Department of Clinical Sciences Malmö, Clinical Memory Research Unit, Lund University, Lund, Sweden.
Department of Neurology, Skåne University Hospital, Lund University, Lund, Sweden.
J Alzheimers Dis. 2023;95(3):805-828. doi: 10.3233/JAD-230119.
Alzheimer's disease (AD) is a prevalent neurodegenerative disorder without a cure. Innovative disease models, such as induced neurons (iNs), could enhance our understanding of AD mechanisms and accelerate treatment development. However, a review of AD human iN studies is necessary to consolidate knowledge.
The objective of this review is to examine the current body of literature on AD human iN cells and provide an overview of the findings to date.
We searched two databases for relevant studies published between 2010 and 2023, identifying nine studies meeting our criteria.
Reviewed studies indicate the feasibility of generating iNs directly from AD patients' fibroblasts using chemical induction or viral vectors. These cells express mature neuronal markers, including MAP-2, NeuN, synapsin, and tau. However, most studies were limited in sample size and primarily focused on autosomal dominant familial AD (FAD) rather than the more common sporadic forms of AD. Several studies indicated that iNs derived from FAD fibroblasts exhibited abnormal amyloid-β metabolism, a characteristic feature of AD in humans. Additionally, elevated levels of hyperphosphorylated tau, another hallmark of AD, were reported in some studies.
Although only a limited number of small-scale studies are currently available, AD patient-derived iNs hold promise as a valuable model for investigating AD pathogenesis. Future research should aim to conduct larger studies, particularly focusing on sporadic AD cases, to enhance the clinical relevance of the findings for the broader AD patient population. Moreover, these cells can be utilized in screening potential novel treatments for AD.
阿尔茨海默病(AD)是一种常见的神经退行性疾病,目前尚无治愈方法。创新的疾病模型,如诱导神经元(iNs),可以增强我们对 AD 机制的理解并加速治疗的发展。然而,有必要对 AD 人类 iN 研究进行综述,以整合相关知识。
本综述旨在检查当前关于 AD 人类 iN 细胞的文献,并概述迄今为止的研究结果。
我们在两个数据库中搜索了 2010 年至 2023 年发表的相关研究,确定了符合我们标准的九项研究。
综述研究表明,使用化学诱导或病毒载体直接从 AD 患者的成纤维细胞中生成 iNs 是可行的。这些细胞表达成熟神经元标志物,包括 MAP-2、NeuN、突触素和 tau。然而,大多数研究的样本量有限,主要集中在常染色体显性家族性 AD(FAD)上,而不是更为常见的散发性 AD 上。一些研究表明,源自 FAD 成纤维细胞的 iNs 表现出异常的淀粉样β代谢,这是人类 AD 的一个特征。此外,一些研究报告称,一些 iNs 中存在高水平的过度磷酸化 tau,这也是 AD 的另一个标志。
尽管目前仅有少数小规模研究可用,但 AD 患者来源的 iNs 作为研究 AD 发病机制的有价值模型具有很大的潜力。未来的研究应旨在开展更大规模的研究,特别是关注散发性 AD 病例,以提高研究结果对更广泛的 AD 患者群体的临床相关性。此外,这些细胞可用于筛选 AD 的潜在新型治疗方法。