Modeling Neurological Disorders in 3D Organoids Using Human-Derived Pluripotent Stem Cells

被引:15
|
作者
Bose, Raj [1 ,2 ,3 ,4 ]
Banerjee, Soumyabrata [1 ,2 ,3 ]
Dunbar, Gary L. [1 ,2 ,3 ,5 ]
机构
[1] Cent Michigan Univ, Field Neurosci Inst Lab Restorat Neurol, Mt Pleasant, MI 48859 USA
[2] Cent Michigan Univ, Dept Psychol, Mt Pleasant, MI 48859 USA
[3] Cent Michigan Univ, Program Neurosci, Mt Pleasant, MI 48859 USA
[4] Karolinska Inst, Dept Neurosci, Stockholm, Sweden
[5] Ascens St Marys, Field Neurosci Inst, Saginaw, MI 48601 USA
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2021年 / 9卷
关键词
neurological disorders; hiPSCs; neural organoids; vascularization; blood-brain barrier; MICROGLIA-LIKE CELLS; BRAIN-BARRIER MODEL; CEREBRAL ORGANOIDS; NEURAL PROGENITORS; IN-VITRO; EFFICIENT GENERATION; PARKINSONS-DISEASE; ENDOTHELIAL-CELLS; DIFFERENTIATION; DERIVATION;
D O I
10.3389/fcell.2021.640212
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Modeling neurological disorders is challenging because they often have both endogenous and exogenous causes. Brain organoids consist of three-dimensional (3D) self-organizing brain tissue which increasingly is being used to model various aspects of brain development and disorders, such as the generation of neurons, neuronal migration, and functional networks. These organoids have been recognized as important in vitro tools to model developmental features of the brain, including neurological disorders, which can provide insights into the molecular mechanisms involved in those disorders. In this review, we describe recent advances in the generation of two-dimensional (2D), 3D, and blood-brain barrier models that were derived from induced pluripotent stem cells (iPSCs) and we discuss their advantages and limitations in modeling diseases, as well as explore the development of a vascularized and functional 3D model of brain processes. This review also examines the applications of brain organoids for modeling major neurodegenerative diseases and neurodevelopmental disorders.
引用
收藏
页数:17
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