Späth G F, Ramadori G, Rittner C, Schneider P M
Institute of Legal Medicine, Johannes Gutenberg University, Mainz, Germany.
Exp Clin Immunogenet. 1995;12(1):53-60.
The three chains of the human complement component C8-alpha, beta and gamma- are encoded by distinct structural genes. C8A and C8B are closely linked on chromosome 1p and C8G is located on chromosome 9q. The biosynthesis and regulation of the gene products were studied in the human hepatoma-derived cell line HepG2 after in vitro induction of the acute-phase response by incubation with the cytokine interleukin IL-6. Analysis of C8 expression by immunoprecipitation and SDS-PAGE of biosynthetically labeled alpha-gamma and beta subunits demonstrated a positive response to this cytokine. The expression pattern observed in the hepatoma cells characterizes C8 in vitro as a positive acute-phase protein. In addition, the comparison of the relative amounts of the C8 transcripts provides evidence for a post transcriptional regulation of the C8 beta subunit. No evidence was obtained for an increased expression of IL-6 or IL-6 receptor mRNA thus excluding autoregulatory mechanisms of the cytokine in HepG2 cells.
人类补体成分C8的三条链——α链、β链和γ链——由不同的结构基因编码。C8A和C8B在1号染色体短臂上紧密连锁,C8G位于9号染色体长臂上。在用细胞因子白细胞介素IL-6体外诱导急性期反应后,在源自人肝癌的细胞系HepG2中研究了这些基因产物的生物合成和调控。通过对生物合成标记的α-γ和β亚基进行免疫沉淀和SDS-PAGE分析C8表达,结果表明对这种细胞因子有阳性反应。在肝癌细胞中观察到的表达模式将体外的C8表征为一种阳性急性期蛋白。此外,对C8转录本相对量的比较为C8β亚基的转录后调控提供了证据。未获得IL-6或IL-6受体mRNA表达增加的证据,因此排除了HepG2细胞中细胞因子的自调控机制。