Department of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
Neuroscience and Cardiovascular Centers of Excellence, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
Neurosci Bull. 2019 Feb;35(1):113-123. doi: 10.1007/s12264-018-0319-2. Epub 2018 Dec 17.
The recent development of tools to decipher the intricacies of neural networks has improved our understanding of brain function. Optogenetics allows one to assess the direct outcome of activating a genetically-distinct population of neurons. Neurons are tagged with light-sensitive channels followed by photo-activation with an appropriate wavelength of light to functionally activate or silence them, resulting in quantifiable changes in the periphery. Capturing and manipulating activated neuron ensembles, is a recently-designed technique to permanently label activated neurons responsible for a physiological function and manipulate them. On the other hand, neurons can be transfected with genetically-encoded Ca indicators to capture the interplay between them that modulates autonomic end-points or somatic behavior. These techniques work with millisecond temporal precision. In addition, neurons can be manipulated chronically to simulate physiological aberrations by transfecting designer G-protein-coupled receptors exclusively activated by designer drugs. In this review, we elaborate on the fundamental concepts and applications of these techniques in research.
最近用于破译神经网络复杂性的工具的发展提高了我们对大脑功能的理解。光遗传学允许评估激活遗传上不同的神经元群体的直接结果。神经元被贴上光敏感通道的标签,然后用适当波长的光进行光激活,以功能上激活或沉默它们,从而在外周产生可量化的变化。捕获和操纵激活的神经元集合是最近设计的一种技术,可以永久标记负责生理功能的激活神经元并对其进行操作。另一方面,可以用遗传编码的 Ca 指示剂转染神经元,以捕获调节自主终点或躯体行为的神经元之间的相互作用。这些技术具有毫秒级的时间精度。此外,通过转染仅由设计药物激活的设计 G 蛋白偶联受体,神经元可以被慢性操纵以模拟生理异常。在这篇综述中,我们详细阐述了这些技术在研究中的基本概念和应用。