Inserm, U769, Univ. Paris-Sud 11, IFR141, Labex Lermit, Châtenay-Malabry, France.
Curr Vasc Pharmacol. 2013 Jul;11(4):497-506. doi: 10.2174/1570161111311040013.
Cardiac hypertrophy arises as a response of the heart to many different pathological stimuli that challenge its work. Regardless of the initial pathologic cause, cardiac hypertrophy shares some characteristics resulting from a genetic reprogramming of several proteins. Recent studies point to Ca2+ as a key signaling element in the initiation of this genetic reprogramming. In fact, besides its important role in excitation-contraction coupling, Ca2+ regulates cardiac growth by activation of Ca2+-dependent transcription factors. This mechanism has been termed excitation-transcription (ET) coupling. Some information about cardiac ET coupling is being gathered from the analysis of cardiac hypertrophy development, where two Ca2+ dependent enzymes are key actors: the Ca2+/calmodulin kinase II (CaMKII) and the phosphatase calcineurin, both activated by Ca2+/Calmodulin. In this review we focus on some neurohormonal signaling pathways involved in cardiac hypertrophy, which could be ascribed as activators of ET coupling, for instance, adrenergic stimulation and the renin-angiotensin-aldosterone system. β-adrenergic receptor (β-AR) produces cAMP, which directly, (through cAMP response element) or indirectly (through activating Epac) induces cardiac hypertrophy. α1 AR and angiotensin receptor type 1 are Gq protein coupled receptors, which when activated, stimulate phospholipase C producing inositol 1,4,5 triphosphate (IP3) and diacylglycerol (DAG). IP3 promotes elevation of [Ca2+] in the nucleus, activating CaMKII/MEF2 (myocyte enhancer factor 2) pathway and may indirectly induce Ca2+ entry through transient receptor potential channels (TRPC). Other TRPC channels are activated by DAG. Ca2+ entry activates calcineurin/NFAT hypertrophic signaling. By promoting L-type Ca2+ channel expression, aldosterone may also have an important role in the genetic reprogramming during hypertrophy.
心肌肥厚是心脏对多种病理刺激的一种反应,这些刺激挑战着心脏的工作。无论最初的病理原因是什么,心肌肥厚都有一些共同的特征,这些特征是由于几种蛋白质的基因重编程所致。最近的研究表明,Ca2+ 是这种基因重编程起始的关键信号元素。事实上,除了在兴奋-收缩偶联中的重要作用外,Ca2+ 通过激活 Ca2+ 依赖性转录因子来调节心脏生长。这种机制被称为兴奋-转录(ET)偶联。在心肌肥厚的发展过程中,通过分析得到了一些关于心脏 ET 偶联的信息,其中两种 Ca2+ 依赖性酶是关键因素:Ca2+/钙调蛋白激酶 II(CaMKII)和磷酸酶钙调神经磷酸酶,两者均被 Ca2+/钙调蛋白激活。在这篇综述中,我们重点介绍了一些参与心肌肥厚的神经激素信号通路,这些信号通路可以被认为是 ET 偶联的激活剂,例如,肾上腺素能刺激和肾素-血管紧张素-醛固酮系统。β-肾上腺素能受体(β-AR)产生 cAMP,它可以直接(通过 cAMP 反应元件)或间接(通过激活 Epac)诱导心脏肥厚。α1AR 和血管紧张素受体 1 是 Gq 蛋白偶联受体,当被激活时,它们会刺激磷脂酶 C 产生肌醇 1,4,5 三磷酸(IP3)和二酰基甘油(DAG)。IP3 促进核内 [Ca2+]的升高,激活 CaMKII/MEF2(肌细胞增强因子 2)途径,并可能通过瞬时受体电位通道(TRPC)间接诱导 Ca2+ 内流。其他 TRPC 通道被 DAG 激活。Ca2+ 内流激活钙调神经磷酸酶/NFAT 肥厚信号。通过促进 L 型 Ca2+通道的表达,醛固酮在肥厚过程中的基因重编程中可能也具有重要作用。