光遗传学
沟道视紫红质
电生理学
心脏电生理学
神经科学
去极化
人口
生物
医学
生物物理学
环境卫生
作者
Marbely C. Fernández,Ramona A. Kopton,Ana Simón-Chica,Josef Madl,Ingo Hilgendorf,Callum M. Zgierski‐Johnston,Franziska Schneider‐Warme
出处
期刊:Methods in molecular biology
日期:2020-08-31
卷期号:: 287-307
被引量:10
标识
DOI:10.1007/978-1-0716-0830-2_17
摘要
Optogenetic approaches have evolved as potent means to investigate cardiac electrophysiology, with research ranging from the study of arrhythmia mechanisms to effects of cardiac innervation and heterocellular structural and functional interactions, both in healthy and diseased myocardium. Most commonly, these studies use channelrhodopsin-2 (ChR2)-expressing murine models that enable light-activated depolarization of the target cell population. However, each newly generated mouse line requires thorough characterization, as cell-type specific ChR2 expression cannot be taken for granted, and the electrophysiological response of its activation in the target cell should be evaluated. In this chapter, we describe detailed protocols for assessing ChR2 specificity using immunohistochemistry, isolation of specific cell populations to analyze electrophysiological effects of ChR2 activation with the patch-clamp technique, and whole-heart experiments to assess in situ effects of optical stimulation.
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