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阿尔茨海默病与海马体成年神经发生;探索共同机制。

Alzheimer's Disease and Hippocampal Adult Neurogenesis; Exploring Shared Mechanisms.

作者信息

Hollands Carolyn, Bartolotti Nancy, Lazarov Orly

机构信息

Department of Anatomy and Cell Biology, College of Medicine, The University of Illinois at Chicago Chicago, IL, USA.

出版信息

Front Neurosci. 2016 May 3;10:178. doi: 10.3389/fnins.2016.00178. eCollection 2016.

Abstract

New neurons incorporate into the granular cell layer of the dentate gyrus throughout life. Neurogenesis is modulated by behavior and plays a major role in hippocampal plasticity. Along with older mature neurons, new neurons structure the dentate gyrus, and determine its function. Recent data suggest that the level of hippocampal neurogenesis is substantial in the human brain, suggesting that neurogenesis may have important implications for human cognition. In support of that, impaired neurogenesis compromises hippocampal function and plays a role in cognitive deficits in Alzheimer's disease mouse models. We review current work suggesting that neuronal differentiation is defective in Alzheimer's disease, leading to dysfunction of the dentate gyrus. Additionally, alterations in critical signals regulating neurogenesis, such as presenilin-1, Notch 1, soluble amyloid precursor protein, CREB, and β-catenin underlie dysfunctional neurogenesis in Alzheimer's disease. Lastly, we discuss the detectability of neurogenesis in the live mouse and human brain, as well as the therapeutic implications of enhancing neurogenesis for the treatment of cognitive deficits and Alzheimer's disease.

摘要

新神经元在整个生命过程中都会融入齿状回的颗粒细胞层。神经发生受行为调节,并在海马可塑性中起主要作用。新神经元与较老的成熟神经元一起构成齿状回,并决定其功能。最近的数据表明,海马神经发生在人类大脑中相当显著,这表明神经发生可能对人类认知具有重要意义。支持这一观点的是,神经发生受损会损害海马功能,并在阿尔茨海默病小鼠模型的认知缺陷中起作用。我们回顾了当前的研究工作,这些研究表明阿尔茨海默病中神经元分化存在缺陷,导致齿状回功能障碍。此外,调节神经发生的关键信号,如早老素-1、Notch 1、可溶性淀粉样前体蛋白、CREB和β-连环蛋白的改变是阿尔茨海默病中神经发生功能障碍的基础。最后,我们讨论了在活体小鼠和人类大脑中检测神经发生的可能性,以及增强神经发生对治疗认知缺陷和阿尔茨海默病的治疗意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cc9/4853383/eee2a0859020/fnins-10-00178-g0001.jpg

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