Bandoh S, Tsukada T, Maruyama K, Ohkura N, Yamaguchi K
Growth Factor Division, National Cancer Center Research Institute, Tokyo, Japan.
Leukemia. 1997 Sep;11(9):1453-8. doi: 10.1038/sj.leu.2400800.
NOR-1, NGFI-B and Nurr1 are closely related transcription factors that constitute a distinct subfamily within the nuclear receptor superfamily. Genes for these proteins are immediate-early genes, and are inducible in diverse cell types by various stimuli. In the present study, we investigated the effect of mechanical agitation on the gene expression of these transcription factors in cultured suspension cells by the quantitative reverse transcription-polymerase chain reaction. We found that mechanical agitation transiently induced NOR-1, NGFI-B and Nurr1 mRNAs in several leukemic cell lines in a dose-dependent manner. This induction was most pronounced in the HL-60 promyelocytic leukemia cell line, but also occurred to a lesser extent in other cell lines including KG-1, THP-1 and U937 cells. The induction was attenuated by serum or albumin, which are shear stress protectants for suspension culture cells. These reagents did not suppress forskolin-induced NOR-1 gene expression. These findings suggest the involvement of fluid shear stress in agitation-induced immediate-early gene expression. Since even moderate agitation could cause the induction, investigators should be cautious when evaluating the expression of immediate-early genes in some leukemic cell lines.
NOR-1、NGFI-B和Nurr1是密切相关的转录因子,它们在核受体超家族中构成一个独特的亚家族。这些蛋白质的基因属于即早基因,可在多种细胞类型中被各种刺激诱导表达。在本研究中,我们通过定量逆转录-聚合酶链反应,研究了机械搅拌对培养的悬浮细胞中这些转录因子基因表达的影响。我们发现,机械搅拌能以剂量依赖的方式在几种白血病细胞系中瞬时诱导NOR-1、NGFI-B和Nurr1的mRNA表达。这种诱导在HL-60早幼粒细胞白血病细胞系中最为明显,但在包括KG-1、THP-1和U937细胞在内的其他细胞系中也有较小程度的发生。血清或白蛋白可减弱这种诱导,血清或白蛋白是悬浮培养细胞的剪切应力保护剂。这些试剂并不抑制福斯高林诱导的NOR-1基因表达。这些发现表明流体剪切应力参与了搅拌诱导的即早基因表达。由于即使适度搅拌也可能导致诱导,因此研究人员在评估某些白血病细胞系中即早基因的表达时应谨慎。