Graduate Program in Neuroscience, Brown University, Providence, RI 02912, USA.
Warren Alpert Medical School of Brown University, Providence, RI 02912, USA; Department of Neuroscience, Brown University, Providence, RI 02912, USA.
Stem Cell Reports. 2021 Apr 13;16(4):681-693. doi: 10.1016/j.stemcr.2021.01.019. Epub 2021 Feb 25.
Cognitive deficits associated with Alzheimer's disease (AD) severely impact daily life for the millions of affected individuals. Progressive memory impairment in AD patients is associated with degeneration of the hippocampus. The dentate gyrus of the hippocampus, a region critical for learning and memory functions, is a site of adult neurogenesis in mammals. Recent evidence in humans indicates that hippocampal neurogenesis likely persists throughout life, but declines with age and is strikingly impaired in AD. Our understanding of how neurogenesis supports learning and memory in healthy adults is only beginning to emerge. The extent to which decreased neurogenesis contributes to cognitive decline in aging and AD remains poorly understood. However, studies in rodent models of AD and other neurodegenerative diseases raise the possibility that targeting neurogenesis may ameliorate cognitive dysfunction in AD. Here, we review recent progress in understanding how adult neurogenesis is impacted in the context of aging and AD.
与阿尔茨海默病(AD)相关的认知缺陷严重影响了数百万受影响个体的日常生活。AD 患者进行性记忆损伤与海马体退化有关。海马体的齿状回是学习和记忆功能的关键区域,也是哺乳动物成年神经发生的部位。最近在人类中的证据表明,海马体神经发生可能在整个生命过程中持续存在,但随着年龄的增长而下降,在 AD 中则明显受损。我们对神经发生如何支持健康成年人学习和记忆的理解才刚刚开始出现。神经发生减少在多大程度上导致衰老和 AD 中的认知能力下降仍知之甚少。然而,AD 及其他神经退行性疾病的啮齿动物模型研究提出了这样一种可能性,即针对神经发生可能改善 AD 中的认知功能障碍。在这里,我们回顾了最近在理解成年神经发生在衰老和 AD 背景下受到的影响方面的进展。