Protective effect of cotransfection of A20 and HO-1 gene against the apoptosis induced by TNF-α in rat islets in vitro

OBJECTIVE: To establish the method for cotransferring human A20 gene and human heme oxygenase-1 (HO-1) gene into the isolated rat islets using lentiviral transfection system, and to study the protective effect of A20 and HO-1 protein against the apoptosis induced by cycloheximide (CHX) and TNF-α, an...

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Veröffentlicht in:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 51(2013), 6 vom: 30. Juni, Seite 420-5
1. Verfasser: Lu, Zhong (VerfasserIn)
Weitere Verfasser: Shen, Shui-xian, Zhi, Di-jing, Xu, Hong, Guo, Li-he, Luo, Fei-hong
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:Journal Article Research Support, Non-U.S. Gov't DNA-Binding Proteins Insulin Intracellular Signaling Peptides and Proteins Nuclear Proteins Tumor Necrosis Factor-alpha HMOX1 protein, human EC 1.14.14.18 Heme Oxygenase-1 mehr... TNFAIP3 protein, human EC 3.4.19.12 Tumor Necrosis Factor alpha-Induced Protein 3 Caspase 3 EC 3.4.22.-
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100 1 |a Lu, Zhong  |e verfasserin  |4 aut 
245 1 0 |a Protective effect of cotransfection of A20 and HO-1 gene against the apoptosis induced by TNF-α in rat islets in vitro 
264 1 |c 2013 
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500 |a Date Completed 10.03.2014 
500 |a Date Revised 25.11.2016 
500 |a published: Print 
500 |a Citation Status MEDLINE 
520 |a OBJECTIVE: To establish the method for cotransferring human A20 gene and human heme oxygenase-1 (HO-1) gene into the isolated rat islets using lentiviral transfection system, and to study the protective effect of A20 and HO-1 protein against the apoptosis induced by cycloheximide (CHX) and TNF-α, and finally to explore the underlying mechanism 
520 |a METHOD: The A20 gene and HO-1 gene were cloned and inserted into the lentiviral transfection system. The efficacy of gene transfer was measured by the intensity of the enhanced green fluorescent protein (EGFP) fluorescence-positive islets. Western blot was applied to verify the expression of the A20 and HO-1 genes. To induce apoptosis in vitro, the isolated islets were treated with CHX+TNF-α, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and the fluorescence-activated cell sorting (FACS) methods were used to evaluate the apoptosis of the islet cells and Western blot was used to detect caspase-3 activation 
520 |a RESULT: (1) A20 and HO-1 genes were introduced into the isolated islets by lentiviral transfection, both of the genes were highly expressed in the islets after 96 hours culture detected by Western blot method. (2) The insulin levels in the cell culture medium from A20 and/or HO-1 transgenic islets were significantly higher than that in non-transgenic controls (P < 0.01). (3)After CHX + TNF-alpha treatment, the cell culture medium insulin concentration in the A20 gene transfected group [(93.58 ± 4.12)µg/ml], HO-1 gene transfected group [(88.98 ± 4.77) µg/ml ] and A20/HO-1 co-transfected group [(103.33 ± 3.16) µg/ml] were significantly higher than that in the EGFP group [(9.03 ± 0.65) µg/ml ] and the control group [(8.86 ± 0.38) µg/ml] (P < 0.001). Minimum expression level of the activated caspase-3 was found in the A20/HO-1 co-transfected group 
520 |a CONCLUSION: The lentiviral gene transfer system was an efficient and stable gene transfer vector, the over-expressed A20 and HO-1 protein delivered via lentivirus could preserve rats' islets function and act against the apoptosis induced by CHX and TNF-α 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a DNA-Binding Proteins  |2 NLM 
650 7 |a Insulin  |2 NLM 
650 7 |a Intracellular Signaling Peptides and Proteins  |2 NLM 
650 7 |a Nuclear Proteins  |2 NLM 
650 7 |a Tumor Necrosis Factor-alpha  |2 NLM 
650 7 |a HMOX1 protein, human  |2 NLM 
650 7 |a EC 1.14.14.18  |2 NLM 
650 7 |a Heme Oxygenase-1  |2 NLM 
650 7 |a EC 1.14.14.18  |2 NLM 
650 7 |a TNFAIP3 protein, human  |2 NLM 
650 7 |a EC 3.4.19.12  |2 NLM 
650 7 |a Tumor Necrosis Factor alpha-Induced Protein 3  |2 NLM 
650 7 |a EC 3.4.19.12  |2 NLM 
650 7 |a Caspase 3  |2 NLM 
650 7 |a EC 3.4.22.-  |2 NLM 
700 1 |a Shen, Shui-xian  |e verfasserin  |4 aut 
700 1 |a Zhi, Di-jing  |e verfasserin  |4 aut 
700 1 |a Xu, Hong  |e verfasserin  |4 aut 
700 1 |a Guo, Li-he  |e verfasserin  |4 aut 
700 1 |a Luo, Fei-hong  |e verfasserin  |4 aut 
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