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From stem cell to red cell: regulation of erythropoiesis at multiple levels by multiple proteins, RNAs, and chromatin modifications

Hattangadi, Shilpa M., Wong, Piu, Zhang, Lingbo, Flygare, Johan, Lodish, Harvey F.·2011·Blood

Abstract

This article reviews the regulation of production of RBCs at several levels. We focus on the regulated expansion of burst-forming unit-erythroid erythroid progenitors by glucocorticoids and other factors that occur during chronic anemia, inflammation, and other conditions of stress. We also highlight the rapid production of RBCs by the coordinated regulation of terminal proliferation and differentiation of committed erythroid colony-forming unit-erythroid progenitors by external signals, such as erythropoietin and adhesion to a fibronectin matrix. We discuss the complex intracellular networks of coordinated gene regulation by transcription factors, chromatin modifiers, and miRNAs that regulate the different stages of erythropoiesis.

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Research works printed but not linked: 106

  1. Palis, 1999, Development of erythroid and myeloid progenitors in the yolk sac and embryo proper of the mouse., Development, 126, 5073, 10.1242/dev.126.22.5073 · DOI
  2. Elliott, 2008, Erythropoietins: a common mechanism of action., Exp Hematol, 36, 1573, 10.1016/j.exphem.2008.08.003 · DOI
  3. Fawcett, 1997, Bloom & Fawcett: Concise Histology
  4. Molineux, 2009, Erythropoiesis and Erythropoietins
  5. Dolznig, 2006, Erythroid progenitor renewal versus differentiation: genetic evidence for cell autonomous, essential functions of EpoR, Stat5 and the GR., Oncogene, 25, 2890, 10.1038/sj.onc.1209308 · DOI
  6. Wu, 1995, Generation of committed erythroid BFU-E and CFU-E progenitors does not require erythropoietin or the erythropoietin receptor., Cell, 83, 59, 10.1016/0092-8674(95)90234-1 · DOI
  7. Kieran, 1996, Thrombopoietin rescues in vitro erythroid colony formation from mouse embryos lacking the erythropoietin receptor., Proc Natl Acad Sci U S A, 93, 9126, 10.1073/pnas.93.17.9126 · DOI
  8. Lin, 1996, Differential effects of an erythropoietin receptor gene disruption on primitive and definitive erythropoiesis., Genes Dev, 10, 154, 10.1101/gad.10.2.154 · DOI
  9. Zhang, 2003, Role of Ras signaling in erythroid differentiation of mouse fetal liver cells: functional analysis by a flow cytometry-based novel culture system., Blood, 102, 3938, 10.1182/blood-2003-05-1479 · DOI
  10. Eshghi, 2007, Alpha4beta1 integrin and erythropoietin mediate temporally distinct steps in erythropoiesis: integrins in red cell development., J Cell Biol, 177, 871, 10.1083/jcb.200702080 · DOI
  11. Lodish, 2009, Signaling by the erythropoietin receptor., 155, 10.1007/978-3-7643-8698-6_10 · DOI
  12. Ghaffari, 2006, AKT induces erythroid-cell maturation of JAK2-deficient fetal liver progenitor cells and is required for Epo regulation of erythroid-cell differentiation., Blood, 107, 1888, 10.1182/blood-2005-06-2304 · DOI
  13. Zhang, 2007, Endogenous K-ras signaling in erythroid differentiation., Cell Cycle, 6, 1970, 10.4161/cc.6.16.4577 · DOI
  14. Socolovsky, 2001, Ineffective erythropoiesis in Stat5a(−/−)5b(−/−) mice due to decreased survival of early erythroblasts., Blood, 98, 3261, 10.1182/blood.V98.12.3261 · DOI
  15. Socolovsky, 1999, Fetal anemia and apoptosis of red cell progenitors in Stat5a−/−5b−/− mice: a direct role for Stat5 in Bcl-X(L) induction., Cell, 98, 181, 10.1016/S0092-8674(00)81013-2 · DOI
  16. Wood, 2009, ID1 promotes expansion and survival of primary erythroid cells and is a target of JAK2V617F-STAT5 signaling., Blood, 114, 1820, 10.1182/blood-2009-02-206573 · DOI
  17. Zhu, 2008, Hematopoietic-specific Stat5-null mice display microcytic hypochromic anemia associated with reduced transferrin receptor gene expression., Blood, 112, 2071, 10.1182/blood-2007-12-127480 · DOI
  18. Sathyanarayana, 2008, EPO receptor circuits for primary erythroblast survival., Blood, 111, 5390, 10.1182/blood-2007-10-119743 · DOI
  19. Cantor, 2002, Transcriptional regulation of erythropoiesis: an affair involving multiple partners., Oncogene, 21, 3368, 10.1038/sj.onc.1205326 · DOI
  20. Kerenyi, 2010, Networking erythropoiesis., J Exp Med, 207, 2537, 10.1084/jem.20102260 · DOI · Paper page
  21. Bauer, 2011, Update on fetal hemoglobin gene regulation in hemoglobinopathies., Curr Opin Pediatr, 23, 1, 10.1097/MOP.0b013e3283420fd0 · DOI
  22. Gilliland, 2004, The molecular basis of leukemia., Hematology Am Soc Hematol Educ Program, 80, 10.1182/asheducation-2004.1.80 · DOI
  23. Tijssen, 2011, Genome-wide analysis of simultaneous GATA1/2, RUNX1, FLI1, and SCL binding in megakaryocytes identifies hematopoietic regulators., Dev Cell, 20, 597, 10.1016/j.devcel.2011.04.008 · DOI
  24. Bresnick, 2005, Developmental control via GATA factor interplay at chromatin domains., J Cell Physiol, 205, 1, 10.1002/jcp.20393 · DOI
  25. Fujiwara, 2009, Discovering hematopoietic mechanisms through genome-wide analysis of GATA factor chromatin occupancy., Mol Cell, 36, 667, 10.1016/j.molcel.2009.11.001 · DOI
  26. Yu, 2009, Insights into GATA-1-mediated gene activation versus repression via genome-wide chromatin occupancy analysis., Mol Cell, 36, 682, 10.1016/j.molcel.2009.11.002 · DOI
  27. Heintzman, 2007, The gateway to transcription: identifying, characterizing and understanding promoters in the eukaryotic genome., Cell Mol Life Sci, 64, 386, 10.1007/s00018-006-6295-0 · DOI
  28. Cui, 2009, Chromatin signatures in multipotent human hematopoietic stem cells indicate the fate of bivalent genes during differentiation., Cell Stem Cell, 4, 80, 10.1016/j.stem.2008.11.011 · DOI
  29. Cheng, 2009, Erythroid GATA1 function revealed by genome-wide analysis of transcription factor occupancy, histone modifications, and mRNA expression., Genome Res, 19, 2172, 10.1101/gr.098921.109 · DOI · Paper page
  30. Kassouf, 2010, Genome-wide identification of TAL1's functional targets: insights into its mechanisms of action in primary erythroid cells., Genome Res, 20, 1064, 10.1101/gr.104935.110 · DOI
  31. Tripic, 2009, SCL and associated proteins distinguish active from repressive GATA transcription factor complexes., Blood, 113, 2191, 10.1182/blood-2008-07-169417 · DOI
  32. Miller, 1993, A novel, erythroid cell-specific murine transcription factor that binds to the CACCC element and is related to the Kruppel family of nuclear proteins., Mol Cell Biol, 13, 2776, 10.1128/MCB.13.5.2776 · DOI
  33. Tallack, 2010, A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells., Genome Res, 20, 1052, 10.1101/gr.106575.110 · DOI
  34. Jackson, 1993, Visualization of focal sites of transcription within human nuclei., EMBO J, 12, 1059, 10.1002/j.1460-2075.1993.tb05747.x · DOI
  35. Schoenfelder, 2010, Preferential associations between co-regulated genes reveal a transcriptional interactome in erythroid cells., Nat Genet, 42, 53, 10.1038/ng.496 · DOI
  36. Capron, 2011, LYL-1 deficiency induces a stress erythropoiesis., Exp Hematol, 39, 629, 10.1016/j.exphem.2011.02.014 · DOI
  37. Maeda, 2009, LRF is an essential downstream target of GATA1 in erythroid development and regulates BIM-dependent apoptosis., Dev Cell, 17, 527, 10.1016/j.devcel.2009.09.005 · DOI
  38. Guenther, 2007, A chromatin landmark and transcription initiation at most promoters in human cells., Cell, 130, 77, 10.1016/j.cell.2007.05.042 · DOI
  39. Muse, 2007, RNA polymerase is poised for activation across the genome., Nat Genet, 39, 1507, 10.1038/ng.2007.21 · DOI
  40. Zeitlinger, 2007, RNA polymerase stalling at developmental control genes in the Drosophila melanogaster embryo., Nat Genet, 39, 1512, 10.1038/ng.2007.26 · DOI
  41. Sawado, 2003, The beta-globin locus control region (LCR) functions primarily by enhancing the transition from transcription initiation to elongation., Genes Dev, 17, 1009, 10.1101/gad.1072303 · DOI
  42. Monteiro, 2011, The gata1/pu.1 lineage fate paradigm varies between blood populations and is modulated by tif1gamma., EMBO J, 30, 1093, 10.1038/emboj.2011.34 · DOI
  43. Bai, 2010, TIF1gamma controls erythroid cell fate by regulating transcription elongation., Cell, 142, 133, 10.1016/j.cell.2010.05.028 · DOI
  44. Suganuma, 2011, Signals and combinatorial functions of histone modifications., Annu Rev Biochem, 80, 473, 10.1146/annurev-biochem-061809-175347 · DOI
  45. Talbert, 2010, Histone variants: ancient wrap artists of the epigenome., Nat Rev Mol Cell Biol, 11, 264, 10.1038/nrm2861 · DOI
  46. Schubeler, 2004, The histone modification pattern of active genes revealed through genome-wide chromatin analysis of a higher eukaryote., Genes Dev, 18, 1263, 10.1101/gad.1198204 · DOI
  47. Feng, 2010, Early mammalian erythropoiesis requires the Dot1L methyltransferase., Blood, 116, 4483, 10.1182/blood-2010-03-276501 · DOI
  48. Orford, 2008, Differential H3K4 methylation identifies developmentally poised hematopoietic genes., Dev Cell, 14, 798, 10.1016/j.devcel.2008.04.002 · DOI
  49. Wong, 2011, Gene induction and repression during terminal erythropoiesis are mediated by distinct epigenetic changes., Blood, 118, e128, 10.1182/blood-2011-03-341404 · DOI · Paper page
  50. Kinross, 2006, E2f4 regulates fetal erythropoiesis through the promotion of cellular proliferation., Blood, 108, 886, 10.1182/blood-2005-09-008656 · DOI
  51. Sankaran, 2010, Advances in the understanding of haemoglobin switching., Br J Haematol, 149, 181, 10.1111/j.1365-2141.2010.08105.x · DOI
  52. Muir, 1958, Erythropoiesis: an electron microscopical study., Q J Exp Physiol Cogn Med Sci, 43, 106
  53. Ji, 2011, Formation of mammalian erythrocytes: chromatin condensation and enucleation., Trends Cell Biol, 21, 409, 10.1016/j.tcb.2011.04.003 · DOI
  54. Palis, 2010, Primitive erythropoiesis in the mammalian embryo., Int J Dev Biol, 54, 1011, 10.1387/ijdb.093056jp · DOI
  55. Jayapal, 2010, Down-regulation of Myc is essential for terminal erythroid maturation., J Biol Chem, 285, 40252, 10.1074/jbc.M110.181073 · DOI
  56. Fujieda, 2005, A putative role for histone deacetylase in the differentiation of human erythroid cells., Int J Oncol, 27, 743
  57. Popova, 2009, Chromatin condensation in terminally differentiating mouse erythroblasts does not involve special architectural proteins but depends on histone deacetylation., Chromosome Res, 17, 47, 10.1007/s10577-008-9005-y · DOI
  58. Ji, 2010, Histone deacetylase 2 is required for chromatin condensation and subsequent enucleation of cultured mouse fetal erythroblasts., Haematologica, 95, 2013, 10.3324/haematol.2010.029827 · DOI
  59. Bartel, 2009, MicroRNAs: target recognition and regulatory functions., Cell, 136, 215, 10.1016/j.cell.2009.01.002 · DOI · Paper page
  60. Guo, 2010, Mammalian microRNAs predominantly act to decrease target mRNA levels., Nature, 466, 835, 10.1038/nature09267 · DOI · Paper page
  61. Lu, 2008, MicroRNA-mediated control of cell fate in megakaryocyte-erythrocyte progenitors., Dev Cell, 14, 843, 10.1016/j.devcel.2008.03.012 · DOI · Paper page
  62. Felli, 2005, MicroRNAs 221 and 222 inhibit normal erythropoiesis and erythroleukemic cell growth via kit receptor down-modulation., Proc Natl Acad Sci U S A, 102, 18081, 10.1073/pnas.0506216102 · DOI · Paper page
  63. Wang, 2008, MicroRNA miR-24 inhibits erythropoiesis by targeting activin type I receptor ALK4., Blood, 111, 588, 10.1182/blood-2007-05-092718 · DOI
  64. Felli, 2009, MicroRNA 223-dependent expression of LMO2 regulates normal erythropoiesis., Haematologica, 94, 479, 10.3324/haematol.2008.002345 · DOI
  65. Dore, 2008, A GATA-1-regulated microRNA locus essential for erythropoiesis., Proc Natl Acad Sci U S A, 105, 3333, 10.1073/pnas.0712312105 · DOI · Paper page
  66. Pase, 2009, miR-451 regulates zebrafish erythroid maturation in vivo via its target gata2., Blood, 113, 1794, 10.1182/blood-2008-05-155812 · DOI
  67. Fu, 2009, Mir-144 selectively regulates embryonic alpha-hemoglobin synthesis during primitive erythropoiesis., Blood, 113, 1340, 10.1182/blood-2008-08-174854 · DOI
  68. Patrick, 2010, Defective erythroid differentiation in miR-451 mutant mice mediated by 14-3-3zeta., Genes Dev, 24, 1614, 10.1101/gad.1942810 · DOI
  69. Rasmussen, 2010, The miR-144/451 locus is required for erythroid homeostasis., J Exp Med, 207, 1351, 10.1084/jem.20100458 · DOI · Paper page
  70. Yu, 2010, miR-451 protects against erythroid oxidant stress by repressing 14-3-3zeta., Genes Dev, 24, 1620, 10.1101/gad.1942110 · DOI
  71. Sankaran, 2011, MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13., Proc Natl Acad Sci U S A, 108, 1519, 10.1073/pnas.1018384108 · DOI
  72. Zhang, 2011, miR-191 regulates mouse erythroblast enucleation by down-regulating Riok3 and Mxi1., Genes Dev, 25, 119, 10.1101/gad.1998711 · DOI
  73. Huarte, 2010, A large intergenic noncoding RNA induced by p53 mediates global gene repression in the p53 response., Cell, 142, 409, 10.1016/j.cell.2010.06.040 · DOI · Paper page
  74. Loewer, 2010, Large intergenic non-coding RNA-RoR modulates reprogramming of human induced pluripotent stem cells., Nat Genet, 42, 1113, 10.1038/ng.710 · DOI
  75. Harandi, 2010, Murine erythroid short-term radioprotection requires a BMP4-dependent, self-renewing population of stress erythroid progenitors., J Clin Invest, 120, 4507, 10.1172/JCI41291 · DOI
  76. McCulloch, 1964, Spleen-colony formation in anemic mice of genotype Ww., Science, 144, 844, 10.1126/science.144.3620.844 · DOI
  77. Hara, 1976, Erthropoietic precursors in mice with phenylhydrazine-induced anemia., Am J Hematol, 1, 453, 10.1002/ajh.2830010410 · DOI
  78. Kreja, 1985, On the role of the spleen in Friend virus (F-MuLV-P) erythroleukemia., Exp Hematol, 13, 623
  79. Slaper-Cortenbach, 1987, Different stimulative effects of human bone marrow and fetal liver stromal cells on erythropoiesis in long-term culture., Blood, 69, 135, 10.1182/blood.V69.1.135.bloodjournal691135 · DOI
  80. Yanai, 1989, Spleen stromal cell lines selectively support erythroid colony formation., Blood, 74, 2391, 10.1182/blood.V74.7.2391.2391 · DOI
  81. Ohneda, 1990, Microenvironment created by stromal cells is essential for a rapid expansion of erythroid cells in mouse fetal liver., Development, 110, 379, 10.1242/dev.110.2.379 · DOI
  82. Flygare, 2007, Diamond-Blackfan anemia: erythropoiesis lost in translation., Blood, 109, 3152, 10.1182/blood-2006-09-001222 · DOI
  83. Vlachos, 2008, Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference., Br J Haematol, 142, 859, 10.1111/j.1365-2141.2008.07269.x · DOI
  84. Bauer, 1999, The glucocorticoid receptor is required for stress erythropoiesis., Genes Dev, 13, 2996, 10.1101/gad.13.22.2996 · DOI
  85. Ganguli, 2002, The p53 tumour suppressor inhibits glucocorticoid-induced proliferation of erythroid progenitors., EMBO Rep, 3, 569, 10.1093/embo-reports/kvf114 · DOI
  86. von Lindern, 1999, The glucocorticoid receptor cooperates with the erythropoietin receptor and c-Kit to enhance and sustain proliferation of erythroid progenitors in vitro., Blood, 94, 550, 10.1182/blood.V94.2.550 · DOI
  87. Flygare, 2011, HIF-1alpha synergizes with glucocorticoids to promote BFU-E progenitor self-renewal., Blood, 117, 3435, 10.1182/blood-2010-07-295550 · DOI
  88. Kolbus, 2003, Cooperative signaling between cytokine receptors and the glucocorticoid receptor in the expansion of erythroid progenitors: molecular analysis by expression profiling., Blood, 102, 3136, 10.1182/blood-2003-03-0923 · DOI
  89. Wessely, 1997, The glucocorticoid receptor is a key regulator of the decision between self-renewal and differentiation in erythroid progenitors., EMBO J, 16, 267, 10.1093/emboj/16.2.267 · DOI
  90. Chou, 2010, Fetal liver hepatic progenitors are supportive stromal cells for hematopoietic stem cells., Proc Natl Acad Sci U S A, 107, 7799, 10.1073/pnas.1003586107 · DOI
  91. Broudy, 1996, Interaction of stem cell factor and its receptor c-kit mediates lodgment and acute expansion of hematopoietic cells in the murine spleen., Blood, 88, 75, 10.1182/blood.V88.1.75.75 · DOI
  92. Huddleston, 2003, Functional p85alpha gene is required for normal murine fetal erythropoiesis., Blood, 102, 142, 10.1182/blood-2002-10-3245 · DOI
  93. Bakker, 2007, Differential regulation of Foxo3a target genes in erythropoiesis., Mol Cell Biol, 27, 3839, 10.1128/MCB.01662-06 · DOI
  94. Munugalavadla, 2005, Repression of c-kit and its downstream substrates by GATA-1 inhibits cell proliferation during erythroid maturation., Mol Cell Biol, 25, 6747, 10.1128/MCB.25.15.6747-6759.2005 · DOI
  95. Hegde, 2007, An intronic sequence mutated in flexed-tail mice regulates splicing of Smad5., Mamm Genome, 18, 852, 10.1007/s00335-007-9074-9 · DOI
  96. Lenox, 2005, BMP4 and Madh5 regulate the erythroid response to acute anemia., Blood, 105, 2741, 10.1182/blood-2004-02-0703 · DOI
  97. Subramanian, 2008, Friend virus utilizes the BMP4-dependent stress erythropoiesis pathway to induce erythroleukemia., J Virol, 82, 382, 10.1128/JVI.02487-06 · DOI
  98. Singbrant, 2010, Canonical BMP signaling is dispensable for hematopoietic stem cell function in both adult and fetal liver hematopoiesis, but essential to preserve colon architecture., Blood, 115, 4689, 10.1182/blood-2009-05-220988 · DOI
  99. Singbrant, 2006, Smad5 is dispensable for adult murine hematopoiesis., Blood, 108, 3707, 10.1182/blood-2006-02-003384 · DOI
  100. Wu, 2010, Hypoxia regulates BMP4 expression in the murine spleen during the recovery from acute anemia., PLoS One, 5, e11303, 10.1371/journal.pone.0011303 · DOI
  101. Millot, 2010, Erythropoietin stimulates spleen BMP4-dependent stress erythropoiesis and partially corrects anemia in a mouse model of generalized inflammation., Blood, 116, 6072, 10.1182/blood-2010-04-281840 · DOI
  102. Perry, 2009, Maintenance of the BMP4-dependent stress erythropoiesis pathway in the murine spleen requires hedgehog signaling., Blood, 113, 911, 10.1182/blood-2008-03-147892 · DOI
  103. Lugus, 2007, GATA2 functions at multiple steps in hemangioblast development and differentiation., Development, 134, 393, 10.1242/dev.02731 · DOI
  104. Fuchs, 2002, Inhibition of Smad5 in human hematopoietic progenitors blocks erythroid differentiation induced by BMP4., Blood Cells Mol Dis, 28, 221, 10.1006/bcmd.2002.0487 · DOI
  105. Perry, 2007, BMP4, SCF, and hypoxia cooperatively regulate the expansion of murine stress erythroid progenitors., Blood, 109, 4494, 10.1182/blood-2006-04-016154 · DOI
  106. Sankaran, 2010, Reversing the hemoglobin switch., N Engl J Med, 363, 2258, 10.1056/NEJMcibr1010767 · DOI

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Metadata

Authors
Hattangadi, S. M., Wong, P., Zhang, L., Flygare, J., & Lodish, H. F.
Affiliations
Whitehead Institute for Biomedical Research, Cambridge, MA;
Venue
Blood
Published
2011-12-08
Volume
118
Issue
24
Pages
6258-6268
ISSN
  • 0006-4971
  • 1528-0020
Cited by
423
References
11
Language
en

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