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Export by red blood cells of nitric oxide bioactivity
Abstract
Previous studies support a model in which the physiological O2 gradient is transduced by haemoglobin into the coordinate release from red blood cells of O2 and nitric oxide (NO)-derived vasoactivity to optimize oxygen delivery in the arterial periphery. But whereas both O2 and NO diffuse into red blood cells, only O2 can diffuse out. Thus, for the dilation of blood vessels by red blood cells, there must be a mechanism to export NO-related vasoactivity, and current models of NO-mediated intercellular communication should be revised. Here we show that in human erythrocytes haemoglobin-derived S-nitrosothiol (SNO), generated from imported NO, is associated predominantly with the red blood cell membrane, and principally with cysteine residues in the haemoglobin-binding cytoplasmic domain of the anion exchanger AE1. Interaction with AE1 promotes the deoxygenated structure in SNO-haemoglobin, which subserves NO group transfer to the membrane. Furthermore, we show that vasodilatory activity is released from this membrane precinct by deoxygenation. Thus, the oxygen-regulated cellular mechanism that couples the synthesis and export of haemoglobin-derived NO bioactivity operates, at least in part, through formation of AE1-SNO at the membrane-cytosol interface.
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“This view changed radically after the discovery of RBC-mediated hypoxic vasodilation: under conditions of decreased oxygen saturation, RBCs were shown to induce vasodilation of vessel strips by exporting NO bioactivity (146).”
From Red Blood Cell Function and Dysfunction: Redox Regulation, Nitric Oxide Metabolism, Anemia (2017) · cites this paper as [146]
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Cites
S-nitrosohaemoglobin: a dynamic activity of blood involved in vascular control
Jia, L., Bonaventura, C., Bonaventura, J., & Stamler, J. S. (1996) · Nature · doi:10.1038/380221a0 · Cited by 1,592
Self-citationBlood Flow Regulation by S -Nitrosohemoglobin in the Physiological Oxygen Gradient
Stamler, J. S., Jia, L., Eu, J. P., McMahon, T. J., Demchenko, I. T., Bonaventura, J., Gernert, K., & Piantadosi, C. A. (1997) · Science · doi:10.1126/science.276.5321.2034 · Cited by 1,050
Self-citation(S)NO Signals: Translocation, Regulation, and a Consensus Motif
Stamler, J. S., Toone, E. J., Lipton, S. A., & Sucher, N. J. (1997) · Neuron · doi:10.1016/s0896-6273(00)80310-4 · Cited by 679
Self-citationReactions between nitric oxide and haemoglobin under physiological conditions
Gow, A. J., & Stamler, J. S. (1998) · Nature · doi:10.1038/34402 · Cited by 562
Self-citationDiffusion-limited reaction of free nitric oxide with erythrocytes
Liu, X., Miller, M. J. S., Joshi, M. S., Sadowska-Krowicka, H., Clark, D. A., & Lancaster, J. R. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.30.18709 · Cited by 512
The oxyhemoglobin reaction of nitric oxide
Gow, A. J., Luchsinger, B. P., Pawloski, J. R., Singel, D. J., & Stamler, J. S. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.16.9027 · Cited by 418
Self-citationLow, P. S. (1986) · Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes · doi:10.1016/0304-4157(86)90009-2 · Cited by 407
Walder, J. A., Chatterjee, R., Steck, T. L., Low, P. S., Musso, G. F., Kaiser, E. T., Rogers, P. H., & Arnone, A. (1984) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)90956-7 · Cited by 302
Erythrocytes Possess an Intrinsic Barrier to Nitric Oxide Consumption
Vaughn, M. W., Huang, K., Kuo, L., & Liao, J. C. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.4.2342 · Cited by 220
Salhany, J. M., Cordes, K. A., & Gaines, E. D. (1980) · Biochemistry · doi:10.1021/bi00548a028 · Cited by 144
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S-Nitrosothiol measurements in biological systems
Gow, A. J., Doctor, A., Mannick, J. B., & Gaston, B. M. (2007) · Journal of Chromatography B · doi:10.1016/j.jchromb.2007.01.052 · Cited by 123
Andrews, D. A., Yang, L., & Low, P. S. (2002) · Blood · doi:10.1182/blood.v100.9.3392 · Cited by 122
Detection and proteomic identification of S-nitrosylated proteins in endothelial cells
Martı́nez-Ruiz, A., & Lamas, S. (2004) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2003.12.006 · Cited by 120
Band 3 anion exchanger and its involvement in erythrocyte and kidney disorders
Tanner, M. J. A. (2002) · Current Opinion in Hematology · doi:10.1097/00062752-200203000-00009 · Cited by 119
The Diversity of Microbial Responses to Nitric Oxide and Agents of Nitrosative Stress
Bowman, L. A. H., McLean, S., Poole, R. K., & Fukuto, J. M. (2011) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/b978-0-12-387661-4.00006-9 · Cited by 118
Myoglobin as a model system for designing heme protein based blood substitutes
Dou, Y., Maillett, D. H., Eich, R. F., & Olson, J. S. (2002) · Biophysical Chemistry · doi:10.1016/s0301-4622(02)00090-x · Cited by 118
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Simmonds, M. J., Detterich, J. A., & Connes, P. (2014) · Biorheology · doi:10.3233/bir-140653 · Cited by 115
S-nitrosylation: integrator of cardiovascular performance and oxygen delivery
Haldar, S. M., & Stamler, J. S. (2013) · Journal of Clinical Investigation · doi:10.1172/jci62854 · Cited by 118
Self-citationZaffagnini, M., Morisse, S., Bedhomme, M., Marchand, C. H., Festa, M., Rouhier, N., Lemaire, S. D., & Trost, P. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.475467 · Cited by 120
Nitric oxide and autonomic control of heart rate: a question of specificity
Paton, J. F. R., Kasparov, S., & Paterson, D. J. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02261-0 · Cited by 116
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Kalinina, E. V., & Novichkova, M. (2021) · Molecules · doi:10.3390/molecules26020435 · Cited by 121
Derakhshan, B., HAO, G., & GROSS, S. (2007) · Cardiovascular Research · doi:10.1016/j.cardiores.2007.04.023 · Cited by 117
Novel Aspects of Endothelium-Dependent Regulation of Vascular Tone
Villar, I. C., Francis, S., Webb, A., Hobbs, A. J., & Ahluwalia, A. (2006) · Kidney International · doi:10.1038/sj.ki.5001680 · Cited by 112
Stimulation of Erythrocyte Phosphatidylserine Exposure by Paclitaxel
Lang, P. A., Huober, J., Bachmann, C., Kempe, D. S., Sobiesiak, M., Akel, A., Niemoeller, O. M., Dreischer, P., Eisele, K., Klarl, B. A., et al. (2006) · Cellular Physiology and Biochemistry · doi:10.1159/000095190 · Cited by 112
A protein microarray-based analysis of S -nitrosylation
Foster, M. W., Forrester, M. T., & Stamler, J. S. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900729106 · Cited by 113
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Bosman, G. J. C. G. M., Lasonder, E., Groenen‐Döpp, Y. A. M., Willekens, F. L. A., & Werre, J. M. (2012) · Journal of Proteomics · doi:10.1016/j.jprot.2012.05.031 · Cited by 109
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Zhang, R., Hess, D. T., Qian, Z., Hausladen, A., Fonseca, F., Chaube, R., Reynolds, J. D. H., & Stamler, J. S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1502285112 · Cited by 107
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Neuroglobin, seven years after
Brunori, M., & Vallone, B. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-7090-2 · Cited by 105
Red Blood Cell Nitric Oxide as an Endocrine Vasoregulator
Datta, B. N., Tufnell-Barret, T., Bleasdale, R. A., Jones, C. J. H., Beeton, I., Paul, V., Frenneaux, M. P., & James, P. E. (2004) · Circulation · doi:10.1161/01.cir.0000124450.07016.1d · Cited by 102
Hemoglobin-Mediated, Hypoxia-Induced Vasodilation via Nitric Oxide
Robinson, J. M., & Lancaster, J. R. (2005) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.f292 · Cited by 104
Nitric oxide reaction with red blood cells and hemoglobin under heterogeneous conditions
Han, T. H., Hyduke, D. R., Vaughn, M. W., Fukuto, J. M., & Liao, J. C. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.122118299 · Cited by 100
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Herold, S., & Röck, G. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210275200 · Cited by 99
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Hausladen, A., Rafikov, R., Angelo, M., Singel, D. J., Nudler, E., & Stamler, J. S. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611191104 · Cited by 96
Self-citationS-Nitrosylation signaling regulates cellular protein interactions
Marozkina, N. V., & Gaston, B. M. (2011) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2011.06.017 · Cited by 98
Suicidal Erythrocyte Death Following Cellular K+ Loss
Schneider, J., Nicolay, J. P., Föller, M., Wieder, T., & Lang, F. J. W. (2007) · Cellular Physiology and Biochemistry · doi:10.1159/000104151 · Cited by 97
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Bicarbonate transport in health and disease
Alka, K., & Casey, J. R. (2014) · IUBMB Life · doi:10.1002/iub.1315 · Cited by 94
Linnarsson, D., Carpenter, J., Fubini, B., Gerde, P., Karlsson, L. L., Loftus, D. J., Prisk, G. K., Staufer, U., Tranfield, E. M., & van Westrenen, W. (2012) · Planetary and Space Science · doi:10.1016/j.pss.2012.05.023 · Cited by 95
Wang, Q., & Zennadi, R. (2021) · Antioxidants · doi:10.3390/antiox10101608 · Cited by 105
Luchsinger, B. P., Rich, E. N., Yan, Y., Williams, E. M., Stamler, J. S., & Singel, D. J. (2005) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2004.12.010 · Cited by 89
Self-citationTemperature-Dependent Studies of NO Recombination to Heme and Heme Proteins
Ionascu, D., Gruia, F., Xiong, Y., Yu, A., Rosca, F., Beck, C. M., Demidov, A., Olson, J. S., & Champion, P. M. (2005) · Journal of the American Chemical Society · doi:10.1021/ja054249y · Cited by 92
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Gladwin, M. T., & Schechter, A. N. (2004) · Circulation Research · doi:10.1161/01.res.0000126697.64381.37 · Cited by 85
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Forrester, M. T., Seth, D., Hausladen, A., Eyler, C. E., Foster, M. W., Matsumoto, A., Benhar, M., Marshall, H. E., & Stamler, J. S. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.057729 · Cited by 87
Self-citationHypoxia limits antioxidant capacity in red blood cells by altering glycolytic pathway dominance
Rogers, S. C., Said, A. S., Corcuera, D., McLaughlin, D., Kell, P. J., & Doctor, A. (2009) · The FASEB Journal · doi:10.1096/fj.09-130666 · Cited by 88
McMahon, T. J., & Doctor, A. (2006) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200507-066bg · Cited by 87
Ülker, P., Yaraş, N., Yalçın, Ö., Çelik-Özenci, Ç., Johnson, P. C., Meiselman, H. J., & Baskurt, O. K. (2011) · Nitric Oxide · doi:10.1016/j.niox.2011.03.003 · Cited by 87
Nagababu, E., Ramasamy, S., & Rifkind, J. M. (2006) · Nitric Oxide · doi:10.1016/j.niox.2006.01.012 · Cited by 86
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Watts, R., Ponka, P., & Richardson, D. R. (2003) · Biochemical Journal · doi:10.1042/bj20021302 · Cited by 84
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Rogers, S. C., Ross, J. G. C., d'Avignon, A., Gibbons, L. B., Gazit, V. A., Hassan, M. N., McLaughlin, D., Griffin, S., Neumayr, T. M., DeBaun, M. R., et al. (2013) · Blood · doi:10.1182/blood-2012-02-414037 · Cited by 85
Signaling by S-nitrosylation in the heart
Murphy, E., Kohr, M., Menazza, S., Nguyen, T., Evangelista, A., Sun, J., & Steenbergen, C. (2014) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2014.01.003 · Cited by 82
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Voss, A. A., Langó, J., Ernst‐Russell, M. A., Morin, D., & Pessah, I. N. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m404290200 · Cited by 83
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Müller, B., Kleschyov, A. L., de Alencar, J. L., Vanin, A. F., & Stoclet, J. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb04063.x · Cited by 78
Samaja, M., Crespi, T., Guazzi, M., & Vandegriff, K. D. (2003) · European Journal of Applied Physiology · doi:10.1007/s00421-003-0954-8 · Cited by 79
Sepsis impairs microvascular autoregulation and delays capillary response within hypoxic capillaries
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Mechanical stimulation of nitric oxide synthesizing mechanisms in erythrocytes
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Xu, X., Cho, M., Spencer, N. Y., Patel, N. K., Huang, Z., Shields, H. W., King, S. B., Gladwin, M. T., Hogg, N., & Kim‐Shapiro, D. B. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2033883100 · Cited by 77
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Chen, Y., Ku, W., Feng, L.-T., Tsai, M.-H., Hsieh, C., Hsu, W.-H., Liaw, W., Hung, C., & Chen, Y. (2008) · Journal of the American Chemical Society · doi:10.1021/ja711494m · Cited by 74
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Stamler, J. S., & Hess, D. T. (2010) · Nature Cell Biology · doi:10.1038/ncb1110-1024 · Cited by 70
Self-citationPall, M. L. (2002) · The FASEB Journal · doi:10.1096/fj.01-0861hyp · Cited by 70
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SULLIVAN, K. J., Kissoon, N. “., Duckworth, L. J., Sandler, E. S., Freeman, B., Bayne, E., Sylvester, J. E., & Lima, J. J. (2001) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.164.12.2012090 · Cited by 69
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Föller, M., Shumilina, E. V., Lam, R. S., Mohamed, W. A., Kasinathan, R. S., Huber, S. M., Chakraborty, T., & Lang, F. J. W. (2007) · Cellular Physiology and Biochemistry · doi:10.1159/000110715 · Cited by 69
Sonveaux, P., Lobysheva, I. I., Féron, O., & McMahon, T. J. (2007) · Physiology · doi:10.1152/physiol.00042.2006 · Cited by 71
Sompong, W., Cheng, H., & Adisakwattana, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129495 · Cited by 68
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Sun, K., D’Alessandro, A., Ahmed, M. H., Zhang, Y., Song, A., Ko, T., Nemkov, T. G., Reisz, J. A., Wu, H., Adebiyi, M. G., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-13667-8 · Cited by 66
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Zhou, H., Grimmett, Z. W., Venetos, N. M., Stomberski, C. T., Qian, Z., McLaughlin, P. J., Bansal, P. K., Zhang, R., Reynolds, J. D. H., Premont, R. T., et al. (2023) · Cell · doi:10.1016/j.cell.2023.11.009 · Cited by 63
Self-citationInhaled nitric oxide in 2003: a review of its mechanisms of action
Wang, T., Kebir, D. E., & Blaise, G. A. (2003) · Canadian Journal of Anesthesia/Journal canadien d anesthésie · doi:10.1007/bf03019384 · Cited by 62
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Storz, J. F., Baze, M. M., Waite, J. L., Hoffmann, F. G., Opazo, J. C., & Hayes, J. P. (2007) · Genetics · doi:10.1534/genetics.107.078550 · Cited by 63
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Metadata
- Authors
- Pawloski, J. R., Hess, D. T., & Stamler, J. S.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Stamler, Jonathan S.
- ORCID
- Stamler, Jonathan S.
- Venue
- Nature
- Published
- 2001-02
- Volume
- 409
- Issue
- 6820
- Pages
- 622-626
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2118023300
- Cited by
- 579
- References
- 28
- Citations by year
- 2026: 2 · 2025: 8 · 2024: 13 · 2023: 13 · 2022: 22 · 2021: 20 · 2020: 17 · 2019: 17 · 2018: 10 · 2017: 19 · 2016: 12 · 2015: 18 · 2014: 16 · 2013: 27 · 2012: 22
- FWCI
- 16.77
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- American Heart Association
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Hemoglobin structure and function
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heme Oxygenase-1 and Carbon Monoxide
- Keywords
- nitric oxide, erythrocytes, S-nitrosothiols, hemoglobin, band 3, oxygen gradients, vasodilation, oxygen delivery, intercellular communication, cysteine residues
- MeSH terms
- Animals, Aorta, Biological Transport, Erythrocyte Membrane, Erythrocytes, Hemoglobins, Humans, Mercaptoethanol, Nitric Oxide, Nitroso Compounds, Rabbits, Vasoconstriction, 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid, Antiporters, S-Nitrosothiols, Chloride-Bicarbonate Antiporters, In Vitro Techniques
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