The effect of local IL-4 delivery or CCL2 blockade on implant fixation and bone structural properties in a mouse model of wear particle induced osteolysis

J Biomed Mater Res A. 2016 Sep;104(9):2255-62. doi: 10.1002/jbm.a.35759. Epub 2016 May 10.

Abstract

Modulation of macrophage polarization and prevention of CCL2-induced macrophage chemotaxis are emerging strategies to reduce wear particle induced osteolysis and aseptic total joint replacement loosening. In this study, the effect of continuous IL-4 delivery or bioactive implant coating that constitutively releases a protein inhibitor of CCL2 signaling (7ND) on particle induced osteolysis were studied in the murine continuous femoral intramedullary particle infusion model. Polyethylene particles with or without IL-4 were infused into mouse distal femurs implanted with hollow titanium rods using subcutaneous infusion pumps. In another experimental group, particles were infused into the femur through a 7ND coated rod. After 4 weeks, fixation of the implant was assessed using a pullout test. The volume of trabecular bone and the geometry of the local cortical bone were assessed by µCT and the corresponding structural properties of the cortical bone determined by torsional testing. Continuous IL-4 delivery led to increased trabecular bone volume as well as enhanced local bone geometry and structural properties, while 7ND implant coating did not have effect on these parameters. The results suggest that local IL-4 treatment is a promising strategy to mitigate wear particle induced osteolysis. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 2255-2262, 2016.

Keywords: CCL2; aseptic loosening; bone structural properties; interleukin-4; macrophage.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Bone-Implant Interface*
  • Chemokine CCL2 / antagonists & inhibitors*
  • Chemokine CCL2 / metabolism
  • Disease Models, Animal
  • Femur / metabolism*
  • Femur / pathology
  • Implants, Experimental / adverse effects*
  • Interleukin-4 / pharmacology*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Osteolysis* / chemically induced
  • Osteolysis* / metabolism
  • Osteolysis* / pathology
  • Polyethylene* / adverse effects
  • Polyethylene* / pharmacology

Substances

  • Ccl2 protein, mouse
  • Chemokine CCL2
  • Interleukin-4
  • Polyethylene