Analysis of Skeletal Muscle Defects in Larval Zebrafish by Birefringence and Touch-evoke Escape Response Assays

Summary

The zebrafish is now an established and powerful tool for modeling muscular dystrophies, congenital myopathies, and related neuromuscular diseases. Birefringence and touch-evoked escape behavior are two common noninvasive assays used to determine the degree of muscular disorganization and locomotive impairment of zebrafish embryos during early development.

Abstract

Zebrafish (Danio rerio) have become a particularly effective tool for modeling human diseases affecting skeletal muscle, including muscular dystrophies^1-3, congenital myopathies^4,5, and disruptions in sarcomeric assembly^6,7, due to high genomic and structural conservation with mammals⁸. Muscular disorganization and locomotive impairment can be quickly assessed in the zebrafish over the first few days post-fertilization. Two assays to help characterize skeletal muscle defects in zebrafish are birefringence (structural) and touch-evoked escape response (behavioral).

Birefringence is a physical property in which light is rotated as it passes through ordered matter, such as the pseudo-crystalline array of muscle sarcomeres⁹. It is a simple, noninvasive approach to assess muscle integrity in translucent zebrafish larvae early in development. Wild-type zebrafish with highly organized skeletal muscle appear very bright amidst a dark background when visualized between two polarized light filters, whereas muscle mutants have birefringence patterns specific to the primary muscular disorder they model. Zebrafish modeling muscular dystrophies, diseases characterized by myofiber degeneration followed by repeated rounds of regeneration, exhibit degenerative dark patches in skeletal muscle under polarized light. Nondystrophic myopathies are not associated with necrosis or regenerative changes, but result in disorganized myofibers and skeletal muscle weakness. Myopathic zebrafish typically show an overall reduction in birefringence, reflecting the disorganization of sarcomeres.

The touch-evoked escape assay involves observing an embryo's swimming behavior in response to tactile stimulation^10-12. In comparison to wild-type larvae, mutant larvae frequently display a weak escape contraction, followed by slow swimming or other type of impaired motion that fails to propel the larvae more than a short distance¹². The advantage of these assays is that disease progression in the same fish type can be monitored in vivo for several days, and that large numbers of fish can be analyzed in a short time relative to higher vertebrates.

Protocol

1. In vivo Analysis of Skeletal Muscle Structure by Birefringence

1. Prepare mating cages separating the male(s) from the female(s) of the desired zebrafish line(s) late in the afternoon after feeding.
   1. Distinguish females by their bigger underbelly and slight blue/white coloration, and males by their slender body shape and pink/yellow hues.
   2. Success with pair-wise crosses (one male and one female) may only be about 50%. For a higher rate of success, mate one male with 2-3 females.
2. Remove cage dividers the next morning shortly after the onset of light and allow the fish to spawn undisturbed.
3. Collect the eggs using a strainer when sufficient numbers of fertilized eggs are laid at the bottom of the tank.
4. Transfer the embryos into a deep Petri dish by rinsing the strainer with fish water and return the parent fish to their tanks. Place dishes of embryos into a 28.5 °C incubator.
5. Clean out the inviable eggs and debris later that day or the following morning, and return the embryos to the incubator for further growth.
6. Embryos/larvae reach the appropriate age to observe birefringence at 3-7 days post-fertilization (dpf), as results prior to 3 dpf may potentially suffer from limited contrast. Wild-type embryos hatch from their chorions between 48-60 hr post-fertilization (hpf), followed by a straightening of the body axis. Late-hatching wild-type or mutant embryos may require manual dechorionation.
   1. Gently make a tear in the chorion with sharp forceps and turn it upside down so that the embryo falls out.
   2. Allow dechorionated embryos to straighten prior to beginning the assay.
   3. Anesthetize embryo(s) with tricaine (0.04% in fish water) to aid in their correct positioning.
7. Fit a dissecting microscope with a polarized lens that can be rotated to adjust the angle of polarized light (Figure 1A).
8. Place dechorionated, anesthetized embryo(s) directly on top of a second polarized lens along the lateral axis of the body. The second lens should be positioned below the top lens, on the microscope stage (Figure 1B). Do not use plastic Petri dishes at any point during the birefringence assay, as plastic is not an appropriate medium for the transmission of refracted light.
9. Rotate the top lens with the embryo of interest in view until the axes of polarization of the two lenses are oriented at 90° from one another and the background is completely dark.
10. The optimum output of the assay is dependent on the orientation of fish between two polarized lenses. Move the fish around to make sure that they are lying as flat as possible.
    1. If the fish is curved, only the segments with this flat orientation will pass the polarized light and exhibit birefringence. In such cases, measure the birefringence in the flat areas and record the birefringence of the corresponding area in the wild-type fish (e.g. somites 1-10 in both wild-type and mutant fish).
11. Observe the birefringent phenotype of the fish.
    1. Wild-type fish with highly organized skeletal muscle show bright birefringence, as the refractive index for the light parallel to the myofilaments is higher than the polarized light perpendicular to these structures.
    2. Fish with disorganized skeletal muscle suggestive of a nondegenerative myopathy or a developmental defect typically show an overall reduction in birefringence.
    3. Fish with disorganized skeletal muscle characteristic of a muscular dystrophy commonly exhibit a patch-like pattern of birefringence, with dark areas representing muscle degeneration among bright areas of normal muscle architecture.
12. Quantify birefringence by taking images of wild-type and mutant fish under polarized light at the same exposure settings and magnification. Save images as .tiff files.
    1. Open birefringence images in ImageJ software (http://rsbweb.nih.gov/ij/).
    2. For each image, select the area of zebrafish muscle by drawing a line around the body using the “Polygon Selections” option from the toolbar.
    3. Use “Set Measurements” under the “Analyze” drop-down menu to select the required statistics for the image.
       1. Minimum selection requires that boxes for “Area,” “Mean gray value,” and “Min & max gray value” are checked.
       2. A maximum gray value of >255 will indicate pixel saturation. Therefore, use images with maximum gray values less than 255.
    4. Normalize the mean intensity with the selected area and repeat this same quantification procedure for each birefringence image.

2. Touch-evoked Escape Behavior Assay

1. Set up mating pairs of the appropriate zebrafish line(s) and collect embryos as described above in steps 1.1-1.5.
2. At 2-7 days post-fertilization, place dechorionated embryos/larvae individually into a deep Petri dish or the chambers of multiwell plates.
3. Working with only one embryo at a time, center the embryo in the field of view of a Nikon SMZ1500 stereomicroscope with a SPOT RT3 digital camera system or similar, and begin sequential imaging.
   1. The same frequency of imaging should be used for both wild-type and mutant fish. Frame rates >30 Hz are recommended, as slower rates will typically not be sufficient to capture the fast swimming of wild-type fish.
4. Deliver mechanosensory stimuli to the embryo by touching the tail with an insect pin.
5. Stop imaging when the embryo has stopped swimming or has swam out of the field of view.
6. Convert sequential images into a video file, or analyze individual frames of time-lapse images off-line, using SPOT 5.1 Advanced software. Similar software packages include Open Lab, NIS Elements, or freely available ImageJ (http://rsbweb.nih.gov/ij/).
7. Quantify swimming behavior by performing the touch-evoked response in multiple embryos.
   1. This can be achieved by averaging the distance embryos are able to swim within a fixed time interval using software or a metric ruler to mark the start and end points of the swimming bout.
   2. Avoid embryos becoming habituated to the touch stimulus over time by performing the assay with a new embryo for each experimental repeat. Behaviors in wild-type and reliable mutant models tend to be highly reproducible.

Results

Birefringence can be used as an efficient, noninvasive assay to shed light on the state of myofibrillar organization in living zebrafish embryos. Examples of wild-type zebrafish as well as zebrafish with decreased expression of genes critical to skeletal muscle development and function are presented. Wild-type zebrafish at 5 dpf display highly birefringent skeletal muscles under polarized light due to the ordered array of myofilaments (Figures 2A-B). In contrast, an age-matched embryo homozygous for a pa...

Discussion

Primary neuromuscular disorders are traditionally classified as dystrophic or nondystrophic processes. Muscular dystrophies are characterized by myofiber degeneration followed by repeated rounds of regeneration, which ultimately leads to an end stage process typified by fibrosis and replacement by adipose tissue¹⁴. Nondystrophic myopathies, in contrast, are not associated with necrosis or regenerative changes, but do result in disorganized myofibers and overall skeletal muscle weakness.

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Tricaine	Sigma	A5040
Petri dishes	Fischer Scientific	0875711Z
Forceps	Fischer Scientific	100189-588
Insect pin	Fischer Scientific	S67375
Polarized lenses	Ritz Camera	Quantaray Tristar Optics C-PL 72mm
Incubator	Fischer Scientific	Isotemp Incubator Model 630D
Microscope	Nikon Instruments Inc.	SMZ 1500
Camera	Diagnostic Instruments Inc.	SPOT RT3
Imaging software	Diagnostic Instruments Inc.	SPOT 5.1 Advanced