The plasma membrane is involved in the visible light-tissue interaction

Photomedicine and Laser Surgery

Volumn 30, Issue 1, 2012, Pages 14-19

  Lavi, Ronit ^a   Ankri, Rinat ^a   Sinyakov, Michael ^a   Eichler, Maor ^a   Friedmann, Harry ^a   Shainberg, Asher ^a   Breitbart, Haim ^a   Lubart, Rachel ^a  

^a BAR ILAN UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

BLUE LIGHT; CELLULAR TARGETS; ELECTRON CHAIN; ELECTRON TRANSFER; ENZYME-CATALYZED REACTIONS; LIGHT-TISSUE INTERACTION; LOW LEVEL; MITOCHONDRIAL CYTOCHROME; NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATES; OXYGEN RADICAL; REACTIVE OXYGEN SPECIES; SPIN-TRAPPING TECHNIQUE; VISIBLE LIGHT; VISIBLE-LIGHT IRRADIATION;

AMIDES; CATALYSIS; CELL MEMBRANES; CHROMOPHORES; DENATURATION; ELECTRON SPIN RESONANCE SPECTROSCOPY; ENZYMES; FREE RADICAL REACTIONS; LIGHT SOURCES; MEMBRANES; OXYGEN; PARAMAGNETIC RESONANCE; PARAMAGNETISM; PHOTOCHEMICAL REACTIONS; PHOTOSENSITIZERS; PLASMAS; SIGNAL TRANSDUCTION; TISSUE;

LIGHT;

5,5 DIMETHYL 1 PYRROLINE 1 OXIDE; 5,5-DIMETHYL-1-PYRROLINE-1-OXIDE; AMINE OXIDE; REACTIVE OXYGEN METABOLITE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE;

ANIMAL; ARTICLE; CELL MEMBRANE; ELECTRON SPIN RESONANCE; LIGHT; MALE; METABOLISM; RADIATION EXPOSURE; SHEEP; SPERMATOZOON; SPIN TRAPPING; ULTRASTRUCTURE;

ANIMALS; CELL MEMBRANE; CYCLIC N-OXIDES; ELECTRON SPIN RESONANCE SPECTROSCOPY; LIGHT; MALE; NADPH OXIDASE; REACTIVE OXYGEN SPECIES; SHEEP; SPERMATOZOA; SPIN TRAPPING;

EID: 84855447548     PISSN: 15495418     EISSN: None     Source Type: Journal    
DOI: 10.1089/pho.2011.3083     Document Type: Article

References (56)

1. Kreisler, M., Christoffers, A.B., Al-Haj, H., Willershausen, B., and d'Hoedt, B. (2002). Low level 809-nm diode laserinduced in vitro stimulation of the proliferation of human gingival fibroblasts. Lasers Surg. Med. 30, 365-369. (Pubitemid 34742332)
2. Moore P., Ridgway T.D., Higbee R.G., Howard E.W., Lucroy M.D. (2005). Effect of wavelength on low-intensity laser irradiation- stimulated cell proliferation in vitro. Lasers Surg. Med,. 36, 8-12. (Pubitemid 40224025)
3. Yu, W., Naim, J.O., and Lanzafame, R.J. (1995). The effect of photo-irradiation (laser) on lymphocyte proliferation and ATP production in vitro. FASEB J. 9, A239.
4. Ben-Dov, N., Shefer, G., Irinitchev, A., Wernig, A., Oron, U., and Halevy, O. (1999). Low-energy laser irradiation affects satellite cell proliferation and differentiation in vitro. Biochim. Biophys. Acta 1448, 372-380. (Pubitemid 29070861)
5. Moore, P., Ridgway, T.D., Higbee, R.G., Howard, E.W., and Lucroy, M.D. (2005). Effect of wavelength on low-intensity laser irradiation-stimulated cell proliferation in vitro. Lasers Surg. Med. 36, 8-12. (Pubitemid 40224025)
6. 2 laser wounds in rats. Photomed. Laser Surg. 24, 389-396. (Pubitemid 44115223)
7. Stein, A., Benayahu, D., Maltz, L., and Oron, U. (2005). Lowlevel laser irradiation promotes proliferation and differentiation of human osteoblasts in vitro. Photomed. Laser Surg. 23, 161-166. (Pubitemid 40720983)
8. 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. (Pubitemid 32808308)
9. Gigo-Benato D., Geuna S. and Rochkind S. (2005). Phototherapy for enhancing peripheral nerve repair: A review of the literature. Muscle & Nerve. 31, 694-701. (Pubitemid 40734677)
10. Oron U. (2004). Photoengineering of tissue repair in skeletal and cardiacmuscles - Review. Photomed. Laser Surg. 24, 2006.
11. Rochkind S., Leider-Trejo L., Nissan M., Shamir M.H., Kharenko O. and Alon M. (2007). Efficacy of 780-nm Laser Phototherapy on Peripheral Nerve Regeneration after Neurotube Reconstruction Procedure (Double-Blind Randomized Study). Photomed. Laser Surg. 25, 137-143. (Pubitemid 47068077)
12. 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. (Pubitemid 128472728)
13. Corral-Baques, M.I., Rigau, T., Rivera, M., Rodriguez, J.E., and Rigau, J. (2005). Effect of 655-nm diode laser on dog sperm motility. Lasers Med. Sci. 20, 28-34. (Pubitemid 41175881)
14. Kipshidze, N., Nikolaychik, V., Keelan, M.H., et al. (2001). Low-power helium: neon laser irradiation enhances production of vascular endothelial growth factor and promote growth of endothelial cells in vitro Lasers Surg. Med. 28, 355-364. (Pubitemid 32411118)
15. Schwartz, F., Brodie, C., Appel, E., Kazimirsky, G., and Shainberg, A. (2002). Effect of helium laser irradiation on nerve growth factor synthesis and secretion in skeletal muscle cultures. Photochem. Photobiol. B. 66, 195-200. (Pubitemid 34449963)
16. Saygun, I., Karacay, S., Serdar, M., Ural, A.U., Sencimen, M., and Kurtis, B. (2008). Effects of laser irradiation on the release of basic fibroblast growth factor (bFGF), insulin like growth factor-1 (IGF-1), and receptor of IGF-1 (IGFBP3) from gingival fibroblasts. Lasers Med. Sci. 23, 211-215. (Pubitemid 351422642)
17. Arany, P.R., Nayak, R.S., Hallikerimath, S., Limaye, A.M., Kale, A.D., and Kondaiah, P. (2007). Activation of latent TGF-b1 by low-power laser in vitro correlates with increased TGF-b1 levels in laser-enhanced oral wound healing. Wound Rep. Reg. 15, 866-874. (Pubitemid 350135237)
18. Hou, J.-f., Zhang, H., Yuan, X., Li, J., Wei, Y-j., and Hu, S-s. (2008). In vitro effects of low-level laser irradiation for bone marrow mesenchymal stem cells: Proliferation, growth factors secretion and myogenic differentiation. Lasers Surg. Med. 40, 726-733.
19. Karu, T. (1999). Primary and secondary mechanisms of action of visible to near-IR radiation on cells. J. Photochem. Photobiol. B. 49, 1-17. (Pubitemid 29229670)
20. 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. (Pubitemid 37069761)
21. Friedmann, H., Lubart, R., Laulicht, I., and Rochkind, S. (1991). A possible explanation of laser-induced stimulation and damage of cells cultures. J. Photochem. Photobiol. B. 11, 87-95.
22. Lubart, R., Wollman, Y., Friedmann, H., Rochkind, S., and Laulicht, I. (1992). Effects of visible and near-infrared lasers on cell cultures. J. Photochem. Photobiol. B. 12, 305-310.
23. Suzuki, Y.J., Forman, H.J., and Sevanian, A. (1997). Oxidants as stimulators of signal transduction. Free Radic. Biol. Med. 22, 269-285. (Pubitemid 26399334)
24. Purohit, S, Kumar, G.P., Laloraya, M, and Laloraya, M.M. (1994). Involvement of superoxide radical in signal transduction regulating stomatal movements. Biochem. Biophys. Res. Commun. 205, 30-37. (Pubitemid 24381586)
25. Davies, K.J. (1999). The broad spectrum of responses to oxidants in proliferating cells: a new paradigm for oxidative stress. IUBMB Life 48, 41-47. (Pubitemid 29512983)
26. Kohli, R., Bose, B., and Gupta, P.K. (2001). Induction of phr gene expression in E. coli strain KY706/pPL-1 by He-Ne laser (632.8 nm) irradiation. J. Photochem. Photobiol. B. 60, 136-142. (Pubitemid 32747245)
27. Kessel, D. (1982). Determinants of hematoporphyrin-catalyzed photosensitization. Photochem. Photobiol. 36, 99-101. (Pubitemid 12017551)
28. Fraikin, G.Y., Strakhovskaya, M.G., and Rubin, A.B. (1996). The role of membrane-bound porphyrin-type compound as endogenous sensitizer in photodynamic damage to yeast plasma membranes. J. Photochem. Photobiol. B. 34, 129-135. (Pubitemid 26355480)
29. Klebanov, G.I., Strashkevich, I.A., Chichuk, T.V., Modestova, T.M., and Vladimirov, Y. (1998). Effects of endogenous photosensitizers on the laser-induced priming of leucocytes. Membr. Cell Biol. 12, 339-354. (Pubitemid 29067241)
30. Pottier, R., and Truscott, T.G. (1986). The photochemistry of haematoporphyrin and related systems. Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med. 50, 421-452. (Pubitemid 16049037)
31. Cunningham, M.L., Krinsky, N.I., Giovanazzi, S.M., and Peak, M.J. (1985). Superoxide anion is generated from cellular metabolites by solar radiation and its components. J. Free Radic. Biol. Med. 1, 381-385. (Pubitemid 17173362)
32. Kim, C.S., and Jung, J. (1992). Iron-sulfur centers as endogenous blue light sensitizers in cells: a study with an artificial non-heme iron protein. Photochem. Photobiol. 56, 63-68.
33. Edwards, A. M. (2006). General properties of flavins, in: Flavin Photochemistry and Photobiology. E. Silva and A. M. Edwards (eds.). Amsterdam: Elsevier Scientific Publishing Co., Inc., pp. 1-11.
34. Massey, V. (2000). The chemical and biological versatility of riboflavin. Biochem. Soc. Trans. 28, 283-296.
35. Aba L., and Wolfgang G. (2011) Old chromophores, new photoactivation paradigms, trendy applications: flavins in blue light-sensing photoreceptors. Photochem. Photobiol. 87, 491-510.
36. Edwards, A.M., and Silva, E. (2001). Effect of visible light on selected enzymes, vitamins and amino acids. J. Photochem. Photobiol. B. 63, 126-131. (Pubitemid 33040730)
37. Jones, R.D., Hancock, J.T., and Morice, A.H. (2000). NADPH oxidase: a universal oxygen sensor? Free Radic. Biol. Med. 29, 416-424.
38. Lubart, R., Friedmann, H., Sinyakov, M., Cohen, N., and Breitbart, H. (1997). Changes in calcium transport in mammalian sperm mitochondria and plasma membranes caused by 780nm irradiation. Lasers Surg. Med. 21, 493-499. (Pubitemid 27481411)
39. Lowry, O.H., Rosenbrough, N.H., Farr, A.L., and Randall, R.J. (1951). Protein measurement with the folin phenol reagent. J. Biol. Chem. 193, 265-275.
40. Finkelstein, E., Rosen, G.M., and Rauckman, E.J. (1980). Spin trapping of superoxide and hydroxyl radical: practical aspects. Arch. Biochem. Biophys. 200, 1-16.
41. Kalyanaraman, B. (1982). Detection of toxic free radicals in biology and medicine, in: Reviews in Biochemical Toxicology. E. Hodgson, J.R. Beudand, and R.M. Philipot (eds.). New York: Elsevier Scientific Publishing Co., Inc., pp. 73-139.
42. Kanofsky, J.R., Hoogland, H., Wever, R., and Weiss, S.J. (1988). Singlet oxygen production by human eosinophils. J. Biol. Chem. 263, 9692-9696.
43. Lurie, Z., Offer, T., Russo, A., Samuni, A., and Nitzan, D. (2003). Do stable nitroxide radicals catalyze or inhibit the degradation of hyaluronic acid? Free Radic. Biol. Med. 35, 169-178. (Pubitemid 36835917)
44. de Lamirande, E., Tsai, C., Harakat, A., and Gagnon, C. (1998). Involvement of reactive oxygen species in human sperm arcosome reaction induced by A23187, lysophosphatidylcholine, and biological fluid ultrafiltrates. J. Androl. 19, 585-594. (Pubitemid 28498450)
45. Pushpan, S.K., Venkatraman, S., Anand, V.G., et al. (2002). Porphyrins in photodynamic therapy - a search for ideal photosensitizers. Curr. Med. Chem. Anti-Canc. Agents 2, 187-207. (Pubitemid 34657137)
46. Girotti, A.W. (2001). Photosensitized oxidation of membrane lipids: reaction pathways, cytotoxic effects, and cytoprotective mechanisms. J. Photochem. Photobiol. B. 63, 103-113. (Pubitemid 33040728)
47. 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. (Pubitemid 41598961)
48. Silva, E., and Godoy, J. (1994). Riboflavin sensitized photooxidation of tyrosine. Int. J. Vitam. Nutr. Res. 64, 253-256.
49. Crane, F.L., Sun, I.L., Clark, M.G., Grebing, C., and Low, H. (1985). Transplasma-membrane redox systems in growth and development. Biochim. Biophys. Acta 811, 233-264. (Pubitemid 15246564)
50. Go, Y.M., and Jones, D.P. (2005). Intracellular proatherogenic events and cell adhesion modulated by extracellular thiol/disulfide redox state. Circulation 111, 2973-2980. (Pubitemid 40814191)
51. Sauer, H., Wartenberg, M., and Hescheler, J. (2001). Reactive oxygen species as intracellular messengers during cell growth and differentiation. Cell Physiol. Biochem. 11, 186.
52. Nakashima, I., Kato, M., Akhand, A.A., et al. (2002). Redoxlinked signal transduction pathways for protein tyrosine kinase activation. Antioxid. Redox. Signal 4, 517-531. (Pubitemid 34753392)
53. Lavi, R., Shainberg, A., 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.
54. O'Flaherty, C., de Lamirande, E., and Gagnon, C. (2006). Positive role of reactive oxygen species in mammalian sperm capacitation: triggering and modulation of phosphorylation events. Free Radic. Biol. Med. 41, 528-540. (Pubitemid 44080504)
55. Ford, W.C.L. (2004). Regulation of sperm function by reactive oxygen species. Hum. Reprod. Update 10, 387-399. (Pubitemid 39232794)
56. Rivlin, J., Mendel, J., Rubinstein, S., Etkovitz, N., and Breitbart, H. (2004). Role of hydrogen peroxide in sperm capacitation and acrosome reaction. Biol. Reprod. 70, 518-522. (Pubitemid 38160116)