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内源性肾小管心房利钠肽的局部作用。

Local action of endogenous renal tubular atrial natriuretic peptide.

作者信息

Lo Chao-Sheng, Chen Chao-Hung, Hsieh Tusty-Jiuan, Lin Kun-Der, Hsiao Pi-Jung, Shin Shyi-Jang

机构信息

Graduate Institute of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.

出版信息

J Cell Physiol. 2009 Jun;219(3):776-86. doi: 10.1002/jcp.21728.

Abstract

Up-regulation of atrial natriuretic peptide (ANP) mRNA in the kidneys in several disorders has been demonstrated; however, evidence that ANP synthesized by the kidney exerts a local function has never been produced. Therefore, we investigated whether endogenous ANP could modulate high glucose-stimulated TGF-beta1, collagen type I and nuclear factor-kappaB (NF-kappaB) in NRK-52E cells using transfection of ANP and ANP small interfering RNA (siANP). NRK-52E cells were grown with or without transfection with ANP plasmid; cells were also transfected with ANP siRNA or control siRNA. These cells were then stimulated with a high glucose concentration to modulate ANP, TGF-beta1, collagen type I, NF-kappaB and IkappaB-alpha, and the results showed that ANP, TGF-beta1, collagen type I and NF-kappaB significantly increased in untransfected cells, and the transfection of ANP significantly attenuated high glucose-activated TGF-beta1, collagen I and NF-kappaB expression. ANP siRNA knocked-down ANP but significantly increased TGF-beta1 and collagen I under normal glucose conditions; ANP siRNA decreased IkappaB-alpha but strongly enhanced high glucose-activated TGF-beta1, collagen type I and NF-kappaB. In contrast, medium from ANP-transfected cells attenuated high glucose-activated TGF-beta1 and collagen type I expression in NRK-52E cells transfected with siANP. In conclusion, our results demonstrated that siANP increased activation of TGF-beta1, collagen type I and NF-kappaB in NRK-52E cells under high glucose conditions, and medium from ANP-transfected cells attenuated high glucose-activated TGF-beta1 and collagen type I. This is the first study to demonstrate the auto/paracrine action of endogenous ANP in renal tubular cells on the attenuation of hyperglycemia-activated TGF-beta1 and NF-kappaB expression. J. Cell. Physiol. 219: 776-786, 2009. (c) 2009 Wiley-Liss, Inc.

摘要

已有研究表明,在多种疾病状态下,肾脏中的心钠素(ANP)mRNA会出现上调;然而,肾脏合成的ANP发挥局部功能的证据却从未得到证实。因此,我们利用ANP和ANP小干扰RNA(siANP)转染技术,研究内源性ANP是否能够调节高糖刺激下NRK-52E细胞中转化生长因子-β1(TGF-β1)、I型胶原蛋白和核因子-κB(NF-κB)的表达。NRK-52E细胞在有无ANP质粒转染的情况下进行培养;细胞还分别用ANP siRNA或对照siRNA进行转染。然后用高糖浓度刺激这些细胞,以调节ANP、TGF-β1、I型胶原蛋白、NF-κB和IκB-α的表达,结果显示,未转染细胞中ANP、TGF-β1、I型胶原蛋白和NF-κB显著增加,而ANP转染显著减弱了高糖激活的TGF-β1、胶原蛋白I和NF-κB的表达。在正常葡萄糖条件下,ANP siRNA敲低了ANP,但显著增加了TGF-β1和胶原蛋白I的表达;ANP siRNA降低了IκB-α的表达,但强烈增强了高糖激活的TGF-β1、I型胶原蛋白和NF-κB的表达。相反,ANP转染细胞的培养基减弱了用siANP转染的NRK-52E细胞中高糖激活的TGF-β1和I型胶原蛋白的表达。总之,我们的结果表明,在高糖条件下,siANP增加了NRK-52E细胞中TGF-β1、I型胶原蛋白和NF-κB的激活,而ANP转染细胞的培养基减弱了高糖激活的TGF-β1和I型胶原蛋白的表达。这是首次证明内源性ANP在肾小管细胞中对高血糖激活的TGF-β1和NF-κB表达的衰减具有自分泌/旁分泌作用的研究。《细胞生理学杂志》2009年第219卷:776 - 786页。(c)2009威利 - 利斯公司。

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