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论文摘要

浓缩生长因子促人脐静脉血管内皮细胞成血管化作用研究

An in vitro study of the angiogenic effects of concentrate growth factor on human umbilical vein endothelial cells

作者:宦俊, 窦磊, 严崎方, 杨德琴

Author:Jun Huan, Lei Dou, Qifang Yan, Deqin Yang

收稿日期:2017-09-25          年卷(期)页码:2018,36(3):247-247-251

期刊名称:华西口腔医学杂志

Journal Name:West China Journal of Stomatology

关键字:浓缩生长因子,人脐静脉血管内皮细胞,增殖,分化,

Key words:concentrate growth factor,human umbilical vein endothelial cells,proliferation,differentiation,

基金项目:国家自然科学基金面上项目(31571508,31371473);2016年重庆高校创新团队建设计划;重庆市高校市级口腔生物医学工程重点实验室资助项目[渝教科2014(55)号]

中文摘要

目的 研究浓缩生长因子(CGF)对人脐静脉血管内皮细胞(HUVECs)的增殖、迁移和分化的作用。方法 取健康志愿者静脉血制成CGF,再用CGF制备浓缩生长因子提取液(CGFe)。体外培养细胞分为2%CGFe组、5%CGFe组、10%CGFe组和对照组。CCK-8和细胞周期实验检测各组细胞增殖活性;划痕实验检测内皮细胞迁移;实时荧光定量聚合酶链反应(qRT-PCR)检测各组细胞血管内皮生长因子(VEGF)、趋化因子受体4(CXCR4)、血小板衍生因子(PDGF)mRNA表达量。结果 CCK-8法和细胞周期结果显示CGFe明显促进细胞增殖(P<0.05),且增殖效应呈CGFe浓度依赖性,各组间均有统计学差异(P<0.05);划痕实验中12 h时实验组划痕愈合效率明显高于对照组,且愈合效率与CGFe浓度呈正比(P<0.05);CGFe明显促进VEGF、CXCR4、PDGF的mRNA表达量,促进效应与浓度呈正比(P<0.05)。结论 CGFe能有效促进HUVECs的增殖、迁移和成血管分化。

英文摘要

ObjectiveThis study aimed to explore the effects of concentrate growth factor extracts (CGFe) on human umbi-lical vein endothelial cells (HUVECs)in vitro.MethodsConcentrate growth factor (CGF) were prepared from the peripheral blood of healthy donors, followed by CGFe. Four groups were designed based on cell culture medium, as follows: 2%CGFe, 5%CGFe, 10%CGFe, and control. The proliferation activity of HUVECs was detected by cell cycle and CCK-8 assays. The migration of HUVECs was detected by scratch assay. The mRNA expression levels of vascular endothelial growth factor (VEGF), chemokine receptor 4 (CXCR4), and platelet derived growth factor (PDGF) were examined by quantitative real time polymerase chain reaction (qRT-PCR).ResultsResults of CCK-8 and cell cycle assays showed that CGFe promoted the proli-feration capability of HUVECs in a dose-dependent manner, and the data had statistical significance among four groups (P<0 .05). the cell migration assay indicated that cgf accelerated wound closure in a dose-dependent manner after 12 h of culture (P<0 .05). the results of qrt-pcr showed that cgf upregulated the expression levels of vegf, cxcr4, and pdgf in huvecs.ConclusionCGFe can promote the proliferation, migration, and angiogenic differentiation of HUVECs. Thus, CGF might be an appropriate cure for dental pulp revascularization.

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