A three-step pathway comprising PLZF/miR-146a/CXCR4 controls megakaryopoiesis

被引:193
作者
Labbaye, Catherine [1 ]
Spinello, Isabella [1 ]
Quaranta, Maria Teresa [1 ]
Pelosi, Elvira [1 ]
Pasquini, Luca [1 ]
Petrucci, Eleonora [1 ]
Biffoni, Mauro [1 ]
Nuzzolo, Eugenia Rosa [1 ]
Billi, Monia [4 ]
Foa, Robin [2 ]
Brunetti, Ercole [3 ]
Grignani, Francesco [4 ]
Testa, Ugo [1 ]
Peschle, Cesare [1 ,5 ]
机构
[1] Ist Super Sanita, Dept Hematol Oncol & Mol Med, I-00161 Rome, Italy
[2] Univ Roma La Sapienza, Div Hematol, Dept Cellular Biotechnol & Hematol, I-00161 Rome, Italy
[3] San Pietro FBF, Ctr Ric AFaR, I-00100 Rome, Italy
[4] Univ Perugia, Dept Gen Pathol, I-06122 Perugia, Italy
[5] IRCCS MultiMed, I-20138 Milan, Italy
关键词
D O I
10.1038/ncb1741
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MicroRNAs ( miRNAs or miRs) regulate diverse normal and abnormal cell functions. We have identified a regulatory pathway in normal megakaryopoiesis, involving the PLZF transcription factor, miR-146a and the SDF-1 receptor CXCR4. In leukaemic cell lines PLZF overexpression downmodulated miR-146a and upregulated CXCR4 protein, whereas PLZF knockdown induced the opposite effects. In vitro assays showed that PLZF interacts with and inhibits the miR-146a promoter, and that miR-146a targets CXCR4 mRNA, impeding its translation. In megakaryopoietic cultures of CD34(+) progenitors, PLZF was upregulated, whereas miR-146a expression decreased and CXCR4 protein increased. MiR-146a overexpression and PLZF or CXCR4 silencing impaired megakaryocytic (Mk) proliferation, differentiation and maturation, as well as Mk colony formation. Mir-146a knockdown induced the opposite effects. Rescue experiments indicated that the effects of PLZF and miR-146a are mediated by miR-146a and CXCR4, respectively. Our data indicate that megakaryopoiesis is controlled by a cascade pathway, in which PLZF suppresses miR-146a transcription and thereby activates CXCR4 translation.
引用
收藏
页码:788 / 801
页数:14
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