Cheng Pingyan, Nefedova Yulia, Corzo Cesar A, Gabrilovich Dmitry I
H. Lee Moffitt Cancer Center, Department of Interdisciplinary Oncology, University of South Florida, MRC 2067, 12902 Magnolia Dr, Tampa, FL 33612, USA.
Blood. 2007 Jan 15;109(2):507-15. doi: 10.1182/blood-2006-05-025601. Epub 2006 Sep 14.
Notch is a major factor mediating interaction between hematopoietic progenitor cells (HPCs) and bone marrow stroma (BMS). However its contribution to dendritic cell (DC) differentiation is controversial. We found that main Notch ligands Delta-1 and Jagged-1 had the opposite effect on DC differentiation. Delta-1 promoted generation of fully differentiated DCs, whereas Jagged-1 stimulated accumulation of DC precursors but prevented their transition to terminally differentiated DCs. BMS expressed a substantially higher level of Jagged-1 than Delta-1. Just the opposite expression pattern was observed in spleen stroma (SS). The BMS effect on DC differentiation was similar to that of Jagged-1, whereas the effect of SS was similar to the effect of Delta-1. Down-regulation of Jagged-1 in BMS substantially increased DC differentiation. Experiments in vivo with adoptive transfer of DC precursors further supported the different roles of BMS and SS in DC development. Jagged-1 and Delta-1 equally activated CBF-1/RBPJkappa transcription factor, which is a major Notch target. However, they produced a different pattern of activation of Notch target gene Hes1. Overexpression of Hes1 resulted in increased DC differentiation from HPCs. Thus, this study not only revealed the different role of Notch ligands in DC differentiation but also may provide a new insight into regulation of DC differentiation by BMS.
Notch是介导造血祖细胞(HPCs)与骨髓基质(BMS)相互作用的主要因子。然而,其对树突状细胞(DC)分化的作用存在争议。我们发现,主要的Notch配体Delta-1和Jagged-1对DC分化具有相反的作用。Delta-1促进完全分化的DC生成,而Jagged-1刺激DC前体的积累,但阻止它们向终末分化DC的转变。BMS中Jagged-1的表达水平显著高于Delta-1。在脾基质(SS)中观察到相反的表达模式。BMS对DC分化的作用类似于Jagged-1,而SS的作用类似于Delta-1。BMS中Jagged-1的下调显著增加了DC分化。DC前体过继转移的体内实验进一步支持了BMS和SS在DC发育中的不同作用。Jagged-1和Delta-1同样激活CBF-1/RBPJkappa转录因子,这是Notch的主要靶点。然而,它们产生了不同的Notch靶基因Hes1激活模式。Hes1的过表达导致HPCs来源的DC分化增加。因此,本研究不仅揭示了Notch配体在DC分化中的不同作用,还可能为BMS对DC分化的调控提供新的见解。