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Erythroblastic islands: niches for erythropoiesis
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Erythroblastic islands, the specialized niches in which erythroid precursors proliferate, differentiate, and enucleate, were first described 50 years ago by analysis of transmission electron micrographs of bone marrow. These hematopoietic subcompartments are composed of erythroblasts surrounding a central macrophage. A hiatus of several decades followed, during which the importance of erythroblastic islands remained unrecognized as erythroid progenitors were shown to possess an autonomous differentiation program with a capacity to complete terminal differentiation in vitro in the presence of erythropoietin but without macrophages. However, as the extent of proliferation, differentiation, and enucleation efficiency documented in vivo could not be recapitulated in vitro, a resurgence of interest in erythroid niches has emerged. We now have an increased molecular understanding of processes operating within erythroid niches, including cell-cell and cell-extracellular matrix adhesion, positive and negative regulatory feedback, and central macrophage function. These features of erythroblast islands represent important contributors to normal erythroid development, as well as altered erythropoiesis found in such diverse diseases as anemia of inflammation and chronic disease, myelodysplasia, thalassemia, and malarial anemia. Coupling of historical, current, and future insights will be essential to understand the tightly regulated production of red cells both in steady state and stress erythropoiesis.
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“Erythroblastic islands are very specialized niches supporting the proliferation and differentiation of erythroblasts.14 Erythroid islands are characterized by a central macrophage that extends cytoplasmic protrusions to a ring of adjacent erythroblasts.The interaction of cells within the island is crucial for early and late stages of erythroid maturation.”
From Inflammatory bone marrow microenvironment (2019) · cites this paper as [14]
Citations
Cites
Effects of an Rb mutation in the mouse
Jacks, T., Fazeli, A., Schmitt, E. M., Bronson, R. T., Goodell, M. A., & Weinberg, R. A. (1992) · Nature · doi:10.1038/359295a0 · Cited by 1,755
F4/80, a monoclonal antibody directed specifically against the mouse macrophage
Austyn, J. M., & Gordon, S. (1981) · European Journal of Immunology · doi:10.1002/eji.1830111013 · Cited by 1,596
Identification of a factor that links apoptotic cells to phagocytes
Hanayama, R., Tanaka, M., Miwa, K., Shinohara, A., Iwamatsu, A., & Nagata, S. (2002) · Nature · doi:10.1038/417182a · Cited by 1,401
Pevny, L., Simon, M. C., Robertson, E., Klein, W. H., Tsai, S.-F., D'Agati, V., Orkin, S. H., & Costantini, F. (1991) · Nature · doi:10.1038/349257a0 · Cited by 1,308
Mice deficient for Rb are nonviable and show defects in neurogenesis and haematopoiesis
Lee, E. Y.-H. P., Chang, C.-Y., Hu, N., Wang, Y.-C. J., Lai, C., Herrup, K., Lee, W., & Bradley, A. (1992) · Nature · doi:10.1038/359288a0 · Cited by 1,264
Requirement for a functional Rb-1 gene in murine development
Clarke, A. R., Maandag, E. R., van ROON, M. A., van der Lugt, N. M. T., van der Valk, M., Hooper, M., Berns, A. J. M., & Rielef, H. T. (1992) · Nature · doi:10.1038/359328a0 · Cited by 1,006
Erythropoietin Retards DNA Breakdown and Prevents Programmed Death in Erythroid Progenitor Cells
Koury, M. J., & Bondurant, M. C. (1990) · Science · doi:10.1126/science.2326648 · Cited by 819
Fujiwara, Y., Browne, C. P., Cunniff, K., Goff, S. C., & Orkin, S. H. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.22.12355 · Cited by 778
Regulation of Iron Metabolism by Hepcidin
Nemeth, E., & Ganz, T. (2006) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.26.061505.111303 · Cited by 756
Weiss, M. J., Keller, G., & Orkin, S. H. (1994) · Genes & Development · doi:10.1101/gad.8.10.1184 · Cited by 541
Research works printed but not linked: 2
- Bessis, 1958, L'ilot erythroblastique. Unite functionelle de la moelle osseuse., Rev Hematol, 13, 8
- Porter, 1983, Erythroid burst promoting activity (BPA)., 81
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Jacobsen, R. N., Perkins, A. C., & Lévesque, J.-P. (2015) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000131 · Cited by 53
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Hayashi, Y., Zhang, Y., Yokota, A., Yan, X., Liu, J., Choi, K., Li, B., Sashida, G., Peng, Y., Xu, Z., et al. (2018) · Cancer Discovery · doi:10.1158/2159-8290.cd-17-1203 · Cited by 54
Ketema, T., & Bacha, K. (2013) · BMC Public Health · doi:10.1186/1471-2458-13-637 · Cited by 52
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Shah, S., Huang, X., & Cheng, L. (2013) · Stem Cells Translational Medicine · doi:10.5966/sctm.2013-0054 · Cited by 53
Boeuf, P., Loizon, S., Awandare, G. A., Tetteh, J. K., ADDAE, M. M., Adjei, G. O., Goka, B. Q., Kurtzhals, J. A. L., Mercereau‐Puijalon, O., Hviid, L., et al. (2012) · Malaria Journal · doi:10.1186/1475-2875-11-253 · Cited by 52
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Longo, F., Piolatto, A., Ferrero, G. B., & Piga, A. G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137229 · Cited by 53
Falchi, M., Varricchio, L., Martelli, F., Masiello, F., Federici, G., Zingariello, M., Girelli, G., Whitsett, C., Petricoin, E. F., Moestrup, S. K., et al. (2014) · Haematologica · doi:10.3324/haematol.2014.114405 · Cited by 51
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Wang, D., Zhang, W., Kalfa, T. A., Grabowski, G. A., Davies, S. M., Malik, P., & Pan, D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908528106 · Cited by 51
Fraser, S. T., Midwinter, R. G., Coupland, L. A., Kong, S., Berger, B. S., Yeo, J. H., Andrade, O. C., Cromer, D., Suarna, C., Lam, M., et al. (2015) · Haematologica · doi:10.3324/haematol.2014.116368 · Cited by 50
FAJTOVA, M., KOVARIKOVA, A., Švec, P., Kankuri, E. M., & Sedlák, J. (2013) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.3109/10428194.2013.781167 · Cited by 50
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Chen, Y., Xiang, J., Qian, F., Tukaramrao, D. B., Ruan, B., Hao, S., Prabhu, K. S., & Paulson, R. F. (2020) · Blood · doi:10.1182/blood.2019003480 · Cited by 49
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Romano, L., Seu, K. G., Papoin, J., Muench, D. E., Konstantinidis, D. G., Olsson, A., Schlum, K., Chetal, K., Chasis, J. A., Mohandas, N., et al. (2022) · Blood · doi:10.1182/blood.2022015724 · Cited by 50
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Bouchnita, A., Eymard, N., Moyo, T. K., Koury, M. J., & Volpert, V. A. (2016) · American Journal of Hematology · doi:10.1002/ajh.24291 · Cited by 47
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Schwarz, E. M., Kato, M., & Sternberg, P. W. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1203045109 · Cited by 46
Erythroid development in the mammalian embryo
Baron, M. H., Vacaru, A. M., & Nieves, J. L. (2013) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2013.07.006 · Cited by 46
Combinatorial and distinct roles of α5 and α4 integrins in stress erythropoiesis in mice
Ulyanova, T., Jiang, Y., Padilla, S., Nakamoto, B., & Papayannopoulou, T. (2010) · Blood · doi:10.1182/blood-2010-05-283218 · Cited by 45
Moss, J., Ben‐Ami, R., Shai, E., Gal-Rosenberg, O., Kalish, Y., Klochendler, A., Cann, G. M., Gläser, B., Arad, A., Shemer, R., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43310-2 · Cited by 43
Ex-vivo expansion of red blood cells: How real for transfusion in humans?
Migliaccio, A. R., Masselli, E., Varricchio, L., & Whitsett, C. (2011) · Blood Reviews · doi:10.1016/j.blre.2011.11.002 · Cited by 44
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Aglialoro, F., Hofsink, N., Hofman, M., Brandhorst, N., & van den Akker, E. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00958 · Cited by 46
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Liu, J., Mohandas, N., & An, X. (2011) · Current Opinion in Hematology · doi:10.1097/moh.0b013e32834521f3 · Cited by 44
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Lombardo, B., Izzo, V., Terracciano, D., Ranieri, A., Mazzaccara, C., Fimiani, F., Cesaro, A., Gentile, L., Leggiero, E., Pero, R., et al. (2019) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm-2018-1107 · Cited by 46
de Kruijf, E.-J. F. M., Fibbe, W. E., & van Pel, M. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14059 · Cited by 43
Concise Review: Early Embryonic Erythropoiesis: Not so Primitive After All
Baron, M. H. (2013) · Stem Cells · doi:10.1002/stem.1342 · Cited by 43
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Luo, S., Zhang, D., Qin, Q., Lu, L., Luo, M., Guo, F., Shi, H., Jiang, L., Shao, B., Li, M., et al. (2017) · Scientific Reports · doi:10.1038/srep38105 · Cited by 41
Combined liver–cytokine humanization comes to the rescue of circulating human red blood cells
Song, Y., Shan, L., Gbyli, R., Liu, W., Strowig, T., Patel, A. J., Fu, X., Wang, X., Xu, M. L., Gao, Y., et al. (2021) · Science · doi:10.1126/science.abe2485 · Cited by 41
Role of Helix-Loop-Helix Proteins during Differentiation of Erythroid Cells
Anantharaman, A., Lin, I., Barrow, J. J., Liang, S. Y., Masannat, J., Strouboulis, J., Huang, S., & Bungert, J. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.01186-10 · Cited by 43
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Dulmovits, B. M., Hom, J., Narla, A., Mohandas, N., & Blanc, L. (2017) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000328 · Cited by 41
Self-citationMikdar, M., González‐Menéndez, P., Cai, X., Zhang, Y., Serra, M., Dembélé, A. K., Boschat, A., Sanquer, S., Chhuon, C., Guerrera, I. C., et al. (2021) · Blood · doi:10.1182/blood.2020007281 · Cited by 42
Self-citationZhu, H., Foretz, M., Xie, Z., Zhang, M., Zhu, Z., Xing, J., Leclerc, J., Gaudry, M., Viollet, B., & Zou, M. (2014) · Autophagy · doi:10.4161/auto.29197 · Cited by 42
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Carden, M. A., Fasano, R. M., & Meier, E. R. (2019) · Blood Reviews · doi:10.1016/j.blre.2019.100637 · Cited by 38
Yang, C., Endoh, M., Tan, D. Q., Nakamura‐Ishizu, A., Takihara, Y., Matsumura, T., & Suda, T. (2021) · British Journal of Haematology · doi:10.1111/bjh.17531 · Cited by 37
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Kim, T. S., Hanak, M. F., Trampont, P. C., & Braciale, T. J. (2015) · Journal of Clinical Investigation · doi:10.1172/jci81919 · Cited by 36
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Boehm, D., Murphy, W. G., & Al‐Rubeai, M. (2009) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2009.08.017 · Cited by 36
Extrinsic and intrinsic control by EKLF (KLF1) within a specialized erythroid niche
Li, X., Galdass, M., Gnanapragasam, M. N., Manwani, D. G., & Bieker, J. J. (2014) · Development · doi:10.1242/dev.103960 · Cited by 36
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Thomson-Luque, R., Wang, C. C. Q., Ntumngia, F. B., Xu, S., Szekeres, K., Conway, A., Adapa, S. R., Barnes, S. J., Adams, J. H., & Jiang, R. H. Y. (2018) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2018.06.004 · Cited by 35
Raducka-Jaszul, O., Bogusławska, D. M., Jędruchniewicz, N., & Sikorski, A. F. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21093325 · Cited by 37
Yang, C., Yokomori, R., Chua, L. H., Tan, S. H., Tan, D. Q., Miharada, K., Sanda, T., & Suda, T. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20220685 · Cited by 35
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Oates, T. C., Moura, P. L., Cross, S., Roberts, K., Baum, H. E., Haydn‐Smith, K. L., Wilson, M. C., Heesom, K. J., Severn, C. E., & Toye, A. M. (2023) · Immunology and Cell Biology · doi:10.1111/imcb.12687 · Cited by 39
Fukumoto, R., Burns, T. M., & Kiang, J. G. (2014) · PLoS ONE · doi:10.1371/journal.pone.0090448 · Cited by 34
Kumkhaek, C., Aerbajinai, W., Liu, W., Zhu, J., Uchida, N., Kurlander, R. J., Hsieh, M. M., Tisdale, J. F., & Rodgers, G. P. (2013) · Blood · doi:10.1182/blood-2011-10-385252 · Cited by 33
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Nagata, S., & Kawane, K. (2011) · Advances in immunology · doi:10.1016/b978-0-12-387663-8.00004-1 · Cited by 32
Dev, A., Fang, J., Sathyanarayana, P., Pradeep, A., Emerson, C., & Wojchowski, D. M. (2010) · Blood · doi:10.1182/blood-2009-12-258947 · Cited by 32
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Lima, F. D. S., & Fock, R. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197084 · Cited by 34
Jordan, S., Ruzsics, Z., Mitrović, M., Baranek, T., Arapović, J., Krmpotić, A., Vivier, É., Dalod, M., Jonjić, S., Dölken, L., et al. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.04.007 · Cited by 33
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Zou, Z., Enis, D. R., Bui, H., Khandros, E., Kumar, V., Jakus, Z., Thom, C. S., Yang, Y., Dhillon, V., Chen, M. Y., et al. (2013) · Blood · doi:10.1182/blood-2012-10-462689 · Cited by 32
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Ma, J., Li, R., Liu, Y., Qu, G., Liu, J. L., Guo, W., Song, H., Li, X., Liu, Y., Xia, T., et al. (2017) · Small · doi:10.1002/smll.201603830 · Cited by 31
Spring, F. A., Griffiths, R. E., Mankelow, T. J., Agnew, C., Parsons, S. F., Chasis, J. A., & Anstee, D. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062654 · Cited by 34
Self-citationGuzniczak, E., Zadeh, M. M., Dempsey, F. C., Jimenez, M., Bock, H., Whyte, G., Willoughby, N. A., & Bridle, H. L. (2017) · Scientific Reports · doi:10.1038/s41598-017-14958-w · Cited by 31
Less known pathophysiological mechanisms of anemia in patients with diabetic nephropathy
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Modeling erythroblastic islands: Using a hybrid model to assess the function of central macrophage
Fischer, S., Kurbatova, P., Bessonov, N., Gandrillon, O., Volpert, V. A., & Fabien Crauste, A. (2012) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2012.01.002 · Cited by 30
EKLF/KLF1 expression defines a unique macrophage subset during mouse erythropoiesis
Mukherjee, K., Li, X., Planutis, A., Gnanapragasam, M. N., Chess, A. J., & Bieker, J. J. (2021) · eLife · doi:10.7554/elife.61070 · Cited by 31
Ferritin H is a novel marker of early erythroid precursors and macrophages
Wang, W., Grier, D. D., Woo, J., Ward, M., Sui, G., Torti, S. V., Torti, F. M., & Beaty, M. W. (2013) · Histopathology · doi:10.1111/his.12101 · Cited by 29
Vidal, M. (2010) · Transfusion Clinique et Biologique · doi:10.1016/j.tracli.2010.05.004 · Cited by 30
New Insights into the Mechanisms of Mammalian Erythroid Chromatin Condensation and Enucleation
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Rhodes, M., Koury, S. T., Kopsombut, P., Alford, C. E., Price, J. O., & Koury, M. J. (2016) · American Journal of Hematology · doi:10.1002/ajh.24421 · Cited by 30
Marcero, J. R., Cox, J. E., Bergonia, H. A., Medlock, A. E., Phillips, J. D., & Dailey, H. A. (2021) · Blood Advances · doi:10.1182/bloodadvances.2021004750 · Cited by 30
Palma, A. D., Roveri, A., Zaccarin, M., Benazzi, L., Daminelli, S., Pantano, G., Buttarello, M., Ursini, F., Gion, M., & Mauri, P. (2010) · Journal of Chromatography A · doi:10.1016/j.chroma.2010.06.045 · Cited by 29
Vitamin‐regulated cytokines and growth factors in the CNS and elsewhere
Scalabrino, G. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06417.x · Cited by 29
Motani, K., & Kosako, H. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.002175 · Cited by 29
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Sinha, S., Pereira-Reis, J., Guerra, A., Rivella, S., & Duarte, D. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8155 · Cited by 29
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Fibach, E. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.604738 · Cited by 29
Freikman, I., & Fibach, E. (2011) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2011.08.014 · Cited by 28
Clearance of Apoptotic Cells and Pyrenocytes
Toda, S., Nishi, C., Yanagihashi, Y., Segawa, K., & Nagata, S. (2015) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2015.07.017 · Cited by 28
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Mohandas, N., & Chasis, J. A. (2010) · Transfusion Clinique et Biologique · doi:10.1016/j.tracli.2010.05.009 · Cited by 27
Self-citationWang, J., Hayashi, Y., Yokota, A., Xu, Z., Zhang, Y., Huang, R., Yan, X., Liu, H., Ma, L., Azam, M., et al. (2017) · Haematologica · doi:10.3324/haematol.2017.172775 · Cited by 27
Migliaccio, A. R., Martelli, F., Verrucci, M., Sanchez, M., Valeri, M., Migliaccio, G., Vannucchi, A. M., Zingariello, M., Baldassarre, A. D., Ghinassi, B., et al. (2009) · Blood · doi:10.1182/blood-2009-03-211680 · Cited by 27
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Rabinovich, G. A., & Vidal, M. (2011) · Current Opinion in Hematology · doi:10.1097/moh.0b013e32834bab18 · Cited by 27
Fan, W., Cao, W., Shi, J., Gao, F., Wang, M., Xu, L., Wang, F., Li, Y., Guo, R., Bian, Z., et al. (2023) · Annals of Hematology · doi:10.1007/s00277-023-05284-5 · Cited by 26
Breda, L., & Rivella, S. (2014) · Hematology/Oncology Clinics of North America · doi:10.1016/j.hoc.2013.12.001 · Cited by 26
Meng, X., Baylink, D. J., Sheng, M. H. ‐., Wang, H., Gridley, D. S., Lau, K. ‐. W., & Zhang, X. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037569 · Cited by 26
Ontogeny of haematopoiesis: recent advances and open questions
Ottersbach, K., Smith, A. M., Wood, A., & Göttgens, B. (2009) · British Journal of Haematology · doi:10.1111/j.1365-2141.2009.07953.x · Cited by 26
The macrophage contribution to stress erythropoiesis: when less is enough
Ulyanova, T., Phelps, S. R., & Papayannopoulou, T. (2016) · Blood · doi:10.1182/blood-2016-05-714527 · Cited by 26
Red Blood Cell Generation by Three-Dimensional Aggregate Cultivation of Late Erythroblasts
Lee, E.-M., Han, S. Y., Choi, H. S., Chun, B.-H., Hwang, B., & Baek, E. J. (2014) · Tissue Engineering Part A · doi:10.1089/ten.tea.2014.0325 · Cited by 26
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Metadata
- Authors
- Chasis, J. A., & Mohandas, N.
- Affiliations
- Lawrence Berkeley National Laboratory (US)
- New York Blood Center (US)
- ORCID
- Mohandas, Narla
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2008-08-01
- Volume
- 112
- Issue
- 3
- Pages
- 470-478
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- PMC
- PMC2481536
- OpenAlex
- W2048719634
- Cited by
- 506
- References
- 101
- Citations by year
- 2026: 12 · 2025: 18 · 2024: 19 · 2023: 31 · 2022: 29 · 2021: 27 · 2020: 34 · 2019: 32 · 2018: 26 · 2017: 29 · 2016: 20 · 2015: 31 · 2014: 33 · 2013: 43 · 2012: 28
- FWCI
- 3.95
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Blood (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Yale University
- National Institutes of Health
- National Heart, Lung, and Blood Institute (T32HL007956, HL7956)
- National Institute of Diabetes and Digestive and Kidney Diseases (P01DK032094, DK56267, R01DK056267, DK32094)
- Topics
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Health Sciences › Medicine › Hematology › Erythropoietin and Anemia Treatment
- Health Sciences › Medicine › Genetics (clinical) › Hemoglobinopathies and Related Disorders
- Keywords
- erythroblastic islands, erythropoiesis, erythroid progenitor cells, erythroblast enucleation, erythroid differentiation, erythropoietin, cell-matrix adhesion, feedback regulation, anemia of chronic disease, myelodysplastic syndrome, thalassemia, malarial anemia, stress erythropoiesis
- MeSH terms
- Bone Marrow, Cell Adhesion, Erythroblasts, Erythropoiesis, Extracellular Matrix, Humans, Macrophages, Feedback, Physiological
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