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SRX17109173: GSM6469639: Stab 6; Rattus norvegicus; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 540.3M spots, 96.2G bases, 30.6Gb downloads

External Id: GSM6469639_r1
Submitted by: Biomedical Engineering, Washington University in St. Louis
Study: Single Cell RNA-Sequence Analyses Reveal Uniquely Expressed Genes and Heterogeneous Immune Cell Involvement in the Rat Model of Intervertebral Disc Degeneration
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Purpose: We used single-cell RNA-sequencing analysis of degenerating tissues of the rat IVD following lumbar disc puncture Methods: Two control, uninjured IVDs (L2-3, L3-4) and two degenerated, injured IVDs (L4-5, L5-6) from each animal were examined either at the two- or eight-week post-operative time points. The cells from these IVDs were extracted and transcriptionally profiled at the single-cell resolution Results: Unsupervised cluster analysis revealed the presence of four known cell types in both non-degenerative and degenerated IVDs based on previously established gene markers: IVD cells, endothelial cells, myeloid cells, and lymphoid cells. As a majority of cells were associated with the IVD cell cluster, sub-clustering was used to further identify the cell populations of the nucleus pulposus, inner and outer annulus fibrosus Conclusions: . Differential gene expression analysis revealed multiple distinct cell types from the myeloid and lymphoid lineages, most notably macrophages and B lymphocytes, and demonstrated a high degree of immune specificity during degeneration. In addition to the heterogenous infiltrating immune cell populations in the degenerating IVD, the increased number of cells in the AF sub-cluster expressing Ngf and Ngfr, encoding for p75NTR, suggest that NGF signaling may be one of the key mediators of the IVD crosstalk between immune and neuronal cell populations Overall design: Rats (n=8, male Sprague-Dawley, 8 weeks) underwent surgery for retroperitoneal exposure of the L4-L6 -lumbar spine. The L4-5 and L5-6 IVDs each received a single stab injury via a 27G needle and allowed to recover postoperatively for either 2 (n=4) or 8 weeks (n=4). Animals were then euthanized and the IVD tissues were isolated and pooled from L4-5 and L5-6 (LDP= lumbar disc puncture), or from L2-3 and L3-4 (CON= control) via dissection, with care to remove unwanted peripheral tissues by microdissection. The separated tissue was digested via pronase and collagenase (< 4h total) to obtain IVD cells (51,655 and 60,626 total cell yield from CON and LDP respectively).
Sample: Stab 6
SAMN30351839 • SRS14684608 • All experiments • All runs
Library:
Name: GSM6469639
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Intervertebrals discs (IVDs) were harvested and tissue was isolated at room temperature; tissue was then immediately transferred into the digestion medium 0.3% pronase and 0.2% Typle 2 collagenase (< 4h total) to obtain IVD cells at 37 degrees Celsius. Once the IVDs were digested into a single cell suspension, the cells were immediately put on ice and expedited to the Genome Technology and Access Center at Washington University in St. Louis. The input samples were submitted to the Washington University Genome Technology Access Center to obtain and sequence the cDNA libraries (10XGenomics, 3'v3.1; Illumina NovaSeq S4) according to established protocols
Runs: 1 run, 540.3M spots, 96.2G bases, 30.6Gb
Run# of Spots# of BasesSizePublished
SRR21095522540,255,54796.2G30.6Gb2022-08-19

ID:
23902565

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