Topologically controlled circuits of human iPSC-derived neurons for electrophysiology recordings

被引:20
|
作者
Girardin, Sophie [1 ]
Clement, Blandine [1 ]
Ihle, Stephan J. [1 ]
Weaver, Sean [1 ]
Petr, Jana B. [1 ]
Mateus, Jose C. [2 ]
Duru, Jens [1 ]
Forro, Csaba [3 ]
Ruff, Tobias [1 ]
Fruh, Isabelle [4 ]
Mueller, Matthias [4 ]
Voeroes, Janos [1 ]
Magdalena [1 ]
机构
[1] Swiss Fed Inst Technol, Lab Biosensors & Bioelect, Inst Biomed Engn, Gloriastr 35, CH-8092 Zurich, Switzerland
[2] Univ Porto, Inst Invest & Inovacao Saude, Rua Alfredo Allen 208, Porto, Portugal
[3] Cui Lab, S285 290 Jane Stanford Way Stanford, Stanford, CA 94305 USA
[4] Novartis Inst BioMed Res, Chem Biol & Therapeut, CH-4002 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
IN-VITRO MODELS; NETWORKS; PLATFORM; DESIGN; CHIP; TERM;
D O I
10.1039/d1lc01110c
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bottom-up neuroscience, which consists of building and studying controlled networks of neurons in vitro, is a promising method to investigate information processing at the neuronal level. However, in vitro studies tend to use cells of animal origin rather than human neurons, leading to conclusions that might not be generalizable to humans and limiting the possibilities for relevant studies on neurological disorders. Here we present a method to build arrays of topologically controlled circuits of human induced pluripotent stem cell (iPSC)-derived neurons. The circuits consist of 4 to 50 neurons with well-defined connections, confined by microfabricated polydimethylsiloxane (PDMS) membranes. Such circuits were characterized using optical imaging and microelectrode arrays (MEAs), suggesting the formation of functional connections between the neurons of a circuit. Electrophysiology recordings were performed on circuits of human iPSC-derived neurons for at least 4.5 months. We believe that the capacity to build small and controlled circuits of human iPSC-derived neurons holds great promise to better understand the fundamental principles of information processing and storing in the brain.
引用
收藏
页码:1386 / 1403
页数:18
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