Houben Sarah, Homa Mégane, Yilmaz Zehra, Leroy Karelle, Brion Jean-Pierre, Ando Kunie
Laboratory of Histology, Neuroanatomy and Neuropathology, UNI (ULB Neuroscience Institute), Faculty of Medicine, Université Libre de Bruxelles, Brussels, Belgium.
Front Neurol. 2021 Feb 10;12:610330. doi: 10.3389/fneur.2021.610330. eCollection 2021.
Adult hippocampal neurogenesis (AHN) has been widely confirmed in mammalian brains. A growing body of evidence points to the fact that AHN sustains hippocampal-dependent functions such as learning and memory. Impaired AHN has been reported in human brain hippocampus of Alzheimer's disease (AD) and is considered to contribute to defects in learning and memory. Neurofibrillary tangles (NFTs) and amyloid plaques are the two key neuropathological hallmarks of AD. NFTs are composed of abnormal tau proteins accumulating in many brain areas during the progression of the disease, including in the hippocampus. The physiological role of tau and impact of tau pathology on AHN is still poorly understood. Modifications in AHN have also been reported in some tau transgenic and tau-deleted mouse models. We present here a brief review of advances in the relationship between development of tau pathology and AHN in AD and what insights have been gained from studies in tau mouse models.
成体海马神经发生(AHN)已在哺乳动物大脑中得到广泛证实。越来越多的证据表明,AHN维持着诸如学习和记忆等依赖海马体的功能。据报道,在阿尔茨海默病(AD)患者的脑海马体中,AHN受损,这被认为是导致学习和记忆缺陷的原因。神经纤维缠结(NFTs)和淀粉样斑块是AD的两个关键神经病理学特征。NFTs由异常的tau蛋白组成,在疾病进展过程中,这些蛋白会在包括海马体在内的许多脑区积累。tau蛋白的生理作用以及tau病理对AHN的影响仍知之甚少。在一些tau转基因和tau基因敲除小鼠模型中也报道了AHN的改变。我们在此简要回顾AD中tau病理发展与AHN之间关系的研究进展,以及从tau小鼠模型研究中获得的见解。