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成年期和衰老过程中的髓鞘可塑性。

Myelin plasticity in adulthood and aging.

机构信息

Department of Biological Sciences, Dartmouth College, Hanover, NH, USA.

Department of Biological Sciences, Dartmouth College, Hanover, NH, USA.

出版信息

Neurosci Lett. 2020 Jan 10;715:134645. doi: 10.1016/j.neulet.2019.134645. Epub 2019 Nov 22.

Abstract

The central nervous system maintains the potential for molecular and cellular plasticity throughout life. This flexibility underlies fundamental features of neural circuitry including the brain's ability to sense, store, and properly adapt to everchanging external stimuli on time scales from seconds to years. Evidence for most forms of plasticity are centered around changes in neuronal structure and synaptic strength, however recent data suggests that myelinating oligodendrocytes exhibit certain forms of plasticity in the adult. This plasticity ranges from the generation of entirely new myelinating cells to more subtle changes in myelin sheath length, thickness, and distribution along axons. The extent to which these changes dynamically modify axonal function and neural circuitry and whether they are directly related to mechanisms of learning and memory remains an open question. Here we describe different forms of myelin plasticity, highlight some recent evidence for changes in myelination throughout life, and discuss how defects in these forms of plasticity could be associated with cognitive decline in aging.

摘要

中枢神经系统在整个生命周期中都保持着分子和细胞可塑性的潜力。这种灵活性是神经回路的基本特征的基础,包括大脑感知、存储和及时适应外部刺激的能力,这些刺激的时间尺度从几秒钟到几年不等。大多数形式的可塑性的证据都集中在神经元结构和突触强度的变化上,然而最近的数据表明,成熟的少突胶质细胞表现出某些形式的可塑性。这种可塑性的范围从产生全新的髓鞘细胞到髓鞘鞘长、厚度和沿轴突分布的更细微变化。这些变化在多大程度上动态地改变轴突功能和神经回路,以及它们是否与学习和记忆的机制直接相关,仍然是一个悬而未决的问题。在这里,我们描述了不同形式的髓鞘可塑性,强调了一生中髓鞘变化的一些最新证据,并讨论了这些形式的可塑性缺陷如何与衰老时的认知能力下降相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d123/6981290/e892bab2da76/nihms-1545255-f0001.jpg

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