Huang Shu, Shen Qun, Mao Wen-Ge, Li Ai-Ping, Ye Jian, Liu Qi-Zhan, Zou Chang-Ping, Zhou Jian-Wei
Department of Molecular Toxicology, The Jiangsu Key Laboratory of Human Functional Genomics and Applied Toxicology, School of Public Health, Nanjing Medical University, 140 Hanzhong Road, Nanjing 210029, China.
Biochem Biophys Res Commun. 2006 Mar 10;341(2):440-50. doi: 10.1016/j.bbrc.2005.12.197. Epub 2006 Jan 11.
Dysregulation of hematopoietic cellular differentiation contributes to leukemogenesis. Unfortunately, relatively little is known about how cell differentiation is regulated. JWA (AF070523) is a novel all-trans retinoic acid (ATRA) responsible gene that initially isolated from ATRA-treated primary human tracheal bronchial epithelial cells. For the notable performance achieved by ATRA in the differentiation induction therapy, we investigated the role of JWA in the induction of differentiation of human myeloid leukemia cells. Our results showed that JWA was not only regulated by ATRA but also by several other differentiation inducers such as phorbol-12-myristate-13-acetate (TPA), arabinoside (Ara-C), and hemin, involved in the mechanisms of differentiation along different lineages of myeloid leukemia cells arrested at different stages of development. Generally, JWA was up-regulated by these inducers in a time-dependent manner. Inhibition of JWA by RNA interference decreased the induced cellular differentiation. However, in NB4 cells treated with ATRA, dissimilar with others, the expression of JWA was down-regulated, and the induced cellular differentiation could be enhanced by silencing of JWA. Collectively, JWA works as a potential critical molecule, associated with multi-directional differentiation of human myeloid leukemia cells. In NB4 cells, JWA may function as a lineage-restricted gene during differentiation along the monocyte/macrophage-like or granulocytic pathway.
造血细胞分化失调有助于白血病的发生。不幸的是,关于细胞分化如何被调控,我们了解得相对较少。JWA(AF070523)是一种新的全反式维甲酸(ATRA)反应基因,最初从经ATRA处理的原代人气管支气管上皮细胞中分离得到。鉴于ATRA在分化诱导治疗中取得的显著成效,我们研究了JWA在人髓系白血病细胞分化诱导中的作用。我们的结果表明,JWA不仅受ATRA调控,还受其他几种分化诱导剂调控,如佛波酯-12-肉豆蔻酸酯-13-乙酸酯(TPA)、阿糖胞苷(Ara-C)和血红素,它参与了处于不同发育阶段的髓系白血病细胞沿不同谱系分化的机制。一般来说,这些诱导剂以时间依赖性方式上调JWA。通过RNA干扰抑制JWA会降低诱导的细胞分化。然而,在用ATRA处理的NB4细胞中,与其他细胞不同,JWA的表达下调,沉默JWA可增强诱导的细胞分化。总体而言,JWA作为一个潜在的关键分子,与人髓系白血病细胞的多向分化相关。在NB4细胞中,JWA在沿单核细胞/巨噬细胞样或粒细胞途径分化过程中可能作为一个谱系限制基因发挥作用。