In vivo rescue of genetic dilated cardiomyopathy by systemic delivery of nexilin.
Yanjiao ShaoCanzhao LiuHsin-Kai LiaoRan ZhangBaolei YuanHanyan YangRonghui LiSiting ZhuXi FangConcepcion Rodriguez EstebanJu ChenJuan Carlos Izpisua BelmontePublished in: Genome biology (2024)
In summary, we demonstrated that a single injection of AAV-Nexn was capable to restore the functions of cardiomyocytes and extended the lifespan of Nexn knockout and G645del mice. Our study represented a long-term gene replacement therapy for DCM that potentially covers all forms of loss-of-function mutations in NEXN.