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海马体中的长期可塑性:突触内的维持与突触间的“标记”

Long-term plasticity in the hippocampus: maintaining within and 'tagging' between synapses.

作者信息

Bin Ibrahim Mohammad Zaki, Benoy Amrita, Sajikumar Sreedharan

机构信息

Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Life Sciences Institute Neurobiology Programme, National University of Singapore, Singapore.

出版信息

FEBS J. 2022 Apr;289(8):2176-2201. doi: 10.1111/febs.16065. Epub 2021 Jun 25.

Abstract

Synapses between neurons are malleable biochemical structures, strengthening and diminishing over time dependent on the type of information they receive. This phenomenon known as synaptic plasticity underlies learning and memory, and its different forms, long-term potentiation (LTP) and long-term depression (LTD), perform varied cognitive roles in reinforcement, relearning and associating memories. Moreover, both LTP and LTD can exist in an early transient form (early-LTP/LTD) or a late persistent form (late-LTP/LTD), which are triggered by different induction protocols, and also differ in their dependence on protein synthesis and the involvement of key molecular players. Beyond homosynaptic modifications, synapses can also interact with one another. This is encapsulated in the synaptic tagging and capture hypothesis (STC), where synapses expressing early-LTP/LTD present a 'tag' that can capture the protein synthesis products generated during a temporally proximal late-LTP/LTD induction. This 'tagging' phenomenon forms the framework of synaptic interactions in various conditions and accounts for the cellular basis of the time-dependent associativity of short-lasting and long-lasting memories. All these synaptic modifications take place under controlled neuronal conditions, regulated by subcellular elements such as epigenetic regulation, proteasomal degradation and neuromodulatory signals. Here, we review current understanding of the different forms of synaptic plasticity and its regulatory mechanisms in the hippocampus, a brain region critical for memory formation. We also discuss expression of plasticity in hippocampal CA2 area, a long-overlooked narrow hippocampal subfield and the behavioural correlate of STC. Lastly, we put forth perspectives for an integrated view of memory representation in synapses.

摘要

神经元之间的突触是可塑的生化结构,会随着时间的推移根据所接收信息的类型而增强或减弱。这种被称为突触可塑性的现象是学习和记忆的基础,其不同形式,即长时程增强(LTP)和长时程抑制(LTD),在强化、重新学习和关联记忆中发挥着不同的认知作用。此外,LTP和LTD都可以以早期短暂形式(早期LTP/LTD)或晚期持续形式(晚期LTP/LTD)存在,它们由不同的诱导方案触发,在对蛋白质合成的依赖性以及关键分子参与者的参与方面也有所不同。除了同突触修饰外,突触之间还可以相互作用。这在突触标记和捕获假说(STC)中有所体现,即表达早期LTP/LTD的突触会呈现一个“标记”,该标记可以捕获在时间上接近的晚期LTP/LTD诱导过程中产生的蛋白质合成产物。这种“标记”现象构成了各种条件下突触相互作用的框架,并解释了短期和长期记忆的时间依赖性关联性的细胞基础。所有这些突触修饰都在受控的神经元条件下发生,受表观遗传调控、蛋白酶体降解和神经调节信号等亚细胞元件的调节。在这里,我们综述了目前对海马体中突触可塑性不同形式及其调节机制的理解,海马体是对记忆形成至关重要的脑区。我们还讨论了海马体CA2区可塑性的表达,CA2区是一个长期被忽视的狭窄海马亚区,也是STC的行为相关因素。最后,我们提出了关于突触中记忆表征的综合观点的展望。

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