Cardiac applications of optogenetics

被引:58
|
作者
Ambrosi, Christina M. [1 ]
Klimas, Aleksandra [1 ]
Yu, Jinzhu [1 ]
Entcheva, Emilia [1 ]
机构
[1] SUNY Stony Brook, Dept Biomed Engn, Stony Brook, NY 11794 USA
来源
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY | 2014年 / 115卷 / 2-3期
关键词
Optogenetics; Channelrhodopsin; Gene delivery; Cell delivery; Cardiomyocytes; Fibroblasts; OPTICAL CONTROL; STEM-CELLS; ISCHEMIC CARDIOMYOPATHY; LIGHT; FLUORESCENCE; EXCITATION; CALCIUM; HEART; CHANNELRHODOPSIN-2; ACTIVATION;
D O I
10.1016/j.pbiomolbio.2014.07.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In complex multicellular systems, such as the brain or the heart, the ability to selectively perturb and observe the response of individual components at the cellular level and with millisecond resolution in time, is essential for mechanistic understanding of function. Optogenetics uses genetic encoding of light sensitivity (by the expression of microbial opsins) to provide such capabilities for manipulation, recording, and control by light with cell specificity and high spatiotemporal resolution. As an optical approach, it is inherently scalable for remote and parallel interrogation of biological function at the tissue level; with implantable miniaturized devices, the technique is uniquely suitable for in vivo tracking of function, as illustrated by numerous applications in the brain. Its expansion into the cardiac area has been slow. Here, using examples from published research and original data, we focus on optogenetics applications to cardiac electrophysiology, specifically dealing with the ability to manipulate membrane voltage by light with implications for cardiac pacing, cardioversion, cell communication, and arrhythmia research, in general. We discuss gene and cell delivery methods of inscribing light sensitivity in cardiac tissue, functionality of the light-sensitive ion channels within different types of cardiac cells, utility in probing electrical coupling between different cell types, approaches and design solutions to all-optical electrophysiology by the combination of optogenetic sensors and actuators, and specific challenges in moving towards in vivo cardiac optogenetics. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:294 / 304
页数:11
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