Scarpa S, Negroni A, Amendola R, Signorelli P, Calabretta B, Modesti A, Raschellà G
Experimental Medicine and Pathology Department, University of Rome La Sapienza, Italy.
J Neurooncol. 1997 Jan;31(1-2):107-14. doi: 10.1023/a:1005749802210.
B-myb gene is expressed in neuroblastoma cells and down-regulated during differentiation. We used B-myb-transfected LAN-5 cells, which constitutively express high level of B-myb, to detect changes at phenotypic and morphological levels in basal and differentiation conditions. Our results demonstrate that the overexpression of B-myb markedly affects the cytoskeletal composition, the pattern of neurotransmitter enzymes and the extracellular matrix expression. In general, B-myb transfected neuroblastoma cells show a broad potentiality without a direction toward a specific neuroectodermal differentiation pathway. On the other hand, we confirm inhibition of the neuronal differentiation upon retinoic acid (RA) treatment of B-myb transfected cells. Furthermore, the ultrastructural analyses are supportive of a change in the metabolism in B-myb transfected cell treated with RA. Our data suggest that B-myb expression is compatible with an early phase of differentiation of neuroectodermal cells, but must be down-regulated for the completion of the differentiative programme.
B-myb基因在神经母细胞瘤细胞中表达,并在分化过程中下调。我们使用组成性表达高水平B-myb的B-myb转染LAN-5细胞,来检测基础条件和分化条件下细胞表型和形态水平的变化。我们的结果表明,B-myb的过表达显著影响细胞骨架组成、神经递质酶模式和细胞外基质表达。一般来说,B-myb转染的神经母细胞瘤细胞显示出广泛的潜能,而不倾向于特定的神经外胚层分化途径。另一方面,我们证实了用视黄酸(RA)处理B-myb转染细胞后,神经元分化受到抑制。此外,超微结构分析支持了用RA处理的B-myb转染细胞代谢发生变化。我们的数据表明,B-myb的表达与神经外胚层细胞分化的早期阶段相容,但为了完成分化程序,其表达必须下调。