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Sample GSM6616797 Query DataSets for GSM6616797
Status Public on Oct 01, 2023
Title WT-STAT5-MSC
Sample type SRA
 
Source name bone marrow
Organism Mus musculus
Characteristics tissue: bone marrow
cell type: stromal
genotype: Vav1-Cre/+STAT5ab+/+
Extracted molecule total RNA
Extraction protocol Bone marrow cells were harvested from the femurs and tibias of 4 Vav1-Cre/+ or Vav1-Cre/+/STAT5abflox/flox (8-12 weeks). The cells were lineage depleted using a mouse lineage cell depletion kit (Miltenyi Biotech, Auburn, CA) and stained with FITC-labeled lineage antibodies (Gr-1, Mac-1, B220, Ter119, CD3, CD4, CD8a), anti-c-Kit-APC, anti-Sca-1-PE-Cy7 (Thermo Fisher Scientific, Norcross, GA), and dead cells were excluded by staining with propidium iodide dye. KLS cells were sorted using BD FACSAria III Cell Sorter. For sorting bone marrow stromal cells, cells were isolated as described [reference: Houlihan, D.D.; Mabuchi, Y.; Morikawa, S.; Niibe, K.; Araki, D.; Suzuki, S.; Okano, H.; Matsuzaki, Y. Isolation of mouse mesenchymal stem cells on the basis of expression of Sca-1 and PDGFR-alpha. Nature protocols 2012, 7, 2103-2111, doi:10.1038/nprot.2012.125]. Briefly, mouse bones (tibia and femur) were isolated and cleaned from 6-8 weeks old mice, then were crushed and cut into tiny pieces with sterile scissors, incubated them in 20 ml of preheated DMEM plus 0.2% (wt/vol; 40 mg) collagenase at 110 rpm at 37°C for 1 hour ). The cell suspension was filtered through a 70-μm cell strainer and bone fragment was further crushed and washed to liberate cells out of the bone into solution. CD45+ cells were depleted with mouse CD45 microbeads from Miltenyi Biotech( Auburn, CA) and stained with anti-Ter119-PE (BD Biosciences, San Jose, CA), anti-CD45-FITC, Anti-CD71-Alexa 700, Anti-Sca-1-PE-Cy7 and Anti-CD140a-APC (Thermo Fisher Scientific, Norcross, GA). CD45negTer119-/lowCD71-Sca-1+CD140a+  cells were sorted using BD FACSAria III Cell Sorter. Sorted cells were immediately processed for single cells RNA sequencing.
Tissue derived single cells were loaded onto the 10X Chromium Controller targeting 3000-6000 cells/sample. Single cell capture, barcoding, GEM-RT, clean-up, cDNA amplification and library construction were performed according to the manufacturers’ instructions for v3 chemistry using 10x Genomics Single Cell 5’ Chromium Chip B kit (PN-1000074) and Chromium Single Cell 3’ GEM, Library & Gel Bead Kit v3 (PN 1000092). Final gene expression library pools were sent to Genewiz (South Plainfield, NJ) and sequenced on an Illumina’s Novaseq6000 instrument with a targeted sequencing depth of 150,000 reads/cell.
 
Library strategy RNA-Seq
Library source transcriptomic single cell
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing Raw sequencing reads were processed by Cell Ranger (10x Genomics) to generate gene expression count matrices for every sample (wild type and knockout samples for KLS and MSC respectively). After sequence alignment to GRCm38/mm10 mouse reference genome, UMI (Unique Molecular Identifiers) counts for each gene per cell formed the gene expression count matrices.
Assembly: GRCm38/mm10
Supplementary files format and content: Cell Ranger output files of barcodes, genes and count matrix
 
Submission date Oct 05, 2022
Last update date Oct 01, 2023
Contact name Peng Qiu
E-mail(s) peng.qiu@bme.gatech.edu
Organization name Georgia Institute of Technology
Street address 950 Atlantic Dr. NW
City Atlanta
State/province GA
ZIP/Postal code 30332
Country USA
 
Platform ID GPL24247
Series (1)
GSE214857 Stromal STAT5-mediated trophic activity regulates hematopoietic multipotent progenitor niche factors
Relations
BioSample SAMN31166757
SRA SRX17806600

Supplementary file Size Download File type/resource
GSM6616797_WT-MSC-barcodes.tsv.gz 3.6 Kb (ftp)(http) TSV
GSM6616797_WT-MSC-genes.tsv.gz 244.7 Kb (ftp)(http) TSV
GSM6616797_WT-MSC-matrix.mtx.gz 2.2 Mb (ftp)(http) MTX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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