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Atherosclerosis Is Attenuated by Limiting Superoxide Generation in Both Macrophages and Vessel Wall Cells
Abstract
Objective— We previously showed that NAD(P)H oxidase deficiency significantly reduces atherosclerosis in apoE −/− mice. The present study was designed to determine the relative contribution of monocyte/macrophage versus vascular wall cell NAD(P)H oxidase to atherogenesis in this model. Methods and Results— Cell-specific NAD(P)H oxidase inhibition was achieved via allogenic, sex-mismatched bone marrow transplantation. Aortic atherosclerosis and superoxide production in apoE −/− mice (Control) with functional NAD(P)H oxidase in both monocytes/macrophages and vascular wall cells was compared with that in apoE −/− mice with nonfunctional monocyte/macrophage NAD(P)H oxidase (BMO) or nonfunctional vessel wall NAD(P)H oxidase (VWO). A significant decrease in superoxide production and atherosclerotic lesions was observed in BMO and VWO mice compared with control mice. Interestingly, BMO mice had significantly lower plasma oxidized LDL levels compared with control and VWO mice, whereas aortic sections of VWO mice showed decreased expression of cellular adhesion molecules compared with control and BMO mice. NAD(P)H oxidase deficiency also attenuated neointimal hyperplasia and mitogenic protein activation in apoE −/− mice after arterial injury. Conclusions— We conclude that (1) both monocyte/macrophages and vessel wall cells play critical roles in atherogenesis; (2) decrease in atherosclerosis results from attenuated superoxide generation in monocyte/macrophages or vessel wall cells; and (3) superoxide generation may impact atherosclerosis, in part, by activating smooth muscle cell mitogenic signaling pathways.
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“In conditions that promote uncoupling, the heme group is usually the main generator of superoxide species through the formation of a ferrous/oxy complex that decays to ferric heme and superoxide (Eq. 20) (FIGURE 11) (250, 901, 973, 1033).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [973]
In the citing paper
“The reaction is observed in the three NOS isoforms (750, 973, 1034).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [973]
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Cites
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
BABIOR, B. M. (1999) · Blood · doi:10.1182/blood.v93.5.1464 · Cited by 2,147
Boring, L., Gosling, J., Cleary, M., & Charo, I. F. (1998) · Nature · doi:10.1038/29788 · Cited by 1,965
Vascular NAD(P)H oxidases: specific features, expression, and regulation
Lassegue, B. P., & Clempus, R. E. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00758.2002 · Cited by 1,026
Napoli, C., D'Armiento, F. P., Mancini, F. P., Postiglione, A., Witztum, J. L., Palumbo, G., & Palinski, W. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119813 · Cited by 1,014
Mechanisms of Increased Vascular Superoxide Production in Human Diabetes Mellitus
Guzik, T. J., Mussa, S., Gastaldi, D., Sadowski, J., Ratnatunga, C., Pillai, R. G., & Channon, K. M. (2002) · Circulation · doi:10.1161/01.cir.0000012748.58444.08 · Cited by 979
Superoxide Production and Expression of Nox Family Proteins in Human Atherosclerosis
Sorescu, D., Weiss, D., Lassègue, B., Clempus, R. E., Szöcs, K., Sorescu, G. P., Valppu, L., Quinn, M. T., Lambeth, J. D., Vega, J. D., et al. (2002) · Circulation · doi:10.1161/01.cir.0000012917.74432.66 · Cited by 847
Gosling, J., Slaymaker, S., Gu, L., Tseng, S., Zlot, C. H., Young, S. G., Rollins, B. J., & Charo, I. F. (1999) · Journal of Clinical Investigation · doi:10.1172/jci5624 · Cited by 657
Vascular Superoxide Production by NAD(P)H Oxidase
Guzik, T. J., West, N. E. J., Black, E., McDonald, D., Ratnatunga, C., Pillai, R. G., & Channon, K. M. (2000) · Circulation Research · doi:10.1161/01.res.86.9.e85 · Cited by 584
Bendall, J. K., Cave, A. C., Heymes, C., Gall, N. P., & Shah, A. M. (2002) · Circulation · doi:10.1161/hc0302.103712 · Cited by 529
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Eelen, G., de Zeeuw, P., Treps, L., Harjes, U., Wong, B. W., & Carmeliet, P. (2017) · Physiological Reviews · doi:10.1152/physrev.00001.2017 · Cited by 614
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Tejero, J., Shiva, S., & Gladwin, M. T. (2019) · Physiological Reviews · doi:10.1152/physrev.00036.2017 · Cited by 541
Evolution of nadph oxidase inhibitors: Selectivity and mechanisms for target engagement
Altenhöfer, S., Radermacher, K. A., Kleikers, P. W. M., Wingler, K., & Schmidt, H. H. H. W. (2015) · Antioxidants & Redox Signaling · doi:10.1089/ars.2013.5814 · Cited by 521
Wenzel, P., Knorr, M., Kossmann, S., Stratmann, J., Hausding, M., Schuhmacher, S., Karbach, S. H., Schwenk, M., Yogev, N., Schulz, E., et al. (2011) · Circulation · doi:10.1161/circulationaha.111.034470 · Cited by 512
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Hopkins, P. N. (2013) · Physiological Reviews · doi:10.1152/physrev.00004.2012 · Cited by 469
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Li, G., Scull, C. M., Özcan, L., & Tabas, I. A. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201006121 · Cited by 310
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Selemidis, S., Sobey, C. G., Wingler, K., Schmidt, H. H. H. W., & Drummond, G. R. (2008) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2008.08.005 · Cited by 249
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Ikeda, K., Shiozawa, A., Ono, N., Kusunoki, T., Hirotsu, M., Homma, H., Saitoh, T., & Murata, J. (2013) · The Laryngoscope · doi:10.1002/lary.24154 · Cited by 218
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Leopold, J. A., & Loscalzo, J. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.09.009 · Cited by 218
Jha, J. C., Ho, F., Dan, C., & Jandeleit-Dahm, K. A. M. (2018) · Clinical Science · doi:10.1042/cs20171459 · Cited by 207
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Sahoo, S., Meijles, D. N., & Pagano, P. J. (2016) · Clinical Science · doi:10.1042/cs20150087 · Cited by 147
Langbein, H., Brunssen, C., Hofmann, A., Cimalla, P., Brux, M., Bornstein, S. R., Deussen, A., Koch, E., & Morawietz, H. (2016) · European Heart Journal · doi:10.1093/eurheartj/ehv564 · Cited by 133
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Elnakish, M. T., Hassanain, H. H., Janssen, P. M. L., Angelos, M. G., & Khan, M. (2013) · The Journal of Pathology · doi:10.1002/path.4255 · Cited by 133
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Niu, X.-L., Madamanchi, N. R., Vendrov, A. E., Tchivilev, I., Rojas, M., Madamanchi, C., Brandes, R. P., Krause, K. H., Humphries, J., Smith, A., et al. (2010) · Circulation · doi:10.1161/circulationaha.109.908319 · Cited by 116
Self-citationMury, P., Chirico, E. N., Mura, M., Millon, A., Canet‐Soulas, E., & Pialoux, V. (2018) · Sports Medicine · doi:10.1007/s40279-018-0996-z · Cited by 112
Möller, P., Mikkelsen, L., Vesterdal, L. K., Folkmann, J. K., Forchhammer, L., Roursgaard, M., Danielsen, P. H., & Loft, S. H. (2011) · Critical Reviews in Toxicology · doi:10.3109/10408444.2010.533152 · Cited by 108
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Sarna, L. K., Wu, N., Hwang, S., Siow, Y. L., & Karmin, O. (2010) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y09-136 · Cited by 108
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Marie, P. K., & Jain, S. K. (2016) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2016.03.002 · Cited by 71
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Xu, S., Chamseddine, A. H., Carrell, S., & Miller, F. J. (2014) · Redox Biology · doi:10.1016/j.redox.2014.04.004 · Cited by 66
Donovan, E. L., McCord, J. M., Reuland, D. J., Miller, B. F., & Hamilton, K. L. (2012) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2012/132931 · Cited by 64
Vendrov, A. E., Sumida, A., Canugovi, C., Lozhkin, A. P., Hayami, T., Madamanchi, N. R., & Runge, M. S. (2018) · Redox Biology · doi:10.1016/j.redox.2018.11.021 · Cited by 63
Self-citationMonaghan-Benson, E., Hartmann, J., Vendrov, A. E., Budd, S., Byfield, G. E., Parker, A., Ahmad, F. I., Huang, W. C., Runge, M. S., Burridge, K., et al. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.090878 · Cited by 60
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Li, J., Newburger, P. E., Gounis, M. J., Dargon, P. T., Zhang, X., & Messina, L. M. (2010) · Gene Therapy · doi:10.1038/gt.2010.69 · Cited by 58
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Liu, Y., Zhao, Y., Shukha, Y., Lu, H., Wang, L., Liu, Z., Liu, C., Zhao, Y., Wang, H. H., Zhao, G., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109420 · Cited by 52
Gutowska, I., Baranowska‐Bosiacka, I., Baskiewicz, M., Milo, B., Siennicka, A., Marchlewicz, M., Wiszniewska, B., Machaliński, B., & Stachowska, E. (2010) · Toxicology Letters · doi:10.1016/j.toxlet.2010.03.1167 · Cited by 47
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Yao, E., Fukuda, N., Matsumoto, T., Katakawa, M., Yamamoto, C., Han, Y., Ueno, T., Kobayashi, N., & Matsumoto, K. (2008) · American Journal of Hypertension · doi:10.1038/ajh.2008.233 · Cited by 47
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Porter, K. M., & Sutliff, R. L. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.03.019 · Cited by 45
Peshavariya, H., Taylor, C. J., Yergin, C. G., Liu, G., Jiang, F., Chan, E. C., & Dusting, G. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060790 · Cited by 46
Khanicheh, E., Qi, Y., Xie, A., Mitterhuber, M., Xu, L., Mochizuki, M., Daali, Y., Jaquet, V., Krause, K. H., Ruggeri, Z. M., et al. (2013) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.113.301710 · Cited by 44
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de Dios, S. T., Sobey, C. G., & Drummond, G. R. (2010) · Springer eBooks · doi:10.1007/978-3-0346-0168-9_3 · Cited by 44
Dávalos, A., de la Peña, G., Sánchez-Martín, C. C., Guerra, M. T., Bartolomé, B., & Lasunción, M. A. (2009) · British Journal Of Nutrition · doi:10.1017/s0007114509382148 · Cited by 44
Sfyri, P., & Matsakas, A. (2017) · Journal of Biomedical Science · doi:10.1186/s12929-017-0346-8 · Cited by 44
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Luo, M., Zheng, Y., Tang, S., Gu, L., Zhu, Y., Ying, R., Liu, Y., Ma, J., Guo, R., Gao, P., et al. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1166178 · Cited by 41
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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
Tung, W.-C., Rizzo, B., Dabbagh, Y., Saraswat, S., Romanczyk, M., Codorniu‐Hernández, E., Rebollido-Rios, R., Needs, P. W., Kroon, P. A., Rakotomanomana, N., et al. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108589 · Cited by 33
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Cerrato, R., Cunnington, C., Crabtree, M. J., Antoniades, C. A., Pernow, J., Channon, K. M., & Böhm, F. (2012) · Life Sciences · doi:10.1016/j.lfs.2012.03.024 · Cited by 33
Arca, M., Conti, B., Montali, A., Pignatelli, P., Campagna, F., Barillà, F., Tanzilli, G., Verna, R., Vestri, A., Gaudio, C., et al. (2008) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.154823 · Cited by 32
Yusuf, A., & Casey, A. (2019) · APOPTOSIS · doi:10.1007/s10495-019-01584-2 · Cited by 32
Cannizzo, B., Quesada, I., Militello, R. D., Sanchez, C. A., Miatello, R. M., Cruzado, M., & Castro, C. (2014) · Free Radical Research · doi:10.3109/10715762.2014.889295 · Cited by 33
Gutowska, I., Baranowska‐Bosiacka, I., Goschorska, M., Kolasa, A., Łukomska, A., Jakubczyk, K., Dec, K., & Chlubek, D. (2015) · Toxicology in Vitro · doi:10.1016/j.tiv.2015.06.024 · Cited by 29
Ono, N., Kusunoki, T., & Ikeda, K. (2012) · Allergy & Rhinology · doi:10.2500/ar.2012.3.0030 · Cited by 29
Riebel, M., Sabel, A., Claus, H., Xia, N., Li, H., König, H., Decker, H., & Fronk, P. (2017) · Food Chemistry · doi:10.1016/j.foodchem.2017.03.003 · Cited by 29
Drebrin attenuates atherosclerosis by limiting smooth muscle cell transdifferentiation
Wu, J., Zhang, L., Nepliouev, I., Brian, L., Huang, T.-Q., Snow, K. P., Schickling, B., Hauser, E. R., Miller, F. J., Freedman, N. J., et al. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab156 · Cited by 27
Nox2 Is Required for Macrophage Chemotaxis towards CSF-1
Chaubey, S., Jones, G. E., Shah, A. M., Cave, A. C., & Wells, C. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054869 · Cited by 28
Oxidative stress, NADPH oxidases, and arteries
Sun, Q.-A., Madamanchi, N. R., & Runge, M. S. (2015) · Hämostaseologie · doi:10.5482/hamo-14-11-0076 · Cited by 29
Self-citationFalco, L., Tessitore, V., Ciccarelli, G., D’Aquino, M. M. C., D’Andrea, A., Imbalzano, E., Golino, P., & Russo, V. (2023) · Antioxidants · doi:10.3390/antiox12061185 · Cited by 29
Endothelial Reprogramming in Atherosclerosis
Zhang, L., Xin, W., & Hong, L. (2024) · Bioengineering · doi:10.3390/bioengineering11040325 · Cited by 23
Shitaw, E. E., AlAhmad, M., & Sivaprasadarao, A. (2025) · Antioxidants · doi:10.3390/antiox14070776 · Cited by 26
Metadata
- Authors
- Vendrov, A. E., Hakim, Z. S., Madamanchi, N. R., Rojas, M., Madamanchi, C., & Runge, M. S.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- ORCID
- Venue
- Arteriosclerosis, Thrombosis, and Vascular Biology
- Published
- 2007-12
- Volume
- 27
- Issue
- 12
- Pages
- 2714-2721
- ISSN
- 1079-5642 (ISSN-L)
- 1524-4636
- OpenAlex
- W2146706268
- Cited by
- 173
- References
- 33
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 5 · 2023: 6 · 2022: 5 · 2021: 6 · 2020: 10 · 2019: 8 · 2018: 9 · 2017: 10 · 2016: 12 · 2015: 9 · 2014: 13 · 2013: 13 · 2012: 14
- FWCI
- 3.72
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Arteriosclerosis Thrombosis and Vascular Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- University of North Carolina at Chapel Hill
- National Heart, Lung, and Blood Institute (HL-57352, R01HL057352)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Keywords
- atherosclerosis, NADPH oxidase, superoxide production, monocytes/macrophages, vascular wall cells, bone marrow transplantation, ApoE-deficient mice, oxidized LDL, adhesion molecules, intimal hyperplasia, atherogenesis
- MeSH terms
- Animals, Aorta, Apolipoproteins E, Dietary Fats, Disease Models, Animal, Endothelium, Vascular, Femoral Artery, Hyperplasia, Lipoproteins, LDL, Macrophages, Muscle, Smooth, Vascular, Oxidation-Reduction, Phosphorylation, RNA, Messenger, Superoxides, Thrombin, Signal Transduction, Cell Adhesion Molecules, Bone Marrow Transplantation, Mice, Knockout, NADPH Oxidases, Mitogen-Activated Protein Kinases, Cell Proliferation, Atherosclerosis, STAT3 Transcription Factor, Mice, Janus Kinase 2
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