Binding of proteins to ultra high molecular weight polyethylene wear particles as a possible mechanism of macrophage and lymphocyte activation
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
20845495
DOI
10.1002/jbm.a.32924
Knihovny.cz E-zdroje
- MeSH
- aktivace lymfocytů * MeSH
- aktivace makrofágů * MeSH
- koncentrace vodíkových iontů MeSH
- krevní proteiny metabolismus MeSH
- kyčelní protézy MeSH
- lidé MeSH
- polyethyleny chemie metabolismus MeSH
- pufry MeSH
- selhání protézy * MeSH
- testování materiálů MeSH
- vazba proteinů MeSH
- velikost částic MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- GUR 4150 HP polyethylene powder MeSH Prohlížeč
- krevní proteiny MeSH
- polyethyleny MeSH
- pufry MeSH
- ultra-high molecular weight polyethylene MeSH Prohlížeč
Binding of five human plasma proteins (IgG, serum albumin, α(1)-acid glycoprotein, holo-transferrin, α(1)-antitrypsin) to ultra high molecular weight polyethylene wear particles (0.1-10 μm) isolated from hip periprosthetic tissues was studied in vitro. All tested plasma proteins were bound to wear particles in a similar way indicating irreversible binding. Analogous interaction was found also between GUR 4120 particles (diameter ∼250 μm) and two tested plasma proteins (human serum albumin and α(1)-acid glycoprotein). The binding was not affected by pH of a buffer or the isoelectric point of bound proteins; thus it was apparently of clearly hydrophobic nature. We hypothesize that the binding causes some unfolding of the bound proteins, thus exposing new determinants with which sensitive cells may react. This could be a mechanism by which polyethylene wear particles trigger, for example, macrophages activity and thence initiate aseptic inflammation and cause the failure of total joint replacements. Results can contribute to the choice of a convenient construction type of prostheses.
Citace poskytuje Crossref.org