Name: laminectomy and spinal cord window implantation in the mouse
Uploaded: 2019-10-23T12:30:00.000+00:00
Duration: 6 min 59 s
Description: Watch this Scientific Journal Video about Laminectomy and Spinal Cord Window Implantation in the Mouse at JoVE.com

S.E. Lutz is supported by the National Center for Advancing Translational Sciences, National Institutes of Health, under Grant KL2TR002002 and University of Illinois Chicago College of Medicine start-up funds. Simon Alford is supported by RO1 MH084874. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. The authors thank Dritan Agalliu in the Department of Neurology at Columbia University Medical Center for the Tg eGFP:Claudin-5 mice, scientific discussions, and insights into the development of the surgical protocol and imaging applications. The authors thank Sunil P. Gandhi in the Department of Neurobiology and Behavior at University of California, Irvine for designing the first prototype of the stereotactic apparatus and animal temperature controller, discussion of the surgical protocol, and training in two-photon microscopy. The authors also thank Steve Pickens (W. Nuhsbaum, Inc.) for assistance in customizing the surgical stereomicroscope, and Ron Lipinski (Whale Manufacturing) for machining stereotactic parts.

All experiments follow the University of Illinois, Chicago Institutional Animal Care and Use Committee protocols. This is a terminal procedure.&#160;
1. Reagent Preparation
<ol>
	<li>Prepare artificial cerebral spinal fluid (aCSF) to contain 125 mM NaCl, 5 mM KCl, 10 mM Glucose, 10 mM HEPES, 2 mM MgCl2&#183;6H2O, 2 mM CaCl2&#183;2H2O in ddH2O. Sterile filter and freeze in individual-use aliquots. Warm aCSF in a water bath to 39 &#176;C before use.</li>
	<li>Warm low melting-point agarose (2%) in aCSF until fully dissolved in a water bath set to 65 &#176;C. During the laminectomy, cool the melted agarose aliquot to 39 &#176;C in a water bath, so that it can ready at close to physiologic temperature for step 5.2. 
	Note: The agarose solution can be stored at -20 &#176;C in single-use aliquots.</li>
	<li>Prepare sterile 50 mg/mL carprofen in bacteriostatic water. Store at 4 &#176;C.</li>
	<li>Clean cover-glasses with 70% ethanol, three washes of ddH2O, and store dry in a dust-free container.</li>
</ol>
2. Backplate 3D Printing
<ol>
	<li>Use 3D CAD software is used to create a model to the dimensions shown in Figure 1. The interior is an ellipse widest at the bottom surface with respect to the printer and cut with a lofted cut to a smaller ellipse forming a lumen at the opposite surface. Two projecting arms with holes to accept screws extend laterally, for attachment to the backplate holding fork. From this 3D structure, create a triangulated 3D mesh file (.STL file). 
	Note: See Figure 1B&#8210;D and Supplementary Files 1 and 2.</li>
	<li>Upload the triangulated 3D mesh file to a 3D printer.</li>
	<li>Print backplates using a 0.4 mm hot-end nozzle and a 0.2 mm layer height. Select nozzle temperature of 205 &#176;C, bed temperature of 45 &#176;C, and printing speed of 45 mm/s.</li>
	<li>Assess the resultant 3D printed backplates visually for structural integrity (Figure 1E); gross structural failure (absent lumen, collapsed wall) indicates printing defects (Figure 1F).</li>
</ol>
3. Surgical Preparation
<ol>
	<li>Preheat the heating pad.</li>
	<li>Load isoflurane into the delivery syringe while working in a chemical fume hood. Attach the delivery syringe to the isoflurane unit.</li>
	<li>Select an 8&#8210;12-week-old mouse. Weigh the animal. Induce anesthesia using 2% isoflurane in an induction chamber. Inject carprofen at 5 mg/kg subcutaneously.</li>
	<li>Position the nose-cone and deliver isoflurane at 2% with a flow rate of 150 mL/min for maintenance of a surgical plane of anesthesia (Figure 2A&#8210;E). Wrap the heating pad with a disposable absorbent pad for ease of cleanup.</li>
	<li>Position an animal on the heating pad at the surgical station and install the nose cone. Lubricate the thermometer with petroleum jelly and insert it 5 mm into the rectum. Tape the thermometer probe to the tail for stability. Apply ophthalmic ointment to eyes of the mouse.</li>
	<li>To maintain hydration, apply 200 &#181;L of lactated Ringer&#8217;s solution by subcutaneous injection every 30 min until termination of the experiment.</li>
	<li>Spray the dorsum with 70% ethanol, remove fur with clippers, and clean the site with povidone-iodine.</li>
</ol>
4. Laminectomy
<ol>
	<li>Position the animal between the ear bars; these maintain the head position of the mouse with respect to the nose-cone.</li>
	<li>Confirm that animal is deeply anesthetized as assessed by lack of interdigital pinch reflex and steady respiratory pattern.</li>
	<li>Make a 1.5 cm rostral-caudal incision at midline over the lower thoracic/upper lumbar region using #11 blade (Figure 2). Separate the skin by grasping it with blunt toothed forceps and/or gloved fingers. Use forceps to separate and peel back any remaining transparent connective tissue underneath the skin. The superficial musculature should now be exposed; displace this with a foam surgical spear.</li>
	<li>Use foam surgical spears (or a curette) to clear away the remaining, deeper musculature of the target vertebra (thoracic 12). To create a seat for the backplate, also clear away muscle from the posterior aspect of thoracic 11, and the anterior aspect of thoracic 13. Control any bleeding by applying gentle pressure with a surgical spear or use a minimal pulse with a cautery gun. Continue to remove the remaining muscle away from the tendons using forceps</li>
	<li>Once muscles are removed, carefully detach the tendons by cutting with forceps. There should be plenty of space for visualizing and manipulating the cord when this step is complete. Check that the dura matter of the inter-vertebral space, the semi-transparent laminar bone, the central superficial blood vessel underneath the bone, and anterior radiating artery are now clearly visible.</li>
	<li>Wet the region with warm aCSF. Use the microdrill to repetitively thin the laminar bone using straight strokes parallel to the long axis of the spinal cord (Figure 2, Figure 3). If desired, utilize a gliding stage to rotate the surgical platform for enhanced ergonomic comfort (for example, a right-handed operator may rotate the surgical platform counterclockwise for the drilling step). 
	Note: The gliding stage used is constructed of an upper aluminum plate that slides &#177;15 mm with respect to the fixed base plate.</li>
	<li>Gently grasp the superficial spinous process with forceps and lift the vertebra; the bone should lift away easily. If there is resistance, repeat bone thinning with the drill and if necessary use iris scissors, being careful to aim the scissor tips upward to avoid damaging the tissue. 
	Note: In order to maintain the dura intact, it is essential not to tug on the bone.</li>
	<li>Use #4 forceps to clear away any bone shards. Use a surgical spear to apply gentle steady pressure to control any bleeding. Rinse tissue with warm aCSF. Do not allow the tissue to dry out.</li>
</ol>
5. Cover-glass Implantation
<ol>
	<li>Gently apply a 3 mm borosilicate cover-glass to the exposed cord.</li>
	<li>Ensure agarose is cooled to 39 &#176;C. Using a small spatula, apply warm 2% agarose/aCSF to the edge of the cover-glass and allow capillary action to draw it under the surface. 
	Note: At temperatures below 39 &#176;C, the agarose may start to gel. If this occurs, rewarm using a water bath or microwave. Some operators prefer to first apply one drop of agarose and lay the cover-glass on top.</li>
	<li>Apply tissue adhesive to the exposed bony articular processes of the intact adjacent vertebra at thoracic level 11 vertebral spine and thoracic level 13 vertebral spine. Apply additional tissue adhesive in a ring around the laminectomy site, over the adjacent tendon and transverse process. 
	Note: Tissue adhesive is required for proper adherence of the dental cement in the subsequent steps. The articular processes form a natural seat on which the backplate can rest stably (Figure 3). Adhesion to the articular processes will form the strongest points of attachment.</li>
	<li>Mix dental cement with accelerant in a porcelain mixing tray. Utilize a small spatula to transfer dental cement onto the tissue adhesive layer. Use dental cement to adhere the backplate to the surgical field, centered over the window. Allow 10 minutes for the dental cement to cure. 
	Note: The firm adhesion of the backplate to the anterior and posterior articular processes provides the fundamental structural stability of the implant.</li>
	<li>Use additional dental cement to fill in the interior base of the backplate, and the underside of the backplate : tissue interface. 
	Note: The extra application of dental cement improves adherence and reduces risk of leakage of microscope objective immersion fluid (saline) out the bottom of the backplate.</li>
	<li>Advance the forked backplate holder to the appropriate position over the window. Secure the backplate into the backplate holder with screws. 
	Note: This protocol utilized a custom-machined backplate holder (Figure 2G&#8210;H).</li>
	<li>Apply saline to the backplate to test for leakage. If any fluid leaks, dry the area and apply more dental cement.</li>
</ol>
6. Imaging Preparation
<ol>
	<li>Transfer the animal on the surgical platform to the optical table. 
	Note: Our surgical platform, backplate holder, and isoflurane nose-cone holder can be transported between surgical and two-photon imaging stations as one unit, while applying continuous isoflurane anesthesia (Figure 2D,H). Similar units can be assembled from holding forks, beams, and supportive pillar posts obtainable from commercial sources (e.g. ThorLabs). For intravital microscopy, there should be at least 11 inches of clearance between the microscope objective and the optical table to accommodate the height of the surgical platform.</li>
	<li>Affix the surgical platform to the optical table using a stainless-steel mounting post and counterbored clamping fork.</li>
	<li>Apply fresh saline into the well of the backplate. Lower a water-immersion lens into the well.</li>
	<li>Use transmitted or epifluorescence light to identify the area of interest and focus. Switch to laser scanning mode and perform in vivo imaging according to the appropriate two-photon laser excitation wavelength, dichroics and bandpass filters for the fluorophores present in the tissue6.</li>
</ol>

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The authors have nothing to disclose.

The method described here allows for stable imaging of the spinal cord in mice through a glass window. This method has been applied to assess BBB remodeling in transgenic eGFP:Claudin5+/- mice that express a fluorescent BBB tight junction protein, but it could be applied equally well for studies of any fluorescent proteins or cells in the spinal cord.
Multiple methods for laminectomy and spinal cord stabilization have been developed. All protocols address stabilizing the spinal cord during ima...

Transgenic animal models expressing fluorescent proteins, when combined with intravital microscopy, provide a powerful platform for addressing biology and pathophysiology. To apply these techniques to the spinal cord, specialized protocols are required to prepare the spinal cord for imaging. One such strategy is to conduct a laminectomy and spinal cord window implantation. The key features of an ideal laminectomy protocol for microscopy include preservation of native tissue structure and function, stability of the imaging field, quick processing time, and reproducibility of results. A particular challenge is to stabilize the imaging field against the motion induced by respiration and heartbeat. Multiple ex vivo and in vivo strategies have been reported to achieve these goals1,2,3,4,5. Most in vivo methods involve clamping the sides of the spinal column2,4 and is often followed by implanting a rigid metal apparatus3,4 for stability during surgery and downstream imaging applications. Clamping the spinal column can potentially compromise blood flow and induce blood-brain barrier (BBB) protein remodeling.
The purpose of this method is to make the intact spinal cord available for optical imaging in the living mouse while minimizing the invasiveness of the protocol and improving outcomes. We describe a single laminectomy and cover-glass implantation procedure paired with a minimally invasive oval plastic 3D-printed backplate that still achieves robust mechanical stability. The backplate is directly adhered to the anterior and posterior vertebral spines with dental cement. The backplate is equipped with lateral extension arms with screw holes that rigidly attach to the microscope stage via a metal arm. This effectively anchors the intact anterior and posterior vertebra to the microscope stage, providing mechanical resistance to the motion artifact that would otherwise be introduced by respiration and heartbeat. The method has been optimized for laminectomy of a single vertebra at thoracic level 12, omitting the clamps utilized in alternative strategies for stability during in vivo imaging. The procedure is rapid, taking approximately 30 min per mouse.
This protocol can be used to study disease mechanisms of the BBB. The BBB is a dynamic microvascular system comprised of endothelial cells, vascular smooth muscle, pericytes, and astrocyte foot processes that provide a highly selective environment for the central nervous system (CNS). Representative data depict the application of this protocol in transgenic mice engineered to express enhanced green fluorescent protein (eGFP):Claudin-5, a BBB tight junction protein. The provided backplate printing files can also be customized for alternative applications.

<table><tbody><tr><td>3D printer</td><td>Raise3D</td><td>Pro2</td><td>For printing backplates</td></tr><tr><td>PLA 3D printing filament</td><td>Inland</td><td>PLA+-175-B</td><td>Black plastic 3D printing material</td></tr><tr><td>3D CAD software</td><td>Dassault Systemes</td><td>Solidworks software</td><td>used to design 3D shapes</td></tr><tr><td>3D printer software</td><td>Raise3D</td><td>Ideamaker software</td><td>software used to interface with the 3D printer</td></tr><tr><td>3D printed oval backplate</td><td>custom</td><td></td><td>Stabilizing imaging field</td></tr><tr><td>Surgical dissecting microscope</td><td>Leica</td><td>M205 C</td><td>Equipped with Leica FusionOptics, Planapo 0.63x M-series objective, and gliding stage</td></tr><tr><td>Microscope camera</td><td>Leica</td><td>MC170</td><td>HD color camera for visualizing surgical field</td></tr><tr><td>Gliding stage</td><td>Leica</td><td>10446301</td><td>The gliding stage is constructed of two metal plates. The base plate is fixed. The upper plate slides on greased interface to allow rotational and linear movement.</td></tr><tr><td>Surgical station and stabilization fork</td><td>Whale Manufactoring</td><td>custom</td><td>Laminectomy</td></tr><tr><td>SomnoSuite low-flow isoflurane delivery unit</td><td>Kent Scientific</td><td>SS-01</td><td>Surgical anesthesia administration with integrated digitial vaporizer</td></tr><tr><td>Stainless steel 1.5 inch mounting post</td><td>ThorLabs</td><td>P50/M</td><td>For mounting surgical station onto optical table for two-photon imaging</td></tr><tr><td>Counterbored Clamping Fork for 1.5&quot; mounting Post</td><td>ThorLabs</td><td>PF175</td><td>For stabilizing surgical station mount onto optical table for two-photon imaging</td></tr><tr><td>Ideal bone microdrill</td><td>Harvard apparatus</td><td>72-6065</td><td>Thinning bone for laminectomy</td></tr><tr><td>Water bath</td><td>Fisher Scientific</td><td>15-462-10</td><td>Warming saline</td></tr><tr><td>Cautery gun</td><td>FST</td><td>18010-00</td><td>Cauterizing minor bleeds</td></tr><tr><td>Heating pad</td><td>Benchmark</td><td>BF11222</td><td>1.9&amp;rdquo; x 4.5&amp;rdquo; silicone heater with 20&amp;rdquo; Teflon leads, 10W, 5V</td></tr><tr><td>K type thermocoupled rectal probe</td><td>Physitemp</td><td>RET3</td><td>Measuring mouse body temperature</td></tr><tr><td>petroleum jelly</td><td>Sigma</td><td>8009-03-8</td><td>Lubricating rectal probe</td></tr><tr><td>Feedback-regulated thermal controller</td><td>custom</td><td>NA</td><td>Commercially available alternatives include the Physitemp TCAT series</td></tr><tr><td>PVA Surgical eye spears</td><td>Beaver-visitec international</td><td>40400-8</td><td>Absorbing blood</td></tr><tr><td>Electric trimmer</td><td>Wahl</td><td>41590-0438</td><td>Trimming mouse fur</td></tr><tr><td>Blade, #11</td><td>FST</td><td>14002-14</td><td>Surgical tool</td></tr><tr><td>Forceps, #5</td><td>FST</td><td>11254-20</td><td>Surgical tool</td></tr><tr><td>Forceps, #4</td><td>FST</td><td>14002-14</td><td>Surgical tool</td></tr><tr><td>Titatnium toothed forceps</td><td>WPI</td><td>555047FT</td><td>Surgical tool</td></tr><tr><td>Titanium Iris scissors</td><td>WPI</td><td>555562S</td><td>Surgical tool</td></tr><tr><td>Vetbond tissue adhesive</td><td>3M</td><td>084-1469SB</td><td>Preparing tissue surface for dental acrylic</td></tr><tr><td>Ceramic mixing tray</td><td>Jack Richeson</td><td>420716</td><td>Mixing dental acrylic agent with accelerant</td></tr><tr><td>Orthojet dental acrylic</td><td>Lang Dental</td><td>1520BLK, 1503BLK</td><td>Permanently bonding backplate to tissue</td></tr><tr><td>Small round cover glass, #1 thickness, 3 mm</td><td>Harvard apparatus</td><td>64-0720</td><td>optical window</td></tr><tr><td>NaCl</td><td>Fisher Scientific</td><td>7647-14-5</td><td>For aCSF</td></tr><tr><td>KCl</td><td>Fisher Scientific</td><td>7447-40-7</td><td>For aCSF</td></tr><tr><td>Glucose</td><td>Fisher Scientific</td><td>50-99-7</td><td>For aCSF</td></tr><tr><td>HEPES</td><td>Sigma</td><td>7365-45-9</td><td>For aCSF</td></tr><tr><td>MgCl2&amp;middot;6H2O</td><td>Fisher Scientific</td><td>7791-18-6</td><td>For aCSF</td></tr><tr><td>CaCl&lt;sub&gt;2&lt;/sub&gt;&amp;middot;2H&lt;sub&gt;2&lt;/sub&gt;O</td><td>Fisher Scientific</td><td>10035-04-8</td><td>For aCSF</td></tr><tr><td>Carprofen</td><td>Rimadyl</td><td>QM01AE91</td><td>Analgesia</td></tr><tr><td>Bacteriostatic water</td><td>Henry Schein</td><td>2587428</td><td>Diluent for carprofen</td></tr><tr><td>Isoflurane</td><td>Henry Schein</td><td>11695-6776-2</td><td>Anesthesia</td></tr><tr><td>Lactated ringer solution</td><td>Baxter</td><td>0338-0117-04</td><td>Hydration for mouse</td></tr><tr><td>Agarose High EEO</td><td>Sigma</td><td>A9793</td><td>gel point 34-37 degrees C</td></tr><tr><td>Opthalmic lubricating ointment</td><td>Akwa Tears</td><td>68788-0697</td><td>Prevent corneal drying</td></tr><tr><td>MOM Two-Photon Microscope</td><td>Sutter</td><td></td><td></td></tr></tbody></table>

laminectomy and spinal cord window implantation in the mouse

This protocol describes a method for spinal cord laminectomy and glass window implantation for in vivo imaging of the mouse spinal cord. An integrated digital vaporizer is utilized to achieve a stable plane of anesthesia at a low-flow rate of isoflurane. A single vertebral spine is removed, and a commercially available cover-glass is overlaid on a thin agarose bed. A 3D-printed plastic backplate is then affixed to the adjacent vertebral spines using tissue adhesive and dental cement. A stabilization platform is used to reduce motion artifact from respiration and heartbeat. This rapid and clamp-free method is well-suited for acute multi-photon fluorescence microscopy. Representative data are included for an application of this technique to two-photon microscopy of the spinal cord vasculature in transgenic mice expressing eGFP:Claudin-5 &#8212; a tight junction protein.

Implanted glass windows and intravital two-photon microscopy provides a useful tool for assessing dynamic changes in CNS proteins. The functional integrity of the BBB is influenced by the expression, subcellular localization, and turnover rates of tight junction proteins7. Previous studies have demonstrated that tight junction proteins undergo rapid and dynamic remodeling at steady state8. The currently described laminectomy and glass window...

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Laminectomy and Spinal Cord Window Implantation in the Mouse

This protocol describes implantation of a glass window onto the spinal cord of a mouse to facilitate visualization by intravital microscopy.

This protocol describes a method for spinal cord laminectomy and glass window implantation for in vivo imaging of the mouse spinal cord. An integrated ...

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12.0K Views.  University of Illinois at Chicago College of Medicine. This protocol describes implantation of a glass window onto the spinal cord of a mouse to facilitate visualization by intravital microscopy.

Video: Laminectomy and Spinal Cord Window Implantation in the Mouse

In vivo Imaging of the Mouse Spinal Cord Using Two-photon Microscopy

In vivo imaging using two-photon microscopy 1 in mice that have been genetically engineered to express fluorescent proteins in specific cell types 2-3 has significantly broadened our knowledge of physiological and pathological processes in numerous tissues in vivo 4-7. In studies of the central nervous system (CNS), there has been a broad application of in vivo imaging in the brain, which has produced a plethora of novel and often unexpected findings about the behavior of cells such as neurons, astrocytes, microglia, under physiological or pathological conditions 8-17. However, mostly technical complications have limited the implementation of in vivo imaging in studies of the living mouse spinal cord. In particular, the anatomical proximity of the spinal cord to the lungs and heart generates significant movement artifact that makes imaging the living spinal cord a challenging task.
We developed a novel method that overcomes the inherent limitations of spinal cord imaging by stabilizing the spinal column, reducing respiratory-induced movements and thereby facilitating the use of two-photon microscopy to image the mouse spinal cord in vivo. This is achieved by combining a customized spinal stabilization device with a method of deep anesthesia, resulting in a significant reduction of respiratory-induced movements. This video protocol shows how to expose a small area of the living spinal cord that can be maintained under stable physiological conditions over extended periods of time by keeping tissue injury and bleeding to a minimum. Representative raw images acquired in vivo detail in high resolution the close relationship between microglia and the vasculature. A timelapse sequence shows the dynamic behavior of microglial processes in the living mouse spinal cord. Moreover, a continuous scan of the same z-frame demonstrates the outstanding stability that this method can achieve to generate stacks of images and/or timelapse movies that do not require image alignment post-acquisition. Finally, we show how this method can be used to revisit and reimage the same area of the spinal cord at later timepoints, allowing for longitudinal studies of ongoing physiological or pathological processes in vivo.

In vivo Imaging of the Mouse Spinal Cord Using Two-photon Microscopy

A minimally invasive protocol to stabilize the mouse spinal column and perform repetitive in vivo spinal cord imaging using two-photon microscopy is described. This method combines a spinal stabilization device and an anesthetic regimen to minimize respiratory-induced movements and produce raw imaging data that require no alignment or other post-processing.

In vivo imaging using two-photon microscopy 1 in mice that have been genetically engineered to express fluorescent proteins in specific cell types 2-3 has ...

Surgical Transplantation of Mouse Neural Stem Cells into the Spinal Cords of Mice Infected with Neurotropic Mouse Hepatitis Virus

Mice infected with the neurotropic JHM strain of mouse hepatitis virus (MHV) develop pathological and clinical outcomes similar to patients with the demyelinating disease Multiple Sclerosis (MS). We have shown that transplantation of NSCs into the spinal cords of sick mice results in a significant improvement in both remyelination and in clinical outcome. Cell replacement therapies for the treatment of chronic neurologic diseases are now a reality and in vivo models are vital in understanding the interactions between the engrafted cells and host tissue microenvironment. This presentation provides an adapted method for transplanting cells into the spinal cord of JHMV-infected mice. In brief, we provide a procedure for i) preparation of NSCs prior to transplant, ii) pre-operative care of mice, iii) exposure of the spinal cord via laminectomy, iv) stereotactic injection of NSCs, and iv) post-operative care.

The transplantation of mouse neural stem cells (NSCs) into the spinal cords of mice with established demyelination is detailed. The preparation of NSCs, the laminectomy of thoracic vertebra 9 (T9), and transplantation of NSCs is outlined along with the pre- and post-operative care of the mice.

Mice infected with the neurotropic JHM strain of mouse hepatitis virus (MHV) develop pathological and clinical outcomes similar to patients with the ...

Implanting Glass Spinal Cord Windows in Adult Mice with Experimental Autoimmune Encephalomyelitis

Experimental autoimmune encephalomyelitis (EAE) in adult rodents is the standard experimental model for studying autonomic demyelinating diseases such as multiple sclerosis. Here we present a low-cost and reproducible glass window implantation protocol that is suitable for intravital microscopy and studying the dynamics of spinal cord cytoarchitecture with subcellular resolution in live adult mice with EAE. Briefly, we surgically expose the vertebrae T12-L2 and construct a chamber around the exposed vertebrae using a combination of cyanoacrylate and dental cement. A laminectomy is performed from T13 to L1, and a thin layer of transparent silicone elastomer is applied to the dorsal surface of the exposed spinal cord. A modified glass cover slip is implanted over the exposed spinal cord taking care that the glass does not directly contact the spinal cord. To reduce the infiltration of inflammatory cells between the window and spinal cord, anti-inflammatory treatment is administered every 2 days (as recommended by ethics committee) for the first 10 days after implantation. EAE is induced only 2-3 weeks after the cessation of anti-inflammatory treatment.
Using this approach we successfully induced EAE in 87% of animals with implanted windows and, using Thy1-CFP-23 mice (blue axons in dorsal spinal cord), quantified axonal loss throughout EAE progression. Taken together, this protocol may be useful for studying the recruitment of various cell populations as well as their interaction dynamics, with subcellular resolution and for extended periods of time. This intravital imaging modality represents a valuable tool for developing therapeutic strategies to treat autoimmune demyelinating diseases such as EAE.

We describe a method for implanting and maintaining glass windows over the exposed spinal cords of adult mice for studying experimental autoimmune encephalomyelitis. These windows provide chronic optical access to the spinal cord for monitoring cell dynamics at the subcellular level in live animals using two-photon microscopy.

Experimental autoimmune encephalomyelitis (EAE) in adult rodents is the standard experimental model for studying autonomic demyelinating diseases such as ...

Medicine

Stereotaxic Injection of a Viral Vector for Conditional Gene Manipulation in the Mouse Spinal Cord

Intraparenchymal injection of a viral vector enables conditional gene manipulation in distinct populations of neurons or particular regions of the central nervous system. We demonstrate a stereotaxic injection technique that allows targeted gene expression or silencing in the dorsal horn of the mouse spinal cord. The surgical procedure is brief. It requires laminectomy of a single vertebra, providing for quick recovery of the animal and unimpaired motility of the spine. Controlled injection of a small vector suspension volume at low speed and use of a microsyringe with beveled glass cannula minimize the tissue lesion. The local immune response to the vector depends on the intrinsic properties of the virus employed; in our experience, it is minor and short-lived when a recombinant adeno-associated virus is used. A reporter gene such as enhanced green fluorescent protein facilitates monitoring spatial distribution of the vector, and the efficacy and cellular specificity of the transfection.

Viral vectors allow for targeted gene manipulation. We demonstrate a method for conditional gene expression or ablation in the mouse spinal cord, using stereotaxic injection of a viral vector into the dorsal horn, a prominent site of synaptic contact between primary somatosensory afferents and neurons of the central nervous system.

Intraparenchymal injection of a viral vector enables conditional gene manipulation in distinct populations of neurons or particular regions of the central ...

Neural Stem Cell Transplantation in Experimental Contusive Model of Spinal Cord Injury

Spinal cord injury is a devastating clinical condition, characterized by a complex of neurological dysfunctions. Animal models of spinal cord injury can be used both to investigate the biological responses to injury and to test potential therapies. Contusion or compression injury delivered to the surgically exposed spinal cord are the most widely used models of the pathology. In this report the experimental contusion is performed by using the Infinite Horizon (IH) Impactor device, which allows the creation of a reproducible injury animal model through definition of specific injury parameters. Stem cell transplantation is commonly considered a potentially useful strategy for curing this debilitating condition. Numerous studies have evaluated the effects of transplanting a variety of stem cells. Here we demonstrate an adapted method for spinal cord injury followed by tail vein injection of cells in CD1 mice. In short, we provide procedures for: i) cell labeling with a vital tracer, ii) pre-operative care of mice, iii) execution of a contusive spinal cord injury, and iv) intravenous administration of post mortem neural precursors. This contusion model can be utilized to evaluate the efficacy and safety of stem cell transplantation in a regenerative medicine approach.

Spinal cord injury is a traumatic condition that causes severe morbidity and high mortality. In this work we describe in detail a contusion model of spinal cord injury in mice followed by a transplantation of neural stem cells.

Spinal cord injury is a devastating clinical condition, characterized by a complex of neurological dysfunctions. Animal models of spinal cord injury can ...

A Procedure for Implanting a Spinal Chamber for Longitudinal In Vivo Imaging of the Mouse Spinal Cord

Studies in the mammalian neocortex have enabled unprecedented resolution of cortical structure, activity, and response to neurodegenerative insults by repeated, time-lapse in vivo imaging in live rodents. These studies were made possible by straightforward surgical procedures, which enabled optical access for a prolonged period of time without repeat surgical procedures. In contrast, analogous studies of the spinal cord have been previously limited to only a few imaging sessions, each of which required an invasive surgery. As previously described, we have developed a spinal chamber that enables continuous optical access for upwards of 8 weeks, preserves mechanical stability of the spinal column, is easily stabilized externally during imaging, and requires only a single surgery. Here, the design of the spinal chamber with its associated surgical implements is reviewed and the surgical procedure is demonstrated in detail. Briefly, this video will demonstrate the preparation of the surgical area and mouse for surgery, exposure of the spinal vertebra and appropriate tissue debridement, the delivery of the implant and vertebral clamping, the completion of the chamber, the removal of the delivery system, sealing of the skin, and finally, post-operative care. The procedure for chronic in vivo imaging using nonlinear microscopy will also be demonstrated. Finally, outcomes, limitations, typical variability, and a guide for troubleshooting are discussed.

A Procedure for Implanting a Spinal Chamber for Longitudinal In Vivo Imaging of the Mouse Spinal Cord

In this video, we describe a procedure for implanting a chronic optical imaging chamber over the dorsal spinal cord of a live mouse. The chamber, surgical procedure, and chronic imaging are reviewed and demonstrated.

Studies in the mammalian neocortex have enabled unprecedented resolution of cortical structure, activity, and response to neurodegenerative insults by ...

Induction of Complete Transection-Type Spinal Cord Injury in Mice

Spinal cord injury (SCI) largely leads to irreversible and permanent loss of function, most commonly as a result of trauma. Several treatment options, such as cell transplantation methods, are being researched to overcome the debilitating disabilities arising from SCI. Most pre-clinical animal trials are conducted in rodent models of SCI. While rat models of SCI have been widely used, mouse models have received less attention, even though mouse models can have significant advantages over rat models. The small size of mice equates to lower animal maintenance costs than for rats, and the availability of numerous transgenic mouse models is advantageous for many types of studies. Inducing repeatable and precise injury in the animals is the primary challenge for SCI research, which in small rodents requires high-precision surgery. The transection-type injury model has been a commonly used injury model over the last decade for transplantation-based therapeutic research, however a standardized method for inducing a complete transection-type injury in mice does not exist. We have developed a surgical protocol for inducing a complete transection type injury in C57BL/6 mice at thoracic vertebral level 10 (T10). The procedure uses a small tip drill instead of rongeurs to precisely remove the lamina, after which a thin blade with rounded cutting edge is used to induce the spinal cord transection. This method leads to reproducible transection-type injury in small rodents with minimal collateral muscle and bone damage and therefore minimizes confounding factors, specifically where behavioral functional outcomes are analyzed.

This protocol describes how to create a precise laminectomy for induction of stable transection-type spinal cord injury in the mouse model, with minimal collateral damage for spinal cord injury research.

Spinal cord injury (SCI) largely leads to irreversible and permanent loss of function, most commonly as a result of trauma. Several treatment options, ...

A Spinal Cord Injury Contusion Device for Accurate Mouse Models

Automated Impactor for Contusive Spinal Cord Injury Model in Mice

Spinal cord injury (SCI) due to traumatic injuries such as car accidents and falls is associated with permanent spinal cord dysfunction. Creation of contusion models of spinal cord injury by impacting the spinal cord results in similar pathologies to most spinal cord injuries in clinical practice. Accurate, reproducible, and convenient animal models of spinal cord injury are essential for studying spinal cord injury. We present a novel automated spinal cord injury contusion device for mice, the Guangzhou Jinan University smart spinal cord injury system, that can produce spinal cord injury contusion models with accuracy, reproducibility, and convenience. The system accurately produces models of varying degrees of spinal cord injury via laser distance sensors combined with an automated mobile platform and advanced software. We used this system to create three levels of spinal cord injury mice models, determined their Basso mouse scale (BMS) scores, and performed behavioral as well as staining assays to demonstrate its accuracy and reproducibility. We show each step of the development of the injury models using this device, forming a standardized procedure. This method produces reproducible spinal cord injury contusion mice models and reduces human manipulation factors via convenient handling procedures. The developed animal model is reliable for studying spinal cord injury mechanisms and associated treatment approaches.

Author Spotlight: Insight Into Innovations in Spinal Cord Injury Research

Presented here is a novel automated spinal cord injury contusion device for mice, which can accurately produce spinal cord injury contusion models with varying degrees.

Spinal cord injury (SCI) due to traumatic injuries such as car accidents and falls is associated with permanent spinal cord dysfunction. Creation of ...

Targeting Mouse Sympathetic Neurons: A Lumbar Sympathectomy Approach

Surgical Lumbar Sympathectomy in Mice

Peripheral nerve injuries are common, and full functional recovery after injury is achieved in only 10% of patients. The sympathetic nervous system plays many critical roles in maintaining bodily homeostasis, but it has rarely been studied in the context of peripheral nerve injury. The extent of postganglionic sympathetic neuronal functions in distal targets in the periphery is currently unclear. To better explore the role of sympathetic innervation of peripheral targets, a surgical &#34;knock-out&#34; model provides an alternative approach. Although this can be achieved chemically, chemical destruction of postganglionic sympathetic neurons can be nonspecific and dose-dependent. The use of a surgical lumbar sympathectomy in mice, once thought to be &#34;virtually not practicable&#34; in small animals, allows for specific targeting of postganglionic sympathetic neurons that innervate the hind limbs. This manuscript describes how to surgically remove the L2-L5 lumbar sympathetic ganglia from a mouse as a survival surgery, which reliably decreases the hind paw sweat response and the number of sympathetic axons in the sciatic nerve.

Author Spotlight: Exploring Plasticity of Sympathetic Neurons

This manuscript presents a protocol for surgically removing the postganglionic lumbar sympathetic neurons from a mouse. This procedure will facilitate a multitude of studies aimed at investigating the role of sympathetic innervation in distal tissue targets.

Peripheral nerve injuries are common, and full functional recovery after injury is achieved in only 10% of patients. The sympathetic nervous system plays ...

Installation of Optical Windows in the Brain of Transgenic Mice to Image Neural Activities

Source: Lin, X., et al. <a href="https://app.jove.com/v/56297">Imaging Neural Activity in the Primary Somatosensory Cortex Using Thy1-GCaMP6s Transgenic Mice.</a> J. Vis. Exp. (2019).
This video demonstrates the brain&#39;s neural activity recording through an optical window in transgenic mice. The mice express a fluorescent protein that enables the detection of neural activities. A small portion of the skull is carefully removed to install an optical window, and the skull is then covered with black cement to block light before imaging.

Instalacja okien optycznych w mózgu myszy transgenicznych w celu zobrazowania aktywności neuronalnej

All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.
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Laminectomy and Spinal Cord Window Implantation in the Mouse

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In vivo Imaging of the Mouse Spinal Cord Using Two-photon Microscopy

Surgical Transplantation of Mouse Neural Stem Cells into the Spinal Cords of Mice Infected with Neurotropic Mouse Hepatitis Virus

Implanting Glass Spinal Cord Windows in Adult Mice with Experimental Autoimmune Encephalomyelitis

Stereotaxic Injection of a Viral Vector for Conditional Gene Manipulation in the Mouse Spinal Cord

Neural Stem Cell Transplantation in Experimental Contusive Model of Spinal Cord Injury

A Procedure for Implanting a Spinal Chamber for Longitudinal In Vivo Imaging of the Mouse Spinal Cord

Induction of Complete Transection-Type Spinal Cord Injury in Mice

Automated Impactor for Contusive Spinal Cord Injury Model in Mice

Surgical Lumbar Sympathectomy in Mice

Instalacja okien optycznych w mózgu myszy transgenicznych w celu zobrazowania aktywności neuronalnej