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Sample GSM4666932 Query DataSets for GSM4666932
Status Public on Jul 09, 2023
Title AAV-GFAP-Gq-DREADD_106
Sample type SRA
 
Source name Hippocampus and Cortex
Organism Mus musculus
Characteristics strain: C57BL/6J
tissue: brain
group: Saccharin
genotype: Gq-DREADD
Treatment protocol Mouse samples 104 and 105 were given CNO in their drinking water for 8 weeks, while sampples 106 and 107 were given saccharin in their drinking water
Extracted molecule polyA RNA
Extraction protocol 8-week old C57BL/6J male mice were injected the AAV-GFAP-hM3D(Gq)-mCherry virus in the hippocampus and cortex using a stereotaxic instrument. They were given either CNO or Saccharin for 8 weeks in their drinking water. Upon tissue collection, the mice were euthanized and perfused using ice-cold PBS. The hippocampal and cortical tissue containing the virus was dissected, minced with a razor blade and incubated for 30 min in ice-cold Accutase at 4 degrees C. The dissociated tissue was centrifuged at 300g for 10 min at 4°C. The pellet was resuspended in ice-cold Hanks’ Balanced Salt solution (Life Technologies, Cat. No. 14025-092) and triturated with a 15 mL serological pipette. This step was repeated until the entire tissue was dissociated. Next, the sample was filtered first through a 70 μm cell strainer, followed by a 40 μm cell strainer. The cells were centrifuged at 300g for 5 min at 4°C. Myelin removal was performed following the Miltenyi’s Myelin Depletion Protocol. In short, the pellet obtained during cell isolation was resuspended in magnetic-activated cell sorting (MACS) buffer (0.5% BSA in PBS, Thermofisher, Cat. No. AM2618), myelin removal beads (Miltenyi Biotec, Cat. No. 130-096-733) were added, and the solution was incubated for 15 min at 4°C. The cells were centrifuged at 300g for 10 min at 4°C, the pellet was resuspended in MACS buffer and the solution was passed through LS columns (Miltenyi Biotec, Cat. No. 130-042-401). The cells were centrifuged at 300g for 15 min at 4°C, the pellet was resuspended in MACS buffer, centrifuged again at 300g for 15 min at 4°C and resuspended in PBS containing 0.01% BSA. The obtained single cells were subjected to droplet-based single cell RNA sequencing. The 10x Genomics ChromiumTM Single Cell 3’ Library & Gel Bead Kit v2 was used per manufacturer’s instructions. The libraries were sequenced on an Illumina NovaSeq 6000 SP.
10x Genomics ChromiumTM Single Cell 3’ Library & Gel Bead Kit v2 protocol
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Description single cell RNA sequencing
Data processing quality control, Cell Ranger Single Cell Software Suite (v.3.0.2)
barcode processing, Cell Ranger Single Cell Software Suite (v.3.0.2)
single-cell 3' gene counting, Cell Ranger Single Cell Software Suite (v.3.0.2)
alignment, Cell Ranger Single Cell Software Suite (v.3.0.2)
Genome_build: mm10
Supplementary_files_format_and_content: Filtered matrix of gene by cell expression, file with barcodes and file with expressed genes. Files are ready to be imported to Seurat package
 
Submission date Jul 10, 2020
Last update date Jul 09, 2023
Contact name Stephanie Philtjens
E-mail(s) sphiltje@iu.edu
Phone 3172786353
Organization name Indiana University School of Medicine
Street address 320 W. 15th Street, NB Bldg Rm 103
City Indianapolis
State/province Indiana
ZIP/Postal code 46202
Country USA
 
Platform ID GPL24247
Series (1)
GSE154208 Chemogenetic activation of astrocytes in the hippocampus and cortex changes the transcriptome of microglia
Relations
BioSample SAMN15504371
SRA SRX8707786

Supplementary file Size Download File type/resource
GSM4666932_106_barcodes.tsv.gz 59.9 Kb (ftp)(http) TSV
GSM4666932_106_features.tsv.gz 272.8 Kb (ftp)(http) TSV
GSM4666932_106_matrix.mtx.gz 38.8 Mb (ftp)(http) MTX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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