Fibulin-3 Attenuates Phosphate-Induced Vascular Smooth Muscle Cell Calcification by Inhibition of Oxidative Stress

被引:57
作者
Luong, Trang T. D. [1 ]
Schelski, Nadeshda [1 ]
Boehme, Beate [1 ]
Makridakis, Manousos [2 ]
Vlahou, Antonia [2 ]
Lang, Florian [3 ]
Pieske, Burkert [1 ,4 ,5 ]
Alesutan, Ioana [1 ,4 ,6 ]
Voelkl, Jakob [1 ,6 ]
机构
[1] Charite, Dept Internal Med & Cardiol, Augustenburgerpl 1, D-13353 Berlin, Germany
[2] Acad Athens, Biomed Res Fdn, Athens, Greece
[3] Eberhard Karls Univ Tubingen, Dept Physiol 1, Tubingen, Germany
[4] BIH, Berlin, Germany
[5] German Heart Inst Berlin, Dept Internal Med & Cardiol, Berlin, Germany
[6] DZHK German Ctr Cardiovasc Res, Partner Site Berlin, Berlin, Germany
关键词
Fibulin-3; Phosphate; Oxidative stress; Vascular calcification; Osteo-/chondrogenic signaling; Vascular smooth muscle cells; OSTEOBLASTIC DIFFERENTIATION; HYDROGEN-PEROXIDE; UP-REGULATION; MODULATION; EXPRESSION; MATRIX-METALLOPROTEINASE-9; PATHOPHYSIOLOGY; TRANSFORMATION; TRANSCRIPTION; PATHOGENESIS;
D O I
10.1159/000489144
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 PA1-1. 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. (C) 2018 The Author(s) Published by S. Karger AG, Basel.
引用
收藏
页码:1305 / 1316
页数:12
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