In vivo Imaging of Fully Active Brain Tissue in Awake Zebrafish Larvae and Juveniles by Skull and Skin Removal

Paul Schramm; Florian Hetsch; Jochen C. Meier; Reinhard W. K&#246;ster

doi:10.3791/62166

JoVE Journal > Neuroscience

Neurociencias

In vivo Imaging of Fully Active Brain Tissue in Awake Zebrafish Larvae and Juveniles by Skull and Skin Removal

Published: February 10, 2021

doi:

10.3791/62166

Paul Schramm¹, Florian Hetsch², Jochen C. Meier³, Reinhard W. Köster¹

¹Cellular and Molecular Neurobiology, Zoological Institute,Technische Universität Braunschweig, ²Institute of Pathophysiology,University Medical Center of the Johannes Gutenberg University, ³Cell Physiology, Zoological institute,Technische Universität Braunschweig

Summary

Here we present a method to image the zebrafish embryonic brain in vivo upto larval and juvenile stages. This microinvasive procedure, adapted from electrophysiological approaches, provides access to cellular and subcellular details of mature neuron and can be combined with optogenetics and neuropharmacological studies for characterizing brain function and drug intervention.

Abstract

Understanding the ephemeral changes that occur during brain development and maturation requires detailed high-resolution imaging in space and time at cellular and subcellular resolution. Advances in molecular and imaging technologies have allowed us to gain numerous detailed insights into cellular and molecular mechanisms of brain development in the transparent zebrafish embryo. Recently, processes of refinement of neuronal connectivity that occur at later larval stages several weeks after fertilization, which are for example control of social behavior, decision making or motivation-driven behavior, have moved into focus of research. At these stages, pigmentation of the zebrafish skin interferes with light penetration into brain tissue, and solutions for embryonic stages, e.g., pharmacological inhibition of pigmentation, are not feasible anymore.

Therefore, a minimally invasive surgical solution for microscopy access to the brain of awake zebrafish is provided that is derived from electrophysiological approaches. In teleosts, skin and soft skull cartilage can be carefully removed by micro-peeling these layers, exposing underlying neurons and axonal tracts without damage. This allows for recording neuronal morphology, including synaptic structures and their molecular contents, and the observation of physiological changes such as Ca²⁺ transients or intracellular transport events. In addition, interrogation of these processes by means of pharmacological inhibition or optogenetic manipulation is feasible. This brain exposure approach provides information about structural and physiological changes in neurons as well as the correlation and interdependence of these events in live brain tissue in the range of minutes or hours. The technique is suitable for in vivo brain imaging of zebrafish larvae up to 30 days post fertilization, the latest developmental stage tested so far. It, thus, provides access to such important questions as synaptic refinement and scaling, axonal and dendritic transport, synaptic targeting of cytoskeletal cargo or local activity-dependent expression. Therefore, a broad use for this mounting and imaging approach can be anticipated.

Introduction

Over the recent decades, the zebrafish (Danio rerio) has evolved as one of the most popular vertebrate model organisms for embryonic and larval developmental studies. The large fecundity of zebrafish females coupled with the rapid ex utero development of the embryo and its transparency during early embryonic developmental stages are just a few key factors that make zebrafish a powerful model organism to adress developmental questions¹. Advances in molecular genetic technologies combined with high resolution in vivo imaging studies allowed for addressing cell biological mechanisms underlying developmental processes². In particular, in the field of neuronal differentiation, physiology, connectivity, and function, zebrafish has shed light on the interplay of molecular dynamics, brain functions and organismic behavior in unprecedented detail.

Yet, most of these studies are restricted to embryonic and early larval stages during the first week of development as transparency of the nervous system tissue is progressively lost. At these stages, brain tissue is prevented from access by high resolution microscopy approaches becoming shielded by skull differentiation and pigmentation³.

Therefore, key questions of neuronal differentiation, maturation, and plasticity such as the refinement of neuronal connectivity or synaptic scaling are difficult to study. These cellular processes are important in order to define cellular mechanisms driving, for example, social behavior, decision making, or motivation-based behavior, areas to which zebrafish research on several weeks' old larvae has recently contributed key findings based on behavioral studies⁴.

Pharmacological approaches to inhibit pigmentation in zebrafish larvae for several weeks are barely feasible or may even cause detrimental effects⁵^,⁶^,⁷^,⁸. Double or triple mutant strains with specific pigmentation defects, such as casper⁹ or crystal¹⁰, have become tremendously valuable tools, but are laborious in breeding, provide few offspring, and pose the danger of accumulating genetic malformations due to excessive inbreeding.

Here, a minimal invasive procedure as an alternative is provided that is applicable to any zebrafish strain. This procedure was adapted from electrophysiological studies to record neuronal activity in living and awake zebrafish larvae. In teleosts, skin and soft skull cartilage can be carefully removed by micro-peeling these layers, because they are not tightly interwoven with the brain vasculature. This allows for exposing brain tissue containing neurons and axonal tracts without damage and for recording neuronal morphology, including synaptic structures and their molecular contents, which in turn include the observation of physiological changes such as Ca²⁺ transients or intracellular transport events for up to several hours. Moreover, beyond descriptive characterizations, the direct access to brain tissue enables interrogation of mature neuronal functions by means of neuropharmacological substance administration and optogenetic approaches. Therefore, true structure function relationships can be revealed in the juvenile zebrafish brain using this brain exposure strategy.

Protocol

All animal work described here is in accordance with legal regulations (EU-Directive 2010/63). Maintenance and handling of fish have been approved by local authorities and by the animal welfare representative of the Technische Universität Braunschweig.

1. Preparation of artificial cerebro spinal fluid (ACSF), low melting agarose and sharp glass needles

Prepare the ACSF by dissolving the listed chemicals at following concentrations in distilled water. 134 mM NaCl (58.44 g/mol), 2.9 mM KCl (74.55 g/mol), 2.1 mM CaCl₂ (110.99 g/mol), 1.2 mM MgCl₂ 6x H₂O (203.3 g/mol), 10 mM HEPES (238.31 g/mol), and 10 mM d-Glucose (180.16 g/mol).
NOTE: For MgCl₂, CaCl₂, and KCl, 1 M stock solutions are prepared in desalted sterile water and stored at 4 °C for subsequently preparing fresh ACSF. Glucose, HEPES, and NaCl are dissolved as solid compounds in the fresh ACSF solution. For dissolving chemicals, follow the manufacturer's instructions.
Adjust the pH of the ACSF to 7.8 with 10 M NaOH. Preparation of ACSF requires precise measurement of chemicals and fine adjustment of pH as it replaces the cerebro spinal fluid and maintains the physiological conditions required for neurons to be fully functional else it might cause brain misfunction and neuronal death.
Store the freshly prepared ACSF at 4 °C for a maximum of 4 weeks. For working conditions, aliquot the required volume of ACSF for the day/experiment and prewarm at 25-28 °C (and optionally oxygenate it, step 2.5)
NOTE: Freshly prepared ASCF is fine for 1 day. If planning to use it over several days, ACSF needs to be sterile filtered.
For later anesthesia of the larvae, prepare a 50 mM stock solution of d-Tubocurarine in distilled water and store the solution at -20 °C as 100 µL aliquots in the freezer until needed.
To embed the fish, prepare 2.5% low melting (LM) agarose by dissolving 1.25 g LM-agarose (Table of Materials) in 50 mL ACSF and boil until the agarose is completely dissolved.
NOTE: Alternatively, higher or lower concentrations of LM-agarose can be used depending on the experimental set-up. However, if the agarose is too soft, it will not be able to hold the fish in position when opening the skull.
Store the agarose at 37 °C waterbath, to avoid solidification and because this temperature will also not harm the larvae when embedding. After the boiled agarose is cooled down to 37 °C in the waterbath, add the necessary amount of d-Tubocurarine to the aliquoted agarose needed for the day to reach a working concentration of 10 µM. For future use, store the left-over agarose at 4 °C to avoid contamination.
Prepare sharp and thin glass needles from glass capillaries (Supplementary Figure 1) using a micropipette puller with the following settings.
1. Puller I, Capillary type 1: Heat 1: 65.8; Heat 2: 55.1; 2-step pulling
  Puller II, Capillary type 2: Heat = 700; Fil = 4; Vel = 55; Del = 130; Pul = 55; 1-step pulling.
  NOTE: The units are specific for each puller and glass capillary used here, respectively (see Table of Materials). Other capillaries and pullers can also be used to prepare the glass needles. But the glass needles should not be too thin as they might break when coming in contact with the skull. Capillary: length: 100 mm (4 inches); OD: 1.5 mm; ID: 0.84 mm; filament: Yes

2. Anesthesia of larvae and preparations for embedding

When starting the experiment for the day, transfer the animals that are needed with a plastic Pasteur pipette to a 90 mm diameter Petri dish, which is filled with either Danieau (for larvae which are still kept in a Petri dish with Danieau) or water from the fish facility (for larvae which are older than 7 dpf and are kept in the fish facility).
1. When pipetting fish older than 2 weeks, make sure the opening of the pipette is large enough to avoid injuring the fish when transferring them. Do not use a net because it will physically damage especially the younger larvae.
Add rotifera or artemia nauplii suited for the size of the larvae kept in the Petri dish, to ensure free access to food and maximum health status of the larvae and to reduce stress.
For embedding, transfer the selected larvae to a 35 mm diameter Petri dish filled with ACSF. Add the necessary volume of d-Tubocurarine to reach a working concentration/effective dose of 10 µM and wait for a few minutes until the larvae are completely immobilized¹¹.
NOTE: When the fish grow older or if a faster full anesthesia is needed (under 5 min), it is possible to increase the concentration of d-Tubocurarine (LD₅₀ for mice is 0.13 mg/kg intravenously¹²). It is also possible to use a different anesthetic, such as α-bungarotoxin (working concentration: 1 mg/mL), which has the same effect as curare and also keeps the brain fully active¹³. If a fully active brain is not necessary for the subject of interest, Tricaine in a non-lethal dose (0.02%) is also an option to fully anesthetize the larvae. However, Tricaine blocks sodium-channels, thereby impairing brain activity¹⁴.
Prepare the mounting chamber by taking the lid of the 35 mm diameter Petri dish, flip the lid upside down, and place a square glass coverslip (24 x 24 mm) on the bottom of the lid. See Figure 1 (upper part) for a schematic description of these steps. The smoother surface of the glass prevents slipping away of the agarose block, which contains the larvae during the skull opening procedure.
Aliquot the amount of ACSF needed for the day in an appropriate vial (e.g., 50 mL tube, beaker, Schott bottle, etc.) and oxygenate it with carbogen (5% CO₂, 95% O₂). If imaging only morphology (e.g., fluorescence patterns) ACSF is still necessary to ensure the integrity of the brain and that cells are not negatively influenced by osmolarity effects but oxygenation of the ACSF is not needed. This step only needs to be performed when full brain activity is necessary for imaging.
NOTE: For optimal oxygen saturation of the medium, add an air stone to the end of the carbogen tube. To guarantee a sufficiently high oxygen level, it is necessary to exchange the ACSF in the imaging chambers with freshly oxygenated ACSF every 20-60 min, depending on the number and age of larvae embedded in the same imaging chamber (e.g., for a single embedded larva ACSF exchange every hour is sufficient. For six larvae older than 14 dpf embedded in parallel, exchanging ACSF every 20 min is necessary) so plan the necessary amount of oxygen saturated ACSF according to the planned experiment.

3. Embedding of the larvae

Transfer the fully anesthetized larvae with a plastic Pasteur pipette to the (in step 2.4) prepared mounting chamber. Then, carefully remove the excess medium to avoid dilution of the LM-agarose. All the following steps should be performed under a stereo microscope with sufficient magnification.
NOTE: Tilting the mounting chamber can help to fully remove the medium.
Proceed immediately to the next step, by adding a sufficiently large LM-agarose drop on top of the larvae (circa 1 mL, depending on the size of the larvae) to protect the animals from drying out and to reduce unnecessary stress.
Orient the larvae in position before the agarose solidifies. Ensure that the dorsal part of the larvae is directed upward. Also, make sure to embed the larvae as close to the surface of the agarose as possible.
NOTE: Depending on the size and number of larvae planned to embed at the same time, it is possible to adjust the agarose concentration. For example, for 1-3 larvae that are 30 dpf old, a concentration of 1.8%-2% LM-agarose is recommended. For 1-4 larvae that are 7 dpf old, it is most practicable to use 2.5% LM-agarose, whereas, for 5-8 larvae, 2% is more suited. If a fully active brain is required, it is recommended to only embed three fish at the same time to reduce the time needed to operate the larvae. In general, it is recommended to use lower concentrations (1.8%-2%) the older the larvae get or the more larvae are planned to be embedded at the same time.
If images will be recorded using an inverted microscope, trim the agarose block containing the larvae into a small cuboid shape. This is important for transferring the larvae to the imaging chamber later on. If using an upright microscope, such trimming is not necessary, because the mounting chamber can also be used as the imaging chamber. In Figure 1 (upper part), one can find a schematic description of these steps.

4. Exposing the brain

NOTE: All the following steps should be performed with greatest care to not unnecessarily injure the larvae. If a fully active brain is required for the experiment, keep in mind that with every second that passes, while the fish is still fully mounted in agarose and has an open skull without oxygenated ACSF, the brain will suffer from a lack of oxygen and also dry out. The effects of oxygen deficiency will become even more dramatic, the older the embedded larvae are. Therefore, it is important to perform the surgery not only within the shortest time possible, but also with maximum precision to not evoke mechanical brain damage with the needle. When trained, steps 4.2-4.4 should not take more than 30 s per fish.

Begin the surgery as soon as the agarose has solidified. First, trim away all of the excess agarose above the brain region of interest to obtain free access to the head and a clear working space. If the dorsal part of the head is already sticking out of the agarose, skip this step.
Depending on the region of interest, pick a spot to begin with the surgery. Take the glass needle and make a small incision through the skin but without penetrating too deep into the tissue. This will be the starting point for peeling away the overlaying skin.
NOTE: For optimal results, never start directly above the region of interest to reduce the risk of damaging important structures. If necessary, it is possible to even start posterior to the hindbrain and from there work forward until the unwanted area of skin is peeled away.
Continue with very small cuts along the part of skin aiming to remove by barely moving the needle just underneath the surface. Most of the time it is not necessary to move completely around the brain and to cut out a circle-like piece of skin and skull, but rather just make two incisions along the head and then push the skin away to one or the other side. Figure 2 shows a schematic representation of the optimal cutting strategy to obtain free access to the cerebellum.
NOTE: This micro-surgery is a delicate procedure and it will most likely need some training to perfectly remove the skin without damaging the underlying brain. It is also recommended to find out the optimal cutting strategy for the brain region of interest and stick with it for the period of the experiment.
Immediately after removing the skin from all embedded larvae, proceed by pouring (oxygenated) ACSF over the agarose to flood away unwanted skin particles and blood and to keep the brain fully active and protect it from drying out.
NOTE: If a healthy brain is needed for the experiment, it is recommended to go for a maximum of three fish at a time.
If using an upright microscope, start directly with imaging.
1. When using an inverted microscope, slide a small spatula underneath the cuboid agarose block (step 3.4).
2. Add a small drop of LM-agarose to the bottom of the imaging chamber (e.g., glass-bottom dish) and immediately flip the agarose block containing the larvae with the spatula for 180° and gently push it to the bottom of the imaging chamber, while the liquid agarose drop acts as glue.
3. When the agarose has solidified, fill up the imaging chamber with (oxygenated) ACSF, then begin imaging. See Figure 1 (lower part) for a schematic description.
When full brain activity is required for the experiment, always make sure that ACSF in the imaging chamber has a sufficiently high oxygen level. To ensure this, exchange the medium carefully with freshly oxygenated ACSF when possible every 20-60 min (depending on the number and size of the fish, size and surface of the imaging chamber, and imaging duration).

Figure 1: Schematic procedure for the preparation of open skull zebrafish for in vivo imaging in a stepwise manner. The working instructions for the different steps can be found in the graphic itself. Graphic designed by Florian Hetsch and adapted by Paul Schramm. Please click here to view a larger version of this figure.

Figure 2: Detailed schematic representation of the micro-surgery performed to remove pieces of skin and skull above the brain region of interest. The red circle marks the spot where the first cut needs to be made. The red-dotted line delineates the optimal path to cut along with the needle to obtain free access to the cerebellum without damaging it. The green arrow marks the direction in which the excessive skin and skull pieces can easily be pushed away. Make sure to never penetrate into the brain tissue during the whole procedure. After successfully peeling away the skin, the brain region of interest (here, cerebellum) will be freely accessible for any kind of high-resolution in vivo imaging. Please click here to view a larger version of this figure.

Representative Results

Figure 3A,C show a 14 dpf larva of the transgenic line Tg[-7.5Ca8:GFP]^bz12[¹⁵^] with the skull still intact. The pigment cells in the overlaying skin are distributed all over the head and are interfering with the fluorescence signal in the region of interest (here, cerebellum). With the larva in this condition, it is not possible to obtain high resolution images of the brain. Figure 3B shows a larva of the same transgenic line after performing the open skull surgery. The area of interest is now freely accessible for the excitation laser and emitted fluorescence light to penetrate the tissue without getting scattered and reflected. Pictures recorded of this larva will result in detailed high-resolution images (Figure 3D), comparable with images of an isolated brain, but with the advantage that the brain is still fully active. Additionally, the brain is not losing any fluorescence intensity that would normally be caused by fixation with para-formaldehyde, as would be the case for a fixed and explanted brain. In a larva with an open skull and, therefore, a freely accessible brain with fully active neurons, which still posseses all physiological connections and receives normal input from the sensory system, it will be also possible to observe short termed events, e.g., synaptogenesis, spine growth, dendritic/axonal migration or local mRNA expression¹⁶ under physiologic conditions. Another advantage of this method is, that it is suited for the application of different pharmacological substances to investigate the effects on the living larva without the diffusion problems caused by the skin and skull or the blood brain barrier, which would normally hinder substances to penetrate the brain (Figure 3E). To demonstrate that, a 14 dpf larva with an open skull was incubated with Hoechst-33342 (5 µg/mL in ACSF) for 10 min and then imaged (Figure 3F–I). Figure 4A,B show 30 dpf old larvae before and after opening the skull. It is the most advanced timepoint tested so far for this method. Even at this developmental stage of the larva, it is possible to obtain high resolution images of single neurons and also subcellular compartments using the method described here (Figure 4C,D). These 30 dpf old larvae were not showing activity deficits after 1 h of imaging. This method is also used for electrophysiological patch clamp analysis of 30 dpf old larvae and there is no sign for the loss of neuronal activity in Purkinje cells (yet cells close to the surface are delicate and vulnerable) during the first 60 min of being embedded with an open skull. By regularly inspecting the amount of blood flow, it is possible to validate that the larva is still in a healthy status. This status can be maintained, by regularly exchanging or oxygenating ACSF during long-term image recording. It is therefore fairly simple to validate whether a larva is still suited for functional brain studies. To prove, that no important blood vessels are damaged during the micro-surgery and also to show that this method allows much deeper penetration of the excitation laser light into brain tissue and the reflection-reduced emission of photons, a 10 dpf old larva of the transgenic strain Tg(flk1:mCherry)_y206Tg¹⁷ was analyzed by this method. These fish contain a fluorescent vasculature in the brain due the expression of the red fluorescent protein mCherry in endothelial cells. A maximum intensity projection of an image stack covering 245 µm in depth reveals the intricate network of the blood vessels meandering through the mid- and hindbrain (Figure 5A). Furthermore, color coding of depth values of the image stack demonstrates that even blood vessels deeply burried in the brain at nearly 250 µm are clearly visible and traceable (Figure 5B). Supplementary Video 1A shows a healthy brain with sufficient blood supply, while Supplementary Video 1B shows a brain with compromised blood flow due to the lack of exchange of ACSF and lack of medium oxygenation.

Figure 3: Skin peeling in zebrafish larvae provides optimal access for in vivo brain imaging. Confocal microscopy analysis of 14 dpf old transgenic Tg(-7.5ca8:GFP]^bz12 larvae. Overview of mid- and hindbrain of non-peeled (A,C) and skin-peeled (B,D) specimens at 20x and 40x magnification respectively. In the latter, the lack of pigment clearly improves image quality and allows for detailed image recording of fluorescent Purkinje cells in the cerebellum. Subcellular imaging and ease of compound administration to the brain is demonstrated by a 10 min incubation period with the nucleic acid fluorescent staining using Hoechst-33342 (5 µg/mL in ACSF). While only skin cells incorporate this dye in non-peeled larvae (E), specimens with lifted skin display intense labeling of their nuclei throughout the brain (F) allowing for visualizing individual nuclei (G) of GFP-fluorescent Purkinje neurons (H, merged image shown in I, 63x optical and 4x digital magnification). Scale bars: A-F: 100 µm, G-I: 5 µm. Larvae were embedded with their head to the left, dorsal is up. Please click here to view a larger version of this figure.

Figure 4: Skin peeling extends access for in vivo brain imaging to juvenile zebrafish. Confocal microscopy analysis of 30 dpf old transgenic Tg(-7.5ca8:GFP]^bz12Tg juveniles. Overview over mid- and hindbrain of non-peeled (A) and and skin-peeled specimens at 10x (B) and 40x (C) and 63x optical magnification with 4x digital zoom (D), respectively. The removal of pigmented skin enables visualization of the cellular organization of the continuous cerebellar Purkinje cell layer and to depict projections of individual neurons (D, white arrows). Scale bars: A-C: 100 µm, D: 5 µm. Larvae were embedded with their head to the left, dorsal is up. Please click here to view a larger version of this figure.

Figure 5: Skin removal permits brain vasculature reconstruction at extended depth in a 10 dpf old Tg(flk1:mCherry)^y206Tg zebrafish larva. (A) Maximum intensity projection of a stack of images (245 images of a thickness of 1 µm at total distance of 245 µm, 20x optical magnification) displays a continuous network of blood vessels throughout these brain areas. (B) Depth color coding reveals that this network of blood vessels can be monitored at depth of 200 µm and beyond. To remove autofluorescence and reflection, the eyes were masked by black color. Scale bar: 100 µm. Larvae were embedded with their head to the left, dorsal is up. Please click here to view a larger version of this figure.

Supplementary Figure 1: Needles made from glass capillaries. (A) Two needle types obtained from two different needle pullers are shown. It is important that the tip is not too long to provide it with sufficient stability and to avoid their breaking when coming in contact with the skin/skull. Yet a sufficient sharpness is needed to allow for making cuts with clean edges. (B) An image of the capillary that is loaded in the needle pullers is shown. Scale bar is 250 µm. Capillary length: 100 mm; OD: 1.5 mm: ID: 0.84 mm; filament: yes. Please click here to download this figure.

Supplementary Video 1: Imaging 7dpf old larva. (A) Real-time Movie recording (30 fps) from a 7 dpf old larva 10 min after the skin above the brain has been removed. The vivid blood flow indicates a healthy state with sufficient blood supply. (B) Real-time Movie recording (30 fps) from the same 7 dpf old larva shown in Supplementary Video 1A, 2 h after the microsurgery without exchange of ACSF and lack of medium oxygenation. Scale bar: 100 µm. Please click here to download this video.

Discussion

The presented method provides an alternative approach to brain isolation or the treatment of zebrafish larvae with pharmaceuticals inhibiting pigmentation for recording high resolution images of neurons in their in vivo environment. The quality of images recorded with this method is comparable to images from explanted brains, yet under natural conditions.

Furthermore, a loss in intensity of fluorescence is avoided, because there is no need for treatment with fixatives¹⁸. Also, this method is not as invasive as isolating a brain and it only consists of one crucial step that could lead to failure, so the chances of a successful preparation are higher compared to brain explantation. The most important advantage is, that this method is suited for in vivo image recording. Provided that the skull opening is performed precisely, fast and successful, and oxygen saturation of ACSF is monitored regularly, the brain should be fully functional and viable for hours. Based on electrophysiological recordings, blood circulation, breathing, and survival of fish for additional days, we consider it likely that skin and skull removal is not majorly detrimental to overall health. Thus, this method can be used for real-time imaging of cellular and subcellular processes in a healthy and functional brain without image-disturbing pigmentation. This method is a standard procedure used for electrophysiological recordings of neuronal activity in vivo in our lab and is also well established in other electrophysiology laboratories around the world¹⁹^,²⁰^,²¹^,²², proving that the function of the brain is not impaired by the micro-surgery. One disadvantage that needs to be mentioned is that this approach is only suited for imaging of dorsal and lateral brain regions and cannot be performed repeatedly with the same specimen.

However, if a fully functional brain is necessary for the experiment, the oxygen saturation should be monitored permanently, and, if required, the ACSF in the imaging chamber should be exchanged with freshly oxygenated ACSF. This means, for long-term recordings, there needs to be an option to exchange the used ACSF with oxygen-saturated ACSF without disturbing the imaging-procedure which could be addressed using a miniature pump.

Of note, if the micro-surgery is not performed correctly or imprecisely, it will lead to brain injury or cerebral hemorrhage resulting in compromised brain physiology. Also, a low oxygen saturation in the ACSF (see Supplementary Video 1) or too much stress for the larvae during this whole procedure can negatively impact the brain²³^,²⁴. Therefore, this method is not suited for high-throughput analysis, but rather for longitudinal or highly detailed image recording of only a few larvae per timepoint. Therefore, this method should not be aimed for drug screening at high throughput, but it could be used to characterize or validate promising pharmacological compounds in detail, where high resolution imaging is informative and necessary. To ensure proper brain health status, it is recommended to not exceed the number of three larvae per trial.

Through the open skull, it is even possible to directly apply substances to the brain tissue without having them to pass through the blood-brain barrier. Overall, the method described here – currently applied for in vivo electrophysiology – is a technique with a high potential in a very broad field of in vivo brain imaging and optogenetics in zebrafish larvae and juveniles and can be coupled with neuropharmacological approaches.

Divulgaciones

The authors have nothing to disclose.

Acknowledgements

We especially thank Timo Fritsch for excellent animal care and Hermann Döring, Mohamed Elsaey, Sol Pose-Méndez, Jakob von Trotha, Komali Valishetti and Barbara Winter for their helpful support. We are also grateful to all the other members of the Köster lab for their feedback. The project was funded in part by the German Research Foundation (DFG, KO1949/7-2) project 241961032 (to RWK) and the Bundesministerium für Bildung und Forschung (BMBF; Era-Net NEURON II CIPRESS project 01EW1520 to JCM) is acknowledged.

Materials

Calcium chloride	Roth	A119.1
Confocal Laser scanning microscope	Leica	TCS SP8
d-Glucose	Sigma	G8270-1KG
d-Tubocurare	Sigma-Aldrich	T2379-100MG
Glass Capillary type 1	WPI	1B150F-4
Glass Capillary type 2	Harvard Apparatus	GC100F-10
Glass Coverslip	deltalab	D102424
HEPES	Roth	9105.4
Hoechst 33342	Invitrogen (Thermo Fischer)	H3570
Imaging chamber	Ibidi	81156
Potassium chloride	Normapur	26764298
LM-Agarose	Condalab	8050.55
Magnesium chloride (Hexahydrate)	Roth	A537.4
Microscope Camera	Leica	DFC9000 GTC
Needle-Puller type 1	NARISHIGE	Model PC-10
Needle-Puller type 2	Sutter Instruments	Model P-2000
Pasteur-Pipettes 3ml	A.Hartenstein	20170718
Sodium chloride	Roth	P029.2
Sodium hydroxide	Normapur	28244262
Tricain	Sigma-Aldrich	E10521-50G
Waterbath	Phoenix Instrument	WB-12
35 mm petri dish	Sarstedt	833900
90 mm petri dish	Sarstedt	821473001

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Schramm, P., Hetsch, F., Meier, J. C., Köster, R. W. In vivo Imaging of Fully Active Brain Tissue in Awake Zebrafish Larvae and Juveniles by Skull and Skin Removal. J. Vis. Exp. (168), e62166, doi:10.3791/62166 (2021).