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| Status |
Public on Apr 25, 2022 |
| Title |
Immue cells from small intestine, cecum and colon of mouse old-1 |
| Sample type |
SRA |
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| Source name |
Lamina Propria
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| Organism |
Mus musculus |
| Characteristics |
cell type: immune cells
strain: C57BL6/J
age: old
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| Growth protocol |
4 Young (1x 8week, 2x 12week and 1x 20week) and 4 old (2x 90week, 1x 92week ,2x 108week) female wild-type C57BL6/J mice were group housed and maintained in a specific pathogen-free animal facility
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| Extracted molecule |
total RNA |
| Extraction protocol |
Immune cells were isolated from lamina propria: tissue (cleared of crypts) was chopped finely with a scalpel and then incubated in 3ml of 1mg/ml collagenase-D (Merck, Cat. 11088866001) and 1mg/ml DNaseI in RPMI medium (ThermoFisherScientific, Cat. 21875091) in 6 well plates in an incubator shaker (80rpm) (VWR, Cat. 444-0732) for 20min at 37°C. Tissue pipetted up and down several times with a cut p1000 tip. The supernatant was passed through a 100μm strainer into 5% FBS in RPMI. Leftover tissue incubated again twice in 3ml collagenase-D/DNaseI RPMI solution in an incubator shaker (80rpm) for 30min at 37°C, collecting filtered supernatant. After the third incubation, the remaining tissue was smashed with a syringe plunger on a Falcon 40μm cell strainer (Corning, Cat. 352340) and washed with 5% FBS/RPMI to collect the maximum number of cells. The supernatant was centrifuged at 300g, 4°C for 5min. The pellet was re-suspended in 40% percoll (Sigma-Aldrich, Cat. P1644-1L) in RPMI. The cell suspension was carefully pipetted over 80% percoll in a falcon tube in order to create a gradient. The falcon tubes were centrifuged at 1600g, RT for 20min (centrifuge break disabled). The immune cells formed a white ring on the border of the two percoll concentrations: they were collected carefully and washed with FSM (2% FBS in PBS). The suspension was centrifuged at 450g, 4°C for 5min. Resulting pellet was resuspended in FSM and transferred for staining.
The 10X Single Cell 3’ v2 or v3.1 reagent kit (10X Genomics) was used for cell partitioning, cDNA amplification and library construction.
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| Library strategy |
RNA-Seq |
| Library source |
transcriptomic |
| Library selection |
cDNA |
| Instrument model |
Illumina NextSeq 500 |
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| Description |
Single cell RNA sequencing
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| Data processing |
The fastq files are mapped against mm10.e87 genome following by counting the UMI and removing duplicates for single cells using 'cellranger count' (https://support.10xgenomics.com/single-cell-gene-expression/software/pipelines/latest/using/count ) with default parameters.
Genome_build: mm10.e87
Supplementary_files_format_and_content: The processed data is a seurat object saved in RDS file with assigned meta data in trascriptome matrix of intesine
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| Submission date |
Mar 22, 2021 |
| Last update date |
Apr 25, 2022 |
| Contact name |
Seyed Mohammd Mahdi Rasa |
| E-mail(s) |
[email protected]
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| Phone |
015258164616
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| Organization name |
Universitätsklinikum Schleswig-Holstein
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| Department |
Institut for Immunology
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| Lab |
Immunology (Prof. Sheffold)
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| Street address |
Michaelisstrasse 5
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| City |
Kiel |
| State/province |
Schleswig-Holstein |
| ZIP/Postal code |
24105 |
| Country |
Germany |
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| Platform ID |
GPL19057 |
| Series (1) |
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| Relations |
| BioSample |
SAMN18426378 |
| SRA |
SRX10412183 |
| Supplementary data files not provided |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data are available on Series record |
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