Cellular chromophores and signaling in low level light therapy

Progress in Biomedical Optics and Imaging - Proceedings of SPIE

Volumn 6428, Issue , 2007, Pages

  Hamblin, Michael R ^a,b,c   Demidova Rice, Tatiana N ^a,d  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c HARVARD MIT DIVISION OF HEALTH SCIENCES AND TECHNOLOGY   (United States)

^d TUFTS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Biostimulation; Cytochrome c oxidase; Low level laser therapy; Mitochondria; Nitric oxide

Indexed keywords

ELECTROMAGNETIC WAVES; NITRIC OXIDE; PHOTODISSOCIATION; PROTEINS; TISSUE;

BIOSTIMULATION; CYTOCHROME C OXIDASE; LOW LEVEL LASER THERAPY; MITOCHONDRIA; REACTIVE OXYGEN SPECIES;

CHROMOPHORES;

EID: 34548238193     PISSN: 16057422     EISSN: None     Source Type: Conference Proceeding    
DOI: 10.1117/12.712885     Document Type: Conference Paper

References (76)

1. A.N. Pereira, P. Eduardo Cde, E. Matson and M.M. Marques, Effect of low-power laser irradiation on cell growth and procollagen synthesis of cultured fibroblasts, Lasers Surg Med 31 (2002) 263-7.
2. J.S. Kana, G. Hutschenreiter, D. Haina and W. Waidelich, Effect of low-power density laser radiation on healing of open skin wounds in rats, Arch Surg 116 (1981) 293-6.
3. J.C. Sutherland, Biological effects of polychromatic light, Photochem Photobiol 76 (2002) 164-70.
4. J.T. Eells, M.T. Wong-Riley, J. VerHoeve, M. Henry, E.V. Buchman, M.P. Kane, L.J. Gould, R. Das, M. Jett, B.D. Hodgson, D. Margolis and H.T. Whelan, Mitochondrial signal transduction in accelerated wound and retinal healing by near-infrared light therapy, Mitochondrion 4 (2004) 559-67.
5. S. Passarella, E. Casamassima, S. Molinari, D. Pastore, E. Quagliariello, I.M. Catalano and A. Cingolani, Increase of proton electrochemical potential and ATP synthesis in rat liver mitochondria irradiated in vitro by helium-neon laser, FEBS Lett 175 (1984) 95-9.
6. M. Greco, G. Guida, E. Perlino, E. Marra and E. Quagliariello, Increase in RNA and protein synthesis by mitochondria irradiated with helium-neon laser, Biochem Biophys Res Commun 163 (1989) 1428-34.
7. D. Pastore, M. Greco, V.A. Petragallo and S. Passarella, Increase in <--H+/e- ratio of the cytochrome c oxidase reaction in mitochondria irradiated with helium-neon laser, Biochem Mol Biol Int 34 (1994) 817-26.
8. W. Yu, J.O. Naim, M. McGowan, K. Ippolito and R.J. Lanzafame, Photomodulation of oxidative metabolism and electron chain enzymes in rat liver mitochondria, Photochem Photobiol 66 (1997) 866-71.
9. K. Surrey and S.A. Gordon, Influence of Light on Phosphate Metabolism in Lettuce Seed: Spectral Response Red, Far-Red Interaction, Plant Physiol 37 (1962) 327-32.
10. S.A. Gordon and K. Surrey, Red and far-red action on oxidative phosphorylation, Radiat Res 12 (1960) 325-39.
11. H. Loevschall and D. Arenholt-Bindslev, Effect of low level diode laser irradiation of human oral mucosa fibroblasts in vitro, Lasers Surg Med 14 (1994) 347-54.
12. T.I. Karu and S.F. Kolyakov, Exact action spectra for cellular responses relevant to phototherapy, Photomed Laser Surg 23 (2005) 355-61.
13. T.I. Karu, L.V. Pyatibrat, S.F. Kolyakov and N.I. Afanasyeva, Absorption measurements of a cell monolayer relevant to phototherapy: Reduction of cytochrome c oxidase under near IR radiation, J Photochem Photobiol B 81 (2005) 98-106.
14. M.T. Wong-Riley, H.L. Liang, J.T. Eells, B. Chance, M.M. Henry, E. Buchmann, M. Kane and H.T. Whelan, Photobiomodulation directly benefits primary neurons functionally inactivated by toxins: role of cytochrome c oxidase, J Biol Chem 280 (2005) 4761-71.
15. M.T. Wong-Riley, X. Bai, E. Buchmann and H.T. Whelan, Light-emitting diode treatment reverses the effect of TTX on cytochrome oxidase in neurons, Neuroreport 12 (2001) 3033-7.
16. J.T. Eells, M.M. Henry, P. Summerfelt, M.T. Wong-Riley, E.V. Buchmann, M. Kane, N.T. Whelan and H.T. Whelan, Therapeutic photobiomodulation for methanol-induced retinal toxicity, Proc Natl Acad Sci U S A 100 (2003) 3439-44.
17. T.I. Karu and N.I. Afanas'eva, Cytochrome c oxidase as the primary photoacceptor upon laser exposure of cultured cells to visible and near IR-range light, Dokl Akad Nauk 342 (1995) 693-5.
18. R.A. Capaldi, F. Malatesta and V.M. Darley-Usmar, Structure of cytochrome c oxidase, Biochim Biophys Acta 726 (1983) 135-48.
19. I. Szundi, G.L. Liao and O. Einarsdottir, Near-infrared time-resolved optical absorption studies of the reaction of fully reduced cytochrome c oxidase with dioxygen, Biochemistry 40 (2001) 2332-9.
20. S. Passarella, He-Ne laser irradiation of isolated mitochondria, J Photochem Photobiol B 3 (1989) 642-3.
21. S. Moneada and J.D. Erusalimsky, Does nitric oxide modulate mitochondrial energy generation and apoptosis?, Nat Rev Mol Cell Biol 3 (2002) 214-20.
22. G.C. Brown, Regulation of mitochondrial respiration by nitric oxide inhibition of cytochrome c oxidase, Biochim Biophys Acta 1504 (2001) 46-57.
23. A.J. Kanai, L.L. Pearce, P.R. Clemens, L.A. Birder, M.M. VanBibber, S.Y. Choi, W.C. de Groat and J. Peterson, Identification of a neuronal nitric oxide synthase in isolated cardiac mitochondria using electrochemical detection, Proc Natl Acad Sci U S A 98 (2001) 14126-31.
24. W. Xu, I.G. Charles and S. Moncada, Nitric oxide: orchestrating hypoxia regulation through mitochondrial respiration and the endoplasmic reticulum stress response, Cell Res 15 (2005) 63-5.
25. V. Darley-Usmar, The powerhouse takes control of the cell; the role of mitochondria in signal transduction, Free Radie Biol Med 37 (2004) 753-4.
26. S. Shiva, J.Y. Oh, A.L. Landar, E. Ulasova, A. Venkatraman, S.M. Bailey and V.M. Darley-Usmar, Nitroxia: the pathological consequence of dysfunction in the nitric oxide-cytochrome c oxidase signaling pathway, Free Radie Biol Med 38 (2005) 297-306.
27. M.D. Brand, The efficiency and plasticity of mitochondrial energy transduction, Biochem Soc Trans 33 (2005) 897-904.
28. G.C. Brown, Nitric oxide and mitochondria, Front Biosci 12 (2007) 1024-33.
29. F. Antunes, A. Boveris and E. Cadenas, On the mechanism and biology of cytochrome oxidase inhibition by nitric oxide, Proc Natl Acad Sci U S A 101 (2004) 16774-9.
30. T.I. Karu, L.V. Pyatibrat and N.I. Afanasyeva, Cellular effects of low power laser therapy can be mediated by nitric oxide, Lasers Surg Med 36 (2005) 307-14.
31. V. Borutaite, A. Budriunaite and G.C. Brown, Reversal of nitric oxide-, peroxynitrite- and S-nitrosothiolinduced inhibition of mitochondrial respiration or complex I activity by light and thiols, Biochim Biophys Acta 1459 (2000) 405-12.
32. B. Moreau, C. Nelson and A.B. Parekh, Biphasic regulation of mitochondrial Ca2+ uptake by cytosolic Ca2+ concentration, Curr Biol 16 (2006) 1672-7.
33. G. Hajnoczky, G. Csordas, S. Das, C. Garcia-Perez, M. Saotome, S. Sinha Roy and M. Yi, Mitochondrial calcium signalling and cell death: approaches for assessing the role of mitochondrial Ca2+ uptake in apoptosis, Cell Calcium 40 (2006) 553-60.
34. A.R. Coombe, C.T. Ho, M.A. Darendeliler, N. Hunter, J.R. Philips, C.C. Chapple and L.W. Yum, The effects of low level laser irradiation on osteoblastic cells, Clin Orthod Res 4 (2001) 3-14.
35. R.A. Vacca, L. Moro, V.A. Petragallo, M. Greco, F. Fontana and S. Passarella, The irradiation of hepatocytes with He-Ne laser causes an increase of cytosolic free calcium concentration and an increase of cell membrane potential, correlated with it, both increases taking place in an oscillatory manner, Biochem Mol Biol Int 43 (1997) 1005-14.
36. E. Alexandratou, D. Yova, P. Handris, D. Kletsas and S. Loukas, Human fibroblast alterations induced by low power laser irradiation at the single cell level using confocal microscopy, Photochem Photobiol Sci 1 (2002) 547-52.
37. K.D. Desmet, D.A. Paz, J.J. Corry, J.T. Eells, M.T. Wong-Riley, M.M. Henry, E.V. Buchmann, M.P. Connelly, J.V. Dovi, H.L. Liang, D.S. Henshel, R.L. Yeager, D.S. Millsap, J. Lim, L.J. Gould, R. Das, M. Jett, B.D. Hodgson, D. Margolis and H.T. Whelan, Clinical and experimental applications of NIR-LED photobiomodulation, Photomed Laser Surg 24 (2006) 121-8.
38. H.L. Liang, H.T. Whelan, J.T. Eells, H. Meng, E. Buchmann, A. Lerch-Gaggl and M. Wong-Riley, Photobiomodulation partially rescues visual cortical neurons from cyanide-induced apoptosis, Neuroscience 139 (2006) 639-49.
39. M. Asahi, M. Hoshimaru, Y. Uemura, T. Tokime, M. Kojima, T. Ohtsuka, N. Matsuura, T. Aoki, K. Shibahara and H. Kikuchi, Expression of interleukin-1 beta converting enzyme gene family and bcl-2 gene family in the rat brain following permanent occlusion of the middle cerebral artery, J Cereb Blood Flow Metab 17 (1997) 11-8.
40. A.C. Salate, G. Barbosa, P. Gaspar, P.U. Koeke, N.A. Parizotto, B.G. Benze and D. Foschiani, Effect of InGa-Al-P diode laser irradiation on angiogenesis in partial ruptures of Achilles tendon in rats, Photomed Laser Surg 23 (2005) 470-5.
41. T. Hagen, C.T. Taylor, F. Lam and S. Moneada, Redistribution of intracellular oxygen in hypoxia by nitric oxide: effect on HIF1alpha, Science 302 (2003) 1975-8.
42. H.H. Marti, Angiogenesis - a self-adapting principle in hypoxia, Exs (2005) 163-80.
43. H.H. Marti, Vascular endothelial growth factor, Adv Exp Med Biol 513 (2002) 375-94.
44. D.E. Richard, E. Berra and J. Pouyssegur, Angiogenesis: how a tumor adapts to hypoxia, Biochem Biophys Res Commun 266 (1999) 718-22.
45. J. Dulak and A. Jozkowicz, Regulation of vascular endothelial growth factor synthesis by nitric oxide: facts and controversies, Antioxid Redox Signal 5 (2003) 123-32.
46. J. Dulak and A. Jozkowicz, Carbon monoxide -a "new" gaseous modulator of gene expression, Acta Biochim Pol 50 (2003) 31-47.
47. S.Y. Yu, J.H. Chiu, S.D. Yang, Y.C Hsu, W.Y. Lui and C.W. Wu, Biological effect of far-infrared therapy on increasing skin microcirculation in rats, Photodermatol Photoimmunol Photomed 22 (2006) 78-86.
48. Y. Maegawa, T. Itoh, T. Hosokawa, K. Yaegashi and M. Nishi, Effects of near-infrared low-level laser irradiation on microcirculation, Lasers Surg Med 27 (2000) 427-37.
49. U. Oron, T. Yaakobi, A. Oron, G. Hayam, L. Gepstein, O. Rubin, T. Wolf and S. Ben Haim, Attenuation of infarct size in rats and dogs after myocardial infarction by low-energy laser irradiation, Lasers Surg Med 28 (2001) 204-11.
50. T.I. Karu, V.V. Lobko, G.G. Lukpanova, I.M. Parkhomenko and I. Chirkov, Effect of irradiation with monochromatic visible light on the cAMP content in mammalian cells, Dokl Akad Nauk SSSR 281 (1985) 1242-4.
51. T.I. Karu, G.G. Lukpanova, I.M. Parkhomenko and O.A. Tiphlova, Effect of irradiation with monochromatic visible light in CAMP content in Chinese hamster fibroblasts, Nuovo Cimento D9 (1987) 1245-1251.
52. F.A. Antoni, Molecular diversity of cyclic AMP signalling, Front Neuroendocrinol 21 (2000) 103-32.
53. D.H. Maurice, D. Palmer, D.G. Tilley, H.A. Dunkerley, S.J. Netherton, D.R. Raymond, H.S. Elbatarny and S.L. Jimmo, Cyclic nucleotide phosphodiesterase activity, expression, and targeting in cells of the cardiovascular system, Mol Pharmacol 64 (2003) 533-46.
54. G.S. McKnight, Cyclic AMP second messenger systems, Curr Opin Cell Biol 3 (1991) 213-7.
55. T. Nakajima, C Uchida, S.F. Anderson, J.D. Parvin and M. Montminy, Analysis of a cAMP-responsive activator reveals a two-component mechanism for transcriptional induction via signal-dependent factors, Genes Dev 11 (1997) 738-47.
56. S. Seino and T. Shibasaki, PKA-dependent and PKA-independent pathways for cAMP-regulated exocytosis, Physiol Rev 85 (2005) 1303-42.
57. M.A. Movsesian and M.R. Bristow, Alterations in cAMP-mediated signaling and their role in the pathophysiology of dilated cardiomyopathy, Curr Top Dev Biol 68 (2005) 25-48.
58. B. Furman, N. Pyne, P. Flatt and F. O'Harte, Targeting beta-cell cyclic 3'5' adenosine monophosphate for the development of novel drugs for treating type 2 diabetes mellitus. A review, J Pharm Pharmacol 56 (2004) 1477-92.
59. J.S. Richards, New signaling pathways for hormones and cyclic adenosine 3',5'-monophosphate action in endocrine cells, Mol Endocrinol 15 (2001) 209-18.
60. E.K. Jackson and R.K. Dubey, Role of the extracellular cAMP-adenosine pathway in renal physiology, Am J Physiol Renal Physiol 281 (2001) F597-612.
61. B.S. Skalhegg, A. Funderud, H.H. Henanger, T.T. Hafte, A.C. Larsen, A.K. Kvissel, S. Eikvar and S. Orstavik, Protein kinase A (PKA) - a potential target for therapeutic intervention of dysfunctional immune cells, Curr Drug Targets 6 (2005) 655-64.
62. I. McPhee, L.C. Gibson, J. Kewney, C Darroch, P.A. Stevens, D. Spinks, A. Cooreman and S.J. MacKenzie, Cyclic nucleotide signalling: a molecular approach to drug discovery for Alzheimer's disease, Biochem Soc Trans 33 (2005) 1330-2.
63. Y. Kawasaki, T. Kohno, Z.Y. Zhuang, G.J. Brenner, H. Wang, C. Van Der Meer, K. Befort, C.J. Woolf and R.R. Ji, Ionotropic and metabotropic receptors, protein kinase A, protein kinase C, and Src contribute to C-fiber-induced ERK activation and cAMP response element-binding protein phosphorylation in dorsal horn neurons, leading to central sensitization, J Neurosci 24 (2004) 8310-21.
64. I. Barlat, B. Henglein, A. Plet, N. Lamb, A. Fernandez, F. McKenzie, J. Pouyssegur, A. Vie and J.M. Blanchard, TGF-beta 1 and cAMP attenuate cyclin A gene transcription via a cAMP responsive element through independent pathways, Oncogene 11 (1995) 1309-18.
65. W.P. Hu, J.J. Wang, C.L. Yu, C.C. Lan, G.S. Chen and H.S. Yu, Helium-Neon Laser Irradiation Stimulates Cell Proliferation Through Photostimulatory Effects in Mitochondria, J Invest Dermatol in press (2007).
66. P. Angel and M. Karin, The role of Jun, Fos and the AP-1 complex in cell-proliferation and transformation, Biochim Biophys Acta 1072 (1991) 129-57.
67. B. Hope, B. Kosofsky, S.E. Hyman and E.J. Nestler, Regulation of immediate early gene expression and AP-1 binding in the rat nucleus accumbens by chronic cocaine, Proc Natl Acad Sci U S A 89 (1992) 5764-8.
68. B. Miotto and K. Struhl, Differential gene regulation by selective association of transcriptional coactivators and bZIP DNA-binding domains, Mol Cell Biol 26 (2006) 5969-82.
69. M. Meyer, R. Schreck and P.A. Baeuerle, H2O2 and antioxidants have opposite effects on activation of NF-kappa B and AP-1 in intact cells: AP-1 as secondary antioxidant-responsive factor, Embo J 12 (1993) 2005-15.
70. M. Greco, R.A. Vacca, L. Moro, E. Perlino, V.A. Petragallo, E. Marra and S. Passarella, Helium-Neon laser irradiation of hepatocytes can trigger increase of the mitochondrial membrane potential and can stimulate c-fos expression in a Ca2+-dependent manner, Lasers Surg Med 29 (2001) 433-41.
71. J. Hirayama, L. Cardone, M. Doi and P. Sassone-Corsi, Common pathways in circadian and cell cycle clocks: light-dependent activation of Fos/AP-1 in zebrafish controls CRY-1a and WEE-1, Proc Natl Acad Sci U S A 102 (2005) 10194-9.
72. T.K. Tamai, A.J. Carr and D. Whitmore, Zebrafish circadian clocks: cells that see light, Biochem Soc Trans 33 (2005) 962-6.
73. E. Abraham, NF-kappaB activation, Crit Care Med 28 (2000) N100-4.
74. Y. Hattori, K. Kasai and S.S. Gross, NO suppresses while peroxynitrite sustains NF-kappaB: a paradigm to rationalize cytoprotective and cytotoxic actions attributed to NO, Cardiovasc Res 63 (2004) 31-40.
75. C.F. Rizzi, J.L. Mauriz, D.S. Freitas Correa, A.J. Moreira, C.G. Zettler, L.I. Filippin, N.P. Marroni and J. Gonzalez-Gallego, Effects of low-level laser therapy (LLLT) on the nuclear factor (NF)-kappaB signaling pathway in traumatized muscle, Lasers Surg Med 38 (2006) 704-13.
76. A.F. Haas, J.W. Wong, C.K. Iwahashi, B. Halliwell, C.E. Cross and P.A. Davis, Redox regulation of wound healing? NF-kappaB activation in cultured human keratinocytes upon wounding and the effect of low energy HeNe irradiation, Free Radic Biol Med 25 (1998) 998-1005.