1. Introduction
Canine spontaneous tumours are considered good models for human disease due to their similar morphology and behavior. Canine tumours may represent a better alternative to rodent tumours for studying cancer biology and therapy [1,2].
Osteosarcoma (OSA) is the most common primary malignant bone tumour in dogs [3,4,5], being characterised by a high metastatic potential and poor prognosis [1,6,7]. Most dogs that develop canine OSA die because of lung metastases. Further, the recurrence rate is high and the median survival time ranges from 3 months to 1 year [8,9,10]. Therefore, new treatments are necessary for canine osteosarcomas, and targeted therapies could be adequate options.
In the search for new therapies for cancer, many natural compounds can be found that have the ability to kill cells. The Bacillus anthracis toxin is one of these compounds. However, due to its highly toxic effect on normal cells, the natural anthrax toxin would not be suitable for treating cancers without causing serious adverse effects.
The natural Bacillus anthracis toxin is composed of three parts: the oedema factor (EF), the lethal factor (LF), and the protective antigen (PA). The PA combined with the LF or EF is toxic to cells and may result in death in animals [11,12]. An alternative effector component, FP59, consists of the N-terminal 254 amino acids of LF fused to the catalytic domain of Pseudomonas exotoxin A. FP59 kills cells by inhibiting protein synthesis. The Bacillus anthracis toxin has been modified to specifically target tumour cells that express matrix metalloproteinases (MMPs) and the urokinase plasminogen activator (uPA) [13,14,15,16]. The reengineered toxin consists of the PA variants PA-U2-R200A and PA-L1-I210A, which cause cell death by disruption of the MAP kinase (MAPK) signalling pathway when combined with the LF.
The modified anthrax toxin is cytotoxic to xenografted human melanomas and carcinomas [17,18]. Recently, our group has shown the efficacy of the reengineered anthrax toxin in canine oral mucosal melanomas, where it resulted in decreased tumour growth and stable disease. In addition, tumours had decreased bleeding, and tumour cells and intratumoral endothelial cells were necrotic [19]. Although the reengineered Bacillus anthracis toxin has shown anticancer properties in carcinomas and melanomas, its effects have not been tested in mesenchymal tumours yet. Since osteosarcomas are so prevalent and aggressive in dogs and there are only a few effective treatments, we aimed to investigate if the reengineered anthrax toxin could exert any inhibitory effects on canine osteosarcoma cells in comparison to human osteosarcoma cells. Based on the in vitro inhibitory effects of this reengineered toxin on canine osteosarcoma cells, further studies will be proposed to investigate if it could be used as a novel therapy for osteosarcomas in vivo.
2. Results
2.1. Canine OSA Tissue Has High Expression of uPA and MMPs
Since it is known that uPA and MMPs are overexpressed in a variety of tumour cells and are rarely present in normal cells [20], we first evaluated their expression in a tissue microarray (TMA) containing 22 canine OSA samples. All of the samples were positive for MMP-2, MT1-MMP, uPA H140, and TIMP 2. These results led us to test the effects of reengineered anthrax toxins on canine OSA cells. Since canine tumours in dogs are considered good models for human cancers, we included both dog and human OSA cells in this study. In addition, a normal canine cell osteoblastic cell line, COBS, was also used in order to test the effect of the anthrax toxin on a non-neoplastic cell line.
2.2. OSA Cells Express Tumour Markers
We performed immunofluorescence assays to check the basal expression patterns of tumour markers in canine (D17) and human (MG63) OSA cell lines and a non-neoplastic canine osteoblastic cell line (COBS). The expression of MMP 2 (Figure 1A), uPA (Figure 1B), and MT1-MMP (Figure 1C) has been observed in both canine and human OSA cell lines. MT1-MMP and MMP2 expressions were also seen at lower intensities in COBS cell line (Figure 1D).
Regarding the immunoexpression of uPA (Figure 1B), it is possible to see cytoplasm positivity in both MG63 and D17, but also dot immunostainings in both cells lines, which we considered as indicator of the positivity of uPA in cell membranes. Although no quantification was performed, apparently D17 has more uPA immunostaining dots in the membrane than MG63.
The non-neoplastic canine osteoblastic cell line (COBS) was established in our laboratory after isolation of cells from a fragment of a dog’s bone fracture. This cell line was previously validated in our lab to express bone markers and has low expression of MMP2 and MTI-MMP [21].
2.3. The Reengineered Anthrax Toxin Is More Cytotoxic to OSA Cells Than to COBS Cells
LF and FP59 were applied to canine and human osteosarcoma cells, and it was observed that neither LF or FP59 alone was cytotoxic in all tested cells. Within a certain dose range, the cell viability was comparable to that of untreated cells, confirming that the toxicity was dependent on the other component of the toxin, the native PA.
We also examined the reengineered anthrax toxin in OSA cells. LF plus PA at all concentrations (15, 49, 494, 1571, and 5000 ng/mL PA) caused significant cytotoxicity after 24 h in the canine OSA cell line D17 when compared to untreated cells (Figure 2A). Combination of LF with PA-U2-R200A and PA-L1-I210A also proved to be significantly cytotoxic at all PA concentrations (5, 15, 49, 155, 494, 1571, and 5000 ng/mL PA) in D17 cells (Figure 2B). When we analysed the combinations of FP59 and PA and FP59 and PA-U2-R200A and PA-L1-I210A in D17 cells, we observed statistically significant cytotoxicity at all applied concentrations (1, 3, 10, 31, 99, 314, and 1000 ng/mL PA) when compared to untreated cells (Figure 2C,D).
We further examined the reengineered anthrax toxin in human OSA cell line MG63. The combination of LF and PA at 5, 49, 155, 494, 1571, and 5000 ng/mL PA was significantly cytotoxic in the human OSA cell line MG63 compared to untreated cells (Figure 3A). The combination of LF with PA-U2-R200A and PA-L1-I210A was also significantly cytotoxic; there was a decrease in the optical density at the two highest PA concentrations (1571 and 5000 ng/mL PA) (Figure 3B). When we analysed the combinations of FP59 and PA and FP59 and PA-U2-R200A/PA-L1-I210A in MG63 cells, we observed statistically significant cytotoxicity at all analysed concentrations (1, 3, 10, 31, 99, 314, and 1000 ng/mL PA) (Figure 3C,D).
We next assessed the cytotoxicity of the reengineered toxin with a fixed concentration of LF and different concentrations of PA. After 24 h of treatment with the reengineered anthrax toxin with 49, 155, 494, 1571, and 5000 ng/mL PA, we observed a significant decrease in COBS cell viability compared to untreated cells (0 ng/mL PA) (Figure 4A). Combinations of LF with PA-U2-R200A and PA-L1-I210A at concentrations of 494 and 5000 ng/mL, respectively, were also significantly cytotoxic (Figure 4B). We also analysed the effects of FP59 plus PA in COBS cells. We observed statistically significant cytotoxicity at PA concentrations of 3, 10, 31, 99, 314, and 1000 ng/mL (Figure 4C). Similar to what we observed with the LF, the combination of FP59 and PA-U2-R200A/PA-L1-I210A caused significant cytotoxicity at all applied concentrations (1, 3, 10, 31, 99, 314, and 1000 ng/mL PA) (Figure 4D).
The cell viability upon treating D17, MG63, and COBS with the toxin parts was analysed in accordance to the IC50 (half minimal inhibitory concentration). As can be seen in Table 1, OSA cell lineages MG63 and D17 have IC50 values lower than the normal cell lineage of COBS, except for the value found for the LF + PA treatment, in which MG63 shows a much higher IC50 value. Cell line D17 showed the highest sensitivity to treatment with reengineered anthrax toxins (Figure 5).
The D17, MG63, and COBS values of viability were normalized and are presented in Figure 5.
In Figure 5A, we have the exposure of cells to the LF + PA fraction of the toxin, which is much more toxic to cell lines. We observed that the human osteosarcoma cell line (MG63) was resistant to the toxin in all concentrations in this treatment (LF + PA), except in the highest concentration (5000 ng/mL). The normal canine osteoblastic lineage (COBS) remained constant for almost all treatment concentrations, thus showing resistance to the toxin at different concentrations. The canine osteosarcoma cell line (D17), on the other hand, showed a decline in cell viability from the concentration of 155 ng/mL onwards, showing itself to be the most sensitive strain to treatment with the toxin LF + PA.
Figure 5B shows the exposure of the cells to the LF + PAL/PAU fraction of the reengineered toxin, a therapeutic portion, which was less toxic to the tested cell lines. We observed that the human osteosarcoma cell line (MG63) was sensitive to treatment with the fraction (LF + PAL/PAU) of the reengineered toxin from the concentration of 155 ng/mL onwards. In the normal canine osteoblastic strain (COBS), we observed a small decline in cell viability, but this viability was stable even during exposure to the highest concentrations of the toxin (LF + PAL/PAU). The canine osteosarcoma cell line (D17) was more sensitive in the first concentrations of the toxin LF + PAL/PAU (5, 15 and 49 ng/mL), but from the concentration 155 ng/mL on wards it showed stability in terms of cell viability.
Figure 5C shows the exposure of cells to the FP + PA fraction of the toxin. This modified FP fraction is 50 times more potent than wild LF, which is used to detect the presence of toxin receptors in the strains analyzed. We observed that the human osteosarcoma cell line (MG63) and the canine osteosarcoma cell line (D17) showed great sensitivity from the concentration of 1 ng/mL onwards when treated with the FP + PA fraction of the toxin, thus demonstrating the presence of receptors that respond to the toxin. The same did not happen with normal canine osteoblastic (COBS), which was not as sensitive to this fraction with the lowest concentrations of the toxin; only after the concentration of 10 ng/mL did it begin to decrease its viability.
In Figure 5D, we observe the exposure of cells to the FP + PAL/PAU fraction of the reengineered toxin. This association showed practically the same results as observed with the FP + PA portion. The canine osteosarcoma cell line (D17) was more sensitive than the other two cell lines, MG63 and COBS.
2.4. The Reengineered Anthrax Toxin Causes Cell Death in OSA Cells
Cell cycle analysis indicated that the reengineered anthrax toxin caused apoptosis in the canine OSA cell line D17 (Figure 6) and in the human OSA cell line MG63 (Figure 7), as can be seen in the representative histograms, which revealed the fractional DNA content (sub-G1peak) and S-phase arrest. In contrast, the reengineered toxin caused arrest in the G1 phase in the non-neoplastic canine osteoblastic COBS cell line when analyzing the cell distribution at each phase of the cell cycle, even at the highest concentration (Figure 8).
2.5. The Reengineered Anthrax Toxin Decreased Migration Capacity in OSA Cells
The wound-healing assay was performed to evaluate the cell migration capacity after treatment with the reengineered anthrax toxin. After 24 h of treatment with only the LF portion of the toxin, the canine OSA cell line D17 had good capacity to grow and migrate into the space left by the wound, partially closing it. This response was similar to that observed in control cells (Figure 8). In contrast, after 24 h of treatment with LF + PA-U2-R200A/PA-L1-I210A, D17 cells lost the ability to migrate into the space left by the wound (Figure 9).
The human OSA cell line MG63 had good migratory capacity after 24 h of treatment with only the LF portion of the toxin, partially closing the wound. This was similar to that observed in the control cells (Figure 10). In contrast, after 24 h of treatment with LF + PA-U2-R200A/PA-L1-I210A, MG63 cells had significantly lost the ability to migrate into the space left by the wound (Figure 9).
3. Discussion
Osteosarcomas are aggressive neoplasms in both dogs and humans. In this study, we aimed to test a possible novel targeted therapy for these tumors in vitro. The Bacillus anthracis toxin is naturally toxic and has been modified to target some components (uPA and metalloproteinases) that are often highly expressed in cancer cells.
New selective therapies have shown encouraging results in the treatment of different types of neoplasms. One such possible selective therapy uses the genetically reengineered B. anthracis toxin. The B. anthracis toxin has three subunits: an EF, a PA, and an LF. The furin proteases cleave the PA at the cell membrane, forming an active heptamer (PA63) bound to the B. anthracis toxin receptor (TEM8 or CMG2). The channel formed by this association allows EF and LF to translocate into the cytosol, causing cell death either by increasing intracellular cAMP levels [11,15,22,23,24,25] or blocking MAPK signaling [3,26,27]. Metalloproteinases and urokinase are mainly expressed in neoplastic cells [17,28,29]. Therefore, the B. anthracis toxin was modified (mutated PA) so as to be activated by uPA and MMPs. Liu et al. synthesized the PA variants PA-L1-I210A and PA-U2-R200A, which can only be cleaved by MMP and uPA, respectively [12,16,22,30]. This modification allowed the toxin to act selectively in cells that express both proteases at their outer membranes, and it has diminished off-target cytotoxicity when compared to the native B. anthracis toxin [16].
Before testing whether this modified toxin would be effective in canine and human OSA cell lines, we first examined the MMP, uPA, and MT1-MMP expression in canine (D17) and human (MG63) OSA by immunofluorescence assay. Immunofluorescence in D17 and MG63 OSA cell lines indicated the expression of MMP2, MT1-MMP, and uPA. Although we did not comparatively quantify the expression of uPA in canine and human OSA cells, apparently the canine OSA has high numbers of immunoflurescent dots, suggesting a higher expression of uPA in these canine cancer cells. The significance of this is unknown. The uPA expression has scarcely been studied in canine tumors, either through immunohistochemistry of selective tumors [31,32,33] or its serum levels [34]. Its functions and importance in cancer, however, seems to be similar, at least in canine mammary tumors [35], and correlated to more aggressive and metastatic tumors.
The expression of uPA and MMP2 suggested that these OSA cell lines could be sensitive to the reengineered B. anthracis toxin, as it was modified to have a selective cytotoxic action. Therefore, we used these lines for toxin cytotoxicity tests. In addition, in our experiments we also used the non-neoplastic canine osteoblastic cell line (COBS). This line has low expression of MMP2 and MMP-MT1 [21]. We must state here that no human osteoblastic cell line was available for our experiments, and that comparisons between canine and human osteosarcoma cell lines and normal canine cell lines were not performed. Every cell line tested had its own controls, represented by treatments with other parts of the reengineered toxin. Our results corroborate those of previous studies [36], which showed a significantly higher expression of these markers in tumour tissues than in normal tissues. These data suggested that the reengineered toxin could be cytotoxic in OSA cell lines, since the action of the toxin is dependent on the presence of proteases, such as MMPs and uPAs. This toxin would also be selective in cancer cells, since normal tissues have low or no expression of these markers.
We observed that the LF and FP59 portions of the toxin alone were not cytotoxic in any of the cell lines, confirming that the reengineered B. anthracis toxin was dependent on the association with PA for cytotoxicity. In the D17 canine OSA cell line, the combination of LF and PA at all PA concentrations (5, 15, 49, 155, 494, 1571, and 5000 ng/mL) was significantly cytotoxic. The combination of LF and PAL1/PAU2, the modified toxin, also proved to be significantly cytotoxic at all concentrations of PA. We also found that combinations of FP59 and PA and FP59 and PA-U2-R200A/PA-L1-I210A were more cytotoxic in D17 cells than the LP combinations. This higher mortality caused by FP59 in relation to LF was expected, since FP59 is 50 times more potent than LF. We observed similar results in the MG63 human OSA cell line. The combination of LF and PA was cytotoxic at 5, 49, 155, 494, 1571, and 5000 ng/mL PA. The combinations of LF and PA-U2-R200A/PA-L1-I210A was also cytotoxic at the two highest PA concentrations (1571 and 5000 ng/mL). As with the D17 cells, the combinations of FP59 and PA and FP59 and PA-U2-R200A/PA-L1-I210A in MG63 cells had even higher cytotoxicity at all PA concentrations examined (1, 3, 10, 31, 99, 314, and 1000 ng/mL). These results indicated that MG63 and D17 cells have receptors for urokinase and metalloproteinases, allowing the B. anthracis toxins to internalise. Cell cycle analysis indicated that this cytotoxicity was due to apoptosis.
The non-neoplastic canine osteoblastic cell line (COBS) showed sensitivity to the reengineered B. anthracis toxin only at two of the three highest concentrations (494 and 5000 ng/mL) of the therapeutic toxin (LF + PA-U2-R200A/PA-L1-I210A). This suggests that this normal cell line has receptors for the B. anthracis toxin (TEM8 or CMG2). However, the expression levels of MMP2 and MT1-MMP are low, which explains the lower sensitivity compared with the two OSA cell lines. In addition, cell cycle analysis showed that the reengineered toxin did not induce apoptosis in COBS cells, unlike in the two OSA cell lines, but only arrested the cells in the G1 phase.
We can conclude that canine and human OSA cells were sensitive to treatment with reengineered B. anthracis toxin, which caused cell death. Further, the LF toxin with PA-U2-R200A/PA-L1-I210A was less aggressive in the normal osteoblastic cell line; therefore, this toxin is selective for cancer cells and has the best therapeutic potential. This cytotoxicity of B. anthrax toxin is due to the action of the LF, which is a zinc metalloproteinase that cleaves Nlrp1 [37] and MAPKK-activated protein kinase in its N-terminal region [26]. The cleavage of Nlrp1 by LF causes activation of inflammasomes, release of IL-1β, and pyroptosis of macrophages in mice and rats [32]. MAPKKK cleavage interrupts several signalling pathways, including the ERK1/2, JNK/SAPK, and p38 pathways. These pathways have important cellular functions, such as proliferation and regulation, but they also regulate immune modulation and survival against insults. Our cell cycle analysis indicated that the cell death observed with reengineered toxin treatment was due to apoptosis. These results corroborate those of previous studies, which showed that B. anthracis toxin interfered with protein synthesis and caused DNA damage, leading to apoptosis [11].
Cell migration analysis was performed to observe the effect of the toxin on migration capacity. In the two OSA cell lines, the migration capacity was compromised after treatment with the therapeutic reengineered B. anthracis toxin at all concentrations. These effects were not described before in studies involving the reengineered B. anthracis toxin and cancer cells, and may indicate that the toxin affects the capacity of cancer cell migration in vivo as well. Since invasion and migration are initial steps towards metastasis, it is possible that the toxin will not only inhibit the local tumour growth but also may affect its metastatic potential.
In this study, we show that the reengineered anthrax toxin determines the inhibitory effects on canine and human osteosarcoma cells. A series of studies have shown similarities between canine and human osteosarcomas [38,39,40] regarding the morphology and molecular alterations. In particular, canine osteosarcomas can be models for pediatric osteosarcomas [41]. Therefore, new drugs that can inhibit canine tumors, including osteosarcomas, can be tested in humans, eventually children, and represent novel therapies for these aggressive diseases.
4. Conclusions
The reengineered anthrax toxin is a promising potential treatment for canine OSA and possibly for other solid tumours that express metalloproteinases and the urokinase plasminogen activator, uPA. The potential to decrease cancer cell migration is indicative that this anthrax toxin has the potential to inhibit the initial steps for metastasis. Therefore, it deserves further research and clinical tests in order to show its safety and efficacy in vivo, so that it can be used to treat canine (and eventually human) osteosarcomas.
5. Materials and Methods
5.1. Cell Lines
The study was performed in accordance with protocols approved by the Committee on Ethics on the Use of Animals of the School of Veterinary Medicine and Animal Science of the University of São Paulo (FMVZ-USP), Brazil, process number 5645170918, 17 April 2019.
Two different OSA cell lines were used—a commercial canine OSA cell line, D17 (Figure 11A), and a commercial human OSA cell line, MG63 (Figure 11B). The canine OSA strain D17 was purchased from the American Type Culture Collection (ATCC) (Manassas, VA, USA) (ATCC® CCL-183™). This cell line comes from a female dog, poodle breed, 11 years old, and was purchased at passage 227. The cells are adherent and have epithelial morphology. The human OSA cell line MG63 was also purchased from the ATCC (code: ATCC® CRL-1427™). This cell line comes from a 14-year-old male. The cells are adherent and have fibroblastic morphology.
We previously established a non-neoplastic canine osteoblastic cell line (COBS) (Figure 11C) from a bone callus scrape from a fracture in the tibia of a female dog, German Spitz dwarf breed, aged 10 months, which we called the COBS cell line. These cells were submitted for karyotyping and have 78 chromosomes, the normal number for canines. They are positive for osteonectin, alkaline phosphatase, osteopontin, and secreted protein, and are acidic and rich in cysteine [21].
The OSA cell lines were cultured in DMEM with 10% foetal bovine serum, 100 μg/mL penicillin and 100 μg/mL streptomycin (Gibco™ Penicillin-Streptomycin (10,000 U/mL, Carlsbad, CA, USA)) in an incubator at 5% CO2 and in a humidified atmosphere at 37 °C. The COBS cell line was isolated and cultivated in a complete medium specific for canine osteoblast growth (canine osteoblast growth medium, code: CN417500, Sigma-Aldrich, Saint-Louis, MO, USA).
5.2. Reengineered Anthrax Toxin
The reengineered anthrax toxin was kindly supplied by Drs. Leppla, Bugge, and Liu [11,17,18] from the Laboratory of Parasitic Diseases of the National Institute of Allergy and Infectious Diseases of the National Institutes of Health in Bethesda, MD, USA. The importation of the toxin was approved by the National Sanitary Surveillance Agency of the Brazilian Ministry of Health to be acquired by the Laboratory of Experimental Oncology of the Department of Pathology at the School of Veterinary Medicine and animal Science of the University of Sao Paulo, USP, and was kept in a freezer at −80 °C.
The following parts of the anthrax toxin were supplied:
The native protective antigen (PA);
The reengineered protective antigen: PA-U2-R200A + PA-L1-I210A;
The lethal factor (LF)
The catalytic domain of Pseudomonas aeruginosa exotoxin A combined with the N-terminal domain of LF (FP59).
5.3. Immunofluorescence
For immunofluorescence, the OSA cell lines and the COBS cell line were grown on cover slips in 6-well plates. After 2 days, the medium was removed and the cells were washed with PBS and fixed with 70% ethanol for 20 min at −20 °C. The cells were subjected to antigenic exposure with EDTA pH 9.0 buffer heated to 90 °C for 20 min. After antigenic exposure, the coverslips were washed with 1 × PBS plus Triton X-100. Then, the coverslips were incubated in a humid chamber overnight at 4 °C with the antibodies, as shown in Table 2. The following day, the slides were washed with PBS containing 0.1% Triton X-100 and incubated with secondary monoclonal or polyclonal antibodies conjugated to Alexa Fluor 488 or 568 (Dako, Carpinteria, CA, USA, 1:100) for 60 min in a humid chamber. Subsequently, the slides were washed with PBS containing 0.1% Triton X-100 and mounted with Vectashield to prevent depletion of fluorescence (Vector Laboratories, Inc., Burlingame, CA, USA) and sealed with enamel.
5.4. In Vitro Cytotoxicity Assay
The D17 and MG63 OSA and COBS cell lines were plated in 96-well plates in 150 µL volumes at a concentration of 0.7 × 104 cells/mL for 24 h before incubation with the reengineered anthrax toxin. We used the reengineered anthrax toxin in the following concentrations: LF (500 ng/mL) + PA (0–5000 ng/mL), LF (500 ng/mL) + PA-U2-R200A + PA-L1-l210 (0–5000 ng/mL), FP59 (100 ng/mL) + PA (0–5000 ng/mL), and FP59 (100 ng/mL) + PA-U2-R200A+PA-L1-l210 (0–5000 ng/mL).
Cell viability was assessed using the MTT assay based on the metabolism of tetrazolium (3-)4,5-dymethylthiazol-2-(yl)-2,5-(diphenyl tetrazolium bromide) salts by the mitochondria of metabolically active cells. The cells were treated with concentrations ranging from 1 ng to 1 mg. After 24 h of treatment, 10 µL/well of MTT (5 mg/mL) was added to 100 µL of medium. The plate was incubated in an incubator at 5% CO2 and 37 °C for 3 h. Then, the plates were centrifuged and 100 µL of HCl solution (0.04 N) in isopropanol was added to each well, followed by slow pipetting to dissolve the crystals. After 10 min, the optical density was read using a spectrophotometer (Multi Skan Thermofisher Scientific, Waltham, MA, USA) at a wavelength of 570 nm [18,39,40].
5.5. Cell Cycle Analysis
The cell cycle analysis was performed using propidium iodide (PI) and flow cytometry. For flow cytometry, 106 cells of each cell line were permeabilised by fixation in ethanol (Merck®, Darmstadt, Germany) or up to 3 days (−20 °C). Then, the cells were washed three times with PBS (5 min, 1200 RPM) and incubated with 200 µL of a solution containing 20 µg/mL IP, 200 µg/mL RNase A, and 0.1% Triton X-100 in PBS. After 15 min of incubation in the dark, 10,000 events were acquired by flow cytometry on the FACSCalibur device (Becton Dickinson, NJ, USA) using the program CellQuestPro. The analysis of fluorescence data and cell percentages in each phase of the cell cycle was performed using Flowjo (Tree Star Inc., Asland, OR, USA) version 10 and Flowjo version 7.6.1 (Tree Star Inc.). The results were expressed as a percentage of cells in the G1, G0/G1, S, and G2/M phases. The data were represented as histograms.
5.6. Apoptosis and Necrosis Assay
The apoptosis rate was determined using flow cytometry of cells labelled with annexin V and PI. A commercial kit containing Alexa® Fluor 488 annexin V (Molecular Probes, Eugene, OR, USA) and PI was used to stain the cells. The kit contained the following components: A: Alexa Fluor® 488 annexin V in 25 mM HEPES solution, 140 mM NaCl, 1 mM EDTA, pH 7.4, and 0.1% bovine serum albumin; B: PI at 1 mg/mL (1.5 mM) in deionised water; and C: 5× annexin binding buffer containing 50 mM HEPES, 700 mM NaCl, and 12.5 mM CaCl2. Component C was diluted in deionised water at a ratio of 1:4 to make the buffer. Component B was diluted in the buffer at a ratio of 1:9, yielding a final PI concentration of 100 µg/mL. The cell labelling solution was prepared by adding 2 µL of component A and 1 µL of PI for each 100 µL of buffer.
The OSA cell lines were cultured in 30 mm dishes (2 × 105 cells) for 24 h. After treatment with the reengineered anthrax toxin, the culture medium was removed and the cells were trypsinised and collected in a tube for flow cytometry. After centrifugation, the cells were resuspended in 100 µL of the annexin/PI solution and incubated for 15 min at room temperature. Cells were sorted on the FACSCalibur® cytometer (Becton Dickinson Immunocytometry System™, San Diego, CA, USA) by measuring the fluorescence emission at 530 and 575 nm with excitation at 488 nm, with at least 10,000 events being observed. The FlowJo® software (Ashland, OR, USA) was used to analyse the data.
5.7. Wound-Healing Assay
The OSA cell lines were cultured in 12-well plates. After reaching 100% confluence, we used a 200 µL tip to create a “scratch” in the monolayer. Then, the culture medium and cellular debris were aspirated. New culture medium was added slowly. A photo was taken at this point to record the initial scratch width (time zero), and cells were treated with either the toxin or control. The plate was placed in an incubator at 37 °C and 5% CO2. After 24 h, another photo was taken under an inverted microscope to assay the wound width. To determine the migration rate, we photographed three fields and measured the total area of the wound in the monolayer in relation to the size of the field at baseline (0 h) and compared the area of the wound in the monolayer in relation to the area of the field after 24 h of treatment. We averaged the three fields and the results were presented as a percentage.
5.8. Statistical Analyses
GraphPad Prism 8 was used to make the graphs and perform the statistical analysis. One-way analysis of variance followed by the Dunnett post-test was used to analyse differences between different treatments. Values were considered statistically significant at p ≤ 0.05.
Author Contributions
Conceptualization, M.K.N., A.T.N., S.L., J.M.W., S.H.L. and M.L.Z.D.; data curation, J.M.d.F. and I.I.M.d.F.; formal analysis, J.M.d.F., I.I.M.d.F. and M.K.N.; investigation, I.I.M.d.F., C.d.O.M., A.N., S.L., J.M.W., T.H.B. and M.L.Z.D.; methodology, J.M.d.F., I.I.M.d.F., M.K.N., S.L., J.M.W., S.H.L. and T.H.B.; project administration, M.L.Z.D.; resources, A.T.N., T.H.B. and M.L.Z.D.; software, S.L.; validation, J.M.d.F., C.d.O.M. and S.L.; visualization, I.I.M.d.F., M.K.N., C.d.O.M. and S.H.L.; eriting—original draft, J.M.d.F.; writing—review and editing, M.L.Z.D. All authors have read and agreed to the published version of the manuscript.
Funding
Jonathan Mackowiak da Fonseca was the recipient of a fellowship (process number 141455/2015-2) from the National Council of Scientific and Technological Development (CNPq) of the Ministry of Science, Technology, Innovation, and Communication of Brazil. Ivone Izabel Mackowiak da Fonseca (process number 2017/12855-1) and Marcia Kazumi Nagamine (process number 2016/20479-7) are recipients of fellowships from the Sao Paulo Research Foundation, (Fundação de Amparo à Pesquisa do Estado de Sao Paulo, FAPESP). This study has been supported with grants from FAPESP (regular support process number 2015/16776-3) under the responsibility of Maria Lucia Zaidan Dagli. T.H.B. and S.H.L. were supported by the National Institue of Dental and Cranial Research (NIDCR) and National Institute of Allergy and Infectious Diseases (NIAID) Intramural Research Programs, respectively.
Acknowledgments
This study is part of the thesis presented by Jonathan Mackowiak da Fonseca to the Interunit Graduate Program on Biotechnology of the University of Sao Paulo.
Conflicts of Interest
The authors declare that they have no conflict of interest.
Figures and Tables
Enlarge this image.Figure 1. Photomicrograph representation of the expression of different markers in canine (D17) and human (MG63) osteosarcoma cell lines and canine osteoblastic (COBS) cell line, as tested by immunofluorescence. (A) Metalloproteinase 2 (MMP2) expression in canine (D17) and human (MG63) osteosarcoma cell lines. (B) The urokinase plasminogen activator (uPA)expression in canine (D17) and human (MG63) osteosarcoma cell lines. (C) Membrane-type 1 matrix metalloproteinase MT1-MMP expression in canine (D17) and human (MG63) osteosarcoma cell lines. (D) Membrane-type 1 matrix metalloproteinase (MT1-MMP) and Metalloproteinase 2 (MMP2) expression in Canine Osteoblast Spitz (COBS) cell line. Note: Alexa Fluor 488: green; DAPI: blue. Original magnification 40×.
Enlarge this image.Figure 2. Response of the canine osteosarcoma cell line (D17) to the reengineered anthrax toxin. (A) D17 cells treated with LF + PA at differing PA concentrations; (B) D17 cells treated with LF + PAL1/PAU2 at differing PA concentrations. (C) D17 cells treated with FP59 + PA at differing PA concentrations. (D) D17 cells treated with FP59 + PAL1/PAU2 at differing PA concentrations. Optical density was compared to that of untreated cells (only LF or FP59). Note: * p < 0.05; *** p < 0.001. LF: lethal factor; PA: protective antigen; PAL1: PA-L1-l210; PAU2: PA-U2-R200A; FP59: the A exotoxin of Pseudomonas aeruginosa combined with the LF.
Enlarge this image.Figure 3. Response of the human osteosarcoma cell line (MG63) to the reengineered anthrax toxin. (A) MG63 cells treated with LF + PA at differing PA concentrations. (B) MG63 cells treated with LF + PAL1/PAU2 at differing PA concentrations. (C) MG63 cells treated with FP59 + PA at differing PA concentrations. (D) MG63 cells treated with FP59 + PAL1/PAU2 at differing PA concentrations. Optical density was compared to that of untreated cells (only LF or FP59). Note: ** p < 0.01; *** p < 0.001. LF: lethal factor; PA: protective antigen; PAL1: PA-L1-l210; PAU2: PA-U2-R200A; FP59: the A exotoxin of Pseudomonas aeruginosa combined with the LF.
Enlarge this image.Figure 4. Response of the non-neoplastic canine osteoblastic cell line (COBS) to the reengineered anthrax toxin. (A) COBS cells treated with LF + PA at differing PA concentrations. (B) COBS cells treated with LF + PAL1/PAU2 at differing PA concentrations. (C) COBS cells treated with FP59 + PA at differing PA concentrations. (D) COBS cells treated with FP59 + PAL1/PAU2 at differing PA concentrations. Optical density was compared to that of untreated cells (only LF or FP59). Note: * p < 0.05; ** p < 0.01; *** p < 0.001. LF: lethal factor; PA: protective antigen; PAL1: PA-L1-l210; PAU2: PA-U2-R200A; FP59: the A exotoxin of Pseudomonas aeruginosa combined with the LF.
Enlarge this image.Figure 5. Graphs showing the cell viability of canine and human osteosarcoma cell lines (D17 and MG63, respectively) and canine osteoblast cell line (COBS) after treatment with reengineered anthrax toxins: (A) LF + PA; (B) LF + PAL1/PAU2; (C) FP + PA; (D) FP + PAL1/PAU2. The IC50 values are shown in Table 1.
Enlarge this image.Figure 6. Cell cycle histograms of the canine osteosarcoma cell line D17 after 24 h of treatment with the reengineered anthrax toxin from Bacillus anthracis: (A) LF only; (B) LF + PAL1/PAU2 50 ng/mL; (C) LF + PAL1/PAU2 500 ng/mL; (D) LF + PAL1/PAU2 5000 ng/mL. LF: lethal factor; PAL1: PA-L1-l210; PAU2: PA-U2-R200A. The black line represents a cell population histogram in respect to iodide propide fluorescence, while the pink line represents the univariate cell cycle model created by FlowJo software to de-convolute the populations in order to assign percentage values to each population, since adjacent populations overlap each other, resulting in the purple, yellow, and green areas, which represent G0/G1, S, and G2/M phases, respectively.
Enlarge this image.Figure 7. Cell cycle histograms of the human osteosarcoma cell line MG63 after 24 h of treatment with the reengineered anthrax toxin from Bacillus anthracis: (A) LF only; (B) LF + PAL1/PAU2 50 ng/mL; (C) LF + PAL1/PAU2 500 ng/mL; (D) LF + PAL1/PAU2 5000 ng/mL. LF: lethal factor; PAL1: PA-L1-l210; PAU2: PA-U2-R200A.
Enlarge this image.Figure 8. Cell cycle histograms of the non-neoplastic COBS cell line after 24 h of treatment with the reengineered anthrax toxin from Bacillus anthracis: (A) LF only; (B) LF + PAL1/PAU2 50 ng/mL: (C) LF + PAL1/PAU2 500 ng/mL; (D) LF + PAL1/PAU2 5000 ng/mL. LF: lethal factor; PAL1: PA-L1-l210; PAU2: PA-U2-R200A.
Enlarge this image.Figure 9. Relative width of the lesion in the wound-healing assay in the canine osteosarcoma cell line D17 with and without treatment of LF + PAL1/PAU2 at a concentration of 5000 ng/mL PA. (A) D17 cells treated with LF + PAL1/PAU2 at 5000 ng/mL PA. (B) Representative images of the wound-healing assay in the canine osteosarcoma cell line D17. Note: *** p < 0.001 in relation to the control at 24 h. LF: lethal factor; PAL1: PA-L1-l210; PAU2: PA-U2-R200A.
Enlarge this image.Figure 10. Relative area of the lesion in the wound-healing assay in the human osteosarcoma cell line MG63 with and without LF + PAL1/PAU2 at 5000 ng/mL PA. (A) MG63 cells treated with LF + PAL1/PAU2 at 5000 ng/mL PA. (B) Representative images of the wound-healing assay in the human osteosarcoma cell line MG63. Note: ** p < 0.01 in relation to the control at 24 h. LF: lethal factor; PAL1: PA-L1-l210; PAU2: PA-U2-R200A.
Enlarge this image.Figure 11. Photomicrograph representative of canine (D17) and human (MG63) osteosarcoma cell lines and canine osteoblastic cell line (COBS) in culture: (A) canine osteosarcoma cell line (D17); (B) human osteosarcoma cell line (MG63); (C) canine osteoblastic cell line (COBS). Original magnification 40×.
IC50 values upon treatment of D17, MG63, and COBS with the toxin parts. The IC50 values were calculated with GraphPad Prism software.
| IC50 | LF + PA (ng/mL) | LF + PAL1/PAU2 (ng/mL) | FP + PA (ng/mL) | FP + PAL1/PAU2 (ng/mL) |
|---|---|---|---|---|
| D17 | 511.2 | 9277 | 1.073 | 1.077 |
| MG63 | 20,439 | 2070 | 1.057 | 1.082 |
| COBS | 3418 | 79,655 | 37.76 | 42.12 |
Antibodies used for the immunofluorescence analysis of canine and human OSA and COBS cells.
| Antibody | Catalogue Number | Mono or Polyclonal | Mouse or Rabbit | Dilution | Subcellular Localisation |
|---|---|---|---|---|---|
| MMP-2–Abcam | Ab86607 | Monoclonal | Mouse | 1:200 | Membrane |
| uPA H140–Santa Cruz | Sc14019 | Polyclonal | Rabbit | 1:200 | Cytoplasm |
| β-catenin-Invitrogen | 138400 | Monoclonal | Mouse | 1:100 | Membrane, cytoplasm, and nucleus |
| p53-Serotec | MCA909 | Monoclonal | Mouse | 1:100 | Nucleus |
| MAPK-Cell Signaling | 2532 | Polyclonal | Rabbit | 1:100 | Cytoplasm |
© 2020 by the authors.
Details
1 Department of Pathology, School of Veterinary Medicine and Animal Science, University of Sao Paulo, Sao Paulo 05508-270, SP, Brazil;
2 Global Vet Pathology, Montgomery Village, MD 20886, USA;
3 Aging Institute and Division of Infectious Diseases, Department of Medicine, University of Pittsburg, Pittsburgh, PA 15261, USA;
4 Microbial Pathogenesis Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA;
5 Proteases & Tissue Remodeling Section, National Institute of Dental and Craniofacial Research, NIH, Bethesda, MD 20892, USA;