Department of Biomedical Sciences, University of California San Diego, La Jolla, CA, USA.
J Cardiovasc Pharmacol. 2010 Dec;56(6):598-603. doi: 10.1097/FJC.0b013e3181e1d263.
The molecular events associated with the development of pathological hypertrophy have been shown to be stimulated through G-protein–coupled receptors that activate Gq signaling pathways in neonatal cardiomyocytes and in transgenic (TG) and knockout mice. We demonstrated that CaMKII, a multifunctional Ca(2+)-regulated protein kinase, was activated through G-protein–coupled receptor and inositol trisphosphate–mediated Ca(2+) release and suggested that CaMKII was a downstream mediator of Gq-coupled hypertrophic signaling. This was supported by the demonstration of CaMKII activation by pressure overload [(transverse aortic constriction (TAC)] and induction of hypertrophy by TG CaMKII expression. CaMKII also phosphorylates Ca(2+) handling proteins including the ryanodine receptor (RyR2), phosphorylation of which markedly increases sarcoplasmic reticulum Ca(2+) leak. Increased RyR2 phosphorylation is associated with heart failure development in CaMKII TG mice, and mice genetically deleted for CaMKII (KO) have attenuated RyR2 phosphorylation, sarcoplasmic reticulum Ca(2+) leak, and heart failure development after long-term TAC. Genetic ablation of CaMKII also decreases development of heart failure in Gq TG mice and decreases infarct size, while improving functional recovery in mice subject to ischemia/reperfusion and preventing adverse remodeling after coronary artery occlusion. The underlying mechanisms are currently under study.
与病理性心肌肥厚发展相关的分子事件已被证实是通过 G 蛋白偶联受体(GPCR)刺激的,这些受体在新生心肌细胞以及转基因(TG)和基因敲除(KO)小鼠中激活 Gq 信号通路。我们证明,钙调蛋白依赖性蛋白激酶 II(CaMKII)是一种多功能 Ca2+ 调节蛋白激酶,通过 GPCR 和肌醇三磷酸(InsP3)介导的 Ca2+ 释放而被激活,并表明 CaMKII 是 Gq 偶联的肥厚信号的下游介质。这一观点得到了以下证据的支持:压力超负荷(通过横主动脉缩窄(TAC))可激活 CaMKII,TG CaMKII 表达可诱导心肌肥厚。CaMKII 还磷酸化 Ca2+ 处理蛋白,包括肌浆网 Ca2+ 释放通道(RyR2),其磷酸化显著增加肌浆网 Ca2+ 泄漏。RyR2 磷酸化增加与 CaMKII TG 小鼠心力衰竭的发展有关,而 CaMKII 基因敲除(KO)小鼠的 RyR2 磷酸化、肌浆网 Ca2+ 泄漏和长期 TAC 后的心力衰竭发展则减弱。CaMKII 的基因缺失还可减少 Gq TG 小鼠心力衰竭的发展,减少梗死面积,改善缺血/再灌注后小鼠的功能恢复,并防止冠状动脉闭塞后的不良重构。目前正在研究其潜在机制。