Zhang Xiongfei, Zhang Jingjing, Yang Xiaomin, Han Xiao
Key Laboratory of Human Functional Genomics of Jiangsu Province, Nanjing, PR China.
Mol Biol Rep. 2007 Sep;34(3):199-206. doi: 10.1007/s11033-007-9085-3. Epub 2007 May 16.
Cyclooxygenase-2 (COX-2) expression is associated with many aspects of physiological and pathological conditions, including pancreatic beta-cell dysfunction. Prostaglandin E2 (PGE2) production, as a consequence of COX-2 gene induction, has been reported to impair beta-cell function. The molecular mechanisms involved in the regulation of COX-2 gene expression are not fully understood. In this report, we used pancreatic beta-cells (RINm5F) to explore the potential transcription factors regulating COX-2 promoter activity. Using promoter screening method, we selected several transcription factors in our study. Through luciferase reporter studies, we found that these factors can regulate COX-2 promoter activity in RINm5F cells. Among these factors, cyclic AMP response-element binding protein (CREB), Ets family members Ets-1 and Elk-1 can positively regulate COX-2 promoter activity. On the contrary, signal transducer and activator of transcription 1 (STAT1) plays a negative role on COX-2 promoter. Our findings will be helpful for better understanding the transcriptional regulation of COX-2 in pancreatic beta-cells. Moreover, these transcriptional regulators of COX-2 expression will be potential targets for the prevention of beta-cell damage mediated by PGE2.
环氧化酶-2(COX-2)的表达与生理和病理状况的许多方面相关,包括胰腺β细胞功能障碍。据报道,COX-2基因诱导产生的前列腺素E2(PGE2)会损害β细胞功能。COX-2基因表达调控所涉及的分子机制尚未完全阐明。在本报告中,我们使用胰腺β细胞(RINm5F)来探索调节COX-2启动子活性的潜在转录因子。通过启动子筛选方法,我们在研究中选择了几种转录因子。通过荧光素酶报告基因研究,我们发现这些因子可以调节RINm5F细胞中COX-2启动子的活性。在这些因子中,环磷酸腺苷反应元件结合蛋白(CREB)、Ets家族成员Ets-1和Elk-1可以正向调节COX-2启动子活性。相反,信号转导子和转录激活子1(STAT1)对COX-2启动子起负向作用。我们的研究结果将有助于更好地理解胰腺β细胞中COX-2的转录调控。此外,这些COX-2表达的转录调节因子将成为预防PGE2介导的β细胞损伤的潜在靶点。