A Cre-Dependent GCaMP3 Reporter Mouse for Neuronal Imaging In Vivo

被引:282
作者
Zariwala, Hatim A. [1 ,2 ]
Borghuis, Bart G. [2 ]
Hoogland, Tycho M. [3 ]
Madisen, Linda [1 ]
Tian, Lin [2 ]
De Zeeuw, Chris I. [3 ,4 ]
Zeng, Hongkui [1 ]
Looger, Loren L. [2 ]
Svoboda, Karel [2 ]
Chen, Tsai-Wen [2 ]
机构
[1] Allen Inst Brain Sci, Seattle, WA 98103 USA
[2] Howard Hughes Med Inst, Ashburn, VA 20147 USA
[3] Royal Netherlands Acad Arts & Sci KNAW, Netherlands Inst Neurosci, NL-1105 BA Amsterdam, Netherlands
[4] Erasmus MC, Dept Neurosci, NL-3015 GE Rotterdam, Netherlands
关键词
FLUORESCENT CA2+ INDICATOR; ENCODED CALCIUM INDICATOR; PRIMARY VISUAL-CORTEX; NEURAL ACTIVITY; CELLULAR RESOLUTION; EXCITATORY NEURONS; GABAERGIC NEURONS; CELLS; EXPRESSION; MICE;
D O I
10.1523/JNEUROSCI.4469-11.2012
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Fluorescent calcium indicator proteins, such as GCaMP3, allow imaging of activity in genetically defined neuronal populations. GCaMP3 can be expressed using various gene delivery methods, such as viral infection or electroporation. However, these methods are invasive and provide inhomogeneous and nonstationary expression. Here, we developed a genetic reporter mouse, Ai38, which expresses GCaMP3 in a Cre-dependent manner from the ROSA26 locus, driven by a strong CAG promoter. Crossing Ai38 with appropriate Cre mice produced robust GCaMP3 expression in defined cell populations in the retina, cortex, and cerebellum. In the primary visual cortex, visually evoked GCaMP3 signals showed normal orientation and direction selectivity. GCaMP3 signals were rapid, compared with virally expressed GCaMP3 and synthetic calcium indicators. In the retina, Ai38 allowed imaging spontaneous calcium waves in starburst amacrine cells during development, and light-evoked responses in ganglion cells in adult tissue. Our results show that the Ai38 reporter mouse provides a flexible method for targeted expression of GCaMP3.
引用
收藏
页码:3131 / 3141
页数:11
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