Titanium particles modulate expression of Toll-like receptor proteins

The role of Toll‐like receptors (TLRs) responding to microbial remnants, indolent biofilms or cellular byproducts in aseptic loosening of joint replacements is unknown. Thus, the effect of titanium (Ti) particles on TLR protein levels was evaluated. To create a model of particle‐induced inflammation...

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Veröffentlicht in:Journal of biomedical materials research. Part A 2010-03, Vol.92A (4), p.1528-1537
Hauptverfasser: Pajarinen, Jukka, Mackiewicz, Zygmunt, Pöllänen, Raimo, Takagi, Michiaki, Epstein, Noah J., Ma, Ting, Goodman, Stuart B., Konttinen, Yrjö T.
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container_end_page 1537
container_issue 4
container_start_page 1528
container_title Journal of biomedical materials research. Part A
container_volume 92A
creator Pajarinen, Jukka
Mackiewicz, Zygmunt
Pöllänen, Raimo
Takagi, Michiaki
Epstein, Noah J.
Ma, Ting
Goodman, Stuart B.
Konttinen, Yrjö T.
description The role of Toll‐like receptors (TLRs) responding to microbial remnants, indolent biofilms or cellular byproducts in aseptic loosening of joint replacements is unknown. Thus, the effect of titanium (Ti) particles on TLR protein levels was evaluated. To create a model of particle‐induced inflammation, an intramedullary stainless steel rod with and without Ti particles was bilaterally placed in the femora of 14 mice. The animals were sacrificed at 2 or 10 weeks postoperatively and paraffin‐embedded femur sections were evaluated for TLR1, 2, 4, 5, 8, and 9 proteins using immunohistochemistry. Decrease in the number of TLR immunoreactive cells was observed between weeks 2 and 10 in both settings. Furthermore, in the presence of Ti particles, the numbers of TLR immunoreactive cells were lower than in the presence of rod only at both time points, suggesting downregulation of TLR expression by Ti‐particles per se. Accordingly, in a short‐term 24 h stimulation, downregulation of TLR4 mRNA (p < 0.02) was observed in vitro in RAW 264.7 cells challenged with Ti particles. Results suggest that after an initial inflammatory stage, TLRs are downregulated in response to Ti particles, possibly to inhibit excessive inflammation, although TLR downregulation might at the same time render tissues more susceptible to pathogens. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res 2010
doi_str_mv 10.1002/jbm.a.32495
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Thus, the effect of titanium (Ti) particles on TLR protein levels was evaluated. To create a model of particle‐induced inflammation, an intramedullary stainless steel rod with and without Ti particles was bilaterally placed in the femora of 14 mice. The animals were sacrificed at 2 or 10 weeks postoperatively and paraffin‐embedded femur sections were evaluated for TLR1, 2, 4, 5, 8, and 9 proteins using immunohistochemistry. Decrease in the number of TLR immunoreactive cells was observed between weeks 2 and 10 in both settings. Furthermore, in the presence of Ti particles, the numbers of TLR immunoreactive cells were lower than in the presence of rod only at both time points, suggesting downregulation of TLR expression by Ti‐particles per se. Accordingly, in a short‐term 24 h stimulation, downregulation of TLR4 mRNA (p &lt; 0.02) was observed in vitro in RAW 264.7 cells challenged with Ti particles. 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Thus, the effect of titanium (Ti) particles on TLR protein levels was evaluated. To create a model of particle‐induced inflammation, an intramedullary stainless steel rod with and without Ti particles was bilaterally placed in the femora of 14 mice. The animals were sacrificed at 2 or 10 weeks postoperatively and paraffin‐embedded femur sections were evaluated for TLR1, 2, 4, 5, 8, and 9 proteins using immunohistochemistry. Decrease in the number of TLR immunoreactive cells was observed between weeks 2 and 10 in both settings. Furthermore, in the presence of Ti particles, the numbers of TLR immunoreactive cells were lower than in the presence of rod only at both time points, suggesting downregulation of TLR expression by Ti‐particles per se. Accordingly, in a short‐term 24 h stimulation, downregulation of TLR4 mRNA (p &lt; 0.02) was observed in vitro in RAW 264.7 cells challenged with Ti particles. Results suggest that after an initial inflammatory stage, TLRs are downregulated in response to Ti particles, possibly to inhibit excessive inflammation, although TLR downregulation might at the same time render tissues more susceptible to pathogens. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res 2010</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19425045</pmid><doi>10.1002/jbm.a.32495</doi><tpages>10</tpages></addata></record>
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subjects Animals
Biocompatibility
Biocompatible Materials - adverse effects
Biocompatible Materials - chemistry
Biological and medical sciences
bone
bone marrow
Bone Marrow Cells - physiology
Cell Line
Cellular
Female
Implants, Experimental
Inflammation - chemically induced
Inflammation - immunology
Macrophages - cytology
Macrophages - physiology
Male
Materials Testing
Medical sciences
Mice
Mice, Inbred C57BL
Microorganisms
Orthopedic surgery
Proteins
Receptors
Reproduction
Stainless Steel
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Surgical implants
Titanium
Titanium - immunology
toll-like receptors
Toll-Like Receptors - genetics
Toll-Like Receptors - metabolism
title Titanium particles modulate expression of Toll-like receptor proteins
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