Mackman N, Sawdey M S, Keeton M R, Loskutoff D J
Department of Immunology, Scripps Research Institute, La Jolla, California 92037.
Am J Pathol. 1993 Jul;143(1):76-84.
Regulation of tissue factor (TF) gene expression was studied in vivo employing a murine model system. In untreated mice, TF mRNA was detected in brain, lung, kidney, and heart by Northern blot analysis. After administration of lipopolysaccharide, steady-state levels of TF mRNA were unchanged in brain, decreased in heart, and increased in both kidney and lung. In the brain, Bergmann glia within the Purkinje cell layer of the cerebellum and neuroglia within the cerebral cortex expressed TF mRNA by in situ hybridization. Epidermal cells of the skin and tongue also expressed TF mRNA. At present, we have not identified the cell type(s) in the kidney and lung responsible for increased TF gene expression. These results demonstrate tissue- and cell-specific TF gene expression in vivo. Lipopolysaccharide-mediated increases in TF expression in the kidney and lung may promote fibrin deposition in these organs during Gram-negative sepsis.
利用小鼠模型系统在体内研究了组织因子(TF)基因表达的调控。在未处理的小鼠中,通过Northern印迹分析在脑、肺、肾和心脏中检测到TF mRNA。给予脂多糖后,脑内TF mRNA的稳态水平未改变,心脏中降低,而肾和肺中均升高。在脑中,小脑浦肯野细胞层内的伯格曼胶质细胞和大脑皮层内的神经胶质细胞通过原位杂交表达TF mRNA。皮肤和舌的表皮细胞也表达TF mRNA。目前,我们尚未确定肾和肺中负责TF基因表达增加的细胞类型。这些结果证明了体内组织和细胞特异性的TF基因表达。脂多糖介导的肾和肺中TF表达增加可能在革兰氏阴性菌败血症期间促进这些器官中的纤维蛋白沉积。