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Series GSE272271 Query DataSets for GSE272271
Status Public on Jul 16, 2024
Title Single-cell RNA-seq of telencephalic organoids from healthy CTRL and HD (Huntington’s disease) hESC (RUES2) grown as mono-culture or co-culture of chimeric organoids
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Huntington's disease (HD) causes selective degeneration of striatal and cortical neurons, resulting in cell mosaicism of coexisting still functional and dysfunctional cells. The impact of non-cell autonomous mechanisms between these cellular states is poorly understood. Here we generated telencephalic organoids with healthy or HD cells, grown separately or as mosaics of the two genotypes. We used single-cell transcriptomics to test early HD selective cellular phenotypes by comparing healthy (CTRL) and pathologic (HD) telencephalic organoids at days 45 and 120 of differentiation. To test the influence and the interactions between healthy and HD cells, mosaic organoids composed of CTRL and HD cells juxtaposed within the same organoid were grown and analyzed by scRNAseq at day 120. Single-cell RNA sequencing revealed neurodevelopmental abnormalities in the ventral fate acquisition of HD organoids, confirmed by cytoarchitectural and transcriptional defects leading to fewer GABAergic neurons, while dorsal populations showed milder phenotypes mainly in the maturation trajectory. Healthy cells in mosaic organoids restored HD cell identity, trajectories, synaptic density, and communication pathways upon cell-cell contact while showing no significant alterations when grown with HD cells. These findings highlight cell-type-specific alterations in HD and beneficial non-cell autonomous effects of healthy cells, emphasizing the therapeutic potential of modulating cell-cell communication in disease progression and treatment.
 
Overall design At DIV 45, 6 individual organoids were independently sequenced for scRNAseq (3 per genotype: the CTRL with 20cag and the HD with 56cag). At DIV 120, 4 pools of 10 mosaic organoids each were collected for FACS sorting to separate the GFP and the TOM cell lines. The 4 pools derived from mono-culture organoids where GFP and TOM cells of the same genotype were grown together (20CAG-GFP with 20CAG-TOM and 56CAG-GFP with 56CAG-TOM) and co-culture organoids by co-culturing cells of different genotypes together (20CAG-GFP with 56CAG-TOM and 20CAG-TOM with 56CAG-GFP). After FACS we obtained and sequenced 8 independent samples. We then merged them as 4 biological conditions: “CTRL_mono” (CTRL cells grown alone); “CTRL_co” (CTRL cells that were grown in the presence of HD cells and then isolated); “HD_co” (HD cells that were grown in the presence of CTRL cells and then isolated); and “HD_mono” (HD cells grown alone, as for CTRL_mono).
 
Contributor(s) Galimberti M, Nucera MR, Bocchi VD, Conforti P, Vezzoli E, Cereda M, Maffezzini C, Iennaco R, Scolz A, Falqui A, Cordiglieri C, Cremona M, Espuny-Camacho I, Faedo A, Felsenfeld DP, Vogt TF, Ranzani V, Zuccato C, Besusso D, Cattaneo E
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Submission date Jul 15, 2024
Last update date Jul 16, 2024
Contact name Maura Galimberti
E-mail(s) maura.galimberti@unimi.it
Organization name University of Milan
Department Bioscience
Lab Cattaneo
Street address Francesco Sforza 35
City Milan
State/province Milan
ZIP/Postal code 20122
Country Italy
 
Platforms (1)
GPL20301 Illumina HiSeq 4000 (Homo sapiens)
Samples (14)
GSM8397568 control,co-culture,rep1
GSM8397569 HD,co-culture,rep1
GSM8397570 control,mono-culture,rep1
Relations
BioProject PRJNA1135995

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
GSE272271_D120matrix.tar.gz 119.6 Mb (ftp)(http) TAR
GSE272271_D45matrix.tar.gz 142.6 Mb (ftp)(http) TAR
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Raw data are available in SRA

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