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作 者:邓定浩 肖永乐 唐健雪 杨鑫[1] 高荣[1] DENG Ding-hao;XIAO Yong-le;TANG Jian-xue;YANG Xing;GAO Rong(Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education,Key Laboratory for Animal Disease Prevention and Food Safety of Sichuan Province,College of Life Sciences,Sichuan University,Chengdu 610064,China)
机构地区:[1]四川大学生命科学学院生物资源与生态环境教育部重点实验室动物疫病防控与食品安全四川省重点实验室
出 处:《中国生物工程杂志》2018年第8期10-18,共9页China Biotechnology
基 金:成都市科技攻关项目(2015NY-02-0028-NC);四川省科技项目(2017HH0023,2016RZ0034);科技部国际合作项目(2011DFA10101103)资助项目
摘 要:目的:为真核表达猪白细胞介素17(IL-17),研究产物在细胞培养下的免疫生物活性。方法:通过PCR扩增出猪IL-17基因并插入到真核表达载体p VAX1,然后转染到IPEC-J2细胞、Ha Ca T细胞和L02细胞中。在转染后第24、48和72h收集细胞,第48h收集上清液。收集细胞通过实时荧光定量PCR检测相关免疫基因的表达水平,收集上清液通过抑菌试验检测相关抗菌肽的生物活性。结果:采用p VAX1载体构建了表达猪IL-17的重组质粒,转染到细胞中。证实IL-17基因能诱导抗菌肽基因(RegⅢ、S100A8和BD2)的表达,显著上调JAK-STAT信号通路基因(JAK1、STAT1和STAT3)和细胞因子基因(IL-6、IL-12和TNF-α)的表达。此外,细胞上清液能够在不同程度上抑制大肠杆菌及金黄色葡萄球菌的增殖。结论:成功将猪IL-17基因真核表达,其表达产物能诱导效应细胞表达多种细胞因子,产生多种抗菌肽,具有抑菌能力;这为进一步研发猪IL-17作为抗菌免疫分子制剂奠定了初步基础。Objective: To study porcine interleukin-17( IL-17) eukaryotic expression and their biologic activity. Methods: The IL-17 gene was amplified by PCR and cloned into eukaryotic expression vector p VAX1,named PV17. PV17 was transfected into IPEC-J2 cells,Ha Ca T cells and L02 cells,thereafter the cells were collected on hours 24,48 and 72,the supernatants were collected on hours 48. Related genes expression levels in cells were analysed by qRT-PCR,bioactivity of antimicrobial peptides in supernatants were analyzed by bacteriostatic test in vitro. Results: The eukaryotic expression plasmid of the porcine IL-17 gene was constructed and transfected into the three eukaryotic cells,and could expressed in target cells. The expression levels of antimicrobial peptide genes( RegⅢ,S100 A8 and BD2),JAK-STAT signaling pathway genes( JAK1,STAT1 and STAT3) and cytokine genes( IL-6,IL-12 and TNF-α) were significantly up-regulated. Furthermore,the supernatants have marked bacteriostatic effect on E. coli and S. aureus. Conclusion: The recombinant plasmid of the porcine IL-17 gene was constructed and expressed in target cells,and the expressed products elicited the significant increases of cytokines and antibacterial peptides,which manifested obvious antibacterial activities against E. coli and S. aureus drug-resistant bacteria,and facilitated the further development of porcine IL-17 as the antibacterial reagent.
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