人剪切修复基因D介导ox-LDL促进HUVEC凋亡作用
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(1.南昌大学第一附属医院心电图室,江西省南昌市 330006;2.南昌大学医学院,江西省南昌市 330006;3.南昌大学第二附属医院心电诊断室,江西省南昌市 330006;4.江西省乐安县人民医院, 江西省抚州市 344300;5.南昌大学第二附属医院心血管内科,江西省南昌市 330006)

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俞菊梅,硕士,住院医师,主要研究方向为心血管疾病的基因治疗,E-mail为363449568@qq.com。

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国家自然科学基金项目(81300348);江西省青年科学基金资助项目(20132BAB215015);江西省卫生厅科技计划项目(20143084)


Hxeroderma pigmentosum mediates the effect of ox-LDL on promoting the apoptosis of HUVEC
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1.Department of ECG, the First Affliated Hospital of Nanchang University, Nanchang, Jiangxi 330006, China;2.Medical school of Nanchang University, Nanchang, Jiangxi 330006, China;3.Department of ECG Diagnosis, the Second Affliated Hospital of Nanchang University, Nanchang, Jiangxi 330006, China;4.People’s Hospital of Le’An County, Fuzhou, Jiangxi 344300, China;5.Deptartment of Cardiovascular, the Second Affliated Hospital of Nanchang University, Nanchang, Jiangxi 330006, China)

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    摘要:

    目的 探讨人剪切修复基因D(XPD)是否介导氧化型低密度脂蛋白(ox-LDL)促进人脐静脉内皮细胞(HUVEC)凋亡。 方法 以ox-LDL建立HUVEC凋亡模型。用脂质体将XPD-siRNA转染HUVEC,给予ox-LDL处理。实验分6组:空白对照组;阴性对照siRNA组;XPD-siRNA组;ox-LDL组;ox-LDL +阴性对照siRNA组;ox-LDL+XPD-siRNA组。MTT测定细胞活力;流式细胞仪检测细胞凋亡率和细胞周期;用RT-PCR和Western blot检测XPD、Bax和Bcl-2的表达。 结果 建立HUVEC凋亡模型ox-LDL的最佳浓度为100 mg/L。与阴性对照siRNA组相比,XPD-siRNA组的细胞凋亡率明显下降(P<0.05),存活率明显增加(P<0.01),G0/G1期细胞减少(P<0.05)、S期细胞增加(P<0.05),XPD、Bax表达降低(P均<0.05),Bcl-2表达增高(P<0.05);与空白对照组相比,ox-LDL组细胞凋亡率明显增加(P<0.01),细胞存活率下降(P<0.05),G0/G1期细胞增加(P<0.05)、S期细胞明显减少(P<0.01),XPD、Bax表达升高(P均<0.05),Bcl-2表达降低(P<0.05);与ox-LDL+阴性对照siRNA组相比,ox-LDL+XPD-siRNA组细胞凋亡率下降(P<0.05),细胞存活率明显增加(P<0.01),G0/G1期细胞减少(P<0.05)、S期细胞增加(P<0.05),XPD、Bax表达降低(P均<0.05),Bcl-2表达增高(P<0.05)。 结论 XPD能介导ox-LDL促进HUVEC凋亡作用。

    Abstract:

    Aim To explore whether the hxeroderma pigmentosum D(XPD) could mediate the apoptosis of human umbilical vein endothelial cells (HUVEC) promoted by oxidized low density lipoprotein (ox-LDL). Methods The model of apoptosis of HUVEC was established by ox-LDL. XPD-siRNA was transfected into HUVEC with liposome,followed by treatment with ox-LDL. This experiment was divided into six groups:blank control group; negative control siRNA group; XPD-siRNA group; ox-LDL group; ox-LDL+negative control siRNA group; ox-LDL+XPD-siRNA group. Cell vitality was detected by MTT; Cell apoptosis rate and cell cycle were assessed with flow cytometry; The expressions of the XPD, Bax and Bcl-2 were detected by RT-PCR and Western blot. Results The optimal concentration of ox-LDL to establish the model of apoptosis of HUVEC was 100 mg/L. Compared with negative control siRNA group, the cell apoptosis rate of XPD-siRNA group was significantly decreased (P<0.05), the survival rate was significantly increased (P<0.01), the cell number in G0/G1 phase decreased (P<0.05), while increased in S phase (P<0.05), the expressions of XPD and Bax were declined (all P<0.05), while the expression of Bcl-2 was elevated (P<0.05); Compared with blank control group, the cell apoptosis rate of ox-LDL group increased significantly (P<0.01), the survival rate was decreased (P<0.05), the cell number in G0/G1 phase increased (P<0.05),while decreased significantly in S phase (P<0.01), the expressions of XPD and Bax were elevated (all P<0.05),while the expression of Bcl-2 was declined (P<0.05). Compared with ox-LDL+negative control siRNA group,the cell apoptosis rate of ox-LDL+XPD-siRNA group was reduced (P<0.05),the survival rate was increased(P<0.01), the cell number in G0/G1 phase decreased (P<0.05),while increased in S phase (P<0.05), the expressions of XPD and Bax were declined (all P<0.05), while the expression of Bcl-2 was elevated (P<0.05). Conclusion XPD can mediate the effect of ox-LDL on promoting the apoptosis of HUVEC.

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俞菊梅,胡利琳,丁颖,元文峰,李菊香,孙国芳.人剪切修复基因D介导ox-LDL促进HUVEC凋亡作用[J].中国动脉硬化杂志,2018,26(1):19~24.

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  • 收稿日期:2017-06-19
  • 最后修改日期:2017-08-14
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  • 在线发布日期: 2018-02-01