Cerebral organoids at the air-liquid interface generate diverse nerve tracts with functional output

被引:419
作者
Giandomenico, Stefano L. [1 ]
Mierau, Susanna B. [2 ]
Gibbons, George M. [3 ,4 ]
Wenger, Lea M. D. [3 ,4 ]
Masullo, Laura [1 ]
Sit, Timothy [2 ]
Sutcliffe, Magdalena [1 ]
Boulanger, Jerome [1 ]
Tripodi, Marco [1 ]
Derivery, Emmanuel [1 ]
Paulsen, Ole [2 ]
Lakatos, Andras [3 ,4 ,5 ]
Lancaster, Madeline A. [1 ]
机构
[1] MRC, Lab Mol Biol, Cambridge Biomed Campus, Cambridge, England
[2] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge, England
[3] Univ Cambridge, John van Geest Ctr Brain Repair, Cambridge, England
[4] Univ Cambridge, Div Stem Cell Neurobiol, Dept Clin Neurosci, Cambridge, England
[5] Wellcome Trust MRC Cambridge Stem Cell Inst, Cambridge Biomed Campus, Cambridge, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金; 英国医学研究理事会; 欧洲研究理事会;
关键词
SELF-ORGANIZATION; AXON GUIDANCE; SPIKE TRAINS; CELL; DYNAMICS; MODEL;
D O I
10.1038/s41593-019-0350-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neural organoids have the potential to improve our understanding of human brain development and neurological disorders. However, it remains to be seen whether these tissues can model circuit formation with functional neuronal output. Here we have adapted air-liquid interface culture to cerebral organoids, leading to improved neuronal survival and axon outgrowth. The resulting thick axon tracts display various morphologies, including long-range projection within and away from the organoid, growth-cone turning, and decussation. Single-cell RNA sequencing reveals various cortical neuronal identities, and retrograde tracing demonstrates tract morphologies that match proper molecular identities. These cultures exhibit active neuronal networks, and subcortical projecting tracts can innervate mouse spinal cord explants and evoke contractions of adjacent muscle in a manner dependent on intact organoid-derived innervating tracts. Overall, these results reveal a remarkable self-organization of corticofugal and callosal tracts with a functional output, providing new opportunities to examine relevant aspects of human CNS development and disease.
引用
收藏
页码:669 / +
页数:14
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