Arakawa T, Laneuville O, Miller C A, Lakkides K M, Wingerd B A, DeWitt D L, Smith W L
Department of Biochemistry, Michigan State University, East Lansing, Michigan 48824, USA.
J Biol Chem. 1996 Nov 22;271(47):29569-75. doi: 10.1074/jbc.271.47.29569.
Prostaglandin endoperoxide H synthase-1 (PGHS-1) is expressed constitutively in murine NIH 3T3 cells and RAW 264.7 cells. PGHS-2 is inducibly expressed in these cells following stimulation with serum or bacterial lipopolysaccharide (LPS), respectively. Reverse transcription-polymerase chain reaction (RT-PCR) analysis established that a variety of G protein-linked and peroxisomal proliferator-activated prostanoid receptors are expressed in both of these cell types. The levels of the EP2 and EP4 prostaglandin E2 (PGE2) receptors and the prostaglandin I2 receptor were changed in these cells by serum or LPS stimulation. Quantitative RT-PCR indicated that the mRNA for the murine EP4 receptor, the butaprost-insensitive PGE2 receptor that couples to Gs, increases 1.5-3-fold in response to serum (NIH 3T3) or LPS (RAW 264.7) with a time course approximating the induction of PGHS-2 expression. To study expression of the EP4 receptor we isolated the mouse EP4 receptor gene; the gene is 10 kilobase pairs (kb) in length and, like other known prostanoid receptor genes, contains three exons and two introns. The first intron is 0.5 kb and is located 16 base pairs (bp) downstream of the translational start site. This is a different location than that of the first introns of other prostanoid receptor genes. The second intron is located immediately following the sixth transmembrane domain at the same position as the second intron of the thromboxane A2 receptor, prostaglandin D2 receptor, prostaglandin I2 receptor, and one of the PGE2 (EP1) receptor genes. A major transcriptional start was detected at -142 bp upstream of the translational start. There are a variety of putative cis-acting elements within 1.5 kb upstream of the translational start site and within the first intron. Promoter analyses of the EP4 receptor gene promoter in RAW 264.7 cells indicated that there is a constitutive negative regulatory region between -992 and -928 bp, a constitutive positive region between -928 and -554 bp, and an LPS/serum-responsive region between -554 and -116 bp.
前列腺素内过氧化物H合酶-1(PGHS-1)在小鼠NIH 3T3细胞和RAW 264.7细胞中组成性表达。PGHS-2分别在血清或细菌脂多糖(LPS)刺激后在这些细胞中诱导表达。逆转录-聚合酶链反应(RT-PCR)分析表明,多种G蛋白偶联和过氧化物酶体增殖物激活的前列腺素受体在这两种细胞类型中均有表达。血清或LPS刺激可改变这些细胞中EP2和EP4前列腺素E2(PGE2)受体以及前列腺素I2受体的水平。定量RT-PCR表明,小鼠EP4受体(与Gs偶联的布他前列素不敏感的PGE2受体)的mRNA在血清(NIH 3T3)或LPS(RAW 264.7)刺激下增加1.5至3倍,其时间进程与PGHS-2表达的诱导相似。为了研究EP4受体的表达,我们分离了小鼠EP4受体基因;该基因长度为10千碱基对(kb),与其他已知的前列腺素受体基因一样,包含三个外显子和两个内含子。第一个内含子为0.5 kb,位于翻译起始位点下游16个碱基对(bp)处。这与其他前列腺素受体基因第一个内含子的位置不同。第二个内含子紧接在第六个跨膜结构域之后,与血栓素A2受体、前列腺素D2受体、前列腺素I2受体以及PGE2(EP1)受体基因之一的第二个内含子位于相同位置。在翻译起始位点上游-142 bp处检测到一个主要转录起始点。在翻译起始位点上游1.5 kb内和第一个内含子内存在多种假定的顺式作用元件。对RAW 264.7细胞中EP4受体基因启动子的分析表明,在-992至-928 bp之间存在一个组成性负调控区域,在-928至-554 bp之间存在一个组成性正调控区域,在-554至-116 bp之间存在一个LPS/血清反应区域。