Spatiotemporal transcriptome analysis reveals critical roles for mechano-sensing genes at the border zone in remodeling after myocardial infarction.
Shintaro YamadaToshiyuki KoSatoshi HatsuseSeitaro NomuraBo ZhangZhehao DaiShunsuke InoueMasayuki KubotaKosuke SawamiTakanobu YamadaTatsuro SassaMikako KatagiriKanna FujitaManami KatohMasamichi ItoMutsuo HaradaHaruhiro TokoNorifumi TakedaHiroyuki MoritaHiroyuki AburataniIssei KomuroPublished in: Nature cardiovascular research (2022)
The underlying mechanisms of ventricular remodeling after myocardial infarction (MI) remain largely unknown. In this study, we performed an integrative analysis of spatial transcriptomics and single-nucleus RNA sequencing (snRNA-seq) in a murine MI model and found that mechanical stress-response genes are expressed at the border zone and play a critical role in left ventricular remodeling after MI. An integrative analysis of snRNA-seq and spatial transcriptome of the heart tissue after MI identified the unique cluster that appeared at the border zone in an early stage, highly expressing mechano-sensing genes, such as Csrp3. AAV9-mediated gene silencing and overexpression of Csrp3 demonstrated that upregulation of Csrp3 plays critical roles in preventing cardiac remodeling after MI by regulation of genes associated with mechano-sensing. Overall, our study not only provides an insight into spatiotemporal molecular changes after MI but also highlights that the mechano-sensing genes at the border zone act as adaptive regulators of left ventricular remodeling.
Keyphrases
- genome wide
- left ventricular
- single cell
- heart failure
- early stage
- rna seq
- dna methylation
- genome wide identification
- acute myocardial infarction
- bioinformatics analysis
- hypertrophic cardiomyopathy
- transcription factor
- aortic stenosis
- signaling pathway
- radiation therapy
- poor prognosis
- atrial fibrillation
- coronary artery disease
- aortic valve
- sentinel lymph node
- gene therapy