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Virus Res ; 104(1): 39-49, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15177891

ABSTRACT

The expression of individual viral genes enables the study of their effects on cellular functions. Our group previously generated stable HeLa cell lines that efficiently express poliovirus proteases 2A (clone 2A7d) and 3C (clone 3C7) under the control of tetracycline [Virology 266 (2000a) 352; J. Virol. 74 (2000b) 2383]. Upon induction of these proteases, the cells undergo drastic morphological alterations and eventually die. The present paper characterizes, in detail, the cellular and molecular events that lead to cell death in these lines. Several signs of apoptosis were observed in both 2A7d- and 3C7-induced cells, such as nuclear fragmentation, DNA breakdown (as determined by TUNEL), and phosphatidylserine translocation. Protease 2A induces the cleavage of poly-ADP-ribose-polymerase (PARP). This is blocked by the caspase-3 inhibitor DEVD in both 2A7d-On and 3C7-On cells suggesting that this enzyme might account for PARP cleavage in both cell lines. The results indicate that both poliovirus proteases induce apoptosis by mechanisms involving caspase activation, although the kinetics of apoptosis differs.


Subject(s)
Caspases/metabolism , Cysteine Endopeptidases/metabolism , Poliovirus/enzymology , Poly(ADP-ribose) Polymerases/metabolism , Viral Proteins/metabolism , 3C Viral Proteases , Caspase Inhibitors , Enzyme Activation/drug effects , Gene Expression , HeLa Cells , Humans , Poliovirus/genetics , Poly(ADP-ribose) Polymerases/genetics , Tetracycline/pharmacology
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