A 3D Spheroid Model for Glioblastoma

Podsumowanie

Here, we describe an easy-to-use invasion assay for glioblastoma. This assay is suitable for glioblastoma stem-like cells. A Fiji macro for easy quantification of invasion, migration, and proliferation is also described.

Streszczenie

Two-dimensional (2D) cell cultures do not mimic in vivo tumor growth satisfactorily. Therefore, three-dimensional (3D) culture spheroid models were developed. These models may be particularly important in the field of neuro-oncology. Indeed, brain tumors have the tendency to invade the healthy brain environment. We describe herein an ideal 3D glioblastoma spheroid-based assay that we developed to study tumor invasion. We provide all technical details and analytical tools to successfully perform this assay.

Wprowadzenie

In most studies using primary or commercially available cell lines, assays are performed on cells grown on plastic surfaces as monolayer cultures. Managing cell culture in 2D represents disadvantages, as it does not mimic an in vivo 3D cell environment. In 2D cultures, the entire cell surface is directly in contact with the medium, altering cell growth and modifying drug availability. Furthermore, the nonphysiological plastic surface triggers cell differentiation¹. Three-dimensional culture models have been developed to overcome these difficulties. They have the advantage of mimicking the multicellular architecture and heterogeneity of tumors², and thus could be considered to be a more relevant model for solid tumors³. The complex morphology of spheroids contributes to better evaluate drug penetrance and resistance⁴. The tumor heterogeneity in the spheroid impacts the diffusion of oxygen and nutrients, and the response to pharmacological agents (Figure 1A). Diffusion of oxygen is altered when the spheroid size reaches 300 µm, inducing a hypoxic environment in the center of the spheroid (Figure 1A,C). Metabolites are also less penetrating through the cell layers and compensating metabolic reactions take place⁵. When the diameter of the spheroid increases, necrotic cores can be observed, further mimicking characteristics found in many solid cancers, including the aggressive brain cancer glioblastoma (GBM)⁶.

Several 2D or 3D invasion assays for glioblastoma have been reported in the literature^7,8. Two-dimensional assays are mainly for studying invasion in a horizontal plane on a thin matrix layer or in a Boyden chamber assay⁹. Three-dimensional assays have been described with 3D spheroid cultures using classical glioblastoma cell lines¹⁰. More complex variants are represented by invasion of brain organoids by tumor spheroids in confrontation cultures¹¹. However, it is still important to develop an easy-to-use and reproducible assay available to any laboratory. We have developed a protocol to generate glioblastoma stem-like cells from patient samples. The quantification of these assays is easily manageable and only requires open-access online software. Briefly, tumor pieces are cut into small pieces and enzymatically digested. Single cells derived from the digestion are cultivated in neurobasal medium. After 4-7 days, spheroid structures form spontaneously. Upon intracranial implantation in mice models, they form tumors exhibiting a necrotic core surrounded by pseudo-palisading cells¹². This closely resembles the characteristics found in GBM patients.

In this article, we describe our protocol to produce spheroids from a determined number of cells to ensure reproducibility. Two complementary matrices can be used for this purpose: Matrigel and collagen type I. Matrigel is enriched in growth factors and mimics the mammalian basal membrane required for cell attachment and migration. On the other hand, collagen type I, a structural element of stroma, is the most common fibrillary extracellular matrix and is used in cell invasion assays. Herein, we illustrate our GBM spheroid model by performing migration and proliferation assays. Analysis was done not only at fixed time points but also by monitoring spheroid expansion and cell movement by live imaging. Furthermore, electron microscopy was done to visualize morphological details.

Protokół

Informed written consent was obtained from all patients (from the Haukeland Hospital, Bergen, Norway according to local ethics committee regulations). Our protocol follows the guidelines of our institution’s human research ethics committee. 

1. Generation of uniform size tumor spheroids

NOTE: Stem-like cells are cultured in neurobasal medium complemented with B27 supplement, heparin, FGF-2, penicillin, and streptomycin, as described in previous articles¹². These cells spontaneously form spheroids in culture.

1. Wash the tumor cells with 5 mL phosphate-buffered saline (PBS) and incubate the cells with 0.5-1 mL dissociation enzyme (see Table of Materials) for 5 minutes at 37 °C.
2. Wash with 4-4.5 mL PBS and add 10 mL of the complete growth medium (complete neurobasal medium, cNBM).
3. Count the cells using an automatic counting technique with trypan blue and a cell counting chamber slide.
4. To generate 100 spheroids with 10⁴ cells per spheroid (according to preferred size), mix 10⁶ cells in 8 mL of NBM with 2 mL of 2% methylcellulose.
5. Transfer the suspension to a sterile system container and dispense 100 µL/well with a multichannel pipette into a 96 well round bottom plate.
6. Incubate the plate at 37 °C, 5% CO₂ and 95% humidity. Equal sized spheroids will form and can be used after 3-4 days.

2. Three-dimensional experiments

1. Proliferation
   1. Preparation
      1. Suspend inhibitors (e.g., rotenone as in Figure 4A) and chemicals in 100 µL of medium and add to the 100 µL of medium in each well (i.e., one spheroid per well).
      2. Incubate the plate at 37 °C, 5% CO₂, and 95% humidity.
   2. Image acquisition and analysis
      1. Take pictures with a video microscope in brightfield to create a series of conditions at T₀ and the following times expected.
      2. Use Fiji to analyze pictures either manually or in a semiautomated manner. To do so manually, draw a circle around the spheroid core with the freehand selection tool and measure the area of each spheroid. To analyze the images in a semiautomated manner, use the macro shown in Supplementary Document 1 with //Core Area only.
2. Invasion
   1. Preparation
      1. Prepare the collagen matrix in a tube on ice with type I collagen at 1 mg/mL final concentration, 1x PBS, 0.023xV_collagen, 1 M sodium hydroxide, and sterile H₂O. Incubate the solution on ice for 30 min.
      2. Collect spheroids from the round bottom well plate in 500 µL tubes and wash 2x with 200 µL 1x PBS.
      3. Pipette the spheroids carefully into 100 µL of the collagen matrix and insert in the center of a well in normal 96 well plates.
      4. Incubate the collagen gel for 30 min at 37 °C and then add cNBM on top of the gel. Inhibitors or activators (e.g., hydrogen chloride as shown in Figure 4B, 4C) can be added to the medium at this step.
   2. Image acquisition and analysis
      1. Take pictures sequentially with a video microscope in brightfield mode 24 h after collagen inclusion.
      2. Use Fiji to analyze pictures either manually or in a semiautomated manner. To do so manually, draw around the core and the total area of the spheroid with the freehand selection tool and measure the invasive area of each spheroid by subtract total area with core area. To analyze the images in a semiautomated manner, use the macro as indicated in Supplementary Document 1 to determine the invasive area.
3. Migration
   1. Preparation
      1. Coat a 6 well plate with Matrigel (0.2 mg/mL) in NBM for 30 min at 37 °C, then remove the Matrigel and add 2 mL of cNBM.
      2. Transfer spheroids into 50 µL of cNBM from the round bottom well plate to the 6 well plate.
      3. Incubate the plate at 37 °C and wait 30 min for the spheroids to adhere.
      4. After 24 h of incubation, stain with 10 ng/mL of Hoechst and incubate 30 min at 37 °C.
   2. Image acquisition and analysis
      1. Obtain images using a video microscope in brightfield. A 405 nm laser is used for visualization of Hoechst staining.
      2. Use Fiji software to analyze pictures and run the macro as indicated in Supplementary Document 1.
         NOTE: Touching the bottom of the well or completely removing the supernatant damages the spheroids. For collagen type I gel handling, keep the gel on ice to avoid collagen polymerization, do not add an acidic component because the change in pH will affect the compactness of the gel, and pipette cells rapidly into the collagen to prevent cell death and the degradation of the gel.

3. Fiji Macro

NOTE: Fiji is an image analysis program developed in the public domain that allows the development of macros to speed up image analysis. Manual analysis is also possible, but this is a slow process and may introduce biases. Images can be imported by drag-and-drop in the software and quantified with the ROI Manager Tools plugin. The procedure used in this study is described below:

1. Open the macro window: Plugins | Macros | Interactive Interpreter.
2. Copy and paste the following adapted purple loop. Keep the purple sentences and add the green sentences of interest (Supplementary Document 1).
3. To analyze the entire series, adjust the parameters in red for a specific quantification and run the macro using Macros | Run Macro or pressing Ctrl+R.
4. Check and, if necessary, manually adapt the region of interest (ROI).

4. Electron microscopy of spheroids

NOTE: Most of the following steps must be done in a chemical hood.

1. Fixation step
   1. Collect the spheroid with a cut pipette tip, put it in a 1.5 mL tube, and wash 1x with 0.1 M phosphate buffer (PB).
   2. Fix the spheroid overnight at 4 °C in 2% glutaraldehyde/2% paraformaldehyde (PFA) in 0.1 M PB.
   3. Replace the fixation solution with a solution of 1% PFA in 0.1 M PB followed by sample preparation.
2. Sample preparation
   1. Transfer the spheroids into a strainer and put them in a glass beaker in order to avoid spheroid damage.
   2. Carefully wash 3x with 0.1 M PB.
   3. Incubate with osmium for 2 h in the dark. Dilute osmium to 4% in 1% 0.1 M PB buffer.
   4. Carefully wash 3x with 0.1 M PB.
      1. Dehydrate as follows: soak in 50% ethanol for 10 min, 70% ethanol for 10 min, 2x 90% ethanol for 15 min, 2x 100% ethanol for 20 min, and 2x acetone for 30 min.
   5. Incubate the samples in a 50/50 mixture of acetone/resin for 2 h. During this step, prepare the EPON resin (Embed-812: 11.25 g; DDSA: 9 g; NMA: 4.5 g).
   6. Discard the acetone/resin mixture, replace with freshly prepared resin and incubate overnight.
   7. Replace the resin by a new one and incubate between 2-6 h.
   8. Add the spheroids in resin into a mold at 60 °C for 48-72 h.

Wyniki

Spheroids were prepared as described in the protocols section and observations were made regarding migration, invasion, proliferation, and microscopy. To measure hypoxia in distinct areas of the spherical structure, carboxic anhydrase IX staining was used for determining hypoxic activity (Figure 1A-C). More CAIX-positive cells were observed in the spheroid center (Figure 1A-C). Hypoxic cells loca...

Dyskusje

Tumor spheroid assays are well adapted to study tumor characteristics including proliferation, invasion, and migration, as well as cell death and drug response. Cancer cells invade the 3D matrix forming an invasive microtumor, as seen in Figure 4B,C. During the invasive process, matrix metalloproteinases (MMP) digest matrices surrounding tumor cells¹³, and MMP inhibitors (e.g., GM6001 or Rebimastat) may impair cell invasion but not migration

Materiały

Name	Company	Catalog Number	Comments
96 well round-bottom plate	Falcon	08-772-212
Accutase	Gibco	A11105-01	Stored at 4 °C, sphere dissociation enzyme
B27	Gibco	12587	Stored at -20 °C, defrost before use
Basic Fibroblast Growth Factor	Peprotech	100-18B	Stored at -20 °C, defrost before use
Countess Cell Counting Chamber Slides	Invitrogen	C10283
DPBS 10X	Pan Biotech	P04-53-500	Stored at 4 °C
Fiji software	ImageJ		Used to analyze pictures
Flask 75 cm2	Falcon	10497302
Matrigel	Corning	354230	Stored at -20 °C, diluted to a final concentration of 0.2 mg/mL in cold NBM
Methylcellulose	Sigma	M0512	Diluted in NBM for a 2% final concentration
NBM	Gibco	21103-049	Stored at 4 °C
Neurobasal medium	Gibco	21103049	Stored at 4 °C
Penicillin - Streptomycin	Gibco	15140-122	Stored at 4 °C
Trypan blue 0.4%	ThermoFisher	T10282	Used to cell counting
Type I Collagen	Corning	354236	Stored at 4 °C