Nord M, Cassel T N, Braun H, Suske G
Department of Medical Nutrition, Karolinska Institute, NOVUM, Huddinge University Hospital, SE-141 86 Huddinge, Sweden.
Ann N Y Acad Sci. 2000;923:154-65. doi: 10.1111/j.1749-6632.2000.tb05527.x.
Clara cell secretory protein/uteroglobin (CCSP/UG) is specifically expressed in the conducting airway epithelium of the lung in a differentiation-dependent manner. The proximal promoter region of the rodent CCSP/UG gene directs Clara cell specificity. Previously, it was shown that the forkhead transcription factors HNF-3 alpha and beta and the homeodomain factor TTF-1 are important transcription factors acting through this region, suggesting that they contribute to cell specificity of the CCSP/UG gene. Members of the C/EBP family of transcription factors can also interact with elements of the proximal rat and mouse CCSP/UG promoters. The onset of C/EBP alpha expression in Clara cells correlates with the strong increase of CCSP/UG expression. Thus, C/EBP alpha may play a crucial role for differentiation-dependent CCSP/UG expression. Transfection studies demonstrate that C/EBP alpha and TTF-1 can synergistically activate the murine CCSP/UG promoter. Altogether, these results suggest that C/EBP alpha, TTF-1, and HNF-3 determine the Clara cell-specific, differentiation-dependent expression of the CCSP/UG gene in murine lung. The relative importance of these three transcription factors, however, differs in rabbits and humans.
克拉拉细胞分泌蛋白/子宫珠蛋白(CCSP/UG)以分化依赖的方式在肺的传导气道上皮中特异性表达。啮齿动物CCSP/UG基因的近端启动子区域决定了克拉拉细胞特异性。此前研究表明,叉头转录因子HNF-3α和β以及同源结构域因子TTF-1是通过该区域起作用的重要转录因子,这表明它们有助于CCSP/UG基因的细胞特异性。转录因子C/EBP家族的成员也可与大鼠和小鼠CCSP/UG近端启动子元件相互作用。克拉拉细胞中C/EBPα表达的起始与CCSP/UG表达的显著增加相关。因此,C/EBPα可能在分化依赖的CCSP/UG表达中起关键作用。转染研究表明,C/EBPα和TTF-1可协同激活小鼠CCSP/UG启动子。总之,这些结果表明,C/EBPα、TTF-1和HNF-3决定了小鼠肺中CCSP/UG基因的克拉拉细胞特异性、分化依赖的表达。然而,这三种转录因子的相对重要性在兔和人中有所不同。