Malignant mesothelioma (MM), is an intractable disease with limited therapeutic options and grim survival rates. Altered metabolic and mitochondrial functions are hallmarks of MM and most other cancers. Mitochondria exist as a dynamic network, playing a central role in cellular metabolism. MM cell lines display a spectrum of altered mitochondrial morphologies and function compared to control mesothelial cells. Fractal dimension and lacunarity measurements are a sensitive and objective method to quantify mitochondrial morphology and most importantly are a promising predictor of response to mitochondrial inhibition. Control cells have high fractal dimension and low lacunarity and are relatively insensitive to mitochondrial inhibition. MM cells exhibit a spectrum of sensitivities to mitochondrial inhibitors. Low mitochondrial fractal dimension and high lacunarity correlates with increased sensitivity to the mitochondrial inhibitor metformin. Lacunarity also correlates with sensitivity to Mdivi-1, a mitochondrial fission inhibitor. MM and control cells have similar sensitivities to cisplatin, a chemotherapeutic agent used in the treatment of MM. Neither oxidative phosphorylation nor glycolytic activity, correlated with sensitivity to either metformin or mdivi-1. Our results suggest that mitochondrial inhibition may be an effective and selective therapeutic strategy in mesothelioma, and identifies mitochondrial morphology as a possible predictor of response to targeted mitochondrial inhibition.
Malignant mesothelioma (MM) is an aggressive disease for which overall outcome is quite poor. The median survival for MM being just 12 months1. Although the use of asbestos has decreased in recent years, its latency period, which can be up to 40 years, means large numbers of new MM patients are still diagnosed each year1,2,3. In the US approximately 3000 new cases are diagnosed each year, with the majority of them being advanced stage. Three histologies are usually identified in MM: epithelioid, which is the most common, biphasic, and sarcomatoid4. There are a number of immunohistochemical markers such as WT-1 and calretinin that differentiate mesothelioma from other tumors such as lung cancer5. In certain subsets of MM, one can detect circulating mesothelin and osteopontin in patient serum6. Recently, a number of genetic alterations in BAP1 and NF2 have been identified, that may be prognostic and potentially predictive of therapeutic response3,7,8,9,10. As an example, loss or mutation of merlin (NF2) may be a predictor of effective targeting by anti-focal adhesion kinase (FAK) therapy11. The standard of care in mesothelioma remains surgery or combination chemotherapy with pemetrexed and cisplatin7. Although new therapies targeting the immune system, PI3kinase and mTOR are emerging more options are needed if improved outcomes and increased survival are to become a reality for MM patients12,13,14.
In MM layering of the pleura leads to the formation of a solid tumor structure4. However tumors are not easily quantified by the conventional metrics of length or volume, therefore we examined the fractal properties of the tumor structure. Fractals are mathematical constructs, which exhibit self-similarity over an infinite scale15,16. Many biological structures are considered to have fractal properties whereby they exhibit self-similarity within a limited scaling window, often 2–3 orders of magnitude17. Objects exhibiting exact, quasi, or statistical self-similarity may be considered fractal. Fractal dimension measurements can be used to indicate the complexity and space-filling properties of a shape18,19,20,21. Lacunarity is another measurement often used in conjunction with fractal dimension to describe the texture of a shape or fractal22,23. In this study fractal dimension and lacunarity measurements were leveraged to differentiate between benign and malignant MM tissues and to classify the different mitochondrial morphologies exhibited by mesothelioma cell lines.
Mitochondria form a dynamic network within the cell, which allows them to respond and adapt as the cell progresses through the cell cycle and to withstand cell stresses such as increased energy demand, nutrient deprivation or hypoxia24,25,26. Mitochondrial networks are often classified as predominately elongated, fragmented or reticulated27,28. These classifications are indicative of the relative rates of fission and fusion occurring within the network and may alter depending of the state of the cell. Mitochondrial dynamics (cycling between mitochondrial fission and fusion) help to maintain mitochondrial integrity and functional ability29. At various points within the normal cell cycle the mitochondria may undergo increased rates of fission (G2-M) or fusion (G1-S)25. Increases in fission are also observed during the initial stages of apoptosis, while increased fusion may aim to preserve mitochondrial function in response to cell stress such as hypoxia and cytotoxicity27,30,31. In the current study we have investigated mitochondrial morphology in MM cell lines and quantified the various morphologies using fractal dimension and lacunarity. We have examined the functional outputs of the various mitochondrial morphologies by measuring the metabolic activity in these cells. Oxidative phosphorylation and glycolysis were measured via oxygen consumption rate (OCR) and extracellular acidification rate (ECAR) respectively. Mitochondrial stress testing allowed us to calculate the oxidative reserve capacity of these cells32. Finally we examined the sensitivity of MM cell lines to conventional chemotherapeutics (cisplatin) and to the mitochondria targeted inhibitors metformin and mdivi-1. Our results indicate that mesothelioma cells show a spectrum of mitochondrial morphologies ranging from elongated, highly reticulated in H2373 and H2596 cells, to a more fragmented and condensed pattern in H28 and H513. These differences were easily and objectively quantified using the fractal dimension and lacunarity measurements. The MM cell lines exhibited a range of metabolic phenotypes, exhibiting increased reliance on glycolytic function (as indicated from the OCR/ECAR ratio) compared to MeT-5A control mesothelial cells, (with the exception of the H2373 and H2461 lines). Mitochondrial morphology showed better correlation with mitochondrial inhibitor sensitivity that metabolic function measured via oxygen consumption rate (OCR) and extracellular acidification rate (ECAR).
Morphology of malignant mesothelioma subtypes
We have utilized fractal dimension and lacunarity analysis as a novel method to differentiate between hyperplastic and malignant mesothelial tissue18,33. A tissue microarray (TMA) was constructed containing duplicate samples of hyperplastic, biphasic and epithelioid mesothelium (Fig. 1a). The hematoxylin and eosin (H&E) stained TMA was then scanned using a 3D- Histech Pannoramic SCAN whole slide scanner and images were analyzed (at 15x magnification) using the ImageJ plugin FracLac to calculate the fractal dimension and lacunarity of each sample. Due to some missing or damaged samples the resulting number of tumors analyzed was 36 epithlioid, 20 biphasic and 12 hyperplastic/benign controls. As shown in Fig. 1b,c biphasic and epithelioid samples had significantly higher fractal dimension and lower lacunarity compared to hyperplastic/benign tissue (p < 0.0001). Although the difference between biphasic and epithelioid tissue was not found to be statistically significant, epithelioid tissue tended to have a slighter higher fractal dimension and lower lacunarity than biphasic tissue. These results suggest that fractal dimension and lacunarity analysis maybe a useful and rapid method to differentiate benign and malignant tissues in malignant mesothelioma. No significant variation was detected between duplicate samples taken from the same tumor (Supplemental Fig. 1). No correlation was found between age, gender or survival with fractal dimension or lacunarity (Data not shown). The diagnostic potential of fractal dimension and lacunarity was determined by receiver operating characteristic (ROC) analysis. The cases of biphasic and epithelioid mesothelioma were differentiated from benign hyperplasia. Analysis indicates fractal dimension and lacunarity as excellent predictors of mesothelioma histology. For fractal dimension the areas under the curve (AUC) for cases of biphasic or epithelioid mesothelioma were 96.97% and 91.84% respectively. For lacunarity the AUC’s for biphasic or epithelioid mesothelioma were 97.06% and 90.00% respectively. Therefore both fractal dimension and lacunarity demonstrated high accuracy as predictors of mesothelioma. ROC curves, sensitivity and specificity results are included in supplemental Figs 2 and 3.
Mitochondrial morphology in mesothelioma
We then applied the fractal dimension and lacunarity analysis to mitochondrial morphology in a panel of mesothelioma cell lines. Staining with the mitochondrial marker TOM20 revealed a spectrum of mitochondrial morphologies in the mesothelioma cell lines (Fig. 2). MeT-5A cells had reticulated and elongated mitochondria distributed throughout the cytoplasm. The mesothelioma cell lines showed a range of alterations, from H28 in which the mitochondria were much more fragmented but still distributed throughout the cytosol, to H513 which had some elongated mitochondria but they were almost exclusively perinuclear. H2052 and H2596 cells had a high level of reticulated mitochondria but with a restricted distribution around the nucleus. In order to quantify these different complex mitochondrial morphologies we calculated the mitochondrial fractal dimension and lacunarity of each cell type using the ImageJ plugin FracLac34. A minimum of 40 cells were analyzed for each cell type and the entire mitochondrial network was analyzed for each cell. Figure 3a illustrate the general relationship between fractal dimension, lacunarity and the types of mitochondrial morphologies observed in the mesothelioma cells. The mesothelioma cell lines all possessed significantly decreased fractal dimensions compared to control MeT-5A cells, with H513 and H2596 showing the largest changes (Fig. 3b). Conversely, lacunarity was increased in the mesothelioma cell lines compared to MeT-5A controls (Fig. 3c). Again H513 and H2596 showed the most significant changes compared to MeT-5A. Fractal dimension and lacunarity takes into account the fission/fusion state of the mitochondria, the diameter of the mitochondrial tubules and the distribution within the cell. Figure 3d shows a morphological profile of the mesothelioma cells based on fractal dimension and lacunarity. We can see that the control MeT-5A cells have a different profile to the mesothelioma cells. H513 is at the opposite end of the spectrum to MeT-5A, its mitochondria are almost completely perinuclear showing limited elongation (Fig. 3d).
Altered expression of mitochondrial proteins in malignant mesothelioma cell lines
Mitochondrial dynamics are regulated in part via the relative expression of fission and fusion proteins including DRP1, MFN2, OPA1 and FIS135,36. To analyze the expression of mitochondrial dynamics proteins in mesothelioma we performed immunoblotting on the panel of mesothelioma cell lines (Fig. 4a). There was a decrease in total DRP1 and MFN2 in mesothelioma cell lines compared to the MeT-5A mesothelium control cells, suggestive of decreased fission/fusion cycling in these cells. However there was also a shift in the relative levels of these proteins in the mesothelioma cell lines towards higher expression of the fission regulator DRP1 compared to MFN2, the fusion regulator (Fig. 2b). This could suggest a higher relative rate of fission in these cells, which would result in a more fragmented mitochondrial network. The expression of TRAP1, an HSP75-like protein involved in the recruitment of DRP1 to the mitochondria was also altered in mesothelioma, although no clear pattern emerged37,38. Expression of COX IV a mitochondrial marker protein was similar in all cell lines indicating no significant changes in total mitochondrial content39. MCT4, which facilitates lactate export from cells, is associated with a glycolytic phenotype40,41. MCT4 was increased in mesothelioma cell lines compared to control MeT-5A cells. This increase was most evident in cell lines expressing low levels of total NF-2 or those with phosphorylated, inactive NF-2, namely H28 and H2461 (Fig. 4a).
We then examined the levels of DRP1 and MFN2 localized to the mitochondria. Mitochondrial fractions were isolated from each cell line and immunoblotted. Similarly to the trend observed in total cell lysates, DRP1 levels were increased relative to MFN2 in mitochondrial fraction of the mesothelioma cells lines (Fig. 2c,d). Protein levels were normalized using expression of the mitochondrial marker protein VDAC1.
Mitochondrial and glycolytic function in mesothelioma
Mitochondrial morphology is also thought to be an indicator of mitochondrial activity. Fusion or elongation of mitochondria is associated with optimization of mitochondria function and preservation of mitochondrial membrane potential, while fission is associated with removal of damaged mitochondrial components and may be an indicator of decreased mitochondrial function26. Given the varied mitochondrial morphologies and altered expression of mitochondrial dynamics associated proteins in mesothelioma we investigated the bioenergetic profile of these cells using a mitochondrial stress test. OCR was measured as an indicator of oxidative phosphorylation while glycolysis was assessed via the ECAR32. An example of a typical mitochondrial stress test in shown in Fig. 5a. Basal OCR was significantly lower in multiple mesothelioma cell lines (p < 0.001 for H28, H2052, H2452, and H2596) compared to control MeT-5A cells (Fig. 5b). Two mesothelioma cell lines, H2373 and H2461, had no change compared to control MeT-5A cells. The majority of mesothelioma cells, with the exception of H513 and H2452, also had significantly reduced levels of reserve oxidative respiratory capacity (calculated as the difference between max OCR stimulated by FCCP treatment and basal OCR levels) (Fig. 5c)32. Basal ECAR, a measure of glycolytic activity was almost unchanged in the mesothelioma cell lines compared to MeT-5A (Fig. 5d). H513 and H2052 exhibited slightly higher ECAR but these did not reach statistical significance. Similarly, the lower ECAR observed in H2372, H2452 and H2461 did not reach significance. Fig. 5e shows the ratios of OCR to ECAR in these cells lines. A lower ratio indicates cells are more dependent on glycolysis compared to oxidative phosphorylation42. The majority of the mesothelioma cell lines tested show a decrease in this ratio indicating an increased dependence on glycolysis compared to Met-5A cells (H28, H513, H2052, H2452, H2596). Two of the cell lines tested (H2373 and H2461) had a higher OCR/ECAR ratio compared to control MeT-5A cells. Figure 6, places the cell lines on the OCR-ECAR plane and gives us a snapshot of the basal bioenergetic profile of these cells and how they relate to the control MeT-5A cells. We can see that MeT-5A cells have relatively high oxidative phosphorylation activity, while H28 and H2452 have lower levels of both oxidative phosphorylation and glycolysis and can therefore be considered as a low energy phenotype. Incidentally these two cell lines had the lowest proliferation rate of the cell lines tested (data not shown).
Cytotoxicity of mitochondrial inhibitors in malignant mesothelioma
Next we examined the cytotoxicity of two different mitochondrial targeted inhibitors, metformin and mdivi-1, and cisplatin, a standard chemotherapeutic agent in mesothelioma cell lines1. The first inhibitor metformin, is reported to inhibit complex I of the electron transport chain and is under investigation for its potential as a cancer therapeutic and preventative agent43. The second inhibitor, mdivi-1 is a specific inhibitor of DRP-1, a key regulator of mitochondrial fission44. Cells were treated with metformin, mdivi-1, cisplatin or vehicle control at the indicated concentrations for 72 hrs (Fig. 7). The EC50 for each drug was then calculated and is shown in Table 1. In the case of cisplatin, H2452 and H28 cells lines showed the highest levels of resistance to cisplatin treatment, with EC50 values of 80.13 μM and 66.63 μM respectively. H513 and H2596 were the most sensitive (EC50 5.5 μM and 6.769 μM). The control cell line MeT-5A was also sensitive to cisplatin toxicity compared to the mesothelioma cell lines with an EC50 of 15.1 μM. However when cells were treated with the mitochondria targeted therapies a different profile emerged. MeT-5A showed the highest resistance to metformin (EC50 67.28 mM) of all cell lines tested. H28 and H2452 were also somewhat resistant to metformin treatment. These two cell lines also had the slowest proliferation rate of the cell lines tested (data not shown). H513 and H2596 were the most sensitive cell lines (EC50 4.762 mM and 15.8 mM) being 14 and 4 times more sensitive than MeT-5A. Cells treated with mdivi-1 showed a similar trend to the metformin treatment. H28 and MeT-5A were the most resistant to treatment (EC50 51.11 μM and 46.0 μM) while H2596 was the most sensitive (EC50 8.722 μM).
Given the spectrum of mitochondrial morphologies and bioenergetic activity observed in the mesothelioma cells we investigated whether any of these factors correlated with the inhibitor sensitivities. We plotted EC50 values for each cell line and inhibitor against basal OCR, ECAR, mitochondrial fractal dimension and lacunarity and calculated the Pearson correlation coefficient. Mitochondrial fractal dimension showed statistically significant correlation with metformin sensitivity (r = 0.8315, p = 0.0105) and a slight but not significant correlation with Mdivi-1 (r = 0.5726, p = 0.138) but did not correlate with cisplatin sensitivity (r = 0.02596, p = 0.915) (Fig. 8a). Mitochondrial lacunarity demonstrated significant inverse correlation with both metformin (r = −0.8974, p = 0.0025) and mdivi-1 (r = −0.7342, p = 0.0381), but no correlation with cisplatin sensitivity (r = −0.4793, p = 0.2294) (Fig. 8b). ECAR demonstrated an inverse correlation with cisplatin sensitivity (r = −0.715, p = 0.0462) but did not correlate with either of the mitochondrial inhibitors (Supplemental data Fig. 4). OCR did not correlate with any of the inhibitors (Supplemental data Fig. 4).
In this study, we have applied the metrics of fractal dimension and lacunarity to the quantification of mesothelioma tumor tissue and mitochondrial morphologies. These measurements were successfully used to differentiate between hyperplastic and malignant mesothelial tissues and to classify various mitochondrial morphologies in MM cell lines. The expression of mitochondrial fission and fusion regulatory proteins (DRP1 and MFN2 being the main regulators) was altered in MM, likely contributing to the various morphologies. The panel of MM cell lines examined displayed a spectrum of bioenergetic profiles, ranging from more oxidative (H2461), to more glycolytic (H28) and with decreased oxidative reserve capacities. MM cell lines exhibited increased sensitivity to mitochondrial-targeted inhibitors, be it metformin (complex 1 inhibitor) or mdivi-1 (DRP1 inhibitor) compared to control MeT-5A cells. Finally we report that mitochondrial morphology measured via fractal dimension or lacunarity correlated with mitochondrial inhibitor (metformin, mdivi-1) sensitivity, whereas OCR or ECAR did not show any correlation (Fig. 8a,b and Supplemental Fig. 4a,b).
Tissue and cell morphologies cannot always be readily and completely quantified using standard Euclidian metrics. For example, automated quantification of mitochondrial morphology within the cells is challenging and often restricted to simple measurements of length or volume45. Other visual methods of classification are heavily dependent on subjective interpretation28. Both of these approaches can be time-consuming and often do not take into account subtle differences in mitochondrial structure and the mitochondrial distribution within the cell. The same is also true of tissue measurements. Therefore we have adopted a more objective and complete quantification method for complex patterns and shapes such as those found in tumor tissues or the mitochondrial network using fractal dimension and lacunarity measurements18,20,21,22. Fractal dimension analysis allows us to quantify the inherent self-similarity in a structure or image. It tells us how the image changes based on the scale used to observe said image15. Lacunarity relates to texture, it quantifies the distribution and size of gaps within an image23. Fractal dimension and lacunarity have previously been utilized to quantify complex morphologies and patterns in a range of biological settings including cell shape, chromatin texture, retinal angiogenesis, neuronal growth and physiological measurements33,46,47,48,49,50. We observed a significant difference in the fractal dimension and lacunarity of hyperplastic compared to malignant mesothelial tissue samples (Fig. 1b,c). ROC analysis indicates fractal dimension and lacunarity as excellent predictors of mesothelioma histology (Supplemental Figs 2 and 3). Further analysis of larger numbers of tissue samples including the sarcomatoid tumors will be necessary to assess if these measurements would also be useful in discriminating between mesothelioma subtypes.
Cell metabolism and mitochondrial function is a crucial facet of MM and an emerging therapeutic target51,52. We undertook an investigation of multiple aspects of the mitochondria in MM including morphology, protein expression and bioenergetic function. Fractal dimension and lacunarity analysis of mitochondrial morphologies revealed significant differences in MM cell lines (Fig. 3b,c). Fractal dimension was correlated with sensitivity to metformin inhibition, while lacunarity was inversely correlated with sensitivity to both metformin and mdivi-1 (Fig. 8). Mitochondrial oxidative phosphorylation measured via OCR did not correlate with any of the inhibitors tested (Supplemental Fig. 4). These results suggest that mitochondrial morphology could be an important predictor of mitochondrial inhibitor sensitivity, even more so than bioenergetic function. Expression of multiple mitochondrial dynamics associated proteins are altered in MM. Expression of both DRP1, a fission regulator and MFN2, a fusion regulator are decreased in MM compared to control MeT-5A cells (Fig. 4a) other fission and fusion regulators FIS1, OPA1 also show differential expression in these cells (Supplemental Fig. 5). This may indicate a decrease in the overall rate of fission-fusion cycling in these cells. When we examined the ratio between DRP1 and MFN2, it indicates that in MM there is an increase in the relative level of DRP1 compared to MFN2, particularly in the mitochondrial fraction (Fig. 4b–d). This would indicate a pro-fission mitochondrial phenotype in these cells. Increased fission is associated with decreased mitochondrial activity26. We have previously reported that lung cancer cells have decreased levels of mitochondrial networking and increased fission44. An overall decrease in the rate of fission-fusion cycling could mean the mitochondria are slower to clear damaged mitochondrial proteins and may be less effective in maintaining the mitochondrial membrane potential. This would result in decreased mitochondrial performance and increased cell death. This could explain the increased sensitivity of MM cells to mitochondrial-targeted inhibitors (Table 1).
Comparing the bioenergetic profile (Fig. 6) with the fractal analysis (Fig. 3d) we observed some clustering of certain cell types in both graphs. H2373 and H2461 both have relatively high levels of OCR and high fractal dimension/low lacunarity, while H28, H2452 exhibit low metabolic activity and relatively low fractal dimension and lacunarity. However we did not detect any significant correlation between mitochondrial morphology measurements (fractal dimension, lacunarity) with OCR or ECAR. The lack of a definitive association between morphology and metabolic activity is not completely unexpected as other factors apart from morphology can affect mitochondrial activity. Substrate availability, reactive oxygen species and multiple signaling pathways can all effect mitochondrial function and activity53.
While the alteration in mitochondrial morphology may in part be due be to altered activity and expression of mitochondrial fission and fusion regulators it may also reflect changes in mitochondrial transport and localization in the cytoplasm. Mitochondria are transported mainly via the microtubule network while the actin cytoskeleton may be involved in mitochondrial anchoring and in regulating fission54,55,56. Regulation of the actin cytoskeleton is quite complex and is influenced by a plethora of signals, particularly during cell migration57. The link between metabolism and/or the mitochondria and cell migration is an area of growing research interest35,58,59,60. Together with the actin cytoskeleton, focal adhesion proteins are another crucial regulator of cell migration. Recently, we have shown that focal adhesion protein paxillin can influence the mitochondrial architecture61. For example, when the mutant A127T paxillin protein, which stimulates focal adhesion formation, is introduced into cells the mitochondrial network appears swollen and more reticulated. This indicates an alteration in the mitochondrial fission-fusion cycling within the cell. In this case it appears that paxillin is downregulated in mesothelioma compared to control cells, which may be indicative of altered migration and focal adhesion regulation in these cells (Fig. 4a). FAK, another crucial regulator of cell migration and emerging therapeutic target in mesothelioma may also be regulated via metabolic stress58. However we did not observe significant alteration in FAK expression in the mesothelioma cell lines, with the exception of H2452 where it was down regulated. Given that mesothelioma cells display a range of mitochondrial morphologies a more systemic investigation of the reciprocal regulation of the cytoskeleton and mitochondrial dynamics and functionality in cell migration is now warranted. It is also possible that differential gene alterations (such as loss or mutation of NF2 or BAP1) can also contribute to metabolic changes and altered mitochondrial morphologies in mesothelioma and should be more thoroughly investigated.
The use of metformin as a cancer preventative and therapeutic agent is an attractive but still largely unproven proposition. While initial observational reports from diabetic patients indicated that metformin treatment could be an effective cancer prevention strategy more formal studies have yet to confirm this62,63,64,65. Further its effectiveness as a cancer therapeutic remains unclear with conflicting reports and no consensus on its use or effects51. Our data indicate that mitochondrial morphology may be an informative metric in the prediction of metformin and even mitochondrial inhibitor sensitivity. Previous reports have indicated that the mitochondria and cell metabolism may be a viable therapeutic target in MM. Inhibition or silencing of peroxirodoxin-3, a mitochondrial oxidoreductase, led to disrupted mitochondrial bioenergetics, cell cycle arrest and reduced MM tumor volumes in vivo52. Here we have also shown the effectiveness of targeting mitochondrial dynamics to inhibit cell viability in MM. We have previously shown that mdivi-1 inhibits cell proliferation in vitro and decreased tumor volumes in vivo in lung cancer44. The data shown here indicate that it may also be effective against MM tumor growth.
In conclusion we have shown that mitochondrial morphology is altered in mesothelioma. This is reflected in altered expression of mitochondrial dynamics regulatory proteins and in altered cell bioenergetics. Classification of mitochondria via fractal dimension and lacunarity is a rapid, robust and objective method to quantify subtle changes in morphology and may be a useful indicator of sensitivity to mitochondrial-targeted inhibition. Going forward, we believe that the mitochondria is a viable target in mesothelioma and that mitochondrial morphology may be a promising predictor of therapeutic response.
Materials and Methods
Cell Culture and Reagents
MeT-5A control transformed non-tumorigenic mesothelial cells (ATCC) were maintained in Medium 199 containing 10% fetal bovine serum (Sigma), 1.5 g/L sodium bicarbonate (Corning), 3.3 nM epidermal growth factor, 400 nM hydrocortisone, 870 nM zinc-free bovine insulin (Lonza), 20 mM HEPES (Sigma), 3.87 μg/L selenious acid, trace elements B liquid (MediaTech) used at 1,000 dilution. Mesothelioma cell lines H28, H513, H2052, H2461 (Epithelioid) and H2373, H2596 (Sarcomatoid) and H2452 (Biphasic) (ATCC) were maintained in RPMI-1640 (Corning), 10% fetal bovine serum (Sigma) as described previously. Metformin, Cisplatin, and mdivi-1 were obtained from Sigma.
A Seahorse Bioscience XF24 Extracellular Flux Analyzer was used to measure OCR and ECAR. Control and mesothelioma cell lines were maintained in normal complete growth media and seeded onto a gelatin coated 24-well XF Flux analyzer assay plate at 80,000 cells/well 24 hrs prior to assay. Cells were switched to serum free XF assay media (Seahorse Biosciences) with 25 mM glucose, 1 mM sodium pyruvate, 2 mM glutamine (Corning) and placed in a CO2-free incubator at least 1 hour prior to start of assay. A Seahorse XF24 Analyzer was then used to measure the cellular bioenergetic profile. Each cycle included 3 min of mixing, a 2 min wait and finally measurement over 2 mins. Four measurements were obtained at baseline and following injection of oligomycin (1 μM; Sigma), FCCP (1 μM; Sigma), and rotenone (1 μM; Sigma). Measurements were normalized to total protein content per well using the Bradford protein assay (Bio-Rad).
Cells were rinsed with PBS and scraped in ice-cold RIPA lysis buffer (Boston BioProducts) and centrifuged at 8,000 rpm for 5 min at 4 °C. A Coomassie Bradford protein assay (Thermo Fisher) was performed and equal amounts of protein were combined with 4x reducing Laemmli sample buffer (Boston Bioproducts) prior to loading on to SDS-page gel. 20 μg of protein was loaded for each sample and separated by SDS–PAGE, and immunoblotted with antibodies to DRP1 (Novus Biologicals), TRAP1, MFN2, MCT4, VDAC1 (Santa Cruz Biotechnology) NF2, phospho-NF2 (Cell Signaling Technology), FAK (Millipore), Paxillin (Invitrogen) Actin (Sigma). After incubation with peroxidase-conjugated secondary antibodies, the signals were visualized by Clarity™ enhanced chemiluminescence (Bio-Rad) according to the manufacturer’s instruction. Protein band intensity was quantified by ImageJ software.
Isolation of Mitochondrial Fraction
The mitochondrial fraction was isolated according to a protocol adapted from Wheaton et al.66. Briefly, cells were rinsed in ice-cold PBS and scraped in mitochondrial isolation buffer (250 mM Sucrose, 50 mM Tris-HCl pH7.4, 0.1 mM EGTA, 5 mMMgCl with protease inhibitors). Cells were disrupted by 30 strokes with a Dounce homogenizer (15 strokes with each pestle) and 5 expulsions through a 28-gauge needle. The lysates were centrifuged at 1000 rpm for 10 min to remove nuclei, followed by centrifugation at 11,000 rpm for 20 min to pellet mitochondria. The mitochondrial pellet was then solubilized in RIPA buffer and the protein concentration determined via Bradford assay (Bio-Rad). Samples were then processed for immunoblotting as described earlier.
The Institutional Review Board at The University of Chicago (Chicago, IL) approved all of the human subjects research performed in this study. Written informed consent was obtained from all patients involved in the study. All methods were carried out in accordance with the respective approved protocol. Duplicate samples from fifty-seven MM tumors including 36 epithelioid, and 20 biphasic were processed into a tissue microarray (TMA) under an institutional review board approved protocol as previously described67. Patient and tumor characteristics are included in Table 2. Control tissues included 15 benign hyperplastic mesothelial samples in duplicate. The TMA was built using the ATA-27 Arrayer from Beecher Instruments. In brief, tissue cores (1-mm punch) from biopsied tissue samples were precisely organized into a grid and embedded in paraffin. The paraffin block was cut and the TMA was processed for H&E staining. Pathologic diagnosis in these cases was reviewed by at least two experienced pathologists. The H&E stained TMA was scanned using a 3D- Histech Pannoramic SCAN whole slide scanner.
Cells were cultured for 24 hrs on glass coverslips and fixed in 4% paraformaldehyde for 10 mins at 37 °C. They were permeabilized in 0.2% Triton PBS for 2 mins and blocked in 5%BSA PBS. Slides were incubated with primary antibody TOM20 (Santa Cruz Biotechnology) for 30 mins at RT followed by Alexa-647 conjugated secondary anti-Rabbit. Slides were then mounted using Prolog Gold anti-Fade mounting media (Life Technologies). Slides were then analyzed and imaged using Leica SP5 II STED-CW superresolution Laser Scanning Confocal.
Fractal dimension and lacunarity analysis
For analysis of the TMA histological samples 15x images of each core were selected from the whole slide scanned images. These images were converted to grayscale and fractal dimension and lacunarity was analyzed using the ImageJ plugin FracLac34. A box-counting grayscale differential analysis returns an intensity fractal dimension based on the difference in pixel intensity in each box. 12 different grid positions were used and the box sizes ranged from a minimum of 2 × 2 pixels and increased until they reached a maximum size of 45% of the selected image area. The estimated fractal dimension is calculated for each grid position from the regression line of a log-log plot of intensity versus box size. The average of these estimates is then calculated as the fractal dimension. Lacunarity was calculated based on the number of positive pixels in each box at the different box sizes.
Immunofluorescent stacks of TOM20-Alexa-647 stained cells were converted to maximum projection images using ImageJ. Background intensity was analyzed for all images and 1000 was subtracted from each image to ensure a zero background prior to fractal dimension analysis. The entire mitochondrial network of each individual cell was selected and saved as a separate image. The FracLac ImageJ plug-in was then used to measure the fractal dimension and lacunarity of each image as described.
To determine specific cytotoxicity, we used cell-permeable Calcein-AM (Santa Cruz). The hydrolysis of Calcein-AM by intracellular esterases produces Calcein, a hydrophilic, strongly fluorescent compound that is well-retained in the cell cytoplasm. Cells were seeded in black walled 96-well plates and allowed to adhere in normal growth media for 24 hrs. Cells were then washed once in PBS and the test compounds were added in 1% serum media at the indicated concentrations for 72 hrs. The media was then removed and replaced with 100 ul of phenol red-free optimem containing 2 μM Calcein-AM and incubated for a further 30 mins. Fluorescence was then measured at 485/535 nm using a Bio-Tek Synergy multi-detection microplate reader.
The Graph Pad Prism 5.0 software package was used for the statistical analysis. One-way ANOVA with Tukey multiple comparison post-test was used as appropriate. EC50 values were calculated by fitting a sigmoidal ‘four parameter logistic’ curve to the normalized log-transformed data. Pearson ‘r’ coefficient was calculated to determine correlation. A p value of less than 0.05 was considered significant. ROC analysis was performed using the STATA12 Data Analysis and Statistical Software.
How to cite this article: Lennon, F. E. et al. Unique fractal evaluation and therapeutic implications of mitochondrial morphology in malignant mesothelioma. Sci. Rep. 6, 24578; doi: 10.1038/srep24578 (2016).
This work was supported by CRF, MARF and NCI grants to RS, and NIH grants HL052233 and DK085006 to JKL.
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