Human stem cell models of polyglutamine diseases: Sources for disease models and cell therapy

被引:6
|
作者
He, Lang [1 ]
Chen, Zhao [1 ,2 ,3 ]
Peng, Linliu [1 ]
Tang, Beisha [1 ,2 ,3 ,4 ]
Jiang, Hong [1 ,2 ,3 ,4 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Neurol, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Key Lab Hunan Prov Neurodegenerat Disorders, Changsha, Hunan, Peoples R China
[3] Cent South Univ, Natl Clin Res Ctr Geriatr Dis, Changsha, Hunan, Peoples R China
[4] Cent South Univ, Lab Med Genet, Changsha, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Polyglutamine diseases; Pluripotent stem cells; Disease modeling; Cell replacement therapy; Gene therapy;
D O I
10.1016/j.expneurol.2020.113573
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Polyglutamine (polyQ) diseases are a group of neurodegenerative disorders involving expanded CAG repeats in pathogenic genes that are translated into extended polyQ tracts and lead to progressive neuronal degeneration in the affected brain. To date, there is no effective therapy for these diseases. Due to the complex pathologic mechanisms of these diseases, intensive research on the pathogenesis of their progression and potential treatment strategies is being conducted. However, animal models cannot recapitulate all aspects of neuronal degeneration. Pluripotent stem cells (PSCs), such as induced pluripotent stem cells (iPSCs) and embryonic stem cells (ESCs), can be used to study the pathological mechanisms of polyQ diseases, and the ability of autologous stem cell transplantation to treat these diseases. Differentiated PSCs, neuronal precursor cells/neural progenitor cells (NPCs) and mesenchymal stem cells (MSCs) are valuable resources for preclinical and clinical cell transplantation therapies. Here, we discuss diverse stem cell models and their ability to generate neurons involved in polyQ diseases, such as medium spiny neurons (MSNs), cortical neurons, cerebellar Purkinje cells (PCs) and motor neurons. In addition, we discuss potential therapeutic approaches, including stem cell replacement therapy and gene therapy.
引用
收藏
页数:16
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