Central nervous system organoids for modeling neurodegenerative diseases

被引:2
|
作者
Hou, Pei-Shan [1 ,2 ]
Kuo, Hung-Chih [3 ,4 ]
机构
[1] Natl Yang Ming Chiao Tung Univ, Inst Anat & Cell Biol, Taipei 11221, Taiwan
[2] Natl Yang Ming Chiao Tung Univ, Brain Res Ctr, Taipei, Taiwan
[3] Acad Sinica, Inst Cellular & Organism Biol, 128,Sec 2,Acad Rd, Taipei 11529, Taiwan
[4] Natl Taiwan Univ, Coll Med, Grad Inst Med Genom & Prote, Taipei, Taiwan
关键词
CNS organoid; disease modeling; drug screen; iPSC; neurodegenerative disorders; PLURIPOTENT STEM-CELLS; HUMAN CORTICAL ORGANOIDS; HUMAN BRAIN-DEVELOPMENT; ALZHEIMERS-DISEASE; SELF-ORGANIZATION; CEREBRAL ORGANOIDS; IPSCS REVEALS; HUMAN ES; NEURONS; ALS;
D O I
10.1002/iub.2595
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent advances in induced pluripotent stem cell (iPSC) technology have allowed researchers to generate neurodegenerative disease-specific iPSCs and use the cells to derive a variety of relevant cell populations for laboratory modeling and drug testing. Nevertheless, these efforts have faced challenges related to immaturity and lack of complex developmental niches in the derived cell populations, limiting the utility of these in vitro models of neurodegenerative disease. Such limitations may be overcome by using human iPSC technology to generate three-dimensional (3D) brain organoids, which better recapitulate in vivo tissue architecture than traditional neuronal cultures to provide more complex and representative disease models and drug testing systems. In this review, we focus on the application of pluripotent stem cell-derived central nervous system (CNS) organoids to model neurodegenerative diseases. We first summarize recent progress in generating and characterizing various CNS organoids from pluripotent stem cells. We then review the application of CNS organoids for modeling several different human neurodegenerative diseases. We also describe several novel pathological mechanisms and drugs that were studied using patient iPSC-derived CNS organoids. Finally, we discuss remaining challenges and emerging opportunities for the use of 3D brain organoids for in vitro modeling of CNS development and neurodegeneration.
引用
收藏
页码:812 / 825
页数:14
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