µTongue: A Microfluidics-Based Functional Imaging Platform for the Tongue In Vivo

Podsumowanie

The article introduces the µTongue (microfluidics-on-a-tongue) device for functional taste cell imaging in vivo by integrating microfluidics into an intravital imaging window on the tongue.

Streszczenie

Intravital fluorescence microscopy is a tool used widely to study multicellular dynamics in a live animal. However, it has not been successfully used in the taste sensory organ. By integrating microfluidics into the intravital tongue imaging window, the µTongue provides reliable functional images of taste cells in vivo under controlled exposure to multiple tastants. In this paper, a detailed step-by-step procedure to utilize the µTongue system is presented. There are five subsections: preparing of tastant solutions, setting up of a microfluidic module, sample mounting, acquiring functional image data, and data analysis. Some tips and techniques to solve the practical issues that may arise when using the µTongue are also presented.

Wprowadzenie

The intravital fluorescence microscope is used widely to study the spatiotemporal dynamics on living tissues. Researchers are rapidly developing genetically encoded sensors that provide specific and sensitive transformations of the biological processes into fluorescence signals - which can be recorded readily using fluorescence microscopes that are widely available^1,2. Although most internal organs in rodents have been investigated using the microscope, its successful application to the tongue has not yet been successful³.

Previous studies on the calcium imaging of taste cells were conducted ex vivo by thin-sectioning a tongue tissue to obtain circumvallate taste buds^4,5,⁶ or by peeling off the taste epithelium to obtain fungiform taste buds^7,8. The preparation of these samples was inevitably invasive, thus the natural microenvironments such as nerves innervation, permeability barriers, and blood circulation, were largely perturbed. The first intravital tongue imaging window was reported in 2015 by Choi et al., but reliable functional recording was not achievable because of the movement and optical artifacts caused by fluidic tastant stimuli⁹.

Recently, microfluidics-on-a-tongue (µTongue) was introduced¹⁰. This device integrates a microfluidic system with an imaging window on the mouse tongue. By attaining a quasi-steady-state flow of tastant stimuli throughout the imaging period, artifacts from fluidic motion could be minimized (Figure 1). The input port is fed by a series of multichannel pressure controllers, whereas the output port is connected to a syringe pump, which maintains 0.3 mL/min. Additionally, optical artifacts caused by the difference in refractive indices of tastant solutions were minimized by ratiometric analysis introducing a calcium-insensitive indicator (tdTomato) as well as the calcium indicator (GCaMP6)¹¹. This design provided microscopic stability of taste cells in vivo even with abrupt switching between fluidic channels. Consequently, the µTongue implement a reliable functional screening of multiple tastants to the mouse taste buds in vivo.

In this protocol, the experimental procedures are explained in detail for calcium imaging of the mouse fungiform taste buds in vivo using µTongue. First, the preparation of artificial saliva and tastant solutions is described. Second, the setting up of the microfluidic system to achieve the quasi-steady-state flow is introduced. Third, the procedures used to mount the mouse tongue on the µTongue to permit image acquisition are delineated. Lastly, each step for image analysis, including correction of lateral motion artifacts and ratiometry, is specified. This protocol can be adapted readily to any research laboratory with a mouse facility and a two-photon microscope or equivalent equipment.

Protokół

All surgical procedures were approved by the Institutional Animal Care and Use Committee (IACUC) of Sungkyunkwan University and Seoul National University.

1. Preparation of solutions: artificial saliva and tastants

1. Prepare artificial saliva by dissolving 2 mM NaCl, 5 mM KCl, 3 mM NaHCO₃, 3 mM KHCO₃, 0.25 mM CaCl₂, 0.25 mM MgCl₂, 0.12 mM K₂HPO₄, 0.12 mM KH₂PO₄, and 1.8 mM HCl in distilled water (>1 L), and adjust the pH of the solution to 7 (see Table of Materials)¹².
2. Prepare tastants, such as sour: 10 mM citric acid; salty: 400 mM NaCl, optionally with 50 µM amiloride; sweet: 40 mM acesulfame K; bitter: a mixture of 5 mM quinine, 5 mM denatonium and 20 µM cycloheximide, by dissolving the tasting chemical in the artificial saliva prepared in step 1.1.

2. Preparation of the microfluidic system

NOTE: Tastants were delivered to the mouse tongue using a pressurized multichannel fluidic delivery system (refer Figure 1 and Table of Materials).

1. Fill the reservoirs of the pressurized flow perfusion system with the artificial saliva and tastants.
2. Connect the compressed air line to the regulator input and set the air pressure between 30 and 50 psi in the fluidic delivery system.
3. Set the output pressure of the regulator to 0.4 psi and check if liquid comes out of the tube under this pressure.
4. Connect the manifold from the reservoirs to the input port of µTongue.
5. Connect the output port of µTongue to a syringe pump and withdraw liquid with ~300 µL∙min^-1 to establish the steady-state condition. Observe the constant volume of a hanging droplet under the µTongue. Adjust the value of the setting parameter depending on the sample height.
6. Disconnect the compressed air line and stop the syringe pump until protocol step 3 is completed.

3. Mouse preparation for in vivo imaging (Figure 2).

NOTE: All animal preparations were carried out during the daytime under aseptic conditions on a laboratory workbench.

1. Mouse anesthesia
   1. Prepare a 7-week-old or older mouse of either sex. Use a genetically modified mouse line that expresses calcium-sensing fluorescence proteins in the taste cells.
   2. The mouse is restrained for anesthesia. A mixture of 100 mg/kg ketamine and 10 mg/kg xylazine is injected intraperitoneally into the mouse¹³.
2. TRITC-dextran (500 kDa) in 2.5% W/V phosphate buffer saline is administrated intravenously into the mouse through a retro-orbital route to observe blood circulation during an imaging session.
3. Attach a head fixer on the mouse skull to minimize movement artifacts.
   1. The mouse head is sprayed with 70% ETOH while the mouse is placed in a supine position. Lift the head skin lightly with forceps and snip off approximately 7 mm² with scissors.
   2. Clean the hair around the scalp, remove the periosteum under the skin, apply an instant adhesive to the skull, and attach a customized head fixer.
   3. After the instant adhesive is hardened, apply dental glue around the head fixer and illuminate with a blue light to solidify dental glue.
4. Place the mouse tongue on the bottom unit of µTongue.
   1. Attach the lower lip of the mouse to the bottom unit of µTongue with an instant adhesive.
   2. Place the mouse on the board (mouse preparation board in Figure 1B) and put the bottom unit of the µTongue to the posts (µTongue hold post in Figure 1B). Make sure that the holes at the edge of the bottom unit are aligned to the post.
   3. Tighten the mouse head fixer to the head fixer holder at the board. Then, adjust the distance between the mouse head and the device. Rotate the mouse head smoothly approximately 45° using the head fixer holder. This process prevents physical contact of the mouse nose with microscope objective.
   4. Draw the mouse tongue gently using plastic tweezers and attach the ventral side of the tongue to the upper side of the bottom unit of the µTongue. Then, wipe the surface of the mouse tongue with a wet cotton swab.
   5. Soak a piece of paper in the artificial saliva and place it on the exposed surface of the mouse tongue to maintain a wet condition.
   6. Place the curved washers on the posts that hold both ends of the bottom part of µTongue.
5. Place the mouse preparation on the microscope stage. Position the exposed mouse tongue under the approximate center of the microscope objective area. Be sure not to deviate from the dynamic range of the stage. Then, tighten the mouse board on the stage with screws.
6. Place the heating pad under the mouse body and maintain the temperature at 36.5 °C-37.5 °C. Monitor the mouse body temperature with a temperature sensor and control the temperature of the heating pad using a feedback signal from the temperature sensor.
7. Twist a thin piece of paper and place it at the mouth of the mouse to prevent liquid from entering the mouse trachea.
8. Remove the wet tissue from the mouse tongue and place the prepared µTongue on the mouse tongue. Put a microfluidic channel on the tongue and adjust its position to observe the surface of the tongue through the imaging window.
9. Secure the µTongue by gently screwing on both ends with minimal compressive pressure.

4. Imaging acquisition

1. Turn on the 920 nm two-photon laser and the microscope in advance of use.
2. Mount the water-immersion objective (16x, NA 0.80 or 25x, NA 1.1) on the microscope. Drop the distilled water on the imaging window of the µTongue and immerse the objective.
3. In camera mode, turn on the light using mercury lamp and illuminate the surface of the tongue.
4. By adjusting the Z-axis, search the autofluorescent signal from the filiform papillae to find the approximate focal plane. Then, using the X and Y adjustment knob, locate a taste bud.
5. Switch to the multiphoton mode. Set the image acquisition conditions as follows: excitation wavelength: 920 nm; emission filter set: 447/60 nm, 525/50 nm, and 607/70 nm; bidirectional raster scan mode, frame size: 512 x 512.
6. Adjust the X and Y positions to place the taste bud on the center of the image window.
7. Search the blood vessels surrounding the taste bud at about two-third height of the taste bud. Visualize the blood circulation by TRITC-dextran (500 kDa) injection from protocol step 3.2. If the blood flow clogs, loosen the fixing screws slightly to allow blood flow.
8. Adjust Z-axis and find the Z-plane of taste bud that contains an adequate number of taste cells.
9. Proceed calcium imaging with 2-6 Hz for 80 s. Provide a taste solution of 20 s by switching on the reservoir of the fluidic system after imaging starts. After 20 s of taste stimulation, switch the reservoir back to artificial saliva.
10. After sequential imaging is finished, wait for about 3-4 min in advance to the next imaging session. Keep the artificial saliva flowing to the mouse tongue to wash away the tastant remanent from the previous imaging session. Depending on the design of the experiment, repeat the session as required.
11. When in vivo calcium imaging is complete, euthanize the mouse according to the IACUC procedure. The mouse under anesthesia is sacrificed in the CO₂ chamber.
    ​NOTE: Check the depth of the anesthesia using a toe-pinch reflex. During an imaging session, artificial saliva from the reservoirs should be provided consistently. If bubbles appear at the imaging window of the µTongue, remove the bubbles by pushing them through the input or the output of the µTongue using strong liquid pressure.

5. Image analysis (Figure 3)

1. Image conversion
   1. Open the raw image files using Fiji¹⁴ or a similar image analysis software.
   2. Convert the image file to a RGB stack file to use the NPL Bud Analyzer code.
      1. Image > Color > Split Channels
      2. Image > Color > Merge Channels and select the image from step 5.2.1.
      3. Image > Color > Stack to RGB
2. Image registration
   NOTE: Use the custom-written code for data analysis. Please refer to https://github.com/neurophotonic/Tastebud-analyzer.
   1. Run the code named Taste_GUI.m; a GUI window named NPL Bud Analyzer will pop up. Click on the New Analysis button on the upper-right corner, then load the converted image from step 5.1. Set the frame rate above the loaded image.
   2. Draw the region of interest (ROI) over the loaded image for registration. Double click on the selected ROI and an auto-calculated registration will start.
3. Obtain the relative fluorescence intensity changes (ΔF/F)
   1. Go back to the NPL Bud Analyzer window to show the registered image from step 5.2 automatically. If the user already has a reg file, click on the Load Data button and select the _reg.tif file.
   2. Click on the CIRCLE or POLYGON button and position the ROI of taste cell over the taste bud image.
   3. This presents the raw fluorescence intensity and the calcium trace (ΔF/F) of the selected taste cell automatically under the taste bud image.
   4. Click on Save Trace to present the calcium trace (ΔF/F) on the right side of the GUI, while ROI is shown over the taste bud image. Repeat steps 5.3.2-5.3.4 until the ROI selection is finished.
      NOTE: Click on the Delete Trace button if the ROI is mis-selected to eliminate the last selected ROI and calcium trace.
   5. After the ROI selection is finished, write the file name on the bottom-right corner, and click on the Finish button to export the ΔF/F calcium trace as an .xls format, and the tase bud image with ROIs in a .bmp format.
4. Analysis of the calcium trace
   1. Analyze the calcium trace obtained from step 5.3. Consider that taste cells have reacted to tastant when fluorescence intensity rises more than two standard deviations of the baseline after the tastant is delivered⁴, and p-values are less than 0.01, using paired or unpaired t-tests¹⁰.
   2. Consider the taste cell as a responder cell, if it responds to a certain tastant more than two times out of three trials(~60%)¹⁵.
   3. Obtain the representative calcium traces by averaging individual calcium traces acquired from step 5.4.1.

Wyniki

The Pirt-GCaMP6f-tdTomato mouse was used to obtain a taste bud image. The surface of the mouse tongue was covered with autofluorescent filiform papillae. Taste buds are spread sparsely over the surface of the tongue (Figure 4A). The images of the taste bud and its structure were acquired using three different filter detectors. Using the 607/70 nm filter set, the tdTomato signal from the taste cells was obtained for ratiometric analysis (Figure 4B). Using the 525...

Dyskusje

Described here is a detailed protocol to apply µTongue to the investigation of functional activities of taste cells in vivo. In this protocol, the functional imaging on the taste cells using genetically encoded calcium indicators is performed. In addition to the use of transgenic mice, the electrophoretic loading of calcium dyes (or voltage sensing dyes) onto the taste cells can be an alternative option.

All the taste solutions less than 1.336 of refractive index were used in thi...

Materiały

Name	Company	Catalog Number	Comments
acesulfame K	Sigma Aldrich	04054-25G	Artificial saliva / tastant
calcium chloride solution	Sigma Aldrich	21115-100ML	Artificial saliva / tastant
citric acid	Sigma Aldrich	C0759-100G	Artificial saliva / tastant
cycloheximide	Sigma Aldrich	01810-5G	Artificial saliva / tastant
denatonium	Sigma Aldrich	D5765-5G	Artificial saliva / tastant
Dental glue	Denkist	P0000CJT-A2	Animal preparation
Image J	NIH	ImageJ	Data analysis
IMP	Sigma Aldrich	57510-5G	Artificial saliva / tastant
Instant adhesive	Loctite	Loctite 4161, Henkel	Animal preparation
K2HPO4	Sigma Aldrich	P3786-100G	Artificial saliva / tastant
KCl	Sigma Aldrich	P9541-500G	Artificial saliva / tastant
Ketamine	Yuhan	Ketamine 50	Animal preparation
KH2PO4	Sigma Aldrich	P0662-25G	Artificial saliva / tastant
KHCO3	Sigma Aldrich	237205-500G	Artificial saliva / tastant
MATLAB	Mathwork	MATLAB	Data analysis
MgCl2	Sigma Aldrich	M8266-100G	Artificial saliva / tastant
MPG	Sigma Aldrich	49601-100G	Artificial saliva / tastant
Mutiphoton microscope	Thorlab	Bergamo II	Microscope
NaCl	Sigma Aldrich	S3014-500G	Artificial saliva / tastant
NaHCO3	Sigma Aldrich	792519-500G	Artificial saliva / tastant
Objective	Nikon	N16XLWD-PF	Microscope
Octaflow	ALA Scientific Instruments	OCTAFLOW II	Fluidic control
PC	LG	Lg15N54	Fluidic control
PH meter	Thermoscientific	ORION STAR AZ11	Artificial saliva / tastant
Phosphate-buffered saline	Sigma Aldrich	806562	Artificial saliva / tastant
quinine	Sigma Aldrich	Q1125-5G	Artificial saliva / tastant
Syringe pump	Havard Apparatus	PHD ULTRA 4400	Fluidic control
TRITC-dextran	Sigma Aldrich	52194-1G	Animal preparation
Ultrafast fiber laser	Toptica	FFultra920 01042	Microscope
Xylazine	Bayer Korea	Rompun	Animal preparation