CAJ | 학술논문

目的构建血管内皮生长因子(VEGF)基因和铜绿假单胞菌外毒素(PE38)基因真核融合表达载体,观察其表达产物对人脐静脉内皮细胞(HUVECs)的影响.方法通过聚合酶链反应(PCR)获得VEGF165基因片段,通过Hind Ⅲ和EcoR Ⅰ双酶切pRB391质粒获得PE38基因.构建两融合基因的真核表达载体plRES2-VEGF165-PE38-EGFP,转染293细胞后用逆转录(RT)-PCR及ELISA检测VEGF165-PE38融合蛋白在293细胞的表达,并检测转染细胞的培养上清对HUVECs的选择性细胞毒作用.结果成功构建VEGF165-PE38融合基因真核表达载体,其可在293细胞表达,ELISA检测表明空质粒转染组、无转染组和重组质粒转染组VEGF浓度分别为(269.0±23.6)、(306.0±29.3)和(1390.0±136.6)ng/L.CCK-8和TUNEL检测表明重组质粒细胞转染上清对HUVECs具有较强的细胞抑制效应,凋亡细胞率分别为8.34%、7.69%和39.88%,差异有统计学意义(P<0.05).结论 VEGF 165-PE38融合基因构建,表达及其功能的初步研究,为肿瘤血管内皮细胞的靶向治疗及临床应用奠定了基础.
목적 구건혈관내피생장인자(VEGF)기인화동록가단포균외독소(PE38)기인진핵융합표체재체,관찰기표체산물대인제정맥내피세포(HUVECs)적영향.방법 통과취합매련반응(PCR)획득VEGF165기인편단,통과Hind Ⅲ화EcoR Ⅰ쌍매절pRB391질립획득PE38기인.구건량융합기인적진핵표체재체plRES2-VEGF165-PE38-EGFP,전염293세포후용역전록(RT)-PCR급ELISA검측VEGF165-PE38융합단백재293세포적표체,병검측전염세포적배양상청대HUVECs적선택성세포독작용.결과 성공구건VEGF165-PE38융합기인진핵표체재체,기가재293세포표체,ELISA검측표명공질립전염조、무전염조화중조질립전염조VEGF농도분별위(269.0±23.6)、(306.0±29.3)화(1390.0±136.6)ng/L.CCK-8화TUNEL검측표명중조질립세포전염상청대HUVECs구유교강적세포억제효응,조망세포솔분별위8.34%、7.69%화39.88%,차이유통계학의의(P<0.05).결론 VEGF 165-PE38융합기인구건,표체급기공능적초보연구,위종류혈관내피세포적파향치료급림상응용전정료기출.
Objective To construct a new recombinant immunotoxin expression vector by fusing human VEGFI65 and a truncated pseudomonas exotoxin A ramification (PE38) gene, and explore the in-fluence of the VEGFI65-PE38 fusion protein on human umbilical vein endothehal cells (HUVECs). Methods VEGFI65 was cloned by polymerase chain reaction (PCR). PE38 gene was gained from a vec- tor plasmid pRB391 by restriction endonuelease digestion, and then inserted to the eukaryotic expression vector plRES2-EGFP. The vector was transfected into 293 cells. RT-PCR and ELISA were used to confirm the expression of the fusion gene in the 293 cells. The selectively killing activities of the immunotoxin in culture supernatant were detected in vitro. Results The fusion gene eukaryotie expression plasmid was constructed successfully. The fusion gene could be expressed in the 293 cells. The VEGF levels of(269.0 ± 23.6 ),(306.0 ± 29.3)and(1390.0 ± 136.6 )ng/ L were secreted into the culture medium by no transfected cells, plRES2-EGFP-transfected cells and VEGFI65PE38 transfeeted cells respectively. VEGF165-PE38-containing supematant was specific to VEGFR-positive HUVECs, and the apoptosis rate was 8. 34% , 7. 69%, and 39. 88% in no transfected group, plRES2-EGFP-transfected group and VEGFI65PE38 transfeeted group respectively. Conclusion The results provide the basis for research of the targeted cytotoxie activity to tumor vascular endothelial cells, and may have some potential values in clinical application.