Brar A K, Kanda Y, Kessler C A, Cedars M I, Handwerger S
Children's Hospital Medical Center, and Department of Obstetrics & Gynecology, University of Cincinnati, Ohio 45229-3039, USA.
In Vitro Cell Dev Biol Anim. 1999 Mar;35(3):150-4. doi: 10.1007/s11626-999-0017-5.
Prolactin gene expression in extrapituitary tissues, such as decidua and lymphocytes, is regulated by a distinct promoter approximately 6 kb upstream of the pituitary prolactin gene transcription start site. Here we describe studies in a human endometrial stromal cell line, N5, that was immortalized by transfection with an SV40 mutant and which expresses the prolactin gene driven by the extrapituitary promoter. The N5 cells have phenotypic features of primary cultures of decidualized human endometrial stromal cells and secrete low levels of prolactin and insulin-like growth factor binding protein-1 (IGFBP-1), both of which are markers of decidualized endometrial stromal cells. As in primary cultures of endometrial stromal cells, treatment of N5 cells with progesterone and estradiol alone or in combination with prostaglandin E2 stimulated the synthesis and release of prolactin. Transient transfection of the N5 cells with an expression vector containing - 2927/ + 66 bp of the decidual prolactin promoter coupled to a luciferase reporter gene resulted in a 20 to 25-fold increase in luciferase activity, a magnitude similar to that which occurs in primary cultures of endometrial stromal cells decidualized in vitro by treatment with progesterone and estradiol. Luciferase expression levels were similar in untreated N5 cells and N5 cells treated with progesterone and estradiol. Taken together, these results indicate that the N5 human endometrial stromal cell line has phenotypic characteristics of normal decidualized stromal cells and is a useful model to study regulation of decidual prolactin gene expression.
催乳素基因在垂体外组织(如蜕膜和淋巴细胞)中的表达,受一个位于垂体催乳素基因转录起始位点上游约6 kb处的独特启动子调控。在此,我们描述了对人子宫内膜基质细胞系N5的研究,该细胞系通过转染SV40突变体而永生化,并且表达由垂体外启动子驱动的催乳素基因。N5细胞具有人蜕膜化子宫内膜基质细胞原代培养物的表型特征,分泌低水平的催乳素和胰岛素样生长因子结合蛋白-1(IGFBP-1),这两者都是蜕膜化子宫内膜基质细胞的标志物。与子宫内膜基质细胞原代培养物一样,单独用孕酮和雌二醇或与前列腺素E2联合处理N5细胞,可刺激催乳素的合成与释放。用含有蜕膜催乳素启动子的-2927 / + 66 bp并与荧光素酶报告基因偶联的表达载体对N5细胞进行瞬时转染,导致荧光素酶活性增加20至25倍,其幅度与经孕酮和雌二醇体外处理蜕膜化的子宫内膜基质细胞原代培养物中发生的幅度相似。在未处理的N5细胞和经孕酮和雌二醇处理的N5细胞中,荧光素酶表达水平相似。综上所述,这些结果表明N5人子宫内膜基质细胞系具有正常蜕膜化基质细胞的表型特征,是研究蜕膜催乳素基因表达调控的有用模型。