Literature DB >> 17236833

Comparison of the roles of IL-1, IL-6, and TNFalpha in cell culture and murine models of aseptic loosening.

Naoya Taki1, Joscelyn M Tatro, Robert Lowe, Victor M Goldberg, Edward M Greenfield.   

Abstract

Pro-inflammatory cytokines, such as IL-1, IL-6, and TNF, are considered to be major mediators of osteolysis and ultimately aseptic loosening. This study demonstrated that synergistic interactions among these cytokines are required for the in vitro stimulation of osteoclast differentiation by titanium particles. In contrast, genetic knock out of these cytokines or their receptors does not protect murine calvaria from osteolysis induced by titanium particles. Thus, the extent of osteolysis was not substantially altered in single knock out mice lacking either the IL-1 receptor or IL-6. Osteolysis also was not substantially altered in double knock out mice lacking both the IL-1 receptor and IL-6 or in double knock out mice lacking both TNF receptor-1 and TNF receptor-2. The differences between the in vivo and the cell culture results make it difficult to conclude whether the pro-inflammatory cytokines contribute to aseptic loosening. One alternative is that in vivo experiments are more physiological and that therefore the current results do not support a role for the pro-inflammatory cytokines in aseptic loosening. We however favor the alternative that, in this case, the cell culture experiments can be more informative. We favor this alternative because the role of the pro-inflammatory cytokines may be obscured in vivo by compensation by other cytokines or by the low signal to noise ratio found in measurements of particle-induced osteolysis.

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Year:  2006        PMID: 17236833      PMCID: PMC1930165          DOI: 10.1016/j.bone.2006.12.053

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  45 in total

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3.  Efficacy of etanercept for wear debris-induced osteolysis.

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4.  Effect of anti-tumor necrosis factor-alpha gene therapy on wear debris-induced osteolysis.

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5.  Titanium particles stimulate bone resorption by inducing differentiation of murine osteoclasts.

Authors:  Y Bi; R R Van De Motter; A A Ragab; V M Goldberg; J M Anderson; E M Greenfield
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Review 8.  Proposed standard nomenclature for new tumor necrosis factor members involved in the regulation of bone resorption. The American Society for Bone and Mineral Research President's Committee on Nomenclature.

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9.  The effect of particle wear debris on NFkappaB activation and pro-inflammatory cytokine release in differentiated THP-1 cells.

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  18 in total

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2.  Wear Particle-induced Priming of the NLRP3 Inflammasome Depends on Adherent Pathogen-associated Molecular Patterns and Their Cognate Toll-like Receptors: An In Vitro Study.

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3.  Tumor necrosis factor alpha and interleukin-6 facilitate corneal lymphangiogenesis in response to herpes simplex virus 1 infection.

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4.  PI3Kγ deletion reduces variability in the in vivo osteolytic response induced by orthopaedic wear particles.

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5.  Co-Cr-Mo alloy particles induce tumor necrosis factor alpha production in MLO-Y4 osteocytes: a role for osteocytes in particle-induced inflammation.

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6.  Direct subcutaneous injection of polyethylene particles over the murine calvaria results in dramatic osteolysis.

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7.  Stimulation of macrophage TNFalpha production by orthopaedic wear particles requires activation of the ERK1/2/Egr-1 and NF-kappaB pathways but is independent of p38 and JNK.

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9.  Lysosomal disruption by orthopedic wear particles induces activation of the NLRP3 inflammasome and macrophage cell death by distinct mechanisms.

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10.  Oestrogen deficiency modulates particle-induced osteolysis.

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