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低密度脂蛋白和氧化型低密度脂蛋白对大鼠系膜细胞中肝素结合表皮生长因子样生长因子基因表达的调控

Regulation of heparin binding-epidermal growth factor like growth factor gene expression by LDL and oxidized-LDL in rat mesangial cells.

作者信息

Tan M S, Lee Y J, Shin S J, Tsai J H

机构信息

Graduate Institute of Medicine, Kaohsiung Medical College, Taiwan, Republic of China.

出版信息

Biochem Biophys Res Commun. 1994 Jul 29;202(2):1001-8. doi: 10.1006/bbrc.1994.2028.

Abstract

The present study was to determine whether low-density lipoprotein (LDL) and oxidized LDL (Ox-LDL) modulate the heparin binding-epidermal growth factor like growth factor (HB-EGF) gene expression in rat mesangial cells (RMC). Using Northern blot analysis, LDL and Ox-LDL stimulated the expression of RMC HB-EGF mRNA in a time- and concentration-dependent manner, and the stimulatory effect of Ox-LDL lasted longer than LDL. In addition, a protein kinase C (PKC) inhibitor-staurosporine and a PKC-depletion condition abolished both of the stimulatory activities of LDL and Ox-LDL, while H-8 (a protein kinase A inhibitor) and cAMP-antagonist (cyclic adenosine-3':5'-monophosphothioate) had little effect. Our data indicate that LDL and Ox-LDL enhance HB-EGF gene expression and both via the PKC pathway in RMC. As HB-EGF is a mitogen for RMC, our results suggest that lipoproteins may regulate RMC function by inducing HB-EGF gene expression and thus contribute to glomerular injury.

摘要

本研究旨在确定低密度脂蛋白(LDL)和氧化型低密度脂蛋白(Ox-LDL)是否调节大鼠系膜细胞(RMC)中肝素结合表皮生长因子样生长因子(HB-EGF)基因的表达。采用Northern印迹分析,LDL和Ox-LDL以时间和浓度依赖性方式刺激RMC的HB-EGF mRNA表达,且Ox-LDL的刺激作用持续时间比LDL长。此外,蛋白激酶C(PKC)抑制剂-星形孢菌素和PKC耗竭条件消除了LDL和Ox-LDL的刺激活性,而H-8(蛋白激酶A抑制剂)和cAMP拮抗剂(环腺苷-3':5'-单磷酸硫代物)影响很小。我们的数据表明,LDL和Ox-LDL通过RMC中的PKC途径增强HB-EGF基因表达。由于HB-EGF是RMC的有丝分裂原,我们的结果表明脂蛋白可能通过诱导HB-EGF基因表达来调节RMC功能,从而导致肾小球损伤。

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