Neuroblastoma cells injected into experimental mature teratoma reveal a tropism for embryonic loose mesenchyme
- S. Jamil
- J. Cedervall
- I. Hultman
- R. Ali
- N. V. Margaryan
- A. Rasmuson
- J. I. Johnsen
- B. Sveinbjörnsson
- T. Dalianis
- L. Kanter
- A. Orrego
- L. Strizzi
- M. J.C. Hendrix
- B. Sandstedt
- P. Kogner
- L. Ährlund-Richter
- Published online on: July 12, 2013 https://doi.org/10.3892/ijo.2013.2014
Key knowledge is still missing for the successful cure of aggressive neuroblastoma (NB), representing one of the most deadly pediatric malignancies (1–4). Neuroblastoma is a small round cell tumor of childhood and is considered to arise from dedifferentiation of primordial neural crest cells that populate the sympathetic trunks and the adrenal medulla (reviewed in ref. 5). During this process, an aberrant response to microenvironment cues may play an important role in modulating the tumor phenotype, and hence also lead to the variable clinical presentations of NB in patients. The clinical presentation spans from a benign type with the ability to spontaneously regress to a variant with a high rate of recurrence, metastatic spread and a high frequency of therapy-resistance. Current consensus supports the importance of a strong interplay with the surrounding tissue promoting tumor growth and spread (6). Thus, pre-clinical studies of childhood NB would for increased relevance benefit from in vivo models better matching the embryonic neoplastic niche in early development from which this tumor is believed to originate.
Pluripotent stem cells (PSC) are defined by their ability to differentiate into any of the three germ layers and ectopic injections into mice repeatedly produce what is described as experimental teratoma (7,8). Although generically referred to as a tumor, others and we have previously reported evidence that pluripotent stem cell-derived teratoma (PSCT) from PSC with normal karyotype can be described as a failed embryonic process including increasingly chaotic embryonic tissues and an emerging organoid development (7,8–11). Despite lacking a developmental axis this process can show striking similarities to the events in the human embryo, including and often dominated by components of early neural development (9,10). When compared to human embryos at diagnosed gestation stages, we observed minor kinetic deviations in the appearances of several organoid structures in PSCT developed from the well-studied human embryonic stem cell line HS181 (10). However, more advanced organoid structures are rare (7–10) and a prolonged immaturity of some neural components is a consistent finding also in benign PSCT induced by PSC with normal karyotype (reviewed in ref. 8). More specifically, such immature neural areas display a strong resemblance with primitive neuroectodermal tumors and a similar histology when appearing in patient samples is considered potentially malignant.
The stem cell induced teratoma environment has earlier been suggested as an experimental platform for studying human tumor cell lines of a variety of origins (ovarian, prostate, lung, glioblastoma, breast, colorectal cancer) (12–14). Similarly, we studied growth from a malignant melanoma cell line in human experimental teratoma and identified a de-differentiated tumor phenotype not present in xenografts from the same cell line (15), possibly indicating an adaptation of the tumor cells to the embryonic microenvironment.
To generate new insights and testing a principle of closer developmental match between the injected tumor and the PSCT microenvironment, we conducted experiments to explore the PSCT milieu specifically for in vivo support of tumors of embryonic origin. Proliferative tumor cells from the injections of three aggressive NB cell lines; IMR-32, Kelly and SK-N-BE(2) could readily be identified and growth was found exclusively integrated into areas of loose mesenchyme, presenting tumors with histological resemblance to clinical NB.
Materials and methods
This study was performed in full accordance with permission for experiments using human embryonic stem cells, from the Local Ethics Committee at Karolinska Institute (114/00), and for animal experimentation from the regional ethics committee (Stockholm Northern Animal Review Board; Dnr S172-03 and N105/07).
The human embryonic stem cell lines HS181 (16) and H9 (17), both of 46:XX karyotype, were maintained in culture as previously described (18). The human male NB cell lines IMR-32, Kelly and SK-N-BE(2) were obtained from ATCC (Manassas, VA, USA). For genetic profile see Table I. All tumor cell lines were cultured in Iscove’s modified Dulbecco’s medium (IMDM) supplied with 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin (all from Invitrogen, Carlsbad, CA, USA), at 37°C, 6.8% CO2, with high humidity.
Animals and generation of PSCT
SCID/Beige (C.B.-17/GbmsTac-scid-bgDF N7; M&B, Ry, Denmark), male mice, 6–8 weeks old, were used. PSCT were generated by injection of 104–105 HS181 under the testicular capsule of mice, as previously described (8,9). PSCT were allowed to progress for 45 days before injected with NB tumor cells. The variations of germ layer formation in separate HS181 PSCT formed under the present conditions have been described previously in more detail and were in all cases minor (9,15).
Injection of NB cells
Cells from the indicated cell lines (1×106 cells in 20 μl PBS), were injected into 45-day-old PSCT, or as a xenograft, directly under the testis capsule of mice anesthetized using isofluran (3%). Injections of NB cells resulted in outgrowth in all cases. For number of injections and frequency of tumor takes see Table I. Animals were sacrificed two weeks after NB tumor cell injection, before reaching the limit of the accepted total size of the PSCT, including NB tumor growth, according to the ethical permit for the recipient animal.
Tumors were harvested after two weeks, fixed in 4% paraformaldehyde at 4°C 24 hours and dehydrated through a graded series of alcohol to xylene, embedded in paraffin, then serially sectioned into 5-μm-thick sections and stained using standard hematoxylin and eosin (H&E) staining for basic histological orientation. For each NB cell line, two xenografts and two PSCT with injected NB tumor were subjected to detailed screening of 10–30 sections each.
Verification of NB tumor growth
Presence of NB tumor cells was verified using genetic identification as described previously (15). Human Y- and X-chromosomes was detected using mixed probes (CEP XY; Vysis Inc, Downers Grove, IL, USA) against the human X- and Y-chromosomes, thus positively separating human from mouse cells in xenografts, as well as separating IMR-32 cells (XX) from PSCT cells (XY), as previously described (15). For the identification of Kelly and SK-N-BE(2), both lacking stable Y-chromosome centromeres, the identification of their genetic MYCN amplification was performed using the probes LSI N-MYC, 2p24 (Vysis Inc).
Areas of identified tumor growth were subjected to immunohistochemistry (IHC) using criterion for histological analysis of NB cell differentiation as those used in daily clinical practice and in other studies (19,20).
Dilutions and conditions for the specific antibodies and secondary detection methods are presented in Table II. The IHC results were verified using positive control slides from tissues known to express the antigen of interest. Negative controls were performed by omitting primary antibody and by using non-specific antibodies as isotype controls in the same concentration as the primary antibody. Species-specificity of the human specific antibody for CD31 was verified internally in each staining, since both xenografts and the PSCT environment contain numerous vessels of murine origin, which were all negative.
Imaging was performed using a Zeiss Axiovert 200M microscope and Openlab 5.0 software. Images were adjusted for auto levels in Photoshop.
Histopathology of NB cell lines in xenografts and PSCT
For all three NB cell lines the injections of 106 cells yielded detectable tumor growth in all animals. The number of injections and frequency of tumor takes are summarized in Table I.
All NB cell lines presented growth in smaller nodules as well as larger areas of cohesive tumor growth. A consistent finding in both xenografts and PSCT was a poorly differentiated tumor with a variable amount of fibrovascular stroma, and no Schwann cell differentiation (Table III and illustrated in Fig. 1A–F for all three NB lines). Further, presence of a neuroendocrine phenotype as reflected by positive staining for synaptophysin and chromogranin A was a consistent finding for all three NB cell lines in both models, as exemplified by SK-N-BE(2) in Figs. 1E,F and 2D.
In vivo histology of IMR-32, Kelly and SK-N-BE(2). Section of PSCT two weeks after injection of NB cells, showing poorly differentiated tumors with a variable amount but mainly little fibrovascular stroma, and no Schwann cell differentiation. In the left hand panels (A, C and E) sections from intra testis xenografts, and in the right hand panels (B, D and F) sections after injections into PSCT. (A and B) IMR-32 cells stained for hematoxylin and eosin (H&E). (C and D) Histology of Kelly tumor, stained for HIF2α. (E and F) Histology of SK-N-BE(2), stained for COX2. Original magnifications, ×40.
Nodular NB growth is in the PSCT located in embryonic loose mesenchyme. (A) Section of PSCT two weeks after injection with IMR-32, stained for hematoxylin and eosin (H&E). Arrows indicate two separate areas with IMR-32 growth. (B) Higher magnification of boxed area. LM, loose mesenchyme. Inserted picture illustrates FISH analysis of adjacent section using human specific probes (green signal, human X-chromosome; red signal, human Y-chromosome) verifying location of IMR-23 cells. (C) Illustration of Kelly nodular growth (indicated by arrows) located in loose mesenchyme and close to vessels staining positive for human CD31. (D) Small groups of SK-N-BE(2) tumor cells staining positive for Chromogranin A, embedded in loose mesenchyme. Original magnifications, (A) ×10; (B, C and D) ×40.
The numbers of mitosis were similar in PSCT and xenografts; IMR-32 showed a proliferation index of >70% in both models, while SK-N-BE and Kelly showed a proliferation index of 40–50%.
Tropism of NB outgrowth in the PSCT microenvironment
For practical reasons the NB cells were injected into random positions in the PSCT cell mass. Small nodules of tumor growth were however detected exclusively in areas compatible with undifferentiated mesenchymal stroma, and never observed in areas with well differentiated somatic tissue i.e. bone, muscle, gut or areas of other easily identifiable tissue types.
Fig. 2A illustrates IMR-32 nodular growth (arrows) located in a loose mesenchyme environment, with the dotted boxed area illustrated at a higher magnification (x40) in Fig. 2B. Fig. 2C illustrates the nodular growth of Kelly, here located next to vessels staining for human CD31. Similarly, Fig. 2D illustrates small groups of SK-N-BE(2) tumor cells, here stained for Chromogranin A, embedded in loose mesenchyme.
Expression of Nodal and Cripto-1 but not Lefty was demonstrated for IMR-32 growth in xenografts (Fig. 3A–C) as well as in the PSCT microenvironment (Figs. 3D–F and 4A–C). Notably, in the PSCT environment, non-tumor areas of Cripto-1 positive condensing mesenchyme with similar histology as NB tumor growth could be shown to exhibit a reciprocal Nodal/Lefty expression pattern (compare Fig. 4A2 and A3 with B2 and B3).
Expression of Nodal and Cripto but not Lefty in IMR-32 tumors. (A–C) Paraffin-embedded serial sections of IMR-32 xenografts, stained for (A) Nodal, (B) Cripto-1 or (C) Lefty. Seminiferous tubules are seen on the upper left side and the testis capsule in lower right corner. (D–F) Paraffin-embedded serial PSCT sections, showing an area of IMR-32 in the middle of the picture, stained positive for (D) Nodal, (E) Cripto-1 but not (F) Lefty. Original magnifications, ×40.
A reciprocal Nodal/Lefty expression of an IMR-32 tumor mirrors that of Cripto-1 positive condensing mesenchyme in PSCT. (A, B and C) Illustrates paraffin-embedded serial sections of PSCT two weeks after injection with IMR-32. Stained for (A) Nodal, (B) Lefty and (C) Cripto-1. Blue arrow indicates nodular growth of IMR-32 as verified by FISH analysis using human specific probes as described in text and Fig. 2 (data not shown). Two separate areas of condensing mesenchyme are indicated with dotted circles (a) and (b), respectively. (A1–3, B1–3 and C1–3) Show higher magnification of the staining in the indicated areas. Original magnifications (A, B and C) ×5; (A1–3, B1–3 and C1–3) ×20.
A comparable histology was observed for the three NB cell lines in the PSCT microenvironment or when growing as xenografts. However, the PSCT environment offered additional information and a conspicuous finding following injections into PSCT was that the smaller nodules of tumor growth, presumably representing the initial manifestation of NB, showed for all three NB cell lines a strict tissue preference between the components of the embryonic process in the stem cell induced mature teratoma. Initial growth was observed exclusively in areas compatible with embryonic loose mesenchymal stroma. There was no evidence for NB cells occurring in areas compatible with bone, muscle, gut or areas of other identifiable tissue types.
An upfront explanation regarding the mechanism behind this tropism could be the ‘open’ nature of the loose mesenchyme, i.e. more easily giving space to new cells compared to other more dense tissues. In this context, a recent report that rigidity of the extracellular matrix may provide a physical cue that can modulate NB differentiation, reduce NB proliferation and MYCN expression (21), is here of particular interest.
The ability of tumors to invade host tissues is dependent on signals mediated by several routes that normally enable important physiological functions, such as morphogenesis and angiogenesis. Notably, the mesenchyme of the early embryo is composed of a matrix of reticular fibers and myxoid ground substance and includes undifferentiated spindle or star shaped mesenchymal cells but also cells from other germ layers, e.g. ectodermal neural crest cells. The loose mesenchyme in PSCT is thus best understood as an embryonic tissue in which all connective tissue cell types may occur. The three main components of loose myxoid ground; glycosaminoglycans, proteoglycans and glycoproteins, are known components in cell-cell interactions and are here ideally situated for trophic factors. Thus, it can also be speculated from the presented findings that embryonic loose mesenchyme may supply developmental cues that attracted or promoted the integration of NB tumor cells in the present study.
Whether the explicit tropism identified for the three NB lines in the present study can be of a more general importance for NB, or specific for the tumors used, remains to be determined using a larger panel of NB tumor lines.
Another typical finding was that the NB cells were regularly found in the immediate proximity of vessels. A homing to the perivascular niche is in line with the notion that NB could be considered a stem cell disease of the sympathetic nervous system (5) and that the perivascular niche supports stem cell self-renewal capacity and an undifferentiated state of neural tumor cells (22).
The cellular origin is not exactly known but NB is assumed to originate from neural crest precursor cells that specifically differentiate into the sympathoadrenal lineage. In this context, it is of interest that the timing of NB tumor cell injections used in this study, day 45 of the developing embryonic process in PSCT, overlaps with the presence in PSCT of neural components compatible with gestation stages immediately preceding the positioning of adrenal sympatical progenitors in embryonic mesenchyme (neural crest development; E25–35) (3,19). Thus, we tentatively hypothesize that day 45 HS181 PSCT may provide a timely embryonic niche for in vivo studies on NB.
Some further indirect support for this hypothesis comes from the findings with the embryonic protein Nodal, member of the TGF-β superfamily. Nodal acts as a morphogen in human early development, balanced by its antagonist Lefty, but is not expressed by most normal adult tissues (23–25). Dysregulated expression has however been detected in several malignancies and expression of Nodal has been linked with invasiveness and metastasis; as reported for melanoma, glioma, and cancers of breast endometrium and prostate (25–28). In a previous study using a melanoma cell line we detected Nodal positive tumor cells invading surrounding mesenchymal stroma in the PSCT model (15). We therefore wanted to know whether expression of Nodal could be similarly identified for NB. For this we selected IMR-32 based on its observed infiltrative growth into the surrounding stroma. Our results demonstrated that aggressive IMR-32 tumor growth indeed showed expression of both Nodal and its co-receptor Cripto-1, but not the antagonist Lefty. Intriguingly, the reciprocal Nodal/Lefty expression of IMR-32 in PSCT mirrored that of nearby Cripto-1 positive areas of condensing mesenchyme. This indicates that the expression of Nodal/Lefty in IMR-32 concurred with Nodal regulation in PSCT early embryonic patterning (24).
In conclusion, aiming for the principle of a closer developmental match between the tumor and the microenvironment this study demonstrates the feasibility of using the embryonic PSCT microenvironment for modeling in vivo growth of childhood neuroblastoma. The exclusive integration of NB cells into embryonic loose mesecnhymal stroma added histology with close recapitulation of NB native presentation in patients. This finding, together with the advantage of a species identity of surrounding stroma, suggests clear benefits for the PSCT model compared to xenotransplantation and the PSCT microenvironment to be an important well-needed complement for pre-clinical studies of NB, facilitating clinical translation. Our continued studies will involve expanding the NB model from cell lines to clinical tumor material from young NB patients. Considering the extremely poor prognosis of malevolent NB, development of new clinically relevant models is of utmost importance.
This work was supported by the Swedish Childhood Cancer Foundation (08/092), the Cancer Research Funds of Radiumhemmet (09 1551 and 09 4271), Little Heroes Pediatric Cancer Research Foundation, Petrus and Augusta Hedlund’s stiftelse and Karolinska Institutet. S. Jamil and R. Ali were supported by stipends from the Higher Education Commission of Pakistan.
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