Maurice J P, Hata J A, Shah A S, White D C, McDonald P H, Dolber P C, Wilson K H, Lefkowitz R J, Glower D D, Koch W J
Department of Surgery, The Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina 27710, USA.
J Clin Invest. 1999 Jul;104(1):21-9. doi: 10.1172/JCI6026.
Exogenous gene delivery to alter the function of the heart is a potential novel therapeutic strategy for treatment of cardiovascular diseases such as heart failure (HF). Before gene therapy approaches to alter cardiac function can be realized, efficient and reproducible in vivo gene techniques must be established to efficiently transfer transgenes globally to the myocardium. We have been testing the hypothesis that genetic manipulation of the myocardial beta-adrenergic receptor (beta-AR) system, which is impaired in HF, can enhance cardiac function. We have delivered adenoviral transgenes, including the human beta2-AR (Adeno-beta2AR), to the myocardium of rabbits using an intracoronary approach. Catheter-mediated Adeno-beta2AR delivery produced diffuse multichamber myocardial expression, peaking 1 week after gene transfer. A total of 5 x 10(11) viral particles of Adeno-beta2AR reproducibly produced 5- to 10-fold beta-AR overexpression in the heart, which, at 7 and 21 days after delivery, resulted in increased in vivo hemodynamic function compared with control rabbits that received an empty adenovirus. Several physiological parameters, including dP/dtmax as a measure of contractility, were significantly enhanced basally and showed increased responsiveness to the beta-agonist isoproterenol. Our results demonstrate that global myocardial in vivo gene delivery is possible and that genetic manipulation of beta-AR density can result in enhanced cardiac performance. Thus, replacement of lost receptors seen in HF may represent novel inotropic therapy.
通过外源性基因传递来改变心脏功能是治疗心力衰竭(HF)等心血管疾病的一种潜在新型治疗策略。在实现改变心脏功能的基因治疗方法之前,必须建立高效且可重复的体内基因技术,以便将转基因有效地全局转移至心肌。我们一直在验证这样一个假设,即对在HF中受损的心肌β-肾上腺素能受体(β-AR)系统进行基因操作可增强心脏功能。我们已采用冠状动脉内给药方法,将包括人β2-AR(腺病毒-β2AR)在内的腺病毒转基因递送至兔心肌。导管介导的腺病毒-β2AR递送产生弥漫性多腔室心肌表达,在基因转移后1周达到峰值。总共5×10¹¹个腺病毒-β2AR病毒颗粒可在心脏中可重复地使β-AR过表达5至10倍,在给药后7天和21天,与接受空腺病毒的对照兔相比,体内血流动力学功能增强。包括作为收缩性指标的dP/dtmax在内的几个生理参数在基础状态下显著增强,并显示出对β-激动剂异丙肾上腺素的反应性增加。我们的结果表明,在体内进行全局心肌基因递送是可行的,并且对β-AR密度进行基因操作可导致心脏性能增强。因此,替代HF中所见的丢失受体可能代表新型正性肌力治疗。