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负鼠肾细胞中的α-肾上腺素能受体与血管紧张素原基因表达

Alpha-adrenoceptors and angiotensinogen gene expression in opossum kidney cells.

作者信息

Wang T T, Lachance S, Delalandre A, Carrière S, Chan J S

机构信息

University of Montreal, Maisonneuve-Rosemont Hospital, Research Center, Quebec, Canada.

出版信息

Kidney Int. 1995 Jul;48(1):139-45. doi: 10.1038/ki.1995.277.

Abstract

To investigate whether alpha (alpha)-adrenoceptor agonists have a stimulatory effect on the expression of the angiotensinogen (Ang) gene in opossum kidney (OK) cells, we used OK 27 cells with a fusion gene containing the 5'-flanking regulatory sequence of the rat angiotensinogen gene fused with a human growth hormone (hGH) gene as a reporter, pOGH (Ang N-1498/+18), permanently integrated into their genomes. The level of expression of the pOGH (Ang N-1498/+18) was quantitated by the amount of immunoreactive-human growth hormone (IR-hGH) secreted into the medium. The addition of iodoclonidine (alpha 2-adrenoceptor agonist, 10(-13) to 10(-9) M) and phorbol 12-myristate 13-acetate (PMA, 10(-13) to 10(-5) M) stimulated the expression of pOGH (Ang N-1498/+18) in a dose-dependent manner, whereas the addition of phenylephrine (alpha 1-adrenoceptor agonist, 10(-13) to 10(-5) M) had no effect. The stimulatory effect of iodoclonidine was blocked by the presence of yohimbine (alpha 2-adrenoceptor antagonist) and staurosporine (an inhibitor of protein kinase C) but not blocked by the presence of prazosin (alpha 1-adrenoceptor antagonist) or Rp-cAMP (an inhibitor of cAMP-dependent protein kinase A). The addition of iodoclonidine, phenylephrine or PMA had no effect on the expression of pTKGH in OK 13 cells, an OK cell line, into which had been stably integrated a fusion gene, pTKGH containing the promoter/enhancer DNA sequence of the viral thymidine-kinase (TK) gene fused with a human growth hormone gene as a reporter.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为研究α-肾上腺素能受体激动剂是否对负鼠肾(OK)细胞中血管紧张素原(Ang)基因的表达有刺激作用,我们使用了OK 27细胞,其基因组中永久整合了一个融合基因pOGH(Ang N-1498/+18),该融合基因包含大鼠血管紧张素原基因的5'侧翼调控序列与人生长激素(hGH)基因融合作为报告基因。通过分泌到培养基中的免疫反应性人生长激素(IR-hGH)的量来定量pOGH(Ang N-1498/+18)的表达水平。加入碘可乐定(α2-肾上腺素能受体激动剂,10^(-13)至10^(-9) M)和佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA,10^(-13)至10^(-5) M)以剂量依赖方式刺激pOGH(Ang N-1498/+18)的表达,而加入去氧肾上腺素(α1-肾上腺素能受体激动剂,10^(-13)至10^(-5) M)则无作用。碘可乐定的刺激作用可被育亨宾(α2-肾上腺素能受体拮抗剂)和星形孢菌素(蛋白激酶C抑制剂)阻断,但不被哌唑嗪(α1-肾上腺素能受体拮抗剂)或Rp-cAMP(cAMP依赖性蛋白激酶A抑制剂)阻断。加入碘可乐定、去氧肾上腺素或PMA对OK 13细胞中pTKGH的表达无影响,OK 13细胞是一种OK细胞系,其基因组中稳定整合了一个融合基因pTKGH,该融合基因包含病毒胸苷激酶(TK)基因的启动子/增强子DNA序列与人生长激素基因融合作为报告基因。(摘要截短于250字)

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