Steel D M, Donoghue F C, O'Neill R M, Uhlar C M, Whitehead A S
Department of Genetics, Trinity College, University of Dublin, Ireland.
Scand J Immunol. 1996 Nov;44(5):493-500. doi: 10.1046/j.1365-3083.1996.d01-341.x.
'Acute phase' and 'constitutive' SAA (A-SAA and C-SAA, respectively) mRNA levels were measured in hepatic and non-hepatic cell lines after treatment with monocyte conditioned medium (MoCM), with or without dexamethasone (Dex). A-SAA mRNAs were detected in MoCM-treated hepatoma cell lines (PLC/PRF/5, HuH7, HepG2, and Hep3B), a fibroblast cell line (MRC5), six epithelial cell lines (RT4/ 31, SW13, Hela Ohio, HCT-8, CaCo2, and KB), and an endothelial cell line ECV304. In KB cells, Dex alone caused a dramatic increase in A-SAA mRNA levels. C-SAA was detected in all hepatic and non-hepatic cell lines. Two differentially regulated size classes of C-SAA mRNA were detected in the hepatoma cell lines. A-SAA mRNA levels were measured in ECV304 cells treated with IL-1 beta, IL-6, TNF alpha and Dex, in various combinations, and revealed different profiles to those seen for hepatic cells. The extent of polyadenylation of A-SAA mRNA in ECV304 and KB cells differed whereas the polyadenylation of C-SAA mRNA remained constant. These data suggest that the parameters that determine the steady state mRNA levels and post-transcriptional regulation of A-SAA and C-SAA mRNAs are different and are cell type specific.
在用单核细胞条件培养基(MoCM)处理后,无论有无地塞米松(Dex),均测定了肝细胞系和非肝细胞系中“急性期”和“组成型”血清淀粉样蛋白A(分别为A-SAA和C-SAA)的mRNA水平。在经MoCM处理的肝癌细胞系(PLC/PRF/5、HuH7、HepG2和Hep3B)、成纤维细胞系(MRC5)、六种上皮细胞系(RT4/31、SW13、俄亥俄Hela、HCT-8、CaCo2和KB)以及内皮细胞系ECV304中检测到A-SAA mRNA。在KB细胞中,单独使用地塞米松会导致A-SAA mRNA水平显著升高。在所有肝细胞系和非肝细胞系中均检测到C-SAA。在肝癌细胞系中检测到两种受不同调控的C-SAA mRNA大小类别。用白细胞介素-1β、白细胞介素-6、肿瘤坏死因子-α和地塞米松以各种组合处理ECV304细胞后,测定了A-SAA mRNA水平,结果显示其与肝细胞中的情况不同。ECV304细胞和KB细胞中A-SAA mRNA的多聚腺苷酸化程度不同,而C-SAA mRNA的多聚腺苷酸化保持不变。这些数据表明,决定A-SAA和C-SAA mRNA稳态水平和转录后调控的参数不同,且具有细胞类型特异性。