Lipoteichoic acid modulates inflammatory response in macrophages after phagocytosis of titanium particles through Toll-like receptor 2 cascade and inflammasomes
Toll‐like receptor 2 (TLR2) and nucleotide‐binding and oligomerization domain‐like receptors with a pyrin domain 3 (NLRP3) inflammasomes have been presumed to participate in the pathogenesis of aseptic implant loosening. The aim of this study is to analyze the cellular localization of TLR2 and NLRP3...
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Veröffentlicht in: | Journal of biomedical materials research. Part A 2016-02, Vol.104 (2), p.435-444 |
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Sprache: | eng |
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Zusammenfassung: | Toll‐like receptor 2 (TLR2) and nucleotide‐binding and oligomerization domain‐like receptors with a pyrin domain 3 (NLRP3) inflammasomes have been presumed to participate in the pathogenesis of aseptic implant loosening. The aim of this study is to analyze the cellular localization of TLR2 and NLRP3 inflammasomes in the periprosthetic tissue from aseptically loose hip implants as well as the expression of these molecules in macrophages stimulated in vitro with titanium particles (Ti) coated with lipoteichoic acid (LTA). Using immunohistochemistry, immunoreactivity of TLR2 and NLRP3 inflammasomes was found in macrophages within the foreign body granulomatosis. Using RAW264.7 cells, stimulation with Ti increased the messenger RNA (mRNA) levels of TLR2 and TNF‐α. Stimulation with LTA‐coated Ti enhanced mRNA levels of NLRP3 and IL‐1β, whereas reinforced secretion of IL‐1β was not detected in spite of marked release of TNF‐α. Finally, the same cells with silenced Irak2, an adaptor protein in the TLR2 cascade, suppressed this NLRP3 upregulation. This study suggests that TLR2 and NLRP3 inflammasomes are factors involved in cross‐talk mediating the foreign body type response to wear particles. In addition, discrepant behavior in the release between TNF‐α and IL‐1β release may explain the variable pathomechanisms of aseptic implant loosening without acute inflammatory reactions. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 435–444, 2016. |
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ISSN: | 1549-3296 1552-4965 |
DOI: | 10.1002/jbm.a.35581 |