GEO series
Methazolamide can treat atherosclerosis
GSE254708
Mus musculus
Expression profiling by high throughput sequencing; Other
12 samples
2024/08/08
GPL24247
Summary
Methoxazolamide (MTZ) has been confirmed to treat atherosclerosis (AS) by inhibiting calcification in aortic tissues. This study investigated the therapeutic mechanism. In this study, ApoE-/- mice were fed a high-fat diet to establish an AS model and then treated with MTZ. The aortic tissues were analyzed using single-cell sequencing. MTZ significantly increased the proportions of B-1/MZB cells, CD8+CD122+ Treg-like cell. Those cells can exert atheroprotective role by suppressing immune response and proinflammation. Meanwhile, MTZ decreased the proportions of nonclassical CD14+CD16++ monocytes and Spp1+ macrophages. Those cells can exert atherogenic role by suppressing proinflammation, calcification and tissue remodeling. The result suggested that MTZ is a potential anti-AS drug that regulates proportions of immunosuppressive cells and proinflammatory cells as well as their calcification-stimulating gene expression.
Download
NCBI GEO page ↗
Paper (PMID 39081633) ↗
{# Names what the click gives you. "Open in finder" meant nothing to a
visitor who arrived from a search engine and has never seen the tool. #}
Find more
mouse RNA-seq datasets →
Similar datasets
- GSE269045 Inflammatory immune modulators of AML lung infiltration and respiratory failure 56 samples
- GSE334689 m6Am-seq profiling of macrophage-specific Pcif1 knockout mice during experimental colitis 8 samples
- GSE337460 Chlamydia serovars in uterus- scRNA-seq, CITE-seq and TCRab 30 samples
- GSE327939 High-Resolution Lineage Tracing in Native Tissue Contexts 79 samples
- GSE249405 Spatial mapping of RNA turnover kinetics in the mouse brain 38 samples
- GSE285147 Astrocyte molecular changes during basolateral amygdala-related emotional behaviors [set2] 23 samples
- GSE327213 Increased mRNA translation delays tumor initiation and exposes a therapeutic vulnerability in lung cancer 16 samples
- GSE314859 The degradation of maternal RNA-binding protein 4E-T regulates translational activation to ensure maternal-to-zygotic transition in mouse embryos 67 samples
Share this dataset
Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.