Method Article

Fluorescent Dye Labeling of Erythrocytes and Leukocytes for Studying the Flow Dynamics in Mouse Retinal Circulation

DOI:

10.3791/55495

⸱

July 3rd, 2017

 ,  ,  ,  ,  , 
1National Healthcare Group Eye Institute, Tan Tock Seng Hospital, 2Singapore Eye Research Institute (SERI), Singapore National Eye Center, 3School of Material Science and Engineering, Nanyang Technological University, 4Department of Ophthalmology, Yong Loo Lin School of Medicine, National University Health Systems, National University of Singapore, 5Ophthalmology Academic Clinical Research Program, DUKE-NUS Graduate Medical School

* These authors contributed equally

In This Article

Summary

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Live-cell imaging of the labeled blood cells in ocular circulation can provide information about inflammation and ischemia in diabetic retinopathy and age-related macular degeneration. A protocol to label blood cells and image the labeled cells in the retinal circulation is described.

Abstract

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The retinal and choroidal blood flow dynamics may provide insight into the pathophysiology and sequelae of various ocular diseases, such as glaucoma, diabetic retinopathy, age-related macular degeneration (AMD) and other ocular inflammatory conditions. It may also help to monitor the therapeutic responses in the eye. The proper labeling of the blood cells, coupled with live-cell imaging of the labeled cells, allows for the investigation of the flow dynamics in the retinal and choroidal circulation. Here, we describe the standardized protocols of 1.5% indocyanine green (ICG) and 1% sodium fluorescein labeling of mice erythrocytes and leukocytes, respectively. Scanning laser ophthalmoscopy (SLO) was applied to visualize the labeled cells in the retinal circulation of C57BL/6J mice (wild type). Both methods demonstrated distinct fluorescently labeled cells in the mouse retinal circulation. These labeling methods can have wider applications in various ocular disease models.

Introduction

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Studying the flow dynamics of the blood cells in the retinal and choroidal circulation is imperative to understanding the pathogenesis of potentially vision-threatening ocular diseases and other ocular inflammatory conditions. However, the conventional angiography techniques, which involve the binding of fluorescent dyes to plasma proteins, do not provide any information regarding the dynamics of the erythrocytes or leukocytes1. The erythrocyte retinal flow dynamics are important for studying metabolically efficient circulation in the retina, and the leukocyte flow dynamics, for understanding the cell migration, recognition, adhesion and destruction in various inflammatory conditions2. There are several fluorescent molecules used in the identification and characterization of various cell types3. The hemodynamics of the blood cells can be measured by staining them with the appropriate fluorescent dyes and applying the proper imaging techniques4.

The presence of inflammatory responses in intraocular diseases like age-related macular degeneration (AMD) and diabetic retinopathy (DR) involve the accumulation of lymphocytes in the diseased area5,6. Tracking the immune cells in the tissues can help understand the complex events involved in the mechanism of disease pathogenesis. Radioactive isotopes like 51Cr and 125I were used as cell tracers in early studies. These dyes are toxic and affect the cell viability. Although the radioactive markers 3H and 14C are less toxic to the cells, due to their lower emission energies, it is difficult to detect their signals in the system7,8. A number of fluorochrome dyes were introduced to overcome the potential problems associated with radioactive markers and track lymphocyte migration in vitro using fluorescent microscopy and flow cytometry9,10. Hoechst 33342 and thiazole orange are DNA binding fluorescent dyes, which are used to track lymphocytes in vivo. Hoechst 33342 binds to AT-rich regions in the DNA, is membrane permeable, retains fluorescent signals for 2 - 4 days and is resistant to quenching9,10. The disadvantages of Hoechst 33342 and thiazole orange are the inhibition of lymphocyte proliferation11 and the short half-life, respectively9.

Calcein-AM, fluorescein diacetate (FDA), 2′,7′-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein, acetoxymethyl ester (BCECF-AM), 5-(and-6)-carboxyfluorescein diacetate (CFDA), and 5-(and-6)-carboxyfluorescein diacetate acetoxymethyl ester (CFDA-AM) are the cytoplasmic fluorescent dyes used for lymphocyte migration studies. However, FDA, CFDA and CFDA-AM have lower retention in the cells9. BCECF-AM reduces the proliferative response and influences the chemotaxis and superoxide production9,12. Calcein-AM is a fluorescent dye and useful for short-term in vivo lymphocyte migration studies. It emits strong fluorescent signals, does not interfere with most of the cellular functions and retains fluorescent signals for up to 3 days12,13. Fluorescein isothiocyanate (FITC) and carboxyfluorescein diacetate succinimidyl ester (CFDA-SE) are covalent coupling fluorescent dyes, which are used for lymphocyte migration studies. FITC exhibits no effect on the cell viability and has a stronger affinity with B lymphocytes than T lymphocytes14,15. The CFDA-SE labeled lymphocytes can be tracked in vivo for more than 8 weeks and up to 8 cell divisions9,16. C18 DiI (1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate), DiO (3,3'-dioctadecyloxacarbocyanine perchlorate), Paul Karl Horan (PKH)2, PKH3, and PKH26 are membrane-inserting fluorescent lipophilic carbocyanine dyes used to label leukocytes and erythrocytes. C18 Dil and DiO exhibit higher signals when incorporated into the cell membrane and are relatively non-toxic12,17. PKH2, PKH3 and PKH26 labeled cells exhibit a good retention of the fluorescent signals with less toxicity18,19,20,21,22. However, PKH2 down regulates the CD62L expression and reduces the lymphocyte viability23.

Most of the above-mentioned studies have been performed for tracking the lymphocyte migration and proliferation in the lymphatics and studying the labeled erythrocytes in the non-ocular circulation. There are very few studies applying the labeling techniques to study the blood cells in the ocular circulation. Application of scanning laser ophthalmoscopy (SLO) has a great advantage in studying the labeled cells in the retinal and choroidal circulation in vivo by fundus angiography24. There are several fluorescent dyes, such as ICG, acridine orange, FITC, sodium fluorescein, and CFDA that are used to study the leukocytes in the retinal circulation by SLO25,26,27,28,29,30,31,32,33,34. The phototoxicity and carcinogenicity of acridine orange26,27, the interference of FITC with the cellular activity, and the requirement of an intravascular contrast agent for the resolution of the retinal and choroidal blood vessels limits their application in in vivo animal experiments29. Sodium fluorescein and ICG are non-toxic, approved by the Food and Drug Administration, and safe for testing on humans32,35. Most of the flow dynamic studies are related to the labeling of the leukocytes or erythrocytes and its visualization in the retinal and choroidal blood vessels36,37,38,39. Here, we describe a standardized protocol of ICG labeling of the erythrocytes, sodium fluorescein labeling of the leukocytes, and tracking the visualized labeled cells in the mouse retinal circulation using SLO.

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Protocol

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The animal protocols used in this study were approved by the Institutional Animal Care and Use Committee of SingHealth, Singapore and are in accordance to the guidelines of the Association for Research in Vision and Ophthalmology (ARVO) Statement for the Use of Animals in Ophthalmic and Vision Research.

1. Labeling of Erythrocytes and Leukocytes with Fluorescent Dyes

  1. Preparation of reagents
    1. Prepare ICG (1.5 mg/mL) by dissolving 3 mg of ICG in 1800 µL of sterilized distilled water. Add 200 µL of 10x phosphate buffered saline (PBS).
    2. Prepare 40% 1x PBS by adding 4 mL of 1x PBS to 6 mL of sterilized distilled water. Prepare 1% bovine serum albumin (BSA) in PBS by adding 100 mg of BSA to 10 mL of 1x PBS. Mix well until the BSA is dissolved.
  2. Isolation of erythrocytes and leukocytes using density gradient centrifugation
    1. Anesthetize the mice (wild type C57BL/6) using a combination of ketamine hydrochloride (50 mg/kg) and xylazine hydrochloride (0.5 mg/kg) (according to schedule 1, under ARVO guidelines). Confirm anesthesia by pedal withdrawal reflex (i.e., toe pinch).
    2. Slowly insert the 29 gauge needle (attached to a 1 mL syringe) at a costal angle directed towards the heart. To confirm that the needle is inside the heart, withdraw the plunger slightly and check if blood is withdrawn into the syringe. Exsanguinate 0.8 - 1 mL of blood directly from the heart.
    3. Immediately transfer the blood into an ethylene diamine tetra acetic acid (EDTA) (1.8 mg/mL of blood) containing blood collection tube and mix gently to prevent coagulation of the blood.
    4. Euthanize the mice by administering pentobarbital (80 mg/kg) by intraperitoneal injection.
    5. Layer the whole blood on top of a polysucrose and sodium diatrizoate solution (1:1 ratio; density 1.077 g/mL) in a 2 mL microcentrifuge tube and centrifuge (450 x g, 30 min) to allow the separation of the leukocytes and erythrocytes from the plasma.
    6. Remove and discard the supernatant (plasma) using a pipette. Carefully transfer the buffy coat (leukocytes) and erythrocytes (red blood cell layer) into new and separate tubes using pipettes.
  3. ICG (1.5%) labeling of erythrocytes
    1. Wash the erythrocytes with 1x PBS to remove any contaminants. Resuspend the erythrocytes in 1x PBS (1:1) to make 50% hematocrit. Aliquot 0.5 mL of 50% hematocrit (~ 250 µL packed erythrocytes) into microcentrifuge tubes. Centrifuge the erythrocytes (750 x g, 5 min) and discard the supernatant.
    2. Add 200 µL of 40% 1x PBS to the pelleted erythrocytes, mix well and incubate at room temperature for 5 min. Add 100 µL of ICG (1.5 mg/mL) to the erythrocyte suspension, mix gently by inverting the tube, and incubate at room temperature for 5 min. Add 300 µL of 1x PBS and incubate at 37 °C in a shaker incubator for 60 min.
    3. Centrifuge the carrier erythrocytes (750 x g, 3 min) and resuspend in 1 mL 1x PBS.
    4. Wash the cells ~ 3 - 5 times with 1x PBS until the supernatant is clear (step 1.3.3). After the last wash, decant the supernatant and add 1% BSA PBS (1:1) to the labeled pre-swelled erythrocytes to achieve a 50% hematocrit (1.25 x 108 cells/mL) of ICG labeled erythrocytes.
  4. Sodium fluorescein (1%) labeling of leukocytes
    1. After separating the buffy coat from the blood using density gradient centrifugation (from step 1.2.6), wash the cells once with 10 mL of 1x PBS by centrifuging at 450 x g for 10 min to remove any contaminants. Resuspend the pellet in 900 µL of 1x PBS.
    2. Add 100 µL of 10% sodium fluorescein to 900 µL of the leukocyte suspension and incubate at room temperature for 2 min. Wash the labeled cells three times with 10 mL 1X PBS by centrifuging (450 x g, 10 min). Resuspend the cells into 100 µL 1x PBS.

2. Live Imaging of Fluorescently Labeled Cells

  1. Live-cell imaging of ICG labeled erythrocytes
    1. To prepare cells for injection via tail vein or retro-orbital route, dilute the 50% hematocrit of ICG labeled erythrocytes by 10-fold and 50-fold with 1x PBS to make 5% and 1% hematocrit cells, respectively.
    2. Place the mouse under the infrared light (250W intensity) for 5 min to let the tail vein dilate. Anesthetize the mouse with ketamine hydrochloride (50 mg/kg) and xylazine hydrochloride (0.5 mg/kg) through intraperitoneal injection (here, according to schedule 1, under ARVO guidelines).
    3. Dilate each pupil of the eyes with a drop of 0.5% tropicamide and 2.5% phenylephrine hydrochloride.
    4. Place the contact lens over one eye for imaging. Use ophthalmic gel as a medium for imaging and to prevent dryness of the cornea. Fix the confocal laser scanning ophthalmoscopy (SLO) camera with +25 diopter lens to compensate for the refraction of the mouse eye.
    5. Place the mouse onto the SLO imaging platform. Ensure that the cornea of the mouse is facing straight towards the optical head of the SLO machine.
    6. Switch on the imaging module. Using the associated imaging module software, click on the "New Patient" button and add animal identification details such as mouse ear tag number, date of birth, percentage of fluorescent dye and labeled cell type.
      1. Position the optic nerve of the animal at the center of the imaging screen by maneuvering the imaging module. Using the associated imaging module software, click on the "Acquire" button to take the infrared (IR) fundus images with the 30° or 15° angle view setting. Ensure that the center of the retina, the pupil and the optical path of the laser are aligned to achieve a best quality image.
        NOTE: The optical path is aligned by maneuvering the joystick to obtain the sharpest image and best lighting exposure.
    7. Take the ICG fundus video.
      1. Turn on the ICG filter (790 nm), set the camera to high speed mode with the 30° or 15° angle view and set the ICG intensity at 85 for all readings for standardization. On the control panel, click on the "Acquire" button to take the video (baseline control) at 8.8/15 frames/s for 1 min.
    8. Load 100 µL of ICG labeled erythrocytes into an insulin syringe attached to a 30 gauge needle.
      1. For the injection via the tail vein route, insert the needle bevel up into the tail vein. Confirm the intravenous access by checking the backflow of the blood into the syringe and inject the labeled cells into the circulation.
      2. For the injection via the retro-orbital route, insert the needle adjacent to the eye into the retro-orbital space. Confirm the retro-orbital access by checking the backflow of the blood into the syringe and inject the labeled cells into the circulation.
    9. After the injection, reposition the mouse and take the IR fundus images (see step 2.1.6.1) and video using the ICG filter (see step 2.1.7.1). The labeled cells in the retinal circulation can be visualized immediately after the injection of the cells.
    10. After acquiring the video frames, extract .tiff images of the video sequences by choosing the .tiff format when exporting the video using the SLO viewing module software. Save the files in a desired folder.
    11. Remove the contact lens, place it over the other eye, and complete the imaging as described in steps 2.1.4 - 2.1.7.
    12. After imaging, place the anesthetized animal under the infrared light (250W) to maintain the body temperature until it recovers from anesthesia. When the animal is fully recovered, place the mouse back into the holding cage.
  2. Live-cell imaging of 1% sodium fluorescein labeled leukocytes
    1. Prepare the mouse and set-up the instrument as described in section 2.1.
    2. Position the mouse and take the IR fundus images as described in steps 2.1.4 - 2.1.6.
      1. Obtain the fluorescein angiogram of the mouse using the fluorescein filter (488 nm) with the high-speed camera mode with the 30° or 15° angle view and fluorescein intensity at 85 for all readings for standardization. Record the video (baseline control) at 8.8/15 frames/s (see step 2.1.7.1).
        NOTE: Here, multiple tracks of videos (1 min videos) were acquired at different time intervals.
    3. Inject 100 µL labeled leukocytes into the mouse through the tail vein or retro-orbital injection as described in section 2.1.8.
    4. Immediately after the injection, position the mouse and take the IR fundus images (see steps 2.1.5 and 2.1.6) and the fluorescein angiogram of the mouse (see section 2.2.2).
    5. Observe the labeled cells in the retina or choroidal blood vessels by adjusting the focal point of the scanning laser by turning the focusing knob on the imaging module.
    6. Acquire the video frames and images using SLO viewing module software (see step 2.1.10) and save it in a desired folder.
    7. After the procedure, follow step 2.1.12 for care of animals.
  3. Image analysis by MtrackJ software
    1. Open the image sequence in ImageJ by clicking on "File". Select "Import" and choose "Image sequence", select the desired image folder, and click "Open". A pop up window called "Sequence options" will appear on the screen. Click "Ok"; the image sequence will open.
    2. Set the frame interval of the image video by clicking on "Image" and select "Properties" for velocity measurements. Here, it is 8.8 frames/s.
    3. Open the MTrackJ plugin by selecting "Plugins". Select "Tracking" and then select "MtrackJ". A menu should appear.
    4. To adjust the tracking settings, select "Tracking" (under menu) and check the box "Move to next time frame index after adding point".
    5. Track the first cell.
      1. Locate one cell and track the same cell in subsequent frames. On the menu click "Add" to add a new track.
      2. Hover the cursor over the image (+ sign) and click on the appropriate cell.
        NOTE: MTrackJ will automatically jump to the next time frame and add a small circle, marking the position of the first point in the trajectory.
      3. Continue clicking on the current position of the cell while moving through the frames of the image sequence.
        NOTE: Occasionally, the circles marking the previous points in the trajectory interfere with the ability to view the current location. If this occurs, proceed to step 2.3.5.3.1.
        1. Change the display option for the trajectory by clicking on "Displaying" in the menu and selecting the option "display only track points at current time". To see all the trajectories, de-select this option.
      4. Continue clicking until the trajectory of the first cell is seen. Then save the track by clicking "Save".
    6. Track the second cell.
      1. In the menu, click "Add" to start a new track. Repeat steps 2.3.5.1 - 2.3.5.4 for tracking the new cell. Click on "Save" to save the second track.
      2. Continue these steps for all trackable cells observed. After tracking the cells, click on "Measure" and "OK" in the menu tab to get the results.
        NOTE: A results window opens up automatically, which can be saved and opened in a spreadsheet for further analysis.

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Results

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Erythrocytes labeled with 1.5% ICG were visualized in the retinal circulation of C57BL/6J mice (wild type). Both 1% and 5% hematocrit of 1.5% ICG labeled erythrocytes were distinguishable in the retinal circulation. However, the individual labeled cells were more clearly visualized with 1% hematocrit of 1.5% ICG labeled erythrocytes (Figure 1). In 5% hematocrit, due to the large number of labeled cells in the retinal vessels, it was not possible to mark the i...

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Discussion

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Studying the hemodynamics in the retinal and choroidal circulation is vital for understanding the pathophysiology of many ocular diseases. The blood flow dynamics in the retinal circulation can be studied by Fourier-domain optical coherence tomography (FD-OCT), laser speckle flowgraphy (LSFG) and retinal oximetry. Although these methods use different approaches to study the total blood flow in the retinal circulation40,41,42

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Disclosures

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The authors have nothing to disclose. No financial or conflict of interest.

Acknowledgements

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The research project was funded under New Investigator grant from the National Medical Research Council (NMRC), Singapore. The team will like to acknowledge the research training provided to Dr Agrawal at Institute of Ophthalmology (IoO), University College London (UCL) under National Medical Research Council (NMRC) Overseas Research Training Fellowship from November 2012 till October 2014 under mentorship of Prof. David Shima. Dr. Agrawal acquired the concept and skills for labelling the cells and live imaging in Dr. Shima's lab. The team will hence like to acknowledge supervision and guidance during the training fellowship from Prof. David Shima, Pro.f Kenith Meissner, Dr. Peter Lundh and Dr. Daiju Iwata.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Cardiogreen polymethine dye (Indocyanine green)Sigma Aldrich12633-50MG
Fluorescein 100 mg/mLNovartisU1705A/H-1330292
10x Phosphate-buffered saline (PBS) Ultra Pure Grade1st BASEBUF-2040-10X1L
Bovine serum albuminSigma AldrichA7906-100G
Microtainer tubes with K2E (K2EDTA) - EDTA concentration - 1.8 mg/mL of bloodBD, USAREF 365974
Histopaque 1077 solutionSigma Aldrich10771
Centrifuge 5810 REppendorf05-413-401
Microcentrifuge tubes 2 mLAxygenMCT-200-C-S
Vortex mixerInsta BioAnalytik pte. ltdFINE VORTEX
Shaker incubatorLab Tech
Ceva Ketamine injection (Ketamine hydrochloride 100 mg/mL)CevaKETALAB03
ILIUM XYLAZIL-20 (Xylazine hydrochloride 20 mg/Ml)Troy Laboratories PTY. LimitedLI0605
1% Mydriacyl 15 mL (Tropicamide 1%)Alcon Laboratories, Inc. USANDC 0998-0355-15
2.5% Mydfrin 5 mL (Phenylephrine hydrochloride 2.5%)Alcon Laboratories, Inc. USANDC 0998-0342-05
Terumo syringe with needle 1 cc/mL TuberculinTerumo (Philippenes) Corporation, PhilippinesSS-01T2613
Vidisic Gel 10 GDr. Gerhard Mann, Chem.-Pharm, Fabrik Gmbh, Berlin, Germany
Alcohol swabsAssure medical disposables7M-004-L-01
Confocal laser scanning angiography system (Heidelberg Retina Angiograph 2)Heidelberg Engineering, GmbH, Heidelberg, Germany
Hiedelberg Spectralis Viewing Module software, v4.0Heidelberg Engineering, GmbH, Heidelberg, Germany
Fluorescent microscopeZEISSModel: axio imager z1

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Erythrocyte LabelingLeukocyte LabelingScanning Laser OphthalmoscopyIndocyanine GreenSodium FluoresceinBlood Cell IsolationFluorescence MicroscopyCell Tracking AnalysisOcular Disease Models

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