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The touch and zap method for in vivo whole-cell patch recording of intrinsic and visual responses of cortical neurons and Glial cells

机译:触摸和zap方法用于体内全细胞贴片记录皮质神经元和胶质细胞的内在和视觉反应

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摘要

Whole-cell patch recording is an essential tool for quantitatively establishing the biophysics of brain function, particularly in vivo. This method is of particular interest for studying the functional roles of cortical glial cells in the intact brain, which cannot be assessed with extracellular recordings. Nevertheless, a reasonable success rate remains a challenge because of stability, recording duration and electrical quality constraints, particularly for voltage clamp, dynamic clamp or conductance measurements. To address this, we describe "Touch and Zap", an alternative method for whole-cell patch clamp recordings, with the goal of being simpler, quicker and more gentle to brain tissue than previous approaches. Under current clamp mode with a continuous train of hyperpolarizing current pulses, seal formation is initiated immediately upon cell contact, thus the "Touch". By maintaining the current injection, whole-cell access is spontaneously achieved within seconds from the cell-attached configuration by a self-limited membrane electroporation, or "Zap", as seal resistance increases. We present examples of intrinsic and visual responses of neurons and putative glial cells obtained with the revised method from cat and rat cortices in vivo. Recording parameters and biophysical properties obtained with the Touch and Zap method compare favourably with those obtained with the traditional blind patch approach, demonstrating that the revised approach does not compromise the recorded cell. We find that the method is particularly well-suited for whole-cell patch recordings of cortical glial cells in vivo, targeting a wider population of this cell type than the standard method, with better access resistance. Overall, the gentler Touch and Zap method is promising for studying quantitative functional properties in the intact brain with minimal perturbation of the cell's intrinsic properties and local network. Because the Touch and Zap method is performed semi-automatically, this approach is more reproducible and less dependent on experimenter technique.
机译:全细胞膜片记录是定量建立大脑功能(尤其是体内)的生物物理学的重要工具。该方法对于研究完整大脑中的皮质神经胶质细胞的功能作用特别感兴趣,而这些功能无法用细胞外记录来评估。然而,由于稳定​​性,记录持续时间和电气质量限制,尤其对于电压钳位,动态钳位或电导率测量,合理的成功率仍然是一个挑战。为了解决这个问题,我们描述了“ Touch and Zap”,这是一种用于全细胞膜片钳记录的替代方法,其目的是比以前的方法对脑组织更简单,更快和更柔和。在电流钳模式下,具有连续的超极化电流脉冲序列,在细胞接触后即刻开始形成密封,即“接触”。通过维持电流注入,当密封阻力增加时,自限膜电穿孔或“ Zap”可自附着细胞后数秒内自发实现全细胞进入。我们提供了从猫和大鼠皮层体内修改后的方法获得的神经元和推定的神经胶质细胞的内在和视觉反应的示例。用触摸和击穿法获得的记录参数和生物物理特性与传统盲贴法获得的记录参数和生物物理特性相比具有优势,表明修订后的方法不会损害记录的细胞。我们发现该方法特别适合于体内皮质神经胶质细胞的全细胞贴片记录,与标准方法相比,该细胞类型的目标人群更广泛,并且具有更好的抗性。总体而言,较温和的“触摸和击键”方法有望用于研究完整大脑中的定量功能特性,而对细胞的固有特性和局部网络的干扰却最小。由于Touch and Zap方法是半自动执行的,因此该方法具有更高的可重复性,并且对实验者技术的依赖性较小。

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