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引导突触可塑性:轴突导向因子 netrin-1 在成年大脑中的突触可塑性和记忆形成中的新作用。

Guiding synaptic plasticity: Novel roles for netrin-1 in synaptic plasticity and memory formation in the adult brain.

机构信息

Department of Neurology & Neurosurgery, Montreal Neurological Institute-Hospital, McGill University, Montreal, QC, H3A 2B4, Canada.

Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, H3A 0C7, Canada.

出版信息

J Physiol. 2021 Jan;599(2):493-505. doi: 10.1113/JP278704. Epub 2020 Mar 12.

Abstract

Adult neural plasticity engages mechanisms that change synapse structure and function, yet many of the underlying events bear a striking similarity to processes that occur during the initial establishment of neural circuits during development. It is a long-standing hypothesis that the molecular mechanisms critical for neural development may also regulate synaptic plasticity related to learning and memory in adults. Netrins were initially described as chemoattractant guidance cues that direct cell and axon migration during embryonic development, yet they continue to be expressed by neurons in the adult brain. Recent findings have identified roles for netrin-1 in synaptogenesis during postnatal maturation, and in synaptic plasticity in the adult mammalian brain, regulating AMPA glutamate receptor trafficking at excitatory synapses. These findings provide an example of a conserved developmental guidance cue that is expressed by neurons in the adult brain and functions as a key regulator of activity-dependent synaptic plasticity. Notably, in humans, genetic polymorphisms in netrin-1 and its receptors have been linked to neurodevelopmental and neurodegenerative disorders. The molecular mechanisms associated with the synaptic function of netrin-1 therefore present new therapeutic targets for neuropathologies associated with memory dysfunction. Here, we summarize recent findings that link netrin-1 signalling to synaptic plasticity, and discuss the implications of these discoveries for the neurobiological basis of memory consolidation.

摘要

成人神经可塑性涉及改变突触结构和功能的机制,但许多潜在事件与发育过程中神经网络初始建立期间发生的过程具有惊人的相似性。长期以来的假说认为,对神经发育至关重要的分子机制也可能调节与成人学习和记忆相关的突触可塑性。Netrins 最初被描述为趋化性导向线索,可在胚胎发育过程中指导细胞和轴突迁移,但它们在成年大脑中的神经元中仍继续表达。最近的研究结果确定了 Netrin-1 在出生后成熟过程中的突触发生以及成年哺乳动物大脑中的突触可塑性中的作用,调节兴奋性突触处 AMPA 谷氨酸受体的运输。这些发现提供了一个保守的发育导向线索的例子,该线索在成年大脑中的神经元中表达,并作为活性依赖性突触可塑性的关键调节剂发挥作用。值得注意的是,在人类中,Netrin-1 及其受体的遗传多态性与神经发育和神经退行性疾病有关。因此,与 Netrin-1 突触功能相关的分子机制为与记忆功能障碍相关的神经病理学提供了新的治疗靶点。在这里,我们总结了将 Netrin-1 信号与突触可塑性联系起来的最新发现,并讨论了这些发现对记忆巩固的神经生物学基础的意义。

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