Promoting Alzheimer's disease research and therapy with stem cell technology

被引:19
作者
Cao, Zimeng [1 ]
Kong, Fanshu [1 ]
Ding, Jiaqi [1 ]
Chen, Chunxia [1 ]
He, Fumei [1 ,2 ]
Deng, Wenbin [1 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Shenzhen Campus, Shenzhen 518107, Peoples R China
[2] Dali Univ, Sch Pharmaceut Sci, Dali 671000, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; Stem cell technology; Disease modeling; Pathogenesis; Neuron-glia interaction; Stem cell-derived therapy; CEREBRAL-CORTEX DEVELOPMENT; AMYLOID-BETA DEPOSITION; IN-VITRO; MOUSE MODEL; MITOCHONDRIAL DYNAMICS; FIBRIN HYDROGELS; HUMAN BRAIN; IPS CELLS; HUMAN ES; MICROGLIA;
D O I
10.1186/s13287-024-03737-w
中图分类号
Q813 [细胞工程];
学科分类号
摘要
BackgroundAlzheimer's disease (AD) is a prevalent form of dementia leading to memory loss, reduced cognitive and linguistic abilities, and decreased self-care. Current AD treatments aim to relieve symptoms and slow disease progression, but a cure is elusive due to limited understanding of the underlying disease mechanisms.Main contentStem cell technology has the potential to revolutionize AD research. With the ability to self-renew and differentiate into various cell types, stem cells are valuable tools for disease modeling, drug screening, and cell therapy. Recent advances have broadened our understanding beyond the deposition of amyloid beta (A beta) or tau proteins in AD to encompass risk genes, immune system disorders, and neuron-glia mis-communication, relying heavily on stem cell-derived disease models. These stem cell-based models (e.g., organoids and microfluidic chips) simulate in vivo pathological processes with extraordinary spatial and temporal resolution. Stem cell technologies have the potential to alleviate AD pathology through various pathways, including immunomodulation, replacement of damaged neurons, and neurotrophic support. In recent years, transplantation of glial cells like oligodendrocytes and the infusion of exosomes have become hot research topics.ConclusionAlthough stem cell-based models and therapies for AD face several challenges, such as extended culture time and low differentiation efficiency, they still show considerable potential for AD treatment and are likely to become preferred tools for AD research.
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页数:34
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