In this study, an in vitro model has been developed to examine the int
eractions of macrophages with ultrahigh molecular-weight polyethylene
(UHMWPE) and high-density polyethylene (HDPE) particles. Polyethylene
particles are the major constituent of the material debris formed as a
result of orthopedic implant wear. However, the study of polyethylene
particle interactions with cells has been limited. UHMWPE (18-20 mu m
) and HDPE (4-10 mu m) were suspended in soluble collagen type I and s
ubsequently solidified on glass coverslips. The particle chemistry was
characterized by Fourier transform infra-red spectroscopy (FT-IR) and
X-ray photoelectron spectroscopy (XPS). Mouse cell line macrophages (
IC-21) were established on the collagen-particle substrata and maintai
ned for up to 24 h. The response of the cells to the particles was exa
mined by light and transmission electron microscopy (LM and TEM), as w
ell as by scanning electron microscopy (SEM), and compared to cells on
control collagen surfaces without particles. Histological analysis of
the samples revealed that the mac macrophages surrounded larger parti
cles (18-20 mu m) and the cells appeared to be attached to the surface
of the particles, and the smaller particles (4-10 mu m) had been phag
ocytosed within 2 h. Inflammatory cytokines (TNF-alpha, IL-1 alpha, IL
-1 beta, and IL-6), lysosomal enzymes (beta-galactosidase and hexosami
nidase), and prostaglandin E-2 were released into the medium, and IL-1
alpha, IL-1 beta, PGE(2), beta-galactosidase, and hexosaminidase leve
ls were significantly increased over collagen control values. The resu
lts demonstrate active phagochemotaxis by macrophages for wear particu
lates and validate this model as a means of studying the specific in v
itro interactions of polyethylene with cells. (C) 1998 John Wiley & So
ns, Inc.