Oxidative stress in Vero cells infected with vesicular stomatitis virus
Viral-induced apoptosis might be mediated by oxidative stress. It has already been described that cell death in vesicular stomatitis virus (VSV)-infected cells occurs by apoptosis. In this study, oxidative stress parameters present in VSV-infected Vero cells were analyzed. Lipid peroxides (LP) were...
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| Otros Autores: | , , , , |
| Formato: | Capítulo de libro |
| Lenguaje: | Inglés |
| Publicado: |
2006
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| Acceso en línea: | Registro en Scopus DOI Handle Registro en la Biblioteca Digital |
| Aporte de: | Registro referencial: Solicitar el recurso aquí |
| LEADER | 09348caa a22010697a 4500 | ||
|---|---|---|---|
| 001 | PAPER-21779 | ||
| 003 | AR-BaUEN | ||
| 005 | 20230518205316.0 | ||
| 008 | 190411s2006 xx ||||fo|||| 00| 0 eng|d | ||
| 024 | 7 | |2 scopus |a 2-s2.0-33747263864 | |
| 024 | 7 | |2 cas |a caspase 3, 169592-56-7; guaiacol, 26638-03-9, 28930-19-0, 90-05-1; superoxide dismutase, 37294-21-6, 9016-01-7, 9054-89-1; Lipid Peroxides; Superoxide Dismutase, EC 1.15.1.1 | |
| 040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
| 030 | |a IVRYA | ||
| 100 | 1 | |a Riva, D.A. | |
| 245 | 1 | 0 | |a Oxidative stress in Vero cells infected with vesicular stomatitis virus |
| 260 | |c 2006 | ||
| 270 | 1 | 0 | |m Riva, D.A.; Department of Biochemistry, School of Science, UBA, 1428 Buenos Aires, Argentina; email: diegor@qb.fcen.uba.ar |
| 506 | |2 openaire |e Política editorial | ||
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| 504 | |a Hobbs, J.A., Schloemer, R.H., Hommel-Berry, G., Brahmi, Z., Caspase-3-like proteases are activated by infection but are not required for replication of vesicular stomatitis virus (2001) Virus Res, 80, pp. 53-65 | ||
| 504 | |a Kopecky, S.A., Willingham, M.C., Lyles, D.S., Matrix protein and another viral component contribute to induction of apoptosis in cells infected with vesicular stomatitis virus (2001) J Virol, 75, pp. 12169-12181 | ||
| 504 | |a Knobil, K., Choi, A.M.K., Weigand, G.W., Jacoby, D.B., Role of oxidants in influenza virus-induced gene expression (1998) Am J Physiol, 274, pp. L134-L142 | ||
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| 504 | |a Lepage, G., Roy, C.C., Improved recovery of fatty acid through direct transesterification without prior extraction or purification (1984) J Lipid Res, 25, pp. 1391-1396 | ||
| 504 | |a Okamoto, O.K., Pinto, E., Latorre, L.R., Bechara, E.J., Colepicolo, P., Antioxidant modulation in response to metal-induced oxidative stress in algal chloroplasts (2001) Arch Environ Contam Toxicol, 40, pp. 18-24 | ||
| 504 | |a Misra, H.P., Fridovich, I., The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase (1972) J Biol Chem, 247, pp. 3170-3175 | ||
| 504 | |a Liao, S.L., Raung, S.L., Chen, C.J., Japanese encephalitis virus stimulates superoxide dismutase activity in rat glial cultures (2002) Neurosci Lett, 324, pp. 133-136 | ||
| 504 | |a Santoro, M.G., Heat shock factors and the control of stress response (2000) Biochem Pharmacol, 59, pp. 55-63 | ||
| 504 | |a Prosniak, M., Hooper, D.C., Dietzschold, B., Koprowski, H., Effect of rabies virus infection on gene expression in mouse brain (2001) Proc Natl Acad Sci, 98, pp. 2758-2763. , USA | ||
| 504 | |a Yu, R., Tan, T.H., Kong, A.T., Butylated hydroxianisole and its metabolite tert-butylhydroquinone differentially regulate mitogen-activated protein kinases (1997) J Biol Chem, 272, pp. 28962-28970 | ||
| 504 | |a Denizot, F., Lang, R., Rapid colorimetric assay for cell growth and survival: Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability (1986) J Inmunol Methods, 89, pp. 271-277 | ||
| 504 | |a Manchester, M., Lisewski, M.K., Atkinson, J.P., Oldstone, M.B., Multiple isoforms of CD46 (membrane cofactor protein) serve as receptors for measles virus (1994) Proc Natl Acad Sci, 91, pp. 2161-2165. , USA | ||
| 504 | |a Pica, F., De Marco, A., De Cesare, F., Santoro, M.G., Inhibition of vesicular stomatitis virus replication by delta 12-protaglandin J2 is regulated at two separate levels and is associated with induction of stress protein synthesis (1993) Antiviral Res, 20, pp. 193-208 | ||
| 504 | |a Gawn, J.M., Greaves, R.F., Absence of IE1 p72 protein function during low-multiplicity infection by human cytomegalovirus results in a broad block to viral delayed-early gene expression (2002) J Virol, 76, pp. 4441-4455 | ||
| 504 | |a Alimonti, J.B., Ball, T.B., Fowke, K.R., Mechanisms of CD4+ T lymphocyte cell death in human immunodeficiency virus infection and AIDS (2003) J Gen Virol, 84, pp. 1649-1661 | ||
| 520 | 3 | |a Viral-induced apoptosis might be mediated by oxidative stress. It has already been described that cell death in vesicular stomatitis virus (VSV)-infected cells occurs by apoptosis. In this study, oxidative stress parameters present in VSV-infected Vero cells were analyzed. Lipid peroxides (LP) were evaluated in cellular extracts and expressed as thiobarbituric acid-reactive substances. LP levels exhibited a rise at different times post infection, according to the multiplicity of infection (MOI), while the presence of cycloheximide determined a reduction on LP. Also, an increase in protein degradation products and a decrease in polyunsaturated fatty acids content was observed, indicating that cellular proteins and lipids began to be susceptible to degradation during VSV infection. In addition, we analyzed cell viability of VSV-infected Vero cells, which were incubated in the presence of butylated hydroxyanisole. This antioxidant was able to protect Vero cells, at least at MOIs assayed in this study, and to reduce viral yield only when VSV infection was done at MOI 0.05. Further, superoxide dismutases, which occupy the first step within the antioxidant enzyme cascade, also exhibit a rise in VSV-infected Vero cells, at different MOI. These results suggest that both an oxidative stress and an antioxidative cell response precede the induction of apoptosis by VSV. Copyright © 2006 S. Karger AG. |l eng | |
| 593 | |a Laboratory of Virology, School of Science, University of Buenos Aires, Buenos Aires, Argentina | ||
| 593 | |a Department of Biochemistry, School of Science, University of Buenos Aires, Buenos Aires, Argentina | ||
| 593 | |a Department of Biochemistry, School of Science, UBA, 1428 Buenos Aires, Argentina | ||
| 690 | 1 | 0 | |a LIPID PEROXIDATION |
| 690 | 1 | 0 | |a SUPEROXIDE DISMUTASE |
| 690 | 1 | 0 | |a VESICULAR STOMATITIS VIRUS |
| 690 | 1 | 0 | |a ANTIOXIDANT |
| 690 | 1 | 0 | |a CASPASE 3 |
| 690 | 1 | 0 | |a CELL PROTEIN |
| 690 | 1 | 0 | |a GUAIACOL |
| 690 | 1 | 0 | |a SUPEROXIDE DISMUTASE |
| 690 | 1 | 0 | |a ANIMAL CELL |
| 690 | 1 | 0 | |a APOPTOSIS |
| 690 | 1 | 0 | |a ARTICLE |
| 690 | 1 | 0 | |a CELL DEATH |
| 690 | 1 | 0 | |a CELL VIABILITY |
| 690 | 1 | 0 | |a ENZYME ACTIVITY |
| 690 | 1 | 0 | |a GENETIC SUSCEPTIBILITY |
| 690 | 1 | 0 | |a LIPID PEROXIDATION |
| 690 | 1 | 0 | |a NONHUMAN |
| 690 | 1 | 0 | |a OXIDATIVE STRESS |
| 690 | 1 | 0 | |a PRIORITY JOURNAL |
| 690 | 1 | 0 | |a PROTEIN DEGRADATION |
| 690 | 1 | 0 | |a PROTEIN LIPID INTERACTION |
| 690 | 1 | 0 | |a VERO CELL |
| 690 | 1 | 0 | |a VESICULAR STOMATITIS VIRUS |
| 690 | 1 | 0 | |a VIRUS INFECTION |
| 690 | 1 | 0 | |a ANIMALS |
| 690 | 1 | 0 | |a CERCOPITHECUS AETHIOPS |
| 690 | 1 | 0 | |a LIPID PEROXIDES |
| 690 | 1 | 0 | |a OXIDATIVE STRESS |
| 690 | 1 | 0 | |a RHABDOVIRIDAE INFECTIONS |
| 690 | 1 | 0 | |a SUPEROXIDE DISMUTASE |
| 690 | 1 | 0 | |a TIME FACTORS |
| 690 | 1 | 0 | |a VERO CELLS |
| 690 | 1 | 0 | |a VESICULAR STOMATITIS-INDIANA VIRUS |
| 690 | 1 | 0 | |a VESICULAR STOMATITIS VIRUS |
| 700 | 1 | |a Ríos De Molina, M.C. | |
| 700 | 1 | |a Rocchetta, I. | |
| 700 | 1 | |a Gerhardt, E. | |
| 700 | 1 | |a Coulombié, F.C. | |
| 700 | 1 | |a Mersich, S.E. | |
| 773 | 0 | |d 2006 |g v. 49 |h pp. 294-298 |k n. 5 |p Intervirology |x 03005526 |w (AR-BaUEN)CENRE-2711 |t Intervirology | |
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