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

被引:161
作者
Andermann, Mark L. [1 ,2 ]
Gilfoy, Nathan B. [4 ]
Goldey, Glenn J. [1 ,2 ]
Sachdev, Robert N. S. [3 ]
Woelfel, Markus [4 ]
McCormick, David A.
Reid, R. Clay [2 ,3 ]
Levene, Michael J. [4 ,5 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Div Endocrinol,Dept Med, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02115 USA
[3] Yale Univ, Sch Med, Dept Neurobiol, Kavli Inst Neurosci, New Haven, CT 06510 USA
[4] Yale Univ, Malone Engn Ctr 312, Dept Biomed Engn, New Haven, CT 06511 USA
[5] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06520 USA
关键词
MOUSE VISUAL-CORTEX; IN-VIVO; RECEPTIVE-FIELDS; NEURAL ACTIVITY; FLUORESCENCE MICROENDOSCOPY; MULTIPHOTON MICROSCOPY; BRAIN-TISSUE; LAYER; CIRCUITS; NEURONS;
D O I
10.1016/j.neuron.2013.07.052
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
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.
引用
收藏
页码:900 / 913
页数:14
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