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肌动蛋白细胞骨架在维持神经元形态和长期记忆中的作用。

Actin Cytoskeleton Role in the Maintenance of Neuronal Morphology and Long-Term Memory.

机构信息

Sagol Department of Neurobiology, Faculty of Natural Sciences, University of Haifa, Haifa 3498838, Israel.

出版信息

Cells. 2021 Jul 15;10(7):1795. doi: 10.3390/cells10071795.

Abstract

Evidence indicates that long-term memory formation creates long-lasting changes in neuronal morphology within a specific neuronal network that forms the memory trace. Dendritic spines, which include most of the excitatory synapses in excitatory neurons, are formed or eliminated by learning. These changes may be long-lasting and correlate with memory strength. Moreover, learning-induced changes in the morphology of existing spines can also contribute to the formation of the neuronal network that underlies memory. Altering spines morphology after memory consolidation can erase memory. These observations strongly suggest that learning-induced spines modifications can constitute the changes in synaptic connectivity within the neuronal network that form memory and that stabilization of this network maintains long-term memory. The formation and elimination of spines and other finer morphological changes in spines are mediated by the actin cytoskeleton. The actin cytoskeleton forms networks within the spine that support its structure. Therefore, it is believed that the actin cytoskeleton mediates spine morphogenesis induced by learning. Any long-lasting changes in the spine morphology induced by learning require the preservation of the spine actin cytoskeleton network to support and stabilize the spine new structure. However, the actin cytoskeleton is highly dynamic, and the turnover of actin and its regulatory proteins that determine and support the actin cytoskeleton network structure is relatively fast. Molecular models, suggested here, describe ways to overcome the dynamic nature of the actin cytoskeleton and the fast protein turnover and to support an enduring actin cytoskeleton network within the spines, spines stability and long-term memory. These models are based on long-lasting changes in actin regulatory proteins concentrations within the spine or the formation of a long-lasting scaffold and the ability for its recurring rebuilding within the spine. The persistence of the actin cytoskeleton network within the spine is suggested to support long-lasting spine structure and the maintenance of long-term memory.

摘要

有证据表明,长期记忆的形成会在特定的神经元网络中导致神经元形态的持久变化,而该网络形成了记忆痕迹。树突棘包含兴奋性神经元中大多数兴奋性突触,通过学习形成或消除。这些变化可能是持久的,并与记忆强度相关。此外,学习引起的现有棘突形态变化也可以促进记忆基础的神经元网络的形成。记忆巩固后改变棘突形态可以消除记忆。这些观察结果强烈表明,学习诱导的棘突修饰可以构成神经元网络内突触连接的变化,从而形成记忆,并且该网络的稳定维持长期记忆。棘突和其他棘突更细微形态变化的形成和消除由肌动蛋白细胞骨架介导。肌动蛋白细胞骨架在棘突内形成支持其结构的网络。因此,人们认为肌动蛋白细胞骨架介导了学习诱导的棘突形态发生。学习引起的棘突形态的任何持久变化都需要保留棘突肌动蛋白细胞骨架网络来支持和稳定新的棘突结构。然而,肌动蛋白细胞骨架具有高度动态性,并且决定和支持肌动蛋白细胞骨架网络结构的肌动蛋白及其调节蛋白的周转率相对较快。这里提出的分子模型描述了克服肌动蛋白细胞骨架的动态性质和快速蛋白周转的方法,并支持棘突内持久的肌动蛋白细胞骨架网络、棘突稳定性和长期记忆。这些模型基于棘突内肌动蛋白调节蛋白浓度的持久变化,或形成持久的支架及其在棘突内反复重建的能力。棘突内肌动蛋白细胞骨架网络的持久性被认为可以支持持久的棘突结构和长期记忆的维持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e9/8305626/9aff5b818057/cells-10-01795-g001.jpg

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