Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited life-threatening arrhythmia leading to syncope and sudden cardiac death at a young age. This disease cell model belongs to CPVT1, an autosomal dominant mutations (P2328S) occur in the RYR2 gene. Generating pluripotent stem cells from foreskin fibroblasts, then differentiate into cardiac myocytes. This disease cell model provides a platform to explore disease mechanisms in human genetic cardiac disorders.
| Specifications | |
|---|---|
| Organ System | Cardiovascular System |
| Disease | CPVT1 |
| Target Gene | RYR2 |
| Gene Function | Ryanodine receptor type 2 gene (RYR2) is a mediator of calcium release in the sarcoplasmic reticulum (SR). |
| Mutation | P2328S |
| Phenotype | Increased EADs and delayed afterdepolarisations (DADs) upon adrenergic stimulation |
| Source | Foreskin fibroblasts |
| Cellular Assays | Whole-cell patch clamp techniques, immunocytochemical staining |
For Research Use Only. Not For Clinical Use.
