Theilgaard-Mönch Kim, Jacobsen Lars Christian, Borup Rehannah, Rasmussen Thomas, Bjerregaard Malene Digmann, Nielsen Finn Cilius, Cowland Jack Bernard, Borregaard Niels
The Granulocyte Research Laboratory, Department of Hematology, Rigshospitalet, University of Copenhagen, 2100 Copenhagen, Denmark.
Blood. 2005 Feb 15;105(4):1785-96. doi: 10.1182/blood-2004-08-3346. Epub 2004 Oct 28.
To characterize the transcriptional program that governs terminal granulocytic differentiation in vivo, we performed comprehensive microarray analyses of human bone marrow populations highly enriched in promyelocytes (PMs), myelocytes/metamyelocytes (MYs), and neutrophils (bm-PMNs). These analyses identified 11 310 genes involved in differentiation, of which 6700 were differentially regulated, including previously unidentified effector proteins and surface receptors of neutrophils. Differentiation of PMs toward MYs was accompanied by a marked decline of proliferative and general cellular activity as defined by down-regulation of E2 promoter binding factor (E2F) target genes; cyclin dependent kinases 2, 4, and 6; and various metabolic, proteasomal, and mitochondrial genes. Expression patterns of apoptosis genes indicated death control by the p53 pathway in PMs and by death receptor pathways in bm-PMNs. Effector proteins critical for host defense were expressed successively throughout granulocytic differentiation, whereas receptors and receptor ligands essential for the activation of the host defense program were terminally up-regulated in bm-PMNs. The up-regulation of ligand-receptor pairs, which are defined inducers as well as target genes of nuclear factor-kappa B (NF-kappa B), suggests a constitutive activation of NF-kappa B in bm-PMNs by autocrine loops. Overall, these results define a granulocytic differentiation model governed by a highly coordinated fail-safe program, which promotes completion of differentiation before cells gain responsiveness toward activating stimuli that accompany infections.
为了描述体内调控终末粒细胞分化的转录程序,我们对人骨髓中早幼粒细胞(PMs)、中幼粒细胞/晚幼粒细胞(MYs)和中性粒细胞(bm-PMNs)高度富集的群体进行了全面的微阵列分析。这些分析鉴定出11310个参与分化的基因,其中6700个基因受到差异调控,包括先前未鉴定的中性粒细胞效应蛋白和表面受体。PMs向MYs的分化伴随着增殖和一般细胞活性的显著下降,这是由E2启动子结合因子(E2F)靶基因、细胞周期蛋白依赖性激酶2、4和6以及各种代谢、蛋白酶体和线粒体基因的下调所定义的。凋亡基因的表达模式表明,PMs中通过p53途径控制死亡,而bm-PMNs中通过死亡受体途径控制死亡。对宿主防御至关重要的效应蛋白在粒细胞分化过程中相继表达,而激活宿主防御程序所必需的受体和受体配体在bm-PMNs中终末上调。配体-受体对上调,它们被定义为核因子-κB(NF-κB)的诱导剂以及靶基因,这表明bm-PMNs中NF-κB通过自分泌环持续激活。总体而言,这些结果定义了一个由高度协调的故障安全程序控制的粒细胞分化模型,该程序在细胞获得对伴随感染的激活刺激的反应性之前促进分化的完成。