MicroRNA-mediated control of cell fate in megakaryocyte-erythrocyte progenitors

被引:284
作者
Lu, Jun [1 ,2 ,3 ]
Guo, Shangqin [4 ,6 ]
Ebert, Benjamin L. [1 ,2 ,3 ,8 ]
Zhang, Hao [1 ,2 ]
Peng, Xiao [1 ,2 ]
Bosco, Jocelyn [1 ,2 ]
Pretz, Jennifer [1 ,2 ]
Schlanger, Rita [4 ,6 ]
Wang, Judy Y. [1 ,2 ]
Mak, Raymond H. [1 ,2 ]
Dombkowski, David M. [5 ]
Preffer, Frederic I. [5 ]
Scadden, David T. [4 ,6 ]
Golub, Todd R. [1 ,2 ,3 ,7 ]
机构
[1] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[2] Harvard Univ, Broad Inst, Cambridge, MA 02142 USA
[3] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02129 USA
[4] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02129 USA
[5] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02129 USA
[6] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[7] Brigham & Womens Hosp, Howard Hughes Med Inst, Boston, MA 02115 USA
[8] Brigham & Womens Hosp, Div Hematol, Boston, MA 02115 USA
关键词
D O I
10.1016/j.devcel.2008.03.012
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lineage specification is a critical issue in developmental and regenerative biology. We hypothesized that microRNAs (miRNAs) are important participants in those processes and used the poorly understood regulation of megakaryocyte-erythrocyte progenitors (MEPs) in hematopoiesis as a model system. We report here that miR-150 modulates lineage fate in MEPs. Using a novel methodology capable of profiling miRNA expression in small numbers of primary cells, we identify miR-150 as preferentially expressed in the megakaryocytic lineage. Through gain- and loss-of-function experiments, we demonstrate that miR-150 drives MEP differentiation toward megakaryocytes at the expense of erythroid cells in vitro and in vivo. Moreover, we identify the transcription factor MYB as a critical target of miR-150 in this regulation. These experiments show that miR-150 regulates MEP fate, and thus establish a role for miRNAs in lineage specification of mammalian multipotent cells.
引用
收藏
页码:843 / 853
页数:11
相关论文
共 37 条
[1]   A clonogenic common myeloid progenitor that gives rise to all myeloid lineages [J].
Akashi, K ;
Traver, D ;
Miyamoto, T ;
Weissman, IL .
NATURE, 2000, 404 (6774) :193-197
[2]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[3]   Transcriptional regulation of erythropoiesis: an affair involving multiple partners [J].
Cantor, AB ;
Orkin, SH .
ONCOGENE, 2002, 21 (21) :3368-3376
[4]   Widespread microRNA repression by Myc contributes to tumorigenesis [J].
Chang, Tsung-Cheng ;
Yu, Duonan ;
Lee, Yun-Sil ;
Wentzel, Erik A. ;
Arking, Dan E. ;
West, Kristin M. ;
Dang, Chi V. ;
Thomas-Tikhonenko, Andrei ;
Mendell, Joshua T. .
NATURE GENETICS, 2008, 40 (01) :43-50
[5]   MicroRNAs modulate hematopoietic lineage differentiation [J].
Chen, CZ ;
Li, L ;
Lodish, HF ;
Bartel, DP .
SCIENCE, 2004, 303 (5654) :83-86
[6]   An RNA interference model of RPS 19 deficiency in Diamond-Blackfan anemia recapitulates defective hematopoiesis and rescue by dexamethasone: identification of dexamethasone-responsive genes by microarray [J].
Ebert, BL ;
Lee, MM ;
Pretz, JL ;
Subramanian, A ;
Mak, R ;
Golub, TR ;
Sieff, CA .
BLOOD, 2005, 105 (12) :4620-4626
[7]   Progression through key stages of haemopoiesis is dependent on distinct threshold levels of c-Myb [J].
Emambokus, N ;
Vegiopoulos, A ;
Harman, B ;
Jenkinson, E ;
Anderson, G ;
Frampton, J .
EMBO JOURNAL, 2003, 22 (17) :4478-4488
[8]   A minicircuitry comprised of MicroRNA-223 and transcription factors NFI-A and C/EBPα regulates human granulopoiesis [J].
Fazi, F ;
Rosa, A ;
Fatica, A ;
Gelmetti, V ;
De Marchis, ML ;
Nervi, C ;
Bozzoni, I .
CELL, 2005, 123 (05) :819-831
[9]   MicroRNAs 221 and 222 inhibit normal erythropoiesis and erythroleukemic cell growth via kit receptor down-modulation [J].
Felli, N ;
Fontana, L ;
Pelosi, E ;
Botta, R ;
Bonci, D ;
Facchiano, F ;
Liuzzi, F ;
Lulli, V ;
Morsilli, O ;
Santoro, S ;
Valtieri, M ;
Calin, GA ;
Liu, CG ;
Sorrentino, A ;
Croce, CM ;
Peschle, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (50) :18081-18086
[10]   MicroRNAs 17-5p-20a-106a control monocytopoiesis through AML1 targeting and M-CSF receptor upregulation [J].
Fontana, Laura ;
Pelosi, Elvira ;
Greco, Paolo ;
Racanicchi, Serena ;
Testa, Ugo ;
Liuzzi, Francesca ;
Croce, Carlo M. ;
Brunetti, Ercole ;
Grignani, Francesco ;
Peschle, Cesare .
NATURE CELL BIOLOGY, 2007, 9 (07) :775-U90