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

被引:7
|
作者
Yue, Chunmei [1 ,2 ]
Feng, Su [1 ,3 ]
Chen, Yingying [1 ]
Jing, Naihe [1 ,3 ,4 ,5 ]
机构
[1] Univ Chinese Acad Sci, Chinese Acad Sci, Shanghai Inst Biochem & Cell Biol, State Key Lab Cell Biol,CAS Ctr Excellence Mol Cel, Shanghai 200031, Peoples R China
[2] Xian Jiaotong Liverpool Univ, Sch Sci, Dept Biol Sci, Suzhou 215000, Peoples R China
[3] Bioland Lab Guangzhou Lab, Guangzhou 510005, Peoples R China
[4] Chinese Acad Sci, Guangzhou Inst Biomed & Hlth, CAS Key Lab Regenerat Biol, Guangdong Prov Key Lab Stem Cell & Regenerat Med, Guangzhou 510530, Peoples R China
[5] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
关键词
Brain disorders; Alzheimer's disease; Stem cell-based replacement therapy; Neural subtype-specific transplantation; Brain region-specific transplantation; Cognitive ability; BLOOD MONONUCLEAR-CELLS; PROGENITOR CELLS; IMPROVE COGNITION; DIRECT CONVERSION; HUMAN FIBROBLASTS; TRANSGENIC MODEL; INTEGRATION-FREE; MOUSE MODEL; TRANSPLANTATION; BRAIN;
D O I
10.1186/s13619-022-00128-5
中图分类号
Q813 [细胞工程];
学科分类号
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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页数:10
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