A Simple Immunofluorescence Method to Characterize Neurodegeneration and Tyrosine Hydroxylase Reduction in Whole Brain of a Drosophila Model of Parkinson’s Disease

Materials and reagents

1. Drosophila melanogaster [Oregon K (OK) flies, procured from the National Drosophila Stock Center, Mysore University, Mysuru, India, were raised in food media containing sucrose, yeast, agar-agar, and propionic acid, and maintained in a fly environment chamber and used in the current study [3,10,13,28]]. Depending on the nature of the experiment, flies with and/or without neurotoxicant treatment (sporadic PD model) and transgenic fly model(s) can be employed.

2. Sterilized 1.5 mL centrifuge tubes (Tarsons, catalog number: 500010)

3. Parafilm^TM wrapping film (Bemis, catalog number: PM996)

4. Conical flask (Borosil, catalog number: 5100)

5. Magnetic stirrer bar #8 mm × 40 mm (Tarsons, catalog number: 4113)

6. SPINNOT^TM digital magnetic stirrer hotplate (Tarsons, catalog number: 6090)

7. Sterilized micro tips (Tarsons, catalog number: 521010)

8. Freshwrapp aluminum foil 9–11 μm (Hindalco, catalog number: HV2241)

9. Glass plate (Suwimut, catalog number: B08FRB2NTM)

10. Fingernail polish (FacesCanada, catalog number: CC4403)

11. Glass spacer (Borosil, catalog number: 9115S01)

12. Microscopy slides #76 mm × 26 mm (ReliGlas, catalog number: 7101)

13. Gold-seal coverslips (22 mm²) (Electron Microscopy Sciences, catalog number: 63765-01)

14. Sucrose (SRL, catalog number: 84973)

15. Agar-agar (HiMedia, catalog number: GRM666)

16. Sugar-tolerant yeast (Angel, catalog number: 5331A201908)

17. Propionic acid (Merck, catalog number: 80060505001730)

18. Whatman^TM filter paper (GE Healthcare, catalog number: 1001917)

19. Paraformaldehyde (PFA) pH 7.4 (Sigma-Aldrich, catalog number: I58127)

20. Phosphate buffered saline (PBS) pH 7.4 (HiMedia, catalog number: ML023)

21. Triton X-100 (Sigma-Aldrich, catalog number: T8787)

22. Normal goat serum (NGS) (Vector Labs, catalog number: S1000)

23. Rabbit anti-tyrosine hydroxylase (anti-TH) polyclonal primary ab (Millipore, catalog number: Ab152)

24. Goat anti-rabbit IgG H&L (TRITC-labeled) polyclonal secondary ab (Abcam, catalog number: Ab6718)

25. VECTASHIELD^® mounting medium (Vector Labs, catalog number: H1000)

1. 4% PFA solution (50 mL) (see Recipes)

2. 0.1% PBST (phosphate buffered saline and Triton X-100) (50 mL) (see Recipes)

3. 0.5% PBST (50 mL) (see Recipes)

4. 5% NGS blocking buffer solution (1 mL) (see Recipes)

5. Anti-TH polyclonal primary ab solution (see Recipes)

6. TRITC-labeled polyclonal secondary ab solution (see Recipes)

Recipes

1. 4% PFA solution (50 mL)

   PFA 2 g

   1× PBS 50 mL

   1. Add PFA in 1× PBS in a conical flask, cover it with parafilm, and shake it thoroughly for 10 min.

   2. Transfer the flask with a magnetic stirrer on the hotplate for heating/boiling with a temperature ranging from 80 °C to 110 °C with moderate stirring at 150 rpm.

   3. Keep the flask on the hotplate until the cloudy solution becomes transparent.

   4. After this, switch off the hotplate but keep the stirring for 15 min. Allow the solution to cool down, aliquot it in a 1.5 mL centrifuge tube, and store it at -80 °C.

   Critical: Do not store the solution for more than a week.

   Caution: PFA is a potential carcinogen; hence, the whole process should be done under a fume hood. Wear hand gloves and a lab coat during handling and preparation of PFA solution.




2. 0.1% PBST (phosphate buffered saline and Triton X-100) (50 mL)

   10× PBS 5 mL

   Autoclaved enzyme-free water 45 mL

   Triton X-100 50 μL

   1. Add 5 mL of 10× PBS in 45 mL of autoclaved enzyme-free water.

   2. Mix 50 μL of Triton X-100 and vortex it for 10 seconds. The solution can be stored at room temperature for one week.




3. 0.5% PBST (50 mL)

   10× PBS 5 mL

   Autoclaved enzyme-free water 45 mL

   Triton X-100 250 μL

   1. Add 5 mL of 10× PBS in 45 mL of autoclaved enzyme-free water.

   2. Mix 250 μL of Triton X-100 and vortex it for 10 s. The solution can be stored at room temperature for one week.




4. 5% NGS blocking buffer solution (1 mL)

   NGS 50 μL

   0.5% PBST 950 μL

   Add 50 μL of NGS in 950 μL of 0.5% PBST and mix it properly by vortexing for 10 s. The solution can be stored at room temperature for 1–2 h.




5. Anti-TH polyclonal primary ab solution

   Anti-TH polyclonal primary ab 5 μL

   5% NGS blocking buffer 1,245 μL

   Take 1,245 μL of 5% NGS blocking buffer and add 5 μL of anti-TH polyclonal primary ab (1:250 dilution). Mix it gently by inverting the tube slowly and place it on the ice until used.




6. TRITC-labeled polyclonal secondary ab solution

   TRITC-labeled polyclonal secondary ab 5 μL

   5% NGS blocking buffer 1,245 μL

   Take 1,245 μL of 5% NGS and add 5 μL of TRITC-labeled polyclonal secondary ab (1:250 dilution). Mix it gently by inverting the tube slowly and store it on ice until used.

Equipment

1. Fly head capsule handling items e.g., needles #31 G × 6 mm (Tentabe BD, catalog number: 324902)

2. Dissecting fine forceps (EMS, catalog number: 78620-4B)

3. Brush (TEYUP, model number: SR-1013)

4. Delicate task Kim wipers (KIMTECH^TM, catalog number: 370080)

5. Micropipette i.e., 1,000 μL, 50 μL, 10 μL, 2 μL (Gilson, catalog number: 30040)

6. Frost-free refrigerator (Whirlpool, model number: FF26 4S)

7. pH/mV meter (Hanna Instruments, model: HI2211-02)

8. -20 °C ES Series refrigerator (Thermo Scientific, model: 50616100444443250)

9. -80 °C ultra-low temperature freezer (New Brunswick Innova, model: U101-86)

10. Stereo zoom microscope (Carl Zeiss, model: Stemi 305)

11. Stereo zoom microscope (Leica, model: E24)

12. Fume hood (BIOMATRIX, Telangana, India)

13. BOD incubator (Percival, model: DR-36VL)

14. Test tube rotator (Tarsons, Rotospin, catalog number: 3070) and disk for 24 × 1.5 mL tube (Tarsons, catalog number: 3071)

15. Axio Imager M2 fluorescence microscope fitted with 100 W Mercury lamp (Carl Zeiss, catalog number: 430004-9902-000)

16. AxioCam ICm1 monochromatic camera (Carl Zeiss, catalog number: 426553-9901-000)

Software and datasets

1. ZEN 2012 SP2 blue edition, version 2.0.14283.302 (Carl Zeiss, Jena, Germany)

2. Microsoft Office Excel Worksheet 2007 (Microsoft Inc., WA, USA)

3. GraphPad Prism, March 7, 2007, version 5.00 (GraphPad Inc., MA, USA)

Procedure

1. Anti-TH immunostaining of the whole Drosophila brain

1. Fix the fly whole head tissue in 1 mL of 4% PFA (pH 7.4) containing 0.5% Triton X-100 in a sterilized 1.5 mL centrifuge tube for 2 h through mixing by using a test tube rotator with constant velocity (10 rpm) at room temperature (RT).

2. Remove PFA after 2 h of fixation by washing the fly head tissue with 1 mL of 0.1% PBST three times for 15 min each at RT.

3. Carry out dissection of brains in 1× PBS (pH 7.4) under a stereo zoom microscope at RT using fine forceps and needles to remove the head capsule and connecting tissues.

4. Then, wash the brains with 0.1% PBST five times for 15 min each at RT.

5. Block the brains with 5% NGS blocking buffer solution for 120 min at RT.

6. Then, incubate/probe brains with anti-TH polyclonal primary ab solution for 72 h at 4 °C through mixing by using a test tube rotator at constant velocity (10 rpm).

7. Wash off excess primary antibodies by 0.1% PBST five times for 15 min each at RT.

8. Incubate brains with TRITC-labeled polyclonal secondary ab solution for 24 h in the dark (Critical: Cover centrifuge tube containing brains with aluminum foil) by thorough mixing with a test tube rotator at a constant velocity (10 rpm) at RT.

9. To eliminate excess secondary antibodies, wash brains again with 0.1% PBST five times for 15 min each at RT.

10. Mount brains in VECTASHIELD^® mounting medium and then top with cover glass.

    Critical: Glass spacers were placed around the VECTASHIELD^® mounting medium to protect brains from being crushed by a coverslip.

    Critical: Brains were scanned in a dorsoventral orientation.

11. Use clear fingernail polish to seal the edges.

12. The sample is ready for image acquisition.




2. Image acquisition

   Steps for the acquisition of Drosophila brain image(s) for quantification of DAergic neurons and FI using a fluorescence microscope with ZEN 2012 SP2 software are as follows:

   1. Observe stained brains under a fluorescence microscope equipped with a 40× objective lens (Figure 1).

      
      

      
      Figure 1. Scanning of the whole brain of Drosophila. Scan the anti-TH immunostained Drosophila brain using Carl Zeiss, Axio Imager M2 (40× objective lens) with ZEN 2012 SP2 software that interactively controls image acquisition, image processing, and analysis of the images.

      
      

   2. Scan and take images using a monochromatic camera with a Rhodamine fluorescence filter (Figure 2).

      
      

      
      Figure 2. Image acquisition and performing the red dot test. For image acquisition, select a monochromatic camera with a Rhodamine filter. Perform a red dot test for visibility of dopaminergic (DAergic) neurons and assessing saturation using a brain, reusing the same exposure time for other samples.

   
   

   3. Perform a red dot test in the acquisition panel (select range indicator from Dimensions and set exposure from Acquisition parameter) for visibility of DAergic neurons and to assess the signal saturation during the image acquisition. Reuse the same exposure time for all brain samples (Figure 2).

   4. Then, perform Z-stack programming with constant intervals of 1.08 μm for each image (Figure 3).

      
      

      
      Figure 3. Selection of images and Z-Stacking

   
   

   5. To generate a 2D image, on the method column apply Ortho and Maximum intensity projection (MIP) from Ortho display with X–Y Plane (Figure 4).

      
      

      
      Figure 4. Creation of 2D image. For creating a 2D merged image, on the Method column, select Maximum intensity projection (MIP) with X-Y Plane.

   
   

   6. Export the 2D image of the brain in .jpg format for presentation (Figure 5).

      
      

      
      Figure 5. Export of 2D brain image to the required format




3. Method for quantification of DAergic neurons

1. Identify clusters from the images/scans obtained through Z-stack programming with constant intervals (Figure 6).

2. Enlarge the image to reveal the cell body/structure (Figure 6).

   
   

   
   Figure 6. Quantification of dopaminergic (DAergic) neuronal number and fluorescence intensity (FI). For the quantification of DAergic neuronal number and FI, select 3D images/scans of Z-Stack with brain regions; PAL, PPL1, PPL2, PPM1/2, and PPM3 (PAL: Protocerebral anterior lateral; PPL: Protocerebral posterior lateral; PPM: Protocerebral posterior medial).




3. Determine/count the number of DAergic neurons in each cluster in an unbiased manner.




4. Method for characterization of FI of DAergic neurons

1. From 3D scan images, chose the PAL, PPL1, PPL2, PPM1/2, PPM3, and VUM (quantifiable DAergic neuronal clusters) regions of the fly brains (Figure 6).

2. Enlarge brain images to see the clear neurites (Figure 7).

   
   

   
   Figure 7. Details of the quantification of the fluorescence intensity (FI). Enlarge the images to see clear neurites, select appropriate tools, draw spline contour from graphics and draw a line around the neuron, and display intensity mean value and area.




3. Select the appropriate graphics tool, draw spline contour, and draw a line to encircle the neuron giving intensity mean and area (Figure 7).

4. Select More measurement options and chose intensity sum by right-clicking inside the neuron (Figure 8).

   
   

   
   Figure 8. Measurement of fluorescence intensity (FI) sum. Select intensity sum by opting for more measurement options (software provides the pixel value upon right-clicking on the neuron).




5. From the Measurement tab on the left side of the panel, select List, All views and Create document (Figure 9).

   
   

   
   Figure 9. Fluorescence intensity (FI) compilation. From the measurement option select list, All views, and create document.




6. Record the area and FI sum for each image of a neuron in .xml format (Figure 10).

   
   

   
   Figure 10. Measuring the FI sum for each scan of a neuron in .xml format




7. For quantification of FI of a single neuron, we considered a total of 11 scans with an interval of 1.08 μm for each scan (cumulative of 11.88 μm width) (Figure 11).

   
   

   
   Figure 11. Compilation of fluorescence intensity (FI) of a single neuron and all the neurons of a cluster. For the characterization of FI of a single neuron, a total of 11 scans with an interval of 1.08 μm for each scan (cumulative 11.88 μm width) were considered. Take the average and find the standard error. Follow the same method/step(s) for all the dopaminergic (DAergic) neurons. The intensity sum of all the neurons in a specific cluster gives the total FI of that particular region (cluster-wise). The total FI is the sum of the FI of all the neurons belonging to all the DAergic neuronal clusters.




8. The intensity sum of all the neurons in a cluster gives the total FI of that particular region (cluster-wise).

9. Total FI is the sum of the FIs of all the neurons belonging to all the DAergic neuronal clusters.




5. Precautions and recommendations

1. Head tissue fixation is critical and should be properly done [use the test tube rotator with constant velocity (10 rpm) for fixing the head tissue gently and thoroughly]. If any issue arises with the working of antibodies (primary ab), the worker should first check if fixation was done thoroughly and properly before investing time in figuring out the efficiency of the antibody.

2. Incubation with primary and secondary antibodies should be done using a test tube rotator with constant velocity (10 rpm).

3. Critical: To prevent brains from being crushed, glass spacers should be used while mounting the brains with a coverslip.

4. Coverslip edges should be thoroughly sealed with nail polish to avoid drying up of the brains.

5. Image acquisition should be done on the same day to avoid bleaching.

6. Care should be taken to capture images from the samples with the same orientation.

7. The red dot test should be carried out carefully.

8. The same setting should be reused to capture the images/scans of different samples.

9. Care should be taken while performing Z-stack programming so that no neuron is left out of scanning.

Data analysis

Analysis of Z-stack scans/images for quantification of DAergic neurons and characterization of FI in Drosophila brain

1. The DAergic neurons were determined/counted from the Z-stack images/scans. The number of DAergic neurons in each cluster was counted in an unbiased manner. A minimum of 10 brains were analyzed for DAergic neuronal number quantification. A merged fly brain 2D image was used for presentation (Figure 12).

   
   

   
   Figure 12. Demonstration of dopaminergic (DAergic) neuronal clusters in the whole brain of a Drosophila. A. Cartoon of Drosophila brain showing the position of different clusters of DAergic neurons. B. Whole-brain mount of Drosophila captured and analyzed using ZEN software of Carl Zeiss fluorescence microscope using fluorescently labeled secondary antibody targeted against the primary anti-TH antibody. The brain of Drosophila has approximately 140 DAergic neurons in each hemisphere, which are arranged into different clusters. Some of them are PAL (4–5 neurons), PPL1 (11–12 neurons), PPL2 (6/7 neurons), PPM1/2 (8/9 neurons), PPM3 (5–6 neurons), and VUM (3 neurons) (PAL: Protocerebral anterior lateral; PPL: protocerebral posterior lateral; PPM: protocerebral posterior medial). Figures 1–12 adapted with modification from Ayajuddin et al. [28].




2. For the characterization of FI of a single neuron, a total of 11 scans with an interval of 1.08 μm for each (cumulative 11.88 μm width) were considered. Then, average and standard error were obtained. The same method/step(s) were followed for all the DAergic neurons. The intensity sum of all neurons in a specific cluster gives the total FI of that particular region (cluster-wise). The total FI is the sum of the FI of all the neurons belonging to all the DAergic neuronal clusters.

3. Data was arranged and plotted using GraphPad Prism for total DAergic neurons and FI of all the DAergic neurons (Figure 13).

   
   

   
   Figure 13. Data analysis and representation of results. A. Data was arranged and plotted using GraphPad Prism for total dopaminergic (DAergic) neurons and fluorescence intensity (FI) of all the neurons. B. Graphical representation of DAergic neurons. C. Graphical representation of total FI of secondary ab tagged against the primary ab (anti-TH) of DAergic neurons in Drosophila brain. Figures 12 and 13 were prepared using Adobe Photoshop CS 6.2 version: 13.0.1.

Validation of protocol

This protocol or parts of it has been used and validated in the following research article:

1. Ayajuddin et al. [28]. Fluorescence microscopy-based sensitive method to quantify dopaminergic neurodegeneration in a Drosophila model of Parkinson’s disease. Front. Neurosci. (Figure 2, Supplementary figures 1–11).

General notes and troubleshooting

1. Utmost care should be exercised while dissecting the head capsule out to avoid damaging the brain, which may damage certain neuronal clusters that will affect FI quantification (may not affect quantification of neuronal number).

2. It is important to pay attention and mix the heads thoroughly and gently while fixing them in PFA.

3. Image acquisition should be done soon after the preparation of slides to minimize the signal bleaching that could influence FI quantification.

4. Care should be taken to scan brains that are oriented in a dorsoventral position.

5. Scanning different brains in different orientations will give variation in FI signal levels.

Acknowledgments

This research was supported by the Department of Biotechnology (DBT), India (R&D grant nos. BT/405/NE/U-Excel/2013; BT/PR16868/NER/95/328/2015 and BT/COE/34/SP28408/2018) and the Science and Engineering Research Board (SERB) of the Department of Science and Technology (DST) India (R&D grant no. EMR/2016/002375, 27-3-2017) awarded to SCY. Part of this work was presented at the Indian Drosophila Research Conference (InDRC)-13-17 December 2021, organized by the Indian Institute of Science Education and Research (IISER-K), Kolkota by RC. RC and MA received DBT-JRF (junior research fellowship); RC received DBT-SRF (senior research fellowship) and ICMR (Indian Council of Medical Research)-SRF.

Original research paper: Ayajuddin, M., Chaurasia, R., Das, A., Modi, P., Phom, L., Koza, Z. and Yenisetti, S.C. (2023). Fluorescence microscopy-based sensitive method to quantify dopaminergic neurodegeneration in a Drosophila model of Parkinson’s disease. Front. Neurosci. 17:1158858 [28].

Competing interests

The author declares no conflicts of interest.

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