维生素 K1 通过肾脏中的基质 Gla 蛋白抑制肾晶体形成

Kidney and Blood Pressure Research Pub Date : 2019-01-01 Epub Date: 2019-10-22 DOI:10.1159/000503300
Yang Li, Xiuli Lu, Baoyu Yang, Jing Mao, Shan Jiang, Daojun Yu, Jichuan Pan, Tiange Cai, Takahiro Yasui, Bing Gao
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引用次数: 5

摘要

背景和目的:维生素 K(VK)在改变骨骼和血管中钙的结合方面发挥着重要作用。了解维生素 K 对肾脏中晶体形成的影响将有助于推进肾结石的治疗和预防:方法:用维生素 K1(VK1)治疗大鼠 8 周。方法:用维生素 K1(VK1)治疗大鼠 8 周,检测 VK1 水平并观察晶体形成。HK2 细胞暴露于一水草酸钙晶体。检测细胞凋亡和细胞活力。用原子吸收法分析晶体沉积。为了阐明 VK1 对晶体形成的影响和机制,构建了表达基质 Gla 蛋白(MGP)和 siMGP 的腺病毒载体。通过 Western 印迹分析了 MGP 在体内和体外的表达。半定量 RT-PCR 检测了单核细胞趋化蛋白-1(MCP-1)和胶原蛋白 I 的 mRNA 水平:结果:使用 VK1 治疗后,全血和肾组织中的 VK1 浓度上升。结果:与对照组相比,VK1治疗组大鼠全血和肾组织中的VK1浓度升高,晶体形成在第2周至第6周受到抑制,晶体形成的频率和质量明显降低,晶体形成的位置受到更大程度的限制。暴露于晶体的 HK2 细胞经华法林处理后,粘附在细胞上的晶体数量和凋亡细胞数量明显增加,细胞活力降低。VK1 治疗逆转了华法林的上述影响。VK1 可抑制晶体负荷下肾组织中 MCP-1 和胶原 I 的上调。VK1 处理可增加体内和体外 MGP 的表达,而 MGP 是 VK1 在细胞内晶体沉积过程中发挥作用的必要条件:结论:VK1治疗可抑制体内肾晶体的形成。结论:VK1 治疗可抑制体内肾晶体的形成。VK1 可增加 MGP 的表达,并通过 MGP 发挥减少晶体在细胞内沉积的作用,从而为细胞提供保护。我们的研究结果表明,VK1 治疗可能是治疗和预防肾炎的一种潜在策略。
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Vitamin K1 Inhibition of Renal Crystal Formation through Matrix Gla Protein in the Kidney.

Background and objectives: Vitamin K (VK) plays a major role in modifying the binding of calcium in bones and blood vessels. Understanding the effect of VK on crystal formation in the kidney would contribute to advancing the treatment and prevention of kidney stones.

Methods: Rats were treated with vitamin K1 (VK1) for 8 weeks. VK1 levels were detected and crystal formation were observed. HK2 cells were exposed to calcium oxalate monohydrate crystals. Apoptosis and cell viability were detected. Crystal deposition was analyzed using atomic absorption assay. The adenovirus vectors expressing matrix Gla protein (MGP) and siMGP were constructed to elucidate the effect and mechanism of VK1 on crystal formation. MGP expression in vivo and in vitro was analyzed by Western blot. The mRNA levels of monocyte chemoattractant protein-1 (MCP-1) and collagen I was measured by semiquantitative RT-PCR.

Results: The concentrations of VK1 in whole blood and kidney tissues rose under treatment with VK1. Crystal formation was inhibited from the second to the 6th week, the frequency and quality of crystal formation decreased significantly, and the location of crystal formation was limited to a greater extent in the rats treated by VK1 compared to the control group. Warfarin treatment in the crystals-exposed HK2 cells significantly increased the number of crystals adhering to cells and the number of apoptotic cells and reduced cell viability. VK1 treatment reversed warfarin's above influence. VK1 inhibited the upregulations of MCP-1 and collagen I in kidney tissues under crystal load. VK1 treatment increased MGP expression in vivo and in vitro, and MGP is necessary for VK1 to play a role in crystal deposition in cells.

Conclusions: VK1 treatment can inhibit the formation of renal crystals in vivo. VK1 increases MGP expression and functions through MGP to reduce crystal deposition in cells and provide cell protection. Our findings suggest that VK1 treatment could be a potential strategy for the treatment and prevention of nephrolithiasis.

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