St Clair Joshua R, Sharpe Emily J, Proenza Catherine
Department of Physiology and Biophysics, University of Colorado - Anschutz Medical Campus, Denver, Colorado; and.
Department of Physiology and Biophysics, University of Colorado - Anschutz Medical Campus, Denver, Colorado; and Department of Medicine, Division of Cardiology - Anschutz Medical Campus, Denver, Colorado
Am J Physiol Heart Circ Physiol. 2015 Aug 1;309(3):H490-8. doi: 10.1152/ajpheart.00068.2015. Epub 2015 May 22.
Pacemaker myocytes in the sinoatrial node of the heart initiate each heartbeat by firing spontaneous action potentials. However, the molecular processes that underlie pacemaking are incompletely understood, in part because of our limited ability to manipulate protein expression within the native cellular context of sinoatrial node myocytes (SAMs). Here we describe a new method for the culture of fully differentiated SAMs from adult mice, and we demonstrate that robust expression of introduced proteins can be achieved within 24-48 h in vitro via adenoviral gene transfer. Comparison of morphological and electrophysiological characteristics of 48 h-cultured versus acutely isolated SAMs revealed only minor changes in vitro. Specifically, we found that cells tended to flatten in culture but retained an overall normal morphology, with no significant changes in cellular dimensions or membrane capacitance. Cultured cells beat spontaneously and, in patch-clamp recordings, the spontaneous action potential firing rate did not differ between cultured and acutely isolated cells, despite modest changes in a subset of action potential waveform parameters. The biophysical properties of two membrane currents that are critical for pacemaker activity in SAMs, the "funny current" (If) and voltage-gated Ca(2+) currents (ICa), were also indistinguishable between cultured and acutely isolated cells. This new method for culture and adenoviral infection of fully-differentiated SAMs from the adult mouse heart expands the range of experimental techniques that can be applied to study the molecular physiology of cardiac pacemaking because it will enable studies in which protein expression levels can be modified or genetically encoded reporter molecules expressed within SAMs.
心脏窦房结中的起搏心肌细胞通过自发产生动作电位引发每次心跳。然而,起搏的分子机制尚未完全明确,部分原因是我们在窦房结心肌细胞(SAMs)的天然细胞环境中操纵蛋白质表达的能力有限。在此,我们描述了一种从成年小鼠培养完全分化的SAMs的新方法,并且我们证明通过腺病毒基因转移可在体外24 - 48小时内实现导入蛋白的强大表达。对培养48小时的SAMs与急性分离的SAMs的形态和电生理特征进行比较,发现体外仅有微小变化。具体而言,我们发现细胞在培养过程中趋于扁平,但保留了总体正常形态,细胞尺寸或膜电容无显著变化。培养的细胞自发搏动,在膜片钳记录中,尽管动作电位波形参数的一个子集中有适度变化,但培养细胞和急性分离细胞的自发动作电位发放率并无差异。对于SAMs起搏活动至关重要的两种膜电流,即“起搏电流”(If)和电压门控钙电流(ICa),其生物物理特性在培养细胞和急性分离细胞之间也没有区别。这种从成年小鼠心脏培养和腺病毒感染完全分化的SAMs的新方法扩展了可用于研究心脏起搏分子生理学的实验技术范围,因为它将使能够进行蛋白质表达水平可被改变或在SAMs内表达基因编码报告分子的研究。