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All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.
- Preparation of the imaging session
- Turn on the imaging setup in advance and let the laser to warm up and stabilize, if necessary.
- Anesthetize the mouse. Place the mouse in the anesthesia induction chamber at 3% isoflurane in 1 L/min O2 and wait until it loses consciousness. Assess anesthesia using the toe pinch reflex test.
- Use forceps to carefully remove the adhesive film from the head holder plate. Hold the mouse in a hand and the head holder plate with the fingers. Remove the film gently, to avoid damaging the preparation.
- Position the mouse under the microscope, over the heating carpet, and secure the head plate to the holder (Figure 1D).
- Position the nose cone to cover the snout and decrease isoflurane to 1.5-2%.
- Apply ophthalmic ointment to the mouse's eyes.
- Clean the imaging cannula by rinsing it with deionized water. Use a syringe and a thin needle to drop water into the cannula and a vacuum pump to remove it.
2. Imaging session
- Use low magnification and long working distance objectives to visually check the cannula for residual water, dirt, integrity, and the presence of fluorescence.
- Align the cannula to the optic axis by adjusting the angles of the head holder arms.
- Switch to the 25X 1.0 NA (numerical aperture), 4 mm WD (working distance), or the 40X 0.8 NA, 3 mm WD, water immersion objectives. Add enough deionized water to fill the cannula and maintain excess water on top of the cannula. Avoid the formation of air bubbles.
- Use two-photon (2P) excitation and image fluorescent signals.
NOTE: The imaging protocol is highly dependent on the time and spatial scales to be imaged. Please refer to the section's representative results and discussion for details about the imaging settings we have used to produce the images shown in this article.