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免疫抑制剂FK506和环孢素A对内皮素-1的差异性转录调控

Differential transcriptional regulation of endothelin-1 by immunosuppressants FK506 and cyclosporin A.

作者信息

Marsen T A, Weber F, Egink G, Suckau G, Baldamus C A

机构信息

Klinik IV für Innere Medizin, University of Cologne, Germany.

出版信息

Fundam Clin Pharmacol. 2000 Jul-Aug;14(4):401-8. doi: 10.1111/j.1472-8206.2000.tb00422.x.

Abstract

Calcineurin antagonists FK506 and CsA, administered to treat organ allograft rejection, exert specific effects on renal vasoconstriction and nephrotoxicity, possibly due to endogenous vasoconstrictor release such as ET-1. We investigated contribution of FK506 and CsA on regulation of prepro ET-1 gene transcription in HUVEC. To conclude on transcriptional regulation, ET-1 mRNA levels were quantified by Northern blot analysis upon stimulation with calcineurin antagonists, and newly transcribed luciferase gene, placed under the control of the rat ET-1 promoter, was quantified by reporter gene assays, where luciferase activity reflects ET-1 promoter activation. Calcium fluorometry was employed to examine calcium dependency of ET-1 promoter-dependent gene transcription. Northern blot analysis shows differential induction of prepro ET-1 mRNA in favour of CsA over FK506. Likewise, luciferase assays demonstrate stronger ET-1 promoter-dependent stimulation of the reporter gene by CsA than by FK506. Transcription of prepro ET-1 gene upon stimulation with both calcineurin antagonists is regulated by intracellular calcium levels. Lack of extra- or intracellular calcium prevents ET-1 promoter-dependent gene transcription and ET-1 mRNA induction. These observations demonstrate that calcineurin antagonists FK506 and CsA differ in quality to induce transcription of prepro ET-1 in HUVEC via calcium-dependent nuclear signalling events. To examine the contribution of ET-1 in nephrotoxicity upon CsA and FK506 immunosuppression the availability of endothelin receptor antagonists or endothelin converting enzyme inhibitors is required.

摘要

用于治疗器官移植排斥反应的钙调神经磷酸酶拮抗剂FK506和环孢素A(CsA),对肾血管收缩和肾毒性有特定影响,这可能是由于内源性血管收缩剂如内皮素-1(ET-1)的释放所致。我们研究了FK506和CsA对人脐静脉内皮细胞(HUVEC)中前内皮素原-1(prepro ET-1)基因转录调控的作用。为了确定转录调控情况,在用钙调神经磷酸酶拮抗剂刺激后,通过Northern印迹分析对ET-1 mRNA水平进行定量,并且通过报告基因分析对置于大鼠ET-1启动子控制下的新转录的荧光素酶基因进行定量,其中荧光素酶活性反映ET-1启动子的激活情况。采用钙荧光测定法检测ET-1启动子依赖性基因转录的钙依赖性。Northern印迹分析显示,与FK506相比,CsA对prepro ET-1 mRNA的诱导作用更强。同样,荧光素酶分析表明,CsA对报告基因的ET-1启动子依赖性刺激比FK506更强。两种钙调神经磷酸酶拮抗剂刺激后,prepro ET-1基因的转录受细胞内钙水平调节。细胞外或细胞内缺乏钙会阻止ET-1启动子依赖性基因转录和ET-1 mRNA诱导。这些观察结果表明,钙调神经磷酸酶拮抗剂FK506和CsA在通过钙依赖性核信号事件诱导HUVEC中prepro ET-1转录的能力上存在差异。为了研究ET-1在CsA和FK506免疫抑制引起的肾毒性中的作用,需要使用内皮素受体拮抗剂或内皮素转化酶抑制剂。

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