Novel methods for studying normal and disordered erythropoiesis

被引:0
作者
LIU Jing [1 ]
HAN Xu [1 ]
AN XiuLi [2 ]
机构
[1] State Key Laboratory of Medical Genetics & School of Life Sciences, Central South University
[2] College of Life Sciences, Zhengzhou University
关键词
erythropoiesis; erythroid progenitors; erythroblast; surface markers; transcriptional profile;
D O I
暂无
中图分类号
R55 [血液及淋巴系疾病];
学科分类号
1002 ; 100201 ;
摘要
Erythropoiesis is a process during which multipotential hematopoietic stem cells proliferate, differentiate and eventually form mature erythrocytes. Interestingly, unlike most cell types, an important feature of erythropoiesis is that following each mitosis the daughter cells are morphologically and functionally different from the parent cell from which they are derived, demonstrating the need to study erythropoiesis in a stage-specific manner. This has been impossible until recently due to lack of methods for isolating erythroid cells at each distinct developmental stage. This review summarizes recent advances in the development of methods for isolating both murine and human erythroid cells and their applications. These methods provide powerful means for studying normal and impaired erythropoiesis associated with hematological disorders.
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页码:1270 / 1275
页数:6
相关论文
共 13 条
[1]  
Abnormal erythropoiesis and the pathophysiology of chronic anemia[J] . Mark J. Koury.Blood Reviews . 2014
[2]   Alloantibodies to a paternally derived RBC KEL antigen lead to hemolytic disease of the fetus/newborn in a murine model [J].
Stowell, Sean R. ;
Henry, Kate L. ;
Smith, Nicole H. ;
Hudson, Krystalyn E. ;
Halverson, Greg R. ;
Park, Jaekeun C. ;
Bennett, Ashley M. ;
Girard-Pierce, Kathryn R. ;
Arthur, C. Maridith ;
Bunting, Silvia T. ;
Zimring, James C. ;
Hendrickson, Jeanne E. .
BLOOD, 2013, 122 (08) :1494-1504
[3]  
Loss of a Rho-Regulated Actin Nucleator, mDia2, Impairs Cytokinesis during Mouse Fetal Erythropoiesis[J] . Sadanori Watanabe,Tihana De Zan,Toshimasa Ishizaki,Shingo Yasuda,Hiroshi Kamijo,Daisuke Yamada,Tomohiro Aoki,Hiroshi Kiyonari,Hiroshi Kaneko,Ritsuko Shimizu,Masayuki Yamamoto,Gohta Goshima,Shuh Narumiya.Cell Reports . 2013 (4)
[4]   Membrane assembly during erythropoiesis [J].
Liu, Jing ;
Mohandas, Narla ;
An, Xiuli .
CURRENT OPINION IN HEMATOLOGY, 2011, 18 (03) :133-138
[5]   A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia [J].
Arnaud, Lionel ;
Saison, Carole ;
Helias, Virginie ;
Lucien, Nicole ;
Steschenko, Dominique ;
Giarratana, Marie-Catherine ;
Prehu, Claude ;
Foliguet, Bernard ;
Montout, Lory ;
de Brevern, Alexandre G. ;
Francina, Alain ;
Ripoche, Pierre ;
Fenneteau, Odile ;
Da Costa, Lydie ;
Peyrard, Thierry ;
Coghlan, Gail ;
Illum, Niels ;
Birgens, Henrik ;
Tamary, Hannah ;
Iolascon, Achille ;
Delaunay, Jean ;
Tchernia, Gil ;
Cartron, Jean-Pierre .
AMERICAN JOURNAL OF HUMAN GENETICS, 2010, 87 (05) :721-727
[6]   Identification of gene networks associated with erythroid differentiation [J].
Peller, Shoshana ;
Tabach, Yuval ;
Rotschild, Miri ;
Garach-Joshua, Osnat ;
Cohen, Yosef ;
Goldfinger, Naomi ;
Rotter, Varda .
BLOOD CELLS MOLECULES AND DISEASES, 2009, 43 (01) :74-80
[7]  
Diamond-Blackfan Anemia: Diagnosis, Treatment, and Molecular Pathogenesis[J] . Jeffrey M. Lipton,Steven R. Ellis.Hematology/Oncology Clinics of North America . 2009 (2)
[8]   Ontogeny of erythropoiesis [J].
Palis, James .
CURRENT OPINION IN HEMATOLOGY, 2008, 15 (03) :155-161
[9]   Advances in the understanding of the congenital dyserythropoietic anaemias [J].
Wickramasinghe, SN ;
Wood, WG .
BRITISH JOURNAL OF HAEMATOLOGY, 2005, 131 (04) :431-446
[10]  
Comparison of mechanisms of anemia in mice with sickle cell disease and β-thalassemia[J] . Leslie S Kean,Laura E Brown,J.Wylie Nichols,Narla Mohandas,David R Archer,Lewis L Hsu.Experimental Hematology . 2002 (5)