INTERFERON-GAMMA REGULATION OF C3-GENE EXPRESSION IN HUMAN ASTROGLIOMA CELLS

被引:41
作者
BARNUM, SR
JONES, JL
BENVENISTE, EN
机构
[1] UNIV ALABAMA,DIV CLIN IMMUNOL & RHEUMATOL,BIRMINGHAM,AL 35294
[2] UNIV ALABAMA,DEPT CELL BIOL,BIRMINGHAM,AL 35294
关键词
ASTROCYTE; COMPLEMENT; INTERFERON-GAMMA; ASTROGLIOMA; C3-PROTEIN;
D O I
10.1016/0165-5728(92)90020-L
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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).
引用
收藏
页码:275 / 282
页数:8
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