Research ID
hum0404-v1Release info
Research title
Elucidation of pathology and therapeutic development using genome analysis, iPS cells, and genome editing for cardiovascular diseases / Elucidation of pathology and development of novel medical technology using iPS cells derived from patients with cardiovascular disease
Research overview
- Aims
- In this study, we analyze the genomic information of samples from patients with various cardiovascular diseases, including severe heart failure, and identify genetic mutations and polymorphisms that are thought to be related to the pathology of cardiovascular diseases. The purpose is to elucidate the underlying mechanism and develop new therapeutic interventions. The source of the genome to be analyzed is mainly peripheral blood, but in some cases, the genome extracted from the myocardial tissue obtained by myocardial biopsy or iPS cells generated from the patient is also used. In the analysis using iPS cells, we repair genetic mutation using genome editing technology such as CRISPR/Cas9 and analyze the pathological phenotypes.
- Methods
- [scRNA-seq] GFP (Control) or S-RBD-sfGFP was added to iPS cell-derived cardiomyocytes and after 48 hours the cells were collected and single-cell RNA sequence analysis was performed.
[WGS] Genomic DNA was extracted from the peripheral blood cells of cardiomyopathy cases and performed whole genome sequencing analysis. - Participants/materials
- iPS cell-derived cardiomyocytes established from a cardiomyopathy case, peripheral blood cells of 3 cardiomyopathy cases
Datasets
| Cart | Dataset ID | Type of data | Analysis method | Access criteria | Date published |
|---|---|---|---|---|---|
| JGAD000749 | NGS (scRNA-seq) |
| Controlled-access (Type I) | 2025-10-01 | |
| E-GEAD-628 | NGS (scRNA-seq) |
| Unrestricted-access | 2023-12-06 | |
| JGAD000837 | NGS (WGS) |
| Controlled-access (Type I) | 2025-10-01 | |
| JGAD000838 | NGS (WGS) |
| Controlled-access (Type I) | 2025-10-01 | |
| JGAD000839 | NGS (WGS) |
| Controlled-access (Type I) | 2025-10-01 |
Data provider
- Principal investigator
- Shuichiro Higo
- Affiliation
- Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine
Research projects
No research projects.
Grants
No grants.
Related publications
| Title | DOI | Dataset ID |
|---|---|---|
SARS-CoV-2 spike receptor-binding domain is internalized and promotes protein ISGylation in human induced pluripotent stem cell-derived cardiomyocytes |
Controlled access users
No use of the controlled access data has been recorded.