Division of Cardiology, Department of Medicine, Columbia University, Vagelos College of Physicians and Surgeons, New York, USA.
Department of Pharmacology, Columbia University, Vagelos College of Physicians and Surgeons.
Channels (Austin). 2020 Dec;14(1):123-131. doi: 10.1080/19336950.2020.1740502.
Activation of protein kinase A by cyclic AMP results in a multi-fold upregulation of Ca1.2 currents in the heart, as originally reported in the 1970's and 1980's. Despite considerable interest and much investment, the molecular mechanisms responsible for this signature modulation remained stubbornly elusive for over 40 years. A key manifestation of this lack of understanding is that while this regulation is readily apparent in heart cells, it has not been possible to reconstitute it in heterologous expression systems. In this review, we describe the efforts of many investigators over the past decades to identify the mechanisms responsible for the β-adrenergic mediated activation of voltage-gated Ca channels in the heart and other tissues.
蛋白激酶 A 被环腺苷酸激活会导致心脏中的 Ca1.2 电流多倍上调,这一现象最初在 20 世纪 70 年代和 80 年代就有报道。尽管人们对此非常感兴趣,并投入了大量资金,但负责这种标志性调节的分子机制 40 多年来一直难以捉摸。这种缺乏理解的一个主要表现是,尽管这种调节在心脏细胞中很容易观察到,但在异源表达系统中还无法对其进行重建。在这篇综述中,我们描述了过去几十年许多研究人员努力识别负责心脏和其他组织中β肾上腺素能介导的电压门控钙通道激活的机制。