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首页> 外文期刊>Cellular Physiology and Biochemistry >Fibulin-3 Attenuates Phosphate-Induced Vascular Smooth Muscle Cell Calcification by Inhibition of Oxidative Stress
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Fibulin-3 Attenuates Phosphate-Induced Vascular Smooth Muscle Cell Calcification by Inhibition of Oxidative Stress

机译:Fibulin-3通过抑制氧化应激减弱磷酸诱导的血管平滑肌细胞钙化。

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Background/Aims Fibulin-3, an extracellular matrix glycoprotein, inhibits vascular oxidative stress and remodeling in hypertension. Oxidative stress is prevalent in chronic kidney disease (CKD) patients and is an important mediator of osteo-/chondrogenic transdifferentiation and calcification of vascular smooth muscle cells (VSMCs) during hyperphosphatemia. Therefore, the present study explored the effects of Fibulin-3 on phosphate-induced vascular calcification. Methods Experiments were performed in primary human aortic smooth muscle cells (HAoSMCs) treated with control or with phosphate without or with additional treatment with recombinant human Fibulin-3 protein or with hydrogen peroxide as an exogenous source of oxidative stress. Results Treatment with calcification medium significantly increased calcium deposition in HAoSMCs, an effect significantly blunted by additional treatment with Fibulin-3. Moreover, phosphate-induced alkaline phosphatase activity and mRNA expression of osteogenic and chondrogenic markers MSX2, CBFA1, SOX9 and ALPL were all significantly reduced by addition of Fibulin-3. These effects were paralleled by similar regulation of oxidative stress in HAoSMCs. Phosphate treatment significantly up-regulated mRNA expression of the oxidative stress markers NOX4 and CYBA, down-regulated total antioxidant capacity and increased the expression of downstream effectors of oxidative stress PAI-1, MMP2 and MMP9 as well as BAX/BLC2 ratio in HAoSMCs, all effects blocked by additional treatment with Fibulin-3. Furthermore, the protective effects of Fibulin-3 on phosphate-induced osteogenic and chondrogenic markers expression in HAoSMCs were reversed by additional treatment with hydrogen peroxide. Conclusions Fibulin-3 attenuates phosphate-induced osteo-/ chondrogenic transdifferentiation and calcification of VSMCs, effects involving inhibition of oxidative stress. Up-regulation or supplementation of Fibulin-3 may be beneficial in reducing the progression of vascular calcification during hyperphosphatemic conditions such as CKD.
机译:背景/目的Fibulin-3是一种细胞外基质糖蛋白,在高血压中抑制血管氧化应激和重塑。氧化应激在慢性肾脏疾病(CKD)患者中普遍存在,并且是高磷酸盐血症期间骨/软骨源性分化和血管平滑肌细胞(VSMC)钙化的重要介质。因此,本研究探讨了Fibulin-3对磷酸盐诱导的血管钙化的影响。方法实验在原代人主动脉平滑肌细胞(HAoSMCs)中进行,原代人主动脉平滑肌细胞经对照或磷酸盐处理,未经过重组人Fibulin-3蛋白或过氧化氢作为外源性氧化应激来源,也未进行其他处理。结果用钙化介质处理可显着增加HAoSMC中的钙沉积,而用Fibulin-3进一步处理则明显减弱了这种作用。此外,添加Fibulin-3显着降低了磷酸盐诱导的碱性磷酸酶活性以及成骨和软骨形成标记MSX2,CBFA1,SOX9和ALPL的mRNA表达。在HAoSMC中,通过类似的氧化应激调节可以达到这些效果。磷酸盐处理显着上调了HAoSMCs中氧化应激标记NOX4和CYBA的mRNA表达,下调了总抗氧化能力,并增加了氧化应激PAI-1,MMP2和MMP9的下游效应子的表达以及BAX / BLC2的比例,用Fibulin-3进一步治疗可阻断所有作用。此外,Fibulin-3对磷酸盐诱导的成骨和成软骨标记在HAoSMCs中的表达的保护作用被过氧化氢进一步处理所逆转。结论Fibulin-3减弱了磷酸盐诱导的VSMCs的骨/软骨源性转分化和钙化,其作用涉及抑制氧化应激。上调或补充Fibulin-3可能有助于减少高磷血症(例如CKD)期间血管钙化的进展。

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