Liggett Stephen B
Cardiopulmonary Genomics Program, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
J Clin Invest. 2006 Apr;116(4):875-7. doi: 10.1172/JCI28234.
Enhanced signaling in myocytes by the G protein Gq has been implicated in cardiac hypertrophy and the transition to heart failure. alpha1-Adrenergic receptors (alpha1-ARs) are members of the 7-transmembrane-spanning domain (7-TM) receptor family and signal via interaction with Gq in the heart. The specific effects of a loss of alpha1-AR signaling in the heart are explored by O'Connell et al. in this issue of the JCI (see the related article beginning on page 1005). Paradoxically, gene ablation of the alpha 1A and alpha 1B subtypes in mice results in a maladaptive form of reactive cardiac hypertrophy from pressure overload, with a predisposition to heart failure. Thus signaling to the alpha1-AR (compared with signaling from other receptors such as angiotensin receptors, which also couple to Gq) appears to be specifically required for a normal hypertrophic response. This represents another example of how receptors that share common G proteins have diversified, developing unique signaling programs. These findings may have particular clinical relevance because of the widespread use of alpha1-AR antagonists in the treatment of hypertension and symptomatic prostate enlargement.
G蛋白Gq介导的心肌细胞信号增强与心脏肥大及向心力衰竭的转变有关。α1-肾上腺素能受体(α1-ARs)属于7跨膜结构域(7-TM)受体家族,在心脏中通过与Gq相互作用来传递信号。奥康奈尔等人在本期《临床研究杂志》(见第1005页开始的相关文章)中探讨了心脏中α1-AR信号缺失的具体影响。矛盾的是,小鼠中α1A和α1B亚型的基因敲除会导致压力超负荷引起的适应性不良的反应性心脏肥大,并易患心力衰竭。因此,与其他也与Gq偶联的受体(如血管紧张素受体)的信号传导相比,α1-AR的信号传导似乎是正常肥大反应所特需的。这代表了共享共同G蛋白的受体如何多样化并形成独特信号程序的又一个例子。由于α1-AR拮抗剂广泛用于治疗高血压和症状性前列腺增生,这些发现可能具有特殊的临床意义。