Barbic Mladen, Moreno Angel, Harris Tim D, Kay Matthew W
Applied Physics and Instrumentation Group, Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, Virginia; and.
Department of Biomedical Engineering, The George Washington University, Washington, District of Columbia.
Am J Physiol Heart Circ Physiol. 2017 Jun 1;312(6):H1248-H1259. doi: 10.1152/ajpheart.00741.2016. Epub 2017 May 5.
Here, we describe new detachable floating glass micropipette electrode devices that provide targeted action potential recordings in active moving organs without requiring constant mechanical constraint or pharmacological inhibition of tissue motion. The technology is based on the concept of a glass micropipette electrode that is held firmly during cell targeting and intracellular insertion, after which a 100-µg glass microelectrode, a "microdevice," is gently released to remain within the moving organ. The microdevices provide long-term recordings of action potentials, even during millimeter-scale movement of tissue in which the device is embedded. We demonstrate two different glass micropipette electrode holding and detachment designs appropriate for the heart (sharp glass microdevices for cardiac myocytes in rats, guinea pigs, and humans) and the brain (patch glass microdevices for neurons in rats). We explain how microdevices enable measurements of multiple cells within a moving organ that are typically difficult with other technologies. Using sharp microdevices, action potential duration was monitored continuously for 15 min in unconstrained perfused hearts during global ischemia-reperfusion, providing beat-to-beat measurements of changes in action potential duration. Action potentials from neurons in the hippocampus of anesthetized rats were measured with patch microdevices, which provided stable base potentials during long-term recordings. Our results demonstrate that detachable microdevices are an elegant and robust tool to record electrical activity with high temporal resolution and cellular level localization without disturbing the physiological working conditions of the organ. Cellular action potential measurements within tissue using glass micropipette electrodes usually require tissue immobilization, potentially influencing the physiological relevance of the measurement. Here, we addressed this limitation with novel 100-µg detachable glass microelectrodes that can be precisely positioned to provide long-term measurements of action potential duration during unconstrained tissue movement.
在此,我们描述了一种新型的可拆卸漂浮玻璃微电极装置,该装置可在活动的器官中进行靶向动作电位记录,而无需对组织运动进行持续的机械约束或药物抑制。该技术基于玻璃微电极的概念,即在细胞靶向和细胞内插入过程中,玻璃微电极被牢固固定,之后,一个100微克的玻璃微电极(一种“微型装置”)被轻轻释放,使其留在活动的器官内。这些微型装置即使在嵌入其的组织进行毫米级运动时,也能提供动作电位的长期记录。我们展示了两种适用于心脏(用于大鼠、豚鼠和人类心肌细胞的尖锐玻璃微型装置)和大脑(用于大鼠神经元的膜片玻璃微型装置)的不同玻璃微电极固定和分离设计。我们解释了微型装置如何能够测量活动器官内的多个细胞,而这通常是其他技术难以做到的。使用尖锐微型装置,在整体缺血 - 再灌注期间,对无约束灌注心脏中的动作电位持续时间进行了连续15分钟的监测,提供了逐搏的动作电位持续时间变化测量。使用膜片微型装置测量了麻醉大鼠海马体中神经元的动作电位,在长期记录过程中提供了稳定的基线电位。我们的结果表明,可拆卸微型装置是一种优雅且强大的工具,能够在不干扰器官生理工作条件的情况下,以高时间分辨率和细胞水平定位记录电活动。使用玻璃微电极在组织内进行细胞动作电位测量通常需要组织固定,这可能会影响测量的生理相关性。在此,我们通过新型的100微克可拆卸玻璃微电极解决了这一限制,这些微电极可以精确放置,以在无约束组织运动期间提供动作电位持续时间的长期测量。