CRISPR-Cas9 adenine base editing of PKCα T497A mutation protected mice from heart failure and improved cardiomyocyte function under stress.
Does CRISPR-Cas9 adenine base editing of PRKCA T497A improve cardiac function and remodeling in mouse models of heart failure and human induced pluripotent stem cell-derived cardiomyocytes?
In vivo CRISPR-Cas9 adenine base editing to introduce a phospho-resistant PKCα mutation protects against heart failure remodeling in mice, suggesting a novel gene therapy approach.
Absolute Event Rate: 0% vs 0%
BACKGROUND: The prevalence of heart failure is increasing globally, with poor prognosis, highlighting the need for novel therapeutic strategies. PKCα (protein kinase C alpha), encoded by PRKCA , plays a central role in heart failure pathogenesis. Phosphorylation of PKCα at threonine 497 (T497) triggers a series of intramolecular phosphorylation events, leading to its activation. Ablation of T497 phosphorylation leads to reduced stability and activity of PKCα. METHODS: We generated mice harboring a phospho-resistant PKCα (T497A) mutation in the germline using CRISPR-Cas9 (clustered regularly interspaced short palindromic repeats/clustered regularly interspaced short palindromic repeat–associated 9)–mediated homology-directed repair. To assess the clinical feasibility of postnatal genome editing, we used CRISPR-Cas9 adenine base editing delivered by adeno-associated virus 9 to introduce the T497A substitution into the Prkca gene ( Prkca T497A ) in wild-type mice. Mice underwent transverse aortic constriction to model heart failure. Cardiac function, hypertrophy, fibrosis, and transcriptional changes were evaluated by echocardiography, wheat germ agglutinin staining, Masson’s trichrome staining, and RNA-sequencing. The editing efficiency of Prkca T497A was assessed using Sanger sequencing and deep amplicon sequencing. To further explore its clinical potential, we introduced the PRKCA T497A mutation into human induced pluripotent stem cells by nucleofection-mediated adenine base editing. Ca 2+ homeostasis was analyzed in Fura-2–loaded human induced pluripotent stem cell–derived cardiomyocytes with PRKCA T497A under chronic AngII (angiotensin II) stimulation. RESULTS: The T497A mutation in PKCα prevented its subsequent phosphorylation and led to PKCα protein degradation. Four weeks after transverse aortic constriction surgery, wild-type mice showed impaired cardiac function, cardiac remodeling, and increased lung weight. In contrast, PKCα phospho-resistant mice showed protection against heart failure–related aberrant changes in cardiac hypertrophy, fibrosis, and cardiac gene expression. Mice administered with adeno-associated virus 9 base editors to prevent T497 phosphorylation exhibited similar cardioprotective effects. In vitro, PKCα-edited induced pluripotent stem cell–derived cardiomyocyte were protected from AngII-induced impairments in contractility and Ca 2+ transients. CONCLUSIONS: The editing of PRKCA T497A through adenine base editing represents a potential therapeutic approach for human cardiac diseases.
Tadokoro et al. (Fri,) reported a other. CRISPR-Cas9 adenine base editing of PKCα T497A mutation protected mice from heart failure and improved cardiomyocyte function under stress.