Isolation of Monocyte-Macrophage Lineage Cells from Rat Bones by Secondary Adherence Method

Podsumowanie

Here we present a protocol for the isolation of BMMs from SD rats, called the secondary adherence method.

Streszczenie

With a decrease of bone mineral density, bones are more likely to fracture, thus negatively affecting a patient's quality of life. The growth and development of bones are mainly regulated by osteoblasts and osteoclasts. It has been widely accepted that osteoclasts are derived from bone marrow monocyte-macrophage cells (BMMs). BMMs and other hematopoietic stem cells are located in the bone marrow cavity. Therefore, isolating single stable BMMs from different and heterogeneous cell populations is a huge challenge. Here we present a protocol for the isolation of BMMs from SD rats, called the secondary adherence method. Adherent cells cultured for 24-48 h in primary culture were collected. Flow cytometric analysis showed that approximately 37.94% of the cells were CD11b/c+ (monocyte-macrophage surface antigen). Tartrate resistant acid phosphatase (TRAP) staining and western blot analysis demonstrated that BMMs could differentiate into osteoclasts in vitro. The above findings suggested that the secondary adherence cells could be considered as a suitable cellular model for osteoclast differentiation research.

Wprowadzenie

It has been reported that monocyte-macrophage lineage cells existing in the bone marrow can differentiate into blood monocytes and tissue macrophages^1,2. The above cells, which can differentiate into osteoclasts to balance bone growth and development, are commonly used as a cell model to induce osteoclasts in vivo^3,4. Bone marrow is a special tissue containing several different types of cells, which include but are not only limited to bone marrow mesenchymal stem cells, bone marrow monocyte-macrophage cells (BMMs), hematopoietic stem cells, endothelial cells, and immune cells. In fact, several previous studies suggested that adherent cells rushed out of the bone marrow cavity of the long bone could differentiate into osteoblasts, osteoclasts, chondrocytes, or adipocytes^5,6,7,8. Although, different isolation and culture methods have been used to produce different homogeneous cell populations, there are still great challenges in isolating and culturing BMMs from a variety of different cell types.

Several methods have been developed to extract bone marrow mononuclear macrophages (BMSCs). However, the majority of these methods are complex^9,10,11. For example, density gradient centrifugation requires a specialized kit and the operation is time-consuming and cumbersome. This method is suitable for the isolation of BMMs from high-volume blood samples, but not from bone marrow samples^9,12,13. In addition, extracting tissue samples using collagenase digestion is a complex and time-consuming procedure; this method is not recommended for the isolation of BMMs from bone marrow samples^14,15. In addition, although flow separation can result in highly purified monocyte/macrophage populations, it requires very large sample sizes and high instrument and equipment requirements^10,16. Additionally, the microbead enrichment method is extremely expensive and is not feasible in a general laboratory¹⁷.

Therefore, in the current study a convenient, fast, and cheap method was proposed for the isolation of mononuclear macrophages from the bone marrow. Bone marrow cells adhered for different time points were used to isolate BMMs using a secondary adherence method. BMMs extracted with the above method could induce the formation of osteoclasts in vitro, thus providing a simple and convenient cell model for the future study of osteoporosis in vitro.

Protokół

All experiments in this study were conducted in accordance with the animal experiment guidelines of the Zhejiang Chinese Medical University Laboratory Animal Research Center (Approval No: IACUC-20181029-11).

1. Cell extraction

1. Put the Sprague-Dawley rats (SD rats, 1-10 days old, male or female) in the euthanasia cages filled with CO₂ at a balanced rate of 30%-70% container volume/minute. After the rats lose consciousness (20-60 min), euthanize the rat by cervical dislocation to ensure a painless death.
2. Immerse the rats in 75% alcohol for 10 min for disinfection.
3. Carefully remove all the limbs of the rat with scissors and forceps, aspirate with PBS using a pipette and flush the blood adhering to the limbs.
4. Add 5 mL of penicillin/streptomycin solution into 500 mL of DMEM and mix well. Take a 50 mL sterile centrifuge tube, add 5 mL of FBS and 45 mL of DMEM medium, and mix thoroughly to obtain a 10% FBS DMEM containing 1% penicillin/streptomycin solution. Add 2 mL of the above culture medium into a 5 mL tube.
5. Transfer the limb bones into the 5 mL tube. Use scissors to cut the limb bones in the tube into small pieces (1-3 mm) and mix the homogenate to re-suspend the bone marrow cells into the culture medium. Stand for 5 min until the tissue fragments settled to the bottom of the tube.
6. Add 10 mL of 10% FBS DMEM into a 100 mm culture dish, and then transfer the supernatant into the culture dish. When aspirating the supernatant, avoid transferring the tissue debris into the culture dish.
7. Incubate at 37 °C and 5% CO₂ for approximately 24 h. After this incubation time, the majority of mesenchymal stem cells will adhere to the culture dish wall and grow slowly, while most BMMs will still be suspended in the culture medium.
8. Transfer the cell suspension in the 100 mm culture dish to a new 25 cm² flask and continue to cultivate the cells at 37 °C and 5% CO₂ for an additional 24 h. BMMs will adhere to the flask wall at 24-48 h of culture. Remove the old medium carefully and replace with fresh medium after BMMs have adhered to the flask wall.
9. Sub-culture when the cells in the flask reached 80%-90% confluency.
   ​NOTE: All the cells were cultured at 37 °C and 5% CO₂. During culture, the cell morphology was gradually unified. Cells were large, irregularly shaped, radially growing and attached to the flask in a form of disc, where multiple nuclei could be observed.

2. FACS staining of the cell

1. Trypsin digest using 1-2 mL of commercial trypsin at 37 °C and 5% CO₂ for 5 min and count secondary adherent cells to ensure a final cell count of 100,000/sample (count cells with Neubauer hemocytometer).
2. Divide the cells into three groups (500 µL of PBS contains 100,000 cells): (1) the blank control group containing unstained cells; (2) the isotype control group; and (3) the experimental group (CD11b/c staining).
3. Incubate primary antibodies (no antibody for the blank control group; anti-CD11 isotype control for the isotype control group, 0.6 µL of antibody/sample, 1 µg/sample; anti-CD11b/c for the experimental group, 1 µL of antibody/sample, 1 µg/sample) on ice for 30 min.
4. Centrifuge at 300-350 x g for 5 min, discard the supernatant, and resuspend the cells with 500 µL of PBS. Repeat the above procedure once to ensure that the unbound primary antibodies are washed away.
5. Incubate the corresponding secondary antibody (no antibody for the blank control group; goat anti-rabbit IgG for the isotype control and the experimental groups, 0.25 µL antibody/sample, 1:2,000) on ice in the dark for 30 min.
6. Centrifuge at 300-350 x g for 5 min, discard the supernatant, and resuspend the cells with 500 µL of PBS. Repeat the above procedure once to ensure that the unbound second antibodies are washed away.
7. Detect the CD11b/c positive cells by flow cytometry (10,000 cells/sample) and analyze the data by software (e.g., FlowJo 7.5).
   ​NOTE: To obtain the final percentage of CD11b/c+ cells, the following formula was used: Percentage of CD11b / c + cells in the experimental group - the percentage of CD11 + cells in the isotype control group.

3. Wright-Giemsa staining

1. Seed the adherent secondary cells that have been passaged three times onto 35 mm² cell climbing sheets (1 × 10⁶ cells/well) and culture at 37 °C and 5% CO₂ for 24 h.
2. Discard the culture medium and wash thrice with PBS.
3. Add Wright-Giemsa dye solution (0.5 mL-0.8 mL) to the cell climbing sheet for 1 min.
4. Mix the dye with distilled water (0.5 mL-0.8 mL) with a cotton swab, and stand for 10 min.
5. Wash the dye solution with distilled water, and then dry for 1-3 min. Observe under a microscope.

4. TRAP staining

1. Seed the adherent secondary cells that have been passaged three times onto 35 mm² cell climbing sheets (1 × 10⁶ cells/well) and culture at 37 °C and 5% CO₂ for 24 h.
2. Replace the old medium with the 10% FBS DMEM or osteoclast induction medium supplemented with 50 ng/mL receptor activator of nuclear factor-κB ligand (RANKL) and 30 ng/mL of macrophage colony-stimulating factor (M-CSF), and culture at 37 °C and 5% CO₂ for an additional 7 days.
3. Stain the cells with the TRAP staining kit according to manufacturer's protocol and observe under a microscope.
   ​NOTE: TRAP-positive cells were defined as osteoclasts, which were purple under a light microscope. The number of TRAP-positive cells was measured using ImageJ software.

5. Western blot

1. Seed the adherent secondary cells that have been passaged three times on 35 mm² cell climbing sheets (1 × 10⁶ cells/well) and culture for 24 h.
2. Replace the old medium with fresh 10% FBS DMEM or osteoclast induction medium (50 ng/mL of RANKL and 30 ng/mL of M-CSF) and culture for an additional 7 days at 37 °C and 5% CO₂.
3. Extract total cellular proteins with RIPA buffer, separate by 10% SDS-PAGE, and transfer to polyvinylidene fluoride membranes^18,19.
4. Block with 5% skimmilk powder (25 mL) for 2 h and wash three times, for 10 min each time, with TBS-Tween 20 (TBST).
5. Incubate primary antibodies at 4 °C overnight (anti-β-actin, anti-TRAP, and anti-cathepsin K; all primary antibodies were diluted 1:1,000, 10 mL diluted antibody/band), and wash thrice with TBST.
6. Incubate the secondary antibody (goat anti-rabbit IgG, 1:2,000 dilution, 10 mL diluted antibody/band) at room temperature for 2 h, and wash thrice with TBST. Visualize the protein bands using a developing solution.
   NOTE: The expression levels of the above proteins were normalized to β-actin.

Wyniki

The secondary adherent cell population was stable and uniform. With the continuous cell proliferation, the majority of cells became larger, with irregular shape and grew into a radial adherent disk (Figure 2C,D). Flow cytometry showed that the percentage of cells expressing CD11b/c, a molecular marker on the surface of monocyte-macrophage lineage cells, was approximately 37.94% (Figure 2A,B). To ...

Dyskusje

Osteoclasts are one of the most significant cell types involved in the occurrence and development of bone diseases, as well as one of the primary objects of bone disease research²⁰. Monocyte/macrophages can differentiate into osteoclasts. Since mononuclear macrophages (RAW264.7 cells) are too expensive to buy and are easily activated during culture, it is difficult to perform in vitro differentiation experiments using this cell line. Although several methods have been developed for extrac...

Materiały

Name	Company	Catalog Number	Comments
35 mm2 cell climbing slices	NEST Biotechnology	80102
Anti-cathepsin K	Abcam	ab19027	1:1,000
Anti-CD11 isotype control	Abcam	ab172730	1 μg/test,1.675 mg/Ml
Anti-CD11b/c	Absin	abs124232	1μg/test, 1 mg/mL
Anti-TRAP	Abcam	ab191406	1:1,000
Anti-β-actin	Beyotime	AF5003	1:1,000
Cell climbing slices	NEST Biotechnology	80102
Cell culture dish	corning	430167
Cell culture flask	corning	430168
Dulbecco's modified eagle medium (DMEM)	Gibco	C11995500BT
Fetal bovine serum (FBS)	Gibco	10099141C
Goat anti-rabbit IgG	Abcam	ab150077	for IF, 1:2,000
goat anti-rabbit IgG	Abcam	ab6721	for WB, 1:2,000
M-CSF	Pepro tech	400-28
PBS	Biosharp	BL302A
RANKL	Pepro tech	400-30
SD rat	Shanghai SLAC Laboratory Animal Co, Ltd		1-10 days old
SDS-PAGE gel preparation kit	Solarbio	P1200
TRAP/ALP Staining Kit	Wako	294-67001
Trypsin-EDTA solution	Biosharp	BL512A
Wright-Giemsa solution	Keygen Biotech	KGA225-1