Enhancement of bone regeneration by dual release of a macrophage recruitment agent and platelet-rich plasma from gelatin hydrogels

Biomaterials. 2014 Jan;35(1):214-24. doi: 10.1016/j.biomaterials.2013.09.103. Epub 2013 Oct 11.

Abstract

Macrophages play an important role in regulating inflammatory responses and tissue regeneration. In the present study, their effect on bone remodeling is investigated by the simultaneous application of a macrophage recruiting agent, SEW2871 of a sphingosine-1 phosphate agonist, and platelet-rich plasma (PRP). The non-water soluble SEW2871 was solubilized in water through micelles formation with l-lactic acid grafted gelatin, and the resulting micelles with PRP were incorporated into gelatin hydrogels. Mixed SEW2871-micelles and PRP were released from gelatin hydrogels in a controlled fashion both in vitro and in vivo. In vitro migration assay revealed that the presence of PRP synergistically promoted SEW2871-induced macrophages migration. When applied to a bone defect of rats, the hydrogels incorporating mixed SEW2871-micelles and PRP recruited a higher number of macrophages than those hydrogels incorporating either SEW2871-micelles or PRP. The hydrogels incorporating mixed SEW2871-micelles and PRP enhanced the level of tumor necrosis factor (TNF)-α of pro-inflammatory cytokine, 3 days after application, while pro-inflammatory responses coupled with a significant increase in the expression level of osteoprotegerin (OPG) and interleukin (IL)-10 and transforming growth factor (TGF)-β1 of anti-inflammatory cytokine were observed 10 days postoperatively. The hydrogels incorporating mixed SEW2871-micelles and PRP promoted bone regeneration to a significant great extent compared with those incorporating PBS and either SEW2871-micelles or PRP. It is concluded that macrophages recruitment contributed to PRP-induced bone regeneration.

Keywords: Bone regeneration; Controlled release; Gelatin hydrogel; Macrophages; Platelet rich plasma (PRP); S1P(1) agonist (SEW2871).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Regeneration*
  • Bone and Bones / metabolism
  • Cell Movement
  • Cytokines / metabolism
  • Gelatin*
  • Hydrogels*
  • Inflammation Mediators / metabolism
  • Macrophages / cytology*
  • Osteoprotegerin / metabolism
  • Platelet-Rich Plasma*
  • Rats
  • Rats, Inbred F344

Substances

  • Cytokines
  • Hydrogels
  • Inflammation Mediators
  • Osteoprotegerin
  • Gelatin