Barnum S R, Jones J L, Benveniste E N
Department of Microbiology, University of Alabama, Birmingham 35294.
J Neuroimmunol. 1992 Jun;38(3):275-82. doi: 10.1016/0165-5728(92)90020-l.
In this report, we show that the human astroglioma cell line, D54-MG, constitutively expresses C3 mRNA and secretes antigenically detectable C3 protein. The cytokine interferon-gamma (IFN-gamma) enhances C3 mRNA and protein expression by D54-MG cells in a dose- and time-dependent manner. C3 mRNA from both D54-MG cells and primary human adult astrocytes has the same apparent size (5.1-5.2 kb) as C3 mRNA from hepatocyte and monocyte cell lines. Constitutive C3 mRNA levels in D54-MG cells and primary human astrocytes are comparable. Primary rat astrocytes also constitutively express C3 mRNA, which is enhanced upon exposure to IFN-gamma. These data are novel since expression of C3 in other cell types is refractory to IFN-gamma. In the central nervous system (CNS), endogenous complement production by astrocytes, and enhancement by the cytokine IFN-gamma, may contribute to the pathogenesis of inflammatory demyelinating diseases such as multiple sclerosis (MS).
在本报告中,我们表明人星形胶质瘤细胞系D54-MG组成性表达C3 mRNA并分泌可通过抗原检测的C3蛋白。细胞因子γ干扰素(IFN-γ)以剂量和时间依赖性方式增强D54-MG细胞的C3 mRNA和蛋白表达。来自D54-MG细胞和原代成人星形胶质细胞的C3 mRNA与来自肝细胞和单核细胞系的C3 mRNA具有相同的表观大小(5.1-5.2 kb)。D54-MG细胞和原代成人星形胶质细胞中的组成性C3 mRNA水平相当。原代大鼠星形胶质细胞也组成性表达C3 mRNA,暴露于IFN-γ后其表达增强。这些数据是新颖的,因为C3在其他细胞类型中的表达对IFN-γ不敏感。在中枢神经系统(CNS)中,星形胶质细胞产生内源性补体以及细胞因子IFN-γ的增强作用可能有助于诸如多发性硬化症(MS)等炎性脱髓鞘疾病的发病机制。