NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE227143 Query DataSets for GSE227143
Status Public on Apr 14, 2023
Title Restoring bone marrow niche function rejuvenates aged hematopoietic stem cells by reactivating the DNA Damage Response [1]
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary The bone marrow (BM) niche comprised of BM endothelial cells (BMECs) and LepR+ mesenchymal stromal cells (MSCs), plays a critical role in preserving the fitness of hematopoietic stem cells (HSCs). Aging is associated with defects in the BM niche that impair their ability to support HSC activity. However, mechanisms underlying age-related defects in the BM niche remain poorly understood. In this study, we identify BM niche derived Netrin-1 (NTN1) as a critical regulator of BM niche cell fitness during aging. Conditional deletion of NTN-1 specifically within BM MSCs or BMECs of young mice resulted in premature aging phenotypes within the BM niche including increased vascular leakiness, hypoxia, DNA damage and adiposity. On the other hand, supplementation of aged mice with NTN1 resulted in restoration of these hallmark niche defects and a rejuvenation of HSC activity. Mechanistically, we identify NTN1 as a critical regulator of DNA Damage Response (DDR) within BM niche cells and HSCs. In this experiment, RNA Seq analysis was performed on BM MSCs and BMECs following conditional deletion of NTN1 within BMECs or MSCs to characterize transcriptional alterations within BM niche cells resulting from a deficiency of niche derived NTN1.
 
Overall design Comparative gene expression profiling analysis of BM niche cells (BM MSCs and BMECs) following deletion of NTN1 in LepR+ MSCs (LepR_NTN1KO) or BMECs (CDH5_NTN1KO) of young (4-6 month old) mice.
 
Contributor(s) Redmond D, Ramalingam P, Poulos M, Butler J
Citation(s) 37037837
Submission date Mar 11, 2023
Last update date May 03, 2023
Contact name David Redmond
E-mail(s) dar2042@med.cornell.edu
Organization name Weill Cornell Medicine
Street address 1300 York Avenue
City New York
State/province New York
ZIP/Postal code 10065
Country USA
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (40)
GSM7092346 LepR_Control_BMEC_1
GSM7092347 LepR_Control_BMEC_2
GSM7092348 LepR_Control_BMEC_3
This SubSeries is part of SuperSeries:
GSE227148 Restoring bone marrow niche function rejuvenates aged hematopoietic stem cells by reactivating the DNA Damage Response
Relations
BioProject PRJNA943403

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE227143_FPKM_Subseries_1_NTN1KO_Niche_cells.txt.gz 1.4 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap