Tracking Cells in GFP-transgenic Zebrafish Using the Photoconvertible PSmOrange System

Summary

We established the photoconvertible PSmOrange system as a powerful, straight-forward and cost inexpensive tool for in vivo cell tracking in GFP transgenic backgrounds. This protocol describes its application in the zebrafish model system.

Abstract

The rapid development of transparent zebrafish embryos (Danio rerio) in combination with fluorescent labelings of cells and tissues allows visualizing developmental processes as they happen in the living animal. Cells of interest can be labeled by using a tissue specific promoter to drive the expression of a fluorescent protein (FP) for the generation of transgenic lines. Using fluorescent photoconvertible proteins for this purpose additionally allows to precisely follow defined structures within the expression domain. Illuminating the protein in the region of interest, changes its emission spectrum and highlights a particular cell or cell cluster leaving other transgenic cells in their original color. A major limitation is the lack of known promoters for a large number of tissues in the zebrafish. Conversely, gene- and enhancer trap screens have generated enormous transgenic resources discretely labeling literally all embryonic structures mostly with GFP or to a lesser extend red or yellow FPs. An approach to follow defined structures in such transgenic backgrounds would be to additionally introduce a ubiquitous photoconvertible protein, which could be converted in the cell(s) of interest. However, the photoconvertible proteins available involve a green and/or less frequently a red emission state¹ and can therefore often not be used to track cells in the FP-background of existing transgenic lines. To circumvent this problem, we have established the PSmOrange system for the zebrafish^2,3. Simple microinjection of synthetic mRNA encoding a nuclear form of this protein labels all cell nuclei with orange/red fluorescence. Upon targeted photoconversion of the protein, it switches its emission spectrum to far red. The quantum efficiency and stability of the protein makes PSmOrange a superb cell-tracking tool for zebrafish and possibly other teleost species.

Introduction

Exponentially improving imaging techniques allow following developmental processes over time periods of up to about four consecutive days³. In zebrafish and many other animal model systems, specific cells, tissues, axonal or vascular structures are marked by transgenic green or sometimes red or yellow fluorescent proteins to facilitate visualization. However, in most transgenic lines the transgene is not specifically expressed in the cells of interest but also additional structures, which hinders the precise tracking of for instance single cells or groups of cells.

Fluorescent photoconvertible proteins are well suited for cell tracking during embryonic development. The prerequisites for the application of such proteins are a long-lived nature, a well-separated emission range upon conversion and bright fluorescence. Available photoconvertible proteins comprise those that change their emission range upon conversion such as Kaede⁴, KiGR⁵, mEos2⁶, PS-CFP2 or Dendra2⁷ and others which are only fluorescent when photoactivated (PAmCherry⁸, PAGFP⁹ or PATagRFP¹⁰). Their applications to track cells in existing FP-transgenic animals are however limited as they often involve a green fluorescent state or do not fulfill all of the above criteria. Only recently, Subach and colleagues reported the PSmOrange protein, which changes its emission from orange/red to far red upon photoconversion and was successfully applied in cells in culture and cultured cells injected into mice².

To investigate the protein's suitability for cell tracking in a living embryo, we generated an expression construct for the microinjection of nuclear-tagged H2B-PSmOrange into zebrafish embryos. We find that the protein fulfills all prerequisites for successful cell tracking in GFP transgenic backgrounds during the first 4 (and possibly more) days of zebrafish embryonic development. During this time, most of the cell migratory events are completed in fish making the PSmOrange system an excellent addition to the zebrafish toolkit.

Protocol

1. H2B-PSmOrange mRNA In Vitro Transcription and mRNA Purification

1. Linearize the H2B-PSmOrange containing pCS2+ plasmid using the NotI restriction enzyme according to manufacturer's instructions.
   Note: Perform the next steps using appropriate protections such as gloves and lab coat to prevent mRNA contamination and degradation.
2. Purify the linearized DNA using a PCR Purification kit or phenol-chloroform based methods according to manufacturers' protocols.
3. Use 1 µg of linearized template DNA for Sp6-mRNA transcription according to manufacturer's instructions.
4. Remove DNA by adding 1.0 U RNase free DNaseI for 10-20 min at 37 °C.
5. Clean up the mRNA using a RNA clean up kit according to manufacturer's protocol.
6. To increase mRNA purity and concentration, precipitate the mRNA by adding 6 µl sodium acetate (3.0 M, pH 5.2) and 150 µl 96% ethanol. Incubate the mixed solution at -20 °C for at least 30 min and up to 24 hr.
7. Collect the mRNA by spinning the solution at 18.407 x g for 45 min at 4 °C. Discard the liquid and resuspend the mRNA in 150 µl 70% ethanol. Mix and centrifuge the solution for an additional 15 min at 4 °C. Discard the liquid, dry the pellet for 5 min on ice and resuspend the mRNA in 20 µl ultrapure RNase free water.
8. Assess the concentration and purity of the mRNA by photometric measurement of a 1:100 mRNA dilution (1 µl mRNA in 99 µl ultrapure RNase free water).
9. For short-term storage, keep the mRNA solution at -20 °C. For long-term storage, keep the mRNA at -80 °C.

2. H2B-PSmOrange mRNA Microinjection into Zebrafish Embryos

1. Set up mating pairs the night before injection using tg(foxD3:GFP); tg(flh:GFP) double transgenic fish (or any other GFP transgenic fish). Leave the fish separated by placing a spacer between them to control the time of mating.
2. Remove the spacer in the morning of injection and let the fish mate for 20 min.
3. During mating time, dilute the H2B-PSmOrange mRNA to the final concentration of 130 pg/nl (in RNase free water) and transfer 6 µl injection solution into a microinjection capillary using a microloader tip. Check the injection volume with a calibrated glass slide. Adjust the injection pressure to inject 2 nl mRNA solution (260 pg).
4. Collect the eggs into a sterilized plastic petri-dish containing 1x Embryo (E3) medium.
5. Transfer 20 to 30 embryos to an injection dish using a plastic pasteur pipette.
6. Inject 2 nl mRNA containing solution into the cell or just below the cell into the yolk at the one-cell stage ¹¹.
7. Transfer injected embryos into a petri-dish containing 1x E3 medium, remove unfertilized or not normally developing embryos and grow them at 28 °C.
   Note: Light protection of the embryos is not required throughout the experiment.
8. Raise zebrafish embryos in 1x E3 medium and add 0.2 mM PTU (1-phenyl-2 thiourea) after gastrulation to inhibit pigmentation. Change the medium twice per day to minimize the danger of bacterial contaminations.

3. Embryo Embedding

1. Select the GFP (green) and PSmOrange (orange/red) co-expressing embryos using a binocular microscope equipped with a fluorescence lamp and appropriate emission filters. Transfer the positive embryos into a sterile petri-dish containing 1x E3 medium.
2. Dechorionate embryos under a stereomicroscope using forceps ¹².
3. Transfer one embryo in a 1.5 ml tube containing 1.0 ml of pre-warmed 1.0% low melting agarose (LMA) prepared in ultrapure water by using a cut-tip pipette (P200). Note: Warm the LMA to 80 °C and cool down for 3-5 min at RT before embedding the embryo.
4. Transfer the embryo in 150 µl LMA into a chambered coverglass and adjust the embryo's orientation, e.g. dorsal side down in the experiment described for the inverted confocal laser scanning microscope A1R+ (or any other suitable microscope), using a fine plastic tip. When the LMA is polymerized, fill the chamber with fish water containing 0.2 mM PTU and 0.02% ethyl 3-aminobenzoate methansulfonate (Tricaine) for anesthesia.
5. Before imaging the sample, wait 15 min to ascertain the effect of Tricaine. The anesthesia prevents embryo movements, which can be monitored using a stereomicroscope equipped with brightfield illumination.
   Note: The chambers can be reused twice.

4. PSmOrange Photoconversion

1. Place the sample under the confocal microscope and scan the specimen to identify the area to photoconvert using 488 nm and 561 nm lasers for imaging GFP and PSmOrange respectively.
   Note: Use the inverted confocal laser scanning microscope A1R+ on the inverted stage TiEcontrolled by the microscope imaging software and equipped with 488 nm, 561 nm and 640 nm lasers for photoconversion and imaging. However, the application is certainly not restricted to this microscope as long as the laser lines for conversion and imaging are available.
   1. Put the 20X air objective into place (NA: 0.75; WD: 1.0 mm; FOV: 0.64 x 0.64 mm).
   2. Use the following microscope settings to detect the PSmOrange protein before photoconversion: 561 nm laser, 0.74 mW measured at the focus plane above the objective.
      Note: This corresponds to 40% on this system (measuring in the focus plane is the only way to determine the effective power). Adjust the laser power according to experimental needs as the efficiency of H2B-PSmOrange injections can vary.
   3. Add zoom factors to highlight the area of interest. Higher magnifications reduce image acquisition time and therefore phototoxicity.
2. Acquire a z-stack covering the structures of interest using 488 nm and 561 nm lasers in sequential mode (line mode 1->4). Fix the z-step between 1.0 and 2.0 µm. Line average and scan frequency can be used to optimize image quality.
3. Scan the sample and select the region of interest (ROI) tool to highlight the area to photoconvert. Fix the ROI as stimulation area. Select the Photo Activation/Bleaching module, activate the 488 nm laser by checking the respective box and set the 488 nm laser to 80% (1 mW laser power measured at the objective). Set the scan speed to 0.5 sec/Frame.
4. Open the photoconversion utility (ND Stimulation) and specify the photoconversion settings.
   1. Click on the "Add" command to specify the photoconversion protocol.
   2. Set "Phase" 1 in the "Acquisition/Stimulation" menu to "Acquisition" and indicate the number of images to be acquired before photoconversion in the "Loops" menu.
   3. Set "Phase" 2 to "Stimulation" and enter the number of stimulation events to be performed.
   4. Adjust "Phase" 3 as described for "Phase" 1. Optionally, insert a waiting "Phase" after "Phase" 2 by entering the time to wait before the last round of image acquisition.
   5. Once all the parameters are set, apply the stimulation setting and run the photoconversion.
      Note: Laser power, frequency of scanning and number of iterations for each round of photoconversion can vary and differ from embryo to embryo. A setting to start with is shown in Table 1.
5. Acquire a final z-stack using 488 nm, 561 nm and 640 nm lasers applying the settings as above. Set the 640 nm laser to visualize the converted PSmOrange using high laser power (up to 4.5 mW).

5. Dismount Embryo from LMA

1. Remove the embryo containing chamber from the microscope. Carefully remove the embryo from the agarose using forceps.
2. Transfer the embryo into a new sterilized plastic petri-dish or into a sterilized 6-well-plate containing 1x E3 and 0.2 mM PTU. Incubate the embryo at 28 °C until the desired stage of development.

6. Analyzing the Fate of Photoconverted PSmOrange Protein Expressing Cells

1. Re-embed the embryo as described under points 3.3 and 3.4.
2. Place the sample under the confocal microscope and scan the specimen to identify photoconverted cells (640 nm) in the GFP transgenic structure of interest (488 nm).
3. Acquire a z-stack covering the structures of interest using 488 nm, 561 nm and 640 nm lasers in sequential mode (line mode 1->4). Fix the z-step between 1.0 and 2.0 µm. Line average and scan frequency can be used to optimize image quality.
4. Use one of the following methods to identify cells, which co-express GFP and the photoconverted protein.
   1. Custom made automatic Fiji ImageJ Macro³
      1. Convolve the original stack using the "GaussianBlur" plugin ( → Process → Filters → GaussianBlur) and subtract the smooth stacks from the original using the "Image Calculator" plugin (→ Process → Image Calculator). Use this step to visualize the structures of interest and reduce the computational time for the analysis.
      2. Apply specific thresholds to the green and far-red channels in order to highlight the photoconverted cells ( → Image → Adjust → Threshold). Use the "Analyze Particles" tool to detect the threshold areas with a suitable setting ( → Analyze → Analyze Particles).
      3. Open the "Image Calculator" plugin and display the overlapping ROIs in the green and far-red channel in yellow ( → Process → Image Calculator).
   2. Microscope imaging software for 3D data evaluation
      1. Display the stack in 3D using the show volume view option ( → 3D Visualization Menu → Show Volume View). Use the graphic interface to select the green, red and far-red channels, adjust the brightness and the contrast and crop the 3D stack to highlight the photoconverted area (Figure 1).
         Note: Similar methods to analyse the data are available in most of the common software for image analysis.

Results

Figure 1 illustrates an example of the PSmOrange photoconversion system. The pineal complex is a conserved structure in the vertebrate dorsal diencephalon. Like in many other vertebrates, this complex consists of the pineal organ in the center of the diencephalon and the left-sided parapineal cells. Elegant but time-consuming uncaging experiments showed that parapineal cells originate in the anterior part of the pineal organ¹³. In tg(foxD3:GFP); tg(flh:GFP) tra...

Discussion

Transgenic embryos carrying fluorescent reporters have helped fundamentally to understand embryonic development. However, there is still the essential need for promoters to facilitate the specific visualization of particular structures. In their absence, researchers rely on techniques such as the photoconversion of fluorescent proteins to find out about the origin and development of their structure of interest. This in turn is a crucial prerequisite to identify the molecular mechanisms involved in its development. Techni...

Materials

Name	Company	Catalog Number	Comments
PCR Purification Kit	Qiagen	28104
mMESSAGE mMACHINE SP6 Transcription kit	Ambion	AM1340
RNeasy MiniElute Cleanup kit	Qiagen	74204
Plastic Pasteur	alpha laboratories	LW4000
Original H2B-PSmOrange Plasmid	Addgene	31920	The plasmid described in the paper is available in the Carl lab
FemtoJet Microinjector	Eppendorf	5247 000.013
Forceps (5 Inox)	NeoLab	2-1633
Lab-Tek II Chambered #1.5 German Coverglass System	Nunc	155382
Nikon A1R+	Nikon GmbH Germany	No Number
Nikon PLAN Apo λ 20X air objective	Nikon GmbH Germany	No Number
NIS Elements AR Software (v. 4.30.02)	Nikon GmbH Germany/Laboratory Imaging	No Number