Human serum opsonization of orthopedic biomaterial particles: Protein‐binding and monocyte/macrophage activation in vitro
- 25 March 2003
- journal article
- research article
- Published by Wiley in Journal of Biomedical Materials Research Part A
- Vol. 65A (2) , 290-298
- https://doi.org/10.1002/jbm.a.10477
Abstract
Wear particles generated after total joint arthroplasty activate monocyte/macrophages and incite formation of a granulomatous periprosthetic tissue associated with bone loss and implant loosening. This study tested the hypothesis that selective opsonization of orthopedic implant biomaterial wear particles by human serum proteins influences monocyte/macrophage activation. Serum protein binding to metallic, polymeric, and ceramic particles was determined by one-dimensional sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). Individual proteins bound to particles were subsequently identified using two-dimensional SDS-PAGE, microsequencing techniques, and SWISS-PROT analysis. Effects of selective protein opsonization on particle-induced monocyte/macrophage activation were assessed by quantification of interleukin-1beta, interleukin-6, and tumor necrosis factor-alpha release. Results from one-dimensional gel analyses revealed distinct serum protein-binding patterns specific for each material tested. Two-dimensional gel analysis together with amino acid sequencing of the prominent protein species confirmed the presence of albumin and alpha-1-antitrypsin bound to all particles tested. In contrast to the metallic particles, apolipoprotein was a major species associated with polymeric particles. Opsonization of PMMA particles with purified preparations of each of the identified proteins showed that albumin significantly enhanced particle-induced monocyte/macrophage activation. These data confirm orthopedic biomaterial specific binding of human serum proteins and demonstrate that albumin exacerbates particle-induced monocyte/macrophage activation. Alterations in the chemical and surface properties of orthopedic biomaterials to modulate protein interactions may improve implant longevity. © 2003 Wiley Periodicals, Inc. J Biomed Mater Res 65A: 290–298, 2003Keywords
This publication has 56 references indexed in Scilit:
- Intracellular Trafficking and Killing ofStreptococcus pneumoniaeby Human Alveolar Macrophages Are Influenced by OpsoninsInfection and Immunity, 2000
- Titanium particles inhibit osteoblast adhesion to fibronectin-coated substratesJournal of Orthopaedic Research, 2000
- Interleukin‐4 inhibits granulocyte‐macrophage colony‐stimulating factor, interleukin‐6, and tumor necrosis factor‐alpha expression by human monocytes in response to polymethylmethacrylate particle challenge in vitroJournal of Orthopaedic Research, 1999
- Interferon-gamma exacerbates polymethylmethacrylate particle-induced interleukin-6 release by human monocyte/macrophagesin vitroJournal of Biomedical Materials Research, 1999
- High levels of expression of collagenase-3 (MMP-13) in pathological conditions associated with a foreign-body reactionThe Journal of Bone and Joint Surgery. British volume, 1998
- Cobalt and Chromium Concentrations in Patients With Metal on Metal Total Hip ReplacementsClinical Orthopaedics and Related Research, 1996
- Metal Levels in Cemented Total Hip ArthroplastyClinical Orthopaedics and Related Research, 1992
- A Clinical-Pathologic-Biochemical Study of the Membrane Surrounding Loosened and Nonloosened Total Hip ArthroplastiesClinical Orthopaedics and Related Research, 1989
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970