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人成骨细胞样细胞在体外对HLA II类决定簇的组成性和诱导性表达

Constitutive and inducible expression of HLA class II determinants by human osteoblast-like cells in vitro.

作者信息

Skjødt H, Hughes D E, Dobson P R, Russell R G

机构信息

Department of Medicine, Sundby Hospital, Copenhagen S, Denmark.

出版信息

J Clin Invest. 1990 May;85(5):1421-6. doi: 10.1172/JCI114586.

Abstract

Activated immune cells release cytokines which modulate the activity of bone cells in vitro. Expression of major histocompatibility complex (HLA in humans) class II determinants on bone surface cells may be important in local immune cell activation. In this study, expression of HLA-DR and DQ by cultured human bone cells (HBC) derived from normal trabecular bone surfaces was assessed by fluorescence-activated cell sorter (FACS) analysis and immunoperoxidase techniques using monoclonal antibodies. A subset of HBC (10-30%) expressed DR constitutively while 5-15% displayed DQ during long-term culture. HBC lacked a number of monocyte and lymphocyte markers. In addition, both DR+ and DR- HBC (FACS separated) produced osteocalcin stimulated by 1,25-dihydroxyvitamin D2 (1,25(OH)2D3). This suggests that both phenotypes belong to the osteoblast lineage. The number of DR+ HBC was increased by interferon-gamma (IFN gamma; 40-95% DR+ cells) whereas DQ+ HBC remained unchanged or was slightly increased (5-20% DQ+ cells). Moreover, 1,25(OH)2D3 enhanced IFN gamma-induced DR expression and at high concentration (10(-7) M) augmented DR expression by itself. Other major osteotropic factors, parathyroid hormone, interleukin 1, and calcitonin, did not affect HBC DR expression. The findings suggest that HBC may participate in activation of the immune system and that some osteotropic factors may regulate this function.

摘要

活化的免疫细胞释放细胞因子,这些细胞因子在体外调节骨细胞的活性。骨表面细胞上主要组织相容性复合体(人类为HLA)II类决定簇的表达可能在局部免疫细胞活化中起重要作用。在本研究中,使用单克隆抗体通过荧光激活细胞分选仪(FACS)分析和免疫过氧化物酶技术评估了源自正常小梁骨表面的培养人骨细胞(HBC)中HLA-DR和DQ的表达。一部分HBC(10%-30%)在长期培养过程中组成性表达DR,而5%-15%表达DQ。HBC缺乏多种单核细胞和淋巴细胞标志物。此外,DR+和DR- HBC(通过FACS分离)在1,25-二羟基维生素D2(1,25(OH)2D3)刺激下均产生骨钙素。这表明这两种表型均属于成骨细胞谱系。干扰素-γ(IFNγ;40%-95%的DR+细胞)可增加DR+ HBC的数量,而DQ+ HBC保持不变或略有增加(5%-20%的DQ+细胞)。此外,1,25(OH)2D3增强了IFNγ诱导的DR表达,并且在高浓度(10(-7) M)时自身可增强DR表达。其他主要的促骨因子,甲状旁腺激素、白细胞介素1和降钙素,均不影响HBC的DR表达。这些发现表明HBC可能参与免疫系统的激活,并且一些促骨因子可能调节这一功能。

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