Summary

Chronic Imaging of Mouse Visual Cortex Using a Thinned-skull Preparation

Published: October 25, 2010
doi:

Summary

In this video and supplemental material, we show a protocol for chronic in vivo imaging of the intact brain using a thinned-skull preparation.

Abstract

In vivo imaging using two-photon laser scanning microscopy (2PLSM) allows the study of living cells and neuronal processes in the intact brain. The technique presented here allows the imaging of the same area of the brain at several time points (chronic imaging) with microscopic resolution allowing the tracking of dendritic spines which are the small structures that represent the majority of postsynaptic excitatory sites in the CNS. The ability to clearly resolve fine cortical structures over several time points has many advantages, specifically in the study of brain plasticity in which morphological changes at synapses and circuit remodeling may help explain underlying mechanisms. In this video and supplementary material, we show a protocol for chronic in vivo imaging of the intact brain using a thinned-skull preparation. The thinned-skull preparation is a minimally invasive approach, which avoids potential damage to the dura and/or cortex, thus reducing the onset of an inflammatory response. When this protocol is performed correctly, it is possible to clearly monitor changes in dendritic spine characteristics in the intact brain over a prolonged period of time.

Protocol

To visualize neurons in the intact brain using two-photon microscopy, a preparation where neurons are labeled with fluorescent markers is used. In the experiments presented here we use the GFP-M transgenic mouse line which labels layer 5 pyramidal cells1. Layer 5 pyramidal cells project dendritic processes into superficial layers, allowing the visualization of dendrites and dendritic spines up to a depth of 300 μm below the level of the pia. An alternate approach is to label cells using viral markers (see Lowery <em…

Discussion

Chronic imaging using two-photon microscopy is becoming an increasingly popular technique to study morphological changes triggered during plasticity2-5. Here we demonstrate a thinned-skull preparation to follow identified dendritic spines in the intact mouse brain on different imaging days. In this protocol, the skull is left intact, causing minimal damage to the cortex and resulting in very low levels of neuroinflammation which may alter brain function6. This allows the animal to be imaged immedia…

Disclosures

The authors have nothing to disclose.

Acknowledgements

This work was supported by Burroughs Wellcome Career Award in the Biomedical Sciences (A.K.M), The Whitehall Foundation Research Grant (A.K.M), Sloan Foundation Fellowship (A.K.M), NIH EY019277 (A.K.M), and an NEI funded, Vision Training Grant, EY013319 (E.A.K.).

Materials

Material Name Type Company Catalogue Number Comment
Fentanyl Citrate   In-house pharmacy   Fentanyl Cocktail: Anesthesic Cocktail;
IP Dose: 0.0125 ml/g

Final cocktail conc.: 0.05 mg/kg
Medetomindine Hydrochloride   In-house pharmacy   Fentanyl Cocktail: Anesthesic Cocktail;
IP Dose: 0.0125 ml/g

Final cocktail conc.: 0.05 mg/kg
Midazolam HCL   In-house pharmacy   Fentanyl Cocktail: Anesthesic Cocktail;
IP Dose: 0.0125 ml/g

Final cocktail conc.: 0.05 mg/kg
2,2,2-tribromoethanol       Avertin Cocktail: Anesthetic;
IP Dose: 0.0075 cc/ g

Final cocktail conc.: 1%
2-methyl-2-butanol (Final concentration: 0.775%)       Avertin Cocktail: Anesthetic;
IP Dose: 0.0075 cc/ g

Final cocktail conc.: .775%
TC-1000 Temp. Control System for Mice   CWE, Inc. TC-1000 Mouse Body Temp. Regulation
Toberadex   In-house pharmacy   Eye Ointment
10% Ferric Chloride   Ricca Chemical, Inc. 3120-32 Thin-skull preparation
Microsurgical Blade   Sable Industries S-6400 Thin-skull preparation
Cyanoacrylate 404,401   Loctite P/N 46551 Thin-skull preparation
Cyanoacrylate 401   Loctite P/N 40140 Thin-skull preparation
Zip Kicker Glue Accelerator   Pacer Technology PT-29 Thin-skull preparation
Micro Drill Steel Burrs 0.7mm tip diameter   Fine Science Tools 19008-07 Thin-skull preparation
Microtorque Control Box and Tech2000 Handpiece   Ram Products, Inc. TECH2000ON/OFF Thin-skull preparation
#6-0 (0.7 metric ) silk suture   Ethicon K8894H Taper C-1
Eye Dressing Forceps, 10cm, tip width 0.5mm, curved Surgical Tools Fine Science Tools 11152-10  
Extra Fine Bonn Scissors, 8.5cm, straight tip, cutting edge 13mm Surgical Tools Fine Science Tools 14084-08  
Standard Pattern Forceps, straight, 2.5mmx1.35mmtip, 12cm Surgical Tools Fine Science Tools 11000-12  

References

  1. Feng, G. Imaging neuronal subsets in transgenic mice expressing multiple spectral variants of GFP. Neuron. 28 (1), 41-51 (2000).
  2. Holtmaat, A. high-resolution imaging in the mouse neocortex through a chronic cranial window. Nat Protoc. 4 (8), 1128-1144 (2009).
  3. Majewska, A. K., Newton, J. R., Sur, M. Remodeling of synaptic structure in sensory cortical areas in vivo. J Neurosci. 26 (11), 3021-3029 (2006).
  4. Mostany, R., Portera-Cailliau, C. A Craniotomy Surgery Procedure for Chronic Brain Imaging. J Vis Exp. , (2008).
  5. Yang, G. Thinned-skull cranial window technique for long-term imaging of the cortex in live mice. Nat Protocols. 5 (2), 201-208 (2010).
  6. Xu, H. T. Choice of cranial window type for in vivo imaging affects dendritic spine turnover in the cortex. Nat Neurosci. 10 (5), 549-551 (2007).
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Cite This Article
Kelly, E. A., Majewska, A. K. Chronic Imaging of Mouse Visual Cortex Using a Thinned-skull Preparation. J. Vis. Exp. (44), e2060, doi:10.3791/2060 (2010).

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