The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.
Circulating cell membrane microparticles transfer heme to endothelial cells and trigger vasoocclusions in sickle cell disease
Open accessAbstract
Key Points: A significant fraction of cell-free heme in plasma is contained in circulating erythrocyte MPs, particularly during hemolysis. Heme-laden MPs can transfer heme to vascular endothelium and mediate oxidative stress, vascular dysfunction, and vasoocclusions.
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Citations
Cites
Cell-free hemoglobin limits nitric oxide bioavailability in sickle-cell disease
Reiter, C. D., Wang, X., Tanus-Santos, J. E., Hogg, N., Cannon, R. O., Schechter, A. N., & Gladwin, M. T. (2002) · Nature Medicine · doi:10.1038/nm1202-799 · Cited by 1,330
Belcher, J. D., Chen, C., Nguyen, J., Milbauer, L., Abdulla, F., Alayash, A. I., Smith, A., Nath, K. A., Hebbel, R. P., & Vercellotti, G. M. (2014) · Blood · doi:10.1182/blood-2013-04-495887 · Cited by 695 · cited 1×
“MP heme might then target cell surface receptors, such as TLR-4 and trigger signaling pathways similar, in part, to those described for soluble heme, including ROS production.(25,26)”
Donadee, C., Raat, N. J. H., Kanias, T., Tejero, J., Lee, J. S., Kelley, E. E., Zhao, X., Liu, C., Reynolds, H., Azarov, I., et al. (2011) · Circulation · doi:10.1161/circulationaha.110.008698 · Cited by 572
Shet, A. S., Aras, O., Gupta, K., Hass, M. J., Rausch, D. J., Saba, N., Koopmeiners, L., Key, N. S., & Hebbel, R. P. (2003) · Blood · doi:10.1182/blood-2003-03-0693 · Cited by 539
Balla, G., Jacob, H. S., Eaton, J. W., Belcher, J. D., & Vercellotti, G. M. (1991) · Arteriosclerosis and Thrombosis: A Journal of Vascular Biology · doi:10.1161/01.atv.11.6.1700 · Cited by 420
Bratosin, D., Estaquier, J., Petit, F., Arnoult, D., Quatannens, B., Tissier, J.-P., Slomianny, C., Sartiaux, C., Alonso, C., Huart, J.-J., et al. (2001) · Cell Death & Differentiation · doi:10.1038/sj.cdd.4400946 · Cited by 394
Heme-induced neutrophil extracellular traps contribute to the pathogenesis of sickle cell disease
Chen, G., Zhang, D., Fuchs, T. A., Manwani, D., Wagner, D. D., & Frenette, P. S. (2014) · Blood · doi:10.1182/blood-2013-10-529982 · Cited by 354
MULLER-EBERHARD, U., JAVID, J., LIEM, H. H., HANSTEIN, A., & HANNA, M. (1968) · Blood · doi:10.1182/blood.v32.5.811.811 · Cited by 328
Physiology and Pathophysiology of Heme: Implications for Kidney Disease
Tracz, M. J., Alam, J., & Nath, K. A. (2007) · Journal of the American Society of Nephrology · doi:10.1681/asn.2006080894 · Cited by 314
Accelerated autoxidation and heme loss due to instability of sickle hemoglobin.
Hebbel, R. P., Morgan, W. T., Eaton, J. W., & Hedlund, B. E. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.1.237 · Cited by 306
Research works printed but not linked: 3
- Mahfoudhi, 2012, Red cells exchanges in sickle cells disease lead to a selective reduction of erythrocytes-derived blood microparticles., Br J Haematol, 156, 545, 10.1111/j.1365-2141.2011.08897.x · doi:10.1111/j.1365-2141.2011.08897.x
- Oztas, 2012, Plasma protein oxidation is correlated positively with plasma iron levels and negatively with hemolysate zinc levels in sickle-cell anemia patients., Int J Lab Hematol, 34, 129, 10.1111/j.1751-553X.2011.01369.x · doi:10.1111/j.1751-553x.2011.01369.x
- LaBrake, 1998, Sickle hemoglobin is more fusogenic than normal hemoglobin at physiological pH and ionic strength conditions., Biochim Biophys Acta, 1406, 152, 10.1016/S0925-4439(97)00093-8 · doi:10.1016/s0925-4439(97)00093-8
Cited by
Pathophysiology of Sickle Cell Disease
Sundd, P., Gladwin, M. T., & Novelli, E. M. (2019) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-012418-012838 · Cited by 813
Intravascular hemolysis and the pathophysiology of sickle cell disease
Kato, G. J., Steinberg, M. H., & Gladwin, M. T. (2017) · Journal of Clinical Investigation · doi:10.1172/jci89741 · Cited by 748
Nader, E., Skinner, S., Romana, M., Fort, R., Lemonne, N., Guillot, N., Gauthier, A., Antoine-Jonville, S., Renoux, C., Hardy-Dessources, M.-D., et al. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01329 · Cited by 502
Zhang, D., Xu, C., Manwani, D., & Frenette, P. S. (2016) · Blood · doi:10.1182/blood-2015-09-618538 · Cited by 413
Inflammation in sickle cell disease
Conran, N., & Belcher, J. D. (2018) · Clinical Hemorheology and Microcirculation · doi:10.3233/ch-189012 · Cited by 294
Metadata
- Authors
- Camus, S. M., De Moraes, J. A., Bonnin, P., Abbyad, P., Le Jeune, S., Lionnet, F., Loufrani, L., Grimaud, L., Lambry, J.-C., Charue, D., Kiger, L., Renard, J.-M., Larroque, C., Le Clésiau, H., Tedgui, A., Bruneval, P., Barja-Fidalgo, C., Alexandrou, A., Tharaux, P.-L., Boulanger, C. M., & Blanc-Brude, O. P.
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2015-06-11
- Volume
- 125
- Issue
- 24
- Pages
- 3805-3814
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W2066856450
- Cited by
- 262
- References
- 51
- FWCI
- 14.67
- Type
- journal article
- Language
- en
- Open access
- green
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- Camus, S. M., De Moraes, J. A., Bonnin, P., Abbyad, P., Le Jeune, S., Lionnet, F., Loufrani, L., Grimaud, L., Lambry, J.-C., Charue, D., Kiger, L., Renard, J.-M., Larroque, C., Le Clésiau, H., Tedgui, A., Bruneval, P., Barja-Fidalgo, C., Alexandrou, A., Tharaux, P.-L., . . . Blanc-Brude, O. P. (2015). Circulating cell membrane microparticles transfer heme to endothelial cells and trigger vasoocclusions in sickle cell disease. Blood. https://doi.org/10.1182/blood-2014-07-589283
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.