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

被引:349
作者
Hattangadi, Shilpa M. [1 ,2 ]
Wong, Piu [1 ]
Zhang, Lingbo [1 ,3 ,4 ]
Flygare, Johan [1 ,5 ]
Lodish, Harvey F. [1 ,6 ,7 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] Childrens Hosp Boston, Div Hematol Oncol, Boston, MA USA
[3] Singapore Massachusetts Inst Technol, Singapore, Singapore
[4] ASTAR, Genome Inst Singapore, Singapore, Singapore
[5] Lund Univ, Dept Mol Med & Gene Therapy, Lund, Sweden
[6] MIT, Dept Biol, Cambridge, MA USA
[7] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
BMP4-DEPENDENT STRESS ERYTHROPOIESIS; PRIMARY ERYTHROID-CELLS; GENOME-WIDE ANALYSIS; MOUSE FETAL LIVER; GLUCOCORTICOID-RECEPTOR; COLONY FORMATION; STROMAL CELLS; C-KIT; TRANSCRIPTION INITIATION; PRIMITIVE ERYTHROPOIESIS;
D O I
10.1182/blood-2011-07-356006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (Blood. 2011;118(24):6258-6268)
引用
收藏
页码:6258 / 6268
页数:11
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