An in vitro model of neuronal ensembles

被引:14
|
作者
Rabadan, M. Angeles [1 ]
De La Cruz, Estanislao Daniel [1 ]
Rao, Sneha B. [2 ]
Chen, Yannan [1 ,3 ]
Gong, Cheng [1 ,3 ]
Crabtree, Gregg [2 ]
Xu, Bin [4 ]
Markx, Sander [4 ]
Gogos, Joseph A. [2 ,5 ,6 ,7 ,8 ]
Yuste, Rafael [1 ]
Tomer, Raju [1 ,2 ,3 ]
机构
[1] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[2] Columbia Univ, Mortimer B Zuckerman Mind Brain & Behav Inst, New York, NY 10027 USA
[3] Columbia Univ, Dept Biomed Engn, New York, NY 10027 USA
[4] Columbia Univ, Vagelos Coll Phys & Surg, Dept Psychiat, New York, NY USA
[5] Columbia Univ, Dept Physiol, New York, NY 10027 USA
[6] Columbia Univ, Dept Neurosci, New York, NY USA
[7] Columbia Univ, Dept Psychiat, New York, NY USA
[8] Columbia Univ, NeuroTechnol Ctr, New York, NY USA
关键词
OF-FUNCTION VARIANTS; MOUSE MODEL; SYNAPTIC PLASTICITY; SCHIZOPHRENIA; DYSFUNCTION; HIPPOCAMPAL; PROTEIN; PATHOPHYSIOLOGY; MECHANISMS; ARC/ARG3.1;
D O I
10.1038/s41467-022-31073-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Advances in 3D neuronal cultures have allowed unprecedented access to the mechanisms underlying brain diseases. This work describes the novel Modular Neuronal Network (MoNNet) system, which enables more complex studies of cortical neuronal ensemble dynamics. Advances in 3D neuronal cultures, such as brain spheroids and organoids, are allowing unprecedented in vitro access to some of the molecular, cellular and developmental mechanisms underlying brain diseases. However, their efficacy in recapitulating brain network properties that encode brain function remains limited, thereby precluding development of effective in vitro models of complex brain disorders like schizophrenia. Here, we develop and characterize a Modular Neuronal Network (MoNNet) approach that recapitulates specific features of neuronal ensemble dynamics, segregated local-global network activities and a hierarchical modular organization. We utilized MoNNets for quantitative in vitro modelling of schizophrenia-related network dysfunctions caused by highly penetrant mutations in SETD1A and 22q11.2 risk loci. Furthermore, we demonstrate its utility for drug discovery by performing pharmacological rescue of alterations in neuronal ensembles stability and global network synchrony. MoNNets allow in vitro modelling of brain diseases for investigating the underlying neuronal network mechanisms and systematic drug discovery.
引用
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页数:17
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