Kaplan D R, Matsumoto K, Lucarelli E, Thiele C J
ABL-Basic Research Program, National Cancer Institute, Frederick Cancer Research and Development Center, Maryland 21702.
Neuron. 1993 Aug;11(2):321-31. doi: 10.1016/0896-6273(93)90187-v.
Retinoic acid (RA) induces the neuronal differentiation of many human neuroblastoma cell lines. In this study, we show that RA treatment of neuroblastoma cells induces the expression of TrkB, the receptor for the neurotrophins BDNF, NT-3, and NT-4/5. BDNF addition to RA-treated SH-SY5Y neuroblastoma cells stimulated the tyrosine phosphorylation of TrkB and neuronal differentiation. RA treatment of KCNR neuroblastoma cells, which constitutively express BDNF mRNA, resulted in the expression of TrkB and differentiation in the absence of added BDNF. Finally, in 15N neuroblastoma cells, which express BDNF mRNA but do not differentiate in response to RA, RA induced only a truncated form of TrkB. 15N cells transfected with full-length TrkB differentiated in the absence of RA. These results indicate that RA induces the neuronal differentiation of neuroblastoma cells by modulating the expression of neurotrophin receptors.
视黄酸(RA)可诱导多种人类神经母细胞瘤细胞系发生神经元分化。在本研究中,我们发现用RA处理神经母细胞瘤细胞可诱导TrkB的表达,TrkB是神经营养因子BDNF、NT-3和NT-4/5的受体。向经RA处理的SH-SY5Y神经母细胞瘤细胞中添加BDNF可刺激TrkB的酪氨酸磷酸化并促进神经元分化。对组成性表达BDNF mRNA的KCNR神经母细胞瘤细胞进行RA处理,在未添加BDNF的情况下导致了TrkB的表达和分化。最后,在表达BDNF mRNA但对RA无反应而不分化的15N神经母细胞瘤细胞中,RA仅诱导出一种截短形式的TrkB。用全长TrkB转染的15N细胞在无RA的情况下发生分化。这些结果表明,RA通过调节神经营养因子受体的表达来诱导神经母细胞瘤细胞的神经元分化。