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Method Article

Cell Migration and Cell Adhesion Assays to Investigate Leishmania-Host Cell Interaction

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DOI:

10.3791/62461

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August 4th, 2021

 ,  ,  ,  ,  ,  ,  , 
1Laboratory of Host - Parasite Interaction and Epidemiology, Gonçalo Moniz Institute

* These authors contributed equally

In This Article

Summary

Here we study implications of Leishmania-host interaction by exploring Leishmania-infected dendritic cells migration. The differentiation and infection of dendritic cells, migration analysis, and the evaluation of adhesion complexes and actin dynamics are described. This method can be applied to other host cell migration studies when infected with Leishmania or other intracellular parasite species.

Abstract

Leishmania is an intracellular protozoan parasite that causes a broad spectrum of clinical manifestations, ranging from self-resolving localized cutaneous lesions to a highly fatal visceral form of the disease. An estimated 12 million people worldwide are currently infected, and another 350 million face risk of infection. It is known that host cells infected by Leishmania parasites, such as macrophages or dendritic cells, can migrate to different host tissues, yet how migration contributes to parasite dissemination and homing remains poorly understood. Therefore, assessing these parasites' ability to modulate host cell response, adhesion, and migration will shed light on mechanisms involved in disease dissemination and visceralization. Cellular migration is a complex process in which cells undergo polarization and protrusion, allowing them to migrate. This process, regulated by actin and tubulin-based microtubule dynamics, involves different factors, including the modulation of cellular adhesion to the substrate. Cellular adhesion and migration processes have been investigated using several models. Here, we describe a method to characterize the migratory aspects of host cells during Leishmania infection. This detailed protocol presents the differentiation and infection of dendritic cells, the analysis of host cell motility and migration, and the formation of adhesion complexes and actin dynamics. This in vitro protocol aims to further elucidate mechanisms involved in Leishmania dissemination within vertebrate host tissues and can also be modified and applied to other cell migration studies.

Introduction

Leishmaniasis, a neglected tropical disease caused by protozoan parasites belonging to the genus Leishmania, results in a wide-ranging spectrum of clinical manifestations, from self-healing localized cutaneous lesions to fatal visceral forms of the disease. It has been estimated that up to one million new leishmaniasis cases arise annually, with a reported 12 million people currently infected worldwide1. Visceral leishmaniasis (VL), which can be fatal in over 95% of cases when left untreated, causes more than 50,000 deaths annually, affecting millions in South America, East Africa, South Asia, and the Mediterranean region2. The main etiological agent of VL in the new world, Leishmania infantum, is transmitted to humans by infected female sandflies during blood-feeding3. These parasites are recognized and internalized by phagocytes, e.g., macrophages and dendritic cells3,4,5. Inside these cells, parasites differentiate into their intracellular forms, known as amastigotes, which will then multiply and be transported via the lymphatic system and bloodstream to different host tissues6,7. However, the mechanisms by which Leishmania parasites are disseminated in the vertebrate host, as well as the role played by host cell migration in this process, remain unclear.

Cell migration is a complex process executed by all nucleated cells, including leukocytes8. According to the classic cycling model of cell migration, this process involves several integrated molecular events that can be divided into five steps: leading-edge protrusion; adhesion of the leading edge to matrix contacts; contraction of cellular cytoplasm; release of the rear edge of the cell from contact sites; and the recycling of membrane receptors from the rear to the front of the cell9.

For cell migration to occur, protrusions must be formed and then stabilized through attachment to the extracellular matrix. Among the different receptor types involved in the promotion of cell migration, integrins are notable. Integrin activation results in migration-related signaling; intracellular signaling then occurs via focal adhesion kinase (FAK) and Src family kinases, in addition to talin, vinculin, and paxillin molecues10,11,12. The phosphorylation of paxillin by activated kinases, including FAK, leads to the recruitment of effector molecules, which transduces external signals that prompt cell migration. It has been shown that paxillin is an intracellular molecule that is crucial to cell adhesion, actin polymerization, and cell migration processes13,14,15.

The actin cytoskeleton plays a central role in the polarization and migration of phagocytes16. During cell migration process, protrusions formed due to actin polymerization become stabilized through cell adhesion to the extracellular matrix. This process may be modulated by integrin receptors associated with the actin cytoskeleton17,18,19. Several actin-binding proteins regulate the rate and organization of actin polymerization in cellular protrusions20. Studies have shown that RhoA, Rac, and Cdc42 regulate actin reorganization after the stimulation of adherent cells by extracellular factors21,22. During migration, Rac1 and Cdc42 are located at the leading edge of the cell, controlling the extension of lamellipodia and filopodia, respectively, while RhoA, located at the rear of the cell, regulates the contraction of the actomyosin cytoskeleton15,23,24,25.

Studies have shown that Leishmania infection modulates host cell functions, such as adhesion to the cellular substrate and migration26,27,28,29,30,31. Immature DCs reside in peripheral tissues; upon interaction with PAMPS, these cells become activated and migrate to the draining lymph nodes, prompting antigen presentation to T cells. A previous study using a mouse model showed that L. amazonensis infection provokes a reduction in the migration of DCs to draining lymph nodes29. It was also demonstrated that the inhibition of the adhesion process reduced DC migration after infection with L. major30. Nonetheless, the impact of DC migration on parasite dissemination in the host, as well as the mechanisms involved in this process, remain poorly understood.

Here we present a compiled step-by-step protocol to perform an in vitro adhesion and migration assay involving human DCs infected by Leishmania. This method comprises not only the differentiation and infection of DCs, but also permits the analysis of host cell motility and migration, the formation of adhesion complexes, as well as actin dynamics. The presently described in vitro protocol allows researchers to further investigate the mechanisms involved in Leishmania dissemination within vertebrate host tissues and can also be manipulated and applied to other cell migration studies.

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Protocol

The procedures described herein were approved by the Institutional Review Board of the Gonçalo Moniz Institute (IGM-FIOCRUZ, protocol no. 2.751.345). Blood samples were obtained from healthy volunteer donors. Animal experimental procedures were conducted in accordance with the Ethical Principles in Animal Research adopted by the Brazilian law 11.784/2008 and were approved and licensed by the Ethical Committee for Animal Research of the Gonçalo Moniz Institute (IGM-FIOCRUZ, protocol no. 014/2019).

1. Isolation and differentiation of human dendritic cells

  1. Pipette 10 mL of the density gradient medium in 50 mL centrifuge tubes.
  2. Label the 50 mL tubes according to each donor's sample.
  3. Collect ~ 50 mL of venous blood from healthy donors and after collection, follow the procedures described below in the flow cabinet.
  4. Carefully transfer the collected blood into centrifuge tubes and dilute in saline solution (0.9% sodium chloride) in a ratio of 1:1 at room temperature.
  5. Slowly overlay the diluted blood on the top of the density gradient medium.
  6. Centrifuge tubes containing the blood and density gradient medium at 400 x g for 30 min at room temperature.
    NOTE: Switch off the brake before centrifuging to prevent the mixing of gradient layers. After the 1st centrifugation, lower the centrifuge temperature to 4 °C.
  7. Carefully remove the tubes from the centrifuge.
  8. Identify the ring of peripheral blood mononuclear cells (PBMC) in the sample (buffy coat); gently remove the residual plasma with a pipette.
    NOTE: After centrifugation, the following gradient layers will have formed: erythrocytes, density gradient medium, PBMC ring, and plasma. The PBMC ring is located between the density gradient medium and plasma layers.
  9. Transfer the cloud-like PBMC layer to a new tube and bring up the volume to 30 mL with saline solution.
  10. Centrifuge the tubes containing cell suspension at 250 x g for 10 min at 4 °C. Discard the supernatant and resuspend the pellet in 1 mL of saline solution.
  11. Collect an aliquot for cell counting with the trypan blue exclusion method. First, dilute at a ratio of 1:1,000. Then, use 10 µL of the diluted cells for trypan blue staining and count cells using a Neubauer chamber to determine cell viability.
  12. Centrifuge again at 200 x g for 10 min under 4 °C.
  13. Resuspend the pellet in MACS buffer. Use 80 µL of the buffer for every 1 x 107 cells.
    NOTE: MACS buffer composition: Prepare a solution containing phosphate-buffered saline (PBS), pH 7.2, 0.5% bovine serum albumin (BSA), and 2 mM EDTA. Dilute the buffer solution at a 1:20 ratio with the rinsing solution. Keep the buffer cold and store at 2-8 °C.
  14. Add CD14 microbeads to the cell suspension prepared in step 1.13. Use 20 µL of CD14 microbeads for every 1 x 107 cells.
    NOTE: CD14 microbeads are used for the positive selection of human monocytes from PBMCs, as beads bind to CD14-positive cells expressed on most monocytes.
  15. Homogenize the solution containing the pellet and microbeads using a pipette. Keep on ice for 15 min.
  16. Centrifuge the suspension at 300 x g for 10 min under 4 °C.
  17. Resuspend cells in MACS buffer. Use 1-2 mL for 1 x 107 cells in the cell microbead mixture.
  18. Centrifuge the suspension at 300 x g for 10 min under 4 °C.
  19. Aspirate the supernatant and resuspend the pellet in 500 µL of MACS buffer.
    NOTE: This is the maximum volume of the cell suspension that can be processed through one column.
  20. Assemble the magnetic column.
  21. Wash the column once by adding 500 µL of MACS buffer. Allow buffer to flow under gravity through the column.
    NOTE: Do not allow the column to dry, as any air that enters can obstruct the column.
  22. Add 500 µL of the cell sample solution from step 1.19 per column. Allow the cell sample solution to flow under gravity through the column.
  23. Wash the column by adding 500 µL of MACS buffer (2x). Only add the fresh buffer when the column reservoir is empty. Avoid drying.
  24. Pipette 1 mL of the MACS bufferonto the column and place it in a new tube underneath. Immediately flush out the magnetically labeled cells by firmly pushing the plunger into the column.
  25. Centrifuge the CD14 enriched cells at 300 x g for 10 min under 4 °C.
  26. Count cells using a Neubauer chamber.
  27. Resuspend cells in 1 mL complete RPMI with interleukin-4 (IL-4) (100 µL/mL) + granulocyte-macrophage colony-stimulating factor (GM-CSF) (50 ng/mL).
    NOTE: GM-CSF is a cytokine secreted by macrophages, T cells, mast cells, natural killer cells, endothelial cells, and fibroblasts that induces the differentiation and proliferation of myeloid progenitors in the bone marrow. GM-CSF and IL-4 are used to induce dendritic cell differentiation32.
  28. Seed cells in a 24 well plate at a concentration of 2 × 105 cells per well in 500 μL of complete RPMI medium containing and incubate the cells for 7 days in the cell culture incubator at 37 °C.

2. Leishmania infantum  cultivation

NOTE: Leishmania infantum (MCAN/BR/89/BA262) parasites are used in this assay. Hamsters were intravenously infected with 20 µL of the solution containing 1 x 106 L. infantum promastigotes in sterile saline. After 1 to 2 months, animals were euthanized and the amastigote forms of Leishmania were recovered from their spleens and differentiated into promastigotes33.

  1. Grow L. infantum promastigotes isolated from previously infected hamster spleens in an inclined 25 cm2 cell culture flask containing 3 mL of Novy-Nicolle-MacNeal medium (NNN) and 5 mL of supplemented Minimum Essential Medium (MEM).
    NOTE: In this assay, MEM medium was supplemented with 10% fetal bovine serum (FBS) and 24.5 nM hemin bovine.
  2. Incubate at 24 °C for 7 days in BOD (Bio-Oxygen Demand) incubator.
  3. Pipette 100 µL of promastigote culture into a new 25 cm2 cell culture flask containing 5 mL of supplemented MEM medium.
  4. Incubate the promastigote culture at 24 °C in BOD incubator until promastigotes reach the stationary phase. Periodically count cultured promastigotes by transferring an aliquot of parasite suspension diluted in saline to a Neubauer chamber (i.e., hemocytometer) to determine the stationary phase of growth.
    NOTE: It is not recommended to use first-passage parasites after cultivation in NNN medium to avoid residual traces of rabbit blood.
  5. Transfer 1 x 105 of stationary growth phase culture of L. infantum promastigotes to a new 25 cm2 cell culture flask and add 5 mL of MEM supplemented medium.
  6. Monitor the growth of the culture periodically for approximately 7 days using a Neubauer chamber until the stationary phase is achieved. Parasites are now ready for use in experimental infection procedures.
    ​NOTE: Promastigote cultures are considered viable for infection for up to 7 passages in vitro; additional passages may induce loss of virulence.

3. Human dendritic cell infection

  1. Inside a biological laminar flow cabinet, transfer all the contents from the parasite culture flask to 50 mL centrifuge tubes.
  2. Add cold saline solution to a final volume of 40 mL.
  3. Centrifuge at 1,600 xg for 10 min under 4 °C.
  4. Discard the supernatant following centrifugation and resuspend the pellet in 1 mL of cold saline solution (Repeat steps 3.3-3.4 three times).
  5. After washing the cells to remove any non-viable parasites, resuspend the pellet in 1 mL of cold saline solution.
  6. Pass the contents slowly through a 1 mL syringe with a 16 G needle 5 times to separate the parasite clusters.
  7. Remove an aliquot to determine the parasite concentration in a hemocytometer (calculate the mean number of parasites in 4 quadrants x dilution factor x 104).
  8. Wash dendritic cells by adding 1 mL of saline solution and centrifuging cells at 300 x g for 10 min at room temperature (3 times).
  9. Calculate the quantity of L. infantum required for the experimental infection; ratio: 20 parasites per cell.
  10. Place the required volume of L. infantum in each well of cell culture plates.
  11. Incubate dendritic cells with parasites for 4 h in an incubator at 37 °C under 5% CO2.
  12. After step 3.11, centrifuge plates at 300 x g for 10 min under 4 °C.

4. Migration assay using cell culture inserts

  1. After infection, wash dendritic cells (infected or not) 3 times with 1 mL of saline solution at room temperature to remove non-internalized parasites. After each wash, centrifuge plates at 300 x g for 10 min under 4 °C.
  2. Once non-internalized parasites are removed, detach cells by adding 200 µL of the cell dissociation reagent in each well and incubate for 15 min. Keep the cells in an incubator at 37 °C under 5% CO2.
  3. Homogenize cells using a 1,000 µL pipette tip to allow cells to loosen.
  4. Transfer the dissociated cells to a 50 mL centrifuge tube.
  5. Centrifuge at 300 x g for 10 min under 4 °C.
  6. Resuspend the pellet in 1 mL of RPMI medium supplemented with 10% FBS.
  7. Pass the contents of each tube slowly through a 1 mL syringe with a 25 G needle 5 times to separate cells.
  8. Remove an aliquot, dilute using trypan blue to determine the cell concentration using a hemocytometer (mean of viable cells in 4 quadrants × dilution factor × 104).
  9. Preparation of cell culture microplate inserts:
    NOTE: Cell culture inserts (5.0 µM pore polycarbonate membrane) are recommended for migration assays using dendritic cells, macrophages, and monocytes, as these inserts allow phagocytes to pass through the membranes.
    1. Remove inserts with sterile tweezers and place in empty wells.
    2. Add 600 µL of RPMI medium supplemented with 10% FBS to each well; add chemoattractant chemokine (C-C motif) ligand 3 (CCL3) (1 µL for every 1 mL of medium).
      NOTE: CCL3 is a chemokine that regulates DC migration34.
    3. Using sterile tweezers, place inserts in wells containing the medium.
  10. Add 2 x 105 dendritic cells (infected or not) in 100 µL of medium to each insert.
  11. Incubate for 4 h to allow cells to migrate.
  12. After 4 h, take the plate out and aspirate the medium. Add 100 µL of 4% paraformaldehyde and incubate for 15 min.
  13. Remove paraformaldehyde and add 100 µL of saline solution.
    NOTE: Plates can be kept at 4 °C for later assembly.
  14. Collect the supernatant from inserts or from wells to count non-migrating cells or those that crossed the membrane, respectively. Incubate with paraformaldehyde 4% for 15 min.
  15. Concentrate cells using a cytocentrifugation technique35.
  16. Add 10 µL of the mounting medium with DAPI to the membranes and place coverslips over the wells.
  17. Assembly of the insert membrane.
    NOTE: This step can be performed outside the biosafety cabinets.
    1. Remove insert membranes from wells.
    2. Scrape the surface of the insert with a swab to remove any cells that have not migrated.
    3. Using a scalpel, remove the membrane from the insert.
    4. Place the membrane on a slide, with cells facing up.
    5. Add 10 µL of mounting medium with DAPI to each membrane and then place overlay coverslips.
    6. Cover plates with aluminum foil.
    7. Incubate plates at room temperature for 30 min, then store at -20 °C
  18. To analyze cell migration, count the number of cells per field (no less than 10 fields) using a fluorescence microscope at a laser excitation wavelength of 405 nm.

5. Adhesion assay and evaluation of actin polymerization by immunofluorescence

NOTE: For this assay, use 24-well plates with coverslips.

  1. After infecting cells for 4 h, wash each well 3 times with sterile saline solution at room temperature to remove any non-internalized parasites.
  2. Centrifuge the plate at 300 x g for 10 min under 4°C. Add 500 µL of 4% paraformaldehyde to each well for 15 min.
  3. Remove paraformaldehyde and add 1 mL of saline solution.
  4. Prepare solutions as described in Table 1.
Primary solutionsChemical compoundDiluent
Ammonium chloride solution0,134 g of NH4Cl50 ml of PBS 1X
Saponin 15%150 mg of saponin1 mL de PBS 1X
Albumin from bovine serum (ABS) 10%1 g of ABS10 mL of PBS 1X
Secondary solutionsComponent 1Component 2Component 3
Saponin 0,15%1mL of saponin 15%100 mL of PBS 1X-
PBS 1X / ABS 3% / Saponin 0,15%13,8 mL of PBS 1X6 mL of ABS 10%200 µL of Saponin 15%
PBS1X / ABS 0,3% / Saponin 0,15%:19,2 mL of PBS 1X0,6 mL of ABS 10%200 µL of Saponin 15%
PBS 1X / ABS 1% / Saponin 0,15%17,8 mL of PBS 1X2 mL of ABS 10%200 µL of Saponin 15%

Table 1: Buffer recipes.

  1. Immunostaining
    ​NOTE: The following steps must be performed under agitation.
    1. Wash coverslips 3 times with 1x PBS for 5 min.
    2. Add 500 µL of ammonium chloride solution per well for 10 min.
    3. Wash coverslips 3 times with 1x PBS for 5 min.
    4. Permeabilize the membrane with Saponin 0.15% for 15 min.
    5. Incubate cells with the blocking solution (PBS 1x / ABS 3% / Saponin 0.15%) for 1 h.
    6. Wash coverslips 3 times with PBS 1x/Saponin 0.15% for 5 min.
    7. Dilute primary antibodies in PBS 1x /ABS 1% /Saponin 0.15% as: Rabbit anti-FAK (pTyr397): 1:500 dilution, Rabbit anti-paxilin (pTyr118): 1:100 dilution. Mouse Anti-Rac1: 1:100 dilution. Rabbit Anti-Cdc42: 1:200 dilution. Rabbit Anti-RhoA: 1:200 dilution.
    8. Incubate cells with primary antibody diluted in PBS 1x/ABS 1% /Saponin 0.15% for 1 h.
      NOTE: FAK and Paxillin are key molecules involved in the formation of adhesion complexes13,14,15. The Rho GTPase family is responsible for the organization of the actin cytoskeleton. RAC1 and Cdc42, located at the front edge of the cell, control the formation of lamellipodia and filopodia, respectively; RhoA is located at the rear of the cell and is involved in cytoskeleton contraction15, 23,24,25.
    9. Wash coverslips 3 times with 1x PBS/Saponin 0.15% for 5 min.
    10. Dilute secondary antibody or phalloidin as follows: Anti-rabbit IgG, Alexa Fluor 568: 1:500 dilution; Anti-mouse IgG, Alexa Fluor 488: 1:500 dilution; Anti-mouse IgG, Alexa Fluor 594: 1:500 dilution; Phalloidin Alexa Fluor 488: 1:1200 dilution.
    11. Incubate cells with secondary antibody or phalloidin diluted in 1x PBS/ABS 0.3% Saponin 0.15% for 45 min.
      NOTE: Incubation of the secondary antibody or phalloidin should be performed in the absence of light. Cover plates with aluminum foil to protect from light during the following steps.
    12. Wash coverslips 3 times with 1x PBS for 5 min.
    13. Remove coverslips from wells.
    14. In the absence of light, add 10 µL of mounting medium with DAPI onto clean microscopic glass slides.
    15. Place coverslips with cells facing down to allow contact between cells and DAPI solution.
      NOTE: Cover slides with aluminum foil to protect from light.
    16. Incubate for 30 min at room temperature.
    17. Store at -20 °C.

6. Confocal microscopy, image acquisition, and quantification using FIJI

NOTE: To acquire/capture immunofluorescence images, use a confocal laser scanning microscope. Oil-immersion 63x objective lens is recommended for optimal resolution.

  1. Allow coverslips to reach room temperature, protected from light, for at least 30 min prior to image acquisition.
  2. Clean the coverslips with absorbent tissue.
  3. Add a drop of immersion oil to the objective and place each slide under the microscope.
  4. Move the objective until the oil touches the slide.
  5. Observe and adjust the microscope focus; select the 63x objective with oil.
  6. Turn on lasers at 488 nm, 552 nm, and 405 nm wavelengths.
  7. Select image resolution: 1024 x 1024.
  8. Click on the Live button, set the Z stack, and press Begin. Repeat the process and then press End.
  9. After selecting the Maximum Projection option in the Tool menu, wait for the image to be acquired.
  10. Save the experiment.
  11. Export images in .lif format on a computer. Use FIJI open-source image analysis software to analyze images.
  12. Select the images to be analyzed and select Duplicate Image.
  13. To have the image in grayscale, select Image | Adjust | Color Threshold. Select 0 and 255 (saturation).
  14. Select the threshold method: Default.
  15. Select threshold color: B and W (black and white).
  16. Do not select Dark background.
  17. Select: Process | Binary | Options and then select the relevant data to be measured: Area, Min, Max, gray value, integrate density.
  18. Select the free hands' tool in the Fiji toolbar and trace each cell manually carefully.
  19. From the Analyze menu, select Set measurements. Make sure to have area integrated intensity and mean grey value selected. Repeat this process for each cell.
  20. Select all data in the Results window and copy and paste into a spreadsheet file.
  21. Calculate the corrected total cell fluorescence (CTCF): CTCF (Integrate density = Area of selected cell x Mean fluorescence of background readings).
  22. Open the file containing data using statistical analysis software to perform statistical analysis.

7. Statistical analysis

  1. Open a New Project when a welcome dialog appears.
  2. Choose the type of graph and medium with SD.
  3. Apply the values obtained from the experimental results to the table.
  4. Select Descriptive Statistics and choose the option column Statistics [all tests] to analyze data distribution.
  5. If data follow a Gaussian distribution, choose the t-test to analyze samples by comparing two pairs. If the distribution is non-Gaussian, analyze data using the Mann-Whitney test.
  6. Choose the best graph option for optimal data representation.

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Results

This protocol described herein enables the evaluation of cell migration and its associated mechanisms, such as actin dynamics and adhesion, thereby providing a tool to determine the migration of Leishmania-infected host cells within the vertebrate host. The results presented here demonstrate that this in vitro assay provides rapid and consistent indications of changes in cellular adhesion, migration, and actin dynamics prior to in vivo experimentation.

First, cells w...

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Discussion

The method described here for evaluating cell migration using the cell culture membrane inserts system allows researchers to study the migratory response of cells in a two-dimensional environment. In this technique, some steps are considered critical. Firstly, the differentiation of human DCs and infection with Leishmania are determinative since the infection rate is donor-dependent. Using more than one donor per experiment and healthy Leishmania cultures will allow for more consistent results. It is al...

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Disclosures

The authors declare they have no competing financial interests.

Acknowledgements

This work was supported by Bahia Research Support Foundation (Fapesb), grant number 9092/2015. The authors acknowledge CNPq, Capes and Fapesb for financial support via scholarships. The authors would like to thank Andris K. Walter for critical analysis, English language revision and manuscript copyediting assistance.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
16 Gauge needleDescarpack353101
24 well cell culture plateJET-BIOFILJ011024
25 Gauge needleDescarpack353601
Albumin from bovine serumSigma AldrichA2153-100G
Ammonium chlorideSigma AldrichA-0171
Anti-mouse IgG, Alexa Fluor 488InvitrogenA32723
Anti-mouse IgG, Alexa Fluor 594InvitrogenA11032
Anti-rabbit IgG, Alexa Fluor 568InvitrogenA11011
CD14 MicroBeadsMACS Myltenyi Biotec130-050-201
Cell Culture Flask 25cm2SPL70125
CellstripperCorning25-056-CI
Confocal microscopeLeicaTCS SP8
Coverslip circles 13mmPerfecta10210013CE
Dissecting ForcepsVWR82027-406
EDTASigma AldrichE6758
Falcon tubeKASVIK19-0051
Fetal Bovine Serumgibco16000044
Fluorescence microscopeOlympus BX51
Glass slide  25,4x76,2mmPerfecta200
Hemin bovineSigma AldrichH2250
HemocytometerPerfecta7302HD
Histopaque® 1077Sigma Aldrich10771
MACS bufferMACS Myltenyi Biotec130-091-221
Minimum Essential MediumGibco41090093
Mouse anti-Rac1BD610650
ParaformaldehydeSigma Aldrich158127
Phalloidin Alexa Fluor 488InvitrogenA12379
Phosphate Buffered SalineThermoFisherAM9624
Polycarbonate Membrane Transwell Inserts - Pore size 5.0 µmCorning3421
ProLong Gold DAPI kitInvitrogenP36931
Rabbit anti-Cdc42InvitrogenPA1-092X
Rabbit anti-FAK (pTyr397)InvitrogenRC222574
Rabbit anti-paxilin (pTyr118)InvitrogenQF221230
Rabbit anti-RhoAInvitrogenOSR00266W
Recombinant Human CCL3R&D Systems270-LD-010
Recombinant Human GM-CSFPeproTech300-03
Recombinant Human IL-4PeproTech200-04
Recombinant Human M-CSFPeproTech300-25
RPMI 1640 MediumGibco21870076
SaponinSigma Aldrich47036 – 50G – F
Syringe 3 mLDescarpack324201
Trypan BlueGibco15250061

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