NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE183839 Query DataSets for GSE183839
Status Public on Nov 17, 2023
Title Single cell transcriptomics and chromatin accessibility profiling elucidate the kidney protective mechanism of mineralocorticoid receptor antagonism [snRNA-seq]
Organism Rattus norvegicus
Experiment type Expression profiling by high throughput sequencing
Summary Mineralocorticoids play a critical role in maintaining sodium and potassium homeostasis and pathophysiological processes including hypertrophy, inflammation and fibrosis. Mineralocorticoid antagonists (MRAs) have shown to protect from kidney and heart disease, however, their molecular mechanism of action is poorly understood. Here we performed single nuclei and bulk transcriptomics and chromatin accessibility analysis to characterize the mode of kidney protection by steroidal and non-steroidal MRA treatment in a rat model of mineralocorticoid-induced cardiorenal end-organ damage. We define mineralocorticoid sensitive cell types and gene network in the kidney. We show that in diseased kidneys specific proximal tubule cells develop an injured profibrotic phenotype expressing Spp1 and Il34. Nonsteroidal finerenone protects from profibrotic differentiation of proximal tubule cells. Profibrotic gene signature can classify human kidney tissue samples and predict prognosis. Our multi-omics approach elucidates target cell types and potential mechanisms of renal protection by finerenone.
 
Overall design We provided three types of datasets of rat kidneys: (i) single nuclei RNA-seq as follows: 3 Control - 3 DOCA treated - 2 DOCA+Finerenone treated - 3 DOCA + Spironolactone treated, (ii) single nuclei ATAC-seq as follows: 1 Control - 1 DOCA treated - 1 DOCA+Finerenone treated - 1 DOCA + Spironolactone treated, and (iii) Bulk RNA-seq as follows: 4 Control - 4 DOCA treated - 4 DOCA+Finerenone treated - 4 DOCA + Spironolactone treated
Web link https://www.jci.org/articles/view/157165
 
Contributor(s) Abedini A, Wu J, Ma Z, Balzer MS, Frederick J, Cernecka H, Kolkhof P, Susztak K
Citation(s) 37906287
Submission date Sep 09, 2021
Last update date Jan 16, 2024
Contact name Katalin Susztak
E-mail(s) ksusztak@pennmedicine.upenn.edu
Organization name University of Pennsylvania
Street address 3400 Civic Center Blvd, SCTR
City Philadelphia
State/province PA
ZIP/Postal code 19104
Country USA
 
Platforms (1)
GPL25947 Illumina NovaSeq 6000 (Rattus norvegicus)
Samples (22)
GSM5572629 Control1_snRNAseq
GSM5572630 Control2_snRNAseq
GSM5572631 Control3_snRNAseq
This SubSeries is part of SuperSeries:
GSE183842 Single cell transcriptomics and chromatin accessibility profiling elucidate the kidney protective mechanism of mineralocorticoid receptor antagonism
Relations
BioProject PRJNA762174
SRA SRP338426

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
GSE183839_EXPORT_snRNAseq_counts.rds.gz 2.1 Gb (ftp)(http) RDS
GSE183839_EXPORT_snRNAseq_metadata.txt.gz 1.7 Mb (ftp)(http) TXT
GSE183839_EXPORT_snRNAseq_umap.txt.gz 5.2 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