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SRX7182785: GSM4176347: GFPpos time 0 rep 3; Mus musculus; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 30.4M spots, 9.1G bases, 3.9Gb downloads

Submitted by: NCBI (GEO)
Study: Sentinel p16INK4a+ cells in the basement membrane form a reparative niche in the lung [RNA-Seq]
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We collected freshly sorted mesenchyme (live CD45-Epcam-CD31-PDGFRa+GFP- or GFP+) from dissociated lung tissue of INKBRITE animals to characterize the transcriptome difference between p16INK4a+ vs p16INK4a- cells at homeostasis and during injury. We used fluorescence activated cell sorting (FACS) to exclude immune (CD45+), epithelial (Epcam+), and endothelial (CD31+) cells and positively select for PDGFRa+ mesenchyme. Cells were sequenced at a depth of average of 45 million reads/sample. The results revealed an increase of senescence associated secretory phenotype (SASP) signature in p16INK4+ cells that becomes refined after injury. We found the expression of an epithelial growth factor epiregulin (ereg) increased in p16INK4a+ cells after injury suggesting a possible role of p16INK4a+ senescence during regeneration of lung epithelium. Overall design: The INKBRITE animals we constructed by inserting a tandem cassette of H2B-GFP expressed in frame with the p16INK4A gene product in the murine Cdkn2a locus into a bacterial artificial chromosome (BAC). The expression of multiple copies of a stable fluorescent protein is driven by p16INK4A promoter. Whole adult murine lung tissue was dissociated to single cells stained with DAPI for live cells selection and subjected to FACS to select live CD45-Epcam-CD31-PDGFRa+GFP+ (p16INK4a+) and CD45-Epcam-CD31-PDGFRa+GFP- (p16INK4a-) cells. We collected p16INK4a+ and – cells from 3 INKBRITE naphthalene injured animals and 3 solvent controls. The RNA was extracted and shipped to GENEWIZ company for sequencing o the Illumina HiSeq instrument. Raw sequence data (.bcl files) generated from Illumina HiSeq was converted into fastq files and de-multiplexed using Illumina's bcl2fastq 2.17 software
Sample: GEO accession GSM4176347 is currently private and is scheduled to be released on Nov 16, 2022.
SAMN13326861 • SRS5689016 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Whole lung was dissected from the adult mouse and tracheally perfused with a digestion cocktail of Collagenase Type I (225 U/ml, Thermo Fisher), Dispase (15 U/ml, Thermo Fisher) and Dnase (50 U/ml, Sigma) and removed from the chest. The lung was further diced with razor blades and the mixture was incubated for 45 mins at 37 ºC and vortexed intermittently. The mixture was then washed with FACS buffer (2% FBS in DMEM-F12). The mixture was passed through a 70 µm cell strainer and resuspended in RBC lysis buffer, before passing through a 40 µm cell strainer. Cells suspensions were incubated with the appropriate antibodies in FACS buffer for 30 min at 4 ºC and washed with FACS buffer. DAPI (0.2 µg/ml) was used to exclude dead cells. Doublets and dead cells were excluded based on forward scatter, side scatter and DAPI fluorescence. CD45-Epcam-CD31-PDGFRa+GFP- or CD45-Epcam-CD31-PDGFRa+GFP+ cells were sorted . Cells were sorted into FACS buffer. FACS analysis was performed by FACSDiva (BD Biosciences). The RNA was extracted by PicoPure RNA Isolation Kit (Applied Biosystems) from the sorted cells, and the amount and quality of extracted RNA was measured by RNA 6000 Pico Kit (Agilent). The Bulk RNA-seq was done in GENEWIZ. RNA libraries were prepared for sequencing using standard Illumina protocols
Experiment attributes:
GEO Accession: GSM4176347
Links:
Runs: 1 run, 30.4M spots, 9.1G bases, 3.9Gb
Run# of Spots# of BasesSizePublished
SRR1049369530,386,3009.1G3.9Gb2022-11-10

ID:
9435519

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