Song Ju Han, Kim Jong Man, Kim Seung Hyun, Kim Hyeoung Joon, Lee Jae Jung, Sung Myung Hui, Hwang Seung Yong, Kim Tae Sung
College of Pharmacy and Research Institute of Drug Development, Chonnam National University, Kwangju, South Korea.
Life Sci. 2003 Aug 15;73(13):1705-19. doi: 10.1016/s0024-3205(03)00515-0.
It is now recognized that precise patterns of differentially expressed genes ultimately direct a particular cell toward a given lineage. In this study, we compared the expression profiles of cancer-related genes by cDNA microarray analysis during the differentiation of human promyelocytic leukemia HL-60 cells into either monocytes or granulocytes. RNA was isolated at times 0, 6, 12, 24, 36, 48, and 72 h following stimulation of differentiation with all-trans retinoic acid (all-trans RA) or 1,25-dihydroxyvitamin D(3) [1,25-(OH)(2)D(3)], and hybridized to the microarray gene chips containing 872 genes related to cell-cycles, oncogenes and leukemias. Several genes were commonly or differentially regulated during cell differentiation into either lineage, as demonstrated by both hierarchical and self-organizing map clustering analysis. At 72 h the expression levels of 45 genes were commonly up- or down-regulated at least a twofold in both lineages. Most importantly, 32 genes including alpha-L-fucosidase gene and adducin gamma subunit gene were up- or down-regulated only in all-trans RA-treated HL-60 cells, while 12 genes including interleukin 1beta and hypoxia-inducible factor 1alpha were up- or down-regulated only in 1,25-(OH)(2)D(3)-treated HL-60 cells. The expression of selected genes was confirmed by Northern blot analysis. As expected, some genes identified have not been examined during HL-60 cell differentiation into either lineage. The identification of genes associated with a specific differentiation lineage may give important insights into functional and phenotypic differences between two lineages of HL-60 cell differentiation.
现在已经认识到,差异表达基因的精确模式最终会引导特定细胞走向特定谱系。在本研究中,我们通过cDNA微阵列分析比较了人类早幼粒细胞白血病HL-60细胞分化为单核细胞或粒细胞过程中癌症相关基因的表达谱。在用全反式维甲酸(全反式RA)或1,25-二羟基维生素D3 [1,25-(OH)2D3]刺激分化后的0、6、12、24、36、48和72小时分离RNA,并与包含872个与细胞周期、癌基因和白血病相关基因的微阵列基因芯片杂交。通过层次聚类和自组织映射聚类分析表明,在细胞分化为任一谱系的过程中,有几个基因受到共同或差异调节。在72小时时,45个基因的表达水平在两个谱系中均普遍上调或下调至少两倍。最重要的是,包括α-L-岩藻糖苷酶基因和内收蛋白γ亚基基因在内的32个基因仅在全反式RA处理的HL-60细胞中上调或下调,而包括白细胞介素1β和缺氧诱导因子1α在内的12个基因仅在1,25-(OH)2D3处理的HL-60细胞中上调或下调。通过Northern印迹分析证实了所选基因的表达。正如预期的那样,在HL-60细胞分化为任一谱系的过程中,尚未对一些已鉴定的基因进行研究。鉴定与特定分化谱系相关的基因可能会为HL-60细胞分化的两个谱系之间的功能和表型差异提供重要见解。