Wang T, Xie K, Lu B
Roche Institute of Molecular Biology, Nutley, New Jersey 07110, USA.
J Neurosci. 1995 Jul;15(7 Pt 1):4796-805. doi: 10.1523/JNEUROSCI.15-07-04796.1995.
Although the effects of neurotrophins on survival and differentiation of various neuronal populations have been well studied, little is known about their role in synaptic development and function. We have investigated the long-term effects of neurotrophins in the maturation of neuromuscular synapses in Xenopus nerve-muscle cocultures. BDNF and NT-3, but not NGF, elicited significant changes in several properties of spontaneous synaptic currents (SSCs), indicative of more mature synapses. Most synapses treated by the neurotrophins exhibited a bell-shaped distribution of SSC amplitudes, which reflects mature quantal secretion. The neurotrophins also potentiated the efficacy and reliability of stimulus-induced synaptic transmission. Moreover, BDNF and NT-3 increased the levels of the synaptic vesicle proteins, synaptophysin, and synapsin 1 in the spinal neurons. The number of varicosities per neuron also showed a significant increase after neurotrophin treatment. The effects of the neurotrophins appear to be mediated by the Trk family of receptor tyrosine kinases, primarily through a presynaptic mechanism. These results suggest that BDNF and NT-3 promote functional maturation of synapses.
尽管神经营养因子对各种神经元群体的存活和分化的影响已得到充分研究,但它们在突触发育和功能中的作用却鲜为人知。我们研究了神经营养因子对非洲爪蟾神经-肌肉共培养物中神经肌肉突触成熟的长期影响。脑源性神经营因子(BDNF)和神经营养因子-3(NT-3),而非神经生长因子(NGF),引起了自发突触电流(SSCs)的几个特性的显著变化,表明突触更成熟。大多数经神经营养因子处理的突触表现出SSC振幅的钟形分布,这反映了成熟的量子分泌。神经营养因子还增强了刺激诱导的突触传递的效能和可靠性。此外,BDNF和NT-3增加了脊髓神经元中突触小泡蛋白、突触素和突触结合蛋白1的水平。神经营养因子处理后,每个神经元的曲张体数量也显著增加。神经营养因子的作用似乎是由受体酪氨酸激酶的Trk家族介导的,主要通过突触前机制。这些结果表明BDNF和NT-3促进突触的功能成熟。