4.8 Article

Chronic Cellular Imaging of Entire Cortical Columns in Awake Mice Using Microprisms

期刊

NEURON
卷 80, 期 4, 页码 900-913

出版社

CELL PRESS
DOI: 10.1016/j.neuron.2013.07.052

关键词

-

资金

  1. NSF [DBI-0953902]
  2. Kavli Center for Neuroscience
  3. Swebilius award
  4. NIH [R01 EY018742, EY010115]
  5. Ludcke Foundation
  6. Pierce Charitable Trust
  7. Smith Family Foundation

向作者/读者索取更多资源

Two-photon imaging of cortical neurons in vivo has provided unique insights into the structure, function, and plasticity of cortical networks, but this method does not currently allow simultaneous imaging of neurons in the superficial and deepest cortical layers. Here, we describe a simple modification that enables simultaneous, long-term imaging of all cortical layers. Using a chronically implanted glass microprism in barrel cortex, we could image the same fluorescently labeled deep-layer pyramidal neurons across their entire somatodendritic axis for several months. We could also image visually evoked and endogenous calcium activity in hundreds of cell bodies or long-range axon terminals, across all six layers in visual cortex of awake mice. Electrophysiology and calcium imaging of evoked and endogenous activity near the prism face were consistent across days and comparable with previous observations. These experiments extend the reach of in vivo two-photon imaging to chronic, simultaneous monitoring of entire cortical columns.

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

4.8
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