Fast two-layer two-photon imaging of neuronal cell populations using an electrically tunable lens

被引:249
作者
Grewe, Benjamin F. [1 ]
Voigt, Fabian F. [1 ]
Van't Hoff, Marcel [1 ]
Helmchen, Fritjof [1 ]
机构
[1] Univ Zurich, Brain Res Inst, Dept Neurophysiol, CH-8057 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
VARIABLE-FOCUS LENS; IN-VIVO; MICROSCOPY; COMPACT;
D O I
10.1364/BOE.2.002035
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Functional two-photon Ca2+-imaging is a versatile tool to study the dynamics of neuronal populations in brain slices and living animals. However, population imaging is typically restricted to a single two-dimensional image plane. By introducing an electrically tunable lens into the excitation path of a two-photon microscope we were able to realize fast axial focus shifts within 15 ms. The maximum axial scan range was 0.7 mm employing a 40x NA0.8 water immersion objective, plenty for typically required ranges of 0.2-0.3 mm. By combining the axial scanning method with 2D acousto-optic frame scanning and random-access scanning, we measured neuronal population activity of about 40 neurons across two imaging planes separated by 40 mu m and achieved scan rates up to 20-30 Hz. The method presented is easily applicable and allows upgrading of existing two-photon microscopes for fast 3D scanning. (C) 2011 Optical Society of America
引用
收藏
页码:2035 / 2046
页数:12
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