Hartmann M, Heumann R, Lessmann V
Department of Molecular Neurobiochemistry, Ruhr University Bochum, NC7-132, D-44780 Bochum, Germany.
EMBO J. 2001 Nov 1;20(21):5887-97. doi: 10.1093/emboj/20.21.5887.
The protein brain-derived neurotrophic factor (BDNF) has been postulated to be a retrograde or paracrine synaptic messenger in long-term potentiation and other forms of activity-dependent synaptic plasticity. Although crucial for this concept, direct evidence for the activity-dependent synaptic release of BDNF is lacking. Here we investigate secretion of BDNF labelled with green fluorescent protein (BDNF-GFP) by monitoring the changes in fluorescence intensity of dendritic BDNF-GFP vesicles at glutamatergic synaptic junctions of living hippocampal neurons. We show that high-frequency activation of glutamatergic synapses triggers the release of BDNF-GFP from synaptically localized secretory granules. This release depends on activation of postsynaptic ionotropic glutamate receptors and on postsynaptic Ca(2+) influx. Release of BDNF-GFP is also observed from extrasynaptic dendritic vesicle clusters, suggesting that a possible spatial restriction of BDNF release to specific synaptic sites can only occur if the postsynaptic depolarization remains local. These results support the concept of BDNF being a synaptic messenger of activity-dependent synaptic plasticity, which is released from postsynaptic neurons.
蛋白质脑源性神经营养因子(BDNF)被认为是长时程增强及其他形式的活动依赖型突触可塑性中的逆行或旁分泌突触信使。尽管这一概念至关重要,但缺乏BDNF活动依赖型突触释放的直接证据。在此,我们通过监测活体海马神经元谷氨酸能突触连接处树突状BDNF-GFP囊泡荧光强度的变化,来研究绿色荧光蛋白标记的BDNF(BDNF-GFP)的分泌情况。我们发现,谷氨酸能突触的高频激活会触发突触定位分泌颗粒释放BDNF-GFP。这种释放依赖于突触后离子型谷氨酸受体的激活以及突触后Ca(2+)内流。在突触外树突囊泡簇中也观察到了BDNF-GFP的释放,这表明只有当突触后去极化保持局部性时,BDNF释放才可能在特定突触位点受到空间限制。这些结果支持了BDNF作为活动依赖型突触可塑性的突触信使,从突触后神经元释放的概念。