Mathematical modeling reveals differential effects of erythropoietin on proliferation and lineage commitment of human hematopoietic progenitors in early erythroid culture

被引:3
|
作者
Ward, Daniel [1 ]
Carter, Deborah [2 ]
Homer, Martin [1 ]
Marucci, Lucia [1 ]
Gampel, Alexandra [2 ]
机构
[1] Univ Bristol, Fac Engn, Dept Engn Math, Bristol BS8 1TH, Avon, England
[2] Univ Bristol, Fac Med & Vet Sci, Sch Biochem, Bristol BS8 1TH, Avon, England
基金
英国工程与自然科学研究理事会;
关键词
STEM-CELLS; EXPRESSION; SURVIVAL; GENE; CSF; SPECIFICATION; MEGAKARYOCYTE; POPULATIONS; GENERATION; MUTATIONS;
D O I
10.3324/haematol.2015.133637
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Erythropoietin is essential for the production of mature erythroid cells, promoting both proliferation and survival. Whether erythropoietin and other cytokines can influence lineage commitment of hematopoietic stem and progenitor cells is of significant interest. To study lineage restriction of the common myeloid progenitor to the megakaryocyte/erythroid progenitor of peripheral blood CD34(+) cells, we have shown that the cell surface protein CD36 identifies the earliest lineage restricted megakaryocyte/erythroid progenitor. Using this marker and carboxyfluorescein succinimidyl ester to track cell divisions in vitro, we have developed a mathematical model that accurately predicts population dynamics of erythroid culture. Parameters derived from the modeling of cultures without added erythropoietin indicate that the rate of lineage restriction is not affected by erythropoietin. By contrast, megakaryocyte/erythroid progenitor proliferation is sensitive to erythropoietin from the time that CD36 first appears at the cell surface. These results shed new light on the role of erythropoietin in erythropoiesis and provide a powerful tool for further study of hematopoietic progenitor lineage restriction and erythropoiesis.
引用
收藏
页码:286 / 296
页数:11
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