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Status |
Public on Nov 02, 2022 |
Title |
Stromal inflammation is a targetable driver of hematopoietic aging [droplet-based scRNAseq] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
To investigate global changes in the structure of the bone marrow niche with age, we performed droplet-based scRNAseq (10X Genomics) of unfractionated endosteal and central marrow stromal cells (Ter119-/CD45-). 8,735 cells passed QC, and hematopoietic clusters of cells were excluded based on marker gene expression, leaving 2359 cells distributed across 9 distinct clusters for final presentation.
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Overall design |
Endosteal and central marrow stromal cells from the bone marrow of young (10 weeks) and old (24 months) wild-type C57BL/6 mice were isolated by flow cytometry and subjected to droplet-based scRNAseq (10X Genomics).
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Contributor(s) |
Verovskaya EV, Mitchell CA, Calero-Nieto FJ, Wang X, Gottgens B, Passegue E |
Citation(s) |
36650381 |
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Submission date |
Mar 09, 2021 |
Last update date |
Feb 02, 2023 |
Contact name |
Emmanuelle Passegue |
E-mail(s) |
ep2828@cumc.columbia.edu
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Organization name |
Columbia University Irving Medical Center
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Department |
Columbia Stem Cell Initiative
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Street address |
650 W 168th St
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City |
New York |
State/province |
NY |
ZIP/Postal code |
10032 |
Country |
USA |
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Platforms (1) |
GPL21103 |
Illumina HiSeq 4000 (Mus musculus) |
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Samples (4)
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This SubSeries is part of SuperSeries: |
GSE169162 |
Stromal niche inflammation mediated by IL-1 signaling is a targetable driver of hematopoietic aging |
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Relations |
BioProject |
PRJNA708338 |
SRA |
SRP310000 |