Chinese Journal of Tissue Engineering Research ›› 2023, Vol. 27 ›› Issue (2): 216-222.doi: 10.12307/2022.928
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Ou Hangjun, Zhao Guangjian, Pan Yujia, Gong Caiwei, Zhao Quanwei, Liu Danan
Received:
2021-12-01
Accepted:
2022-01-29
Online:
2023-01-18
Published:
2022-06-20
Contact:
Liu Danan, MD, Professor, Chief physician, Master’s/Doctoral supervisor, Department of Cardiology, Affiliated Hospital of Guizhou Medical University, Institute of Medical Sciences, Guizhou Medical University, Guiyang 550004, Guizhou Province, China
About author:
Ou Hangjun, Master candidate, Department of Cardiology, Affiliated Hospital of Guizhou Medical University, Institute of Medical Sciences, Guizhou Medical University, Guiyang 550004, Guizhou Province, China
Supported by:
CLC Number:
Ou Hangjun, Zhao Guangjian, Pan Yujia, Gong Caiwei, Zhao Quanwei, Liu Danan. Construction of a lentiviral vector overexpressing fibronectin type III domain containing 5 to inhibit apoptosis of endothelial cells[J]. Chinese Journal of Tissue Engineering Research, 2023, 27(2): 216-222.
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挑选目的基因阳性克隆,送菌液pLenti-EF1-EGFP-P2A-Puro-CMV-FNDC5-3xFLAG-WPRE测序,测序结果经 Chromas 比对显示测序结果与设计序列一致,表明FNDC5过表达慢病毒载体构建成功。 2.2 慢病毒包装并转染人脐静脉内皮细胞结果 将质粒pLenti-EF1-EGFP-P2A-Puro-CMV-FNDC5-3xFLAG-WPRE转染293T细胞,48 h后倒置荧光显微镜下可见大量绿色荧光,表明质粒pLenti-EF1-EGFP-P2A-Puro-CMV-FNDC5-3xFLAG-WPRE已成功导入293T细胞;收集细胞上清液,通过 RT-PCR 法定量测定上清液中的病毒滴度为2.67×108 TU/mL,证实病毒包装成功。然后将慢病毒包装的pLenti-EF1-EGFP-P2A-Puro-CMV-FNDC5-3xFLAG-WPRE表达质粒分别按照感染复数值为20,40,80转染人脐静脉内皮细胞,得到最适感染复数值为40。然后以40的感染复数值转染人脐静脉内皮细胞,72 h后能观察到明显绿色荧光,再经嘌呤霉素筛选7 d后,可观测到成片的稳定表达的绿色荧光,见图2,得到FNDC5稳定过表达的人脐静脉内皮细胞系。 "
加入氧化型低密度脂蛋白1,2 h后,实验组细胞活力高于空白组、对照组(P < 0.05),空白组与对照组细胞活力比较差异无显著性意义(P > 0.05);加入氧化型低密度脂蛋白1,4 h后,3组细胞活力比较差异无显著性意义(P > 0.05)。结果表明,FNDC5过表达能够改善氧化型低密度脂蛋白诱导的人脐静脉内皮细胞活性下降。 2.5 各组人脐静脉内皮细胞凋亡检测结果 流式细胞术检测结果显示,加入氧化型低密度脂蛋白24 h后,实验组早期及晚期凋亡细胞率均低于空白组、对照组(P < 0.05),空白组与对照组早期及晚期凋亡细胞率比较差异无显著性意义(P > 0.05),见图5A。 Hoechst 33342/PI双染检测结果显示,加入氧化型低密度脂蛋白24 h后,实验组凋亡细胞数量少于空白组、对照组,空白组与对照组凋亡细胞数量无明显差异,见图5B。凋亡细胞能够被PI试剂染色,发红色荧光,正常细胞只能发蓝色荧光,故过表达FNDC5可以抑制人脐静脉内皮细胞凋亡,这也与流式检测结果一致。 "
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