IDG-SW3 Cell Culture in a Three-Dimensional Extracellular Matrix

Podsumowanie

Here, we present a protocol for culturing IDG-SW3 cells in a three-dimensional (3D) extracellular matrix.

Streszczenie

Osteocytes are considered to be nonproliferative cells that are terminally differentiated from osteoblasts. Osteoblasts embedded in the bone extracellular matrix (osteoid) express the Pdpn gene to form cellular dendrites and transform into preosteocytes. Later, preosteocytes express the Dmp1 gene to promote matrix mineralization and thereby transform into mature osteocytes.This process is called osteocytogenesis. IDG-SW3 is a well-known cell line for in vitro studies of osteocytogenesis. Many previous methods have used collagen I as the main or the only component of the culturing matrix. However, in addition to collagen I, the osteoid also contains a ground substance, which is an important component in promoting cellular growth, adhesion, and migration. In addition, the matrix substance is transparent, which increases the transparency of the collagen I-formed gel and, thus, aids the exploration of dendrite formation through imaging techniques. Thus, this paper details a protocol to establish a 3D gel using an extracellular matrix along with collagen I for IDG-SW3 survival. In this work, dendrite formation and gene expression were analyzed during osteocytogenesis. After 7 days of osteogenic culture, an extensive dendrite network was clearly observed under a fluorescence confocal microscope. Real-time PCR showed that the mRNA levels of Pdpn and Dmp1 continually increased for 3 weeks. At week 4, the stereomicroscope revealed an opaque gel filled with mineral particles, consistent with the X-ray fluorescence (XRF) assay. These results indicate that this culture matrix successfully facilitates the transition from osteoblasts to mature osteocytes.

Wprowadzenie

Osteocytes are terminally differentiated cells derived from osteoblasts^1,2. Once the osteoblast is buried by the osteoid, it undergoes osteocytogenesis and expresses the Pdpn gene to form preosteocytes, the Dmp1^{gene to mineralize the osteoid, and the} Sost and Fgf23 genes to function as a mature osteocyte in bone tissue³. Here, a 3D culturing system is introduced to identify dendrite extension and marker gene expression in the osteocytogenesis process.

IDG-SW3 cells are an immortalized primary cell line derived from transgenic mice and can expand or replicate osteoblast to late osteocyte differentiation when cultured in different media⁴. Compared with MLO-A5, MLO-Y4, and other cell lines, the expression profile of functional proteins, the ability to perform calcium salt deposition, and the responses to various hormones in IDG-SW3 cells are more likely to be the same as those of primary osteocytes in the bone tissue⁴.

Compared to 2D systems, 3D culturing systems are more capable of mimicking the in vivo cellular growth environment, including the nutrient gradient, low mechanical stiffness, and surrounding mechanical range (Table 1). Most of the previous methods for culturing osteoblastic cells in a 3D system used collagen I as the unique component in formulations^4,5,6, because collagen I fibers serve as the site of calcium and phosphorus deposition. However, an indispensable constituent in the osteoid, the extracellular matrix, contains a large group of cellular factors that promote cellular growth, adhesion, and migration^7,8 and is transparent and convenient for imaging observation. Thus, this protocol uses Matrigel (hereafter referred to as basement membrane matrix) as a secondary component for the osteocytogenesis study.

Protokół

This protocol is suitable for culturing cells in four wells of 24-well plates. If preparing multiple samples or plates, the amounts of the reagents should be increased accordingly.

1. Preparation of the collagen I mixture

NOTE: Collagen I and basement membrane matrix gel quickly at room temperature. Therefore, collagen should be handled on ice (2 °C to 8 °C). All the tips and tubes used must be prechilled unless otherwise indicated. All the procedures should be performed in a safety hood.

1. Place all the reagents and centrifuge tubes on ice.
2. Slowly pipette 0.48 mL of collagen I (5 mg/mL) and 0.1 mL of 10x minimum essential medium (MEM) (with phenol red) into a sterile 15 mL centrifuge tube kept on ice. Mix well by pipetting up and down gently.
3. According to the color palette of the phenol red indicator, use an appropriate volume of 7.5% (w/v) NaHCO₃ (approximately 0.2 mL) to adjust the phenol red indicator to orange, which indicates that the pH value is in the range of 7.0-7.4.
   NOTE: Depending on the pH of the medium, a volume of NaHCO₃ is used to bring the pH to approximately 7.0-7.4. Additionally, NaOH is used for pH neutralization.
4. Bring the final volume of the mixture up to 1 mL by adding an appropriate volume of ddH₂O. Mix well by pipetting gently up and down to prepare for use.
   ​NOTE: The final volume of ddH₂O will depend on the amount of NaHCO₃ or NaOH used in step 1.3.

2. Preparation of the cell-matrix mixture

1. Slowly pipette 0.9 mL of basement membrane matrix into a new 15 mL centrifuge tube on the ice.
2. Culture the IDG-SW3 cells in a T25 flask with 4 mL of complete medium (alpha-MEM containing 10% fetal bovine serum [FBS]) supplemented with 50 U/mL INF-γ at 33 °C.
3. Once the IDG-SW3 cells reach 90% confluency, remove the medium, and wash the cells with phosphate-buffered saline (PBS, pH 7.4 throughout the protocol) with a pipette. Digest the cells with 0.5 mL of 0.25% trypsin-ethylenediaminetetraacetic acid (EDTA) at 37 °C for 30 s.
4. Inactivate the trypsin by adding 3.5 mL of complete medium (alpha-MEM containing 10% fetal bovine serum [FBS]). Transfer the 4 mL cell suspension to a 15 mL centrifuge tube.
5. Spin down the cell suspension at 300 × g for 5 min at 4 °C. Discard the supernatant and resuspend the cell pellet in 1 mL of the complete medium on ice.
6. Count the cells using a hemocytometer and adjust the final cell density with the complete medium to 4 × 10⁵ cells/mL. Add 0.1 mL of the prepared cell suspension to 0.9 mL of the extracellular matrix from step 2.1. Mix well by pipetting gently up and down.
   NOTE: If a cell-free control is needed, add 0.1 mL of the complete medium to 0.9 mL of extracellular matrix as a negative control.

3. Plating the cell-gel mixture

1. Gently, mix well the two mixtures from step 2.6 and step 1.4 to 2 mL by pipetting up and down on the ice. Pipette 0.5 mL of the final mixture into each well (four wells of a 24-well plate). Incubate at 37 °C for 1 h to form a cell-gel mixture.
2. Add 0.5 mL of osteogenic medium (complete medium containing 50 µg/mL ascorbic acid and 4 mM β-glycerophosphate, also known as osteogenic induction medium)⁴ to the cell-gel mixture in each well to start the osteogenic differentiation at 37 °C. Consider this as Day 0.
3. Every 2 days, replace half the medium with fresh osteogenic medium maintained at 37 °C. Continue the culturing for 35 days.

4. Identifying the cell viability and cellular dendrites using a confocal microscope

1. Cell staining
   NOTE: Calcein acetoxymethyl ester (calcein AM) is a cell-permeant dye that can be used to determine cell viability. Ethidium homodimer-I (EthD-1) does not cross the membrane of intact/viable cells⁹. Thus, calcein AM/EthD-1 can be used to identify cell viability and cellular dendrites.
   1. On Day 1 and Day 7 of the culture, remove the calcein AM stock solution (4 mM in DMSO) and EthD-1 stock solution (2 mM in DMSO/H₂O 1:4 [v/v]) from the freezer, and allow them to warm to room temperature.
      NOTE: The mineralized matrix has a strong autofluorescence signal, so the preosteocyte stage without Dmp1 expression within 7 days of culturing⁴ is more suitable for the observation of cell staining.
   2. Add 4 µL of the 2 mM EthD-1 stock solution and 5 µL of the 4 mM calcein AM stock solution to 2 mL of Dulbecco's phosphate-buffered saline (D-PBS), and mix well. This gives approximately 2 µM calcein AM and 4 µM EthD-1 as working solutions.
   3. Pipette 0.5 mL of the working solution into the wells in the 24-well plate. Incubate for 30-45 min at room temperature to stain the cell-gel matrix.
   4. After incubation, add approximately 0.5 mL of fresh D-PBS to a new 35 mm glass-bottom culture dish. Cover the dish to prevent contamination or drying of the samples.
   5. Using elbow-tipped forceps, carefully transfer the stained cell-gel matrix from step 4.1.3 into the 35 mm culture dish from step 4.1.4. Avoid damaging or shearing the cell-gel matrix.
   6. View the labeled cells under a laser confocal fluorescence microscope.
2. Microscope scanning set
   1. Place the 35 mm dish on the stage. Select the regions of the cell-gel matrix to be scanned through the eyepiece using a 10x objective. Higher-magnification objectives are not recommended due to the size of the extended dendrites.
   2. Select the optical filters. Calcein can be viewed as green with a standard fluorescein bandpass filter, and EthD-1 can be viewed as red with filters for propidium iodide or Texas Red dye. Select the "line mode" for scanning and set the "pinhole" to 2 µm.
   3. Select a data depth of 8 bit data depth and an image resolution of 1,024 pixels x 1,024 pixels.
   4. Image using sequential line scanning with the optimal laser and detector settings (keep a minimal laser energy to avoid potential photobleaching).
      NOTE: The optimal detector setting depends on the final fluorescence signals.
3. Collecting a "z-stack" of images
   1. According to the green channel signal, define the top and bottom positions of the cell-gel matrix to be scanned by focusing through the sample while continuously scanning, .
   2. Once the top and bottom of the sample have been specified, select the desired scanning frame. Start scanning. The sample will be scanned from the top to the bottom with the selected settings from step 4.2, generating a gallery of images.
4. Cell viability identification.
   1. Select one slice from step 4.3. The green and red channels indicate live and dead cells, respectively.
5. Cell dendrite identification.
   1. Select the single green channel to generate 3D reconstructions with the image acquisition software. The depth information is displayed as a series of rainbow pseudocolor images. The dendrites located at the bottom of the gel are displayed in red, whereas those at the top are displayed in blue.

5. Identifying appearance using a stereomicroscope

1. On Day 1, Day 7, Day 21, and Day 35 of the culture, remove the culturing medium, and wash the gels in the plate twice with D-PBS. Add 0.5 mL of 4% (v/v) paraformaldehyde in D-PBS to the well to fix the cell-gel matrix in the plate for 10 min at room temperature.
2. Remove the paraformaldehyde in the well and wash the cell-gel matrix two more times with D-PBS in the plate. Leave 0.5 mL of D-PBS in each well for imaging.
3. Place the plate on the stage and select the optimal position through the eyepiece using a 0.5x objective. Image the full-field view of the cell-gel matrix in the plate individually using "automatic exposure" under the bright field.

6. Identifying mineral deposition with an XRF assay

1. On Day 35 of the culture, check whether the liquid nitrogen is sufficient. Start the XRF system. Open the sample room and transfer the gels with elbow-tipped forceps from the plate to the middle of the sample stage of the instrument. Close the sample room and wait for 30 min to allow the instrument to cool before use.
2. Set the "Exposure time" to 35 ms, the "Spectrum range" to 0-40 keV, and the "Electric current" to 770 µA for acquisition setup.
3. Choose three to five scanning sites for analysis by moving the sample stage.
4. Select the elements (Ca and P) for detection. Start the detection and export the results.
   ​NOTE: Ca and P are the most abundant elements in hydroxyapatite.

7. Identifying functional gene expression

1. On Day 1, Day 7, Day 21, Day 28, and Day 35 of the culture, remove the culturing medium and wash the cell-gel matrix twice with ice-cold D-PBS in the plate.
2. Transfer the gels with elbow-tipped forceps from the plate to a 2.0 mL tube (according to the culture time, the cell-gel matrix will gradually shrink to approximately 0.1 mL on Day 35). Make sure one gel is placed in one tube. Add 1 mL of phenol-chloroform and two sterile stainless-steel beating beads (4 mm, as a lysing matrix) into each tube. Place the tubes symmetrically into the prechilled sample slot of the mechanical beating homogenizer.
3. Set the beating to a frequency of 55 Hz and an amplitude of 1 cm in each 1 min of mechanical beating with a 10 s pause, with six cycles in total. Start the bead-beating.
4. Extract the total RNA from the cell-gel matrix using the phenol-chloroform-isoamylachohol method. Reverse-transcribe 2 µg of total RNA to cDNA with random hexamer primers.
5. Design primers targeting β-actin, Pdpn, Dmp1, Sost, and Fgf23 for real-time PCR (Table 2). β-Actin is the housekeeping gene used for normalization. The Pdpn¹⁰ and Dmp1¹¹ genes are mainly expressed in pre-osteocytes and mineralized osteocytes, whereas Sost¹² and Fgf23¹³ are mainly expressed in mature osteocytes.
6. Place the tube on a thermocycler with the heated lid set to 105 °C and perform PCR amplification using the following PCR cycling settings: 95 °C for 5 s and 60 °C for 30 s for 35 cycles with an initial denaturation step at 95 °C for 5 min and a final extension step at 60 °C for 30 s. Analyze the fold changes with the ΔΔCt method.

Wyniki

After live/dead cell staining, the cells were visualized using a confocal laser microscope. All the cells were calcein AM-positive (green color), and there were almost no EthD-1-positive cells (red color) in the field, indicating that the gel system made by this method is highly suitable for osteocytogenesis (Figure 1A, left). To better determine the spatial distribution of the cells, a pseudocolor image was chosen to display the cell dendrites at different depths of the gel; red shows the d...

Dyskusje

A critical point in this protocol is that steps 1 and step 2 must be performed on ice to prevent spontaneous coagulation. In this method, the final concentration of collagen I was 1.2 mg/mL. Thus, an optimal ddH₂O volume should be calculated to match the different collagens from various manufacturers.

In vivo, osteocytogenesis involves a polar movement of osteoblasts from the surface to the interior of trabecular bone¹⁴. This protocol frees cells fro...

Materiały

Name	Company	Catalog Number	Comments
0.25% Trypsin-ethylenediaminetetraacetic acid	Hyclone	SH30042.01
15 mL tubes	Corning, NY, USA	430791
7.5% (w/v) Sodium bicarbonate	Sigma-Aldrich, MO, USA	S8761
ascorbic acid	Sigma-Aldrich, MO, USA	A4544
Collagen I	Thermo Fisher Scientific	A10483-01
fetal bovine serum	Thermo Fisher Scientific	10099141
homogenizer	BiHeng  Biotechnology, Shanghai, China	SKSI
laser confocal fluorescence microscopy	Carl Zeiss, Oberkochen, Germany	LSM 800
Live/Dead Cell Imaging kit	Thermo Fisher Scientific	R37601
Matrigel matrix	Corning, NY, USA	356234
MEM (10X), no glutamine	Thermo Fisher Scientific	21430079
paraformaldehyde	Sigma-Aldrich, MO, USA	158127
phosphate buffered saline	Hyclone	SH30256.FS
stereo microscope	Carl Zeiss, Oberkochen, Germany	Zeiss Axio ZOOM.V16
Trizol	Thermo Fisher Scientific	15596026
X-ray fluorescence	EDAX, USA	EAGLE III
β-glycerophosphate	Sigma-Aldrich, MO, USA	G9422