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Series GSE217558 Query DataSets for GSE217558
Status Public on Dec 31, 2022
Title Signature analyses for circulating extracellular vesicle in chronic kidney disease
Platform organism synthetic construct
Sample organism Rattus norvegicus
Experiment type Non-coding RNA profiling by array
Summary Chronic kidney disease (CKD) accelerates vascular calcification (VC) via phenotypic switching of vascular smooth muscle cells (VSMCs). We investigated the roles of circulating small extracellular vesicles (sEVs) between the kidneys and VSMCs and uncovered relevant sEV-propagated microRNAs (miRNAs) and their biological signaling pathways. We established CKD models in rats and mice by adenine-induced tubulointerstitial fibrosis. The miRNA transcriptome of sEVs revealed a depletion of several miRNAs in CKD. Their expression levels in sEVs from CKD patients were correlated to kidney function. This study revealed the transcriptomic landscape of miRNAs propagated in sEVs in CKD. We investigated the therapeutic potential of miRNAs in VC.
 
Overall design Eight samples derived from small extracellular vesicles of control (n = 4) and CKD model rats (n = 4).
 
Citation(s) 36700539
Submission date Nov 08, 2022
Last update date Apr 01, 2023
Contact name Shintaro Mandai
Organization name Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences
Street address 1-5-45 Yushima
City Bunkyo
State/province Tokyo
ZIP/Postal code 113-8519
Country Japan
 
Platforms (1)
GPL21572 [miRNA-4] Affymetrix Multispecies miRNA-4 Array [ProbeSet ID version]
Samples (8)
GSM6721729 ExtracellularVesicles_control1
GSM6721730 ExtracellularVesicles_control2
GSM6721731 ExtracellularVesicles_control3
Relations
BioProject PRJNA899545

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
GSE217558_RAW.tar 4.8 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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