Intercellular communication plays a critical role in the ever-evolving landscape of invasive cancers. Recent studies have elucidated the potential role of tunneling nanotubes (TNTs) in this function. TNTs are long, filamentous, actin-based cell protrusions that mediate direct cell-to-cell communication between malignant cells. In this study, we investigated the formation of TNTs in response to variable concentrations of the chemotherapeutic drug doxorubicin, which is used extensively in the treatment of cancer patients. Doxorubicin stimulated an increased formation of TNTs in pancreatic cancer cells, and this occurred in a dose-dependent fashion. Furthermore, TNTs facilitated the intercellular redistribution of this drug between connected cells in both pancreatic and ovarian cancer systems in vitro. To provide supportive evidence for the relevance of TNTs in pancreatic cancer in vivo, we performed multiphoton fluorescence microscopy and imaged TNTs in tumor specimens resected from three human patients with pancreatic adenocarcinoma, and one with neuroendocrine carcinoma. In sum, TNT formation was upregulated in aggressive forms of pancreatic carcinoma, was further stimulated after chemotherapy exposure, and acted as a novel method for drug efflux. These findings implicate TNTs as a potential novel mechanism of drug resistance in chemorefractory forms of cancer.
Cancer cells are, in part, characterized by their capacity for invasion. They reside in a context of heterogeneous and stroma-rich tumor microenvironments. The concept of tumor heterogeneity to drug resistance in cancer treatment is well-established1. This property includes heterogeneity within the same cancer type between patients, inter-tumoral heterogeneity between different tumors (primary or metastatic) within the same patient, and intra-tumoral heterogeneity within any given single tumor. Tumor-stromal proportion may vary widely and correlates with patient prognosis2,3,4. The relationship and interaction between malignant and stromal cells is dynamic and in constant flux, as cancer cells react and respond to metabolic and physiologic stressors from each other and from the surrounding environment.
Intercellular communication has gained increasing attention as a critical factor to induce heterogeneity in the tumor microenvironments. The effects of direct cell-to-cell transfer of signals (via horizontal transfer) have long been understood to occur via soluble signals such as chemokines and cytokines. More recently, they have been investigated via cellular channels or carriers such as gap junctions and extracellular vesicles (EVs), including exosomes and microvesicles. These physical modes of cellular communication are responsible for transmission of key signals of cellular proliferation and growth that permit tumor progression. Also, their expression appears to be modulated in response to external signals, including exposure to drugs administered with therapeutic intent.
A relatively new form of intercellular communication known as tunneling nanotubes (TNTs) represents an addition to the cadre of physical mechanisms of cellular signaling5,6. These structures are long, thin (50–1000 nm in width) F-actin-based cellular protrusions, allowing cells connected by TNTs to perform efficient and direct cell-to-cell transfer of cytoplasmic signals, including mitochondria, microRNAs, and other cellular components7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30. TNTs are upregulated in invasive forms of cancer as compared to stromal or non-malignant cells19,31 and are induced in vitro after exposure to metabolic or physiologic forms of stress, including serum-deprivation, hypoxia, hyperglycemia, and hydrogen peroxide19,32,33,34. We hypothesized that TNTs may be further upregulated after exposure to chemotherapeutic drugs and may represent a unique form of cellular stress response that permits cells to redistribute drugs, thereby reducing the overall kill rate of cancer cells. Here, we present data demonstrating variable formation of TNTs after exposure to the anthracycline chemotherapeutic agent, doxorubicin, in pancreatic and ovarian cancer models and examine the effects of intercellular redistribution of doxorubicin via TNTs. Our findings show that TNTs have the ability to effectively redistribute a chemotherapeutic drug. Such redistribution via TNTs could be a potential mechanism for emergence of chemotherapeutic drug resistance in cancer.
TNTs can be visualized in intact malignant pancreatic tumors resected from human patients: supportive evidence that TNTs are an in vivo phenomenon
There is significant heterogeneity in tumor-stroma proportions between patients, even within the same type of cancer. This biologic characteristic poses a challenge to achieving uniform efficacy of targeted therapeutics in many solid tumor types. This is especially true in pancreatic carcinomas, in which the stromal matrix is particularly dense as a result of desmoplastic reaction that takes places throughout the process of tumor formation35,36. As a direct result, malignant cells are often separated by distance, and thus they are not located in immediate proximity; this characteristic makes reliance on gap junction-mediated intercellular communication prohibitive. Furthermore, the vast majority (90–95%) of pancreatic adenocarcinomas harbor mutant forms of the KRAS oncogene37,38,39. Cells harboring mutant KRAS do not form connexin-lined gap junctions40,41,42,43. Exosomes have been implicated as one form of long-distance cellular signaling in pancreatic cancer44. In this context, there is also a clear niche for long-range cell communication that can be further explained by formation of TNTs.
As a demonstration of the potential in vivo relevance of TNT investigations to human pancreatic adenocarcinomas, we obtained primary tumor specimens from four patients with resected malignant pancreatic tumors at the time of Whipple surgery (pancreaticoduodenectomy) (Figs 1 and 2). The first specimen, as shown in Fig. 1, was resected from a 75-year-old patient with a pathologically staged T3 tumor (invasive pancreatic carcinoma extending beyond the pancreas, with invasion of duodenal submucosa and peripancreatic adipose tissue), exhibiting poor prognostic features including lymphovascular and perineural invasion and positive lymph nodes in the setting of chronic pancreatitis. This patient received neoadjuvant chemotherapy treatment (gemcitabine) prior to surgical resection.
Imaging this sample revealed the dense stromatous microenvironment that is characteristic of the desmoplastic reaction seen in pancreatic carcinomas. The thickness of this environment presented more challenges in visualizing TNTs/TNT-like structures in this context, compared to other invasive solid tumor malignancies. For this reason, we further adapted our protocol by using finely sectioned thin tumor slices (100 and 300 µm in thickness), and were able to visualize more distinct TNTs connecting cells in tumors resected from two additional patients with localized pancreatic adenocarcinoma, as well as a fourth patient with pancreatic neuroendocrine tumor in the setting of chronic pancreatitis (Fig. 2). The median TNT length was determined from serial images to be 30–40 µm in length in these tumors (Supplementary Fig. 1).
Pancreatic adenocarcinoma cells form more TNTs than pancreatic ductal epithelium
We have previously quantitatively examined the formation of TNTs in a variety of cancer cell types in vitro, including malignant pleural mesothelioma and ovarian cancer31,32. To determine the TNT index (i.e., average number of TNTs per cell), we cultured four commonly used pancreatic adenocarcinoma cell lines (MIA PaCa-2, S2013, CAPAN-1, and CAPAN-2) in medium previously reported to stimulate formation of TNTs (Fig. 3A)19,31. Of these cell lines, 2 are derived from primary pancreatic tumors (MIA PaCa-2, CAPAN-2) and the other 2 are derived from metastatic lesions (S2013, CAPAN-1). For comparison to non-malignant cells, we also evaluated HPDE, a cell line derived from pancreatic ductal epithelium. Formation of TNTs was negligible in HPDE cells.
TNTs and cells were counted at 24, 48, 72, and 96 hours; data were summarized as the median number of TNTs/cell at these time intervals since TNT formation is not normally distributed (Fig. 3A; cell proliferation curve in Supplementary Fig. 2). Further viewing the data graphed using the mean values of TNTs/cell also demonstrated the differences in TNT formation between malignant cell lines S2013, CAPAN-1, and CAPAN-2 as compared to HPDE cells; formation of TNTs in the MIA PaCa-2 cell line was negligible (Supplementary Fig. 3). We detected heterogeneity in the rates of TNT formation across malignant cell lines, consistent with prior reports from our group of such heterogeneity in cell lines from similarly invasive cancers such as malignant mesothelioma31. For HPDE cells, the TNT indices were significantly greater at 72 hours (p = 0.02) and 96 hours (p < 0.0001) than at 24 hours, but not significantly different between 48 and 24 hours (p = 1.00). In a separate experiment, we compared HPDE cells grown in standard culture medium (Keratinocyte-SFM supplemented with epidermal growth factor (EGF) and bovine pituitary extract), compared with HPDE cells grown in TNT-inducing medium, and found no difference in TNT formation between these two conditions (Supplementary Fig. 4).
There were no statistically significant differences in TNTs/cell over time between the metastatic and primary-derived malignant cell lines. For comparison of TNT formation over time, we specifically analyzed the differences between S2013 and MIA PaCa-2 over time as follows: for S2013, TNT indices were significantly greater at 48 hours (p = 0.02), 72 hours (p < 0.0001), and 96 hours (p < 0.0001) than at 24 hours. For MIA PaCa-2, TNT indices were significantly greater at 48 hours (p < 0.0001), 72 hours (p < 0.0001), and 96 hours (p < 0.0001) than at 24 hours.
To assess the distance across which the cells were forming TNTs, we measured TNT lengths over time. Of the cell lines used in this study, we were able to identify enough TNTs in randomly acquired images for S2013 and CAPAN-2 to measure TNT lengths every 24 hours over a 96-hour period. Data are presented as box plots to illustrate the range of TNT lengths during this duration (Fig. 3B). We found the TNTs were longest for both S2013 and CAPAN-2 at 48-hours. Although the lengths varied, the difference in the median TNT length for the individual cell lines was not significant over the entire 96-hour period. However, consistent with heterogeneity shown in other cancer types in our previously reported evaluation of TNT lengths31, the CAPAN-2 cell line formed longer TNTs than S2013 by 48-hours in culture. An example of a particularly long TNT, exceeding 500 µm and nearly 4-fold the length of the diameters of the cells it is connecting, is shown as a visual example of the distance that some TNTs can traverse (Fig. 3C).
TNTs form in a dose-dependent fashion after exposure to doxorubicin
Having confirmed a higher rate of TNT formation in pancreatic carcinoma cell lines as compared with ductal epithelial cells, we next examined the effects of chemotherapeutic drug exposure on formation of TNTs between these cells. We focused on examining MIA PaCa-2 and S2013 as we had found statistically significant differences in TNT formation at baseline. We cultured these malignant cells in the presence of six different concentrations of doxorubicin, an anthracycline chemotherapeutic drug that has been used extensively for in vitro studies of pancreatic cancer (Fig. 4A). The TNT index was assessed at 24, 48, 72, and 96 hours after initial incubation (median values are shown in Fig. 4B,C; raw data are provided in Supplementary Table 1). At 24 hours, none of the comparisons of TNT index was statistically significant. However, we did observe a heterogeneous response to variable concentrations of this drug at 48 and 72 hours. P-values from direct comparisons of S2013 TNT index data at 48 hours are presented in Supplementary Table 2. We detected a peak in TNT index occurring at the 800 ng/ml dose by 72 hours for both cell lines (Fig. 4B,C). The difference in TNT formation between the most stimulating (800 ng/ml) as compared to that for the least stimulating (1200 ng/ml) doses was 3-fold by this last time-point in the S2013 cell line (p = 0.02) and 1.5-fold in the Mia PaCa-2 cell line (p < 0.0001). There was also a significant difference noted in the S2013 TNT index between 800 ng/ml and 1000 ng/ml at 72 hours (p < 0.0001).
For MIA PaCa-2, significant differences in TNT index were observed when comparing the following doses at the 24-hour timepoint: 0 and 1200 ng/ml (p = 0.002); 200 and 600 ng/ml (p < 0.0001); 400 and 600 ng/ml (p = 0.01); 400 and 1200 ng/ml (p = 0.03); 600 and 800 ng/ml (p = 0.01); 600 and 1000 ng/ml (p < 0.0001); 600 and 1200 ng/ml (p < 0.0001); and 800 and 1200 ng/ml (p = 0.0001). P-values for all comparisons by dose at 48 and 72 hours for this cell line can be found in Supplementary Table 3. Median cell proliferation values over time are provided in distribution box plot format in Supplementary Fig. 5, and direct statistical comparisons are provided in Supplementary Table 4.
TNTs facilitate intercellular redistribution/efflux of doxorubicin between chemoresistant and chemosensitive cancer cells
TNTs are known to facilitate the intercellular transfer of many cytosolic components, including but not limited to mitochondria, Golgi vesicles, microRNAs, exosomes, and even nuclei19,22,45,46,47. Our group recently reported that TNTs can facilitate direct cell-to-cell transfer and redistribution of therapeutic cancer-targeting treatments specifically oncolytic viruses engineered to selectively target cancer cells48. Furthermore, we also demonstrated that after infection with an oncolytic virus, TNTs also mediated intercellular distribution of the viral thymidine kinase-activated nucleoside analog ganciclovir. This transport of cytotoxic drug from non-virus infected to virus-infected cells resulted in increased cell-kill48, representing a newly described form of bystander effect in the treatment of cancer.
If sensitive cells expel drugs to resistant cells via TNTs, this could potentially allow drug-treated cells to survive by minimizing drug exposure. Conversely, resistant cells expelling drugs to sensitive cells via TNTs could induce cell death, thereby enriching the population of drug-resistant cells and allowing them to thrive with reduced competition in the microenvironment. The chemotherapeutic drug doxorubicin, which was the focus of the current study, auto-fluoresces (excitation: 480 nm, emission: 560–590 nm) and can be easily examined using fluorescence microscopy49. Taking advantage of this drug’s unique property, we attempted to capture microscopy evidence of cancer cells harnessing TNTs as conduits for intercellular redistribution of doxorubicin after short-term treatment. We initially determined that S2013 cells readily internalized the doxorubicin via fluorescence microscopy (Fig. 5A). We then performed automated time-lapse microscopy by taking images every 10 minutes for 5 hours to track movement of the drug. We confirmed the formation of TNTs and the successful transfer of doxorubicin from doxorubicin-positive cells to TNT-connected recipient cells (composite images and schematic shown in Fig. 5A and Supplementary Movie 1). To quantify the relative amount of transfer of this auto-fluorescing drug, we analyzed the intensity of fluorescence within the TNT over time using ImageJ, reported as arbitrary units (a.u) (Supplementary Fig. 6). The transfer occurred between the time intervals of 160 and 250 minutes of the total duration of the time-lapse experiment. The total TNT fluorescence fluctuated over time, providing further supportive evidence that the drug was being transported rather than remaining stationary within the TNT.
To confirm this finding in an additional cancer model, we repeated the experiment using chemoresistant ovarian cancer cells that form TNTs at differential rates based on chemoresistant vs chemosensitive status of co-cultured cells32. In this experiment, we treated SKOV3 (multi-drug resistant ovarian carcinoma cells) with doxorubicin and co-cultured them with untreated A2780 cells, which are known to be sensitive to doxorubicin. Using time-lapse microscopy, we analyzed images for TNT formation between the cell populations. In one particularly striking instance, we observed transfer of fluorescing doxorubicin granules from a SKOV3 cell to an A2780 cell via a TNT (Fig. 5B, and Supplementary Movie 2). Notably, only a minimal amount of effluxed drug was required for the recipient chemosensitive A2780 cell to undergo cell death within 3 hours of drug transfer via the TNT.
Chemoresistance remains a significant clinical problem, yet the underlying cellular mechanisms remain unclear despite advances in the field of cancer treatment. Our studies were designed to evaluate the formation of TNTs — a unique form of cellular protrusion implicated in long-distance cell communication — as a cellular stress response. We found that the response after exposure of pancreatic cancer cells to doxorubicin was dose-dependent, and that TNTs facilitate a novel and direct form of cell-to-cell drug efflux among pancreatic and ovarian cancer cells through transport of a cytotoxic drug (doxorubicin). To our knowledge, direct cell-to-cell transfer and efflux of chemotherapy agents via TNTs has been reported in one other instance, in an in vitro model of acute myelogenous leukemia. In that study, researchers detected localization of the drug daunorubicin to lysosomes and visualized cell-to-cell transfer of the drug via TNTs50. In 2012, we reported that TNTs, or at least TNT-like structures, could be visualized connecting cells in intact tumors resected from human patients with malignant pleural mesothelioma19,31. Additional tumor types for which we have reported similar findings include lung carcinomas, ovarian carcinomas, osteosarcomas, breast carcinomas, neuroendocrine tumors, and colon cancers19,32,47,51. Here, we provide visual evidence that pancreatic adenocarcinomas as well as neuroendocrine carcinomas can be added to this growing list of aggressive cancer types that are capable of forming TNTs for mediating long-range intercellular communication in vivo. Detection of TNTs, or TNT-like structures, in this setting further supports the notion that the in vitro findings reported in this paper have potential clinical relevance.
We used doxorubicin, an anthracycline chemotherapeutic drug in extensive clinical use for a variety of epithelial malignancies including breast and ovarian cancers, because of its wide use in cancer chemotherapy-based treatment and in vitro autofluorescent properties49. Its primary mechanism of action involves DNA intercalation and topoisomerase inhibition. Our observations underscore a possible role for TNTs in drug-efflux of either chemo-naïve or in more advanced chemorefractory cancers. We exposed cells to varied concentrations of this drug (200, 400, 600, 800, 1000, and 1200 ng/mL) and compared the results to no drug. In a clinical setting, doxorubicin follows a fast distribution phase followed by a slow elimination phase; the drug reaches a peak concentration of ~600 ng/ml before being distributed to other tissues after intravenous administration52,53. Adding an optimized concentration of the drug (low enough not to induce immediate toxicity leading to cell death, but high enough to be detected using fluorescent microscopy) allowed us to perform time-lapse imaging over 24–48 hours. We visualized direct outgrowth of TNTs from drug-treated chemoresistant (SKOV3) cells to chemosensitive (A200) ovarian cancer cells, confirming that resistant cells were capable of initiating this unique form of cellular interaction. After co-culture of doxorubicin-treated SKOV3 cells with A2780 cells, we visualized a TNT connecting these cells and facilitating transfer of a minimal amount of this autofluorescent drug. Within hours, the recipient chemosensitive (A2780) cell involuted and underwent cell death. As we have previously reported, when these cells were co-cultured, formation of TNTs from chemoresistant to chemosensitive ovarian cancer cells constituted the fewest number of interactions, as compared with sensitive-to-resistant, resistant-to-resistant, or sensitive-to-sensitive32. The finding that a drug can be redistributed via TNTs poses a potential new paradigm for cellular mechanisms of drug efflux and the development of drug resistance in cancers. We speculate that this finding suggests TNTs may serve as an alternative mechanism capable of exporting chemotherapeutic drugs in an efficient manner between connected cells.
In 2013, we published a review of the potential impact of intercellular communication on tumor heterogeneity in pancreatic cancer54. At that time, we speculated on the role that TNTs could play in tumor-tumor interactions in this particularly heterogeneous tumor microenvironment. Our current study supports the notion that TNTs represent a non-genetic intercellular stress response by which tumors can survive despite exposure to cytotoxic chemotherapeutic drugs in a hypoxic tumor microenvironment. In 2015, Ware et al. reported a similar finding of upregulated TNT formation between malignant pancreatic cells following a different therapeutic modality (radiofrequency ablation; RFA)55. In examining the percent of TNT-forming cells prior to and following RFA, the investigators discovered significantly increased formation of TNTs in PANC-1 and AsPc-1 malignant cells and, as in our case, proposed this action as a stress response following that form of treatment. Interestingly, they too used HPDE as a non-malignant comparison, and the percent of TNT-forming cells was relatively negligible both before and after RF treatment55. The findings from both studies support the notion that physiologic or metabolic stressors in the microenvironment can induce or activate other forms of cellular protrusions as well, including invadopodia responsible for invasive cancer cell migration56. Based on these as well as our findings, we speculate that the ability of TNTs to form in response to stress induced by either chemotherapeutic drug or other non-pharmacologic interventions may, at least in part, explain the early emergence of drug resistance. Further, the ability of TNTs to mediate intercellular efflux, or redistribution, of drugs — potentially to subtherapeutic levels — may allow cells connected via these cellular ‘networks’ to protect each other from drug susceptibility. In this potential model, with continued administration of chemotherapy over time, the cells that adapt best to chemotherapeutic stress would survive and overtake other clonal subpopulations.
There is precedence for evolution of drug efflux in cancer cells, as development of chemoresistance via overexpression of P-glycoprotein (P-gp) is already well established57. This protein is a member of the ABC transporter family; when overexpressed, it becomes embedded within the plasma membrane, serving effectively as an ATP-dependent pump for efflux of chemotherapeutic agents58,59. The potential for intercellular transfer of P-gp to occur, and for the protein to remain functional after this horizontal transfer, has also been demonstrated18,60. Furthermore, P-gp has been studied in the context of TNTs, and specifically in ovarian cancer61. TNT-mediated transfer of both mitochondria and P-gp has been demonstrated in breast and ovarian cancer cell lines, in addition to transfer mediated without cell-to-cell contact via microparticles; this transfer has been associated with chemoresistance18,45,61. Several recent studies have in fact confirmed cell-to-cell transport of chemotherapeutic drugs via cellular microparticles or exosomes62. As compared with TNTs, exosomes are diffusible vessels of cell transport but may not be as efficient for cargo delivery as TNTs, which act as nanoscale pipelines between distant cells that cannot be connected via connexin-lined (gap junction) channels. Our results support the notion that TNTs represent a newly identified mechanism of drug efflux, which comprises both cytoplasm-to-cytoplasm extrusion of drug via TNTs. Intercellular transfer of P-gp has been examined in other cancer models (e.g., in bladder cancer); at least one study concluded that cell-to-cell contact is not necessary for this transfer to take place and mediate drug resistance63. The authors concluded microparticles were the most likely mode of transfer in that study. In this context, TNT-mediated transfer of P-gp may play a more complementary or secondary role to cytoplasm-to-extracellular environment extrusion via P-gp/multidrug resistance (MDR) channels.
We have shown that TNT formation is significantly higher in malignant pancreatic cells as compared to pancreatic ductal (non-malignant) epithelial cells. This result and difference in TNTs between malignant and benign cells is consistent with our data in other invasive cancers, such as malignant pleural mesothelioma among others31. We have previously speculated that TNTs play a role in cancers that may allow us to harness them as conduits for more effective drug delivery51,61. This concept would be particularly intriguing and applicable to pancreatic cancer, in which effective drug penetration remains a challenge due to dense desmoplastic reaction and thick hyaluronan coats that preclude diffusion of drugs into tumors54,62. Here, we found that the length of TNTs was notably much longer in pancreatic cancer cell lines cultured in vitro, as compared to their counterparts within human tumors. We speculate that this finding is due to the magnitude of this stromal density in vivo.
Interestingly, TNTs have been shown to provide mesenchymal stem cell rescue of cardiomyocytes damaged after exposure to anthracycline drugs by TNT-mediated transfer of mitochondria64. In the setting of cancer, the effects may actually be reversed, in which chemotherapeutic damage and the resultant rise in TNT formation leads to redistribution of the drug to other cells — in an effort for the affected cells to save themselves — or induce a stress response that leads damaged cells to “offer” their mitochondria and other vital cell components to other neighboring cells as a “sacrifice” to benefit the overall cancer cell population. The niche of TNTs and drug delivery is thought-provoking and one that we predict will gain increased interest.
In summary, TNT formation as a response to chemotherapeutic drug exposure is dose-dependent, with the highest rate of formation occurring at physiologically relevant concentrations. This differential response represents a potential cellular stress response that facilitates increased rates of intercellular TNT-mediated communication and transfer of cytotoxic drugs, such as doxorubicin. We postulate that this novel form of long-range drug efflux redistributes these drugs, and may or may not result in cell death of chemosensitive recipient cells. This study provides preliminary insight into the potential pathophysiologic role of TNTs in facilitating drug redistribution, and their formation as a stress response, and will need to be substantiated through further in-depth investigations. In this context, TNTs may provide a potential new and additional mechanism by which cells propagate drug chemoresistance in invasive cancers.
Materials and Methods
Cell lines and cell culture
MIA PaCa-2 (ATCC CRL-1420)65, S2013 (also known as S2-013 or SUIT.201366,67, CVCL_B280), CAPAN-1 (ATCC HTB79)65, and CAPAN-2 (ATCC HTB-80)65 cells were derived from human pancreatic adenocarcinoma, and HPDE cells from human ductal epithelium (CVCL_4376)63. MIA PaCa-2 and CAPAN-2 are derived from primary pancreatic tumors; S2013 and CAPAN-1 are derived from metastatic tumors. S2013 was obtained from ThermoFisher Scientific (Grand Island, NY); MIA PaCa-2, CAPAN-1, and CAPAN-2 cell lines were obtained from the American Type Culture Collection (ATCC).
A2780 and SKOV3 cell lines were kindly provided by Dr. Sundaram Ramakrishnan at the University of Minnesota. A2780 is a malignant human epithelial cell line derived from an endometrioid ovarian tumor. SKOV3 cells were derived from the ovarian adenocarcinoma ascites (peritoneal metastasis) of an untreated patient. SKOV3 cells are resistant to cisplatin, TNF, diphtheria toxin, and doxorubicin24. Cell lines were authenticated using sequence tandem repeat genotype profiling (Johns Hopkins University, STR Profiling for Human Cell Line Authentication) (MIA PaCa-2, S2013) or used immediately following acquisition from ATCC (CAPAN-2). Ovarian cancer cell genotypes were confirmed by comparison to available genetic profiles using the University of Colorado database (website: http://dnasequencingcore.ucdenver.edu/pdf-Files/Korch%20et%20al%20-%20Table%20S4%20Ovarian%20profiles.pdf).
All cancer cell lines were cultured in RPMI-1640 medium (Thermo Fisher Scientific, Waltham, MA, USA). All media was supplemented with 10% (v/v) fetal bovine serum (FBS) and 1% (v/v) Antibiotic-Antimycotic (Thermo Fisher Scientific, Waltham, MA, USA) at 37 °C in a humidified 5% CO2/95% air atmosphere. HPDE cells were cultured in defined keratinocyte medium supplemented by epidermal growth factor and bovine pituitary extract (Invitrogen Catalog #: 17005042) (Life Technologies, Inc., Grand Island, NY), with 1x antibiotic-antimycotic (Gibco Catalog #15240-062); for Supplementary Fig. 4, this medium is referred to as the “native culture medium.”
Cell lines were passaged every 2–3 days using trypsin-0.53 mM EDTA solution, kept in T-75 cm2 tissue culture flasks, and confirmed to be negative for mycoplasma infection. To stimulate TNT formation for in vitro examination, cells were grown in what our group refers to as “TNT-inducing medium”19 [2.5% FCS in RPMI-1640 containing 50 mM glucose, supplemented with 1% P-S, 2% L-glutamine with 10 mM ammonium lactate] (Sigma Aldrich, St. Louis, Missouri) and acidification of medium to pH 6.6, per our prior study19. Cell cultures were done in 75 cm2 tissue culture flasks (Falcon, Becton Dickson, Oxnard, CA) at 37 °C in 5% CO2.
Quantification of TNT index
TNTs were visually identified and quantified as previously described19,25,31,46. Briefly, these parameters included (i) lack of adherence to the substratum of tissue culture plates, including visualization of TNTs passing over adherent cells; (ii) TNTs connecting two cells or extending from one cell were counted if the width of the extension was estimated to be <1000 nm; and (iii) a narrow base at the site of extrusion from the plasma membrane. Cellular extensions not clearly consistent with the above parameters were excluded. An Olympus IX70 inverted microscope (Olympus Corporation) with 20x objective lens was used to count the number of TNTs and cells in 10 randomly chosen fields of each 6-well plate at 24, 48, 72, and 96 hours. Representative images of each field were taken at all time points in each well. Experiments were performed in triplicate for each cell line. To determine TNT formation, cells were plated at a density of 2.5 × 105 cells/well in 6-well adherent tissue culture plates (Fisher Scientific, Pittsburgh, PA) at 37 °C in 5% CO2 with TNT-inducing medium19. TNTs and cells were counted manually, and the TNT index was calculated as the number of TNTs per cell (TNTs/cell) using previously described methods31.
Pharmacologic treatment of cell lines
Doxorubicin (Doxo) (D-4000, LC Laboratories) is an anthracycline chemotherapeutic drug. It was used in this study for its autofluorescent properties.
Incubation with doxorubicin
MIA PaCa-2 and S2013 cells were cultured in T-flasks before trypsinization. Cells were then treated for 8 minutes in suspension with either 0, 200, 400, 600, 800, 1000, or 1200 ng/mL doxorubicin (D-4000, LC Laboratories, Woburn, MA) in RPMI media. Cells were then washed, pelleted, and plated into 12-well plates (0.1 × 106 cells/well), marking time point 0 hours. Cells were cultured at 37 °C in a humidified 5% CO2/95% air atmosphere for either 24, 48, or 72 hours. A2780 and SKOV3 cell lines were treated with doxorubicin for time-lapse imaging experiments. Doxorubicin was used at optimized concentrations to maximize its autofluorescent properties.
Imaging and TNT quantification
An Olympus IX70 inverted microscope (Olympus Corporation, Waltham, MA) with 20x objective lens was used to identify TNTs using the aforementioned criteria via live imaging. For each cell line, concentration, and time point, 3 fields of view (FOV) were taken from each of 5 wells, in triplicate.
To visualize doxorubicin transfer via TNTs, we performed time-lapse microscopy imaging every 15 minutes for 24 hours (ovarian cancer experiment) or every 10 minutes for 5 hours (pancreatic cancer experiment). Cells were first allowed 12 hours to settle and adhere to the plates prior to imaging. For time-lapsed imaging, multiple 20x fields of view containing evenly distributed cells were chosen using a wide-field Zeiss Axio200M microscope costume-fitted with a stage incubator that maintains environmental conditions at 37 °C and 5% CO2.
Quantification of doxorubicin intensity
Individual images were selected from the time-lapse experiment that documented intercellular of transfer of doxorubicin between pancreatic cancer cells via a TNT. The images were selected based on the times that doxorubicin could be visually identified within the TNT (between timepoints 160 and 250 minutes) and analyzed using ImageJ software. The TNT was traced and marked using the Freehand Selection tool of ImageJ, which measured the total TNT fluorescence based on examination of pixels, reported as an arbitrary unit which we graphed as shown in Supplementary Fig. 6.
Imaging TNTs/TNT-like structures in pancreatic tumor specimens
Ethical approval and informed consent
Tumor specimens from four patients with pancreatic cancer were obtained from the University of Minnesota (UMN) Tissue Procurement Facility under the auspices of a UMN IRB-approved protocol. Informed written consent was obtained, and patient identifiers were removed to ensure anonymity. All procedures for tumor procurement were in compliance with ethical regulations for obtaining and using human tissue.
The images shown in Fig. 1 represent our initial attempt to image TNTs in pancreatic tumor tissue from a human patient. Tumor sections (100–300 mm thick) were cut using a Vibratome and then stained using Hoechst 33342 (10 mg/ml) and MitoTracker Orange dyes (500 nM). Stained sections were mounted between two glass coverslips and imaged as previously described. 3D reconstructions were performed using Nikon NIS elements AR software.
We further refined the protocol to improve detection of TNTs in context of the dense and highly stromatous tumor microenvironment. For the images shown in Fig. 2, formalin-fixed pancreatic tumor specimens from three additional patients were submerged in optimal cutting temperature (OCT) embedding medium and placed on dry ice for three minutes. Specimen-OCT blocks were cut into 100 µm and 300 µm sections with a Leica CM1850 cryostat. Sections were added to 9-well PYREX™ glass plates and rinsed three times with 1X Phosphate-Buffered Saline (PBS). Our lab investigated how to optimize a new tumor imaging protocol, so staining solution reagent concentrations and cryostat slice thickness varied. Tumors were carefully sectioned to either 100 µm or 300um slices as indicated in the corresponding figure legend, and stained using either Alexa Fluor™ 488 Phalloidin or MitoTracker™ Orange CMTMRos per manufacturer’s instructions. All staining solutions contained 1% donkey serum (D9663 Sigma-Aldrich), 0.1% Triton-X in PBS, and 0.12 µM PureBlu™ Hoechst 33342 dye. After applying staining solutions, PYREX plates were covered with aluminum foil for ten minutes. To make agar, 0.38 g noble agar and 25 mL distilled H2O were added to an Erlenmeyer flask and placed in a beaker of boiling water until dissolved. Tumor sections were mounted to glass coverslips and placed in a coverslip boat rack. To dehydrate, coverslip boats were immersed in 75% EtOH within a glass container for 30 minutes. This step was repeated twice more with 95% and 100% EtOH. DPX mounting medium was generously applied to pre-labeled microscope slides. Tissue-mounted coverslips were then mounted to slides and allowed to dry undisturbed, protected from light for 48 hours. Slides were imaged with the Nikon A1R Multiphoton confocal microscope at the University of Minnesota Imaging Center. Parameters for 3-dimensional imaging included obtaining 40 z-stack slices, with 0.3 µm step size.
TNT indices and lengths were not normally distributed and therefore Wilcoxon Rank Sum tests were used to compare TNT indices and lengths for each combination of dose and time measurements within each cell line. P-values were conservatively adjusted for multiple comparisons within each experiment using Bonferroni correction. Analyses were conducted in SAS version 9.4 (Cary, NC), and p-values < 0.05 were considered statistically significant.
Supporting data are available in the main text and in the Supplementary Online Files section, and upon request.
Ethical approval and informed consent
As stated in further detail in Material and Methods: the use of human tumor samples was carried out in accordance with relevant guidelines and regulations, with approval from the University of Minnesota’s Institutional Review Board (IRB). Informed consent was obtained from all participants.
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We would like to thank Guillermo Marques, Ph.D., and Mark Sanders, Ph.D., for assistance with confocal microscopy performed at the University Imaging Centers at the University of Minnesota; Michael Franklin, M.S., for helpful critiques and editorial suggestions; and Beshay Zordoky, Ph.D., for helpful discussion regarding pharmacologic activity and properties of doxorubicin. This research was supported by a National Pancreas Foundation Research Grant (provided in partnership with the National Pancreas Foundation, several NPF Chapters and the Horvitz/Lebovitz Research Fund) (E.L.); the University of Minnesota Deborah E. Powell for Women’s Health Interdisciplinary Seed Grant support (Grant #PCWH-2013-002) (E.L.); Institutional Research Grant #118198-IRG-58-001-52-IRG94 from the American Cancer Society (E.L.); the Mezin-Koats Colon Cancer Research Award (E.L.); The Randy Shaver Cancer Research and Community Fund (E.L.); the Litman Family Fund for Cancer Research; Family and Friends of G. Huntington; Central Society for Clinical and Translational Research Early Career Development Award (E.L.); Minnesota Masonic Charities; Minnesota Medical Foundation/University of Minnesota Foundation (E.L.); the Masonic Cancer Center and Department of Medicine, Division of Hematology, Oncology and Transplantation, University of Minnesota (E.L.); and the NIH Clinical and Translational Science KL2 Scholar Award 8UL1TR000114 (to E.L.). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.