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SRX1539837: GSM2043746: 130115 0629-453 Acute ILC2; Homo sapiens; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 3.4M spots, 218.8M bases, 86.4Mb downloads

Submitted by: NCBI (GEO)
Study: Time course RNA-Seq of Innate Lymphoid Cells in Early Acute HIV Infection
show Abstracthide Abstract
We apply RNA-seq to limited populations of Innate Lymphoid Cells type 2 and type 3 (ILC2s and ILC3s, respectively) in human individuals infected with acute HIV in the FRESH study. We measured the whole transcriptome of ILC2s and ILC3s in both untreated (n=2) and ART treated (n=2) individuals over the course of infection, in order to compare these populations at key points during infection, namely: viral detection, peak viremia, and weeks past peak viremia (6-7 weeks post detection). Lacking true biological replicates, HIV- patients in the same study (n=9) were used as replicates to conduct Differential Expression (DE) analysis between time points in both ILC2s and ILC3s on a patient by patient basis. In untreated patients, ILC2s and ILC3s differentially expressed genes associated with apoptosis and cell death between peak viremia and viral detection, while ART treated patients' ILC2s and ILC3s demonstrated a mitigated response. Comparing 6-7 weeks after detection with peak viremia revealed a relative decrease in genes associated in cell death in untreated patients, while ART treated patients showed varied responses where several DE genes were associated with immune response. Overall design: RNA-seq of two Innate Lymphoid Cell populations in 2 HIV+ untreated patients, 2 HIV+ ART treated patients, and 9 HIV- patients (control, replicates).
Sample: 130115 0629-453 Acute ILC2
SAMN04432855 • SRS1256313 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Due to low cell counts, lysates were treated as single cells in an adapted SMART-Seq II protocol (Trombetta et al., Current Protocols in Molecular Biology, 2014, 107:II:4:22). Briefly, mRNA was extracted from lystates using SPRI beads and then reverse transcribed and amplified using a poly-adenylated RT primer and template switching SMART oligo. Library construction followed from the protocol above (Trombetta et al.,).
Experiment attributes:
GEO Accession: GSM2043746
Links:
Runs: 1 run, 3.4M spots, 218.8M bases, 86.4Mb
Run# of Spots# of BasesSizePublished
SRR31115983,418,792218.8M86.4Mb2016-02-03

ID:
2182930

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