Ishikawa Tomo-O, Jain Naveen, Herschman Harvey R
Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, UCLA, 341 Boyer Hall, 611 Charles E. Young Drive East, Los Angeles, CA 90095, USA.
Biochem Biophys Res Commun. 2009 Jan 16;378(3):534-8. doi: 10.1016/j.bbrc.2008.11.099. Epub 2008 Dec 4.
Cyclooxygenase-2 (COX-2) is a rate-limiting enzyme for prostaglandin biosynthesis. Its inducible expression is regulated by complex pathways. To monitor Cox-2 transcriptional activity in vivo, we generated a knock-in mouse expressing a firefly luciferase reporter. In this study we examined, by comparing luciferase activity of Cox-2(luc/+) and Cox-2(luc/-) cells and mice, effects of prostanoid products on Cox-2 promoter transcriptional activation. In peritoneal macrophages, luciferase induction by LPS in Cox-2(luc/-) cells was less than that of Cox-2(luc/+) cells. However, in the presence of PGE(2), induction was comparable, suggesting positive Cox-2 feedback regulation by PGE(2) occurs for macrophages. In contrast, feedback modulation was not observed in TPA-induced Cox-2(luc/+) and Cox-2(luc/-) mouse embryonic fibroblasts (MEFs). Using non-invasive in vivo imaging, we observed negative feedback regulation of Cox-2 expression during paw inflammation in living mice. Our results suggest Cox-2 expression is regulated by cell type specific feedback mechanisms, both in cultured cells and in living animals.
环氧化酶-2(COX-2)是前列腺素生物合成的限速酶。其诱导性表达受复杂途径调控。为了在体内监测Cox-2的转录活性,我们构建了一种表达萤火虫荧光素酶报告基因的基因敲入小鼠。在本研究中,我们通过比较Cox-2(luc/+)和Cox-2(luc/-)细胞及小鼠的荧光素酶活性,研究了前列腺素产物对Cox-2启动子转录激活的影响。在腹腔巨噬细胞中,LPS诱导Cox-2(luc/-)细胞产生的荧光素酶低于Cox-2(luc/+)细胞。然而,在PGE(2)存在的情况下,诱导情况相当,这表明巨噬细胞中存在PGE(2)对Cox-2的正反馈调节。相反,在佛波酯(TPA)诱导的Cox-2(luc/+)和Cox-2(luc/-)小鼠胚胎成纤维细胞(MEF)中未观察到反馈调节。通过非侵入性体内成像,我们观察到在活体小鼠爪部炎症期间Cox-2表达的负反馈调节。我们的结果表明,在培养细胞和活体动物中,Cox-2的表达受细胞类型特异性反馈机制的调节。