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神经营养因子的自分泌信号形成了一个突触前正反馈回路。

Autocrine signaling by an neurotrophin forms a presynaptic positive feedback loop.

机构信息

Department of Neuroscience, Columbia University, New York, NY 10032;

Department of Biology, Kyushu University, 812-8581 Fukuoka, Japan.

出版信息

Proc Natl Acad Sci U S A. 2018 Nov 20;115(47):E11168-E11177. doi: 10.1073/pnas.1810649115. Epub 2018 Nov 5.

Abstract

Whereas short-term plasticity is often initiated on one side of the synapse, long-term plasticity involves coordinated changes on both sides, implying extracellular signaling. We have investigated the possible signaling role of an neurotrophin (ApNT) in facilitation induced by serotonin (5HT) at sensory-to-motor neuron synapses in culture. ApNT is an ortholog of mammalian BDNF, which has been reported to act as either an anterograde, retrograde, or autocrine signal, so that its pre- and postsynaptic sources and targets remain unclear. We now report that ApNT acts as a presynaptic autocrine signal that forms part of a positive feedback loop with ApTrk and PKA. That loop stimulates spontaneous transmitter release, which recruits postsynaptic mechanisms, and presynaptic protein synthesis during the transition from short- to intermediate-term facilitation and may also initiate gene regulation to trigger the transition to long-term facilitation. These results suggest that a presynaptic ApNT feedback loop plays several key roles during consolidation of learning-related synaptic plasticity.

摘要

虽然短期可塑性通常发生在突触的一侧,但长期可塑性涉及到两侧的协调变化,暗示了细胞外信号的参与。我们研究了神经营养因子(ApNT)在培养中的感觉神经元-运动神经元突触中 5-羟色胺(5HT)诱导的易化作用中的可能信号作用。ApNT 是哺乳动物脑源性神经营养因子(BDNF)的同源物,据报道它可以作为顺行、逆行或自分泌信号,因此其突触前和突触后来源和靶点仍不清楚。我们现在报告说,ApNT 作为一种突触前自分泌信号,与 ApTrk 和 PKA 形成正反馈回路的一部分。该回路刺激自发递质释放,在从短期到中期易化的转变过程中招募突触后机制和突触前蛋白合成,并且可能还启动基因调控以触发向长期易化的转变。这些结果表明,在与学习相关的突触可塑性的巩固过程中,突触前 ApNT 反馈环发挥了几个关键作用。

相似文献

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Autocrine signaling by an neurotrophin forms a presynaptic positive feedback loop.神经营养因子的自分泌信号形成了一个突触前正反馈回路。
Proc Natl Acad Sci U S A. 2018 Nov 20;115(47):E11168-E11177. doi: 10.1073/pnas.1810649115. Epub 2018 Nov 5.

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