Ji Chun-Yan, Cui Cai-San, Ma Dao-Xin, Zhao Jian-Qiang, Guo Nong-Jian, Zhang Mao-Hong
Institute of Hematology, Qilu Hospital, Shandong University, Jinan 250012, China.
Chin Med J (Engl). 2004 Nov;117(11):1687-92.
Notch activation leads to transcriptional suppression of lineage-specific genes, inhibiting differentiation in response to inductive signals. The Notch signal system contains three parts: Notch molecules, Notch ligands and effectors. Delta4 is a newly-discovered Notch ligand which has received the attention of few detailed studies. This study sought to explore the biological function of Delta4 and observe its effects on 32D cell differentiation.
Delta4-expressing vector pTracer.CMV.Delta4.FLAG was constructed using molecular biological techniques. CHO cells stably transfected with pTracer.CMV.Delta4.FLAG were confirmed to have a Delta4 protein band via Western blotting. High-expression Delta4-CHO clones were selected for the following functional studies. Notch1-CHO and Notch2-CHO were used as host cells. After transiently transfecting with transition protein 1 (TP1), Delta4 activity was compared in both cell lines by means of luciferase analysis. CHO cells were incubated with Notch1-32D cells that had been transfected with Notch1 and were observed for granulocyte colony-stimulating factor (G-CSF)-induced differentiation. Jagged2-CHO and Delta4-CHO cells transfected with the Notch ligands Jagged2 and Delta4, respectively, were incubated with Notch1-32D cells to observed inhibition of Notch on G-CSF-induced differentiation.
The vector pTracer.CMV.Delta4.FLAG was constructed successfully. CHO cells were stably transfected with the vector pTracer.CMV.Delta4.FLAG. Two CHO cell lines expressing Delta4 at high levels were selected for use in the study. Delta4 was found to induce signal activity via both Notch1 and Notch2 and the induction of signaling activity was stronger in Notch2 cells than in Notch1 cells. Compared with other Notch ligands, Delta4 was slightly weaker than Jagged2, but stronger than Delta1 and Jagged1 in terms of Notch1 ligands. In terms of Notch2, Delta4 had a strong signaling activity, but was weaker than Delta1, Jagged1, and Jagged2. Jagged2 could inhibit Notch1-32D cell differentiation induced by G-CSF, but Delta4 could not.
Delta4 induces both Notch1 and Notch2 activity and is a ligand for both of them. The effect of Delta4 is stronger on Notch2 than that on Notch1. Jagged2 can inhibit Notch1-32D cell differentiation induced by G-CSF, but Delta4 cannot.
Notch激活导致谱系特异性基因的转录抑制,抑制对诱导信号的分化反应。Notch信号系统包含三个部分:Notch分子、Notch配体和效应器。Delta4是一种新发现的Notch配体,很少有详细研究关注它。本研究旨在探索Delta4的生物学功能,并观察其对32D细胞分化的影响。
采用分子生物学技术构建表达Delta4的载体pTracer.CMV.Delta4.FLAG。通过蛋白质免疫印迹法证实稳定转染pTracer.CMV.Delta4.FLAG的CHO细胞有Delta4蛋白条带。选择高表达Delta4的CHO克隆用于以下功能研究。以Notch1-CHO和Notch2-CHO作为宿主细胞。用过渡蛋白1(TP1)瞬时转染后,通过荧光素酶分析比较两种细胞系中的Delta4活性。将CHO细胞与转染了Notch1的Notch1-32D细胞共同培养,并观察粒细胞集落刺激因子(G-CSF)诱导的分化情况。分别用Notch配体Jagged2和Delta¬¬4转染Jagged2-CHO和Delta4-CHO细胞,然后与Notch1-32D细胞共同培养,观察Notch对G-CSF诱导分化的抑制作用。
成功构建载体pTracer.CMV.Delta4.FLAG。用该载体稳定转染CHO细胞。选择两个高表达Delta4的CHO细胞系用于研究。发现Delta4可通过Notch1和Notch2诱导信号活性,且在Notch2细胞中信号活性的诱导强于Notch1细胞。与其他Notch配体相比,Delta4作为Notch1配体时略弱于Jagged2,但强于Delta1和Jagged1。就Notch2而言,Delta4具有较强的信号活性,但弱于Delta1、Jagged1和Jagged2。Jagged2可抑制G-CSF诱导的Notch1-32D细胞分化,但Delta4不能。
Delta4可诱导Notch1和Notch2活性,是它们二者的配体。Delta4对Notch2的作用强于对Notch1的作用。Jagged2可抑制G-CSF诱导的Notch1-32D细胞分化,但Delta4不能。