This work was supported by Grant-in-Aid for Transformative Research Areas (A) &#39;Glial Decoding&#39; (JP21H05621 to SM), JSPS KAKENHI (JP19K06883 to SM, 15KK0340 to ES, JP22H00432, JP22H05160, JP17H06312 to HB, and JP17H06313 to KK), Grant-in-Aid for Brain Mapping by Integrated Neurotechnologies for Disease Studies (Brain/MINDS) (JP19dm0207079h0002 to SM, JP19dm0207079 to HB, and JP19dm0207080 to KK), Narishige Neuroscience Research Foundation (to SM), Grant for Young Researcher from Yamanashi Prefecture (to SM), and Takeda Science Foundation (to SM) and partially supported by The Frontier Brain Research Grant from Univ. Yamanashi.
We thank N. Yaguchi and K. Okazaki for animal care and technical assistance and members of the Kitamura lab for helpful discussions.

The experimental procedures were approved by the Animal Experiment Committee of University of Yamanashi. Wild-type (C57BL/6J, Japan SLC) and transgenic mice expressing membrane-anchored GECI (Lck-GCaMP6f) in astrocytes were used in this study. The transgenic mice were obtained by crossing AldH1l1-CreERT2 mice [B6N.FVB-Tg(Aldh1l1-cre/ERT2)1Khakh/J, commercially obtained, see Table of Materials] and Flx-Lck-GCaMP6f mice [C57BL/6N-Gt(ROSA)26Sor&#60;tm1(CAG-GCaMP6f)Khak&#62;/J, commercially obtained] mice. The transgenic mice were treated with tamoxifen (20 mg/mL) for 5 days (0.05 mL/10 g bw, i.p.) to express GCaMP6f. All mice used were males and females at least 4 weeks old. The schematic of the window is shown in Figure 1A, and the surgical procedure is summarized in Figure 1B.
1. Preparation for cranial window surgery
<ol>
	<li>Anesthetize mice with isoflurane (induction: 3%, surgery: 1%-1.5%, flow rate: 0.2-0.3 L/min). Confirm the depth of anesthesia by the loss of tail or toe pinch reflex. Maintain the body temperature using a heating pad (36-38 &#176;C). Apply eye ointment with a cotton swab to prevent the eyes of mice from drying out under anesthesia.</li>
	<li>Inject 15% mannitol solution (see Table of Materials) intraperitoneally (3 mL/100 g body weight). Fix the head of the mouse on a stereotaxic frame with ear bars. Remove hair from the head of the mouse using a shaver and hair removal cream.</li>
	<li>Disinfect the skin surface with povidone-iodine and alcohol three times.&#160;Apply Lidocaine topically to provide preemptive analgesia. Remove the skin over the area of interest with surgical scissors and expose the skull (size: 15 x 15 mm). If bleeding is present, use a cotton swab to stop the bleeding. 
	NOTE: In this study, the skin was removed to observe the prefrontal cortex to the visual cortex.</li>
	<li>Remove the periosteum over the exposed skull using a micro curette and dry the skull surface to firmly attach the head plate to the skull with dental cement (see Table of Materials) (Figure 2B). 
	NOTE: The custom-made head plate is created using a 3D printer. The design file is deposited to the Github repository (https://github.com/Satoshi-Manita/Head-plates).</li>
	<li>Attach the head plate using dental cement (Figure 2C). Wait at least 20 min for the cement to harden. Secure the head plate with the head plate holder35.</li>
</ol>
2. Making the cranial window
<ol>
	<li>Remove the extra cement over the skull with a dental drill (see Table of Materials). Be careful not to drill through the bone and damage the brain by drilling.</li>
	<li>Mark the area to be cut with a pen and cut into the bone with a scalpel. Blunt the tip of the scalpel to ensure that the tip does not penetrate the skull (Supplementary Figure 1). Reference the brain atlas to determine where to make the window. 
	NOTE: For the present study, a window was created between -2 mm and +4 mm from bregma in the anteroposterior axis and from sagittal suture to +3 mm in the mediolateral axis, including the motor, somatosensory, and visual cortices.</li>
	<li>Scrape the bone repeatedly with a scalpel to deepen the groove until the bone in the area to be trimmed moves well when lightly touched.</li>
	<li>Remove the incised bone with fine tweezers. Do not push the bone flap into the brain, which may damage the brain (Figure 1Ba). 
	NOTE: If bleeding is observed after removing the bone, immediately apply and aspirate artificial cerebrospinal fluid (ACSF, see Table of Materials) and repeat this process until the bleeding stops. Alternatively, place a hemostatic gelatin sponge (about 3 mm square cubes) soaked in the ACSF on the bleeding point.</li>
	<li>If the dura is not removed, proceed to step 2.7.</li>
	<li>Remove the dura mater following the steps below.
	<ol>
		<li>Remove the dura, for example, in the following situations; transfection using the fibroin-AAV film method36 and observing small structures such as dendritic spines.</li>
		<li>Cut the dura using a pulled glass pipette with a tapered tip of about 10 &#181;m. To expand this cut over the entire window, use a U-shaped needle.</li>
		<li>Set the stereomicroscope zoom to 60-100x and remove the severed dura mater with ultrafine tweezers. If removing the dura mater causes bleeding, rinse with ACSF or use a gelatin sponge to stop the bleeding.</li>
	</ol>
	</li>
	<li>Cut out the PVDC wrap.
	<ol>
		<li>Sterilize a large (for example, 10 x 15 mm) piece of PVDC wrap (about 11 &#956;m, see Table of Materials, Figure 2Aa) by autoclaving and with 70% ethanol.</li>
		<li>Under a stereomicroscope, use tweezers and a scalpel to cut out a wrap of the required size. 
		NOTE: The wrap size needs to be approximately 10 mm larger than the size of the cranial window but smaller than the opening of the head plate. For a 6 x 3 mm2 cranial window, prepare a 15 x 10 mm2 wrap.</li>
	</ol>
	</li>
	<li>Place the wrap accurately following the steps below.
	<ol>
		<li>Place the wrap on the brain surface, leaving the ACSF on the surface. Suck out the ACSF from the edge of the wrap, allowing the wrap to stick firmly to the brain surface (Figure 1Bb,c). 
		NOTE: The wrap used is wrinkle-resistant, so just placing it on the brain&#39;s surface produces almost no wrinkles.</li>
		<li>Trim the wrap with a scalpel and tweezers so that there is approximately a 1 mm margin between the edge of the cranial window and the wrap (Figure 1Bd).</li>
		<li>Once the wrap is in place, glue the edge of the wrap to the skull with a biological adhesive (see Table of Materials, Figure 2D). Allow the adhesive to dry for about 30 min.</li>
	</ol>
	</li>
	<li>Apply the transparent silicone elastomer.
	<ol>
		<li>Apply the commercially available transparent silicone elastomer (see Table of Materials) on top of the wrap using a dispenser with a mixing tip (Figure 1Be, 2Ab-d) and place the cover glass (0.12-0.17 mm thickness) on top (Figure 2E).</li>
		<li>Seal the perimeter of the cover glass with waterproof film, superglue, or dental cement (Figure 1Bf).</li>
	</ol>
	</li>
	<li>After surgery, monitor the mouse until it regains consciousness to maintain sternal recumbency. After that, keep the mice individually, and allow them to recover in their home cage for at least 7 days.
	<ol>
		<li>To reduce stress and pain, administer anti-inflammatory and analgesic agents (e.g., dexamethasone and ketoprofen, 5 mg/kg each, i.p.).</li>
	</ol>
	</li>
	<li>Monitor the mice regularly for infection. If an infection is confirmed, administer an antimicrobial drug (e.g., 10 % enrofloxacin, 1.7 &#181;L/mL) in the drinking water until the infection is eliminated (typically less than 4 weeks).</li>
</ol>
3. Making AAV film on plastic wrap using fibroin solution
NOTE: Step 3 is optional.
<ol>
	<li>Prepare fibroin solution from silkworm cocoons following a previously published method37.
	<ol>
		<li>In brief, boil commercially available normal silkworm cocoons (5 g, see Table of Materials) in sodium carbonate solution (0.02 M, 2 L). Wash the cocoons in ultrapure water and dry overnight.</li>
		<li>Dissolve the dried cocoons in lithium bromide solution (9.3 M, 20% w/v fibroin) while heating in an oven at 60 &#176;C for 4 h. Dialyze the dissolved cocoon solution, centrifuge (twice at 12,700 x g, at 4 &#176;C for 20 min)37, and collect the supernatant.</li>
	</ol>
	</li>
	<li>Prepare the fibroin-AAV film following the steps below.
	<ol>
		<li>Mix fibroin and AAV solutions20 in a 1:4 ratio in a small sample tube using a micropipette. Drop an aliquot of the mixed fibroin-AAV solution onto the plastic wrap for the cranial window, and dry it for at least 3 h. 
		NOTE: For expression in an area of 3 mm in diameter, apply a 5 &#181;L drop of fibroin-AAV solution. This ratio determines the amount of solution for a given area.</li>
		<li>After drying, cut the plastic wrap into the required size for the window (for example, 10 x 15 mm) and place it on the brain surface. Then, follow the abovementioned method from step 2.8.1 onward. 
		NOTE: Before placing the wrap on the brain surface, remove the ACSF on the brain surface as much as possible. This is because the ACSF is expected to dissolve the fibroin-AAV film and reduce the concentration of AAV particles.</li>
		<li>Wait about 2-4 weeks after creating the AAV-treated window until the GECIs are expressed sufficiently. During this process, check the condition of the mice and windows regularly.</li>
	</ol>
	</li>
</ol>
4. Calcium imaging and analysis
NOTE: For details on the imaging and analysis, please see previously published reports1,2,38.
<ol>
	<li>Perform wide-field imaging following the steps below.
	<ol>
		<li>Immobilize the mouse using a head fixation device under a tandem lens fluorescence macroscope (see Table of Materials).</li>
		<li>Illuminate the cerebral cortex of mice with excitation light from a 465 nm LED light source through an excitation filter, dichroic mirror, and objective lens.</li>
		<li>Collect the fluorescence images of the cerebral cortex by a CCD camera through an objective lens (1.0x), dichroic mirror, emission filter, and imaging lens (2.0x). The combination of these lenses gives a total magnification of about 0.5x.</li>
		<li>Acquire images at a sampling frequency of 50 Hz. After data acquisition, analyze the images using ImageJ software. Select the region of interest (ROI) manually. Calculate fluorescence change in each ROI as &#916;F/F = (Ft - F0) / F0, where Ft is the raw fluorescence value of each frame and F0 is the mean fluorescence value obtained from an average image of all frames. 
		NOTE: A macro program for ImageJ is deposited to GitHub (https://github.com/Satoshi-Manita/ImageJ-macro), which calculates &#916;F/F images from calcium imaging data.</li>
	</ol>
	</li>
	<li>Perform two-photon imaging following the steps below.
	<ol>
		<li>Immobilize the mouse under a two-photon microscope using a head fixation device. Identify the area to be imaged using the microscope in bright-field mode with a low magnification (5x) objective lens.</li>
		<li>Switch to two-photon imaging. Use a high magnification objective lens (16x or 25x) and illuminate the laser for two-photon excitation. 
		NOTE: Green Lck-GCaMP6f22 and red XCaMP-R36 were excited by an ultrafast laser at excitation wavelengths of 920 nm and 1070 nm, respectively.</li>
		<li>Acquire fluorescence images at 30 Hz. After data acquisition, correct motion artifacts by the registration function of the suite2p software39. Obtain ROI and &#916;F/F from images using the same method for wide-field imaging.</li>
	</ol>
	</li>
	<li>Plot the data using python with the following libraries: NumPy, Matplotlib, and Pandas (see Table of Materials).</li>
</ol>

The authors have nothing to disclose.

This article presents an inexpensive method of creating a large cranial window using a PVDC plastic wrap, transparent silicone, and cover glass. Using this method, we showed that wide-field calcium imaging could be performed over a wide area of the cerebral cortex. Two-photon calcium imaging can be performed from several different cortical regions in the same mouse that has undergone wide-field imaging. Furthermore, it has been shown that a fibroin-AAV film on the plastic wrap used for the window could express GECI over a wide area of the cortex.
Critical steps 
It is important to avoid infection and damage to the brain when making cranial windows using plastic wrap. In these conditions, neural and glial activity cannot be observed, and imaging of deeper areas is impossible. Injury to blood vessels also results in bleeding, making imaging impossible due to blood. To avoid infection, making the brain surface and the wrap attached as tightly as possible is critical by sucking out the ACSF. Mannitol administration is important to avoid brain and blood vessel damage by preventing increased brain pressure during surgery. This maintains the space between the surface of the brain and the dura mater and prevents the brain and blood vessels from being touched during the removal of the skull and dura mater. A stereo microscope with high magnification and tweezers with sharp tips are also effective for accurate surgery.
In the fibroin-AAV method, it is essential to use flesh silkworm cocoons, not to freeze fibroin solution, to dry the fibroin-AAV solution sufficiently, and to apply enough volume of solution (5 &#181;L per 3 mm diameter). When older cocoons were used, expression efficiency was lower. This is because fibroin from old cocoons may be denatured easily. When fibroin solution was frozen at -80 &#176;C and thawed at the time of use, expression efficiency was poor. This may be due to the denaturation of the protein due to freezing and thawing. Since fibroin solutions stored at 4 &#176;C can be effectively used until gelation, it is recommended that fibroin solutions are kept refrigerated and purified from cocoons again after gelation. The fibroin-AAV solution should be dried for at least 3 h, as the expression is poor after less than 3 h. Finally, the area of expression depends on the amount of fibroin-AAV solution used. In the example in Figure 3M, the amount was small (5 &#181;L); thus, the fibroin-AAV film only covered the upper half of the window, resulting in non-uniform expression over the window. If a sufficient amount of fibroin-AAV is used, the expression will be uniform over the whole window.
Modifications of the technique 
The novel cranial window technique allows one to examine the macroscopic activity of cortical circuits and their underlying single-cell-level activity in the same mouse. Thus, the method can be applied to a variety of neuroscience studies. For example, it can be used to observe cortical activity during decision-making tasks, motor learning, and in mouse models of brain injury and disease. We also believe that the method can be applied not only to rodents but also to non-human primates.
This paper demonstrates that the large cranial window is effective for imaging transgenic mice and mice injected with AAV expressing functional proteins. In particular, it is shown that the fibroin-AAV film on the wrap is much easier than a conventional AAV injection method to express GECIs across the wide area of the cortex. Using a mixture of two AAVs encoding GECIs of different colors41, the correlation between neuron and glial cell activity can be simultaneously imaged over a wide area of the cortex. Furthermore, the fibroin-AAV film method can also be applied to other genetically-encoded biosensors42,43,44,45,46,47.
The larger cranial window, which can image both hemispheres, is also possible. Two-photon microscopes with a much wider field of view (~25 mm2) have recently been developed25,26,27,28,29. Combining this two-photon imaging technique with one-photon wide-field imaging using the wide cranial window described here will allow us to examine the relationship between population activity and single-cell activity from unprecedented scales.
Limitations 
The food wrap does not allow any substances to pass through. This makes the method difficult to be used for pharmacological experiments. It is also difficult to remove the wrap, making it impossible to insert a glass pipette or electrode. Therefore, it is hard to implement experiments combined with other methods such as simultaneous calcium imaging and electrophysiological recordings, and local administration of drugs using a glass pipette. A possible solution for these limitations is to use the wrap and glass window with a hole. This allows access to the brain via a glass pipette or a recording electrode while keeping the cranial window sterile for a long period48.

Wide-field calcium imaging effectively investigates the spatiotemporal activity pattern over a large area of the animal brain1,2,3. Wide-field imaging has been extensively used to observe rodents&#39; entire cortical surface since their cortex is relatively flat2,3,4,5,6,7,8,9,10. Transgenic mice or mice injected with adeno-associated virus (AAV), which specifically express GECIs in various cells such as neurons and glial cells, can be used for wide-field calcium imaging11,12,13. However, the spatial resolution of this technique is usually not enough to resolve the activity of individual cells in vivo14. It is also not suitable for imaging cells located in deeper layers.
On the other hand, two-photon calcium imaging can observe the activity of multiple cells simultaneously with subcellular spatial resolution, allowing the observation of the activity of individual cells even in neuronal dendrites and glial processes15,16,17,18,19,20,21,22. It can also observe cells in deeper layers of the cerebral cortex23,24. Although recent technological advances in two-photon microscopy enable imaging from millimeter-wide cortical regions25,26,27,28,29, it is still difficult to observe an area comparable to wide-field imaging by two-photon imaging.
To understand the physiological relevance of brain activity from single-cell to whole-brain, it is critical to bridge the gap between the activity of cortical regions over the entire cortex and that at single-cell resolution in local neural circuits. Therefore, a combination of wide-field and two-photon calcium imaging performed in the same mouse is especially effective. To realize this, a wide and stable cranial window must be created, ideally over a long period.
Previously, several techniques for making cranial windows have been developed to allow wide-field and two-photon imaging to be performed in the same mouse30,31. Trapezoidal-shaped cover glass windows (crystal skull), which are molded into the shape of the cortical surface to replace the removed bone, allow optical access over the entire cortex32. Alternatively, polymer-based cranial windows can be made with polyethylene terephthalate (PET)33 or polyethylene-oxide-coated amorphous fluoropolymers nanosheet34. Each method has been shown to maintain a stable window for more than 1 month. However, producing these windows is not easy, and the materials and equipment used are often expensive.
The present study describes a new method for making a large cranial window using the PVDC film (plastic food wrap) (Figure 1). Using this window, in vivo wide-field and two-photon imaging experiments can be performed in the same mice. It has also been shown that GECIs could be expressed in neurons over a wide area of the cortex of mice by forming a thin layer of film containing AAV particles on the wrap.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>4% paraformaldehyde phosphate buffer solution</td>
			<td>NACALAI TESQUE, Kyoto, Japan</td>
			<td>TritonX</td>
			<td>Expression efficiency of the wrap with the fibroin-AAV film method</td>
		</tr>
		<tr>
			<td>50 mL beaker</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Acquisition software</td>
			<td>Brain vision</td>
			<td>BV_Ana</td>
			<td>For wide-field calcium imaging of GCaMP6f</td>
		</tr>
		<tr>
			<td>Acquisition software</td>
			<td>Hamamatsu photonics</td>
			<td>High speed recording software: HSR</td>
			<td>For wide-field calcium imaging of XCaMP-R</td>
		</tr>
		<tr>
			<td>Acquisition software</td>
			<td>Vibrio Technologies</td>
			<td>scanImage</td>
			<td>For two-photon calcium imaging</td>
		</tr>
		<tr>
			<td>ACSF (artificial cerebrospinal fluid)</td>
			<td></td>
			<td></td>
			<td>150 mM NaCl, 2.5 mM KCl, 10 mM HEPES, 2 mM CaCl2, 1 mM MgCl2, pH = 7.4 with 1M NaOH</td>
		</tr>
		<tr>
			<td>ACSF aspiration needle</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Adeno-associated virus</td>
			<td>VectorBuilder</td>
			<td>custom-made</td>
			<td>AAV-DJ/8-Syn1-XCaMP-R</td>
		</tr>
		<tr>
			<td>Adhesives for biological use</td>
			<td>Daiichi Sankyo</td>
			<td>Aron Alpha-A</td>
			<td></td>
		</tr>
		<tr>
			<td>Anesthesia machine</td>
			<td>Shinano seisakusho</td>
			<td>SN-487</td>
			<td></td>
		</tr>
		<tr>
			<td>Anesthetic</td>
			<td>Kyoritsu Seiyaku Corporation</td>
			<td>pentobarbital</td>
			<td>Expression efficiency of the wrap with the fibroin-AAV film method</td>
		</tr>
		<tr>
			<td>Auxiliary ear bar</td>
			<td>Narishige</td>
			<td>EB-5N</td>
			<td></td>
		</tr>
		<tr>
			<td>CCD camera</td>
			<td>Brain vision</td>
			<td>MiCAM02-HR</td>
			<td>For wide-field calcium imaging of GCaMP6f</td>
		</tr>
		<tr>
			<td>Clear vinyl polysiloxane</td>
			<td>GC</td>
			<td>Exaclear</td>
			<td></td>
		</tr>
		<tr>
			<td>CMOS camera</td>
			<td>Hamamatsu photonics</td>
			<td>ORCA-spark</td>
			<td>For wide-field calcium imaging of XCaMP-R</td>
		</tr>
		<tr>
			<td>Cotton swab</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Cover glass</td>
			<td>Matsunami</td>
			<td>18 x 18 NO.1</td>
			<td>Size: 18 x 18 mm, Thickness: 0.13-0.17 mm, Borosilicate glass</td>
		</tr>
		<tr>
			<td>DAPI</td>
			<td>Thermo Fisher</td>
			<td>D1306</td>
			<td>Expression efficiency of the wrap with the fibroin-AAV film method</td>
		</tr>
		<tr>
			<td>Ddialysis cassette</td>
			<td>3.5K MWCO, Slide-A-Lyzer</td>
			<td>ThermoFisher</td>
			<td></td>
		</tr>
		<tr>
			<td>Dental adhesive resin cement</td>
			<td>SUN MEDICAL</td>
			<td>Super-Bond</td>
			<td></td>
		</tr>
		<tr>
			<td>Dental drill</td>
			<td>Nakanishi</td>
			<td>VOLVERE Vmax</td>
			<td></td>
		</tr>
		<tr>
			<td>Digital scale</td>
			<td>Dretec</td>
			<td>KS-243</td>
			<td></td>
		</tr>
		<tr>
			<td>Filters</td>
			<td>Brain vision</td>
			<td></td>
			<td>EM: BP466/40-25, DM: DM506, EX: BP520/36-50</td>
		</tr>
		<tr>
			<td>Filters</td>
			<td>Olympus</td>
			<td></td>
			<td>U-MRFPHQ, EM: BP535-555HQ, DM: DM565HQ, Ex: BA570-625HQ</td>
		</tr>
		<tr>
			<td>Fluorescence microscope</td>
			<td>Keyence</td>
			<td>BZ-X810</td>
			<td>Expression efficiency of the wrap with the fibroin-AAV film method</td>
		</tr>
		<tr>
			<td>Fluorescent beads</td>
			<td>Fluoresbrite YG Carboxylate Microspheres</td>
			<td>0.1 &#181;m</td>
			<td>Evaluation of the point spread function under the conventional and the new cranial windows in two-photon imaging</td>
		</tr>
		<tr>
			<td>Forceps</td>
			<td>FST</td>
			<td>No. 11252-20</td>
			<td>thin-tipped, for removal of dura mater</td>
		</tr>
		<tr>
			<td>Forceps</td>
			<td>KFI</td>
			<td>K-7, No.J 18-8</td>
			<td>for general use</td>
		</tr>
		<tr>
			<td>Gelatin for hemostasis</td>
			<td>Johnson &#38; Johnson</td>
			<td>Spongostan</td>
			<td></td>
		</tr>
		<tr>
			<td>Gentamicin sulfate</td>
			<td>Iwaki seiyaku</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Glass pipette</td>
			<td>custom-made</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Hair remover</td>
			<td>Reckitt Japan</td>
			<td>Veet</td>
			<td></td>
		</tr>
		<tr>
			<td>Head fixing device</td>
			<td>custom-made</td>
			<td></td>
			<td>Craniotomy for Cortical Voltage-sensitive Dye Imaging in Mice. Suzuki, T., and Murayama, M. Bio-protocol 2016 6:e1722.</td>
		</tr>
		<tr>
			<td>Head plate</td>
			<td>custom-made</td>
			<td></td>
			<td>aluminum or resin, size: 40 x 25 mm, thickness: 1.5 mm or 2 mm, hole in the center: 15 x 10 mm (head_plate_06 v3.f3d)</td>
		</tr>
		<tr>
			<td>Heating pad</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Image processing software (for calcium imaging data analysis)</td>
			<td></td>
			<td>ImageJ</td>
			<td>https://imagej.net</td>
		</tr>
		<tr>
			<td>Isoflurane</td>
			<td>Pfizer</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Light source</td>
			<td>Hayashi-repic</td>
			<td>LA-HDF108AA</td>
			<td></td>
		</tr>
		<tr>
			<td>Light source</td>
			<td>Brain vision</td>
			<td>LEX2-LZ4-B</td>
			<td>For wide-field calcium imaging of GCaMP6f</td>
		</tr>
		<tr>
			<td>Light source</td>
			<td>Olympus</td>
			<td>U-HGLGPS</td>
			<td>For wide-field calcium imaging of XCaMP-R</td>
		</tr>
		<tr>
			<td>Mannitol solution (15% with saline)</td>
			<td>Sigma-Aldrich (Merck)</td>
			<td>M4125</td>
			<td></td>
		</tr>
		<tr>
			<td>Micro curette</td>
			<td>FST</td>
			<td>No. 10080-05</td>
			<td></td>
		</tr>
		<tr>
			<td>Microscope</td>
			<td>Brain vision</td>
			<td></td>
			<td>For wide-field calcium imaging of GCaMP6f</td>
		</tr>
		<tr>
			<td>Microscope</td>
			<td>Olympus</td>
			<td>MVX10</td>
			<td>For wide-field calcium imaging of XCaMP-R</td>
		</tr>
		<tr>
			<td>Microscope</td>
			<td>Sutter Instruments</td>
			<td>MOM</td>
			<td>For two-photon calcium imaging</td>
		</tr>
		<tr>
			<td>Microslicer</td>
			<td>Dosaka EM</td>
			<td>DTK-1000N</td>
			<td>Expression efficiency of the wrap with the fibroin-AAV film method</td>
		</tr>
		<tr>
			<td>Mixing tip</td>
			<td>GC</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Needle (30 G)</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Polyethylens spoids</td>
			<td>AS ONE</td>
			<td>1-4656-01</td>
			<td></td>
		</tr>
		<tr>
			<td>Polyvinylidene chloride (PVDC) film</td>
			<td>Asahi Kasei</td>
			<td>Asahi Wrap (or Saran Wrap)</td>
			<td></td>
		</tr>
		<tr>
			<td>Povidone-iodine</td>
			<td>Mundipharma</td>
			<td>Isodine</td>
			<td></td>
		</tr>
		<tr>
			<td>Python libralies</td>
			<td></td>
			<td>NumPy</td>
			<td>package for scientific computing, https://numpy.org/doc/stable/index.html#</td>
		</tr>
		<tr>
			<td></td>
			<td></td>
			<td>Matplotlib</td>
			<td>library for visualizations, https://matplotlib.org/stable/index.html#</td>
		</tr>
		<tr>
			<td></td>
			<td></td>
			<td>pandas</td>
			<td>data analysis and manipulation tool, https://pandas.pydata.org</td>
		</tr>
		<tr>
			<td>Scalpel</td>
			<td>Kai</td>
			<td>No. 11</td>
			<td></td>
		</tr>
		<tr>
			<td>Shaver for animal</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Silicone dispensers</td>
			<td>GC</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Silkworm cocoon</td>
			<td>Satoyama Craft News</td>
			<td></td>
			<td>https://sato-yama.jp/</td>
		</tr>
		<tr>
			<td>Stereomicroscope</td>
			<td>LEICA</td>
			<td>MZ6</td>
			<td>objective lens: 0.63x, eyepiece: 25x</td>
		</tr>
		<tr>
			<td>Surfactant</td>
			<td>NACALAI TESQUE</td>
			<td>TritonX</td>
			<td>Expression efficiency of the wrap with the fibroin-AAV film method</td>
		</tr>
		<tr>
			<td>Surgical Scissors</td>
			<td>FST</td>
			<td>No. 91460-11</td>
			<td></td>
		</tr>
		<tr>
			<td>Syringe for mannitol injection</td>
			<td>Terumo</td>
			<td>1mL</td>
			<td></td>
		</tr>
		<tr>
			<td>Transdermal anesthetic</td>
			<td>AstraZeneca</td>
			<td>Lidocaine</td>
			<td></td>
		</tr>
		<tr>
			<td>Transgenic mice used for calcium imaging of astrocytes</td>
			<td></td>
			<td></td>
			<td>The mice were obtained by the following method. 
			AldH1l1-CreERT2 mice: B6N.FVB-Tg(Aldh1l1-cre/ERT2)1Khakh/J (The Jackson laboratory, strain #: 031008) 
			Tamoxifen-inducible Cre recombinase expression directed at high levels to the vast majority of astrocytes 
			Flx-Lck-GCaMP6f mice: C57BL/6N-Gt(ROSA)26Sor[tm1(CAG-GCaMP6f)Khak]/J (The Jackson laboratory, strain #: 029626) 
			Cre-dependent expression of a plasma membrane-targeted GCaMP6f. 
			A mouse born from crossbreeding these mice were treated with tamoxifen (20 mg/mL) for 5 days (0.05 mL/10g bw, i.p.) to express GCaMP6f.</td>
		</tr>
		<tr>
			<td>Tunable ultrafast lasers</td>
			<td>Spectra-Physics</td>
			<td>InSight X3</td>
			<td>For two-photon calcium imaging</td>
		</tr>
		<tr>
			<td>Waterproof film</td>
			<td>Nichiban</td>
			<td>BFR5</td>
			<td></td>
		</tr>
		<tr>
			<td>Wild-type mice</td>
			<td>Japan SLC</td>
			<td>C57BL/6J</td>
			<td>Male and femalek, &#62;4 weeks old</td>
		</tr>
	</tbody>
</table>

in vivo wide-field and two-photon calcium imaging from a mouse using a large cranial window

Wide-field calcium imaging from the mouse&#39;s neocortex allows one to observe cortex-wide neural activity related to various brain functions. On the other hand, two-photon imaging can resolve the activity of local neural circuits at the single-cell level. It is critical to make a large cranial window to perform multiple-scale analysis using both imaging techniques in the same mouse. To achieve this, one must remove a large section of the skull and cover the exposed cortical surface with transparent materials. Previously, glass skulls and polymer-based cranial windows have been developed for this purpose, but these materials are not easily fabricated. The present protocol describes a simple method for making a large cranial window consisting of commercially available polyvinylidene chloride (PVDC) wrapping film, a transparent silicone plug, and a cover glass. For imaging the dorsal surface of an entire hemisphere, the window size was approximately 6 x 3 mm2. Severe brain vibrations were not observed regardless of such a large window. Importantly, the condition of the brain surface did not deteriorate for more than one month. Wide-field imaging of a mouse expressing a genetically-encoded calcium indicator (GECI), GCaMP6f, specifically in astrocytes, revealed synchronized responses in a few millimeters. Two-photon imaging of the same mouse showed prominent calcium responses in individual astrocytes over several seconds. Furthermore, a thin layer of an adeno-associated virus was applied to the PVDC film and successfully expressed GECI in cortical neurons over the cranial window. This technique is reliable and cost-effective for making a large cranial window and facilitates the investigation of the neural and glial dynamics and their interactions during behavior at the macroscopic and microscopic levels.

Evaluation of a large cranial window made using the PVDC wrap methods 
Immediately after the surgery, success or failure can be checked at a glance by the condition of the cortical surface, such as bleeding and color change due to damage or ischemia. A long time after surgery, the cortical surface may be covered with an opaque white membrane due to infection, or blood may cover the window due to bleeding (Figure 2G). In these cases, the cortex may not be in healthy condition, and imaging may not be possible. These could be caused by partially severed wraps or insufficient fixation of the wrap by the adhesive. If the infection is repeatedly observed, it may be effective to apply antibiotics, for example, gentamicin sulfate (10 &#181;L, 50 mg/mL), over the brain surface at window placement. Regeneration of meninges or bones is also seen when the vertical gap between the cortical surface and the wrap is large. To prevent this, applying the wrap as tightly as possible to the brain surface during window preparation is crucial. This can be achieved by placing plastic wrap on the brain surface and sucking out as much ACSF as possible. In the absence of ACSF, it can be done by simply placing the plastic wrap on the brain surface. The brain and blood vessels are determined to be undamaged by the fact that the color of the brain is not discolored and blood vessels are not severed.
The longevity of the window largely depends on the quality of the surgery. When the condition is good, there is no sign of infection, bleeding, or regeneration more than 1 month after surgery (Figure 2F and Figure 3B). In 8 of 10 mice, the window could be maintained clear up to 10 weeks or longer. Windows in two of the mice could not be properly maintained due to infection or bleeding. Although the large window may be prone to mechanical stress or impact, broken or cracked windows were not observed.
To evaluate the imaging quality of the new cranial window with the wrap, silicone, and glass, the point spread function was compared under the new window with that under the conventional glass window by imaging 0.1 &#181;m fluorescent beads in agar (see Supplementary File 1). The results showed no difference in full width at half maximum (FWHM) for both conditions. [X-axis (&#181;m): glass only, 1.99 &#177; 0.07, wrap, 1.76 &#177; 0.13, Y-axis (&#181;m): glass only, 2.11 &#177; 0.27, wrap, 1.90 &#177; 0.15, Z-axis (&#181;m): glass only, 25.29 &#177; 0.71, wrap, 26.64 &#177; 1.02, N = 7 beads, p &#62; 0.05, the Mann-Whitney U test, Supplementary Figure 2A,B]. Therefore, the new elements added (wrap and silicone) did not deteriorate the imaging quality.
Vibration artifacts caused by respiration, heartbeat, and body movement are present in wide-field and two-photon imaging. To determine how much the new cranial window vibrates, a small fluorescent particle was selected from the in vivo two-photon imaging data and examined how much its image moved during 60 s. It was found that the standard deviation of the centroid of that fluorescent particle was about 0.3 &#181;m, which is comparable to that under a conventional glass window (Supplementary Figure 2C). This indicates that because the brain was held down by a transparent silicone plug and cover glass, the vibrations were comparable to that observed in conventional smaller windows, and offline image registration was sufficient to eliminate vibration artifacts.
In wide-field calcium imaging, the cortical activity could be observed propagating across the cortex induced by sensory stimulation (Figure 3A-D,K-N). Two-photon imaging allowed the observation of single-cell fluorescence images specific to neurons and glial cells (Figure 3E,O). Fluorescence changes induced by sensory stimulation could be observed in individual cells (Figure 3E-J,O-T).
Expression of genetically-encoded calcium indicators (GECIs) in a wide area of the cerebral cortex using the PVDC wrap and AAV 
The PVDC wrap for the window could be applied to express functional proteins in a wide area of the cortex. This is achieved using AAV and fibroin, a component protein of silkworm cocoons that have been widely applied as biomaterials37. A previous study showed that fibroin could be mixed with AAVs, forming films implanted in the brain to express functional proteins such as photoactivable opsins or GECIs36. In the present study, AAV expressing GECI and fibroin were mixed and dried on the wrap, and AAV-coated wrap was used for the cranial window. This resulted in the expression of GECI over the broad area of the cortex 2-4 weeks after surgery (Figure 3K-M). Since the window was large, different cortical areas of the same mouse can be imaged (Figure 3M-T).
To confirm the expression efficiency of this method, the number of cells expressing GECI was counted in the fixed brain (Supplementary Figure 2D). It was found that the present strategy using the wrap with fibroin-AAV resulted in the expression of GECI with an efficiency of approximately 20% in both superficial and deeper layers (L2/3: 20.78%, XCaMP-R expressing cell: 32 cells, DAPI: 154 locations, L5: 20.08%, XCaMP-R expressing cell: 51 cells, DAPI: 254 locations). Thus, this method expressed GECIs in cells not only in surface layers but also in deeper layers.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/64224/64224fig01.jpg" /> 
Figure 1: Conceptual diagram of the large cranial window. (A) Left, schematic drawing of the new cranial window. It is larger than the conventional window (3 mm diameter). Right, Cross-sectional view. The method for making a large cranial window uses food wrap, transparent silicone elastomer, and cover glass, allowing wide-field and two-photon imaging from the same mouse. (B) Cranial window fabrication procedure: (a) Bone removal. (b) Removal of ACSF under the wrap. (c) Adherence of the wrap to the brain surface by removing ACSF. (d) Cutting away the excess wrap. (e) Applying transparent silicone. (f) Affixing cover glass. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/64224/64224fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/64224/64224fig02.jpg" /> 
Figure 2: Overview of cranial window surgery. (A)&#160;Materials and equipment required for the cranial window. (a) Polyvinylidene chloride (PVDC) wrapping film. (b) A dispenser of transparent silicone elastomer with a mixing tip. (c) Cover glass. (d) Transparent silicone placed between two pieces of the cover glass. (B) Photograph of mouse head skin incised to expose the skull. The mouse was anesthetized, and the head of the mouse was immobilized using ear bars. The head was then dehaired, treated with local analgesia, and the skin was incised. (C) Photograph after installation of a head plate. A head plate (made of resin from a 3D printer) was attached to the head of the mouse with dental cement. (D) Photograph of a cranial window. The cranial window was created in the cortex of the right hemisphere of the mouse brain. The dura mater was removed, and the wrap was glued in place. (E) A photo of the window made of the wrap with the transparent silicone and cover glass on top. (F) A typical example of a successful window (right hemisphere, 7 weeks after surgery). (G) Example of failed window (both hemispheres, 5 weeks after surgery). <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/64224/64224fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/64224/64224fig03.jpg" /> 
Figure 3: The large window allows wide-field and two-photon calcium imaging from the same mouse. (A) Calcium imaging was performed in a transgenic mouse expressing membrane-anchored GECI (Lck-GCaMP6f) in astrocytes40. (B) Left, a large window was created with plastic wrap, transparent silicone, and cover glass. Wide-field imaging was performed through this window. Right, a photo was captured 79 days after the installation of the cranial window. (C) When air-puff stimulation was applied to the contralateral whiskers, fluorescence changes were observed. (D) The time course of the fluorescence change in the somatosensory cortex (red square in C) was plotted. Red and blue bars indicate air puff timing and &#34;before&#34;, &#34;during&#34;, and &#34;after&#34; timing in (C), respectively. (E) The field of view (FOV 1 in C) of two-photon calcium imaging. Because GCaMP6f was expressed to localize to the membrane, the regions of interest (white squares) were manually placed to detect the local response in astrocyte processes. (F) The fluorescence changes in the colored squares in (E) are plotted. (G) The fluorescence changes in all squares of (E) are plotted. Horizontal and vertical axes indicate time and cell number, respectively. (H-J) Data for FOV 2 (in the visual cortex) in (C) are shown. The FOV 2 was imaged after the imaging in the FOV 1. (K) Red GECI, XCaMP-R, was expressed in neurons by the fibroin-AAV method in the wild-type mouse. (L) Photograph captured two&#160;weeks after surgery in which the window was created using the fibroin film. (M) Wide-field calcium imaging was performed on this mouse. (N)&#160;The fluorescence change evoked by whisker stimulation was plotted from the most prominent site (somatosensory cortex, red square in (M)). Red and blue lines indicate air puff timing and &#34;before&#34; and &#34;during&#34; timing in (M), respectively. (O) Field of view (somatosensory cortex, FOV 1 in (M)) of two-photon calcium imaging at 300 &#181;m depth. ROIs were manually placed at neuronal somata. (P) The fluorescence changes in the colored squares in (O) are plotted. (Q) The fluorescence changes in all squares of (O) are plotted in color. (R-T) Data for FOV 2 in (M) located in the parietal cortex are shown. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/64224/64224fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Supplementary Figure 1: Tips for scalpels. The tip of the new scalpel (top) compared to the scalpel used to cut the skull with a blunted tip (bottom). <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/64224/Supplementary Figure 1.zip" target="_blank">Please click here to download this File.</a>
Supplementary Figure 2: Validation of the new cranial window and the fibroin-AAV expression method. (A) Fluorescence intensity profile of the 0.1 &#181;m fluorescent beads in agar. The top row shows data from a condition in which only cover glass was placed over fluorescent beads mixed in agar, and the bottom row shows data from a condition in which wrap, transparent silicone, and cover glass were placed. The gray traces show the Gaussian fit to the fluorescence intensity profile for each bead, and the red traces show their average values (n = 7). (B) Summary of data in (A). Each graph shows the full width at half maximum (FWHM) of the point spread function on the XYZ axis. The gray plot shows the data for each bead, and the red shows their mean and standard error. (C) From the 2,000 frames (60 s recording) of in vivo imaging data, a small fluorescent particle was selected and examined how much the image moved during the 60 s. The fluorescent image in the center represents the average of 2,000 frames. The images were projected by averaging in the X- and Y-axis directions. The histograms show the distribution of the centroid in each frame. The standard deviations of the centroid were X: 0.36 and Y: 0.315 &#181;m. (D) Example of GECI expression by the fibroin-AAV method. Left: A slice of cerebral cortex applied the fibroin-AAV expression method. Red and blue indicate fluorescence from XCaMP-R and DAPI, respectively; XCaMP-R was expressed not only in layer 2/3 cells but also in layer 5 cells. Center and right. Magnified views of the layers 2/3, and 5 in the left figure (cyan squares), respectively. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/64224/Supplementary Figure 2.zip" target="_blank">Please click here to download this File.</a>
Supplementary File 1: (A) Expression efficiency of the wrap with the fibroin-AAV film method and (B) Evaluation of the point spread function during two-photon imaging. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/64224/Supplementary File 1_FINAL.zip" target="_blank">Please click here to download this File.</a>

Watch this Scientific Journal Video about In Vivo Wide-Field and Two-Photon Calcium Imaging from a Mouse Using a Large Cranial Window at JoVE.com

In Vivo Wide-Field and Two-Photon Calcium Imaging from a Mouse Using a Large Cranial Window

The present protocol describes making a large (6 x 3 mm2) cranial window using food wrap, transparent silicone, and cover glass. This cranial window allows in vivo wide-field and two-photon calcium imaging experiments in the same mouse.

In Vivo Wide-Field and Two-Photon Calcium Imaging from a Mouse Using a Large Cranial Window

Wide-field calcium imaging from the mouse&#39;s neocortex allows one to observe cortex-wide neural activity related to various brain functions. On the ...

in-vivo-wide-field-two-photon-calcium-imaging-from-mouse-using-large

Universidad de Cartagena UDEC

Research

JoVE Journal

Neuroscience

6.2K Views.  University of Yamanashi. The present protocol describes making a large (6 x 3 mm2) cranial window using food wrap, transparent silicone, and cover glass. This cranial window allows in vivo wide-field and two-photon calcium imaging experiments in the same mouse.

Video: In Vivo Wide-Field and Two-Photon Calcium Imaging from a Mouse Using a Large Cranial Window

A Thin-skull Window Technique for Chronic Two-photon In vivo Imaging of Murine Microglia in Models of Neuroinflammation

Traditionally in neuroscience, in vivo two photon imaging of the murine central nervous system has either involved the use of open-skull1,2 or thinned-skull 3 preparations. While the open-skull technique is very versatile, it is not optimal for studying microglia because it is invasive and can cause microglial activation. Even though the thinned-skull approach is minimally invasive, the repeated re-thinning of skull required for chronic imaging increases the risks of tissue injury and microglial activation and allows for a limited number of imaging sessions. Here we present a chronic thin-skull window method for monitoring murine microglia in vivo over an extended period of time using two-photon microscopy. We demonstrate how to prepare a stable, accessible, thinned-skull cortical window (TSCW) with an apposed glass coverslip that remains translucent over the course of three weeks of intermittent observation. This TSCW preparation is far more immunologically inert with respect to microglial activation than open craniotomy or repeated skull thinning and allows an arbitrary number of imaging sessions during a time period of weeks. We prepare TSCW in CX3CR1 GFP/+ mice 4 to visualize microglia with enhanced green fluorescent protein to &le;150 &mu;m beneath the pial surface. We also show that this preparation can be used in conjunction with stereotactic brain injections of the HIV-1 neurotoxic protein Tat, adjacent to the TSCW, which is capable of inducing durable microgliosis. Therefore, this method is extremely useful for examining changes in microglial morphology and motility over time in the living brain in models of HIV Associated Neurocognitive Disorder (HAND) and other neurodegenerative diseases with a neuroinflammatory component.

A Thin-skull Window Technique for Chronic Two-photon In vivo Imaging of Murine Microglia in Models of Neuroinflammation

We describe a method for repeatedly visualizing murine microglia and circulating monocytes in vivo over hours, days or weeks using transcranial two-photon microscopy. We demonstrate how to prepare a thinned-skull window that allows intermittent observation of quiescent microglia that can be activated by adjacent stereotactic injection of the HIV-1 regulatory protein Tat.

Traditionally in neuroscience, in vivo two photon imaging of the murine central nervous system has either involved the use of open-skull1,2 or ...

Intravital Microscopy of the Mouse Brain Microcirculation using a Closed Cranial Window

This experimental model was designed to assess the mouse pial microcirculation during acute and chronic, physiological and pathophysiological hemodynamic, inflammatory and metabolic conditions, using in vivo fluorescence microscopy. A closed cranial window is placed over the left parieto-occipital cortex of the mice. Local microcirculation is recorded in real time through the window using epi and fluorescence illumination, and measurements of vessels diameters and red blood cell (RBC) velocities are performed. RBC velocity is measured using real-time cross-correlation and/or fluorescent-labeled erythrocytes. Leukocyte and platelet adherence to pial vessels and assessment of perfusion and vascular leakage are made with the help of fluorescence-labeled markers such as Albumin-FITC and anti-CD45-TxR antibodies. Microcirculation can be repeatedly video-recorded over several days. We used for the first time the close window brain intravital microscopy to study the pial microcirculation to follow dynamic changes during the course of Plasmodium berghei ANKA infection in mice and show that expression of CM is associated with microcirculatory dysfunctions characterized by vasoconstriction, profound decrease in blood flow and eventually vascular collapse.

Intravital microscopy to follow temporal and spatial hemodynamic and inflammatory events in the pial microcirculation.

This experimental model was designed to assess the mouse pial microcirculation during acute and chronic, physiological and pathophysiological hemodynamic, ...

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 ...

In Vivo Two-photon Imaging Of Experience-dependent Molecular Changes In Cortical Neurons

The brain's ability to change in response to experience is essential for healthy brain function, and abnormalities in this process contribute to a variety of brain disorders1,2. To better understand the mechanisms by which brain circuits react to an animal's experience requires the ability to monitor the experience-dependent molecular changes in a given set of neurons, over a prolonged period of time, in the live animal. While experience and associated neural activity is known to trigger gene expression changes in neurons1,2, most of the methods to detect such changes do not allow repeated observation of the same neurons over multiple days or do not have sufficient resolution to observe individual neurons3,4. Here, we describe a method that combines in vivo two-photon microscopy with a genetically encoded fluorescent reporter to track experience-dependent gene expression changes in individual cortical neurons over the course of day-to-day experience. 
One of the well-established experience-dependent genes is Activity-regulated cytoskeletal associated protein (Arc)5,6. The transcription of Arc is rapidly and highly induced by intensified neuronal activity3, and its protein product regulates the endocytosis of glutamate receptors and long-term synaptic plasticity7. The expression of Arc has been widely used as a molecular marker to map neuronal circuits involved in specific behaviors3. In most of those studies, Arc expression was detected by in situ hybridization or immunohistochemistry in fixed brain sections. Although those methods revealed that the expression of Arc was localized to a subset of excitatory neurons after behavioral experience, how the cellular patterns of Arc expression might change with multiple episodes of repeated or distinctive experiences over days was not investigated. 
In vivo two-photon microscopy offers a powerful way to examine experience-dependent cellular changes in the living brain8,9. To enable the examination of Arc expression in live neurons by two-photon microscopy, we previously generated a knock-in mouse line in which a GFP reporter is placed under the control of the endogenous Arc promoter10. This protocol describes the surgical preparations and imaging procedures for tracking experience-dependent Arc-GFP expression patterns in neuronal ensembles in the live animal. In this method, chronic cranial windows were first implanted in Arc-GFP mice over the cortical regions of interest. Those animals were then repeatedly imaged by two-photon microscopy after desired behavioral paradigms over the course of several days. This method may be generally applicable to animals carrying other fluorescent reporters of experience-dependent molecular changes4.

In Vivo Two-photon Imaging Of Experience-dependent Molecular Changes In Cortical Neurons

Experience-dependent molecular changes in neurons are essential for the brain's ability to adapt in response to behavioral challenges. An in vivo two-photon imaging method is described here that allows the tracking of such molecular changes in individual cortical neurons through genetically encoded reporters.

The brain's ability to change in response to experience is essential for healthy brain function, and abnormalities in this process contribute to a variety ...

Two-Photon in vivo Imaging of Dendritic Spines in the Mouse Cortex Using a Thinned-skull Preparation

In the mammalian cortex, neurons form extremely complicated networks and exchange information at synapses. Changes in synaptic strength, as well as addition/removal of synapses, occur in an experience-dependent manner, providing the structural foundation of neuronal plasticity. As postsynaptic components of the most excitatory synapses in the cortex, dendritic spines are considered to be a good proxy of synapses. Taking advantages of mouse genetics and fluorescent labeling techniques, individual neurons and their synaptic structures can be labeled in the intact brain. Here we introduce a transcranial imaging protocol using two-photon laser scanning microscopy to follow fluorescently labeled postsynaptic dendritic spines over time in vivo. This protocol utilizes a thinned-skull preparation, which keeps the skull intact and avoids inflammatory effects caused by exposure of the meninges and the cortex. Therefore, images can be acquired immediately after surgery is performed. The experimental procedure can be performed repetitively over various time intervals ranging from hours to years. The application of this preparation can also be expanded to investigate different cortical regions and layers, as well as other cell types, under physiological and pathological conditions.

Two-Photon in vivo Imaging of Dendritic Spines in the Mouse Cortex Using a Thinned-skull Preparation

Time-lapse imaging in the living animal provides valuable information on structural reorganization in the intact brain. Here, we introduce a thinned-skull preparation that allows transcranial imaging of fluorescently labeled synaptic structures in the living mouse cortex by two-photon microscopy.

In the mammalian cortex, neurons form extremely complicated networks and exchange information at synapses. Changes in synaptic strength, as well as ...

A Large Lateral Craniotomy Procedure for Mesoscale Wide-field Optical Imaging of Brain Activity

The craniotomy is a commonly performed procedure to expose the brain for in vivo experiments. In mouse research, most labs utilize a small craniotomy, typically 3 mm x 3 mm. This protocol introduces a method for creating a substantially larger 7 mm x 6 mm cranial window exposing most of a cerebral hemisphere over the mouse temporal and parietal cortices (e.g., bregma 2.5 - 4.5 mm, lateral 0 - 6 mm). To perform this surgery, the head must be tilted approximately 30&#176; and much of the temporal muscle must be retracted. Due to the large amount of bone removal, this procedure is intended only for acute experiments with the animal anesthetized throughout the surgery and experiment.
The main advantage of this innovative large lateral cranial window is to provide simultaneous access to both medial and lateral areas of the cortex. This large unilateral cranial window can be used to study the neural dynamics between cells, as well as between different cortical areas by combining multi-electrode electrophysiological recordings, imaging of neuronal activity (e.g., intrinsic or extrinsic imaging), and optogenetic stimulation. Additionally, this large craniotomy also exposes a large area of cortical blood vessels, allowing for direct manipulation of the lateral cortical vasculature.

This protocol presents a method for creating a large unilateral craniotomy over the temporal and parietal regions of the mouse cerebral cortex. This is especially useful for real time imaging over an expansive area of a cortical hemisphere.

The craniotomy is a commonly performed procedure to expose the brain for in vivo experiments. In mouse research, most labs utilize a small craniotomy, ...

Two-photon Calcium Imaging in Neuronal Dendrites in Brain Slices

Calcium (Ca2+) imaging is a powerful tool to investigate the spatiotemporal dynamics of intracellular Ca2+ signals in neuronal dendrites. Ca2+ fluctuations can occur through a variety of membrane and intracellular mechanisms and play a crucial role in the induction of synaptic plasticity and regulation of dendritic excitability. Hence, the ability to record different types of Ca2+ signals in dendritic branches is valuable for groups studying how dendrites integrate information. The advent of two-photon microscopy has made such studies significantly easier by solving the problems inherent to imaging in live tissue, such as light scattering and photodamage. Moreover, through combination of conventional electrophysiological techniques with two-photon Ca2+ imaging, it is possible to investigate local Ca2+ fluctuations in neuronal dendrites in parallel with recordings of synaptic activity in soma. Here, we describe how to use this method to study the dynamics of local Ca2+ transients (CaTs) in dendrites of GABAergic inhibitory interneurons. The method can be also applied to studying dendritic Ca2+ signaling in different neuronal types in acute brain slices.

We present a method combining whole-cell patch-clamp recordings and two-photon imaging to record Ca2+ transients in neuronal dendrites in acute brain slices.

Calcium (Ca2+) imaging is a powerful tool to investigate the spatiotemporal dynamics of intracellular Ca2+ signals in neuronal dendrites. Ca2+ ...

Ablation of a Neuronal Population Using a Two-photon Laser and Its Assessment Using Calcium Imaging and Behavioral Recording in Zebrafish Larvae

To identify the role of a subpopulation of neurons in behavior, it is essential to test the consequences of blocking its activity in living animals. Laser ablation of neurons is an effective method for this purpose when neurons are selectively labeled with fluorescent probes. In the present study, protocols for laser ablating a subpopulation of neurons using a two-photon microscope and testing of its functional and behavioral consequences are described. In this study, prey capture behavior in zebrafish larvae is used as a study model. The pretecto-hypothalamic circuit is known to underlie this visually-driven prey catching behavior. Zebrafish pretectum were laser-ablated, and neuronal activity in the inferior lobe of the hypothalamus (ILH; the target of the pretectal projection) was examined. Prey capture behavior after pretectal ablation was also tested.

Here, we present a protocol to ablate a genetically labeled subpopulation of neurons by a two-photon laser from Zebrafish larvae.

To identify the role of a subpopulation of neurons in behavior, it is essential to test the consequences of blocking its activity in living animals. Laser ...

Visualizing Protein Kinase A Activity In Head-fixed Behaving Mice Using In Vivo Two-photon Fluorescence Lifetime Imaging Microscopy

Neuromodulation exerts powerful control over brain function. Dysfunction of neuromodulatory systems results in neurological and psychiatric disorders. Despite their importance, technologies for tracking neuromodulatory events with cellular resolution are just beginning to emerge. Neuromodulators, such as dopamine, norepinephrine, acetylcholine, and serotonin, trigger intracellular signaling events via their respective G protein-coupled receptors to modulate neuronal excitability, synaptic communications, and other neuronal functions, thereby regulating information processing in the neuronal network. The above mentioned neuromodulators converge onto the cAMP/protein kinase A (PKA) pathway. Therefore, in vivo PKA imaging with single-cell resolution was developed as a readout for neuromodulatory events in a manner analogous to calcium imaging for neuronal electrical activities. Herein, a method is presented to visualize PKA activity at the level of individual neurons in the cortex of head-fixed behaving mice. To do so, an improved A-kinase activity reporter (AKAR), called tAKAR&#945;, is used, which is based on F&#246;rster resonance energy transfer (FRET). This genetically-encoded PKA sensor is introduced into the motor cortex via in utero electroporation (IUE) of DNA plasmids, or stereotaxic injection of adeno-associated virus (AAV). FRET changes are imaged using two-photon fluorescence lifetime imaging microscopy (2pFLIM), which offers advantages over ratiometric FRET measurements for quantifying FRET signal in light-scattering brain tissue. To study PKA activities during enforced locomotion, tAKAR&#945; is imaged through a chronic cranial window above the cortex of awake, head-fixed mice, which run or rest on a speed-controlled motorized treadmill. This imaging approach will be applicable to many other brain regions to study corresponding behavior-induced PKA activities and to other FLIM-based sensors for in vivo imaging.

A procedure is presented to visualize protein kinase A activities in head-fixed, behaving mice. An improved A-kinase activity reporter, tAKAR&#945;, is expressed in cortical neurons and made accessible for imaging through a cranial window. Two-photon fluorescence lifetime imaging microscopy is used to visualize PKA activities in vivo during enforced locomotion.

Neuromodulation exerts powerful control over brain function. Dysfunction of neuromodulatory systems results in neurological and psychiatric disorders. ...

Transpupillary Two-Photon In Vivo Imaging of the Mouse Retina

The retina transforms light signals from the environment into electrical signals that are propagated to the brain. Diseases of the retina are prevalent and cause visual impairment and blindness. Understanding how such diseases progress is critical to formulating new treatments. In vivo&#160;microscopy in animal models of disease is a powerful tool for understanding neurodegeneration and has led to important progress towards treatments of conditions ranging from Alzheimer&#39;s disease to stroke. Given that the retina is the only central nervous system structure inherently accessible by optical approaches, it naturally lends itself towards in vivo imaging. However, the native optics of the lens and cornea present some challenges for effective imaging access.
This protocol outlines methods for in vivo two-photon imaging of cellular cohorts and structures in the mouse retina at cellular resolution, applicable for both acute- and chronic-duration imaging experiments. It presents examples of retinal ganglion cell (RGC), amacrine cell, microglial, and vascular imaging using a suite of labeling techniques including adeno-associated virus (AAV) vectors, transgenic mice, and inorganic dyes. Importantly, these techniques extend to all cell types of the retina, and suggested methods for accessing other cellular populations of interest are described. Also detailed are example strategies for manual image postprocessing for display and quantification. These techniques are directly applicable to studies of retinal function in health and disease.

In vivo imaging is a powerful tool for the study of biology in health and disease. This protocol describes transpupillary imaging of the mouse retina with a standard two-photon microscope. It also demonstrates different in vivoimaging methods to fluorescently label multiple cellular cohorts of the retina.

The retina transforms light signals from the environment into electrical signals that are propagated to the brain. Diseases of the retina are prevalent ...

In Vivo Wide-Field and Two-Photon Calcium Imaging from a Mouse Using a Large Cranial Window

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Chapters in this video

A Thin-skull Window Technique for Chronic Two-photon In vivo Imaging of Murine Microglia in Models of Neuroinflammation

Intravital Microscopy of the Mouse Brain Microcirculation using a Closed Cranial Window

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

In Vivo Two-photon Imaging Of Experience-dependent Molecular Changes In Cortical Neurons

Two-Photon in vivo Imaging of Dendritic Spines in the Mouse Cortex Using a Thinned-skull Preparation

A Large Lateral Craniotomy Procedure for Mesoscale Wide-field Optical Imaging of Brain Activity

Two-photon Calcium Imaging in Neuronal Dendrites in Brain Slices

Ablation of a Neuronal Population Using a Two-photon Laser and Its Assessment Using Calcium Imaging and Behavioral Recording in Zebrafish Larvae

Visualizing Protein Kinase A Activity In Head-fixed Behaving Mice Using In Vivo Two-photon Fluorescence Lifetime Imaging Microscopy

Transpupillary Two-Photon In Vivo Imaging of the Mouse Retina