Chronic cranial window with access port for repeated cellular manipulations, drug application, and electrophysiology

被引:62
作者
Roome, Christopher J. [1 ]
Kuhn, Bernd [1 ]
机构
[1] Grad Univ, Okinawa Inst Sci & Technol, Opt Neuroimaging Unit, Onna Son, Okinawa 9040495, Japan
关键词
imaging; in vivo; access port; chronic cranial window; two-photon; silicone plug; LONG-TERM; IN-VIVO; NEURONS; RECORDINGS; NEOCORTEX; DYNAMICS;
D O I
10.3389/fncel.2014.00379
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Chronic cranial windows have been instrumental in advancing optical studies in vivo, permitting long-term, high resolution imaging in various brain regions. However, once a window is attached it is difficult to regain access to the brain under the window for cellular manipulations. Here we describe a simple device that combines long term in vivo optical imaging with direct brain access via glass or quartz pipettes and metal, glass, or quartz electrodes for cellular manipulations like dye or drug injections and electrophysiological stimulations or recordings while keeping the craniotomy sterile. Our device comprises a regular cranial window glass coverslip with a drilled access hole later sealed with biocompatible silicone. This chronic cranial window with access port is cheap, easy to manufacture, can be mounted just as the regular chronic cranial window, and is self-sealing after retraction of the pipette or electrode. We demonstrate that multiple injections can be performed through the silicone port by repetitively bolus loading calcium sensitive dye into mouse barrel cortex and recording spontaneous cellular activity over a period of weeks. As an example to the extent of its utility for electrophysiological recording, we describe how simple removal of the silicone seal can permit patch pipette access for whole cell patch clamp recordings in ova During these chronic experiments we do not observe any infections under the window or impairment of animal health.
引用
收藏
页数:8
相关论文
共 30 条
[1]   Long-Term Imaging Reveals Dynamic Changes in the Neuronal Composition of the Glomerular Layer [J].
Adam, Yoav ;
Mizrahi, Adi .
JOURNAL OF NEUROSCIENCE, 2011, 31 (22) :7967-7973
[2]   Chronic cellular imaging of mouse visual cortex during operant behavior and passive viewing [J].
Andermann, Mark L. ;
Kerlin, A. M. ;
Reid, R. C. .
FRONTIERS IN CELLULAR NEUROSCIENCE, 2010, 4
[3]   Dural substitute for long-term imaging of cortical activity in behaving monkeys and its clinical implications [J].
Arieli, A ;
Grinvald, A ;
Slovin, H .
JOURNAL OF NEUROSCIENCE METHODS, 2002, 114 (02) :119-133
[4]   Optical imaging combined with targeted electrical recordings, microstimulation, or tracer injections [J].
Arieli, A ;
Grinvald, A .
JOURNAL OF NEUROSCIENCE METHODS, 2002, 116 (01) :15-28
[5]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[6]   Functional Clustering of Neurons in Motor Cortex Determined by Cellular Resolution Imaging in Awake Behaving Mice [J].
Dombeck, Daniel A. ;
Graziano, Michael S. ;
Tank, David W. .
JOURNAL OF NEUROSCIENCE, 2009, 29 (44) :13751-13760
[7]   Dendritic spine changes associated with hippocampal long-term synaptic plasticity [J].
Engert, F ;
Bonhoeffer, T .
NATURE, 1999, 399 (6731) :66-70
[8]   HIGH-RESOLUTION OPTICAL IMAGING OF FUNCTIONAL BRAIN ARCHITECTURE IN THE AWAKE MONKEY [J].
GRINVALD, A ;
FROSTIG, RD ;
SIEGEL, RM ;
BARTFELD, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (24) :11559-11563
[9]   Deep tissue two-photon microscopy [J].
Helmchen, F ;
Denk, W .
NATURE METHODS, 2005, 2 (12) :932-940
[10]   Transient and persistent dendritic spines in the neocortex in vivo [J].
Holtmaat, AJGD ;
Trachtenberg, JT ;
Wilbrecht, L ;
Shepherd, GM ;
Zhang, XQ ;
Knott, GW ;
Svoboda, K .
NEURON, 2005, 45 (02) :279-291