Division of Biology, Office of Science and Engineering Laboratories (OSEL), Center for Devices and Radiological Health (CDRH), Food and Drug Administration (FDA), USA.
Cell Immunol. 2013 Mar;282(1):53-65. doi: 10.1016/j.cellimm.2013.04.003. Epub 2013 Apr 24.
Metal orthopedic implant debris-induced osteolysis of hip bone is a major problem in patients with prosthetic-hips. Although macrophages are the principal targets for implant-wear debris, the receptor(s) and mechanisms underlying these responses are not fully elucidated. We examined whether the TLR4 pathway mediates immune response to metal-on-metal (MoM) implant-generated wear particles. Human monocytes (THP-1) were exposed to Co-alloy particles at increasing particle:cell ratio for 24 h. Challenge with particles caused up-regulation of IL-1β, TNF-α and IL-8, and mediated degradation of cytosolic I-κB and nuclear translocation of NF-κB. Blocking antibodies against TLR4 or gene silencing of MyD88 and IRAK-1 prevented particle-induced I-κB/NF-κB activation response and markedly inhibited IL-8 release. Particle-mediated IL-8 response was not observed in TLR4-negative HEK293T cells; whereas transfection-based TLR4-overexpression in HEK293T enabled particle-sensitivity, as observed by I-κB degradation and IL-8 expression in response to particles. Results demonstrate that Co-alloy particles trigger immune response via the TLR4-MyD88-dependent signaling pathway.
金属骨科植入物磨损颗粒诱导的髋骨骨溶解是人工髋关节患者的主要问题。虽然巨噬细胞是植入物磨损碎片的主要靶标,但这些反应的受体(和机制)尚未完全阐明。我们研究了 TLR4 途径是否介导对金属对金属(MoM)植入物产生的磨损颗粒的免疫反应。将人单核细胞(THP-1)在 24 小时内暴露于 Co 合金颗粒,增加颗粒:细胞的比例。颗粒的挑战导致 IL-1β、TNF-α 和 IL-8 的上调,并介导细胞溶质 I-κB 的降解和 NF-κB 的核易位。针对 TLR4 的阻断抗体或 MyD88 和 IRAK-1 的基因沉默可防止颗粒诱导的 I-κB/NF-κB 激活反应,并显著抑制 IL-8 的释放。在 TLR4 阴性的 HEK293T 细胞中未观察到颗粒介导的 IL-8 反应;而基于转染的 TLR4 过表达使 HEK293T 对颗粒敏感,如颗粒诱导的 I-κB 降解和 IL-8 表达所示。结果表明,Co 合金颗粒通过 TLR4-MyD88 依赖性信号通路触发免疫反应。