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Sample GSM8389459 Query DataSets for GSM8389459
Status Public on Jul 11, 2024
Title Human donor 1, baseline, scRNAseq
Sample type SRA
 
Source name Peripheral Blood
Organism Homo sapiens
Characteristics tissue: Peripheral Blood
cell line: primary human iNKT
cell type: iNKT cells
strain: healthy, male
age: 26 year old
treatment: Freshly isolated
Extracted molecule total RNA
Extraction protocol iNKT scRNA-seq libraries were prepared from both freshly purified iNKTs and matched iNKT cellular products at the end of the expansion. Each library was generated from 10,000 cells with viability >90% as confirmed by Trypan Blue. Human and canine iNKT cells were immunomagnetically purified from PBMCs using PE-conjugated human CD1d tetramers loaded with the αGC analogue PBS57 (NIH Tetramer Core Facility) and anti-PE microbeads (Miltenyi Biotec). After purification, cells were resuspended in PBS with 0.04% w/v BSA for scRNAseq library preparation. For canine and human iNKT expansion, CD1d+ artificail antgen presenting cells were pulsed overnight with αGC 100ng/ml (KRN7000, Cayman Chemicals) and irradiated on the following day (i-aAPC, 10,000 rad). Purified iNKT cells were seeded in round-bottom 96-wells at 1:1 ratio with i-aAPC and maintained at 38-38.8˚C in IMDM medium containing 25 mM Hepes (Gibco), 10% heat inactivated FBS (Atlanta Biologicals), 1% Pen/Strep (Gibco), 1% glutamax (Gibco), 1% non-essential amino acids (Gibco), 1mM sodium pyruvate (Gibco) and 50µM 2-Mercaptoethanol (Gibco). Cross-reactive human IL-15 (Miltenyi Biotec, 30 ng/ml) was supplemented 24-48h after stimulation. Human IL-15 and human IL-2 (Miltenyi Biotec, 30 ng/ml and 100 IU/ml respectively), human IL-7 and human IL-21 (Peprotech, 10 ng/ml) were added 6 days after stimulation and then every other day. To generate clinical scale iNKT products, iNKTs were restimulated twice, i.e., during the second and third week of expansion.8 days after the last restimulation, 10,000 iNKTs were resuspended in PBS with 0.04% w/v BSA for scRNA-seq library preparation.
Library was performed according to the manufacter’s instructions (single cell 3’ v2 protocol, 10x Genomics). Briefly, iNKT cells were resuspended in the master mix and loaded together with partitioning oil and gel beads into the chip to generate the gel bead-in-emulsion (GEM). The poly-A RNA from the cell lysate contained in every single GEM was retrotranscripted to cDNA, which contains an Ilumina R1 primer sequence, Unique Molecular Identifier (UMI) and the 10x Barcode. The pooled barcoded cDNA was then cleaned up with Silane DynaBeads, amplified by PCR and the apropiated sized fragments were selected with SPRIselect reagent for subsequent library construction. During the library construction Ilumina R2 primer sequence, paired-end constructs with P5 and P7 sequences and a sample index were added.
 
Library strategy RNA-Seq
Library source transcriptomic single cell
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Description 10x Genomics
Data processing The demultiplexing, barcode processing, gene counting and aggregation were made using the Cell Ranger software v6.0.2 (https://support.10xgenomics.com/single-cell-gene-expression/software/pipelines/latest/what-is-cell-ranger)
Assembly: CanFam6 and GRCh38
Supplementary files format and content: Tab-separated values files and matrix files
 
Submission date Jul 10, 2024
Last update date Jul 11, 2024
Contact name Antonia Rotolo
E-mail(s) antonia.rotolo@pennmedicine.upenn.edu
Phone 2674696507
Organization name University of Pennsylvania
Street address 3900 Chestnut Street, Apt 521
City Philadelphia
State/province PA
ZIP/Postal code 19104
Country USA
 
Platform ID GPL18573
Series (1)
GSE229457 Comparative gene expression profile of canine and human invariant Natural Killer T (iNKT) cells at single cell level [scRNA-seq]
Relations
BioSample SAMN42397074
SRA SRX25267585

Supplementary file Size Download File type/resource
GSM8389459_H1B.barcodes.tsv.gz 52.2 Kb (ftp)(http) TSV
GSM8389459_H1B.features.tsv.gz 325.6 Kb (ftp)(http) TSV
GSM8389459_H1B.matrix.mtx.gz 58.1 Mb (ftp)(http) MTX
SRA Run SelectorHelp
Raw data are available in SRA

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