Ambrosi Christina M, Klimas Aleksandra, Yu Jinzhu, Entcheva Emilia
Department of Biomedical Engineering, Stony Brook University, Stony Brook, NY 11794-8661, USA.
Department of Biomedical Engineering, Stony Brook University, Stony Brook, NY 11794-8661, USA.
Prog Biophys Mol Biol. 2014 Aug;115(2-3):294-304. doi: 10.1016/j.pbiomolbio.2014.07.001. Epub 2014 Jul 15.
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.
在复杂的多细胞系统中,如大脑或心脏,能够在细胞水平上以毫秒级时间分辨率选择性地扰动并观察单个组件的反应,对于从机制上理解其功能至关重要。光遗传学利用对光敏感性的基因编码(通过表达微生物视蛋白),以细胞特异性和高时空分辨率提供通过光进行操纵、记录和控制的能力。作为一种光学方法,它本质上可扩展用于在组织水平对生物功能进行远程和平行询问;借助可植入的小型化设备,该技术特别适合于体内功能跟踪,如在大脑中的众多应用所示。其在心脏领域的拓展一直较为缓慢。在这里,我们结合已发表研究的实例和原始数据,重点关注光遗传学在心脏电生理学中的应用,具体涉及通过光操纵膜电压的能力及其对心脏起搏、心脏复律、细胞通讯和心律失常研究的普遍影响。我们讨论了在心脏组织中赋予光敏感性的基因和细胞递送方法、不同类型心脏细胞内光敏离子通道的功能、探测不同细胞类型之间电耦合的效用、通过光遗传学传感器和致动器组合实现全光学电生理学的方法和设计方案,以及向体内心脏光遗传学发展过程中的具体挑战。