Effects of RNA interference on expression of tumor necrosis factor-α in lipopolysaccahride-activated mouse macrophages
DU Yan-le
Abstract
DU Yan-le
Abstract
Objective To investigate the effects of siRNAs targeting mouse tumor necrosis factor (TNF)-α gene on the expression of TNF-α mRNA and protein in the LPS activated macrophages.Methods Mouse macrophages of the line RAW264.7 were cultured.Three siRNA sequences targeting different sites of mouse TNF-α gene(siRNA 1-3)and a fluorescein-labeled double-stranded RNA(dsRNA)oligomer (siRNA 4),as negative control,were designed and chemically synthesized.All siRNAs were transfected into the mouse macrophages.0,3,6,9,12,15,and 18 hours after the transfection samples of supernatant were collected.Inverse microscopy was used to observe the efficacy of transfection.Then the microphages were co-incubated with LPS for 9 hours.Macrophages stimulated by LPS only and macrophages without transfection and LPS stimulation were used as controls.Then samples of supernatant were collected.TNF-α protein expression was detected by ELISA.Real time PCR was used to detect the TNF-α mRNA expression. Results The transfection rate was 72%-80%.The TNF-α mRNA expression levels of the LPS+siRNA2 and LPS+siRNA3 groups were 0.158±0.031 and 0.114±0.028 respectively,both significantly lower than that of the LPS control group(0.294±0.147,P0.05 and P0.01 respectively),however,the TNF- αmRNA expression level of the LPS+siRNA1 and LPS+siRNA4 groups were not significantly different from that of the LPS control group.The TNF-αmRNA expression inhibition rates of the LPS+siRNA and LPS+ siRNA3 groups were 46.0% and 61.2% respectively.The TNF-α protein expression levels of the LPS+ siRNA2 and LPS+siRNA3 group were(1358±348)pg/ml and(817±138)pg/ml,both significantly lower than that of the LPS control group[(2104±32)pg/ml,P0.05 and P0.01],and the TNF-α mRNA expression levels of the LPS+siRNA1 and LPS+siRNA4 groups were not significantly different from that of the LPS control group.Conclusion LPS time-dependently increases the expression of TNF-α in macrophages.SiRNAs targeting TNF-α inhibit the expression levels of TNF-α mRNA and protein in macrophages treated with LPS.
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Objective To investigate the effects of siRNAs targeting mouse tumor necrosis factor (TNF)-α gene on the expression of TNF-α mRNA and protein in the LPS activated macrophages.Methods Mouse macrophages of the line RAW264.7 were cultured.Three siRNA sequences targeting different sites of mouse TNF-α gene(siRNA 1-3)and a fluorescein-labeled double-stranded RNA(dsRNA)oligomer (siRNA 4),as negative control,were designed and chemically synthesized.All siRNAs were transfected into the mouse macrophages.0,3,6,9,12,15,and 18 hours after the transfection samples of supernatant were collected.Inverse microscopy was used to observe the efficacy of transfection.Then the microphages were co-incubated with LPS for 9 hours.Macrophages stimulated by LPS only and macrophages without transfection and LPS stimulation were used as controls.Then samples of supernatant were collected.TNF-α protein expression was detected by ELISA.Real time PCR was used to detect the TNF-α mRNA expression. Results The transfection rate was 72%-80%.The TNF-α mRNA expression levels of the LPS+siRNA2 and LPS+siRNA3 groups were 0.158±0.031 and 0.114±0.028 respectively,both significantly lower than that of the LPS control group(0.294±0.147,P0.05 and P0.01 respectively),however,the TNF- αmRNA expression level of the LPS+siRNA1 and LPS+siRNA4 groups were not significantly different from that of the LPS control group.The TNF-αmRNA expression inhibition rates of the LPS+siRNA and LPS+ siRNA3 groups were 46.0% and 61.2% respectively.The TNF-α protein expression levels of the LPS+ siRNA2 and LPS+siRNA3 group were(1358±348)pg/ml and(817±138)pg/ml,both significantly lower than that of the LPS control group[(2104±32)pg/ml,P0.05 and P0.01],and the TNF-α mRNA expression levels of the LPS+siRNA1 and LPS+siRNA4 groups were not significantly different from that of the LPS control group.Conclusion LPS time-dependently increases the expression of TNF-α in macrophages.SiRNAs targeting TNF-α inhibit the expression levels of TNF-α mRNA and protein in macrophages treated with LPS.
Key concepts: Small interfering RNA, Transfection, Tumor necrosis factor alpha, Molecular biology, Messenger RNA, RNA interference, Gene silencing, Gene expression