Evaluation of the Cell Invasion and Migration Process: A Comparison of the Video Microscope-based Scratch Wound Assay and the Boyden Chamber Assay

Summary

This study reports two different methods for the analysis of cell invasion and migration: the Boyden chamber assay and the in vitro video microscope-based wound-healing assay. The protocols for these two experiments are described, and their benefits and disadvantages are compared.

Abstract

The invasion and migration abilities of tumor cells are main contributors to cancer progression and recurrence. Many studies have explored the migration and invasion abilities to understand how cancer cells disseminate, with the aim of developing new treatment strategies. Analysis of the cellular and molecular basis of these abilities has led to the characterization of cell mobility and the physicochemical properties of the cytoskeleton and cellular microenvironment. For many years, the Boyden chamber assay and the scratch wound assay have been the standard techniques to study cell invasion and migration. However, these two techniques have limitations. The Boyden chamber assay is difficult and time consuming, and the scratch wound assay has low reproducibility. Development of modern technologies, especially in microscopy, has increased the reproducibility of the scratch wound assay. Using powerful analysis systems, an "in-incubator" video microscope can be used to provide automatic and real-time analysis of cell migration and invasion. The aim of this paper is to report and compare the two assays used to study cell invasion and migration: the Boyden chamber assay and an optimized in vitro video microscope-based scratch wound assay.

Introduction

Cell invasion and migration are involved in the dissemination of cancer cells, which is the main cause of resistance to treatment¹ and can lead to locoregional or metastatic recurrence after cancer treatment². The epithelial-mesenchymal transition (EMT) is the initial process of cell invasion-migration in which cancer cells switch from an epithelial to a mesenchymal phenotype. E-Cadherin is an extracellular marker of the epithelial phenotype³, and increased expression of N-cadherin and vimentin is characteristic of the mesenchymal phenotype⁴. Migration also depends on the intrinsic capacity of cancer cells to invade the extracellular matrix (ECM) through the action of matrix metalloproteases⁵.

This invasion–migration mechanism has been described for cancer at many locations, particularly in head and neck cancer⁶. Many researchers have focused on the migration and invasion processes to understand better how cancer cells disseminate in the hope that this knowledge will lead to new treatment strategies. It is crucial that these studies are performed using reliable and reproducible assays.

In vitro analysis of cell motility can be challenging. Developed many years ago, the Boyden chamber assay is considered to be the standard for invasion–migration analysis⁷. However, it is time consuming and is often inaccurate. A second test is the wound-healing assay⁸, which involves making a scratch on a cell monolayer culture and capturing images of cell invasion and migration at fixed time intervals. This technique has been criticized widely because of the large variations between the results of two successive tests. However, the application of modern technologies, especially in microscopy, has improved the reproducibility of the scratch wound assay. Video microscopes can be easily introduced in incubators and can generate real-time images of cell migration. These devices record microscopic data and provide automatic analysis of wound cell confluence over time. The aim of this paper is to describe the Boyden chamber assay and the optimized scratch wound assay, and to discuss the advantages and weaknesses of each approach.

Protocol

NOTE: The Boyden chamber and scratch assays without inclusion of the ECM are referred to as the migration assay, and the same assays with the ECM is referred to as the invasion assay.

1. Boyden Chamber Assay

NOTE: This protocol is adapted for the SQ20B cell line, which is derived from a recurrent Head and Neck Squamous Cell Carcinoma (HNSCC) laryngeal cancer and was obtained from John Little (Boston, MA, USA).

Day 1

1. Cell Seeding
   1. Seed 2 10⁶ SQ20B cells in 12 mL of culture medium (CM) in a 175 cm² flask 72 h before day one and allow the cells to grow to 80% cell confluence.
      1. To prepare CM for SQ20B cells, supplement Dulbecco's modified Eagle medium (DMEM) with 10% fetal calf serum (FCS), 0.04 mg/mL hydrocortisone, 100 U/mL penicillin, and 0.1 g/L streptomycin.
   2. Under a laminar flow hood, trypsinize the cells. Remove the medium, wash the cells with sterile phosphate-buffered saline (PBS), and add 2.5 mL of trypsin ethylenediaminetetraacetic acid (EDTA) (0.5 g/L). Incubate the cells for 5 min at 37 °C and then stop the reaction by adding 12.5 mL of CM warmed to 37 °C. Count the number of cells using a cell counter.
   3. Seed the cells in a 25 cm² flask at a cell density of 6 10⁵ cells for each condition to be evaluated. Incubate the cells for 24 h in 3 mL of CM.

Day 2

2. Cell starvation and preparation of coated chambers
   1. Starve the cells by replacing the medium in each flask with 3 mL of low-fetal bovine serum (FBS) medium using 0.1% bovine serum albumin (BSA) instead of FBS. Starve the cells for 24 h in the incubator.
      1. To prepare starvation CM (s-CM), supplement DMEM with 0.1% BSA, 0.04 mg/mL hydrocortisone, 100 U/mL penicillin, and 0.1 g/L streptomycin.
   2. For the migration assay, go to step 1.3.
   3. For the invasion assay, 12 h before day 3, prepare the coated Boyden chambers by adding 500 μL of s-CM to each coated chamber. Use commercially prepared coated Boyden chambers and keep them at 4 °C before use. Place each Boyden chamber in the companion plate and set it in the incubator at 37 °C overnight.

Day 3

3. Cell seeding in the Boyden chamber
   1. Use the companion plate to prepare the chemoattractant.Fill each well of the 24-well companion plate with 750 μL of complete medium with 10% FBS, 0.04 mg/mL hydrocortisone, 100 U/mL penicillin, and 0.1 g/L streptomycin.
      1. Adapt the chemoattractant for each cell line and each treatment condition. To prepare the chemoattractant CM (ca-CM), supplement DMEM with 10% FCS, 0.4 mg/mL hydrocortisone, 100 U/mL penicillin, and 0.1 g/L streptomycin.
   2. Transfer the upper chamber into the prefilled companion plate, taking care to avoid bubbles.
   3. For the invasion assay, carefully remove 450 μL of CM from each Boyden chamber.
   4. Under a laminar flow hood, trypsinize the cells. Remove the medium, wash the cells with sterile PBS, add 0.5 mL of trypsin EDTA (0.5 g/L), and then incubate the cells for 5 min at 37 °C. Stop the reaction by adding CM warmed to 37 °C. Count the number of cells using a cell counter.
   5. Seed 3 10⁴ SQ20B cells in 500 μL of 0.1% BSA medium, giving a final dilution of 6 10⁴ cells/mL.
      NOTE: The cell concentration should be adapted for each cell line.
   6. Place the plate into the incubator at 37 °C for 24 h.

Day 4

4. Cell fixation and staining
   1. Fix the cells before the doubling time specific to that cell line. Fix SQ20B cells before 24 h.
   2. Remove each insert from the companion plate and carefully remove the cells from the upper chamber using a cotton swab. It is particularly important to remove all cells located in the upper chamber.
   3. Fix and stain each insert individually to obtain May-Grunwald Giemsa coloration⁹ using the staining kit provided. Alternatively, use 4% paraformaldehyde in another companion plate for a 30 min fixation.
   4. Keep the inserts in an empty 24-well companion plate under a laboratory hood to dry each chamber.

Day 5

5. Microscopic analysis
   1. Insert the companion plate with the inserts onto a 20 phase-contrast microscope and count each migrated cell on the lower part of the membrane. Optimize the right focus position by moving the objective from the bottom to the top, and stop the position on the bottom part of the membrane.
   2. Calculate the ratio between the numbers of migrated cells and seeded cells. Repeat each count for each treatment condition in triplicate.

2. Scratch Wound Assay: Cell Migration

NOTE: Instructions must be adapted for each type of cell.

Day 1

1. Cell Seeding
   1. Seed 2 x 10⁶ SQ20B cells in 12 mL of CM in a 175 cm² flask 72 h before day one and allow the cells to grow to 80% cell confluence.
   2. Under a laminar flow hood, trypsinize the cells. Remove the medium, wash the cells with sterile PBS, add 2.5 mL of trypsin EDTA (0.5 g/L), and incubate the cells for 5 min at 37 °C. Stop the reaction by adding 12.5 mL of CM warmed to 37 °C. Count the number of cells using a cell counter.
   3. Generate a prediluted sample at a cell density of 4 x 10⁵/mL, giving a final density of 4 10⁴ cells per 100 μL in each well. This concentration must be adapted for each cell line and should be in the range of 1 x 10⁴ to 6 10⁴ cells.
   4. Seed cells into each well of a 96-well plate by depositing 100 μL of the solution prepared in step 2.1.2.
   5. Leave the plate at room temperature for 5 min to disperse the cells evenly on the bottom of the wells.
   6. Place the plate into the incubator and allow the cells to adhere to the plate for 12 to 16 h (maximum) at 37 °C.

Day 2

2. Scratch wound assay
   1. Remove the plates prepared in step 2.1 from the incubator.
   2. Under the hood, make a wound using the commercial wounding device according to the manufacturer's protocol.
   3. Immediately remove the medium from each well using a pipette with an adapted conical tip, taking care not to touch the wound.
   4. Wash the cells twice by repeating the aspiration and using 100 μL of CM warmed to 37 °C for each well.
   5. Remove the CM using a pipette with an adapted conical tip after the washing steps.
   6. Add 100 μL of medium specific for each treatment condition to each well.
   7. Try to avoid creating any bubbles in the wells. A reverse-pipetting technique may be helpful here. Alternatively, remove bubbles with a syringe needle.
   8. Place the plate into the adapted rack of the video microscope.
   9. To improve the image quality, allow the plate to warm for at least 15 min before the first scan to avoid condensation on the lower side of the plate.
   10. Program the schedule of scans, using the video microscope software at one image per well. A maximum 2-h interval is required for an invasion-migration experiment. If the objective of the experiment is to produce a video, an interval of 30 min maximum is preferred.
   11. At the end of the experiment, wash the wounding device carefully and follow each of the four washing steps indicated by the manufacturer.

Days 3, 4, and 5

3. Analysis of migration using the video microscope
   1. For a minimum of 24 h and up to 5 days, monitor and check the cell migration.
   2. Use an appropriate cell mask adapted for each cell type to analyze cell migration. To obtain a cell mask adapted for each cell line, generate a cell processing definition from the software using a specific cell image collection.
   3. Trace the curves and export the data to a spreadsheet, which can be used to analyze and compare the results.

3. Scratch Wound Assay: Cell Invasion

NOTE: Instructions must be adapted for each type of cell.

Day 1

1. Cell Seeding
   1. Use the same protocol for cell seeding as described in step 2.1.

Day 2

2. Preparing the ECM
   1. Defrost the matrix for at least 12 h before use at 4 °C. Make sure that no aggregates are visible. If aggregates are visible, keep the matrix at 4 °C for a longer period until the aggregates disappear. Keep the matrix on ice. Use precooled pipette tips.
      NOTE: The matrix will solidify if not kept at 4 °C.
   2. Chill the microcentrifuge tubes on ice for 5 min.
   3. Take CM cooled to 4 °C from the refrigerator and dilute the matrix in the precooled microcentrifuge tubes to obtain a final concentration of 300 μg/mL.
   4. Return the microcentrifuge tubes with prediluted matrix to the refrigerator at 4 °C.
      NOTE: A cooling rack adapted for microcentrifuge tubes is helpful for maintaining the tubes at 4°C throughout the experiment.

Day 2

3. Scratch Wound Assay and Treatment of the ECM
   1. Remove the plate prepared in step 3.1 from the incubator.
   2. Under the hood, make the wound using the commercial wounding device according to the manufacturer's protocol.
   3. Immediately remove the medium from each well using a pipette with an adapted conical tip taking care not to touch the wound.
   4. Wash the cells twice by repeating the aspiration procedure and using 100 μL of CM warmed to 37 °C.
   5. After the second wash, place the plate on the 4 °C incubator to equilibrate its temperature for 5 min.
   6. Remove the cold medium from each well with the aspiration pipette with a conical tip, taking care to pipette carefully from the edge and to avoid touching the wound.
   7. Add 50 μL of prediluted matrix to each well using precooled conical tips at 4 °C.
   8. Place the plate in the incubator at 37 °C for 30 min.
      NOTE: A prewarmed support rack at 37 °C is helpful to accelerate the warming of the 96-well plate.
   9. Remove the plate from the incubator and add 100 μL of the adapted CM to each well as indicated for each treatment condition.
   10. Try to avoid creating any bubbles in the wells. A reverse-pipetting technique may be helpful here. Alternatively, remove bubbles with a syringe needle.
   11. Place the plate into the adapted rack in the video microscope.
   12. To improve the image quality, allow the plate to warm for at least 15 min before the first scan to avoid condensation on the lower side of the plate.
   13. Program the schedule of scans, using the video microscope software at one image per well, in the Scratch Wound scan mode. A maximum 2-h interval in required for an invasion-migration experiment. If the objective of the experiment is to produce a video, an interval of 30 min maximum is preferred.
   14. At the end of the experiment, wash the wounding device carefully and follow each of the four washing steps indicated by the manufacturer.

Days 3, 4, and 5

4. Analysis of cell invasion using a video microscope.
   1. Repeat step 2.3.

Results

We report here two different methods to analyze cell invasion and migration. Figure 1 shows the Boyden chamber experiment. The inserts are placed into a companion plate with chemoattractant medium, and the cells are seeded in CM. The membrane can be uncoated (migration assay) or coated (invasion assay). Cells are seeded into the upper chamber in s-CM. The lower chamber is filled with CM as a chemoattractant. The cells are fixed before the doubling time.

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Discussion

We report here two different modalities to study the cell invasion and migration process. The analysis of this process is important to understanding the factors involved in metastatic recurrence, which might be explained by increased motility of a subpopulation of cancer cells called cancer stem cells^10,11.

The Boyden chamber experiment is one the most frequently used techniques to explore cell invasion and migration. One advantage of ...

Materials

Name	Company	Catalog Number	Comments
Fetal Calf Serum Gold	GE Healthcare	A15-151
Hydrocortisone water soluble	Sigma-Aldrich	H0396-100MG
Penicillin/Streptomycin 100 X	Dominique Dutscher	L0022-100
DMEM	Gibco	61965-026
F12 Nut Mix (1X) + GlutaMAX-I	Gibco	31765-027
EGF	Promega	G5021	The solution must be prepared just before use because it is very unstable
Z1 coulter particle	Beckman Coulter	6605698
Optical microscope	Olympus	CKX31
SQ20B cell line	Gift from the John Little’s Laboratory	-
Wound Maker	Essen Bioscience	4494	Store in safe and dry place
96-well ImageLock Plate	Essen Bioscience	4379
CoolBox 96F System with CoolSink 96F	Essen Bioscience	1500-0078-A00
CoolBox with M30 System	Essen Bioscience	1500-0078-A00
Boyden Insert	Dominique Dutcher	353097
Boyden Coated Insert	Dominique Dutcher	354483	Store at -20 °C
Companion 24-well Plate	Dominique Dutcher	353504
BD Matrigel standard	BD BioScience	BD 354234	Store at -20°C.
RAL 555 Staining Kit	RAL Diagnostics	361550	Store in safe and dry place
Microcentrifuge tubes	Eppendorf	33511