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Series GSE265931 Query DataSets for GSE265931
Status Public on Sep 21, 2024
Title Thymic stromal lymphopoietin modulates T cell response to improve cardiac repair post-myocardial infarction
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary The inflammatory response is associated with cardiac repair and ventricular remodeling after myocardial infarction (MI). The key inflammation regulatory factor thymic stromal lymphopoietin (TSLP) plays a critical role in various diseases. However, its role in cardiac repair after MI remains uncertain. In this study, we elucidated the biological function and mechanism of action of TSLP in cardiac repair and ventricular remodeling following MI. Wild-type and TSLP receptor (TSLPR)-knockout (Crlf2-/-) mice underwent MI induction via ligation of the left descending artery. TSLP expression was upregulated in the infarcted heart, with a peak observed on day 7 post-MI. TSLP expression was enriched in the cardiomyocytes of infarcted hearts, with the highest expression observed in dendritic cells. Crlf2-/- mice exhibited significantly reduced survival and worsened cardiac function, increased interstitial fibrosis and cardiomyocyte cross-sectional area, and reduced CD31+ staining, with no change in the proportion of apoptotic cardiomyocytes within the border zone. Mechanistically, a reduction in regulatory T cells and more innate immune cells and their subsets were observed in the infarcted hearts of Crlf2-/- mice, accompanied by a systemic reduction in T cell activation and proliferation. Simultaneously, RNA sequencing analysis of the infarcted hearts revealed significant downregulation of genes in Crlf2-/- mice. Our findings indicate that TSLP plays a pivotal role in regulating T cell responses, specifically T regulatory cells, thus promoting cardiac repair, which may provide a potential novel therapeutic approach for managing heart failure after MI.
 
Overall design To investigate the differential gene expression in the heart tissue of mice 7 days after myocardial infarction caused by defects in the TSLP/TSLPR signaling pathway.
 
Contributor(s) Wang X, Tang T, Zha L, Cheng X
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Submission date Apr 26, 2024
Last update date Sep 21, 2024
Contact name wang Xuhong
E-mail(s) wxh2018@hust.edu.cn
Organization name Huazhong University of Science and Technology Tongji Medical College Affiliated Union Hospital
Street address 1277 Jiefang Avenue
City wuhan
ZIP/Postal code 430014
Country China
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (6)
GSM8232179 WT_1
GSM8232180 WT_2
GSM8232181 WT_3
Relations
BioProject PRJNA1104986

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
GSE265931_processed_data_file.txt.gz 2.7 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA

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