NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE109753 Query DataSets for GSE109753
Status Public on Jun 14, 2018
Title The fate of CD8+ T cells during infection is linked to their developmental origin [VirtualMemory_and_TrueNaïve_timestamp]
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary During immune ontogeny the thymus is colonized by distinct waves of hematopoietic stem cells that give rise to unique lineages of immune cells. In this report, we asked whether the developmental origin of CD8+ T cells influences their response to infection later in adulthood. To answer this question, we developed a system to ‘timestamp’ CD8+ T cells in situ at various stages of development (1d and 28d) and examined their behavior after post-thymic differentiation. We found that neonatal-derived CD8+ T cells have an intrinsic propensity to become virtual memory cells prior to infection and are the first cells to proliferate and become effectors after microbial challenge. These data indicate that there are developmental layers in the adult CD8+ T cell response to infection and that the heterogeneity in the effector pool is linked to the variation in the developmental origins of the responding cells. This dataset profiles gene expression in 1day- and 28day-timestamped virtual memory (CD44hi) and "true naive" (CD44 lo) CD8+ T cells in cells that had undergone the same amount of post-thymic maturation (4 weeks, transgenic mice, different sorts).
 
Overall design Gene expression profiling of virtual memory (CD44hi) and "true naïve" (CD44lo) CD8+ T cells (gBT-I TCR transgenic) after 4 weeks of post-thymic maturation, comparing three types of samples: virtual memory cells made at 1 day or 28 days of life, and true naïve cells made at 28 days of life (each in duplicate).
 
Contributor(s) Smith N, Rudd B, Grenier J
Citation(s) 29909981
Submission date Jan 28, 2018
Last update date Mar 25, 2019
Contact name Jennifer K Grenier
Organization name Cornell University
Department Biomedical Sciences
Lab Biotechnology Building rm 333
Street address 526 Campus Rd
City Ithaca
State/province NY
ZIP/Postal code 14853
Country USA
 
Platforms (1)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (6)
GSM2966336 Virtual memory CD8 cells timestamped at day 1, rep 1
GSM2966337 Virtual memory CD8 cells timestamped at day 1, rep 2
GSM2966338 Virtual memory CD8 cells timestamped at day 28, rep 1
This SubSeries is part of SuperSeries:
GSE97802 The fate of CD8+ T cells during infection is linked to their developmental origin
Relations
BioProject PRJNA431918
SRA SRP131622

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
GSE109753_gene_exp.diff.gz 1.5 Mb (ftp)(http) DIFF
GSE109753_genes.read_group_tracking.txt.gz 1.3 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap