Generation and Downstream Analysis of Single-Cell and Single-Nuclei Transcriptomes in Brain Organoids

被引:0
|
作者
Wandres, Miriam [1 ,2 ]
Aigner, Denise [1 ,2 ]
Kastelic, Nicolai [1 ,3 ]
Boltengagen, Anastasiya [1 ]
Rybak-Wolf, Agnieszka [1 ,3 ]
Rajewsky, Nikolaus [1 ,2 ]
机构
[1] Max Delbruck Ctr Mol Med MDC, Berlin Inst Med Syst Biol BIMSB, Berlin, Germany
[2] Humboldt Univ, Inst Biol, Berlin, Germany
[3] Max Delbruck Ctr Mol Med MDC, Berlin Inst Med Syst Biol BIMSB, Organoid Platform, Berlin, Germany
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2024年 / 205期
关键词
CEREBRAL ORGANOIDS;
D O I
10.3791/66225
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
Over the past decade, single -cell transcriptomics has significantly evolved and become a standard laboratory method for simultaneous analysis of gene expression profiles of individual cells, allowing the capture of cellular diversity. In order to overcome limitations posed by difficult -to -isolate cell types, an alternative approach aiming at recovering single nuclei instead of intact cells can be utilized for sequencing, making transcriptome profiling of individual cells universally applicable. These techniques have become a cornerstone in the study of brain organoids, establishing them as models of the developing human brain. Leveraging the potential of single -cell and single -nucleus transcriptomics in brain organoid research, this protocol presents a step-by-step guide encompassing key procedures such as organoid dissociation, single -cell or nuclei isolation, library preparation and sequencing. By implementing these alternative approaches, researchers can obtain high -quality datasets, enabling the identification of neuronal and non -neuronal cell types, gene expression profiles, and cell lineage trajectories. This facilitates comprehensive investigations into cellular processes and molecular mechanisms shaping brain development.
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页数:12
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