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本文引用的文献

1
Gene induction and repression during terminal erythropoiesis are mediated by distinct epigenetic changes.终末红细胞生成过程中的基因诱导和抑制是由不同的表观遗传变化介导的。
Blood. 2011 Oct 20;118(16):e128-38. doi: 10.1182/blood-2011-03-341404. Epub 2011 Aug 22.
2
Dynamics of the epigenetic landscape during erythroid differentiation after GATA1 restoration.GATA1 恢复后红系分化过程中的表观遗传景观动态变化。
Genome Res. 2011 Oct;21(10):1659-71. doi: 10.1101/gr.125088.111. Epub 2011 Jul 27.
3
Formation of mammalian erythrocytes: chromatin condensation and enucleation.哺乳动物红细胞的形成:染色质浓缩和去核。
Trends Cell Biol. 2011 Jul;21(7):409-15. doi: 10.1016/j.tcb.2011.04.003. Epub 2011 May 17.
4
Genome-wide analysis of simultaneous GATA1/2, RUNX1, FLI1, and SCL binding in megakaryocytes identifies hematopoietic regulators.全基因组分析巨核细胞中 GATA1/2、RUNX1、FLI1 和 SCL 的同时结合,鉴定造血调控因子。
Dev Cell. 2011 May 17;20(5):597-609. doi: 10.1016/j.devcel.2011.04.008.
5
Signals and combinatorial functions of histone modifications.组蛋白修饰的信号和组合功能。
Annu Rev Biochem. 2011;80:473-99. doi: 10.1146/annurev-biochem-061809-175347.
6
LYL-1 deficiency induces a stress erythropoiesis.LYL-1 缺乏导致应激性红细胞生成。
Exp Hematol. 2011 Jun;39(6):629-42. doi: 10.1016/j.exphem.2011.02.014. Epub 2011 Mar 21.
7
The gata1/pu.1 lineage fate paradigm varies between blood populations and is modulated by tif1γ.Gata1/pu.1 谱系命运范式在血液群体之间存在差异,并受 tif1γ 调节。
EMBO J. 2011 Mar 16;30(6):1093-103. doi: 10.1038/emboj.2011.34. Epub 2011 Feb 18.
8
MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13.miRNA-15a 和 miRNA-16-1 通过 MYB 作用升高 13 三体综合征患者胎儿血红蛋白的表达。
Proc Natl Acad Sci U S A. 2011 Jan 25;108(4):1519-24. doi: 10.1073/pnas.1018384108. Epub 2011 Jan 4.
9
miR-191 regulates mouse erythroblast enucleation by down-regulating Riok3 and Mxi1.miR-191 通过下调 Riok3 和 Mxi1 来调控小鼠红细胞去核。
Genes Dev. 2011 Jan 15;25(2):119-24. doi: 10.1101/gad.1998711. Epub 2010 Dec 31.
10
HIF1alpha synergizes with glucocorticoids to promote BFU-E progenitor self-renewal.低氧诱导因子 1α与糖皮质激素协同作用促进红系爆式集落形成单位祖细胞自我更新。
Blood. 2011 Mar 24;117(12):3435-44. doi: 10.1182/blood-2010-07-295550. Epub 2010 Dec 21.

从干细胞到红细胞:多种蛋白质、RNA 和染色质修饰在多个层面上调节红细胞生成。

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

机构信息

Whitehead Institute for Biomedical Research, Cambridge, MA, USA.

出版信息

Blood. 2011 Dec 8;118(24):6258-68. doi: 10.1182/blood-2011-07-356006. Epub 2011 Oct 12.

DOI:10.1182/blood-2011-07-356006
PMID:21998215
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3236116/
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.

摘要

本文综述了红系造血在多个层面的调控。我们重点关注糖皮质激素和其他因子在慢性贫血、炎症和其他应激条件下对红系爆式集落形成单位-红系祖细胞的增殖调控,同时也强调了在外部信号(如促红细胞生成素和黏附于纤维连接蛋白基质)的协调调控下,定向的红系集落形成单位-红系祖细胞的末端增殖和分化对红细胞生成的快速作用。我们讨论了转录因子、染色质修饰因子和 miRNAs 等协调基因调控的复杂细胞内网络,这些因子调节着红细胞生成的不同阶段。