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Shear stress attenuates endothelin and endothelin-converting enzyme expression through oxidative stress.

机译:剪应力通过氧化应激减弱了内皮素和内皮素转化酶的表达。

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Shear stress is known to dilate blood vessels and exert an antiproliferative effect on vascular walls. These effects have partly been ascribed to shear stress-induced regulation of the secretion of endothelium-derived vasoactive substances. In this study, to elucidate the role of shear stress in endothelin production by endothelial cells, we examined the effect of physiological shear stress on the mRNA expression of endothelin-converting enzyme-1 (ECE-1) as well as endothelin-1 (ET-1) in cultured bovine carotid artery endothelial cells (BAECs) and human umbilical vein endothelial cells (HUVECs), using a parallel plate-type flow chamber.ECE-1 mRNA expression was significantly down-regulated by shear stress in an intensity- and time-dependent manner within the physiological range (1.5 to 15 dyn/cm(2)). ET-1 mRNA expression decreased together with ECE-1 mRNA expression. Shear stress at 15 dyn/cm(2) for 30 min induced a significant increase in the intracellular peroxide concentration, and the down-regulation of ECE-1 and ET-1 mRNA expression by shear stress was attenuated almost completely on treatment with N-acetyl cysteine (NAC), an antioxidant (20 mM). Furthermore, when H(2)O(2) (0.5 to 2 mM) was added to BAECs in static culture, the ECE-1 as well as ET-1 mRNA expression was attenuated in proportion to the concentration of H(2)O(2). It is suggested that endothelial cells sense shear stress as oxidative stress and transduce signal for the regulation of the gene expression of ECE as well as ET to attenuate vascular tone and inhibit the proliferation of vascular smooth muscle cells.
机译:已知剪应力会扩张血管并在血管壁上发挥抗增殖作用。这些作用部分归因于剪切应力诱导的内皮来源的血管活性物质分泌的调节。在这项研究中,为了阐明剪切应力在内皮细胞产生内皮素中的作用,我们研究了生理剪切应力对内皮素转化酶1(ECE-1)和内皮素1(ET -1)在培养的牛颈动脉内皮细胞(BAEC)和人脐静脉内皮细胞(HUVEC)中,使用平行板式流动室.ECE-1 mRNA表达在剪切强度和强度下显着下调。在生理范围内(1.5至15 dyn / cm(2))随时间变化的方式。 ET-1 mRNA表达与ECE-1 mRNA表达一起下降。 15 dyn / cm(2)的剪切应力持续30分钟会导致细胞内过氧化物浓度显着增加,而用N-处理几乎可以完全消除剪切应力对ECE-1和ET-1 mRNA表达的下调。乙酰半胱氨酸(NAC),抗氧化剂(20 mM)。此外,当将H(2)O(2)(0.5至2 mM)添加到静态培养的BAEC中时,ECE-1和ET-1 mRNA表达随H(2)O浓度的增加而减弱。 (2)。提示内皮细胞将切应力感知为氧化应激并转导信号以调节ECE和ET的基因表达,从而减弱血管紧张度并抑制血管平滑肌细胞的增殖。

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