
鼠IL-10基因腺病毒载体的构建及在骨髓间充质干细胞中的表达
Construction of rat interleukin-10 adenoviral vector and its expression in bone marrow mesenchymal stem cells
目的 构建携带鼠IL-10(rIL-10)基因重组腺病毒载体,并探讨其能否在鼠骨髓间充质干细胞(MSCs)中稳定表达。方法 rIL-10引物经PCR扩增rIL-10 cDNA序列,将回收到的656 bp rIL-10 DNA片段克隆入pcDNA3.1载体中,构建pcDNA3.1-IL-10,将其与腺病毒载体共转染HEK293细胞,进行细胞内同源重组,经测序及聚合酶链反应(PCR)鉴定重组是否成功;反复冻融裂解HEK293细胞,将获得的含rIL-10基因的病毒液感染MSCs,Western blot法检测rIL-10在MSCs中的表达。结果 经测序及PCR验证,rIL-10基因腺病毒载体构建成功,病毒滴度达4×109 PFU/mL。含rIL-10基因的病毒液体外感染MSCs后,可检测到IL-10的表达。结论 构建重组腺病毒能够介导rIL-10基因在MSCs中的稳定表达,为下一步基因移植治疗炎症性肠病提供基础。
Objective To construct the recombinant adenoviral vector carrying the rat interleukin-10 (rIL-10) gene, and to investigate whether it is stably expressed in bone marrow mesenchymal stem cells. Methods The rIL-10 gene was amplified by PCR from template rIL-10 cDNA, and the recovered 656 bp rIL-10 DNA fragment was cloned into pcDNA3.1 to construct pcDNA3.1-IL-10. Then HEK293 cells were transfected with pcDNA3.1-IL-10 and adenoviral vector for homologous recombination, and sequencing and PCR were used to evaluate whether recombination was successful. HEK293 cells were lysed by repeated freeze-thaw cycles, and bone marrow mesenchymal stem cells were infected with the virus solution containing the rIL-10 gene. Western blot was used to measure the expression of rIL-10 in bone marrow mesenchymal stem cells. Results Sequencing and PCR verified that the rIL-10 adenoviral vector was successfully constructed, with a virus titer of 4×109 PFU/mL. The expression of IL-10 was detected after bone marrow mesenchymal stem cells were infected by the virus solution containing the rIL-10 gene. Conclusions The constructed rIL-10 recombinant adenovirus can mediate the stable expression of rIL-10 gene in bone marrow mesenchymal stem cells, which provides a basis for gene transplantation therapy of inflammatory bowel disease.
炎症性肠病 / IL-10基因 / 腺病毒载体 / 骨髓间充质干细胞 / 大鼠
Inflammatory bowel disease / Interleukin-10 gene / Adenoviral vector / Bone marrow mesenchymal stem cell / Rats
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湖南省卫生厅(B2012-102)。