Induced Pluripotent Stem Cells for Disease Modeling and Drug Discovery in Neurodegenerative Diseases

被引:34
作者
Cao, Lei [1 ]
Tan, Lan [1 ,2 ,3 ]
Jiang, Teng [1 ]
Zhu, Xi-Chen [1 ]
Yu, Jin-Tai [1 ,2 ,3 ,4 ]
机构
[1] Nanjing Med Univ, Qingdao Municipal Hosp, Dept Neurol, Nanjing, Jiangsu, Peoples R China
[2] Qingdao Univ, Dept Neurol, Sch Med, Qingdao Municipal Hosp, Qingdao 266071, Peoples R China
[3] Ocean Univ China, Qingdao Municipal Hosp, Dept Neurol, Coll Med & Pharmaceut, Qingdao, Peoples R China
[4] Univ Calif San Francisco, Dept Neurol, Memory & Aging Ctr, San Francisco, CA USA
基金
中国国家自然科学基金;
关键词
Chemical genomics; Drug screening; Drug target; High-throughput technologies; Induced pluripotent stem cells; AMYOTROPHIC-LATERAL-SCLEROSIS; HUNTINGTONS-DISEASE; ALZHEIMERS-DISEASE; NEUROLOGICAL DISEASES; REGENERATIVE MEDICINE; PARKINSONS-DISEASE; MOTOR-NEURONS; CHALLENGES; PATIENT; FIBROBLASTS;
D O I
10.1007/s12035-014-8867-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although most neurodegenerative diseases have been closely related to aberrant accumulation of aggregation-prone proteins in neurons, understanding their pathogenesis remains incomplete, and there is no treatment to delay the onset or slow the progression of many neurodegenerative diseases. The availability of induced pluripotent stem cells (iPSCs) in recapitulating the phenotypes of several late-onset neurodegenerative diseases marks the new era in in vitro modeling. The iPSC collection represents a unique and well-characterized resource to elucidate disease mechanisms in these diseases and provides a novel human stem cell platform for screening new candidate therapeutics. Modeling human diseases using iPSCs has created novel opportunities for both mechanistic studies as well as for the discovery of new disease therapies. In this review, we introduce iPSC-based disease modeling in neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, Huntington's disease, and amyotrophic lateral sclerosis. In addition, we discuss the implementation of iPSCs in drug discovery associated with some new techniques.
引用
收藏
页码:244 / 255
页数:12
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