- Open Access
Transient TNF regulates the self-renewing capacity of stem-like label-retaining cells in sphere and skin equivalent models of melanoma
© Ostyn et al.; licensee BioMed Central Ltd. 2014
- Received: 1 July 2014
- Accepted: 26 August 2014
- Published: 17 September 2014
It is well established that inflammation promotes cancer, including melanoma, although the exact mechanisms involved are less known. In this study, we tested the hypothesis that inflammatory factors affect the cancer stem cell (CSC) compartment responsible for tumor development and relapse.
Using an inducible histone 2B-GFP fusion protein as a tracer of cell divisional history, we determined that tumor necrosis factor (TNF), which is a classical pro-inflammatory cytokine, enlarged the CSC pool of GFP-positive label-retaining cells (LRCs) in tumor-like melanospheres. Although these cells acquired melanoma stem cell markers, including ABCB5 and CD271, and self-renewal ability, they lost their capacity to differentiate, as evidenced by the diminished MelanA expression in melanosphere cells and the loss of pigmentation in a skin equivalent model of human melanoma. The undifferentiated cell phenotype could be reversed by LY294002, which is an inhibitor of the PI3K/AKT signaling pathway, and this reversal was accompanied by a significant reduction in CSC phenotypic markers and functional properties. Importantly, the changes induced by a transient exposure to TNF were long-lasting and observed for many generations after TNF withdrawal.
We conclude that pro-inflammatory TNF targets the quiescent/slow-cycling melanoma SC compartment and promotes PI3K/AKT-driven expansion of melanoma SCs most likely by preventing their asymmetrical self-renewal. This TNF effect is maintained and transferred to descendants of LRC CSCs and is manifested in the absence of TNF, suggesting that a transient exposure to inflammatory factors imprints long-lasting molecular and/or cellular changes with functional consequences long after inflammatory signal suppression. Clinically, these results may translate into an inflammation-triggered accumulation of quiescent/slow-cycling CSCs and a post-inflammatory onset of an aggressive tumor.
- Cancer stem cells
- Label-retaining cell
Human malignant melanoma is an extremely aggressive and drug-resistant skin cancer with poor prognosis if detected at an invasive stage. Despite advances in melanoma research and drug development, 10-20% of clinically disease-free patients relapse 5–10 years following an initial treatment ,. This phenomenon, which is known as tumor dormancy , has been related to the existence of therapy-resistant cells with stem-like activity -. Recent findings suggest that cancer stem cells, in response to chemotherapy, enter protective, prolonged, but reversible, quiescence  and remain dormant without causing any clinical manifestations until activated . Once activated, cancer stem cells (CSCs) are responsible for melanoma re-initiation, tumor progression and increased tumor aggressiveness. Mechanisms that control quiescent tumor cell activation remain poorly understood; however, cellular interactions, the immediate microenvironment of various diffusible factors or immune surveillance may be responsible. The relatively well documented connection between the incidence of cancer and chronic inflammation , prompt us to study whether pro-inflammatory Tumor Necrosis Factor (TNF) is involved in the phenotypic switch of quiescent tumor cells into their active proliferative state in melanoma. This cytokine, which was discovered by Carswell et al. , is considered one of the major mediators of inflammation responsible for the development of many cancers ,, including melanoma, upon exposure to ultraviolet radiation . Using an inducible H2B-GFP tracing system, we demonstrated for the first time that TNF increases the sub-population of quiescent or slow-cycling melanoma stem-like cells. This increase was associated with the increased self-renewal and sphere-forming abilities of melanoma cells in vitro and their tumor-like founding capacity in an in vivo-like model of human skin equivalents (SEs). More importantly, by a serial transplantation of SE-tumor cells using sphere-forming assays, we found that the tumor-founding cells maintain these TNF-induced properties for generations after first exposure and that this activity may be mediated by the PI3K/AKT signaling pathway.
Detection of label-retaining melanoma cancer stem cells in vitro
Pro-inflammatory TNF increases the proportion of label-retaining melanoma stem cells
TNF inhibits melanoma cell differentiation and induces transferable changes affecting the size of the melanoma SC pool in 3D tumor-like sphere and organotypic skin models
To gain insight into the possible cellular mechanism(s) by which TNF maintained its effect, we recapitulated melanoma in an in vivo-like , skin equivalent (SE) model, which is an alternative to animal models, using sorted quiescent (GFPhigh) and fast-cycling (GFPlow) cells in the presence or absence of systemic TNF for 3 weeks. Interestingly, control GFPhigh HBL-H2B-GFP cells (Figure 4D) and, to a lesser extent, SK-Mel28-H2B-GFP (not shown) cells were capable of developing into the highly pigmented assembly of cells resembling melanoma tumor in vivo. TNF apparently limited this process in GFPhigh SEs and had no effect on GFPlow SEs, which contained only a few pigmented spots. These data underline the superior tumor regeneration potential of the GFPhigh cells over their GFPlow counterparts and suggests that chronic TNF either specifically eradicates the majority of GFPhigh cells in SEs or suppresses their differentiation. The presence of some pigmented spots in all SEs independent of the condition indicates a differential cellular response to environmental clues and suggests that both GFPhigh and GFPlow cell compartments are heterogeneous and that the GFPlow compartment contains a small subpopulation of cells with SC activity but are phenotypically undistinguishable from the non-stem GFPlow cells, ratifying our earlier findings .
To resolve whether TNF eradicates or blocks GFPhigh cell differentiation, SE cells were recovered and assayed for their sphere-forming abilities. Apparently, GFPhigh cells were not eradicated because these cells initiated the formation of more spheres (Figure 4E) when derived from TNF-treated SEs. Consistent with a study by Landsberg et al. , this result indicates that TNF inhibited the melanoma GFPhigh cell differentiation fate. However, in Landsberg et al. study, this effect was massively reversible at the molecular level. We concluded that the TNF-induced changes targeting melanoma SC compartment are irreversible, at least at the functional level, because the TNF-reduced pigmentation was linked to a steadily increasing number of secondary and tertiary spheres formed by the sorted GFPhigh cells dissociated from the first generation TNF-treated melanosphere in the absence of TNF (Figure 4E). A small effect of TNF on GFPlow and unexposed melanosphere cells confirms the existence of actively dividing CSCs , within the non-SC GFPlow cell subset. However, their number tended to decrease with further generations, suggesting that the GFPlow cells in the TNF-free environment progressively exhaust their sphere-initiation and repopulation capacity, which is apparently well preserved by the GFPhigh cell subset that seems to attain a TNF-exposure “memory”. Interestingly, these capacities appear to be specifically restricted by the SE environment since unexposed GFPlow SE cells generated fewer spheres then unexposed GFPlow sphere cells (Figure 4B vs 4E). Collectively, all the above data demonstrated that melanoma cell lines contain a small pool of GFPhighABCB5highCD271high, quiescent/slow-cycling, self-renewing, melanoma stem-like cells that lose their ability to differentiate when targeted by TNF, even transiently, and that these cells appear to transfer this effect to further generations and manifest post-TNF exposure.
Inactivation of the PI3K/AKT signaling pathway abolishes the TNF effect on the melanoma stem cell compartment
Reversible cellular quiescence is a hallmark of SCs. This ability protects these cells from a harsh environment and prevents their exhaustion imposed by constant cycling ,,. CSC entry into cellular quiescence and their post-therapeutic persistence in an apparently dormant state may be one reason why curing cancer remains difficult. Dormant cells can be activated and re-initiate tumor growth locally and in distant metastatic sites ,. The exact molecular factors and cellular mechanisms governing the quiescence and activation of dormant CSCs have been intensely investigated but remain unclear, highlighting the requirement for additional research in this area. Because inflammation has been functionally related to cancer evolution and because inflammatory signals have been shown to regulate the quiescence/activation of cancer and normal SCs ,,,, but not much is known concerning the circuitries connecting inflammation to melanoma development, we examined the effect of TNF, which is one of the major mediators of cancer-related inflammatory responses , on melanoma cell quiescence and melanoma development in 3D tumor-like sphere and in vivo-like reconstructed skin models. Using an inducible H2B-GFP system to trace the cell divisional history in vitro, we identified quiescent/slow-cycling GFPhigh label-retaining CSCs in melanoma cell lines and showed that transient and chronic TNF suppresses melanoma SC differentiation while enriching for a GFPhigh melanosphere-initiating CSC subpopulation many generations after TNF withdrawal. This finding is consistent with a model in which inflammatory TNF signals imprint transferrable changes in the melanoma SC subpopulation, permanently affecting their fate and function and, consequentially, their progressive post-TNF expansion. Because the size of the CSC compartment is directly linked to a tumor burden , by enlarging this compartment, TNF may cause a predisposition to melanoma development and evolution. Our findings suggest that TNF may achieve this effect by activating the PI3K/AKT signaling pathway.
AKT signaling, which is often constitutively active in melanoma cells and in other cancer cells, regulates many cellular processes, including cell survival, metabolism and cell cycle progression ,,. Interestingly, recent findings indicate that AKT is a particularly important determinant of SC function because AKT controls SC quiescence, propagation and fate -. Recently, we demonstrated that quiescent melanoma SCs exit the G0 phase of the cell cycle in response to transient AKT inactivation; however, their cycling subset enters the quiescent state, whereas sustained AKT inhibition suppresses cell cycle progression . In the present study, we found that LY294002, which is an inhibitor of PI3K/AKT, specifically blocked the TNF-driven enrichment of melanospheres in GFPhigh label-retaining cells with the CSC phenotype and activity. This inhibition was accompanied by the acquisition of dendritic cell morphology and by the overexpression of the melanocyte differentiation marker MelanA. These data demonstrate that PI3K/AKT inactivation stimulated melanoma GFPhigh cell differentiation, suggesting that TNF suppresses their commitment to the differentiation fate by activating AKT, consequently preventing asymmetric self-renewal and promoting symmetric self-renewal of GFPhigh melanoma SCs. This interpretation is consistent with the observed TNF-driven increase in the proportion of GFPhigh cells and in the sphere-forming efficiency as well as with the inhibition of GFPhigh CSC melanogenesis in SEs and with the simultaneous acquisition of sphere-forming abilities by the SE melanoma cells. Therefore, it appears that one mechanism by which TNF and, in general, inflammation may cause cancer predisposition is a blockage of the differentiation fate in CSCs, at least partially preventing the generation of their fast-cycling destined-to-differentiate progeny. Logically, this mechanism would maintain CSCs in their primitive, quiescent/slow-cycling state and lead to their slow, but continuous, accumulation particularly because the TNF-induced changes seem to be perpetuated in the offspring of CSCs after TNF withdrawal. Currently, the mechanism of this event is unknown. Very recently Wilson et al.  have reported that melanoma SC maintenance is dependent on ABCB5-dependent secretion of Il1β another inflammatory cytokine. Is TNF-induced ABCB5 part of this regulatory circuit? Importantly however, the precedence of the transient induction of heritable changes after removing a stimulus has already been linked to the epithelial-to-mesenchymal transition process, creating self-renewing breast cancer stem cells from a non-stem cell population ,. In another study, a “memory” of transitory FGF had a long-lasting effect on the fibroblast response to the secondary FGF stimulation; this memory reduced rather than increased their proliferation . These findings underscore epigenetics and chromatin structure in controlling long-term responses, including the generation of CSCs and their phenotypic plasticity . Whether similar molecular and cellular changes can be ascribed to the TNF long-lasting action remains to be investigated. However, TNF was shown to induce EMT and to create a permissive environment for a “non-CSC to CSC” conversion in breast cancer , and our data do not exclude the possibility that this mechanism could be responsible for the TNF-induced changes in the melanoma SC compartment. Notably, recent data provided evidence for cell competition as yet another mechanism leading to the selection and expansion of the best-fitted cell (review see -), which could theoretically also be responsible for the selection of the best-fitted melanoma SC in the TNF environment and their post-TNF expansion. Nevertheless, although the above mechanisms are possible, in the absence of evidence, these mechanisms remain yet to be proven options.
The TNF-induced differentiation repressing mechanism, which is mediated by the PI3K/AKT signaling pathway, seems to be the most probable explanation of our results and is strongly supported by the findings of other researchers. For example, TNF was shown to induce the reversible dedifferentiation of melanoma cells  and an increased melanocyte number while inhibiting their differentiation-related pigmentation . Similarly, TNF promotes neural stem (NSC) cell proliferation but inhibits their differentiation  and maintains osteosarcomas in their undifferentiated state . Additionally, in the hematopoietic system, TNF was shown to have a stimulatory growth effect on hematopoietic stem cells (HSCs) but to negatively regulate the growth of their more mature progenitors in vitro. In contrast, recent findings revealed that TNF suppresses cycling HSCs and their long-term repopulating activity in vivo and in vitro, indicating that although the TNF pathway is a critical regulator of HSC maintenance and function (reviewed in ), the stimulatory and/or repressive effect of TNF will depend on cell types, the responding compartment and the cell status within each compartment. Little is known concerning the effect of TNF on the melanoma SC compartment. We  and others  have shown that this compartment is heterogeneous and, as we suggested, that this compartment is composed of CSCs in at least 3 different states: quiescent, slow-cycling and fast-cycling, which are each identified by distinct phenotypes and which each have a different mode of response to environmental changes. Roesch et al.  determined that the slow-cycling melanoma cells, which were identified in our study as GFPhigh cells, have the particular ability to switch between these phenotypes by assuming a distinct epigenetic state regulated by histone demethylase. Melanoma tumor growth depends on the presence of these cells. Consistently, the GFPhigh cells in our reconstitution assay using an in vivo-like skin equivalent model were significantly more efficient in reproducing pigmented lesions resembling melanoma in vivo than their faster proliferating counterparts. This ability was suppressed by TNF, which simultaneously induced the number of melanosphere-inducing GFPhigh cells. In melanospheres, these cells co-existed with their GFPlow progeny and persisted, although many divisions were required to form a melanosphere. This finding indicates that TNF, while blocking the differentiation fate of slow-cycling cells, reverses at least some of these cells into a quiescent state to prevent their exhaustion. These data strongly suggest that TNF maintains melanoma SCs in their primitive state and controls their plasticity. One pathway that is responsible for this effect is PI3K/AKT signaling, which regulates “stemness” in many stem cell systems  and was shown to be selectively inactivated in one of the symmetrically dividing cells to induce quiescence in one daughter while another continues to divide .
In conclusion, we determined that transient TNF suppresses the PI3K/AKT-mediated melanoma SC differentiation and enlarges a GFPhigh melanosphere-initiating CSC subpopulation that preserves the TNF-instigated changes, reinforcing their post-TNF capacity to form tumor-like melanospheres. These findings may have important clinical consequences because an acute inflammation may activate and expand pre-existing altered cells that remain clinically silent for generations until these cells emerge in a post-inflammatory environment as a primary or metastatic tumor in a more aggressive form.
Cell line and cell culture
The human cutaneous melanoma cell line HBL was established in Professor Ghanem’s laboratory from a nodular malignant melanoma . These cells were maintained in RPMI (Gibco®, Life Technologies™, France) supplemented with 10% fetal bovine serum (FBS) (Lonza, Verviers, Belgium) and 1% penicillin/streptomycin (Gibco®, Life Technologies™, France) in a humidified 5% CO2 incubator at 37°C. The medium was changed every 3 days. The SK-Mel28 cells were purchased from ATCC (HTB-72) and grown as recommended. Primary keratinocyte and fibroblast cultures were established using specimens of adult skin discarded after breast plastic surgery (Hôpital Roger Salengro, CHRU, Lille, France) as described previously . The storage and use of human biological samples were declared and performed according to the local Person’s Protection Committee and to the ethical rules approved by the Department of Health, France. Keratinocytes were maintained in defined K-SFM (Gibco®, Life Technologies™, France) supplemented with 1% penicillin/streptomycin (Gibco®, Invitrogen™, France). Fibroblasts were cultured in RPMI supplemented with 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin.
Construction of plasmids and generation of stable transfectants expressing inducible H2B-GFP
To accomplish the tetracycline-inducible expression of fused histone 2B-green fluorescent protein (H2B-GFP), we cloned the Taq polymerase-amplified H2B-GFP gene from Addgene into the PCR8/GW/TOPO entry vector and then into the pT-Rex DEST30 destination vector using the Invitrogen Gateway cloning system and Clonase II enzyme mix. The constructed pT-Rex DEST30-H2B-GFP plasmid was used for the Lipofectamine-mediated transfection of human melanoma HBL and SK-Mel28 clones that were previously modified and preselected in the 0.5 μg/ml blasticidin-containing medium to express high levels of tetracycline-sensitive repressor (TetR) from the pcDNA 6/TR Invitrogen plasmid. HBL and SK-Mel28 cells expressing both plasmids were preselected in 400 μg/ml geneticin (G418 sulfate) and 0.5 μg/ml blasticidin and cloned using serial dilution assay. The presence of two plasmids, pT-Rex DEST30-H2B-GFP and pcDNA 6/TR, in the individual clones was verified by RT-PCR, and H2B-GFP expression was confirmed by flow cytometry. To induce H2B-GFP expression, cells were incubated for 24 h with 1 μg/ml tetracycline, which inactivated TetR and derepressed the tetracycline operator 2X TetO2 (Tet-ON system), permitting H2B-GFP transcription from the CMV promoter. Clones that expressed high, but not toxic, levels of H2B-GFP were chosen for further experimentation. Stably transfected cells were grown in the presence of blasticidin and geneticin to maintain TetR and H2B-GFP genes. Blasticidin was obtained from Gibco®, Life Technologies™, France, and geneticin was obtained from Santa Cruz Biotechnology. RNA extraction was performed following the manufacturer’s protocol (RNeasy Kit, Qiagen, Courtaboeuf, France). Primers were designed to amplify 305 bp cDNA fragments for the pcDNA6/TR plasmid and 187 bp cDNA fragments for the pT-Rex DEST30-H2B-GFP plasmid as follows: 1st plasmid: 5’CTGGTCATCATCCTGCCTTT3’ and 5’GGCGAGTTTACGGGTTGTTA3’; 2nd plasmid: 5’ACGTAAACGGCCACAAGTTG3’ and 5’AAGTCGTGCTGCTTCATGTG3’. RNA was transcribed into cDNA using random hexamers, recombinant RNasin® ribonuclease inhibitor (Promega, France) and M-MLV reverse transcriptase (Promega, France). PCR was performed using GoTaq® Flexi DNA polymerase (Promega, France).
Generation of melanospheres
To generate primary spheres, 4 ± 103 cells were plated on 24-well plates coated with a 0.5 mg/ml poly-2-hydroxyethylmetacrylate (polyHEMA) ethanol solution (Sigma-Aldrich, France) to prevent cell attachment and cultured in DMEM/F12 medium (Gibco®, Life Technologies™, France), which was supplemented with 20 ng/ml EGF (Stem Cells Biotechnologies, Vancouver, BC, Canada), 1:50 B27-supplement (Gibco®, Invitrogen™, France), and 20 ng/ml rHu bFGF (PromoKine-PromoCell GmbH, Heidelberg, Germany), in a humidified 5% CO2 incubator at 37°C for 7 days. Tumor Necrosis Factor α (TNF) (0.5 μg/ml) from Immunotools, Germany, and/or an inhibitor of the PI3K/AKT signaling, 10 μm LY294002, or an inhibitor of NFκB signaling, 1 μm BAY 11-7082, which were both obtained from Calbiochem, France, were added at the time of sphere seeding and not re-added during the 7 days of sphere formation. Spheres were dissociated by a brief incubation with trypsin/EDTA solution (Gibco®, Life Technologies™, France) and then used as a single cell suspension for all the experiments. Cell viability was evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay (Sigma-Aldrich, France). After complete solubilization, the presence of blue formazan was evaluated spectrophotometrically by measuring the absorbance at 562 nm. For the LRC-assay, cells were treated with tetracycline (1 μg/ml) for 24 hours at 37°C in adherent culture and plated as above. Spheres (larger than ~50 cells) were counted under the microscope, and sphere-forming units (SFUs) (%) were estimated according to the formula: number of spheres/number of plated live cells ± 100.
Spheres containing GFPhigh cells were dissociated, and single cell suspensions (2 ± 105 cells/500 μl) of HBL or SK-Mel28 cells were incubated for 45 min on ice in 100 μl of RPMI medium with the following primary antibodies: anti-ABCB5 (Rockland, Tebu-Bio, France), which was used at a 1:215 dilution, and anti-VEGFR1 (Abcam), anti-Notch (Santa Cruz Biotech), and anti-CD57 (HNK-1) (gift from Dr E. Dupin, Vision Institute, Paris or from Santa Cruz Biotech), which were used at a 1:50 dilution. After incubation, the cells were rinsed with RPMI, centrifuged and resuspended in 100 μl of RPMI with a secondary antibody, Cy5® goat anti-rabbit IgG (H + L) or goat anti-mouse (Molecular Probes®, Life Technology™, France), which was used at a 1:2000 dilution for 30 min on ice in dark. After incubation, the cells were rinsed with RPMI, centrifuged, resuspended in 500 μl of RPMI, and placed on ice before being analyzed by flow cytometry. Propidium iodide (PI)-positive dead cells were gated out and excluded from the analysis. Acquisition was performed on an EPICS-CYAN flow cytometer (Beckman Coulter France S.A.S.) and analyzed using Summit 4.3 software. GFP fluorescence intensities were recorded on the FL1 channel. Quadrants were determined based on negative control staining with a corresponding isotype antibody. FACS sorting: Cell sorting was performed on an FACS-ALTRA sorter (Beckman Coulter France S.A.S.). Spheres were dissociated, and the single cell suspension was adjusted to a concentration of 106 cells/ml in RPMI. After excluding cell debris, the collection gates were set according to the negative (GFPlow) control containing cells untreated with tetracycline. Cells with positive fluorescence constituted the GFPhigh cell subset. The collected cells were centrifuged, rinsed and re-plated for sphere and colony generation.
Generation of human skin equivalents
Skin equivalents (SEs) were prepared as described previously . Briefly, dermal equivalents (DEs) were prepared using primary human fibroblasts (3 ± 105/DE) in RPMI with heat-deactivated fetal bovine serum (FBS), 1 mM NAOH and collagen I (rat tail collagen type I, BD Biosciences, France), which were placed into 6-well plates and allowed to contract for several days until their radii reached 5 mm. To regenerate melanoma cells in a reconstructed epidermis, a mixture of primary keratinocytes (1 ± 105/SE) and 1 ± 104/SE human melanoma cells with or without sorting were seeded onto DEs and cultured for 7 days in DMEM (Gibco®, Life Technologies™, France) supplemented with 10% FBS in the presence or absence of 0.5 μg/ml TNF. Then, the cultures were lifted at the air-liquid interface to stimulate keratinocyte differentiation. The medium, which was supplemented with 0.5 μg/ml hydrocortisone, was changed every 2–3 days. After 21–23 days of culture, skin equivalents were dissociated using 4 mg/ml collagenase for 30 min at 37°C and trypsin/EDTA for an additional 5 min. Then, melanoma cells were counted and plated on 24-well plates coated with polyHEMA in DMEM/F12 for sphere formation.
EdU incorporation by melanosphere cells
An Alexa Fluor® 647 Click-iT Edu Flow Cytometry Assay Kit (Life Technologies) and its accompanied recommendations were used to estimate the proportion of GFP-positive and -negative melanosphere cells in S phase. Non-cytotoxic 10 μm EdU (5-ethynyl-2’-desoxyuridine) was added for 2 hours to melanosphere cultures before harvesting. Melanospheres were dissociated with trypsin/EDTA, and a suspension of 1 ± 106 individual cells was centrifuged, washed twice with PBS/1% BSA buffer and fixed in 4% paraformaldehyde solution for 15 minutes at RT in the dark. The fixed cells were permeabilized with saponin solution and incubated with Alexa Fluor® 7 azide in the supplied buffer for 30 minutes in the dark. Labeled cells were analyzed by flow cytometry. For the detection of EdU with Alexa Fluor® 647 azide, we used 633/635 nm excitation with a red emission filter (660/620 nm). The proportion of melanoma cells that were both EdU-positive and GFP-positive or GFP-negative was estimated by a flow cytometry quadrant analysis determining the percentage of each subpopulation. Negative control was gated using EdU unstained and tetracycline uninduced cells.
HBL-H2BGFP melanospheres were cultured for 7 days in the presence or absence of TNF (0.5 μg/ml) and/or LY294002 (10 μm), which were both added at seeding. The dissociated melanosphere cells were plated on Lab-Tek chamber glass coverslips (Millicell EZ SLIDE 8-well glass, sterile Merck Milipore, Darmstadt, Germany) at a density of 15 000 cells per well. After 24 hours, the adherent cells were fixed in PAF solution, and immunocytochemistry was performed according to the standard procedure. A monoclonal anti-Melan A antibody, which was purchased from Santa Cruz Biotech, was used at a dilution of 1:100, and positive cells were detected with a secondary AlexaFluor 594 goat anti-mouse (Life Technologies), which was used at a dilution of 1:2000. Negative controls were performed by replacing the primary antibody with an irrelevant isotype. Nuclei were counterstained with DAPI. All slides were mounted under a coverslip with Vectashield mounting medium (Vector Laboratories, Nanterre, France) and were photographed using a Leica DMRB LAS3.7 fluorescence microscope.
Western blot analysis
Western blot analysis was performed using ready-to-use NuPAGE 4%-12% Bis-Tris polyacrylamide gels according to the supplier’s instructions (Invitrogen™, St. Aubin, Paris, France). Blots were probed with the primary antibodies against Actin (Sigma-Aldrich, St. Quentin Fallavier, France), Akt and pAkt (Cell Signaling, France), followed by a horseradish peroxidase-conjugated secondary antibody (Bio-Rad, Marne-la-Coquette, France). Corresponding isotypes were used as controls. Immunodetection was performed using an ECL + chemiluminescence kit from Amersham. The band intensities in immunoblotting were analyzed and quantified using ImageJ and user-supplied algorithms.
The results are expressed as the mean ± standard error of the mean (SEM) of at least 3 independent experiments each combining spheres from 24 wells unless indicated otherwise. A comparison between means was performed using Student’s t-test for unpaired data. When unequal variance was observed, Welch’s correction was applied. A comparison between several groups was performed using a one-way analysis of variance, followed by Dunnett’s multiple comparison test, using an appropriate control group as the reference. The statistical analyses were performed using GraphPad Prism 4.0 software. A p value of < 0.05 was considered significant.
PO and REM: design of experiments, collection and assembly of data, data analysis and interpretation. SB, NK, JV, and PF: collection and assembly of data, data analysis and interpretation. PS and BM: collection and assembly of data. PF: interpretation and discussion. YT and RP: conception and design, data analysis and interpretation, preparation and writing of the manuscript. All authors read and approved the final version of the manuscript.
The authors thank Nathalie Jouy (BiCell-IFR114 flow cytometry platform) for her assistance with the flow cytometry analyses and FACS sorting. The authors are grateful to the Department of Plastic Surgery at the Roger Salengro Hospital for providing skin specimens. This research was supported by the Institut National de la Sante et de la Recherche Medicale (INSERM), the Institut National du Cancer (National Cancer Institute) of France and the SILAB-Jean Paufique Corporate Foundation. Y. Touil was supported by the Institut Pour la Recherche sur le Cancer de Lille (IRCL) and by SIRIC ONCOLille R. El Machhour was supported by the Ligue Nationale Contre le Cancer. P. Flamenco was supported by the CPER (Contrat de Plan Etat/Région) program of the Nord - Pas de Calais region. P. Ostyn’s graduate study was financed by CHRU Lille and the Region Nord-Pas de Calais.
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