Ito Hisanori, Nakajima Aki, Nomoto Hiroshi, Furukawa Shoei
Laboratory of Molecular Biology, Gifu Pharmaceutical University, Gifu, Japan.
J Neurosci Res. 2003 Mar 1;71(5):648-58. doi: 10.1002/jnr.10532.
Neurogenesis is promoted by basic helix-loop-helix (bHLH) transcription factors Mash1, Math1, or NeuroD but suppressed by another set, Hes1 and Hes5. It remains unknown what kinds of extracellular signals are involved in their regulation; therefore, the effects of neurotrophins on the expression of bHLH factors and neuronal differentiation were investigated by the use of cultured mouse neural stem cells. Each neurotrophin increased Mash1 and Math1 mRNAs of the stem cells growing in the presence of fibroblast growth factor-2 (FGF-2), but did not alter Hes1, Hes5, or NeuroD mRNA levels. Simultaneously, most of the cells expressed nestin but not microtubule-associated protein 2 (MAP2), and remained undifferentiated. FGF-2 removal from the medium reduced the levels of Hes1 and Hes5 mRNAs and increased those of Mash1, Math1, and NeuroD mRNAs, resulting in substantial neuronal differentiation. When the cells were pretreated with brain-derived neurotrophic factor, a neurotrophin, FGF-2 removal enhanced earlier NeuroD expression and generated many more MAP2-positive cells. The high level of Mash1 and Math1 that had been elevated at FGF-2 withdrawal accelerated NeuroD expression in cooperation with the reduced Hes1 and Hes5 expression. Our present results suggest that neurotrophins stimulate neuronal differentiation by altering the balance of expression of various bHLH transcription factors.
碱性螺旋-环-螺旋(bHLH)转录因子Mash1、Math1或NeuroD可促进神经发生,但另一组转录因子Hes1和Hes5则起抑制作用。目前尚不清楚哪些细胞外信号参与了它们的调控;因此,我们利用培养的小鼠神经干细胞研究了神经营养因子对bHLH因子表达和神经元分化的影响。在存在成纤维细胞生长因子-2(FGF-2)的情况下,每种神经营养因子均可增加干细胞的Mash1和Math1 mRNA水平,但不改变Hes1、Hes5或NeuroD mRNA水平。同时,大多数细胞表达巢蛋白,但不表达微管相关蛋白2(MAP2),仍未分化。从培养基中去除FGF-2可降低Hes1和Hes5 mRNA水平,并增加Mash1、Math1和NeuroD mRNA水平,从而导致大量神经元分化。当细胞用一种神经营养因子脑源性神经营养因子预处理后,去除FGF-2可增强NeuroD的早期表达,并产生更多的MAP2阳性细胞。在FGF-2撤除时升高的高水平Mash1和Math1与降低的Hes1和Hes5表达协同作用,加速了NeuroD的表达。我们目前的结果表明,神经营养因子通过改变各种bHLH转录因子的表达平衡来刺激神经元分化。