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类 Kruppel 因子 KLF4 是单核细胞分化的关键调节因子。

The Kruppel-like factor KLF4 is a critical regulator of monocyte differentiation.

作者信息

Feinberg Mark W, Wara Akm Khyrul, Cao Zhuoxiao, Lebedeva Maria A, Rosenbauer Frank, Iwasaki Hiromi, Hirai Hideyo, Katz Jonathan P, Haspel Richard L, Gray Susan, Akashi Koichi, Segre Julie, Kaestner Klaus H, Tenen Daniel G, Jain Mukesh K

机构信息

Department of Medicine, Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.

出版信息

EMBO J. 2007 Sep 19;26(18):4138-48. doi: 10.1038/sj.emboj.7601824. Epub 2007 Aug 30.

Abstract

Monocyte differentiation involves the participation of lineage-restricted transcription factors, although the mechanisms by which this process occurs are incompletely defined. Within the hematopoietic system, members of the Kruppel-like family of factors (KLFs) play essential roles in erythrocyte and T lymphocyte development. Here we show that KLF4/GKLF is expressed in a monocyte-restricted and stage-specific pattern during myelopoiesis and functions to promote monocyte differentiation. Overexpression of KLF4 in HL-60 cells confers the characteristics of mature monocytes. Conversely, KLF4 knockdown blocked phorbol ester-induced monocyte differentiation. Forced expression of KLF4 in primary common myeloid progenitors (CMPs) or hematopoietic stem cells (HSCs) induced exclusive monocyte differentiation in clonogenic assays, whereas KLF4 deficiency inhibited monocyte but increased granulocyte differentiation. Mechanistic studies demonstrate that KLF4 is a target gene of PU.1. Consistently, KLF4 can rescue PU.1-/- fetal liver cells along the monocytic lineage and can activate the monocytic-specific CD14 promoter. Thus, KLF4 is a critical regulator in the transcriptional network controlling monocyte differentiation.

摘要

单核细胞分化涉及谱系特异性转录因子的参与,尽管这一过程发生的机制尚未完全明确。在造血系统中,Kruppel样因子家族(KLFs)成员在红细胞和T淋巴细胞发育中发挥着重要作用。在此我们表明,KLF4/GKLF在骨髓生成过程中以单核细胞特异性且阶段特异性的模式表达,并发挥促进单核细胞分化的作用。在HL-60细胞中过表达KLF4赋予其成熟单核细胞的特征。相反,敲低KLF4可阻断佛波酯诱导的单核细胞分化。在克隆形成试验中,在原代普通髓系祖细胞(CMPs)或造血干细胞(HSCs)中强制表达KLF4可诱导单核细胞特异性分化,而KLF4缺陷则抑制单核细胞分化但增加粒细胞分化。机制研究表明,KLF4是PU.1的靶基因。一致地,KLF4可挽救PU.1基因敲除的胎肝细胞沿单核细胞谱系的分化,并可激活单核细胞特异性CD14启动子。因此,KLF4是控制单核细胞分化的转录网络中的关键调节因子。

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