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Oxidative Medicine and Cellular Longevity
Volume 2013, Article ID 452546, 8 pages
http://dx.doi.org/10.1155/2013/452546
Research Article

Oxidative Stress and Free-Radical Oxidation in BCG Granulomatosis Development

1Research Center of Clinical and Experimental Medicine, USA
2University of Michigan School of Medicine, USA
3Novosibirsk State Medical University, Russia

Received 9 February 2013; Revised 30 March 2013; Accepted 1 April 2013

Academic Editor: Manikandan Panchatcharam

Copyright © 2013 Elena Menshchikova et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. V. A. Shkurupiy, Tuberculous Granulomatosis. Cytophysiology and Targeted Therapy, Moscow, Russia, 2007.
  2. D. L. Boros, Ed., Granulomatous Infections and Inflammations: Cellular and Molecular Mechanisms, ASM Press, Washington, DC, USA, 2003.
  3. E. B. Menshchikova, N. K. Zenkov, V. Z. Lankin et al., Oxidative Stress. Pathological States and Diseases, ARTA, Novosibirsk, Russia, 2008.
  4. T. Finkel, “Signal transduction by reactive oxygen species,” Journal of Cell Biology, vol. 194, no. 1, pp. 7–15, 2011. View at Publisher · View at Google Scholar · View at Scopus
  5. A. Trivedi, N. Singh, S. A. Bhat et al., “Redox biology of tuberculosis pathogenesis,” Advances in Microbial Physiology, vol. 60, pp. 263–324, 2012. View at Publisher · View at Google Scholar
  6. A. Kumar, A. Farhana, L. Guidry et al., “Redox homeostasis in mycobacteria: the key to tuberculosis control?” Expert Reviews in Molecular Medicine, vol. 13, article e39, 2011. View at Google Scholar
  7. P. P. W. Lee, K. W. Chan, L. Jiang et al., “Susceptibility to mycobacterial infections in children with x-linked chronic granulomatous disease: a review of 17 patients living in a region endemic for tuberculosis,” Pediatric Infectious Disease Journal, vol. 27, no. 3, pp. 224–230, 2008. View at Publisher · View at Google Scholar · View at Scopus
  8. R. K. Verma, A. K. Singh, M. Mohan et al., “Inhalable microparticles containing nitric oxide donors: saying NO to intracellular Mycobacterium tuberculosis,” Molecular Pharmacology, vol. 9, no. 11, pp. 3183–3189, 2012. View at Publisher · View at Google Scholar
  9. L. W. Hedlund and G. A. Johnson, “Morphology of the small-animal lung using magnetic resonance microscopy,” Proceedings of the American Thoracic Society, vol. 2, no. 6, pp. 481–483, 501–502, 2005. View at Publisher · View at Google Scholar · View at Scopus
  10. D. L. Laskin, B. Weinberger, and J. D. Laskin, “Functional heterogeneity in liver and lung macrophages,” Journal of Leukocyte Biology, vol. 70, no. 2, pp. 163–170, 2001. View at Google Scholar · View at Scopus
  11. N. Rieber, A. Hector, T. Kuijpers et al., “Current concepts of hyperinflammation in chronic granulomatous disease,” Clinical and Developmental Immunology, vol. 2012, Article ID 252460, 6 pages, 2012. View at Publisher · View at Google Scholar
  12. B. H. Segal, P. Veys, H. Malech, and M. J. Cowan, “Chronic granulomatous disease: lessons from a rare disorder,” Biology of Blood and Marrow Transplantation, vol. 17, supplement, no. 1, pp. S123–S131, 2011. View at Publisher · View at Google Scholar · View at Scopus
  13. F. Facchetti, W. Vermi, S. Fiorentini et al., “Expression of inducible nitric oxide synthase in human granulomas and histiocytic reactions,” American Journal of Pathology, vol. 154, no. 1, pp. 145–152, 1999. View at Google Scholar · View at Scopus
  14. A. L. Pereira-Suarez, C. Estrada-Chavez, C. Arriaga-Diaz, P. Espinosa-Cueto, and R. Mancilla, “Coexpression of NRAMP1, iNOS, and nitrotyrosine in bovine tuberculosis,” Veterinary Pathology, vol. 43, no. 5, pp. 709–717, 2006. View at Publisher · View at Google Scholar · View at Scopus
  15. S. Ahmad, “Pathogenesis, immunology, and diagnosis of latent mycobacterium tuberculosis infection,” Clinical and Developmental Immunology, vol. 2011, Article ID 814943, 2011. View at Publisher · View at Google Scholar · View at Scopus
  16. M. V. Palmer, W. R. Waters, and T. C. Thacker, “Lesion development and immunohistochemical changes in granulomas from cattle experimentally infected with Mycobacterium bovis,” Veterinary Pathology, vol. 44, no. 6, pp. 863–874, 2007. View at Publisher · View at Google Scholar · View at Scopus
  17. M. R. Kreuger, D. R. Tames, and M. Mariano, “Expression of NO-synthase in cells of foreign-body and BCG-induced granulomata in mice: influence of L-NAME on the evolution of the lesion,” Immunology, vol. 95, no. 2, pp. 278–282, 1998. View at Publisher · View at Google Scholar · View at Scopus
  18. H. S. Choi, P. R. Rai, H. W. Chu, C. Cool, and E. D. Chan, “Analysis of nitric oxide synthase and nitrotyrosine expression in human pulmonary tuberculosis,” American Journal of Respiratory and Critical Care Medicine, vol. 166, no. 2, pp. 178–186, 2002. View at Publisher · View at Google Scholar · View at Scopus
  19. S. Hanna, B. Gharib, H. Lepidi, J. C. Montet, H. Dumon, and M. De Reggi, “Experimental schistosomiasis, protective aspects of granulomatous reaction in the mouse liver,” Parasitology Research, vol. 96, no. 1, pp. 6–11, 2005. View at Publisher · View at Google Scholar · View at Scopus
  20. S. O'Brien, P. S. Jackett, D. B. Lowrie, and P. W. Andrew, “Guinea-pig alveolar macrophages kill Mycobacterium tuberculosis in vitro, but killing is independent of susceptibility to hydrogen peroxide or triggering of the respiratory burst,” Microbial Pathogenesis, vol. 10, no. 3, pp. 199–207, 1991. View at Publisher · View at Google Scholar · View at Scopus
  21. D. K. Roy, K. T. Mani Senthil Kumar, Zothanpuia et al., “Pharmacological studies on Indian black tea (leaf variety) in acute and chronic inflammatory conditions,” Phytotherapy Research, vol. 22, no. 6, pp. 814–819, 2008. View at Publisher · View at Google Scholar · View at Scopus
  22. K. S. Kilgore, M. M. Imlay, J. P. Szaflarski et al., “Neutrophils and reactive oxygen intermediates mediate glucan-induced pulmonary granuloma formation through the local induction of monocyte chemoattractant protein-1,” Laboratory Investigation, vol. 76, no. 2, pp. 191–201, 1997. View at Google Scholar · View at Scopus
  23. A. I. Zhuravlyov, Quantum Biophysics of Animals and Humans, Binom, Moscow, Russia, 2011.
  24. O. M. S. Abdallahi, S. Hanna, M. de Reggi, and B. Gharib, “Visualization of oxygen radical production in mouse liver in response to infection with Schistosoma mansoni,” Liver, vol. 19, no. 6, pp. 495–500, 1999. View at Google Scholar · View at Scopus
  25. J. G. Egen, A. G. Rothfuchs, C. G. Feng, N. Winter, A. Sher, and R. N. Germain, “Macrophage and T cell dynamics during the development and disintegration of mycobacterial granulomas,” Immunity, vol. 28, no. 2, pp. 271–284, 2008. View at Publisher · View at Google Scholar · View at Scopus