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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >ProBDNF and mature BDNF as punishment and reward signals for synapse elimination at mouse neuromuscular junctions
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ProBDNF and mature BDNF as punishment and reward signals for synapse elimination at mouse neuromuscular junctions

机译:ProBDNF和成熟的BDNF作为惩罚和奖励信号,用于消除小鼠神经肌肉连接处的突触

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摘要

During development, mammalian neuromuscular junctions (NMJs) transit from multiple-innervation to single-innervation through axonal competition via unknown molecular mechanisms. Previously, using an in vitro model system, we demonstrated that the postsynaptic secretion of pro-brain-derived neurotrophic factor (proBDNF) stabilizes or eliminates presynaptic axon terminals, depending on its proteolytic conversion at synapses. Here, using developing mouse NMJs, we obtained in vivo evidence that proBDNF and mature BDNF (mBDNF) play roles in synapse elimination. We observed that exogenous proBDNF promoted synapse elimination, whereas mBDNF infusion substantially delayed synapse elimination. In addition, pharmacological inhibition of the proteolytic conversion of proBDNF to mBDNF accelerated synapse elimination via activation of p75 neurotrophin receptor (p75NTR). Furthermore, the inhibition of both p75NTR and sortilin signaling attenuated synapse elimination. We propose a model in which proBDNF and mBDNF serve as potential "punishment" and "reward" signals for inactive and active terminals, respectively, in vivo.
机译:在发育过程中,哺乳动物神经肌肉接头(NMJs)通过轴突竞争通过未知的分子机制从多重神经转变为单一神经。以前,使用体外模型系统,我们证明了前脑衍生的神经营养因子(proBDNF)的突触后分泌稳定或消除了突触前轴突末端,具体取决于其在突触中的蛋白水解转化。在这里,使用发育中的小鼠NMJ,我们获得了体内证据,证明proBDNF和成熟BDNF(mBDNF)在突触消除中起作用。我们观察到外源性proBDNF促进突触消除,而mBDNF输注实质上延迟了突触消除。此外,药理学抑制proBDNF到mBDNF的蛋白水解转化通过激活p75神经营养因子受体(p75NTR)加速突触消除。此外,p75NTR和sortilin信号的抑制作用减弱了突触消除。我们提出了一个模型,其中proBDNF和mBDNF分别作为体内无活性和活性末端的潜在“惩罚”和“奖励”信号。

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