miRNA-based mechanism for the commitment of multipotent progenitors to a single cellular fate

被引:96
作者
Mann, Mati [1 ,2 ]
Barad, Omer [2 ]
Agami, Reuven [3 ]
Geiger, Benjamin [1 ]
Hornstein, Eran [2 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[3] Netherlands Canc Inst, Gene Regulat Div, NL-1066 CX Amsterdam, Netherlands
基金
以色列科学基金会; 美国国家卫生研究院;
关键词
microRNA; miR-155; differentiation; osteoclast; macrophage; MICROPHTHALMIA TRANSCRIPTION FACTOR; OSTEOCLAST DIFFERENTIATION; GENE-EXPRESSION; MICRORNA; TARGET; PROTEIN; PU.1; MIR-155; IMPACT; LIGAND;
D O I
10.1073/pnas.0915022107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
When stem cells and multipotent progenitors differentiate, they undergo fate restriction, enabling a single fate and blocking differentiation along alternative routes. We herein present a mechanism whereby such unequivocal commitment is achieved, based on micro-RNA (miRNA)-dependent repression of an alternative cell fate. We show that the commitment of monocyte RAW264.7 progenitors to active macrophage differentiation involves rapid up-regulation of miR-155 expression, which leads to the suppression of the alternative pathway, namely RANK ligand-induced osteoclastogenesis, by repressing the expression of MITF, a transcription factor essential for osteoclast differentiation. A temporal asymmetry, whereby miR-155 expression precedes and overrides the activation of the osteoclast transcriptional program, provides the means for coherent macrophage differentiation, even in the presence of osteoclastogenic signals. Based on these findings, we propose that miRNA may provide a general mechanism for the unequivocal commitment underlying stem cell differentiation.
引用
收藏
页码:15804 / 15809
页数:6
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