TY - JOUR
T1 - Titanium and zirconia particle-induced pro-inflammatory gene expression in cultured macrophages and osteolysis, inflammatory hyperalgesia and edema in vivo
AU - Obando-Pereda, G. A.
AU - Fischer, L.
AU - Stach-Machado, D. R.
N1 - Funding Information:
This study was supported by Grants 07/58796-4 and 07/56731-2 from the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) . L.F. is a recipient of a fellowship from the Fundação Araucária, Governo do Estado do Paraná, Brazil .
PY - 2014/3/3
Y1 - 2014/3/3
N2 - Aims The biological reaction to wear debris is critical to the osteolysis underlying aseptic loosening of joint prosthetic implants. In an attempt to reduce aseptic loosening, ceramics have been introduced. This study was designed to evaluate, compare and correlate the expression of Toll-like receptors (TLRs), their intracellular adaptors and proinflammatory cytokines in cultured macrophages challenged with titanium or zirconia particles, as well as particle-induced osteolysis in calvaria and hyperalgesia and edema in hind paw. Main methods TLRs and their adaptors were evaluated at the mRNA level by RT-PCR, and cytokine expression was evaluated at the mRNA and protein levels. Osteolysis and hyperalgesia and edema were evaluated in vivo, in calvaria and hind paw, respectively. Key findings Cultured macrophages challenged with zirconia or titanium particles expressed increased mRNA for TLRs 2, 3, 4 and 9, and their adaptors MyD88, TRIF and NF-κB and cytokines TNF-α, IL-1β and IL-6, which were also increased at protein level. Quantitative differences are evident and, in general, zirconia particle-induced pro-inflammatory gene expression was lower than that induced by titanium particles. In in vivo experiments, exposition to titanium or zirconia particles induced osteolysis in calvaria and hyperalgesia and edema in hind paw; however those induced by zirconia particles were significantly lower. There is a strong and positive correlation between the expressions of mRNA for TLR4, NF-κB, TNF-α, IL-1β and IL-6. Significance Collectively, our data suggest that zirconia ceramic particles are less bioactive than titanium particles.
AB - Aims The biological reaction to wear debris is critical to the osteolysis underlying aseptic loosening of joint prosthetic implants. In an attempt to reduce aseptic loosening, ceramics have been introduced. This study was designed to evaluate, compare and correlate the expression of Toll-like receptors (TLRs), their intracellular adaptors and proinflammatory cytokines in cultured macrophages challenged with titanium or zirconia particles, as well as particle-induced osteolysis in calvaria and hyperalgesia and edema in hind paw. Main methods TLRs and their adaptors were evaluated at the mRNA level by RT-PCR, and cytokine expression was evaluated at the mRNA and protein levels. Osteolysis and hyperalgesia and edema were evaluated in vivo, in calvaria and hind paw, respectively. Key findings Cultured macrophages challenged with zirconia or titanium particles expressed increased mRNA for TLRs 2, 3, 4 and 9, and their adaptors MyD88, TRIF and NF-κB and cytokines TNF-α, IL-1β and IL-6, which were also increased at protein level. Quantitative differences are evident and, in general, zirconia particle-induced pro-inflammatory gene expression was lower than that induced by titanium particles. In in vivo experiments, exposition to titanium or zirconia particles induced osteolysis in calvaria and hyperalgesia and edema in hind paw; however those induced by zirconia particles were significantly lower. There is a strong and positive correlation between the expressions of mRNA for TLR4, NF-κB, TNF-α, IL-1β and IL-6. Significance Collectively, our data suggest that zirconia ceramic particles are less bioactive than titanium particles.
KW - Aseptic loosening
KW - Cytokines
KW - Macrophage
KW - Osteolysis
KW - Titanium particles
KW - Toll-like receptors
KW - Zirconia particles
UR - http://www.scopus.com/inward/record.url?scp=84894034269&partnerID=8YFLogxK
U2 - 10.1016/j.lfs.2013.11.008
DO - 10.1016/j.lfs.2013.11.008
M3 - Article
C2 - 24252315
AN - SCOPUS:84894034269
SN - 0024-3205
VL - 97
SP - 96
EP - 106
JO - Life Sciences
JF - Life Sciences
IS - 2
ER -