Ma G-F, Liljeström M, Ainola M, Chen T, Tiainen V-M, Lappalainen R, Konttinen Y T, Salo J
Department of Medicine/Invärtes Medicin, P.O. Box 700, FIN-00029 Helsinki University Central Hospital, Finland.
Rheumatology (Oxford). 2006 Jul;45(7):808-14. doi: 10.1093/rheumatology/kel003. Epub 2006 Jan 17.
To investigate the involvement of a disintegrin and the metalloproteinase ADAM9 (meltrin-gamma) in the formation of multinuclear giant cells and osteoclasts in aseptic loosening of hip replacement implants.
We used in situ hybridization, immunohistochemical staining and western blotting of interface membrane surrounding loosened hip implants, macrophage-colony stimulating factor (M-CSF) and receptor activator of nuclear factor kappaB ligand (RANKL) costimulation and polymethyl methacrylate (PMMA) particle stimulation of human monocytes followed by immunofluorescence staining and flow cytometric analysis.
Morphometric analysis revealed that the ADAM9+ area in the revision total hip replacement (THR) interface was larger than in primary THR samples (37.6+/-5.1 vs 5.2+/-0.8%, P=0.002). Double immunofluorescence staining showed that CD68+ interface tissue macrophages and multinuclear giant cells were ADAM9+. ADAM9 mRNA containing mononuclear and multinuclear cells was often seen in a close spatial relationship with other ADAM9+ cells. Western blotting disclosed a 50 kDa ADAM9 band in tissue extracts. Upon M-CSF and RANKL costimulation of human monocytes, the ADAM9 staining pattern changed over time and ADAM9+ cells formed bi- and multinuclear cells. Flow cytometry disclosed that cells of the monocyte/macrophage lineage changed from ADAM9-negative cells into strongly positive cells during a 3-day culture.
ADAM9 is expressed in interface tissues around aseptically loosened THR implants. ADAM9 may play a role as a fusion molecule in the formation of multinuclear giant cells and osteoclasts from mononuclear precursors in diseases characterized by bone tissue destruction.
研究去整合素和金属蛋白酶ADAM9(黑素瘤金属蛋白酶γ)在髋关节置换植入物无菌性松动过程中多核巨细胞和破骨细胞形成中的作用。
我们对松动的髋关节植入物周围的界面膜进行原位杂交、免疫组织化学染色和蛋白质印迹分析,用人单核细胞进行巨噬细胞集落刺激因子(M-CSF)和核因子κB受体活化因子配体(RANKL)共刺激以及聚甲基丙烯酸甲酯(PMMA)颗粒刺激,随后进行免疫荧光染色和流式细胞术分析。
形态计量分析显示,翻修全髋关节置换术(THR)界面中的ADAM9阳性区域大于初次THR样本(37.6±5.1%对5.2±0.8%,P=0.002)。双重免疫荧光染色显示,CD68阳性的界面组织巨噬细胞和多核巨细胞为ADAM9阳性。常可见含ADAM9 mRNA的单核和多核细胞与其他ADAM9阳性细胞在空间上紧密相关。蛋白质印迹分析在组织提取物中发现一条50 kDa 的ADAM9条带。在人单核细胞接受M-CSF和RANKL共刺激后,ADAM9染色模式随时间变化,ADAM9阳性细胞形成双核和多核细胞。流式细胞术显示,在3天培养过程中,单核细胞/巨噬细胞系细胞从ADAM9阴性细胞转变为强阳性细胞。
ADAM9在无菌性松动的THR植入物周围的界面组织中表达。在以骨组织破坏为特征的疾病中,ADAM9可能作为融合分子在单核前体细胞形成多核巨细胞和破骨细胞的过程中发挥作用。