Blue laser irradiation generates intracellular reactive oxygen species in various types of cells

Photomedicine and Laser Surgery

Volumn 31, Issue 3, 2013, Pages 95-104

  Kushibiki, Toshihiro ^a   Hirasawa, Takeshi ^a   Okawa, Shinpei ^a   Ishihara, Miya ^a  

^a NATIONAL DEFENSE MEDICAL COLLEGE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOCARCINOMA CELLS; AFTER-TREATMENT; BLUE LASERS; DIRECT MEASUREMENT; FLOW-CYTOMETER; FLUOROMETRIC ASSAY; FUNCTIONAL REGULATION; INSULINOMA CELLS; LEUKEMIA CELLS; LOW LEVEL LASER THERAPY; LUNG CANCER CELLS; MESENCHYMAL STROMAL CELLS; MYOBLASTS; NEAR-INFRARED LASER IRRADIATION; NEAR-INFRARED LASERS; PHORBOL ESTERS; POTENTIAL SOURCES; PREADIPOCYTES; REACTIVE OXYGEN SPECIES; RED LASERS; ROS GENERATIONS; WAVELENGTH LASERS;

CELL CULTURE; INFRARED DEVICES; INFRARED LASERS; IRRADIATION; LASER SURGERY; OXYGEN; PROBES;

CELLS;

REACTIVE OXYGEN METABOLITE;

ANIMAL; ARTICLE; CELL CULTURE; HUMAN; LOW LEVEL LASER THERAPY; METABOLISM; MOUSE; RADIATION EXPOSURE; RADIATION RESPONSE; RAT;

ANIMALS; CELLS, CULTURED; DOSE-RESPONSE RELATIONSHIP, RADIATION; HUMANS; LASER THERAPY, LOW-LEVEL; MICE; RATS; REACTIVE OXYGEN SPECIES; LOW-LEVEL LIGHT THERAPY;

EID: 84874748575     PISSN: 15495418     EISSN: None     Source Type: Journal    
DOI: 10.1089/pho.2012.3361     Document Type: Article

References (72)

1. Gao, X., and Xing, D. (2009). Molecular mechanisms of cell proliferation induced by low power laser irradiation. J. Biomed. Sci. 16, 4.
2. Karu, T. (1999). Primary and secondary mechanisms of action of visible to near-IR radiation on cells. J. Photochem. Photobiol. B. 49, 1-17.
3. Lavi, R., Shainberg, A., and Friedmann, H., et al. (2003). Low energy visible light induces reactive oxygen species generation and stimulates an increase of intracellular calcium concentration in cardiac cells. J. Biol. Chem. 278, 40,917-40,922.
4. Breitbart, H., Levinshal, T., Cohen, N., Friedmann, H., and Lubart, R. (1996). Changes in calcium transport in mammalian sperm mitochondria and plasma membrane irradi- ated at 633nm (He-Ne laser). J. Photochem. Photobiol. B. 34, 117-121.
5. Kokoska, E.R., Wolff, A.B., Smith, G.S., and Miller, T.A. (2000). Epidermal growth factor-induced cytoprotection in human intestinal cells involves intracellular calcium signaling. J. Surg. Res. 88, 97-103.
6. Krizaj, D., and Copenhagen, D.R. (2002). Calcium regulation in photoreceptors. Front. Biosci. 7, d2023-d2044.
7. Duan, R., Liu, T.C-Y., Li, Y., Guo, H., and Yao L-B. (2001). Signal transduction pathways involved in low intensity He- Ne laser-induced respiratory burst in bovine neutrophils: a potential mechanism of low intensity laser biostimulation. Lasers Surg. Med. 29, 174-178.
8. Lubart, R., Friedmann, H., Sinykov, M., Cohen, N., and Breitbart, H. (1997). Changes in calcium transport in mammalian sperm mitochondria and plasma membranes caused by 780 nm irradiation. Lasers Surg. Med. 21, 493- 499.
9. Cohen, N., Lubart, R., Rubinstein, S., and Breitbart, H. (1998). Light irradiation of mouse spermatozoa: stimulation of in vitro fertilization and calcium signals. Photochem. Photobiol. 68, 407-413.
10. Gavish, L., Asher, Y., Becker, Y., and Kleinman, Y. (2004). Low level laser irradiation stimulates mitochondrial membrane potential and disperses subnuclear promyelocytic leukemia protein. Lasers Surg. Med. 35, 369-376.
11. Wong-Riley, M.T., Bai, X., Buchmann, E., and Whelan, H.T. (2001). Light-emitting diode treatment reverses the effect of TTX on cytochrome oxidase in neurons. NeuroReport 12, 3033-3037.
12. Castano, A.P., Dai, T., and Yaroslavsky, I. et al. (2007). Low-level laser therapy for zymosan-induced arthritis in rats: Importance of illumination time. Lasers Surg. Med. 39, 543-550.
13. Oren, D.A., Charney, D., Lavie, R., Sinyakov, M., and Lubart, R. (2001). Stimulation of reactive oxygen species production by an antidepressant visible light source. Biol. Psychiatry 49, 464-467.
14. Sauer, H., Wartenberg, M., and Hescheler, J. (2001). Reactive oxygen species as intracellular messengers during cell growth and differentiation. Cell Physiol. Biochem. 11, 173-186.
15. Nemoto, S., Takeda, K., Yu, Z.X., Ferrans, V.J., and Finkel, T. (2000). Role for mitochondrial oxidants as regulators of cellular metabolism. Mol. Cell Biol. 20, 7311-7318.
16. Das D.K. (2001). Redox regulation of cardiomyocyte survival and death. Antioxid. Redox Signal 3, 23-37.
17. Hawkins, D., and Abrahamse, H. (2006). Effect of multiple exposures of low-level laser therapy on the cellular responses of wounded human skin fibroblasts. Photomed. Laser Surg. 24, 705-714.
18. Hu, W-P., Wang, J-J., Yu, C-L., Lan, C-CE. Chen, G-S., and Yu, H-S. (2007). Helium-Neon laser irradiation stimulates cell proliferation through photostimulatory effects in mitochondria. J. Invest. Dermatol. 127, 2048-2057.
19. Alexandratou, E., Yova, D., Handris, P., Kletsas, D., and Loukas S. (2002). Human fibroblast alterations induced by low power laser. irradiation at the single cell level using confocal microscopy. Photochem. Photobiol. Sci. 1, 547-552.
20. Lubart, R., and Breitbart H. (2000). Biostimulative effects of low energy lasers and their implications for medicine. Drug Dev. Res. 50, 471-475.
21. Karu, T. (2008). Mitochondrial signaling in mammalian cells activated by red and near-ir radiation. Photochem. Photobiol. 84, 1091-1099.
22. Kushibiki, T., and Awazu, K. (2008). Controlling osteogenesis and adipogenesis of mesenchymal stromal cells by regulating a circadian clock protein with laser irradiation. Int. J. Med. Sci. 5, 319-326.
23. Kushibiki, T., and Awazu, K. (2009). Blue laser irradiation enhances extracellular calcification of primary mesenchymal stem cells. Photomed. Laser Surg. 27, 493-498.
24. Kushibiki, T., Tajiri, T., Ninomiya, Y., and Awazu, K. (2010). Chondrogenic mRNA expression in prechondrogenic cells after blue laser irradiation. J. Photochem. Photobiol. B. 98, 211-215.
25. Donati, Y.R.A., Slosman, D.O., and Polla, B.S. (1990). Oxidative injury and the heat shock response. Biochem. Pharmacol. 40, 2571-2577.
26. Morimoto, R.I., Tissieres, A., and Georgopoulos, C. (1990). The stress response, function of the proteins, and perspectives, in: Stress Proteins in Biology and Medicine. R.I. Morimoto, A. Tissieres, and C. Georgopoulos, eds. Cold Spring Harbor, NY: Cold Spring Harbor, pp. 1-36.
27. Crawford, L.E., Milliken, D.D., Kaidobad, I., et al. (1996). Superoxide-mediated actin response in post-hypoxic endothelial cells. J. Biol. Chem. 271, 26,863-26,867.
28. Finkel, T. (1998). Oxygen radicals and signaling. Curr. Opin. Cell Biol. 10, 248-253.
29. Young, S., Bolton, P., Dyson, M., and Harvey, W. (1989). Diamantopoulos C. Macrophage responsiveness to light therapy. Lasers Surg. Med. 9, 497-505.
30. el Sayed, S.O., and Dyson, M. (1990). Comparison of the effect of multi-wavelength light produced by a cluster of semiconductor diodes and of each individual diode on mast cell number and degranulation in intact and injured skin. Lasers Surg. Med. 10, 559-568.
31. Sayed, S.O., and Dyson M. (1996). Effect of laser pulse repetition rate and pulse duration on mast cell number and degranulation. Lasers Surg. Med. 19, 433-437.
32. Karu, T., Tiphlova, O., Esenaliev, R., and Letokhov V. (1994). Two different mechanisms of low-intensity laser photobiological effects on Escherichia coli. J. Photochem. Photobiol. B. 24, 155-161.
33. Breitbart, H., Levinshal, T., Cohen, N., Friedmann, H., and Lubart, R. (1996). Changes in calcium transport in mammalian sperm mitochondria and plasma membrane irradiated at 633 nm (HeNe laser) J. Photochem. Photobiol. B. 34, 117-121.
34. Agaiby, A.D., Ghali, L.R., Wilson, R., and Dyson, M. (2000). Laser modulation of angiogenic factor production by Tlymphocytes. Lasers Surg. Med. 26, 357-363.
35. Duan, R., Liu, T.C., Li, Y., Guo, H., and Yao L.B. (2001). Signal transduction pathways involved in low intensity He-Ne laser-induced respiratory burst in bovine neutrophils: a potential mechanism of low intensity laser biostimulation. Lasers Surg. Med. 29, 174-178.
36. Karu, T., Pyatibrat, L.V., and Kalendo, G.S. (2001). Cell attachment to extracellular matrices is modulated by pulsed radiation at 820nm and chemicals that modify the activity of enzymes in the plasma membrane. Lasers Surg. Med. 29, 274-281.
37. Nussbaum, E.L., Lilge, L., and Mazzulli T. (2002). Effects of 810nm laser irradiation on in vitro growth of bacteria: comparison of continuous wave and frequency modulated light. Lasers Surg. Med. 31, 343-351.
38. Schindl, A., Merwald, H., Schindl, L., Kaun, C., and Wojta J. (2003). Direct stimulatory effect of low-intensity 670nm laser irradiation on human endothelial cell proliferation. Br. J. Dermatol. 148, 334-336.
39. Kushibiki, T., Tajiri, T., Tomioka, Y., and Awazu, K. (2010). Photodynamic therapy induces interleukin secretion from dendritic cells. Int. J. Clin. Exp. Med. 3, 110-114.
40. Kushibiki, T. (2010). Photodynamic therapy induces micro- RNA-210 and - 296 expression in HeLa cells. J. Biophotonics 3, 368-372.
41. Tomioka, Y., Kushibiki, T., and Awazu, K. (2010). Evaluation of oxygen consumption of culture medium and in vitro photodynamic effect of talaporfin sodium in lung tumor cells. Photomed. Laser Surg. 28, 385-390.
42. Kushibiki, T., Sakai, M., and Awazu, K. (2008). Differential effects of photodynamic therapy on morphologically distinct tumor cells derived from a single precursor cell. Cancer Lett. 268, 244-251.
43. Grzelak, A., Rychlik, B., and Bartosz, G. (2001). Lightdependent generation of reactive oxygen species in cell culture media. Free Radic. Biol. Med. 30, 1418-1425.
44. Edwards, A., and Silva, E. (2001). Effect of visible light on selected enzymes, vitamins and amino acids. J. Photochem. Photobiol. B. 63, 126-131.
45. Eichler, M., Lavi, R., Shainberg, A., and Lubart, R. (2005). Flavins are source of visible-light-induced free radical formation in cells. Lasers Surg. Med. 37, 314-319.
46. Eichler, M., Lavi, R., Friedmann, H., Shainberg, A., and Lubart, R. (2007). Red light-induced redox reactions in cells observed with TEMPO. Photomed. Laser Surg. 25, 170-174.
47. Freeman, B.A., and Crapo, J.D. (1982). Biology of disease: free radicals and tissue injury. Lab. Invest. 47, 412-426.
48. Tyler, D.D. (1975). Polarographic assay and intracellular distribution of superoxide dismutase in rat liver. Biochem. J. 147, 493-504.
49. Chance, B., Sies, H., and Boveris, A. (1979). Hydroperoxide metabolism in mammalian organs. Physiol. Rev. 59, 527- 605.
50. Banki, K., Hutter, E., Gonchoroff, N.J., and Perl A. (1999). Elevation of mitochondrial transmembrane potential and reactive oxygen intermediate levels are early events and occur independently from activation of caspases in Fas signaling. J. Immunol. 162, 1466-1479.
51. Cai, J., and Jones, D.P. (1998). Superoxide in apoptosis. Mitochondrial generation triggered by cytochrome c loss. J. Biol. Chem. 273, 11,401-11,404.
52. Chandel, N.S., and Schumacker, P.T. (1999). Cells depleted of mitochondrial DNA (rho0) yield insight into physiological mechanisms. FEBS Lett. 454, 173-176.
53. Lee, H.C., and Wei, Y.H. (2000). Mitochondrial role in life and death of the cell. J. Biomed. Sci. 7, 2-15.
54. Li, AE., Ito, H., Rovira, II, et al. (1999). A role for reactive oxygen species in endothelial cell anoikis. Circ. Res. 85, 304-310.
55. Von Harsdorf, R., Li, P.F., and Dietz, R. (1999). Signaling pathways in reactive oxygen species-induced cardiomyocyte apoptosis. Circulation 99, 2934-2941.
56. Sidoti-de Fraisse, C., Rincheval, V., Risler, Y., Mignotte, B., and Vayssiere J.L. (1998). TNF-alpha activates at least two apoptotic signaling cascades. Oncogene 17, 1639-1651.
57. Singh, I., Pahan, K., Khan, M., and Singh, A.K. (1998). Cytokine-mediated induction of ceramide production is redox-sensitive. Implications to proinflammatory cytokinemediated apoptosis in demyelinating diseases. J. Biol. Chem. 273, 20,354-20,362.
58. Wissing, D., Mouritzen, H., and Jaattela, M. (1998). TNFinduced mitochondrial changes and activation of apoptotic proteases are inhibited by A20. Free Radic. Biol. Med. 25, 57-65.
59. Chandel, N.S., Maltepe, E., Goldwasser, E., Mathieu, C.E., Simon, M.C., and Schumacker, P.T. (1998). Mitochondrial reactive oxygen species trigger hypoxia-induced transcription. Proc. Natl. Acad. Sci. U.S.A. 95, 11,715-11,720.
60. Duranteau, J., Chandel, N.S., Kulisz, A., Shao, Z., and Schumacker, P.T. (1998). Intracellular signaling by reactive oxygen species during hypoxia in cardiomyocytes. J. Biol. Chem. 273, 11,619- 11,624.
61. McKelvey, T.G., Hollwarth, M.E., Granger, D.N., Engerson, T.D., Landler, U., and Jones, H.P. (1988). Mechanisms of conversion of xanthine dehydrogenase to xanthine oxidase in ischemic rat liver and kidney. Am. J. Physiol. Gastrointest. Liver Physiol. 254, G753-G760.
62. Parks, D.A., Williams, T.K., and Beckman, J.S. (1988). Conversion of xanthine dehydrogenase to oxidase in ischemic rat intestine: a reevaluation. Am. J. Physiol. Gastrointest. Liver Physiol. 254, G768-G774.
63. Heldin, C.H. (1995). Dimerization of cell surface receptors in signal transduction. Cell, 80, 213-223.
64. Rosette, C., and Karin, M. (1996). Ultraviolet light and osmotic stress: activation of the JNK cascade through multiple growth factor and cytokine receptors. Science 274, 1194-1197.
65. Sachsenmaier, C., Radler-Pohl, A., Zinck, R., Nordheim, A., Herrlich, P., and Rahmsdorf, H.J. (1994). Involvement of growth factor receptors in the mammalian UVC response. Cell 78, 963-972.
66. Huang, R.P., Wu, J.X., Fan, Y., and Adamson, E.D. (1996). UV activates growth factor receptors via reactive oxygen intermediates. J. Cell Biol. 133, 211-220.
67. Peus, D., Meves, A., Vasa, R.A., Beyerle, A., O'Brien, T., and Pittelkow, M.R. (1999). H2O2 is required for UVB-induced EGF receptor and downstream signaling pathway activation. Free Radic. Biol. Med. 27, 1197-1202.
68. Gamou, S., and Shimizu, N. (1995). Hydrogen peroxide preferentially enhances the tyrosine phosphorylation of epidermal growth factor receptor. FEBS Lett. 357, 161-164.
69. Goldkorn, T., Balaban, N., Matsukuma, K., et al. (1998). EGF receptor phosphorylation and signaling are targeted by H2O2 redox stress. Am. J. Respir. Cell Mol. Biol. 19, 786-798.
70. Gonzalez-Rubio, M., Voit, S., Rodriguez-Puyol, D., Weber, M., and Marx, M. (1996). Oxidative stress induces tyrosine phosphorylation of PDGF-a and -b receptors and pp60c-src in mesangial cells. Kidney Int. 50, 164-173.
71. Cunnick, J.M., Dorsey, J.F., Standley, T., et al. (1998). Role of tyrosine kinase activity of epidermal growth factor receptor in the lysophosphatidic acid-stimulated mitogen-activated protein kinase pathway. J. Biol. Chem. 273, 14,468-14,475.
72. Bae, YS., Kang, S.W., Seo, M.S., et al. (1997). Epidermal growth factor (EGF)-induced generation of hydrogen peroxide. Role in EGF receptor-mediated tyrosine phosphorylation. J. Biol. Chem. 272: 217-221.