Human iPSC-Derived Neural Models for Studying Alzheimer's Disease: from Neural Stem Cells to Cerebral Organoids

被引:52
作者
Barak, Martin [1 ]
Fedorova, Veronika [1 ]
Pospisilova, Veronika [1 ]
Raska, Jan [1 ]
Vochyanova, Simona [1 ]
Sedmik, Jiri [1 ,2 ]
Hribkova, Hana [1 ]
Klimova, Hana [1 ]
Vanova, Tereza [1 ,2 ]
Bohaciakova, Dasa [1 ,2 ]
机构
[1] Masaryk Univ Brno, Fac Med, Dept Histol & Embryol, Brno, Czech Republic
[2] St Annes Fac Hosp Brno, Int Clin Res Ctr, Brno, Czech Republic
关键词
iPSCs; Neural differentiation; Alzheimer's disease; In vitro differentiation; Neural stem cells; Neural progenitors; Neurons; Astrocytes; Microglia; Cerebral organoids; OLIGODENDROCYTE PROGENITOR CELLS; DIFFERENTIATION IN-VITRO; GAMMA-SECRETASE ACTIVITY; MICROGLIA-LIKE CELLS; A-BETA; HUMAN FIBROBLASTS; AMYLOID-BETA; HUMAN ES; EFFICIENT GENERATION; FUNCTIONAL-NEURONS;
D O I
10.1007/s12015-021-10254-3
中图分类号
Q813 [细胞工程];
学科分类号
摘要
During the past two decades, induced pluripotent stem cells (iPSCs) have been widely used to study mechanisms of human neural development, disease modeling, and drug discovery in vitro. Especially in the field of Alzheimer's disease (AD), where this treatment is lacking, tremendous effort has been put into the investigation of molecular mechanisms behind this disease using induced pluripotent stem cell-based models. Numerous of these studies have found either novel regulatory mechanisms that could be exploited to develop relevant drugs for AD treatment or have already tested small molecules on in vitro cultures, directly demonstrating their effect on amelioration of AD-associated pathology. This review thus summarizes currently used differentiation strategies of induced pluripotent stem cells towards neuronal and glial cell types and cerebral organoids and their utilization in modeling AD and potential drug discovery.
引用
收藏
页码:792 / 820
页数:29
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