells of HA-coated implants, with or without Li(+). Significantly higher β-catenin expression and significantly lower COL2A1 expression were observed in peri-implant bone cells from HA with 14 ng cm(-2) released Li(+). Interestingly, Ti implants showed a significantly larger bone area (BA) in the threads than HA with 39 ng cm(-2) released Li(+), but had a lower BIC than any HA-coated implant. This study shows that HA, with or without Li(+), is a strong activator of the Wnt signaling pathway, and may to some degree explain its high bone induction capacity.

Keywords: Gene expression; Hydroxyapatite; Lithium; Osseointegration; Wnt signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone and Bones / drug effects
  • Bone and Bones / ultrastructure
  • Cell Adhesion / drug effects
  • Cell Adhesion / genetics
  • Coated Materials, Biocompatible / pharmacology*
  • Durapatite / pharmacology*
  • Enzyme-Linked Immunosorbent Assay
  • Gene Expression Regulation / drug effects
  • Immunohistochemistry
  • Implants, Experimental*
  • Male
  • Rats, Sprague-Dawley
  • Torque
  • Wnt Signaling Pathway / drug effects*
  • Wnt Signaling Pathway / genetics
  • Wound Healing / drug effects*
  • beta Catenin / metabolism

Substances

  • Coated Materials, Biocompatible
  • beta Catenin
  • Durapatite