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作 者:Lingyun Li Jing Chi Feng Zhou Dandan Guo Fang Wang Genyan Liu Chun Zhang Kun Yao
机构地区:[1]Department of Microbiology and Immunology,Nanjing Medical University,Nanjing,Jiangsu 210029,China [2]Department of Developmental Genetics,Nanjing Medical University,Nanjing,Jiangsu 210029,China [3]Department of Laboratory Medicine,the First Affiliated Hospital of Nanjing Medical University,Nanjing,Jiangsu 210029,China
出 处:《The Journal of Biomedical Research》2010年第6期444-451,共8页生物医学研究杂志(英文版)
基 金:supported by the National Natural Science Foundationof China (No. 30771961 and No. 30901344);Science Development Foundation of Nanjing Medical University (No. 08NMUZ003);Jiangsu Province Laboratory of Pathogen Biology (No. 08bykf01)
摘 要:Apoptosis plays an important role in the pathogenesis of viral infections.In this study,we investigated the cell death processes during productive HHV-6A infection and the underlying mechanisms.Annexin V-PI staining and electron microscopy indicated that HHV-6A is a strong inducer of apoptosis.HHV-6A infection decreased mitochondrial transmembrane potential and led to morphological changes of mitochondria.The cell death was associated with activation of caspase-3 and cleavage of DNA repair enzyme poly (ADP-ribose) polymerase,which is known to be an important substrate for activated caspase-3.Caspase-9 was activated significantly in HHV-6A-infected cells,whereas caspase-8 was not activated obviously.Moreover,HHV-6A infection upregulated Bax and downregulated Bcl-2.This is the first demonstration of mitochondrion-mediated,caspase-dependent apoptosis in HHV-6A-infected cells.Apoptosis plays an important role in the pathogenesis of viral infections.In this study,we investigated the cell death processes during productive HHV-6A infection and the underlying mechanisms.Annexin V-PI staining and electron microscopy indicated that HHV-6A is a strong inducer of apoptosis.HHV-6A infection decreased mitochondrial transmembrane potential and led to morphological changes of mitochondria.The cell death was associated with activation of caspase-3 and cleavage of DNA repair enzyme poly (ADP-ribose) polymerase,which is known to be an important substrate for activated caspase-3.Caspase-9 was activated significantly in HHV-6A-infected cells,whereas caspase-8 was not activated obviously.Moreover,HHV-6A infection upregulated Bax and downregulated Bcl-2.This is the first demonstration of mitochondrion-mediated,caspase-dependent apoptosis in HHV-6A-infected cells.
关 键 词:human herpesvirus 6 APOPTOSIS CASPASE mitochondrion-mediated
分 类 号:Q255[生物学—细胞生物学] S858.315.3[农业科学—临床兽医学]
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