Liang Raymond, Ghaffari Saghi
Department of Developmental & Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Developmental and Stem Cell Biology Multidisciplinary Training Area, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Br J Haematol. 2016 Sep;174(5):661-73. doi: 10.1111/bjh.14194. Epub 2016 Jul 21.
Anaemia or decreased blood haemoglobin is the most common blood disorder often characterized by reduced red blood cell (RBC) numbers. RBCs are produced from differentiation and commitment of haematopoietic stem cells to the erythroid lineage by a process called erythropoiesis. Coordination of erythropoietin receptor signalling with several erythroid transcription factors including GATA1 is essential for this process. A number of additional players that are critical for RBC production have been identified in recent years. Major technological advances, such as the development of RNA interference, genetically modified animals, including zebrafish, and imaging flow cytometry have led to these discoveries; the emergence of -omics approaches in combination with the optimization of ex vivo erythroid cultures have also produced a more comprehensive understanding of erythropoiesis. Here we summarize studies describing novel regulators of erythropoiesis that modulate erythroid cell production in the context of human erythroid disorders involving hypoxia, iron regulation, immune-related molecules, and the transcription factor FOXO3.
贫血或血液血红蛋白水平降低是最常见的血液疾病,通常表现为红细胞(RBC)数量减少。红细胞由造血干细胞通过称为红细胞生成的过程分化并定向为红系谱系而产生。促红细胞生成素受体信号传导与包括GATA1在内的多种红系转录因子的协调对于这一过程至关重要。近年来,已经确定了许多对红细胞生成至关重要的其他因素。重大技术进步,如RNA干扰的发展、包括斑马鱼在内的基因改造动物以及成像流式细胞术促成了这些发现;“组学”方法的出现与体外红系培养的优化相结合,也使人们对红细胞生成有了更全面的认识。在这里,我们总结了一些研究,这些研究描述了在涉及缺氧、铁调节、免疫相关分子和转录因子FOXO3的人类红系疾病背景下调节红系细胞生成的红细胞生成新调节因子。