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空间和时间分子网络在长期记忆诱导及其潜在突触可塑性中的作用

The Contribution of Spatial and Temporal Molecular Networks in the Induction of Long-term Memory and Its Underlying Synaptic Plasticity.

作者信息

Mirisis Anastasios A, Alexandrescu Anamaria, Carew Thomas J, Kopec Ashley M

机构信息

Center for Neural Science, New York University, New York, NY, USA; Department of Biology, New York University, New York, NY, USA.

Center for Neural Science, New York University, New York, NY, USA; Department of Neuroscience and Physiology, New York University School of Medicine, New York, NY, USA.

出版信息

AIMS Neurosci. 2016;3(3):356-384. doi: 10.3934/Neuroscience.2016.3.356. Epub 2016 Oct 22.

Abstract

The ability to form long-lasting memories is critical to survival and thus is highly conserved across the animal kingdom. By virtue of its complexity, this same ability is vulnerable to disruption by a wide variety of neuronal traumas and pathologies. To identify effective therapies with which to treat memory disorders, it is critical to have a clear understanding of the cellular and molecular mechanisms which subserve normal learning and memory. A significant challenge to achieving this level of understanding is posed by the wide range of distinct temporal and spatial profiles of molecular signaling induced by learning-related stimuli. In this review we propose that a useful framework within which to address this challenge is to view the molecular foundation of long-lasting plasticity as composed of unique spatial and temporal molecular networks that mediate signaling both within neurons (such as via kinase signaling) as well as between neurons (such as via growth factor signaling). We propose that evaluating how cells integrate and interpret these concurrent and interacting molecular networks has the potential to significantly advance our understanding of the mechanisms underlying learning and memory formation.

摘要

形成持久记忆的能力对生存至关重要,因此在动物界中高度保守。由于其复杂性,这种相同的能力容易受到多种神经元创伤和病理状况的干扰。为了确定治疗记忆障碍的有效疗法,清楚了解支持正常学习和记忆的细胞和分子机制至关重要。学习相关刺激所诱导的分子信号具有广泛不同的时空特征,这给达到这种理解水平带来了重大挑战。在本综述中,我们提出应对这一挑战的一个有用框架是,将持久可塑性的分子基础视为由独特的时空分子网络组成,这些网络介导神经元内(如通过激酶信号传导)以及神经元间(如通过生长因子信号传导)的信号传递。我们提出,评估细胞如何整合和解读这些同时存在且相互作用的分子网络,有可能显著推进我们对学习和记忆形成潜在机制的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f881/5096789/d32481b68b8f/nihms825962f1.jpg

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