Yang J, Hou H Y, Bian W, Lin Q S, Jing N H
Shanghai Institute of Biochemistry, Chinese Academy of Sciences, Shanghai 200031.
Sheng Li Xue Bao. 1998 Dec;50(6):671-8.
Wnt signals have been shown to play an important role in the development of the central nervous system (CNS) of mouse. In our previous work, it was demonstrated that Wnt signal could initiate differentiation of P19 EC cells. In the present investigation, it was examined with RT-PCR whether expression of beta-catenin, a downstream gene of Wnt in its signal transduction pathway, is regulated. It was found that the level of protein or transcript beta-catenin during P19 neuronal differentiation was not changed. However, immunostaining data showed that beta-catenin was translocalized into nuclei after retinoic acid induced P19 cell aggregates were trypsinized and cultured in serum free N2 medium for 2 and 4 d. In this period, transcription of En-2, a downstream target gene of Wnt signal, increased evidently. The above data suggest that Wnt signals are involved in the early stage of neuronal differentiation process of P19 cell. Meanwhile, the distribution of beta-catenin on the neurites indicates that this protein may also be involved in neuritis outgrowth process.
Wnt信号已被证明在小鼠中枢神经系统(CNS)发育中起重要作用。在我们之前的工作中,已证明Wnt信号可启动P19胚胎癌细胞的分化。在本研究中,用逆转录聚合酶链反应(RT-PCR)检测了Wnt信号转导途径中其下游基因β-连环蛋白的表达是否受到调控。结果发现,在P19细胞向神经元分化过程中,β-连环蛋白的蛋白质或转录本水平未发生变化。然而,免疫染色数据显示,在视黄酸诱导P19细胞聚集体经胰蛋白酶消化并在无血清N2培养基中培养2天和4天后,β-连环蛋白转位至细胞核。在此期间,Wnt信号的下游靶基因En-2的转录明显增加。上述数据表明,Wnt信号参与了P19细胞神经元分化过程的早期阶段。同时,β-连环蛋白在神经突上的分布表明该蛋白可能也参与了神经突生长过程。