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SRX24126789: GSM8182735: NC_01; Rattus norvegicus; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 86.3M spots, 25.9G bases, 9Gb downloads

External Id: GSM8182735_r1
Submitted by: First Clinical College, Shandong University of Traditional Chinese Medicine
Study: CLCF1/NF-?B Signaling Pathway Regulates Macrophage Efferocytosis to Ameliorate Neural Damage and Cognitive Dysfunction After CO Poisoning.
show Abstracthide Abstract
Severe carbon monoxide (CO) poisoning can cause structural damage to the nervous system, leading to long-term cognitive dysfunction in patients. Correctly terminating the inflammatory response caused by neuronal damage is a prerequisite for tissue repair. Macrophages can clear the cell corpses/fragments caused by brain injury through efferocytosis, and produce cytokines to coordinate the immune response, promoting neuronal repair and regeneration. However, in the microenvironment of the nervous system affected by CO poisoning, the function of macrophages is inhibited. Our research found that CLCF1 can regulate the secretion of cytokines such as TNF-a, IL-1ß, and IL-10 through the NF-?B signaling pathway, thereby affecting neural cell repair and regeneration. Simultaneously, CLCF1 can regulate the efferocytosis function of macrophages, thus controlling the degree of inflammation and assisting in the repair of the damaged nervous system. In experiments, it was observed that targeting the regulation of macrophage CLCF1 expression led to improvements in memory, learning, and motor abilities in rats poisoned with CO. Overall design: Rats were used to create an acute carbon monoxide (CO) poisoning model, following the method described by Li et al.[1]. The rats were placed in a sealed experimental chamber and initially inhaled CO gas with a concentration of 1000 ppm for 40 minutes; this was followed by inhalation of CO gas at a concentration of 3000 ppm for 20 minutes. The model was considered successful for acute severe CO poisoning if the rats exhibited symptoms of impaired consciousness accompanied by high carboxyhemoglobin (HbCO) concentrations (>60%). Brain tissue cell suspensions were extracted from three CO-poisoned rats and three normal control (NC) group rats for single-cell sequencing. Gel beads containing barcode sequences were mixed with the samples and combined with oil surfactants to form Gel Bead-In-Emulsions (GEMs). The GEMs were collected into a reservoir for constructing 10x single-cell transcriptome libraries. An Illumina NovaSeq PE150 sequencing strategy was employed, targeting 50,000-100,000 reads per cell, corresponding to 15-30M data points per cell. Each experimental group was repeated three times to verify the reliability of the results. The raw data were mapped to the Rnor_6.0 rat reference genome using CellRanger (10x Genomics).
Sample: NC_01
SAMN40722938 • SRS20912260 • All experiments • All runs
Library:
Name: GSM8182735
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC SINGLE CELL
Selection: cDNA
Layout: PAIRED
Construction protocol: Under sterile conditions, fresh rat brain tissue is first placed in pre-cooled phosphate-buffered saline (PBS) and transferred to a sterile workbench for processing. Then, the tissue is digested with PBS containing 0.25% trypsin and 0.1% DNAse I, gently shaking in a 37°C water bath for 15-30 minutes, with the time adjusted based on the actual digestion results. To terminate digestion, an equal volume of DMEM culture medium containing 10% fetal bovine serum (FBS) is added, and the mixture is filtered through a 40-70μm cell strainer to remove undigested tissue and cell clumps. Subsequently, the cells are centrifuged at 1300 rpm at 4°C for 5 minutes and resuspended in pre-cooled PBS, repeating the washing until the supernatant is clear. Cell density is measured using a cell counting plate or an automatic cell counter, and cell viability is assessed using a 0.4% trypan blue exclusion test, ensuring a viability rate of over 90%. This series of meticulous operations aims to obtain high-quality single-cell suspensions from rat brain tissue, laying the foundation for subsequent single-cell transcriptome analysis. The key technology of the 10x Genomics Chromium™ system leverages millions of unique Barcodes to tag different samples (long DNA molecules/single cells). Initially, Gel beads containing Barcode sequences are mixed with a mixture of samples and enzymes, then combined with an oil surfactant to form GEMs (Gel Bead-In-Emulsions, meaning oil droplets encapsulating Gel beads, samples, and enzyme mixture). The GEMs are collected and flow into a reservoir, where Gel beads dissolve to release Barcode sequences, starting the sample tagging process. The products containing Barcode information from each droplet are mixed together to construct a standard sequencing library.
Runs: 1 run, 86.3M spots, 25.9G bases, 9Gb
Run# of Spots# of BasesSizePublished
SRR2852598986,301,01425.9G9Gb2024-04-07

ID:
32437291

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