Regulation of cell proliferation and apoptosis in neuroblastoma cells by ccp1, a FGF2 downstream gene
© Pellicano et al; licensee BioMed Central Ltd. 2010
Received: 6 May 2010
Accepted: 30 November 2010
Published: 30 November 2010
Coiled-coil domain containing 115 (Ccdc115) or coiled coil protein-1 (ccp1) was previously identified as a downstream gene of Fibroblast Growth Factor 2 (FGF2) highly expressed in embryonic and adult brain. However, its function has not been characterised to date. Here we hypothesized that ccp1 may be a downstream effecter of FGF2, promoting cell proliferation and protecting from apoptosis.
Forced ccp1 expression in mouse embryonic fibroblast (MEF) and neuroblastoma SK-N-SH cell line, as well as down-regulation of ccp1 expression by siRNA in NIH3T3, was used to characterize the role of ccp1.
Ccp1 over-expression increased cell proliferation, whereas down-regulation of ccp1 expression reduced it. Ccp1 was able to increase cell proliferation in the absence of serum. Furthermore, ccp1 reduced apoptosis upon withdrawal of serum in SK-N-SH. The mitogen-activated protein kinase (MAPK) or ERK Kinase (MEK) inhibitor, U0126, only partially inhibited the ccp1-dependent BrdU incorporation, indicating that other signaling pathway may be involved in ccp1-induced cell proliferation. Induction of Sprouty (SPRY) upon FGF2 treatment was accelerated in ccp1 over-expressing cells.
All together, the results showed that ccp1 regulates cell number by promoting proliferation and suppressing cell death. FGF2 was shown to enhance the effects of ccp1, however, it is likely that other mitogenic factors present in the serum can also enhance the effects. Whether these effects are mediated by FGF2 influencing the ccp1 function or by increasing the ccp1 expression level is still unclear. At least some of the proliferative regulation by ccp1 is mediated by MAPK, however other signaling pathways are likely to be involved.
A previously uncharacterized gene named Coiled-coil domain containing 115 (Ccdc115) or coiled coil protein 1 (ccp1) (GeneID: 69668), has been recently identified downstream of Fibroblast Growth Factor 2 (FGF2) by microarray analysis and its expression pattern was characterized . The ccp1 transcript was up-regulated upon FGF2 stimulation in primary cortical neuron culture (CNC) derived from mouse embryonic telencephalon at embryonic day 14.5 (E14.5) and in neuroblastoma cell line, SK-N-SH. In situ hybridizations revealed that ccp1 was expressed in the ventricular zone (VZ), a region of the developing cerebral cortex known to be composed of progenitor cells undergoing proliferation .
The mechanism by which cell proliferation is controlled in the VZ is still not fully understood. A number of factors, including FGFs, have been shown to regulate the proliferation of progenitor cells in embryonic Central Nervous System (CNS) in vitro [3–7]. FGFs are a family of 22 polypeptides known to play various roles in neural development [8, 9]. FGF signals are mainly mediated by high-affinity receptor-type tyrosine kinases, FGF receptors (FGFRs). FGF signaling plays variety of roles in neural development and in pathogenesis of developmental diseases. FGFs are a class of molecules that regulate proliferation by controlling the length of the G1 phase. Addition of FGF2 in primary culture prepared from developing cortex at E14-E16 showed shortening of the G1 length and increase in proliferative divisions, indicating that FGF2 controls cell proliferation via its control of G1 length . Regulation of cell proliferation is mediated by a complex system of signaling pathways. One of the core pathways downstream of FGF is the mitogen-activated protein kinase (MAPK) pathway , which has a central role in transmitting cell proliferation and survival signals . In this pathway, RAS promotes activation of the serine/threonine protein kinases Raf1 and MEK1. In addition to controlling RAF kinases, MAPK may also directly regulate several other signaling pathway, such as the phosphatidylinositol 3 (PI3) kinase .
In this study, ccp1 function was investigated using a retroviral over-expression system and RNA interference (RNAi) in vitro. We analysed the effects of altered ccp1 expression in cell proliferation and apoptosis in mouse embryonic fibroblast (MEF), a neuroblastoma cell line SK-N-SH, and in NIH3T3. Since ccp1 expression is found regulated by FGF2, we also investigated the effects of FGF2 and compared them to those of the serum in ccp1-expressing cells. Furthermore, by specifically inhibiting the MAPK pathway with the pharmacological inhibitor U0126, we further investigated the involvement of this pathway in ccp1-induced cell proliferation. Our results showed that ccp1 regulates cell number by promoting proliferation and suppressing cell death.
SK-N-SH and MEF cells were maintained in D-MEM, 10% fetal bovine serum (FBS) and 2 mM glutamine. NIH3T3 were maintained in D-MEM, 10% DCS and 2 mM glutamine. The natural immortalised MEFs were originally from Dr Nick Dyson (Massachusetts General Hospital Cancer Center/Harvard Medical School, Charlestown, MA . Cells were maintained at 37°C in 5% CO2. When required, cells were starved in media without serum for 24 h and treated with FGF2 and heparin as indicated.
Retroviral-mediated expression of ccp1
Single strand cDNA was synthesized as described in . The retrovirus expression vector pLPC was obtained from Dr S. Lowe. Phoenix packaging cells were transfected with pLPC/eGFP or pLPC-ccp1/eGFP-N vectors using Lipofectamine 2000 (Invitrogen). Cells were incubated ON in 20% fetal bovine serum (FBS) media in order to allow virus production. Immortalized MEF and SK-N-SH cells were infected with the Phoenix-supernatant. The infection was repeated three times at intervals of 12 h each. After the last infection, cells were selected in the presence of 25 mg/ml of puromycin.
RNA interference (RNAi)
Transfection was performed using Lipofectamine 2000 reagent in Optimem media (Gibco) according to the manufacturer's instructions (Invitrogen). 50 nM/well of pre-designed and annealed siRNAs (Ambion) were used: siRNAi1, sense 5'-aguugaagccuuugacuuctt-3', anti sense 5'-gaagucaaaggcuucaacutc-3'; siRNAi2, sense 5'-ggcaugaaguugaguuaugtt-3', anti sense 5'- cauaacucaacuucaugcctc-3'. Scramble siRNA was purchased from Ambion. After 24 h, cells were harvested and RNA was extracted and used for semi-quantitative RT-PCR. The primers used were F-338 and R-1096 . Primers were designated against a DNA sequence with very high homology between mouse and human DNA.
BrdU assay was performed using BrdU labeling and detection Kit I (Roche). Cells were exposed to BrdU for 1 h and fixed in ethanol for 20 minutes (min) at -20°C. Anti-BrdU antibody was applied for 30 min at 37°C, and the fluorescein-conjugated secondary antibody for 30 min. Coverslips were mounted with 4',6 diamidino-2-phenylindole (DAPI). Photographs were taken using a Zeiss Axioskop microscope and Axiovision software.
Cells were lysed in Laemmli sample buffer (Biorad) and analysed on 12% SDS-PAGE. The proteins transferred to Hybond ECL nitrocellulose membranes (Amersham) were blocked with 10% dried milk in TBST (20 mM Tris, pH 7.6, 13.7 mM NaCl, 0.1% Tween 20) for 2 h. Incubation with the primary antibody was at 4°C overnight, and with the secondary, for 1 h at room temperature. Detection was with ECL (Amersham) exposed to X-ray film (Fuji). Antibodies were anti-ccp1 (1:500; anti-rabbit and anti mouse; Beatson Laboratories Antibody Services), anti-ERK, anti-p-ERK (Cell signaling), anti-Sprouty (Invitrogen) and anti-GFP (Abcam). Densitometry analysis was carried out by Quantity One program (Biorad).
TUNEL assays were performed using the In situ Cell Death Kit-AP (Roche). Cells were serum starved overnight and then fixed in 4% paraformaldehyde for 1 h at -20°C and permeabilised in 0.1% Triton X-100, 0.1% sodium citrate for 2 min at 4°C. The DNA strand breaks were fluorescently labeled via the TUNEL reaction for 1 h at 37°C. TUNEL-positive cells were detected by fluorescence (FITC, 520 nm).
Student's t-test was performed to test the significance of difference in numerical data as appropriate.
Our research conformed to the Helsinki Declaration and to local legislation.
Morphological changes of the cell upon ccp1 over-expression
In order to identify cellular localization of the ccp1 protein, analysis with confocal microscopy was carried out in MEF and SK-N-SH stably expressing ccp1/eGFP-N protein using an anti-GFP antibody (Figure 1C, a-b, e-f). While control cells expressing eGFP showed only diffuse fluorescence signals throughout the cells, the ccp1/eGFP-N protein was observed in a localized and punctate pattern. Although ccp1 was mainly present in the cytoplasm in MEF cells, SK-N-SH cells showed expression also in the nucleus and peri-nuclear region as observed in primary CNC .
Signaling through FGF/FGFR is known to result in morphological transformation of fibroblasts in vitro, which may be associated with tumor progression [15, 16]. Morphological transformation of the cell was observed upon stable expression of ccp1 in MEF and SK-N-SH (Figure 1C, c-d, g-h). Cells expressing ccp1/eGFP-N appeared smaller and had a spindle-like phenotype compared to the control cells. Morphological transformation in MEF stably expressing ccp1/eGFP-N protein was also shown by cytoskeletal staining of the actin filaments, in which actin cytoskeleton actin cytoskeleton actin cytoskeletonMembrane ruffling is visualized by staining the actin cytoskeleton actin remodelling and membrane ruffling was indicated upon ccp1 over-expression (Figure 1C, i-j).
Stable expression of ccp1 leads to an increase in cell number
In order to determine whether ccp1 could actually induce cell proliferation independent of growth factor stimulations, growth of cells were examined in MEF expressing ccp1/eGFP-N in the absence of serum (Figure 2C). Control MEF showed a mild increase in cell number for up to 4 days. In contrast, MEF stably expressing ccp1/eGFP-N showed a three-fold increase in cell number at 3 days in culture and then a decrease was observed on the 4th day. Similarly, BrdU assay was performed in MEF cells stably expressing ccp1/eGFP-N and cultured in the absence of serum (Figure 2D). As expected control parental MEF showed a marked decrease in BrdU incorporation when compared to cells grown in the presence of serum (Figure 2B and 2D). Interestingly, however, MEF expressing ccp1 showed an obvious increase in the number of cells in the S phase compared to that in control parental MEF even in the absence of serum.
These data indicated that ccp1 over-expression promoted cell proliferation in both the presence and absence of serum.
FGF2 treatment increases the proliferative effect of ccp1
We showed that ccp1 expression in MEF and SK-N-SH cells caused a change in cell morphology (Figure 1C). Here we addressed whether FGF2 played a role in ccp1-induced changes in cell morphology, compared to the effect of serum. Control parental MEF and MEF expressing ccp1/eGFP-N were starved overnight and treated with either 50 ng/ml FGF2 in the presence of 10 μg/ml heparin, or serum, for 24 h (Figure 3B). The morphological changes observed in ccp1-expressing cells became more prominent upon stimulation with FGF2 (Figure 3B, c-d) and changes were similar upon treatment with serum (Figure 3B, e-f).
BrdU incorporation is inhibited when ccp1 expression is knocked down by RNAi
Ccp1 stable expression protects cells from apoptosis
Effects of MEK inhibitor, U0126, in cell proliferation upon ccp1 over-expression
Control MEF expressing eGFP and MEF expressing ccp1/eGFP-N were cultured overnight in the absence of serum, in the presence and absence of 20 μM U0126 (Figure 6B). The effectiveness of U0126 was addressed in these cells by Western blotting and densitometry analysis, which confirmed reduced phosphorylated ERK upon treatment (Figure 6E). In the absence of U0126, an increase in BrdU incorporation was detected in the MEF stably expressing ccp1 compared to the control MEF (Figure 6B). Upon treatment by U0126, although BrdU incorporation remained similar in control MEF, a decrease was observed in MEF expressing ccp1. The effects of MEK inhibition was also analysed in cells treated with FGF2 and 10 μg/ml heparin (Figure 6C), as well as with 10% serum (Figure 6D). BrdU incorporation was partially inhibited in control MEF and in MEF expressing ccp1. This indicates that MAPK may play a partial role in cell proliferation promoted by ccp1 over-expression, however there are signaling pathways other than MAPK that are likely to be also involved in this process.
MAPK signaling upon ccp1 over-expression
MAPK signaling events are regulated by a negative-feedback loop through Sprouty (SPRY) proteins . SPRY expression is induced by MAPK signaling upon growth factor stimulation, such as FGF2 . Therefore we addressed whether ccp1 could induce SPRY feedback regulatory activity. Levels of SPRY were analysed by Western blotting in control and ccp1 expressing MEF using a pan-SPRY antibody followed by densitometry analysis (Figure 7D). MEF expressing ccp1 were cultured in the absence of serum overnight and treated with 50 ng/ml FGF2 in the presence of 10 μg/ml heparin for up to 24 h. In the control MEF, the level of SPRY was low at time 0 and gradually increased upon FGF2 stimulation over the time. In contrast, in the MEF expressing ccp1, the level of SPRY was higher than in the control MEF from the time point 0 and reached the maximum level observed in the presence of FGF2 at 6 hours.
In this study, we have investigated the potential role of ccp1, with a hypothesis that ccp1 may be a downstream effecter of FGF2, promoting cell proliferation and protecting from apoptosis. We show here that ccp1, a gene expressed in embryonic and adult brain , may regulate cell morphology, proliferation and programmed death in normal fibroblast and in neuroblastoma cells.
We have demonstrated that morphological transformation occurred in MEF and SK-N-SH cells under stable over-expression of ccp1 (Figure 1). This effect was observed both in the presence or absence of FGF2 or serum (Figure 3). A long-term culture, for example, of neurite outgrowth or growth of cells in soft agar, may further clarify the effect of ccp1 in morphological transformation in the presence or absence of FGF2 in the future. Growth curve and BrdU incorporation in the presence of serum showed that ccp1 expression is able to promote proliferation up to 5 days in culture (Figure 2). Similar results were observed in the absence of serum, suggesting that ccp1 is able to induce proliferation without mitogen stimulation (Figure 2 and 3). Reduction of ccp1 level by RNAi dramatically reduced SK-N-SH cell proliferation, providing further evidence that ccp1 can induce cell proliferation (Figure 4). In addition, we have showed that ccp1 plays a role in suppressing cell death (Figure 5). Whether extrinsic from intrinsic pathways are involved in the suppression of apoptosis by ccp1 is unknown and will need further investigation.
Although both FGF2 and serum treatment enhanced the increase in cell proliferation upon ccp1 over-expression, the effect of FGF2 did not reach that of the serum (Figure 3 and 6). Therefore it is likely that other mitogenic factors present in the serum can also enhance this ccp1 activity. In addition, it was shown that in the absence of serum, ccp1-induced proliferation was partially inhibited by U0126 (Figure 6B). In contrast, in cells treated with FGF2, the inhibition was less prominent in MEF expressing ccp1 than control MEF (Figure 6C, D). This indicates that MAPK may play only a partial role in cell proliferation promoted by ccp1 over-expression, and that there are signaling pathways other than MAPK that are likely to be also involved in this process. For example, ccp1 activity could be regulated by several signaling pathways, such as the PI3K/AKT pathway. The use of inhibitors of the AKT pathway, such as an mTor inhibitor, rapamycin, may be useful in the future to clarify this point.
It is still unclear how ccp1-induced proliferation is enhanced by FGF2 or serum, in particular, either as a consequence of an increased expression of endogenous ccp1 induced by mitogens such as FGF2 , or functional enhancement of ccp1 activity by these factors.
Ccp1 expression was able to increase ERK phosphorylation immediately after the treatment with FGF2 (Figure 7B). This could be the bases of ccp1-induced cell proliferation observed in Figure 6. However, ccp1-expressing MEF showed a decrease in ERK phosphorylation in the steady state culture under serum (Figure 7A). As the decrease in MAPK signaling could be due to the presence of the feedback loop such as Sprouty (SPRY) proteins , we analysed the SPRY levels (Figure 7D). In MEF expressing ccp1, the level of SPRY was already higher than in the control MEF at the time point 0, however at 6 hours, it reached the maximum level observed in the presence of FGF2. This may indicate that ccp1 expression accelerated the induction of SPRY level, possibly due to activation of MAPK signaling. However it is remains unclear, why pERK was suppressed upon ccp1 over-expression in the steady state of culture. On the other hand, maintained increase in SPRY levels in ccp1-overexpressing cells (Figure 7D) may explain the decrease in cell growth observed in the absence of serum at 4 days of treatment (Figure 2C).
Aberrant activation of FGFs and their receptors lead to several pathologies, including cancer . Study of ccp1 function in promoting proliferation and suppressing cell death would be interesting in aiming a better understanding of tumor formation. Further experiments using knockdown system of ccp1 are necessary to address the requirement of ccp1 in mediating FGF signaling in cell proliferation and apoptosis, possibly using multiple cell lines. Although unlikely, a potential cannot be excluded that the siRNA regulates the protein level of ccp1 differently from that of the mRNA. This has to be addressed in the future experiments.
This study has shown that ccp1 regulates cell proliferation and cell death. Although FGF2 enhanced the effects of ccp1, other mitogenic factors such as MAPK, are likely taking part in enhancing the effects of ccp1.
Coiled Coil protein 1
Cortical Neuron Culture
Enhanced Green Fluorescent Protein
Extracellular-signal Regulated Kinase
Fibroblast Growth Factor
mouse embryonic fibroblast
MAPK or ERK Kinase
messenger Ribonucleic Acid
Mitogen-Activated Protein Kinase.
We thank Biological Services, Molecular Technology and Technology Services of the Beatson Laboratories for Cancer Research for their kind technical support. We thank Prof Kevin Ryan for providing cell and reagents. This work is supported by the start up fund of University of Glasgow.
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