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Expression of Cytokines in Mouse Hepatitis B Virus X Gene-transfected Model

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【作者】 孙丽芳史川袁璐孙云姚欣欣马婧薇黄春梅朱慧芬雷萍沈关心

【Author】 Li-fang SUN 1,2,Chuan SHI 1,Lu YUAN 1,Yun SUN 3,Xin-xin YAO 1 ,Jing-wei MA 1,Chun-mei HUANG 1,Hui-fen ZHU 1,Ping LEI 1,Guan-xin SHEN 11 Department of Immunology,School of Basic Medical Sciences,Tongji Medical College,Huazhong University of Science and Technology,Wuhan 430030,China 2 Department of Laboratory,3 Department of Neurosurgery,Union Hospital,Tongji Medical College,Huazhong University of Science and Technology,Wuhan 430022,China

【机构】 Department of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Laboratory,Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Neurosurgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

【摘要】 The expression profile in the mouse hepatitis B virus X (HBx)-transfected model was investigated in order to lay a foundation for further study on the implication of cytokines expression in hepatitis B virus (HBV) infection.Hydrodynamic injection method via the tail vein was used to establish the animal HBx-transfected model.By using microassay,the differential expression of gene in each group was analyzed,which was further confirmed by using real-time PCR and semi-quantitative PCR.Most of chemokine genes such as Ccl2,Ccl5,Ccl9,MIG and IP-10 were up-regulated in the HBx-transfected mouse model versus the control mice,which was coincided with the microarray results.Western blotting and immunohistochemistry were applied to detect the expression of MIG and IP-10 in the liver tissues.Simultaneously,ELISA was adopted to measure the content of IFN-γ in the liver tissues.DNA microassay revealed that the expression of 611 genes changed in HBx-transfected mice as compared with that in pCMV-tag2B-transfected mice,and most of the screened chemokines were up-regulated (including MIG and IP-10).Additionally,IFN-γ protein levels were increased by 20.7% (P<0.05) in pCMV-tag2B-HBx-transfected mice as compared with the untreated mice.IFN-γ protein levels were reduced by 53.9% (P<0.05) in pCMV-tag2B-transfected mice as compared with the untreated mice,which was consistent with the up-regulation of MIG and IP-10.It was suggested HBx transfection could induce the expression of MIG and IP-10 in the liver tissues,which might play the roles in HBV-related liver immunity and cytokines-mediated antiviral effect.

【Abstract】 The expression profile in the mouse hepatitis B virus X (HBx)-transfected model was investigated in order to lay a foundation for further study on the implication of cytokines expression in hepatitis B virus (HBV) infection.Hydrodynamic injection method via the tail vein was used to establish the animal HBx-transfected model.By using microassay,the differential expression of gene in each group was analyzed,which was further confirmed by using real-time PCR and semi-quantitative PCR.Most of chemokine genes such as Ccl2,Ccl5,Ccl9,MIG and IP-10 were up-regulated in the HBx-transfected mouse model versus the control mice,which was coincided with the microarray results.Western blotting and immunohistochemistry were applied to detect the expression of MIG and IP-10 in the liver tissues.Simultaneously,ELISA was adopted to measure the content of IFN-γ in the liver tissues.DNA microassay revealed that the expression of 611 genes changed in HBx-transfected mice as compared with that in pCMV-tag2B-transfected mice,and most of the screened chemokines were up-regulated (including MIG and IP-10).Additionally,IFN-γ protein levels were increased by 20.7% (P<0.05) in pCMV-tag2B-HBx-transfected mice as compared with the untreated mice.IFN-γ protein levels were reduced by 53.9% (P<0.05) in pCMV-tag2B-transfected mice as compared with the untreated mice,which was consistent with the up-regulation of MIG and IP-10.It was suggested HBx transfection could induce the expression of MIG and IP-10 in the liver tissues,which might play the roles in HBV-related liver immunity and cytokines-mediated antiviral effect.

【基金】 supported by grants from Program for Changjiang Scholars and Innovative Research Team in University(No.IRT1131);State Project on Major Infectious Diseases Prevention Grant(No.2012ZX10002006-003)
  • 【文献出处】 Journal of Huazhong University of Science and Technology(Medical Sciences) ,华中科技大学学报(医学英德文版) , 编辑部邮箱 ,2013年02期
  • 【分类号】R512.62
  • 【下载频次】26
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