|
| Status |
Public on Jul 23, 2024 |
| Title |
Control |
| Sample type |
SRA |
| |
|
| Source name |
spinal cord
|
| Organism |
Mus musculus |
| Characteristics |
tissue: spinal cord
gender: female
age: 2-3 months
strain: C57BL6/J
treatment: spinal cord injury + PBS
|
| Treatment protocol |
Before being assigned to surgery, the body weight of mice was assessed and mice lighter than 19 grams were removed. Mice were anesthetized with a ketamine (100 mg kg-1)–xylazine (10 mg kg-1) mixture. The hair on the back was shaved and cleaned with betadine and alcohol. A 15-mm midline skin incision was performed over the T6-T13 vertebra, and the connective and muscle tissues were bluntly dissected to expose the lamina. A laminectomy was performed using rongeurs at T9 to expose the dorsal spinal cord. The vertebral column was stabilized with angled clamps attached to the T7 and T12 and a calibrated contusion injury of the spinal cord was induced at T9 by an Infinite Horizon Impactor (IH-0400 Impactor Precision Systems and Instrumentation) at a force of 80K dynes. After the injury, the muscles and skin were sutured separately and mice were allowed to recover from anesthesia on heating pads. After recovering from anesthesia, mice were injected intra-subcutaneously with buprenorphine (0.05 mg kg-1) daily for the first three days. Water containing sulfamethoxazole and trimethoprime oral suspension (200 mg/ 40 mg L-1) was supplied. Soft food and nutra-gel diet (S5769-TRAY, Bio-Serv) were supplied daily. Bladders of all mice were manually voided twice a day during the experiments.
|
| Extracted molecule |
total RNA |
| Extraction protocol |
10x Genomics Chromium single-cell preparation.
NGS Illumina Next Seq.
|
| |
|
| Library strategy |
RNA-Seq |
| Library source |
transcriptomic single cell |
| Library selection |
cDNA |
| Instrument model |
Illumina NovaSeq 6000 |
| |
|
| Description |
RNA was isolated from the spinal cords of 4 mice.
total mRNA
3' RNAseq
|
| Data processing |
Illumina bcl2fastq software used for basecalling.
UMI count matrices generated using the Cellranger count pipeline 6.0.0. The output from the cellranger count pipeline has been uploaded as a folder containing count, barcode, and gene matrices.
Assembly: mm10
Supplementary files format and content: *.tar archives contain the raw UMI count matrices for each sample, as well as matrices with gene symbols and barcodes.
|
| |
|
| Submission date |
Oct 23, 2022 |
| Last update date |
Jul 23, 2024 |
| Contact name |
Jonathan Kipnis |
| Organization name |
Washington University in Saint Louis
|
| Department |
Pathology and Immunology
|
| Lab |
Kipnis Lab
|
| Street address |
4515 McKinley Ave
|
| City |
Saint Louis |
| State/province |
MO |
| ZIP/Postal code |
63110 |
| Country |
USA |
| |
|
| Platform ID |
GPL24247 |
| Series (2) |
| GSE216389 |
Engineered T cell therapy for central nervous system injury [CD45+ scRNA-seq] |
| GSE216391 |
Engineered T cell therapy for central nervous system injury |
|
| Relations |
| BioSample |
SAMN31422153 |
| SRA |
SRX17999846 |
