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PARTICIPATION OF REDOX SIGNALIZATION IN NITRIC OXIDE-, CARBON MONOXIDE- AND HUDROGEN SULFIDE-MEDIATED REGULATION OF APOPTOSIS AND CELL CYCLE

https://doi.org/10.20538/1682-0363-2013-1-49-54

Abstract

The study has demonstrated that proapoptic concentrations of donors of NO (100 mmol SNP and 100 µmol NOC-5), H2 (10 mmol NaHS), and CO (50 µmol CORM-2) gases caused an increase in the intracellular level of active forms of oxygen in Jurkat cells. As this took place, the activation of redox-dependent transcription factor р53 was observed as Jurkat cells were exposed to 100 mmol SNP and 10 mmol NaHS. In the case of 100 µmol NOC-5 and 50 µmol CORM-2, an increase of р53 was not observed, but the expression of target gens of this transcription factor р21 (under the effect of NO and СО) and bax (under the effect of NO) increased. The antiproliferative concentration of hydrogen sulfide donor (50 µmol ) did not cause an increase in the intracellular production of active forms of oxygen and the activation of redox-dependent signal mechanisms.

About the Authors

Ye. G. Starikova
Siberian State Medical University, Tomsk
Russian Federation


L. A. Tashireva
Siberian State Medical University, Tomsk
Russian Federation


O. A. Vasilieva
Siberian State Medical University, Tomsk
Russian Federation


V. D. Yakushina
Siberian State Medical University, Tomsk
Russian Federation


V. V. Novitsky
Siberian State Medical University, Tomsk
Russian Federation


N. V. Ryazantseva
Siberian State Medical University, Tomsk
Russian Federation


References

1. Pletyushkina O.Yu., Fetisova Ye.K., Lyamzayev K.G. Bio-chemistry, 2006, vol. 71, no. 1, pp. 75–84.

2. Ryazantseva N.V., Novitsky V.V., Chasovskikh N.Yu., Starikova Ye.G., Kaigorodova Ye.V., Starikov Yu.V., Radzivil T.T., Krat I.V. Cytology, 2009, vol. 51, no. 4, pp. 329–334.

3. Ryazantseva N.V., Novitsky V.V., Chasovskikh N.Yu., Kai-gorodova Ye.V., Starikova E.G., Starikov Yu.V. Russian Physiological Journal named after I.M. Sechenov, 2008, vol. 94, no. 6, pp. 710–718.

4. Ryazantseva N.V., Starikova Ye.G., Novitsky V.V., Kleptso-va L.A., Yakushina V.D., Kaigorodova Ye.V. Bulletin of Ex-perimental Biology and Medicine, 2011, vol. 151, no. 6, pp. 656–659.

5. Starikova Ye.G., Ryazantseva N.V., Novitsky V.V., Tashi-reva L.A., Starikov Yu.V., Stepovaya Ye.A., Osikhov I.A., Vasil'eva O.A., Yakushina V.D. Bulletin of Siberian Medi-cine, 2011, no. 6, pp. 40–44.

6. Starikova Ye.G., Tashireva L.A., Bel'dyagina Ye.V., Ryazantse¬va N.V., Novitsky V.V. Siberian Journal of On-cology, 2012, vol. 52, no. 4, pp. 48–51.

7. Butte A.J. Further defining housekeeping, or “maintenance”, genes focus on a compendium of gene expression in normal human tissues. Physiol. Genomics, 2001, vol. 7, no. 2, pp. 95–96.

8. Dornan D., Wertz I., Shimizu H., Arnott D. The ubiquitin ligase COP1 is a critical negative regulator of p53. Nature, 2004, vol. 429, pp. 86–92.

9. Gartel A.L., Tyner A.L. The role of the cyclin-dependent ki-nase inhibitor p21 in apoptosis. Molecular Cancer Therapeu-tics, 2002, vol. 1, pp. 639–649.

10. Kajimura M., Fukuda R., Bateman R.M. Interactions of mul-tiple gas-transducing systems: hallmarks and uncertainties of CO, NO and H2S gas biology. Antioxidants & Redox signaling, 2010, vol. 13, pp. 157–193.

11. Kimura Y., Goto Y-I., Kimura H. Hydrogen sulfide increases glutathione production and suppresses oxidative stress in mitochondria. Antioxid Redox Signal, 2010, vol. 12, pp. 1–13.

12. Koppenol W.H. Chemistry of peroxynitrite and its relevance to biological systems. Met Ions Biol. Syst., 1999, vol. 36, pp. 597–619.

13. Pacher P., Beckman J. S., Liaudet L. Nitric oxide and peroxynitrite in health and disease. Physiol. Rev., 2007, vol. 87, pp. 315–424.

14. Predmore B.L., Lefer D.J. Development of hydrogen sulfide-based therapeutics for cardiovascular disease. J. Cardiovasc Transl Res., 2010, vol. 3, pp. 487–498.

15. Sen N., Snyder S.H. Protein modifications involved in neu-rotransmitter and gasotransmitter signaling. Trends Neurosci, 2010, vol. 33, pp. 493–502.

16. Wang R. The gasotransmitter role of hydrogen sulfide. Antioxid Redox Signal, 2003, vol. 5, pp. 493–501.

17. Webley K., Jane A., Bond I. Posttranslational modifications of p53 in replicative senescence overlapping but distinct from those induced by DNA damage. Molecular and Cellular Biology, 2000, vol. 20, pp. 2803–2808.

18. Wink D.A., Cook J.A., Kim S. Superoxide modulates the ox-idation and nitrosation of thiols by nitric oxide derived reactive intermediates. J. Biol. Chem., 1997, vol. 272, pp. 11147–11151.

19. Yang G., Sun X., Wang R. Hydrogen sulfide-induced apop-tosis of human aorta smooth muscle cells via the activation of MAP kinases and caspase-3. FASEB J., 2004, vol. 18, pp. 1782–1784.

20. Zhao R., Gish K., Murphy M. Analysis of p53-regulated gene expression patterns using oligonucleotide arrays. Genes Dev, 2000, vol. 8, pp. 981–993.


Review

For citations:


Starikova Ye.G., Tashireva L.A., Vasilieva O.A., Yakushina V.D., Novitsky V.V., Ryazantseva N.V. PARTICIPATION OF REDOX SIGNALIZATION IN NITRIC OXIDE-, CARBON MONOXIDE- AND HUDROGEN SULFIDE-MEDIATED REGULATION OF APOPTOSIS AND CELL CYCLE. Bulletin of Siberian Medicine. 2013;12(1):49-54. (In Russ.) https://doi.org/10.20538/1682-0363-2013-1-49-54

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ISSN 1682-0363 (Print)
ISSN 1819-3684 (Online)