4.4 Article

Using Affordable LED Arrays for Photo-Stimulation of Neurons

期刊

出版社

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/3379

关键词

Neuroscience; Issue 57; Adult neurogenesis; Channelrhodopsin; Neural stem cells; Plasticity; Synapses; Electrophysiology

资金

  1. life insurance company AG2R-La-Mondiale
  2. Ecole des Neurosciences de Paris (ENP)
  3. Agence Nationale de la Recherche in the frame of ERA-NET NEURON of FP7 program by the European Commission [ANR-09-NEUR-004]
  4. Pasteur Foundation
  5. Letten Foundation

向作者/读者索取更多资源

Standard slice electrophysiology has allowed researchers to probe individual components of neural circuitry by recording electrical responses of single cells in response to electrical or pharmacological manipulations(1,2). With the invention of methods to optically control genetically targeted neurons (optogenetics), researchers now have an unprecedented level of control over specific groups of neurons in the standard slice preparation. In particular, photosensitive channelrhodopsin-2 (ChR2) allows researchers to activate neurons with light(3,4). By combining careful calibration of LED-based photostimulation of ChR2 with standard slice electrophysiology, we are able to probe with greater detail the role of adult-born interneurons in the olfactory bulb, the first central relay of the olfactory system. Using viral expression of ChR2-YFP specifically in adult-born neurons, we can selectively control young adult-born neurons in a milieu of older and mature neurons. Our optical control uses a simple and inexpensive LED system, and we show how this system can be calibrated to understand how much light is needed to evoke spiking activity in single neurons. Hence, brief flashes of blue light can remotely control the firing pattern of ChR2-transduced newborn cells.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据