Construction of the adenovirus expressing NF-κB SiRNA in rats and its effect on Kupffer cells reaction to LPS
Feixiang Wu, Xin Luan, Yuming Sun
Abstract
Feixiang Wu, Xin Luan, Yuming Sun
Abstract
Objective To construct the incompetent-replication adenovirus expressing NF-κB siRNA in rats and identify its effect on Kupffer cells reaction to lipopolysaccharide (LPS) in vitro. Meth-ods The complementary DNA containing both sense and antisense Oligo DNA of the targeting sequence was cloned into the pShuttleHl vector. Linearized pShuttleH1-siNF-κB of 0. 5 μg was transformed into E. coli BJ5183 cells containing backbone plasmid pAdEasy-1 by electroporation. The recombinant plasmid of 4 μg was transfected into 293 cells to package the adenovirus Ad-siNF-κB. The titers of adenovirus were determined using the specific 50% tissue culture infection dosage (TCID50) method. After virus infected the cultured Kupffer cells with MOI = 10, the effect on LPS-induced NF-κB mRNA and TNF-α, IL-6 ex-pression was observed. Results It was identified that the sequence of gene was correctly inserted into the genome of virus. The titer of recombinant adenovirus was 5.32×109 pfu/ml. NF-κB mRNA and TNF-α, IL-6 expression was greatly reduced after virus infection. Conclusion The recombinant adenovirus ex-pressing NF-κB siRNA in rats were successfully constructed, which probably can be further used in re-search on anti-inflammation effect in vivo. Key words: NF-κB; RNA interference ; Adenovirus ; Tumor necrosis faetor-α; Kupffer cells
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Objective To construct the incompetent-replication adenovirus expressing NF-κB siRNA in rats and identify its effect on Kupffer cells reaction to lipopolysaccharide (LPS) in vitro. Meth-ods The complementary DNA containing both sense and antisense Oligo DNA of the targeting sequence was cloned into the pShuttleHl vector. Linearized pShuttleH1-siNF-κB of 0. 5 μg was transformed into E. coli BJ5183 cells containing backbone plasmid pAdEasy-1 by electroporation. The recombinant plasmid of 4 μg was transfected into 293 cells to package the adenovirus Ad-siNF-κB. The titers of adenovirus were determined using the specific 50% tissue culture infection dosage (TCID50) method. After virus infected the cultured Kupffer cells with MOI = 10, the effect on LPS-induced NF-κB mRNA and TNF-α, IL-6 ex-pression was observed. Results It was identified that the sequence of gene was correctly inserted into the genome of virus. The titer of recombinant adenovirus was 5.32×109 pfu/ml. NF-κB mRNA and TNF-α, IL-6 expression was greatly reduced after virus infection. Conclusion The recombinant adenovirus ex-pressing NF-κB siRNA in rats were successfully constructed, which probably can be further used in re-search on anti-inflammation effect in vivo. Key words: NF-κB; RNA interference ; Adenovirus ; Tumor necrosis faetor-α; Kupffer cells
Key concepts: Recombinant DNA, Transfection, Molecular biology, Electroporation, Tumor necrosis factor alpha, Biology, Plasmid, Sense (electronics)