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Hydrogen Peroxide Activates Endothelial Nitric-oxide Synthase through Coordinated Phosphorylation and Dephosphorylation via a Phosphoinositide 3-Kinase-dependent Signaling Pathway
Open accessAbstract
Endothelial nitric-oxide synthase (eNOS) is an important component of vascular homeostasis. During vascular disease, endothelial cells are exposed to excess reactive oxygen species that can alter cellular phenotype by inducing various signaling pathways. In the current study, we examined the implications of H(2)O(2)-induced signaling for eNOS phosphorylation status and activity in porcine aortic endothelial cells. We found that H(2)O(2) treatment enhanced eNOS activity and NO bioactivity as determined by the conversion of l-[(3)H]arginine to l-[(3)H]citrulline and cellular cGMP content. Concomitant with eNOS activation, H(2)O(2) also activated Akt, increased eNOS phosphorylation at Ser-1177, and decreased eNOS phosphorylation at Thr-495. H(2)O(2)-induced promotion of eNOS activity and modulation of the eNOS phosphorylation status at Ser-1177 and Thr-495 were significantly attenuated by selective inhibitors of Src kinase, the ErbB receptor family, and phosphoinositide 3-kinase (PI 3-K). We found that Akt activation, eNOS Ser-1177 phosphorylation, and eNOS activation by H(2)O(2) were calcium-dependent, whereas eNOS dephosphorylation at Thr-495 was not, suggesting a branch point in the signaling cascade downstream from PI 3-K. Consistent with this, overexpression of a dominant negative isoform of Akt inhibited H(2)O(2)-induced phosphorylation of eNOS at Ser-1177 but not dephosphorylation of eNOS at Thr-495. Together, these data indicate that H(2)O(2) promotes calcium-dependent eNOS activity through a coordinated change in the phosphorylation status of the enzyme mediated by Src- and ErbB receptor-dependent PI 3-K activation. In turn, PI 3-K mediates eNOS Ser-1177 phosphorylation via a calcium- and Akt-dependent pathway, whereas eNOS Thr-495 dephosphorylation does not involve calcium or Akt. This response may represent an attempt by endothelial cells to maintain NO bioactivity under conditions of enhanced oxidative stress.
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“An emerging paradigm proposes that intermediate levels (50–300 nM) can activate a range of positive and negative responses from wound healing to oncogenic pathways”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [938]
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“Higher concentrations of NO (>1 μM) can lead not only to oxidative stress but also nitrative and nitrosative stress via the generation of peroxynitrite and nitrosating species”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [938]
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Cites
Activation of nitric oxide synthase in endothelial cells by Akt-dependent phosphorylation
Dimmeler, S., Fleming, I., Fisslthaler, B., Hermann, C., Busse, R., & Zeiher, A. M. (1999) · Nature · doi:10.1038/21224 · Cited by 3,591
Mechanism of activation of protein kinase B by insulin and IGF‐1.
Alessi, D. R., Andjelković, M., Caudwell, B., Cron, P. D., MORRICE, N. A., Cohen, P., & Hemmings, B. A. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb01045.x · Cited by 3,014
NAD(P)H Oxidase: Role in Cardiovascular Biology and Disease
Griendling, K. K., Sorescu, D., & Ushio-Fukai, M. (2000) · Circulation Research · doi:10.1161/01.res.86.5.494 · Cited by 2,886
Regulation of endothelium-derived nitric oxide production by the protein kinase Akt
Fulton, D. J., Gratton, J., McCabe, T. J. D., Fontana, J. T., Fujio, Y., Walsh, K. X., Franke, T. F., Papapetropoulos, A., & Sessa, W. C. (1999) · Nature · doi:10.1038/21218 · Cited by 2,616
Requirement for Generation of H 2 O 2 for Platelet-Derived Growth Factor Signal Transduction
Sundaresan, M., Yu, Z.-X., Ferrans, V. J., Irani, K., & Finkel, T. (1995) · Science · doi:10.1126/science.270.5234.296 · Cited by 2,520
Paradoxical Vasoconstriction Induced by Acetylcholine in Atherosclerotic Coronary Arteries
Ludmer, P. L., Selwyn, A. P., Shook, T., Wayne, R. R., Mudge, G. H., Alexander, R. W., & Ganz, P. (1986) · New England Journal of Medicine · doi:10.1056/nejm198610233151702 · Cited by 2,422
Garg, U. C., & Hassid, A. (1989) · Journal of Clinical Investigation · doi:10.1172/jci114081 · Cited by 2,154
Role of endothelium-derived nitric oxide in the regulation of blood pressure.
Rees, D. D., Palmer, R. M. J., & Moncada, S. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.9.3375 · Cited by 1,827
Hypercholesterolemia increases endothelial superoxide anion production.
Ohara, Y., Peterson, T. E., & Harrison, D. G. (1993) · Journal of Clinical Investigation · doi:10.1172/jci116491 · Cited by 1,765
Fruman, D. A., Meyers, R. E., & Cantley, L. C. (1998) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.67.1.481 · Cited by 1,382
Flagged first, then by citations
Research works printed but not linked: 3
- Govers, 2001, Am. J. Physiol., 280, F193
- Fleming, 2001, Circ. Res., 88, E68
- Shimizu, 1997, Res. Commun. Mol. Pathol. Pharmacol., 95, 227
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Poh, T. W., & Pervaiz, S. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-0152 · Cited by 88
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Sartoretto, J. L., Kalwa, H., Pluth, M. D., Lippard, S. J., & Michel, T. M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1111331108 · Cited by 86
Stocker, R., Huang, A., Jeranian, E., Hou, J. Y., Wu, T. T., Thomas, S. R., & Keaney, J. F. (2004) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000143388.20994.fa · Cited by 84
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Acute exercise activates AMPK and eNOS in the mouse aorta
Cacicedo, J. M., Gauthier, M., LeBrasseur, N. K., Jasuja, R., Ruderman, N. B., & Ido, Y. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01279.2010 · Cited by 81
Hiền, T. T., Kim, N. D., Pokharel, Y. R., Oh, S. J., Lee, M. Y., & Kang, K. W. (2010) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2010.05.008 · Cited by 82
HIF‐1: hypoxia‐inducible factor or dysoxia‐inducible factor?
López‐Lázaro, M. (2006) · The FASEB Journal · doi:10.1096/fj.05-5168hyp · Cited by 82
Visfatin causes endothelium-dependent relaxation in isolated blood vessels
Yamawaki, H., Hara, N., Okada, M., & Hara, Y. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.04.074 · Cited by 81
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Østergaard, L., Stankevıčıus, E., Andersen, M. R., Eskildsen-Helmond, Y. E. G., Ledet, T., Mulvany, M. J., & Simonsen, U. (2007) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01230.2006 · Cited by 80
Ndiaye, M., Chataigneau, T., Chataigneau, M., & Schini‐Kerth, V. B. (2004) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0705774 · Cited by 80
Witting, P. K., Rayner, B. S., Wu, B. J., Ellis, N. A., & Stocker, R. (2007) · Cellular Physiology and Biochemistry · doi:10.1159/000107512 · Cited by 77
Shafique, E., Choy, W. C., Liu, Y., Feng, J., Cordeiro, B., Lyra, A., Arafah, M., Yassin-Kassab, A., Zanetti, A. V. D., Clements, R., et al. (2013) · Aging · doi:10.18632/aging.100569 · Cited by 76
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Rocca, G. L., Stefano, A. D., Eleuteri, E., Anzalone, R., Magno, F., Corrao, S., Loria, T., Martorana, A., Gangi, C. D., Colombo, M., et al. (2008) · Basic Research in Cardiology · doi:10.1007/s00395-008-0761-9 · Cited by 67
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Trott, D. W., Seawright, J. W., Luttrell, M. J., & Woodman, C. R. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01037.2010 · Cited by 57
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Row, S., Peng, H., Schlaich, E. M., Koenigsknecht, C., Andreadis, S. T., & Swartz, D. D. (2015) · Biomaterials · doi:10.1016/j.biomaterials.2015.01.045 · Cited by 57
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Yan, H., Mi, X., Midgley, A. C., Du, X., Huang, Z., Wei, T., Liu, R., Ma, T., Zhi, D., Zhu, D., et al. (2020) · Advanced Science · doi:10.1002/advs.201903516 · Cited by 56
Kumar, S., Sud, N., Fonseca, F. V., Hou, Y., & Black, S. M. (2009) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00290.2009 · Cited by 56
Visible light induces no formation in sperm and endothelial cells
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Pandolfi, A., Grilli, A., Cilli, C., Patruno, A., Giaccari, A., Silvestre, S. D., Lutiis, M. A. D., Pellegrini, G., Capani, F., Consoli, A., et al. (2003) · Journal of Cellular Physiology · doi:10.1002/jcp.10325 · Cited by 55
Usatyuk, P. V., & Natarajan, V. (2005) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00211.2005 · Cited by 55
Ladurner, A., Schmitt, C. A., Schachner, D., Atanasov, A. G., Werner, E. R., Dirsch, V. M., & Heiss, E. H. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.03.022 · Cited by 54
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Yan, T., Li, Q., Zhang, X., Wei-kang, W., Sun, J., Li, L., Zhang, Q., & Tan, H. (2010) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2010.05438.x · Cited by 50
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Nuntharatanapong, N., Chen, K., Sinhaseni, P., & Keaney, J. F. (2005) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00901.2004 · Cited by 49
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Wang, M., Chen, Y., Xiong, Z., Yu, S., Zhou, B., Ling, Y., Zheng, Z., Shi, G., Wu, Y., & Qian, X. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.7710 · Cited by 43
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Self-citationWitting, P. K., Song, C., Hsu, K., Hua, S., Parry, S. N., Aran, R., Geczy, C. L., & Freedman, S. B. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.06.031 · Cited by 37
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Tracy, E. P., Hughes, W. E., Beare, J. E., Rowe, G., Beyer, A., & LeBlanc, A. J. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0031 · Cited by 39
Tian, J., Hou, Y., Lü, Q., Wiseman, D. A., Fonseca, F. V., Elms, S. C., Fulton, D. J., & Black, S. M. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.03.023 · Cited by 35
Metadata
- Authors
- Thomas, S. R., Chen, K., & Keaney, J. F.
- Affiliations
- Boston University (US)
- Corresponding author
- Keaney, John F.
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2002-02
- Volume
- 277
- Issue
- 8
- Pages
- 6017-6024
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2119043221
- Cited by
- 381
- References
- 47
- Citations by year
- 2026: 2 · 2025: 8 · 2024: 4 · 2023: 5 · 2022: 10 · 2021: 12 · 2020: 7 · 2019: 8 · 2018: 9 · 2017: 14 · 2016: 13 · 2015: 20 · 2014: 21 · 2013: 17 · 2012: 19
- FWCI
- 16.21
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01dk055656-03)
- National Heart, Lung, and Blood Institute (P01HL060886, HL-60886)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK-55656)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- hydrogen peroxide, endothelial nitric oxide synthase, eNOS phosphorylation, phosphatidylinositol 3-kinase, Akt signaling, Src kinase, ErbB receptors, calcium signaling, nitric oxide bioactivity, cyclic GMP, reactive oxygen species
- MeSH terms
- Animals, Aorta, Arginine, Cells, Cultured, Chromones, Citrulline, Egtazic Acid, Endothelium, Vascular, Enzyme Activation, Enzyme Inhibitors, Hydrogen Peroxide, Kinetics, Morpholines, Nitric Oxide, Phosphorylation, Phosphoserine, Phosphothreonine, Quinazolines, Swine, Signal Transduction, Nitric Oxide Synthase, Phosphatidylinositol 3-Kinases, Calcium Signaling, Tyrphostins, Nitric Oxide Synthase Type III
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