Regulated expression of microRNAs in normal and polycythemia vera erythropoiesis

被引:175
作者
Bruchova, Hana
Yoon, Donghoon
Agarwal, Archana M.
Mendell, Joshua
Prchal, Josef T.
机构
[1] Univ Utah, Sch Med, Div Hematol, Dept Pathol, Salt Lake City, UT 84132 USA
[2] Inst Hematol & Blood Transfus, CR-12820 Prague, Czech Republic
[3] Dept Pathophysiol, Prague, Czech Republic
[4] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
关键词
D O I
10.1016/j.exphem.2007.08.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Polycythemia vera (PV) is a myeloproliferative disorder, arising from the acquired mutation(s) of a hematopoietic stem cell. The JAK2 V617F somatic mutation is found in most PV patients; however, it is not the disease-initiating mutation. Because microRNAs (miRNAs) play a regulatory role in hematopoiesis, we studied miRNA expressions in PV and normal erythropoiesis. Methods. Peripheral blood mononuclear cells were cultured in a three-phase liquid system resulting in synchronized expansion of erythroid progenitors. Using gene-expression profiling by CombiMatrix MicroRNArray, we searched for PV-specific changes at days 1, 14, and 21. Twelve miRNA candidates were then reevaluated by quantitative real-time polymerase chain reaction in a larger number of samples obtained from progenitors at the same stage of differentiation. Results. A significant difference in miR-150 expression was found in PV. In normal erythropoiesis, three expression patterns of miRNAs were observed: progressive downregulation of miR-150, miR-155, miR-221, miR-222; upregulation of miR-451, miR-16 at late stages of erythropoiesis; and biphasic regulation of miR-339, miR-378. The miR-451 appears to be erythroidspecific. Conclusions. We identified the miRNAs with regulated expression in erythropoiesis; one appeared to be PV-specific. Their miRNA expression levels define early, intermediate, and late stages of erythroid differentiation. The validity of our findings was confirmed in nonexpanded peripheral blood cells. (C) 2007 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc.
引用
收藏
页码:1657 / 1667
页数:11
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