Low intensity light stimulates nitrite-dependent nitric oxide synthesis but not oxygen consumption by cytochrome c oxidase: Implications for phototherapy

被引:86
作者
Ball, Kerri A. [1 ]
Castello, Pablo R. [1 ]
Poyton, Robert O. [1 ]
机构
[1] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
基金
美国国家卫生研究院;
关键词
Nitrite; Nitric oxide; Mitochondria; Cytochrome c oxidase; Phototherapy; Photobiomodulation; ENERGY LASER IRRADIATION; NEAR-INFRARED LIGHT; HELIUM-NEON LASER; REDUCTASE-ACTIVITY; IN-VIVO; GENE-EXPRESSION; PHOTODYNAMIC THERAPY; CELL-PROLIFERATION; IR RADIATION; MITOCHONDRIA;
D O I
10.1016/j.jphotobiol.2010.12.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytochrome c oxidase (Cco) has been reported to be a receptor for some of the beneficial effects of low intensity visible and near-infrared light on cells and tissues. Here, we have explored the role of low intensity light in affecting a newly described function of Cco, its ability to catalyze nitrite-dependent nitric oxide (NO) synthesis (Cco/NO). Using a new assay for Cco/NO we have found that both yeast and mouse brain mitochondria! Cco produce NO over a wide range of oxygen concentrations and that the rate of NO synthesis increases as the oxygen concentration decreases, becoming optimal under hypoxic conditions. Low intensity broad-spectrum light increases Cco/NO activity in an intensity-dependent fashion but has no effect on oxygen consumption by Cco. By using a series of bandpass filters and light emitting devices (LEDs) we have determined that maximal stimulation of Cco/NO activity is achieved by exposure to light whose central wavelength is 590 +/- 14 nm. This wavelength of light stimulates Cco/NO synthesis at physiological nitrite concentrations. These findings raise the interesting possibility that low intensity light exerts a beneficial effect on cells and tissues by increasing NO synthesis catalyzed by Cco and offer a new explanation for the increase in NO bioavailability experienced by tissue exposed to light. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:182 / 191
页数:10
相关论文
共 78 条
[1]   ISOFORMS OF YEAST CYTOCHROME-C-OXIDASE SUBUNIT-V AFFECT THE BINUCLEAR REACTION-CENTER AND AFTER THE KINETICS OF INTERACTION WITH THE ISOFORMS OF YEAST CYTOCHROME-C [J].
ALLEN, LA ;
ZHAO, XJ ;
CAUGHEY, W ;
POYTON, RO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (01) :110-118
[2]   A photosensitive vascular smooth muscle store of nitric oxide in mouse aorta: no dependence on expression of endothelial nitric oxide synthase [J].
Andrews, KL ;
McGuire, JJ ;
Triggle, CR .
BRITISH JOURNAL OF PHARMACOLOGY, 2003, 138 (05) :932-940
[3]   Nitrite Reductase Activity of Cytochrome c [J].
Basu, Swati ;
Azarova, Natalia A. ;
Font, Michael D. ;
King, S. Bruce ;
Hogg, Neil ;
Gladwin, Mark T. ;
Shiva, Sruti ;
Kim-Shapiro, Daniel B. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (47) :32590-32597
[4]   Regulation of cytochrome c oxidase by adenylic nucleotides.: Is oxidative phosphorylation feedback regulated by its end-products? [J].
Beauvoit, B ;
Rigoulet, M .
IUBMB LIFE, 2001, 52 (3-5) :143-152
[5]   ELECTRON-PARAMAGNETIC-RES STUDIES OF THE PHOTO-DISSOCIATION REACTIONS OF CYTOCHROME-C OXIDASE NITRIC-OXIDE COMPLEXES [J].
BOELENS, R ;
RADEMAKER, H ;
PEL, R ;
WEVER, R .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 679 (01) :84-94
[6]   REACTIONS OF NITRIC-OXIDE WITH CYTOCHROME-C OXIDASE [J].
BRUDVIG, GW ;
STEVENS, TH ;
CHAN, SI .
BIOCHEMISTRY, 1980, 19 (23) :5275-5285
[7]   Nitric oxide and the respiratory enzyme [J].
Brunori, Maurizio ;
Forte, Elena ;
Arese, Marzia ;
Mastronicola, Daniela ;
Giuffre, Alessandro ;
Sarti, Paolo .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2006, 1757 (9-10) :1144-1154
[8]   Cellular targets and mechanisms of nitros(yl)ation:: An insight into their nature and kinetics in vivo [J].
Bryan, NS ;
Rassaf, T ;
Maloney, RE ;
Rodriguez, CM ;
Saijo, F ;
Rodriguez, JR ;
Feelisch, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (12) :4308-4313
[9]   P-31 NMR SATURATION-TRANSFER AND C-13 NMR KINETIC-STUDIES OF GLYCOLYTIC REGULATION DURING ANAEROBIC AND AEROBIC GLYCOLYSIS [J].
CAMPBELLBURK, SL ;
DENHOLLANDER, JA ;
ALGER, JR ;
SHULMAN, RG .
BIOCHEMISTRY, 1987, 26 (23) :7493-7500
[10]   Yeast flavohemoglobin, a nitric oxide oxidoreductase, is located in both the cytosol and the mitochondrial matrix [J].
Cassanova, N ;
O'Brien, KM ;
Stahl, BT ;
McClure, T ;
Poyton, RO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (09) :7645-7653