An In Vivo Functional Screen Uncovers miR-150-Mediated Regulation of Hematopoietic Injury Response

被引:44
作者
Adams, Brian D. [1 ,2 ]
Guo, Shangqin [1 ,2 ]
Bai, Haitao [1 ,2 ,6 ]
Guo, Yanwen [1 ,2 ]
Megyola, Cynthia M. [1 ,2 ]
Cheng, Jijun [1 ,2 ]
Heydari, Kartoosh [3 ]
Xiao, Changchun [4 ]
Reddy, E. Premkumar [5 ]
Lu, Jun [1 ,2 ]
机构
[1] Yale Univ, Yale Canc Ctr, Dept Genet, Yale Stem Cell Ctr, New Haven, CT 06520 USA
[2] Yale Univ, Yale Ctr RNA Sci & Med, New Haven, CT 06520 USA
[3] Yale Univ, Dept Immunobiol, Yale Flow Cytometry Core Facil, New Haven, CT 06520 USA
[4] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
[5] Mt Sinai Sch Med, Dept Oncol Sci, New York, NY 10029 USA
[6] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 1, Dept Hematol, Shanghai 200080, Peoples R China
来源
CELL REPORTS | 2012年 / 2卷 / 04期
基金
美国国家卫生研究院;
关键词
C-MYB EXPRESSION; CELL-DEVELOPMENT; SELF-RENEWAL; MICRORNAS; MIR-150; DIFFERENTIATION; MECHANISMS; IDENTIFY; LIBRARY;
D O I
10.1016/j.celrep.2012.09.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hematopoietic stem and progenitor cells are often undesired targets of chemotherapies, leading to hematopoietic suppression requiring careful clinical management. Whether microRNAs control hematopoietic injury response is largely unknown. We report an in vivo gain-of-function screen and the identification of miR-150 as an inhibitor of hematopoietic recovery upon 5-fluorouracil-induced injury. Utilizing a bone marrow transplant model with a barcoded microRNA library, we screened for barcode abundance in peripheral blood of recipient mice before and after 5-fluorouracil treatment. Overexpression of screen-candidate miR-150 resulted in significantly slowed recovery rates across major blood lineages, with associated impairment of bone marrow clonogenic potential. Conversely, platelets and myeloid cells from miR-150 null marrow recovered faster after 5-fluorouracil treatment. Heterozygous knockout of c-myb, a conserved target of miR-150, partially phenocopied miR-150-forced expression. Our data highlight the role of microRNAs in controlling hematopoietic injury response and demonstrate the power of in vivo functional screens for studying microRNAs in normal tissue physiology.
引用
收藏
页码:1048 / 1060
页数:13
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