摘要
目的:克隆表达赖型钩端螺旋体溶血素基因hlyX,观察其表达产物对人脐静脉内皮细胞(HU-VECs)通透性的影响,并初步探讨其机制。方法:将hlyX基因插入原核表达载体pET32a(+),构建重组质粒pET-hlyX,转化大肠杆菌BL21(DH3)以高效表达携带组氨酸标签的Trx-HlyX融合蛋白,并作亲和层析纯化。采用生物素标记白蛋白的酶联免疫吸附法测定目的蛋白对HUVECs单细胞层通透性的影响,并以流式细胞术及Ho-echst 33258荧光染色方法检测其作用于HUVECs后的细胞凋亡率。结果:成功构建了重组质粒pET-hlyX并高效表达出Trx-HlyX融合蛋白;与对照组相比较,蛋白Trx-HlyX作用于HUVECs后,明显增加其通透性(P<0.05),细胞凋亡率显著增加(P<0.05)。结论:重组质粒pET-hlyX高效表达出Trx-HlyX融合蛋白,纯化后的融合蛋白对HUVECs通透性有影响,且对HUVECs具有细胞毒性作用。
AIM: To clone and express the hemolysin gene hlyX of Leptospira interrogans serovar Lai and to investigate the effect of the expression product on the permeability of human umbilical vein endothelial cells(HUVECs).METHODS: The recombinant plasmid pET-hlyX was constructed by inserting the hlyX gene into prokaryotic expression vector pET32a(+),and transformed into E.coli BL21(DH3) to express the fusion protein Trx-HlyX with a His-tag.The fusion protein was purified using HisTrap affinity columns.The permeability of the monolayer HUVECs was measured by enzyme-linked immunosorbent assay for biotin-labeled albumin.Flow cytometry and Hoechst 33258 staining were applied to measure the apoptotic rate of HUVECs after incubation with Trx-HlyX.RESULTS: The recombinant plasmid pET-HlyX was successfully constructed and the fusion protein Trx-HlyX was highly expressed.Compared with the control cells,the purified recombinant protein Trx-HlyX significantly increased the permeability of transfected cells and promoted apoptosis of HUVECs(P0.05).CONCLUSION: The recombinant plasmid pET-hlyX highly expresses the fusion protein Trx-HlyX.Purified protein Trx-HlyX influences the permeability and has cytotoxicity on HUVECs.
出处
《中国病理生理杂志》
CAS
CSCD
北大核心
2011年第9期1682-1686,共5页
Chinese Journal of Pathophysiology
基金
国家自然科学基金资助项目(No.30771908)
关键词
钩端螺旋体
HlyX
通透性
细胞凋亡
人脐静脉内皮细胞
Leptospira interrogans
HlyX
Permeability
Apoptosis
Human umbilical vein endothelial cells