| First Author | Lu F | Year | 2024 |
| Journal | Nat Biomed Eng | PubMed ID | 39237710 |
| Mgi Jnum | J:358080 | Mgi Id | MGI:7764573 |
| Doi | 10.1038/s41551-024-01253-z | Citation | Lu F, et al. (2024) Virally delivered CMYA5 enhances the assembly of cardiac dyads. Nat Biomed Eng |
| abstractText | Cardiomyocytes derived from human induced pluripotent stem cells (hiPSC-CMs) lack nanoscale structures essential for efficient excitation-contraction coupling. Such nanostructures, known as dyads, are frequently disrupted in heart failure. Here we show that the reduced expression of cardiomyopathy-associated 5 (CMYA5), a master protein that establishes dyads, contributes to dyad disorganization in heart failure and to impaired dyad assembly in hiPSC-CMs, and that a miniaturized form of CMYA5 suitable for delivery via an adeno-associated virus substantially improved dyad architecture and normalized cardiac function under pressure overload. In hiPSC-CMs, the miniaturized form of CMYA5 increased contractile forces, improved Ca(2+) handling and enhanced the alignment of sarcomere Z-lines with ryanodine receptor 2, a protein that mediates the sarcoplasmic release of stored Ca(2+). Our findings clarify the mechanisms responsible for impaired dyad structure in diseased cardiomyocytes, and suggest strategies for promoting dyad assembly and stability in heart disease and during the derivation of hiPSC-CMs. |
