Buchman V L, Davies A M
Department of Anatomy, St. George's Hospital Medical School, Tooting, London, UK.
Development. 1993 Jul;118(3):989-1001. doi: 10.1242/dev.118.3.989.
To investigate if different neurotrophins regulate the survival of neurons at successive developmental stages, we studied the effect of nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF) and neurotrophin-3 (NT-3) on the survival of mouse trigeminal neurons at closely staged intervals in development. We show that during the earliest stages of target field innervation trigeminal neurons display a transitory survival response to BDNF and NT-3. This response is lost as the neurons become NGF-dependent shortly before neuronal death begins in the trigeminal ganglion. BDNF and NT-3 mRNAs are expressed in the peripheral trigeminal target field before the arrival of the earliest axons and the onset of NGF mRNA expression. The levels of BDNF and NT-3 mRNAs peak during the early stages of target field innervation and decline shortly after the loss of neuronal responsiveness to BDNF and NT-3. Our study provides the first clear evidence that different target-derived neurotrophins can act sequentially to promote the survival of developing neurons.
为了研究不同的神经营养因子是否在连续的发育阶段调节神经元的存活,我们研究了神经生长因子(NGF)、脑源性神经营养因子(BDNF)和神经营养因子-3(NT-3)在发育过程中紧密间隔阶段对小鼠三叉神经元存活的影响。我们发现,在靶场神经支配的最早阶段,三叉神经元对BDNF和NT-3表现出短暂的存活反应。随着神经元在三叉神经节开始死亡前不久变得依赖NGF,这种反应消失。在最早的轴突到达和NGF mRNA表达开始之前,BDNF和NT-3 mRNA在外周三叉靶场中表达。BDNF和NT-3 mRNA的水平在靶场神经支配的早期达到峰值,并在神经元对BDNF和NT-3的反应性丧失后不久下降。我们的研究提供了第一个明确的证据,即不同的靶源性神经营养因子可以依次作用,促进发育中神经元的存活。