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Series GSE261157 Query DataSets for GSE261157
Status Public on Apr 07, 2024
Title Aberrant neurodevelopment in human iPS cell-derived neural organoid model of Alexander disease
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary 3D-cultured unguided neural and cortical organoids derived from human iPS cells carrying a GFAP (R239C) mutation - an identified cause of Alexander disease (AxD) - and their isogenic controls were analyzed with scRNA-seq to investigate the effect of the GFAP mutation on brain development, cell type composition, and gene expression. Results of this analysis showed impaired astro- and neurogenesis in both types of organoids (unguided and cortical), including a lack of cells acquiring the astrocyte fate, and an increased abundance of cells differentiating into lineages other than neuroectodermal. The results also suggested dysregulation of extracellular matrix, membrane, and cytoskeleton components, which might have also affected their differentiation trajectories.
 
Overall design The AxD cell line with a GFAP (R239C) mutation originated in Alexander disease patient fibroblasts, and an isogenic control cell line was prepared by mutation correction with CRISPR/Cas9, as described previously (Battaglia et al. 2019). 3D organoids were prepared using either unguided neural protocol (resulting in more diverse cell composition) and more targeted cortical protocol (DUAL SMAD inhibition directing cells towards cortical lineage). Organoids were harvested after 165 days in culture, with a variety of cell types including astrocytes present at this stage. Fixed single-cell suspensions from four samples (unguided control and AxD, cortical control and AxD) were prepared with 10X Genomics pipeline and scRNA-seq was performed to investigate changes in cell type composition, gene expression, and cell-cell interaction between the AxD cell line and controls.
 
Contributor(s) Matusova Z, Dykstra W, de Pablo Y, Zetterdahl O, Canals I, van Gelder CA, Vos HR, Perez-Sala D, Kubista M, Abaffy P, Ahlenius H, Valihrach L, Hol EM, Pekny M
Citation(s) 39308436
Submission date Mar 08, 2024
Last update date Sep 26, 2024
Contact name Zuzana Matusova
E-mail(s) zuzana.matusova@ibt.cas.cz
Organization name Institute of Biotechnology of the Czech Academy of Sciences
Department Laboratory of Gene Expression
Street address Prumyslova 595
City Vestec
ZIP/Postal code 25250
Country Czech Republic
 
Platforms (1)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (4)
GSM8136543 CTX CTRL
GSM8136544 CTX AxD
GSM8136545 UNG CTRL
This SubSeries is part of SuperSeries:
GSE261158 Aberrant neurodevelopment in human iPS cell-derived models of Alexander disease.
Relations
BioProject PRJNA1085644

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE261157_metadata_CER.csv.gz 795.9 Kb (ftp)(http) CSV
GSE261157_metadata_Ctx.csv.gz 508.3 Kb (ftp)(http) CSV
GSE261157_preprocessed_data.txt.gz 138.3 Mb (ftp)(http) TXT
GSE261157_processed_data_CER.txt.gz 715.3 Mb (ftp)(http) TXT
GSE261157_processed_data_Ctx.txt.gz 497.7 Mb (ftp)(http) TXT
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Raw data are available in SRA

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