Human Astrocytes Model Derived from Induced Pluripotent Stem Cells

被引:32
|
作者
Leventoux, Nicolas [1 ]
Morimoto, Satoru [1 ]
Imaizumi, Kent [1 ]
Sato, Yuta [2 ,3 ]
Takahashi, Shinichi [1 ,4 ]
Mashima, Kyoko [1 ]
Ishikawa, Mitsuru [1 ]
Sonn, Iki [1 ]
Kondo, Takahiro [1 ]
Watanabe, Hirotaka [1 ]
Okano, Hideyuki [1 ]
机构
[1] Keio Univ, Dept Physiol, Sch Med, Tokyo 1608582, Japan
[2] Keio Univ, Grad Sch Sci & Technol, Yokohama, Kanagawa 2238522, Japan
[3] RIKEN, Lab Marmoset Neural Architecture, Ctr Brain Sci, Wako, Saitama 3510198, Japan
[4] Saitama Med Univ, Dept Neurol & Stroke, Int Med Ctr, 1397-1 Yamane, Hidaka, Saitama 3501298, Japan
基金
日本学术振兴会;
关键词
astrocytes; iPSC; cell culture; disease modeling; neurodegenerative diseases; SYNAPSIN-I; NEURONAL DIFFERENTIATION; GLUTAMATE TRANSPORTERS; FUNCTIONAL MATURATION; CULTURED ASTROCYTES; EXPRESSION; BRAIN; SPECIFICATION; MATURE; DEGENERATION;
D O I
10.3390/cells9122680
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Induced pluripotent stem cell (iPSC)-based disease modeling has a great potential for uncovering the mechanisms of pathogenesis, especially in the case of neurodegenerative diseases where disease-susceptible cells can usually not be obtained from patients. So far, the iPSC-based modeling of neurodegenerative diseases has mainly focused on neurons because the protocols for generating astrocytes from iPSCs have not been fully established. The growing evidence of astrocytes' contribution to neurodegenerative diseases has underscored the lack of iPSC-derived astrocyte models. In the present study, we established a protocol to efficiently generate iPSC-derived astrocytes (iPasts), which were further characterized by RNA and protein expression profiles as well as functional assays. iPasts exhibited calcium dynamics and glutamate uptake activity comparable to human primary astrocytes. Moreover, when co-cultured with neurons, iPasts enhanced neuronal synaptic maturation. Our protocol can be used for modeling astrocyte-related disease phenotypes in vitro and further exploring the contribution of astrocytes to neurodegenerative diseases.
引用
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页数:20
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