The therapeutic prospects and challenges of human neural stem cells for the treatment of Alzheimer's Disease

被引:0
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作者
Chunmei Yue
Su Feng
Yingying Chen
Naihe Jing
机构
[1] Chinese Academy of Sciences,State Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology
[2] University of Chinese Academy of Sciences,Department of Biological Sciences, School of Science
[3] Xi’an Jiaotong-Liverpool University,CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health
[4] Bioland Laboratory/Guangzhou Laboratory,School of Life Science and Technology
[5] Chinese Academy of Sciences,undefined
[6] ShanghaiTech University,undefined
来源
关键词
Brain disorders; Alzheimer's disease; Stem cell-based replacement therapy; Neural subtype-specific transplantation; Brain region-specific transplantation; Cognitive ability;
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摘要
Alzheimer's disease (AD) is a multifactorial neurodegenerative disorder associated with aging. Due to its insidious onset, protracted progression, and unclear pathogenesis, it is considered one of the most obscure and intractable brain disorders, and currently, there are no effective therapies for it. Convincing evidence indicates that the irreversible decline of cognitive abilities in patients coincides with the deterioration and degeneration of neurons and synapses in the AD brain. Human neural stem cells (NSCs) hold the potential to functionally replace lost neurons, reinforce impaired synaptic networks, and repair the damaged AD brain. They have therefore received extensive attention as a possible source of donor cells for cellular replacement therapies for AD. Here, we review the progress in NSC-based transplantation studies in animal models of AD and assess the therapeutic advantages and challenges of human NSCs as donor cells. We then formulate a promising transplantation approach for the treatment of human AD, which would help to explore the disease-modifying cellular therapeutic strategy for the treatment of human AD.
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