Virally mediated MafB transduction induces the monocyte commitment of human CD34+hematopoietic stem/progenitor cells

被引:63
作者
Gemelli, C. [1 ]
Montanari, M. [1 ]
Tenedini, E. [1 ]
Marani, T. Zanocco [1 ]
Vignudelli, T. [1 ]
Siena, M. [1 ]
Zini, R. [1 ]
Salati, S. [1 ]
Tagliafico, E. [1 ]
Manfredini, R. [1 ]
Grande, A. [1 ]
Ferrari, S. [1 ]
机构
[1] Univ Modena & Reggio Emilia, Dipartimento Sci Biomed, Sez Chim Biol, I-41100 Modena, Italy
关键词
MafB; monocyte commitment; CD34+cells;
D O I
10.1038/sj.cdd.4401860
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Upregulation of specific transcription factors is a generally accepted mechanism to explain the commitment of hematopoietic stem cells along precise maturation lineages. Based on this premise, transduction of primary hematopoietic stem/progenitor cells with viral vectors containing the investigated transcription factors appears as a suitable experimental model to identify such regulators. Although MafB transcription factor is believed to play a role in the regulation of monocytic commitment, no demonstration is, to date, available supporting this function in normal human hematopoiesis. To address this issue, we retrovirally transduced cord blood CD34+ hematopoietic progenitors with a MafB cDNA. Immunophenotypic and morphological analysis of transduced cells demonstrated the induction of a remarkable monomacrophage differentiation. Microarray analysis confirmed these findings and disclosed the upregulation of macrophage-related transcription factors belonging to the AP-1, MAF, PPAR and MiT families. Altogether our data allow to conclude that MafB is a key regulator of human monocytopoiesis.
引用
收藏
页码:1686 / 1696
页数:11
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