Comparison of control of Listeria by nitric oxide redox chemistry from murine macrophages and no donors: Insights into listeriocidal activity of oxidative and nitrosative stress (688 views)
Free Radic Biol Med (ISSN: 0891-5849, 0891-5849linking, 1873-4596electronic), 2001 Feb 1; 30(3): 268-276.
Export to BibTeX Export to EndNote
Paper type: Journal Article,
Impact factor: 5.082, 5-year impact factor: 5.983
Url: http://www.scopus.com/inward/record.url?eid=2-s2.0-0035252335&partnerID=40&md5=bbb99f2c05823ff09e0d838ab6de7b11
Keywords: Free Radicals, Listeria, Nitrosation Stress, Gamma Interferon, Hypoxanthine, Lipopolysaccharide, Nitric Oxide, Nitric Oxide Donor, Reactive Oxygen Metabolite, Tumor Necrosis Factor Alpha, Virulence Factor, Xanthine Oxidase, Animal Cell, Animal Experiment, Animal Model, Article, Bacterial Growth, Bactericidal Activity, Cell Stimulation, Chemical Reaction, Concentration Response, Controlled Study, Cytostasis, Listeria Monocytogenes, Listeriosis, Macrophage, Mouse, Nonhuman, Oxidation Reduction Reaction, Oxidative Stress, Priority Journal, Survival, 2-Naphthylamine, Cell Line, Hydrazines, Interferon Type Ii, Knockout, Nitric Oxide Synthase, Nitric Oxide Synthase Type Ii, Nitrites, Oxidation-Reduction, Reactive Oxygen Species, Tumor Necrosis Factor-Alpha, Murinae,
Affiliations:
*** IBB - CNR ***
Radiation Biology Branch, National Cancer Institute, Bethesda, MD, United States
Department of Immunology, Uniform Services Health Science University, Bethesda, MD, United States
References:
Nathan, C.F., Hibbs J.B., Jr., Role of nitric oxide synthesis in macrophage antimicrobial activity (1991) Curr. Opin. Immunol., 3, pp. 65-7
Fang, F.C., Perspectives series: Host/pathogen interactions. Mechanisms of nitric oxide-related antimicrobial activity (1997) J. Clin. Invest., 99, pp. 2818-2825
Reiss, C.S., Komatsu, T., Does nitric oxide play a role in viral infections? (1998) J. Virol., 72, pp. 4547-4551
Bogdan, C., Of microbes, macrophages and nitric oxide (1997) Behring Inst. Mitt., 99, pp. 58-72
Granger, D.L., Hibbs J.B., Jr., High-output nitric oxide: Weapon against infection? (1996) Trends Microbiol., 4, pp. 46-47
Pacelli, R., Wink, D.A., Cook, J.A., Krishna, M.C., DeGraff, W., Friedman, N., Tsokos, M., Mitchell, J.B., Nitric oxide potentiates hydrogen peroxide-induced killing of Escherichia coli (1995) J. Exp. Med., 182, pp. 1469-1479
Kaplan, S.S., Lancaster, J.R., Basford, R.E., Simmons, R.L., Effect of nitric oxide on staphylococcal killing and interactive effect with superoxide (1996) Infect. Immun., 64, pp. 69-76
Godfrey, R.W., Wilder, M.S., Relationships between oxidative metabolism, macrophage activation, and antilisterial activity (1984) J. Leukoc. Biol., 36, pp. 533-543
Beckerman, K.P., Rogers, H.W., Corbett, J.A., Schreiber, R.D., McDaniel, M.L., Unanue, E.R., Release of nitric oxide during the T cell-independent pathway of macrophage activation. Its role in resistance to Listeria monocytogenes (1993) J. Immunol., 150, pp. 888-895
Boockvar, K.S., Granger, D.L., Poston, R.M., Maybodi, M., Washington, M.K., Hibbs J.B., Jr., Kurlander, R.L., Nitric oxide produced during murine listeriosis is protective (1994) Infect. Immun., 62, pp. 1089-1100
Gregory, S.H., Wing, E.J., Hoffman, R.A., Simmons, R.L., Reactive nitrogen intermediates suppress the primary immunologic response to Listeria (1993) J. Immunol., 150, pp. 2901-2909
Shiloh, M.U., MacMicking, J.D., Nicholson, S., Brause, J.E., Potter, S., Marino, M., Fang, F.C., Nathan, C., Phenotype of mice and macrophages deficient in both phagocyte oxidase and inducible nitric oxide synthase (1999) Immunity, 10, pp. 29-38
Kaufmann, S.H., Immunity to intracellular bacteria (1993) Annu. Rev. Immunol., 11, pp. 129-163
Portnoy, D.A., Schreiber, R.D., Connelly, P., Tilney, L.G., Gamma interferon limits access of Listeria monocytogenes to the macrophage cytoplasm (1989) J. Exp. Med., 170, pp. 2141-2146
Conlan, J.W., North, R.J., Neutrophil-mediated dissolution of infected host cells as a defense strategy against a facultative intracellular bacterium (1991) J. Exp. Med., 174, pp. 741-744
Dunn, P.L., North, R.J., Early gamma interferon production by natural killer cells is important in defense against murine listeriosis (1991) Infect. Immun., 59, pp. 2892-2900
Harty, J.T., Bevan, M., Specific immunity to Listeria monocytogenes in the absence of IFN gamma (1995) Immunity, 3, pp. 109-117
Kaufmann, S.H., Ladel, C.H., Role of T cell subsets in immunity against intracellular infections of knockout mice with Listeria monocytogenes, and Mycobacterium bovis BCG (1994) Immunobiology, 191, pp. 509-516
Maragos, C.M., Morley, D., Wink, D.A., Dunams, T.M., Saavedra, J.E., Hoffman, A., Bove, A.A., Keefer, L.K., Complexes of NO with nucleophiles as agents for the controlled biological release of nitric oxide. Vasorelaxant effects (1991) J. Med. Chem., 34, pp. 3242-3247
Hrabie, J., Klose, J., Wink, D.A., Keefer, L.K., New nitric oxide-releasing zwitterion derived polyamines (1993) J. Org. Chem., 58, pp. 1472-1476
Fridovich, I., Xanthine oxidase , pp. 213-215. , Greenwald, R. A., ed. Handbook of methods for oxygen radical research. Boca Raton, FL: CRC PressBergmeyer, H.U., (1985) Methods in enzymatic analysis (2nd ed.), 1, pp. 521-522. , Deerfield Beach, FL: Verlag Chemie Int
Cox, G.W., Mathieson, B.J., Gandino, L., Blasi, E., Radzioch, D., Varesio, L., Heterogeneity of hematopoietic cells immortalized by v-myc/v-raf recombinant retrovirus infection of bone marrow or fetal liver (1989) J. Natl. Cancer Inst., 81, pp. 1492-1496
Miles, A.M., Wink, D.A., Cook, J.C., Grisham, M.B., Determination of nitric oxide using fluorescence spectroscopy (1996) Methods Enzymol, 268, pp. 105-120
Mocci, S., Dalrymple, S.A., Nishinakamura, R., Murray, R., The cytokine stew and innate resistance to L. monocytogenes (1997) Immunol. Rev., 158, pp. 107-114
Samsom, J.N., Langermans, J.A., Groeneveld, P.H., Van Furth, R., Acquired resistance against a secondary infection with Listeria monocytogenes in mice is not dependent on reactive nitrogen intermediates (1996) Infect. Immun., 64, pp. 1197-1202
Leenen, P.J., Canono, B.P., Drevets, D.A., Voerman, J.S., Campbell, P.A., TNF-alpha and IFN-gamma stimulate a macrophage precursor cell line to kill Listeria monocytogenes in a nitric oxide-independent manner (1994) J. Immunol., 153, pp. 5141-5147
Ohya, S., Tanabe, Y., Makino, M., Nomura, T., Xiong, H., Arakawa, M., Mitsuyama, M., The contributions of reactive oxygen intermediates and reactive nitrogen intermediates to listericidal mechanisms differ in macrophages activated pre- and postinfection (1998) Infect. Immun., 66, pp. 4043-4049
Endres, R., Luz, A., Schulze, H., Neubauer, H., Futterer, A., Holland, S.M., Wagner, H., Pfeffer, K., Listeriosis in p47(phox-/-) and TRp55-/- mice: Protection despite absence of ROI and susceptibility despite presence of RNI (1997) Immunity, 7, pp. 419-432
Dai, W.J., Bartens, W., Kohler, G., Hufnagel, M., Kopf, M., Brombacher, F., Impaired macrophage listericidal and cytokine activities are responsible for the rapid death of Listeria monocytogenes-infected IFN-gamma receptor-deficient mice (1997) J. Immunol., 158, pp. 5297-5304
Miles, A.M., Gibson, M., Krishna, M., Cook, J.C., Pacelli, R., Wink, D.A., Grisham, M.B., Effects of superoxide on nitric oxide-dependent N-nitrosation reactions (1995) Free Radic. Res., 23, pp. 379-390
Gaston, B., Nitric oxide and thiol groups (1999) Biochim. Biophys. Acta., 1411, pp. 323-333
Vodovotz, Y., Chesler, L., Chong, H., Kim, S.J., Simpson, J.T., DeGraff, W., Cox, G.W., Barcellos-Hoff, M.H., Regulation of transforming growth factor beta1 by nitric oxide (1999) Cancer Res., 59, pp. 2142-2149
Wink, D.A., Mitchell, J.B., Chemical biology of nitric oxide: Insights into regulatory, cytotoxic, and cytoprotective mechanisms of nitric oxide (1998) Free Radic. Biol. Med., 25, pp. 434-456
Persichini, T., Colasanti, M., Lauro, G.M., Ascenzi, P., Cysteine nitrosylation inactivates the HIV-1 protease (1998) Biochem. Biophys. Res. Commun., 250, pp. 575-576
Gergel, D., Cederbaum, A.I., Inhibition of the catalytic activity of alcohol dehydrogenase by nitric oxide is associated with S nitrosylation and the release of zinc (1996) Biochemistry, 35, pp. 16186-16194
Braun, J.S., Novak, R., Gao, G., Murray, P.J., Shenep, J.L., Pneumolysin, a protein toxin of Streptococcus pneumoniae, induces nitric oxide production from macrophages (1999) Infect. Immun., 67, pp. 3750-3756
Welch, R.A., Pore-forming cytolysins of gram-negative bacteria (1991) Mol. Microbiol., 5, pp. 521-528
Murray, H.W., Nathan, C.F., Macrophage microbicidal mechanisms in vivo: Reactive nitrogen versus oxygen intermediates in the killing of intracellular Leishmania donovani (1999) J. Exp. Med., 189, pp. 741-746
Prada, J., Muller, S., Bienzle, U., Kremsner, P.G., Upregulation of reactive oxygen and nitrogen intermediates in Plasmodium berghei infected mice after rescue therapy with chloroquine or artemether (1996) J. Antimicrob. Chemother., 38, pp. 95-102
Karupiah, G., Xie, Q.W., Buller, R.M., Nathan, C., Duarte, C., MacMicking, J.D., Inhibition of viral replication by interferon-gamma-induced nitric oxide synthase (1993) Science, 261, pp. 1445-1448
Nathan, C. F., Hibbs J. B., Jr., Role of nitric oxide synthesis in macrophage antimicrobial activity (1991) Curr. Opin. Immunol., 3, pp. 65-7
Fang, F. C., Perspectives series: Host/pathogen interactions. Mechanisms of nitric oxide-related antimicrobial activity (1997) J. Clin. Invest., 99, pp. 2818-2825
Reiss, C. S., Komatsu, T., Does nitric oxide play a role in viral infections? (1998) J. Virol., 72, pp. 4547-4551
Granger, D. L., Hibbs J. B., Jr., High-output nitric oxide: Weapon against infection? (1996) Trends Microbiol., 4, pp. 46-47
Kaplan, S. S., Lancaster, J. R., Basford, R. E., Simmons, R. L., Effect of nitric oxide on staphylococcal killing and interactive effect with superoxide (1996) Infect. Immun., 64, pp. 69-76
Godfrey, R. W., Wilder, M. S., Relationships between oxidative metabolism, macrophage activation, and antilisterial activity (1984) J. Leukoc. Biol., 36, pp. 533-543
Beckerman, K. P., Rogers, H. W., Corbett, J. A., Schreiber, R. D., McDaniel, M. L., Unanue, E. R., Release of nitric oxide during the T cell-independent pathway of macrophage activation. Its role in resistance to Listeria monocytogenes (1993) J. Immunol., 150, pp. 888-895
Boockvar, K. S., Granger, D. L., Poston, R. M., Maybodi, M., Washington, M. K., Hibbs J. B., Jr., Kurlander, R. L., Nitric oxide produced during murine listeriosis is protective (1994) Infect. Immun., 62, pp. 1089-1100
Gregory, S. H., Wing, E. J., Hoffman, R. A., Simmons, R. L., Reactive nitrogen intermediates suppress the primary immunologic response to Listeria (1993) J. Immunol., 150, pp. 2901-2909
Shiloh, M. U., MacMicking, J. D., Nicholson, S., Brause, J. E., Potter, S., Marino, M., Fang, F. C., Nathan, C., Phenotype of mice and macrophages deficient in both phagocyte oxidase and inducible nitric oxide synthase (1999) Immunity, 10, pp. 29-38
Kaufmann, S. H., Immunity to intracellular bacteria (1993) Annu. Rev. Immunol., 11, pp. 129-163
Portnoy, D. A., Schreiber, R. D., Connelly, P., Tilney, L. G., Gamma interferon limits access of Listeria monocytogenes to the macrophage cytoplasm (1989) J. Exp. Med., 170, pp. 2141-2146
Conlan, J. W., North, R. J., Neutrophil-mediated dissolution of infected host cells as a defense strategy against a facultative intracellular bacterium (1991) J. Exp. Med., 174, pp. 741-744
Dunn, P. L., North, R. J., Early gamma interferon production by natural killer cells is important in defense against murine listeriosis (1991) Infect. Immun., 59, pp. 2892-2900
Harty, J. T., Bevan, M., Specific immunity to Listeria monocytogenes in the absence of IFN gamma (1995) Immunity, 3, pp. 109-117
Kaufmann, S. H., Ladel, C. H., Role of T cell subsets in immunity against intracellular infections of knockout mice with Listeria monocytogenes, and Mycobacterium bovis BCG (1994) Immunobiology, 191, pp. 509-516
Maragos, C. M., Morley, D., Wink, D. A., Dunams, T. M., Saavedra, J. E., Hoffman, A., Bove, A. A., Keefer, L. K., Complexes of NO with nucleophiles as agents for the controlled biological release of nitric oxide. Vasorelaxant effects (1991) J. Med. Chem., 34, pp. 3242-3247
Cox, G. W., Mathieson, B. J., Gandino, L., Blasi, E., Radzioch, D., Varesio, L., Heterogeneity of hematopoietic cells immortalized by v-myc/v-raf recombinant retrovirus infection of bone marrow or fetal liver (1989) J. Natl. Cancer Inst., 81, pp. 1492-1496
Miles, A. M., Wink, D. A., Cook, J. C., Grisham, M. B., Determination of nitric oxide using fluorescence spectroscopy (1996) Methods Enzymol, 268, pp. 105-120
Samsom, J. N., Langermans, J. A., Groeneveld, P. H., Van Furth, R., Acquired resistance against a secondary infection with Listeria monocytogenes in mice is not dependent on reactive nitrogen intermediates (1996) Infect. Immun., 64, pp. 1197-1202
Leenen, P. J., Canono, B. P., Drevets, D. A., Voerman, J. S., Campbell, P. A., TNF-alpha and IFN-gamma stimulate a macrophage precursor cell line to kill Listeria monocytogenes in a nitric oxide-independent manner (1994) J. Immunol., 153, pp. 5141-5147
Dai, W. J., Bartens, W., Kohler, G., Hufnagel, M., Kopf, M., Brombacher, F., Impaired macrophage listericidal and cytokine activities are responsible for the rapid death of Listeria monocytogenes-infected IFN-gamma receptor-deficient mice (1997) J. Immunol., 158, pp. 5297-5304
Miles, A. M., Gibson, M., Krishna, M., Cook, J. C., Pacelli, R., Wink, D. A., Grisham, M. B., Effects of superoxide on nitric oxide-dependent N-nitrosation reactions (1995) Free Radic. Res., 23, pp. 379-390
Wink, D. A., Mitchell, J. B., Chemical biology of nitric oxide: Insights into regulatory, cytotoxic, and cytoprotective mechanisms of nitric oxide (1998) Free Radic. Biol. Med., 25, pp. 434-456
Braun, J. S., Novak, R., Gao, G., Murray, P. J., Shenep, J. L., Pneumolysin, a protein toxin of Streptococcus pneumoniae, induces nitric oxide production from macrophages (1999) Infect. Immun., 67, pp. 3750-3756
Welch, R. A., Pore-forming cytolysins of gram-negative bacteria (1991) Mol. Microbiol., 5, pp. 521-528
Murray, H. W., Nathan, C. F., Macrophage microbicidal mechanisms in vivo: Reactive nitrogen versus oxygen intermediates in the killing of intracellular Leishmania donovani (1999) J. Exp. Med., 189, pp. 741-746
Free Radic Biol Med (ISSN: 0891-5849, 0891-5849linking, 1873-4596electronic), 2001 Feb 1; 30(3): 268-276.
Export to BibTeX Export to EndNote
Paper type: Journal Article,
Impact factor: 5.082, 5-year impact factor: 5.983
Url: http://www.scopus.com/inward/record.url?eid=2-s2.0-0035252335&partnerID=40&md5=bbb99f2c05823ff09e0d838ab6de7b11
Keywords: Free Radicals, Listeria, Nitrosation Stress, Gamma Interferon, Hypoxanthine, Lipopolysaccharide, Nitric Oxide, Nitric Oxide Donor, Reactive Oxygen Metabolite, Tumor Necrosis Factor Alpha, Virulence Factor, Xanthine Oxidase, Animal Cell, Animal Experiment, Animal Model, Article, Bacterial Growth, Bactericidal Activity, Cell Stimulation, Chemical Reaction, Concentration Response, Controlled Study, Cytostasis, Listeria Monocytogenes, Listeriosis, Macrophage, Mouse, Nonhuman, Oxidation Reduction Reaction, Oxidative Stress, Priority Journal, Survival, 2-Naphthylamine, Cell Line, Hydrazines, Interferon Type Ii, Knockout, Nitric Oxide Synthase, Nitric Oxide Synthase Type Ii, Nitrites, Oxidation-Reduction, Reactive Oxygen Species, Tumor Necrosis Factor-Alpha, Murinae,
Affiliations:
*** IBB - CNR ***
Radiation Biology Branch, National Cancer Institute, Bethesda, MD, United States
Department of Immunology, Uniform Services Health Science University, Bethesda, MD, United States
References:
Nathan, C.F., Hibbs J.B., Jr., Role of nitric oxide synthesis in macrophage antimicrobial activity (1991) Curr. Opin. Immunol., 3, pp. 65-7
Fang, F.C., Perspectives series: Host/pathogen interactions. Mechanisms of nitric oxide-related antimicrobial activity (1997) J. Clin. Invest., 99, pp. 2818-2825
Reiss, C.S., Komatsu, T., Does nitric oxide play a role in viral infections? (1998) J. Virol., 72, pp. 4547-4551
Bogdan, C., Of microbes, macrophages and nitric oxide (1997) Behring Inst. Mitt., 99, pp. 58-72
Granger, D.L., Hibbs J.B., Jr., High-output nitric oxide: Weapon against infection? (1996) Trends Microbiol., 4, pp. 46-47
Pacelli, R., Wink, D.A., Cook, J.A., Krishna, M.C., DeGraff, W., Friedman, N., Tsokos, M., Mitchell, J.B., Nitric oxide potentiates hydrogen peroxide-induced killing of Escherichia coli (1995) J. Exp. Med., 182, pp. 1469-1479
Kaplan, S.S., Lancaster, J.R., Basford, R.E., Simmons, R.L., Effect of nitric oxide on staphylococcal killing and interactive effect with superoxide (1996) Infect. Immun., 64, pp. 69-76
Godfrey, R.W., Wilder, M.S., Relationships between oxidative metabolism, macrophage activation, and antilisterial activity (1984) J. Leukoc. Biol., 36, pp. 533-543
Beckerman, K.P., Rogers, H.W., Corbett, J.A., Schreiber, R.D., McDaniel, M.L., Unanue, E.R., Release of nitric oxide during the T cell-independent pathway of macrophage activation. Its role in resistance to Listeria monocytogenes (1993) J. Immunol., 150, pp. 888-895
Boockvar, K.S., Granger, D.L., Poston, R.M., Maybodi, M., Washington, M.K., Hibbs J.B., Jr., Kurlander, R.L., Nitric oxide produced during murine listeriosis is protective (1994) Infect. Immun., 62, pp. 1089-1100
Gregory, S.H., Wing, E.J., Hoffman, R.A., Simmons, R.L., Reactive nitrogen intermediates suppress the primary immunologic response to Listeria (1993) J. Immunol., 150, pp. 2901-2909
Shiloh, M.U., MacMicking, J.D., Nicholson, S., Brause, J.E., Potter, S., Marino, M., Fang, F.C., Nathan, C., Phenotype of mice and macrophages deficient in both phagocyte oxidase and inducible nitric oxide synthase (1999) Immunity, 10, pp. 29-38
Kaufmann, S.H., Immunity to intracellular bacteria (1993) Annu. Rev. Immunol., 11, pp. 129-163
Portnoy, D.A., Schreiber, R.D., Connelly, P., Tilney, L.G., Gamma interferon limits access of Listeria monocytogenes to the macrophage cytoplasm (1989) J. Exp. Med., 170, pp. 2141-2146
Conlan, J.W., North, R.J., Neutrophil-mediated dissolution of infected host cells as a defense strategy against a facultative intracellular bacterium (1991) J. Exp. Med., 174, pp. 741-744
Dunn, P.L., North, R.J., Early gamma interferon production by natural killer cells is important in defense against murine listeriosis (1991) Infect. Immun., 59, pp. 2892-2900
Harty, J.T., Bevan, M., Specific immunity to Listeria monocytogenes in the absence of IFN gamma (1995) Immunity, 3, pp. 109-117
Kaufmann, S.H., Ladel, C.H., Role of T cell subsets in immunity against intracellular infections of knockout mice with Listeria monocytogenes, and Mycobacterium bovis BCG (1994) Immunobiology, 191, pp. 509-516
Maragos, C.M., Morley, D., Wink, D.A., Dunams, T.M., Saavedra, J.E., Hoffman, A., Bove, A.A., Keefer, L.K., Complexes of NO with nucleophiles as agents for the controlled biological release of nitric oxide. Vasorelaxant effects (1991) J. Med. Chem., 34, pp. 3242-3247
Hrabie, J., Klose, J., Wink, D.A., Keefer, L.K., New nitric oxide-releasing zwitterion derived polyamines (1993) J. Org. Chem., 58, pp. 1472-1476
Fridovich, I., Xanthine oxidase , pp. 213-215. , Greenwald, R. A., ed. Handbook of methods for oxygen radical research. Boca Raton, FL: CRC PressBergmeyer, H.U., (1985) Methods in enzymatic analysis (2nd ed.), 1, pp. 521-522. , Deerfield Beach, FL: Verlag Chemie Int
Cox, G.W., Mathieson, B.J., Gandino, L., Blasi, E., Radzioch, D., Varesio, L., Heterogeneity of hematopoietic cells immortalized by v-myc/v-raf recombinant retrovirus infection of bone marrow or fetal liver (1989) J. Natl. Cancer Inst., 81, pp. 1492-1496
Miles, A.M., Wink, D.A., Cook, J.C., Grisham, M.B., Determination of nitric oxide using fluorescence spectroscopy (1996) Methods Enzymol, 268, pp. 105-120
Mocci, S., Dalrymple, S.A., Nishinakamura, R., Murray, R., The cytokine stew and innate resistance to L. monocytogenes (1997) Immunol. Rev., 158, pp. 107-114
Samsom, J.N., Langermans, J.A., Groeneveld, P.H., Van Furth, R., Acquired resistance against a secondary infection with Listeria monocytogenes in mice is not dependent on reactive nitrogen intermediates (1996) Infect. Immun., 64, pp. 1197-1202
Leenen, P.J., Canono, B.P., Drevets, D.A., Voerman, J.S., Campbell, P.A., TNF-alpha and IFN-gamma stimulate a macrophage precursor cell line to kill Listeria monocytogenes in a nitric oxide-independent manner (1994) J. Immunol., 153, pp. 5141-5147
Ohya, S., Tanabe, Y., Makino, M., Nomura, T., Xiong, H., Arakawa, M., Mitsuyama, M., The contributions of reactive oxygen intermediates and reactive nitrogen intermediates to listericidal mechanisms differ in macrophages activated pre- and postinfection (1998) Infect. Immun., 66, pp. 4043-4049
Endres, R., Luz, A., Schulze, H., Neubauer, H., Futterer, A., Holland, S.M., Wagner, H., Pfeffer, K., Listeriosis in p47(phox-/-) and TRp55-/- mice: Protection despite absence of ROI and susceptibility despite presence of RNI (1997) Immunity, 7, pp. 419-432
Dai, W.J., Bartens, W., Kohler, G., Hufnagel, M., Kopf, M., Brombacher, F., Impaired macrophage listericidal and cytokine activities are responsible for the rapid death of Listeria monocytogenes-infected IFN-gamma receptor-deficient mice (1997) J. Immunol., 158, pp. 5297-5304
Miles, A.M., Gibson, M., Krishna, M., Cook, J.C., Pacelli, R., Wink, D.A., Grisham, M.B., Effects of superoxide on nitric oxide-dependent N-nitrosation reactions (1995) Free Radic. Res., 23, pp. 379-390
Gaston, B., Nitric oxide and thiol groups (1999) Biochim. Biophys. Acta., 1411, pp. 323-333
Vodovotz, Y., Chesler, L., Chong, H., Kim, S.J., Simpson, J.T., DeGraff, W., Cox, G.W., Barcellos-Hoff, M.H., Regulation of transforming growth factor beta1 by nitric oxide (1999) Cancer Res., 59, pp. 2142-2149
Wink, D.A., Mitchell, J.B., Chemical biology of nitric oxide: Insights into regulatory, cytotoxic, and cytoprotective mechanisms of nitric oxide (1998) Free Radic. Biol. Med., 25, pp. 434-456
Persichini, T., Colasanti, M., Lauro, G.M., Ascenzi, P., Cysteine nitrosylation inactivates the HIV-1 protease (1998) Biochem. Biophys. Res. Commun., 250, pp. 575-576
Gergel, D., Cederbaum, A.I., Inhibition of the catalytic activity of alcohol dehydrogenase by nitric oxide is associated with S nitrosylation and the release of zinc (1996) Biochemistry, 35, pp. 16186-16194
Braun, J.S., Novak, R., Gao, G., Murray, P.J., Shenep, J.L., Pneumolysin, a protein toxin of Streptococcus pneumoniae, induces nitric oxide production from macrophages (1999) Infect. Immun., 67, pp. 3750-3756
Welch, R.A., Pore-forming cytolysins of gram-negative bacteria (1991) Mol. Microbiol., 5, pp. 521-528
Murray, H.W., Nathan, C.F., Macrophage microbicidal mechanisms in vivo: Reactive nitrogen versus oxygen intermediates in the killing of intracellular Leishmania donovani (1999) J. Exp. Med., 189, pp. 741-746
Prada, J., Muller, S., Bienzle, U., Kremsner, P.G., Upregulation of reactive oxygen and nitrogen intermediates in Plasmodium berghei infected mice after rescue therapy with chloroquine or artemether (1996) J. Antimicrob. Chemother., 38, pp. 95-102
Karupiah, G., Xie, Q.W., Buller, R.M., Nathan, C., Duarte, C., MacMicking, J.D., Inhibition of viral replication by interferon-gamma-induced nitric oxide synthase (1993) Science, 261, pp. 1445-1448
Nathan, C. F., Hibbs J. B., Jr., Role of nitric oxide synthesis in macrophage antimicrobial activity (1991) Curr. Opin. Immunol., 3, pp. 65-7
Fang, F. C., Perspectives series: Host/pathogen interactions. Mechanisms of nitric oxide-related antimicrobial activity (1997) J. Clin. Invest., 99, pp. 2818-2825
Reiss, C. S., Komatsu, T., Does nitric oxide play a role in viral infections? (1998) J. Virol., 72, pp. 4547-4551
Granger, D. L., Hibbs J. B., Jr., High-output nitric oxide: Weapon against infection? (1996) Trends Microbiol., 4, pp. 46-47
Kaplan, S. S., Lancaster, J. R., Basford, R. E., Simmons, R. L., Effect of nitric oxide on staphylococcal killing and interactive effect with superoxide (1996) Infect. Immun., 64, pp. 69-76
Godfrey, R. W., Wilder, M. S., Relationships between oxidative metabolism, macrophage activation, and antilisterial activity (1984) J. Leukoc. Biol., 36, pp. 533-543
Beckerman, K. P., Rogers, H. W., Corbett, J. A., Schreiber, R. D., McDaniel, M. L., Unanue, E. R., Release of nitric oxide during the T cell-independent pathway of macrophage activation. Its role in resistance to Listeria monocytogenes (1993) J. Immunol., 150, pp. 888-895
Boockvar, K. S., Granger, D. L., Poston, R. M., Maybodi, M., Washington, M. K., Hibbs J. B., Jr., Kurlander, R. L., Nitric oxide produced during murine listeriosis is protective (1994) Infect. Immun., 62, pp. 1089-1100
Gregory, S. H., Wing, E. J., Hoffman, R. A., Simmons, R. L., Reactive nitrogen intermediates suppress the primary immunologic response to Listeria (1993) J. Immunol., 150, pp. 2901-2909
Shiloh, M. U., MacMicking, J. D., Nicholson, S., Brause, J. E., Potter, S., Marino, M., Fang, F. C., Nathan, C., Phenotype of mice and macrophages deficient in both phagocyte oxidase and inducible nitric oxide synthase (1999) Immunity, 10, pp. 29-38
Kaufmann, S. H., Immunity to intracellular bacteria (1993) Annu. Rev. Immunol., 11, pp. 129-163
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Comparison of control of Listeria by nitric oxide redox chemistry from murine macrophages and no donors: Insights into listeriocidal activity of oxidative and nitrosative stress
The physiological function of nitric oxide (NO) in the defense against pathogens is multifaceted. The exact chemistry by which NO combats intracellular pathogens such as Listeria monocytogenes is yet unresolved. We examined the effects of NO exposure, either delivered by NO donors ol generated in situ within ANA-1 murine macrophages. on L. monocytogenes growth. Production of NO by the two NONOate compounds PAPA/NO (NH2(C3H6)(N[N(O)NO]C3H7)) and DEA/NO (Na(C2H5)(2)N[N(O)NO]) resulted in L. monocytogenes cytostasis with minimal cytotoxicity. Reactive oxygen species generated from xanthine oxidase/hypoxanthine were neither bactericidal nor cytostatic and did not alter the action of NO. L. monocytogenes growth was also suppressed upon internalization into ANA-1 murine macrophages primed with interferon-gamma (INF-gamma) + tumor necrosis factor-alpha TNF-alpha or INF-gamma + lipid polysaccharide (LPS). Growth suppression correlated with nitrite formation and nitrosation of 2,3-diaminonaphthalene elicited by stimulated murine macrophages. This: nitrosative chemistry was not dependent upon nor mediated by interaction with reactive oxygen species (ROS), but resulted solely from NO and intermediates related to nitrosative stress. The role of nitrosation in controlling L. monocytogenes was further examined by monitoring the effects of exposure to NO on an important virulence factor, Listeriolysin O, which was inhibited under nitrosative conditions. These results suggest that nitrosative stress mediated by macrophages is an important component of the immunological arsenal in controlling L. monocytogenes infections. (C) 2001 Elsevier Science Inc.
The physiological function of nitric oxide (NO) in the defense against pathogens is multifaceted. The exact chemistry by which NO combats intracellular pathogens such as Listeria monocytogenes is yet unresolved. We examined the effects of NO exposure, either delivered by NO donors ol generated in situ within ANA-1 murine macrophages. on L. monocytogenes growth. Production of NO by the two NONOate compounds PAPA/NO (NH2(C3H6)(N[N(O)NO]C3H7)) and DEA/NO (Na(C2H5)(2)N[N(O)NO]) resulted in L. monocytogenes cytostasis with minimal cytotoxicity. Reactive oxygen species generated from xanthine oxidase/hypoxanthine were neither bactericidal nor cytostatic and did not alter the action of NO. L. monocytogenes growth was also suppressed upon internalization into ANA-1 murine macrophages primed with interferon-gamma (INF-gamma) + tumor necrosis factor-alpha TNF-alpha or INF-gamma + lipid polysaccharide (LPS). Growth suppression correlated with nitrite formation and nitrosation of 2,3-diaminonaphthalene elicited by stimulated murine macrophages. This: nitrosative chemistry was not dependent upon nor mediated by interaction with reactive oxygen species (ROS), but resulted solely from NO and intermediates related to nitrosative stress. The role of nitrosation in controlling L. monocytogenes was further examined by monitoring the effects of exposure to NO on an important virulence factor, Listeriolysin O, which was inhibited under nitrosative conditions. These results suggest that nitrosative stress mediated by macrophages is an important component of the immunological arsenal in controlling L. monocytogenes infections. (C) 2001 Elsevier Science Inc.
Comparison of control of Listeria by nitric oxide redox chemistry from murine macrophages and no donors: Insights into listeriocidal activity of oxidative and nitrosative stress
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Comparison of control of Listeria by nitric oxide redox chemistry from murine macrophages and no donors: Insights into listeriocidal activity of oxidative and nitrosative stress
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Molinaro A, Holst O, Lorenzo FD, Callaghan M, Nurisso A, D'Errico G, Zamyatina A, Peri F, Berisio R, Jerala R, Jiménez-Barbero J, Silipo A, Martín-Santamarí S
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Speciale I, Paciello I, Fazio LL, Sturiale L, Palmigiano A, Lanzetta R, Parrilli M, Garozzo D, Lemaitre B, Bernardini ML, Molinaro A, De Castro C
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Di Lorenzo F, Silipo A, Bianconi I, Lore' NI, Scamporrino A, Sturiale L, Garozzo D, Lanzetta R, Parrilli M, Bragonzi A, Molinaro A
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Avitabile C, D'Andrea LD, Romanelli A
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Musumeci D, Roviello GN, Montesarchio D
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Impact Factor: 9.723
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Nold-Petry CA, Rudloff I, Baumer Y, Ruvo M, Marasco D, Botti P, Farkas L, Cho SX, Zepp JA, Azam T, Dinkel H, Palmer BE, Boisvert WA, Cool CD, Taraseviciene-Stewart L, Heinhuis B, Joosten LA, Dinarello CA, Voelkel NF, Nold MF
* IL-32 Promotes Angiogenesis (768 views)
J Immunol (ISSN: 0022-1767), 2014 Jan 15; 192(2): 589-602.
Impact Factor: 4.922
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Montefusco S, Esposito R, D'Andrea L, Monti MC, Dunne C, Dolan B, Tosco A, Marzullo L, Clyne M
* Copper promotes TFF1-mediated Helicobacter pylori colonization (488 views)
Plosone (ISSN: 1932-6203, 1932-6203electronic, 1932-6203linking), 2013 Nov 13; 8(11): e79455-e79455.
Impact Factor: 3.534
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Madonna S, Scarponi C, Doti N, Carbone T, Cavani A, Scognamiglio PL, Marasco D, Albanesi C
* Therapeutical potential of a peptide mimicking the SOCS1 kinase inhibitory region in skin immune responses (584 views)
Eur J Immunol (ISSN: 0014-2980), 2013 Jul; 43(7): 1883-1895.
Impact Factor: 4.518
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Avitabile C, Netti F, Orefice G, Palmieri M, Nocerino N, Malgieri G, D'Andrea LD, Capparelli R, Fattorusso R, Romanelli A
* Design, structural and functional characterization of a Temporin-1b analog active against Gram-negative bacteria (488 views)
Bba-Gen Subjects (ISSN: 0304-4165, 0006-3002, 0925-4439), 2013 Jun; 1830(6): 3767-3775.
Impact Factor: 3.829
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Perrino C, Schiattarella GG, Sannino A, Pironti G, Petretta MP, Cannavo A, Gargiulo G, Ilardi F, Magliulo F, Franzone A, Carotenuto G, Serino F, Altobelli GG, Cimini V, Cuocolo A, Lombardi A, Goglia F, Indolfi C, Trimarco B, Esposito G
* Genetic deletion of uncoupling protein 3 exaggerates apoptotic cell death in the ischemic heart leading to heart failure (428 views)
J Am Heart Assoc Journal Of The American Heart Association (ISSN: 2047-9980), 2013 May 20; 2(3): e000086-e000086.
Impact Factor: 2.882
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Scalia M, Satriano C, Greca R, Stella AM, Rizzarelli E, Spina-Purrello V
* PARP-1 inhibitors DPQ and PJ-34 negatively modulate proinflammatory commitment of human glioblastoma cells (422 views)
Neurochemical Research (ISSN: 1573-6903, 0364-3190), 2013 Jan; 38(1): 50-58.
Impact Factor: 2.551
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Sorriento D, Fusco A, Ciccarelli M, Rungi A, Anastasio A, Carillo A, Dorn II GW, Trimarco B, Iaccarino G
* Mitochondrial G protein coupled receptor kinase 2 regulates proinflammatory responses in macrophages (385 views)
Febs Lett (ISSN: 0014-5793, 0014-5793print, 1873-3468electronic), 2013; 587(21): 3487-3494.
Impact Factor: 3.341
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Dolga AM, Letsche T, Gold M, Doti N, Bacher M, Chiamvimonvat N, Dodel R, Culmsee C
* Activation of KCNN3/SK3/K(Ca)2. 3 channels attenuates enhanced calcium influx and inflammatory cytokine production in activated microglia (552 views)
Glia (ISSN: 1098-1136), 2012 Dec; 60(12): 2050-2064.
Impact Factor: 5.466
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Berisio R
* Learning from pathogens: Exploiting host-pathogen liaison for therapeutic development (493 views)
Curr Protein Pept Sci (ISSN: 1389-2037, 1389-2037linking), 2012 Dec; 13(8): 697-698.
Impact Factor: 2.326
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Galdiero S, Falanga A, Cantisani M, Tarallo R, della Pepa ME, D'Oriano V, Galdiero M
* Microbe-Host Interactions: Structure and Role of Gram-Negative Bacterial Porins (629 views)
Curr Protein Pept Sci (ISSN: 1389-2037, 1389-2037linking), 2012 Dec; 13(8): 843-854.
Impact Factor: 2.326
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Berisio R
* Editorial: cell processes in bacterial diseases (409 views)
Protein Pept Lett (ISSN: 0929-8665, 1875-5305), 2012 Oct; 19(10): 1011-1012.
Impact Factor: 1.994
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Doti N, Scognamiglio PL, Madonna S, Scarponi C, Ruvo M, Perretta G, Albanesi C, Marasco D
* New mimetic peptides of the kinase-inhibitory region (KIR) of SOCS1 through focused peptide libraries (994 views)
Biochemical Journal, 2012 Apr 1; 443: 231-240.
Impact Factor: 4.779
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D'Agata R, Spoto G
* Artificial DNA and surface plasmon resonance (534 views)
Artificial Dna Pna & Xna (ISSN: 1949-095x), 2012 Apr; 3(2): N/D-N/D.
Impact Factor: 0
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De Simone G
* Editorial: Zinc Metallo-Enzymes As Target For Drug Design (423 views)
Curr Med Chem (ISSN: 0929-8673, 1875-533x, 1875-533xelectronic), 2012 Feb; 19(6): 820-1012.
Impact Factor: 4.07
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Musumeci D, Bucci EM, Roviello GN, Sapio R, Valente M, Moccia M, Bianchi ME, Pedone C
* DNA-based strategies for blocking HMGB1 cytokine activity: Design, synthesis and preliminary in vitro/in vivo assays of DNA and DNA-like duplexes (462 views)
Mol Biosyst (ISSN: 1742-206x, 1742-2051, 1742-2051electronic), 2011 May; 7(5): 1742-1752.
Impact Factor: 3.534
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Spina-Purrello V, Giliberto S, Barresi V, Nicoletti VG, Giuffrida Stella AM, Rizzarelli E
* Modulation of PARP-1 and PARP-2 expression by L-carnosine and trehalose after LPS and INFγ-induced oxidative stress (429 views)
Neurochemical Research (ISSN: 0364-3190, 1573-6903), 2010 Dec; 35(12): 2144-2153.
Impact Factor: 2.608
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Visco AM, Campo N, Vagliasindi LI, Tabbì G
* STUDY OF THE RADICAL SPECIES INDUCED BY ELECTRON-BEAM IRRADIATION IN VACUUM ON BIOMEDICAL UHMWPE (268 views)
International Journal Of Polymer Analysis And Characterization (ISSN: 1023-666x), 2010; 15(7): 424-437.
Impact Factor: 0.814
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Sorriento D, Ciccarelli M, Santulli G, Campanile A, Altobelli GG, Cimini V, Galasso G, Astone D, Piscione F, Pastore L, Trimarco B, Iaccarino G
* The G-protein-coupled receptor kinase 5 inhibits NFκB transcriptional activity by inducing nuclear accumulation of IκBα (438 views)
P Natl Acad Sci Usa (ISSN: 0027-8424, 1091-6490, 0027-8424print), 2008; 105(46): 17818-17823.
Impact Factor: 9.38
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Nicoletti VG, Santoro AM, Grasso G, Vagliasindi LI, Giuffrida ML, Cuppari C, Purrello VS, Stella AMG, Rizzarelli E
* Carnosine interaction with nitric oxide and astroglial cell protection (647 views)
Journal Of Neuroscience Research (ISSN: 0360-4012), 2007 Sep 1; 85(10): 2239-2245.
Impact Factor: 3.268
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Calabrese V, Colombrita C, Guagliano E, Sapienza M, Ravagna A, Cardile V, Scapagnini G, Santoro AM, Mangiameli A, Butterfield DA, Giuffrida Stella AM, Rizzarelli E
* Protective effect of carnosine during nitrosative stress in astroglial cell cultures (379 views)
Neurochemical Research (ISSN: 0364-3190, 1573-6903), 2005 Jun; 30(6-7): 797-807.
Impact Factor: 2.187
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Paesano N, Marzocco S, Vicidomini C, Saturnino C, Autore G, De Martino G, Sbardella G
* Synthesis and biological evaluation of 3-benzyl-1-methyl- and 1-methyl-3-phenyl-isothioureas as potential inhibitors of iNOS (433 views)
Bioorganic & Medicinal Chemistry Letters (ISSN: 0960-894x), 2005 Feb 1; 15(3): 539-543.
Impact Factor: 2.478
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Improta R, Barone V
* Interplay of electronic, environmental, and vibrational effects in determining the hyperfine coupling constants of organic free radicals (295 views)
Chem Rev (ISSN: 0009-2665), 2004 Mar; 104(3): 1231-1253.
Impact Factor: 20.233
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Galdiero M, Vitiello M, Galdiero S
* Eukaryotic cell signaling and transcriptional activation induced by bacterial porins (459 views)
Fems Microbiology Letters (ISSN: 0378-1097), 2003 Sep 12; 226(1): 57-64.
Impact Factor: 1.932
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Esposito G, Ligresti A, Izzo AA, Bisogno T, Ruvo M, Di Rosa M, Di Marzo V, Iuvone T
* The endocannabinoid system protects rat glioma cells against HIV-1 Tat protein-induced cytotoxicity: Mechanism and regulation (471 views)
Jbc Papers (ISSN: 0021-9258, 1083-351x, 0021-9258linking), 2002 Dec 27; 277(52): 50348-50354.
Impact Factor: 6.696
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Tabbì G, Cassino C, Cavigiolio G, Colangelo D, Ghiglia A, Viano I, Osella D
* Water stability and cytotoxic activity relationship of a series of ferrocenium derivatives. ESR insights on the radical production during the degradation process (642 views)
J Med Chem (ISSN: 0022-2623, 1520-4804, 0022-2623print), 2002 Dec 19; 45(26): 5786-5796.
Impact Factor: 4.566
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Langella E, Improta R, Barone V
* Conformational and spectroscopic analysis of the tyrosyl radical dipeptide analogue in the gas phase and in aqueous solution by a density functional/continuum solvent model (545 views)
J Am Chem Soc (ISSN: 0002-7863, 0002-2786, 1520-5126), 2002 Sep 25; 124(38): 11531-11540.
Impact Factor: 6.201
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Wink DA, Vodovotz Y, Grisham MB, DeGraff W, Cook JC, Pacelli R, Krishna M, Mitchell JB
Antioxidant effects of nitric oxide (351 views)
Method Enzymol (ISSN: 0076-6879, 1557-7988electronic), 1998; 301: 413-424.
Impact Factor: 2.823
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38 Records (36 excluding Abstracts).
Total impact factor: 164.785 (161.903 excluding Abstracts).
Total 5 year impact factor: 200.704 (197.822 excluding Abstracts).
Total impact factor: 164.785 (161.903 excluding Abstracts).
Total 5 year impact factor: 200.704 (197.822 excluding Abstracts).
688 views. Last view on Sunday 19 March 2023, 14:21:07
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