Kopton Ramona A, Buchmann Cinthia, Moss Robin, Kohl Peter, Peyronnet Rémi, Schneider-Warme Franziska
Institute for Experimental Cardiovascular Medicine, University Heart Center Freiburg-Bad Krozingen, Medical Center-University of Freiburg; Faculty of Medicine, University of Freiburg; Faculty of Biology, University of Freiburg;
Institute for Experimental Cardiovascular Medicine, University Heart Center Freiburg-Bad Krozingen, Medical Center-University of Freiburg; Faculty of Medicine, University of Freiburg.
J Vis Exp. 2020 Mar 5(157). doi: 10.3791/60490.
Over the past two decades, optogenetic tools have been established as potent means to modulate cell-type specific activity in excitable tissues, including the heart. While Channelrhodopsin-2 (ChR2) is a common tool to depolarize the membrane potential in cardiomyocytes (CM), potentially eliciting action potentials (AP), an effective tool for reliable silencing of CM activity has been missing. It has been suggested to use anion channelrhodopsins (ACR) for optogenetic inhibition. Here, we describe a protocol to assess the effects of activating the natural ACR GtACR1 from Guillardia theta in cultured rabbit CM. Primary readouts are electrophysiological patch-clamp recordings and optical tracking of CM contractions, both performed while applying different patterns of light stimulation. The protocol includes CM isolation from rabbit heart, seeding and culturing of the cells for up to 4 days, transduction via adenovirus coding for the light-gated chloride channel, preparation of patch-clamp and carbon fiber setups, data collection and analysis. Using the patch-clamp technique in whole-cell configuration allows one to record light-activated currents (in voltage-clamp mode, V-clamp) and AP (current-clamp mode, I-clamp) in real time. In addition to patch-clamp experiments, we conduct contractility measurements for functional assessment of CM activity without disturbing the intracellular milieu. To do so, cells are mechanically preloaded using carbon fibers and contractions are recorded by tracking changes in sarcomere length and carbon fiber distance. Data analysis includes assessment of AP duration from I-clamp recordings, peak currents from V-clamp recordings and force calculation from carbon fiber measurements. The described protocol can be applied to the testing of biophysical effects of different optogenetic actuators on CM activity, a prerequisite for the development of a mechanistic understanding of optogenetic experiments in cardiac tissue and whole hearts.
在过去二十年中,光遗传学工具已成为调节可兴奋组织(包括心脏)中细胞类型特异性活动的有力手段。虽然通道视紫红质-2(ChR2)是使心肌细胞(CM)膜电位去极化、潜在引发动作电位(AP)的常用工具,但一直缺少可靠沉默CM活性的有效工具。有人建议使用阴离子通道视紫红质(ACR)进行光遗传学抑制。在此,我们描述了一种方案,用于评估激活来自嗜热四膜虫的天然ACR GtACR1对培养的兔CM的影响。主要读数是电生理膜片钳记录和CM收缩的光学跟踪,这两者都是在应用不同光刺激模式时进行的。该方案包括从兔心脏分离CM、接种并培养细胞长达4天、通过编码光门控氯离子通道的腺病毒进行转导、制备膜片钳和碳纤维装置、数据收集和分析。使用全细胞配置的膜片钳技术可以实时记录光激活电流(电压钳模式,V钳)和AP(电流钳模式,I钳)。除了膜片钳实验外,我们还进行收缩性测量,以在不干扰细胞内环境的情况下对CM活性进行功能评估。为此,使用碳纤维对细胞进行机械预加载,并通过跟踪肌节长度和碳纤维距离的变化来记录收缩。数据分析包括从I钳记录评估AP持续时间、从V钳记录评估峰值电流以及从碳纤维测量计算力。所描述的方案可应用于测试不同光遗传学激活剂对CM活性的生物物理效应,这是对心脏组织和全心光遗传学实验形成机制性理解的先决条件。