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Journal of Virology, September 1998, p. 7669-7675, Vol. 72, No. 9
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Caspase Activation and Specific Cleavage of
Substrates after Coxsackievirus B3-Induced Cytopathic Effect in
HeLa Cells
Christopher M.
Carthy,1
David J.
Granville,1,2
Kathleen A.
Watson,1
Daniel R.
Anderson,1,3
Janet E.
Wilson,1
Decheng
Yang,1
David W. C.
Hunt,1,2 and
Bruce M.
McManus1,*
Department of Pathology and Laboratory
Medicine, University of British Columbia
St. Paul's
Hospital,1 and
QLT PhotoTherapeutics
Inc.,2 Vancouver, British Columbia, Canada, and
Department of Pathology and Microbiology, University of
Nebraska Medical Center, Omaha, Nebraska3
Received 9 January 1998/Accepted 21 May 1998
Coxsackievirus B3 (CVB3), an enterovirus in the family
Picornaviridae, induces cytopathic changes in cell culture
systems and directly injures multiple susceptible organs and tissues in vivo, including the myocardium, early after infection. Biochemical analysis of the cell death pathway in CVB3-infected HeLa cells demonstrated that the 32-kDa proform of caspase 3 is cleaved subsequent to the degenerative morphological changes seen in infected HeLa cells.
Caspase activation assays confirm that the cleaved caspase 3 is
proteolytically active. The caspase 3 substrates poly(ADP-ribose) polymerase, a DNA repair enzyme, and DNA fragmentation factor, a
cytoplasmic inhibitor of an endonuclease responsible for DNA fragmentation, were degraded at 9 h following infection, yielding their characteristic cleavage fragments. Inhibition of caspase activation by benzyloxycarbonyl-Val-Ala-Asp-fluoromethylketone (ZVAD.fmk) did not inhibit the virus-induced cytopathic effect, while
inhibition of caspase activation by ZVAD.fmk in control apoptotic cells
induced by treatment with the porphyrin photosensitizer benzoporphyrin
derivative monoacid ring A and visible light inhibited the apoptotic
phenotype. Caspase activation and cleavage of substrates may not be
responsible for the characteristic cytopathic effect produced by
picornavirus infection yet may be related to late-stage alterations of
cellular homeostatic processes and structural integrity.
*
Corresponding author. Mailing address: Department of
Pathology and Laboratory Medicine, Cardiovascular Research Laboratory, University of British Columbia, St. Paul's Hospital, 1081 Burrard St.,
Vancouver, B.C., Canada V6Z 1Y6. Phone: (604) 631-5200. Fax: (604)
631-5208. E-mail: mcmanus{at}unixg.ubc.ca.
Journal of Virology, September 1998, p. 7669-7675, Vol. 72, No. 9
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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