The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.
Impaired Superoxide Production Due to a Deficiency in Phagocyte NADPH Oxidase Fails to Inhibit Atherosclerosis in Mice
Abstract
Abstract—Superoxide, the reduced form of molecular oxygen, has been implicated in the genesis of vascular disease. One potential mechanism involves oxidation of low density lipoprotein into an atherogenic particle. A second involves reaction with nitric oxide to generate peroxynitrite, a highly oxidizing intermediate. A third involves regulation of signal transduction in artery wall cells. One well-characterized pathway for superoxide production resides in macrophages, the cellular hallmark of the early atherosclerotic lesion. Macrophages contain a membrane-bound NADPH oxidase that reduces oxygen to superoxide. In the current studies, we used mice that are deficient in the gp91-phox subunit of the NADPH oxidase–a model of chronic granulomatous disease (CGD)–to explore the role of superoxide in atherosclerotic vascular disease. Wild-type and CGD mice on the C57BL/6 background received a high-fat diet for 20 weeks to induce hypercholesterolemia. At the end of this period, the 2 strains of mice had comparable plasma lipid levels, and their atherosclerotic lesions were similar in size. We also crossed CGD mice with apolipoprotein E–deficient (apoE−/−) mice to generate spontaneously hypercholesterolemic animals that lacked functional NADPH oxidase. After 24 weeks, the CGD-apoE−/− animals had lower plasma cholesterol and triglyceride levels than did the apoE−/− animals, but there was no difference in the extent of atherosclerotic plaque. Our findings suggest that superoxide generated by the NADPH oxidase of phagocytes does not promote atherosclerosis in mice with either diet-induced or genetic forms of hypercholesterolemia.
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“The combination of NOX2−/− with ApoE−/− can decrease the atherosclerotic lesions (475), but this is not always the case (508).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [508]
Citations
Cites
Nitric oxide: physiology, pathophysiology, and pharmacology.
Moncada, S., Palmer, R. M., & Higgs, E. A. (1991) · Pharmacological Reviews · doi:10.1016/s0031-6997(25)06663-3 · Cited by 15,525
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
The reaction of NO with superoxide
Huie, R. E., & Padmaja, S. (1993) · Free Radical Research Communications · doi:10.3109/10715769309145868 · Cited by 2,121
Homocysteine and Atherothrombosis
Welch, G. N., & Loscalzo, J. (1998) · New England Journal of Medicine · doi:10.1056/nejm199804093381507 · Cited by 1,997
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
Cell transformation by the superoxide-generating oxidase Mox1
Suh, Y.-A., Arnold, R. S., Lassegue, B., Shi, J., Xu, X., Sorescu, D., Chung, A. B., Griendling, K. K., & Lambeth, J. D. (1999) · Nature · doi:10.1038/43459 · Cited by 1,480
The role of oxidized lipoproteins in atherogenesis
Berliner, J. A., & Heinecke, J. W. (1996) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(95)02173-6 · Cited by 1,369
Self-citation[23] Oxidative chemistry of peroxynitrite
Beckman, J. S., Chen, J., Ischiropoulos, H., & Crow, J. P. (1994) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(94)33026-3 · Cited by 973
Pollock, J. D., Williams, D. A., Gifford, M. A. C., Li, L. L., Du, X., Fisherman, J., Orkin, S. H., Doerschuk, C. M., & Dinauer, M. C. (1995) · Nature Genetics · doi:10.1038/ng0295-202 · Cited by 921
Self-citationSuperoxide and peroxynitrite inatherosclerosis.
White, C. R., Brock, T. A., Chang, L. Y., Crapo, J. D., BRISCOE, P. M., Ku, D. D., Bradley, W. A., Gianturco, S. H., Gore, J. Z., & Freeman, B. Α. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.3.1044 · Cited by 684
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Items 101–169 of 169
Oxidized lipoproteins and macrophages
Jessup, W., Wilson, P., Gaus, K., & Kritharides, L. (2002) · Vascular Pharmacology · doi:10.1016/s1537-1891(02)00174-x · Cited by 51
Sfyri, P., & Matsakas, A. (2017) · Journal of Biomedical Science · doi:10.1186/s12929-017-0346-8 · Cited by 44
Siu, K. L., Gao, L., & Cai, H. “. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.713149 · Cited by 44
Lekshmi, V. S., & Kurup, G. M. (2019) · Journal of Functional Foods · doi:10.1016/j.jff.2019.01.004 · Cited by 39
Husemann, J., Obstfeld, A. E., Febbraio, M., Kodama, T., & Silverstein, S. C. (2001) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/hq0801.095150 · Cited by 38
NOX enzymes and diabetic complications
Kakehi, T., & Yabe‐Nishimura, C. (2008) · Seminars in Immunopathology · doi:10.1007/s00281-008-0122-7 · Cited by 38
Dialysis-related systemic microinflammation is associated with specific genomic patterns
Zaza, G., Pontrelli, P., Pertosa, G. B., Granata, S., Rossini, M., Porreca, S., Staal, F. J. T., Gesualdo, L., Grandaliano, G., & Schena, F. P. (2007) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfm804 · Cited by 39
Assessment of Atherosclerosis in Chronic Granulomatous Disease
Sibley, C. T., Estwick, T., Zavodni, A. E. H., Huang, C., Kwan, A. C., Soule, B. P., Priel, D. A. L., Remaley, A. T., Spergel, A. K. R., Turkbey, E. B., et al. (2014) · Circulation · doi:10.1161/circulationaha.113.006824 · Cited by 37
Functional alterations of myeloid cell subsets in hyperlipidaemia: relevance for atherosclerosis
Soehnlein, O., Drechsler, M. D., Hristov, M., & Weber, C. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00965.x · Cited by 37
A copy number variation in human NCF1 and its pseudogenes
Brunson, T., Wang, Q., Chambers, I., & Song, Q. (2010) · BMC Genetics · doi:10.1186/1471-2156-11-13 · Cited by 36
Gain and Loss of Function for Glutathione Synthesis
Callegari, A., Liu, Y., White, C. C., Chait, A., Gough, P. J., Raines, E. W., Cox, D., Kavanagh, T. J., & Rosenfeld, M. E. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.229765 · Cited by 35
Self-citationRegulation of Monocyte Adhesion and Migration by Nox4
Lee, C. F., Ullevig, S. L., Kim, H. S., & Asmis, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0066964 · Cited by 35
Clarity on the Isoform-Specific Roles of NADPH Oxidases and NADPH Oxidase-4 in Atherosclerosis
Fulton, D. J., & Barman, S. A. (2016) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.116.307096 · Cited by 34
Sobey, C. G., Judkins, C. P., Rivera, J., Lewis, C. V., Diep, H., Lee, H. W., Kemp-Harper, B. K., Broughton, B. R. S., Selemidis, S., Gaspari, T. A., et al. (2015) · Free Radical Research · doi:10.3109/10715762.2014.992893 · Cited by 33
Lee, S.-H., Park, D., Park, S. C., Park, Y.-K., Hong, S. Y., Kim, J.-R., Lee, C., & Baek, S. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900503 · Cited by 33
Vidal, J., Verchere, C. B., Andrikopoulos, S., Wang, F., Hull, R. L., Cnop, M., Olin, K., LeBoeuf, R. C., O’Brien, K. D., Chait, A., et al. (2003) · Diabetologia · doi:10.1007/s00125-002-0984-5 · Cited by 30
Self-citationNauseef, W. M. (2001) · Journal of Clinical Investigation · doi:10.1172/jci11713 · Cited by 30
Schultz, D. W., & Harrison, D. G. (2000) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.20.6.1412 · Cited by 29
The Pathophysiological Role of NOX2 in Hypertension and Organ Damage
Forte, M., Nocella, C., FALCO, E. D., Palmerio, S., Schirone, L., Valenti, V., Frati, G., Carnevale, R., & Sciarretta, S. (2016) · High Blood Pressure & Cardiovascular Prevention · doi:10.1007/s40292-016-0175-y · Cited by 29
Deletion of NoxO1 limits atherosclerosis development in female mice
Buchmann, G., Schürmann, C., Warwick, T., Schulz, M. H., Spaeth, M., Müller, O. J., Schröder, K., Jo, H., Weißmann, N., & Brandes, R. P. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101713 · Cited by 26
The Ins and Outs of Small GTPase Rac1 in the Vasculature
Marinković, G., Heemskerk, N., van Buul, J. D., & de Waard, V. (2015) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.115.223610 · Cited by 25
Călin, M., Mânduțeanu, I., Butoi, E. D., Dragan, E., Nicolae, M., Gan, A., & Simionescu, M. (2009) · Cell and Tissue Research · doi:10.1007/s00441-009-0765-2 · Cited by 23
The role of NOX2-derived reactive oxygen species in collagenase-induced osteoarthritis
van Dalen, S. C. M., Kruisbergen, N. N. L., Walgreen, B., Helsen, M. M., Sloetjes, A. W., Cremers, N. A. J., Koenders, M. I., van de Loo, F. A. J., Roth, J., Vogl, T., et al. (2018) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2018.08.014 · Cited by 22
Brandes, R. P. (2003) · Circulation Research · doi:10.1161/01.res.0000066880.62205.b0 · Cited by 22
Tan, C., Day, R. T., Bao, S. S., TURK, J. W., & Zhao, Q. D. (2014) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.113.302847 · Cited by 21
Grahl, D. A., Axelsson, J., Nordfors, L., Heimbürger, O., Barany, P. F., Qureshi, A. R., Kato, S., Watanabe, M., Suliman, M., RIELLA, M. C., et al. (2007) · Blood Purification · doi:10.1159/000100419 · Cited by 21
Oxidative Stress in Cardiovascular Disease
Aviram, M., & Rosenblat, M. (2003) · Oxidative stress and disease · doi:10.1201/9780203912874.ch25 · Cited by 18
A protective player in the vascular response to injury
Schwartz, S. M. (2001) · Nature Medicine · doi:10.1038/89019 · Cited by 18
Endothelial NADPH oxidase 2: when does it matter in atherosclerosis?
Haendeler, J., Eckers, A., Lukosz, M., Unfried, K., & Altschmied, J. (2012) · Cardiovascular Research · doi:10.1093/cvr/cvs106 · Cited by 15
Xu, F., Liu, Y., Shi, L., Liu, W., Zhang, L., Cai, H., Qi, J., Cui, Y., Wang, W., & Hu, Y. (2015) · Journal of Translational Medicine · doi:10.1186/s12967-015-0407-2 · Cited by 15
Anti-oxidative and Anti-inflammatory Effects of Genistein in BALB/c Mice Injected with LPS
Cho, H.-Y., Noh, K., Cho, M.-K., Jang, J., Lee, M.-O., Kim, S., & Song, Y. (2008) · Journal of the Korean Society of Food Science and Nutrition · doi:10.3746/jkfn.2008.37.9.1126 · Cited by 13
Cloning and sequencing of rabbit leukocyte NADPH oxidase genes reveals a unique p67phoxhomolog
Gauss, K. A., Mascolo, P. L., Siemsen, D. W., Nelson, L. K., Bunger, P. L., Pagano, P. J., & Quinn, M. T. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.71.2.319 · Cited by 13
Sethy-Coraci, I., Crock, L. W., & Silverstein, S. C. (2005) · Journal of Leukocyte Biology · doi:10.1189/jlb.0205101 · Cited by 11
Modified Low-Density Lipoproteins and High-Density Lipoproteins
Koller, E., Volf, I., Gurvitz, A., & Koller, F. (2006) · Pathophysiology of Haemostasis and Thrombosis · doi:10.1159/000093225 · Cited by 10
Altered vascular activation due to deficiency of the NADPH oxidase component p22phox
Wang, H., Albadawi, H., Siddiquee, Z., Stone, J. M., Panchenko, M. P., Watkins, M. T., & Stone, J. R. (2013) · Cardiovascular Pathology · doi:10.1016/j.carpath.2013.08.003 · Cited by 10
Nakamura‐Utsunomiya, A., Tsumura, M., Okada, S., Kawaguchi, H., & Kobayashi, M. (2020) · PLoS ONE · doi:10.1371/journal.pone.0230665 · Cited by 9
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Weber, D. S., & Griendling, K. K. (2003) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0705353 · Cited by 7
Tawfik, M. K., Abo–Elmatty, D. M., & Ahmed, A. A. M. (2009) · PubMed · Cited by 7
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Miller, F. J. (2015) · European Heart Journal · doi:10.1093/eurheartj/ehv518 · Cited by 6
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Vechoropoulos, M., Ish‐Shalom, M., Shaklai, S., Sack, J., Stern, N., & Tordjman, K. M. (2014) · PPAR Research · doi:10.1155/2014/124583 · Cited by 5
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Pappas, K. D., Arnaoutoglou, E., & Papadopoulos, G. (2004) · Heart · doi:10.1136/hrt.2003.026559 · Cited by 5
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Pinheiro, C. H. D. J., Masi, L. N., & Curi, R. (2014) · CRC Press eBooks · doi:10.1201/b16653-12 · Cited by 3
Gerber, C. E., Bruchelt, G., Ledinski, G., Greilberger, J., NIETHAMMER, D., & Jürgens, G. (2002) · Redox Report · doi:10.1179/135100002125000343 · Cited by 3
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Youn, J. Y., Siu, K. L., Li, Q., Harrison, D. G., & Cai, H. “. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_43 · Cited by 3
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Metadata
- Authors
- Kirk, E. A., Dinauer, M. C., Rosen, H., Chait, A., Heinecke, J. W., & LeBoeuf, R. C.
- Affiliations
- University of Washington (US)
- From the Departments of Pathobiology and Nutritional Sciences (E.A.K., R.C.L.) and Medicine (E.A.K., H.R., A.C., R.C.L.), University of Washington, Seattle; the Departments of Pediatrics and Medical and Molecular Genetics (M.C.D.), Indiana University Medical Center, Indianapolis; and the Departments of Medicine and Molecular Biology and Pharmacology (J.W.H.), Washington University School of Medicine, St. Louis, Mo.
- Venue
- Arteriosclerosis, Thrombosis, and Vascular Biology
- Published
- 2000-06
- Volume
- 20
- Issue
- 6
- Pages
- 1529-1535
- ISSN
- 1079-5642 (ISSN-L)
- 1524-4636
- OpenAlex
- W2097082675
- Cited by
- 171
- References
- 49
- Citations by year
- 2025: 1 · 2021: 2 · 2020: 4 · 2019: 3 · 2018: 4 · 2017: 5 · 2016: 4 · 2015: 11 · 2014: 12 · 2013: 9 · 2012: 8
- FWCI
- 9.48
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Arteriosclerosis Thrombosis and Vascular Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (7r01ag015013-06, 5r01ag012293-05)
- National Institute on Aging (AG12293, AG 15013)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 02456)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Keywords
- superoxide, NADPH oxidase, gp91phox, chronic granulomatous disease, atherosclerosis, macrophages, phagocytes, hypercholesterolemia, apolipoprotein E deficiency, high-fat diet, peroxynitrite, nitric oxide, LDL oxidation, serum cholesterol, triglycerides
- MeSH terms
- Animals, Apolipoproteins E, Arteriosclerosis, Cholesterol, Female, Male, Mice, Inbred C57BL, NADH, NADPH Oxidoreductases, Phagocytes, RNA, Messenger, Sex Characteristics, Superoxides, Triglycerides, Gene Expression, NADPH Oxidases, Mice
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