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SRX10417552: GSM5201851: fetal lungs, ILRA-blockade-1; Macaca mulatta; RNA-Seq
2 ILLUMINA (Illumina NovaSeq 6000) runs: 468.4M spots, 59.5G bases, 18.1Gb downloads

Submitted by: NCBI (GEO)
Study: Single-cell RNA-Seq of premature Rhesus macaques lungs with intra-uterine inflammation and therapuetic blockade
show Abstracthide Abstract
Intrauterine inflammation/infection (IUI), which is present in up to 40% of premature births, leads to elevated levels of pro-inflammatory mediators and microbial products within the amniotic fluid, which come in close contact to fetal mucosae. Yet, knowledge on the fetal mucosal responses to IUI exposure remains limited. To address these questions, we used a non-human primate model of IUI, in which pregnant Rhesus macaques received intra-amniotic (IA) LPS, compared with saline IA. We found that IA LPS exposure induced a robust and rapid inflammation of the fetal lung. Overall design: Single-cell RNA-Seq was performed in the premature Rhesus macaques lung in the presence and absence of LPS. Therapuetic intervention was tested in LPS animals with IL-1R, TNF-alpha or combination blockade.
Sample: fetal lungs, ILRA-blockade-1
SAMN18435253 • SRS8538504 • All experiments • All runs
Organism: Macaca mulatta
Library:
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: The fetal lung was removed, and left lobe was processed into single cell suspensions as described previously 56. The large airways were removed and approximately ~500mg of airway free tissue was collected in a gentleMACS C-tube (Miltenyi Biotec, Auburn, CA) and 5mL digest buffer was added and placed on a gentleMACS octo dissociator for programmed runs. Following dissociation, the cell suspension was passed through a 100µm filter and washed with PBS. After washing, cells underwent red cell lysis (eBioscience, San Diego, CA) along with another pass through a 40um filter after neutralization. ~50,000 cells per lung were submitted for single cell sequencing at the Cincinnati Children's Hospital Medical Center DNA Sequencing and Genotyping Core. Approximately ~16,000 cells were loaded into one channel of the Chromium system using the 3 prime v3 single cell reagent kit (10X Genomics, Pleasanton, CA). Following capture and lysis, cDNA was synthesized and amplified as per the manufacturer's protocol (10X Genomics). The amplified cDNA was used to construct Illumina sequencing libraries that were each sequenced using an Illumina HiSeq 4000 machine.
Experiment attributes:
GEO Accession: GSM5201851
Links:
Runs: 2 runs, 468.4M spots, 59.5G bases, 18.1Gb
Run# of Spots# of BasesSizePublished
SRR14041295233,392,02529.6G9Gb2021-09-27
SRR14041296234,985,72829.8G9.1Gb2021-09-27

ID:
13735703

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