Modulation of integrin-linked kinase (ILK) expression in human oesophageal squamous cell carcinoma cell lines by the EGF and TGFβ1 growth factors
© Driver and Veale; licensee BioMed Central Ltd. 2006
Received: 08 November 2005
Accepted: 27 April 2006
Published: 27 April 2006
Integrin-linked kinase (ILK) is a ubiquitously expressed protein kinase that has emerged as one of the points of convergence between integrin- and growth factor-signalling pathways.
In this study we identify the ILK isoform expressed in five human oesophageal squamous cell carcinoma cell lines of South African origin as ILK1, and demonstrate its cellular distribution. ILK expression, although similar in the majority of the cell lines, did show variation. Furthermore, the ILK expressed was shown to be catalytically functional. The effect of growth factors on ILK expression was examined. An increase in ILK expression, following EGF and TGFβ1 exposure, was a trend across all the five oesophageal carcinoma cell lines tested.
These results suggest that growth factor modulation of ILK expression relies on the internalisation/recycling of growth factor receptors and stimulation of the PI3K pathway, which may have implications with regards to cell adhesion and tumourigenesis.
While responsiveness to growth factors is central to a host of normal cellular events, aberrant activity plays a key role in tumour development [1–3]. Among the numerous growth factors identified, epidermal growth factor (EGF) and transforming growth factor-1 (TGFβ1) are key players in neoplastic progression [2, 4]. The action of EGF has been implicated in malignant transformation in squamous cancers of the bladder, breast and lung , whereas colon, gastric, endometrial, ovarian and cervical malignancies exhibit loss of response to TGFβ1 as a growth inhibitor [6, 7]. Regarding carcinoma of the oesophagus in particular, reduced TGFβ1 has been correlated with depth of invasion, lymph node metastasis and poor prognosis .
In normal epithelial cells, appropriate cellular attachment is necessary for signalling pathways to be elicited [9, 10]. More specifically, the response to growth factors can be potentiated by the integrin class of adhesion receptors through the integrin-associated protein, integrin-linked kinase (ILK) [1, 7, 11].
The ILK protein is a ubiquitously expressed serine/threonine protein kinase that is activated in response to PI3K stimulation [9, 11–17]. Once activated, ILK couples integrins to downstream signalling pathways that are involved in the suppression of apoptosis and in promoting cell cycle progression [9, 13, 15, 18–21]. The functional significance of ILK in malignancies is highlighted by the fact that ILK is overexpressed in several human tumours, including Ewing's sarcoma, primitive neuroectodermal tumour and medullablastoma [11, 22, 23]. Furthermore, ILK has been shown to induce an invasive phenotype in prostate and brain tumour cell lines [19, 24].
Since our focus concerns oesophageal carcinoma, ILK expression is particularly intriguing since this tumour has a propensity to invade and metastasise. Carcinoma of the oesophagus has an extremely high incidence with high mortality and a poor prognosis [25–27]. It has the widest variation in incidence by geographical location of any neoplasm occurring in China, the Transkei region of South Africa, France and northern Iran [25–27]. In the cell lines under investigation, EGF is of particular relevance, stemming from the demonstration that these cell lines overexpress the EGF receptor . It therefore becomes necessary to consider the effects of growth factors when examining the regulatory mechanisms of ILK expression. This report demonstrates novel data for the expression of ILK in five human oesophageal carcinoma cell lines and that this expression is modulated by EGF and TGFβ1.
ILK1 in Human Oesophageal SCC cell lines (HOSCCs)
ILK protein expression under standard culture conditions
Densitometric analysis revealed that ILK expression levels were comparatively similar across the WHCO3, WHCO5 and SNO cell lines (per μg of total cellular protein extracted). However, differences in expression were observed for cell lines WHCO1 (1.3 fold higher) and WHCO6 (1.5 fold lower) than the average (Figure 3B).
Localisation of ILK in HOSCCs
ILK expression following time-dependent exposure to EGF in oesophageal SCC cell lines
In the case of the WHCO1 cell line, highest ILK expression was noted after 1 hour EGF exposure where a fold increase of 1.8 fold was observed. This increase was maintained though to 24 hours where a 1.3 fold increase in ILK expression was seen. The WHCO3, WHCO5 and WHCO6 cell lines produced similar trends in ILK expression following time dependent exposure to EGF. ILK expression levels continued to increase following increased exposure to EGF in the WHCO3 cell line, reaching a substantial increase of 4.5 fold after 24 hours EGF treatment. Similarly, in the WHCO5 and WHCO6 cell lines, a large increase was observed following 0.5 hours EGF treatment of 3 and 2.7 fold respectively. Increased ILK expression levels remained constant and highest ILK expression was observed following 24 hours EGF exposure of 3.4 and 2.9 fold respectively (figure 6B).
The SNO cell line was somewhat outstanding in that this cell line elicited greatest ILK expression of 2.2 fold following 0.5 hours EGF exposure. Thereafter, a less substantial increase was noted at 1 hour of 1.5 fold, which was maintained through to 24 hours (Figure 6B).
ILK expression following time-dependent exposure to TGFβ1 in oesophageal SCC cell lines
The WHCO3, WHCO5 and WHCO6 cell lines demonstrated a similar trend in increasing ILK expression in response to TGFβ1 treatment. The WHCO3 cell line produced a substantial increase in ILK expression reaching and maintaining a 7 fold increase over 3 hours exposure. Surprisingly, exposure to TGFβ1 for 6 hours did not produce a higher increase in ILK expression, although ILK expression was still 5.6 fold higher than the untreated control (Figure 7B). ILK expression continued to decrease at 24 hours TGFβ1 exposure but still producing a 4.4 fold increase. Exposure to TGFβ1 for 0.5 hours in the WHCO5 and WHCO6 cell lines caused an increase in ILK expression of 2.5 and 2.4 fold respectively, which was maintained continued to increase reaching 2.8 (WHCO5) and 4 (WHCO6) fold. ILK expression reached peak levels at 6 hours of 4.3 (WHCO5) and 6.4 (WHCO6) fold (Figure 7B). By 24 hours, ILK levels decreased producing a much reduced increase of 2.9 (WHCO5) and 1.9 (WHCO6) fold.
EGF and TGFβ1 downregulate ILK Activity in HOSCCs
Interestingly, it was observed that treatment of cell cultures with 10 ng/ml EGF and TGFβ1 for a period of 24 hours resulted in a decline in ILK kinase activity of 1 to 3 fold in cell lines WHCO1, WHCO6 and SNO (established by densitometry, figure 8C and 8D). However, paradoxical results were obtained in the case of the WHCO5 cell line, where treatment with TGFβ1 reduced ILK activity, whereas EGF augmented ILK activity. The addition of growth factors had the greatest effects on the WHCO3 line, which showed a dramatic increase in activity to both EGF (3 fold) and, TGFβ1 (3.5 fold). Although TGFβ1 treatment had a similar effect to that of EGF, its effect on ILK activity was more profound. When considering growth factor effects upon ILK expression and activity, it became apparent that increased ILK expression induced by growth factors did not necessarily imply a similar response in ILK activity.
Despite data being available for ILK expression in a variety of tumour types (prostate, breast, and colorectal, [11, 12, 19, 22, 23], the same cannot be said for carcinoma of the oesophagus. Moreover, since the cell lines examined here are known to overexpress the EGF receptor , determining the effects of growth factors on ILK expression is pertinent to our understanding of the adhesion/signalling role of ILK in the moderately differentiated class of oesophageal SCC.
The two mRNA isoforms of ILK (ILK1 and ILK2), share similar structural and functional properties but, whereas ILK1 is expressed in all normal tissues, ILK2 has only been identified in two highly metastatic fibrosarcoma and melanoma cell lines . Here we established that the ILK1 isoform predominates in HOSCCs, and is catalytically functional. In addition to ILK demonstrating a typical focal adhesion localisation, ILK was also observed in the nuclear and cytoplasmic compartments. The nuclear distribution of ILK is somewhat surprising but has been demonstrated previously and may be attributable to an impairment of the ILK association with either PINCH or caveolin [21, 23]. These data therefore provided the baseline for examining the effects of growth factor on ILK protein expression in HOSCC cells.
With the exception of the WHCO1 and WHCO6 cell lines, the expression levels of ILK were relatively similar among the WHCO3, WHCO5 and SNO cell lines (see figure 3B). However, since ILK expression levels were not uniform across all five HOSCCs, being somewhat higher in the WHCO1 cell line and lower in the WHCO6 cell line, we could not consider the observed ILK expression as peculiar to the moderately differentiated oesophageal phenotype.
ILK acts as a molecular scaffold during a host of signalling events, mediating crosstalk between integrins and the growth factor response , thus eliciting downstream events that impinge upon vital aspects of cellular function [10, 31]. Although many of the signals elicited by ILK are a direct result of growth factor signalling, the effect of growth factors on ILK protein expression and kinase activity has not been considered to any great extent. In these HOSCCs, the general response of ILK to both EGF and TGFβ1 treatment was an increase in ILK protein expression levels over the duration of growth factor exposure (see figures 6B and 7B). It is likely that this stimulation occurs via activation of the PI3K pathway, which has been shown to be activated in response to these growth factors [32, 33]. The only other report of EGF and TGFβ1 effects on ILK expression, showed stimulation of ILK expression in a human melanoma cell line following exposure to EGF and TGFβ1 for 24 and 48 hours . However, since a rapid response in ILK expression to both EGF and TGFβ1 by most cells has been shown previously [4, 34], the present study concentrated on shorter exposure times in addition to the longer exposure times.
The noted variations in ILK expression among the cell lines suggest that a receptor recycling mechanism occurs in response to these growth factors depending on the time exposure. In the instances where ILK expression decreased abruptly, the decrease could be attributable to a reduction in the number of receptors at the membrane as a result of receptor internalisation . It is widely accepted that, although EGFR localises primarily at the cell surface, they constantly recycle through the cell . Furthermore, rates in recycling can be accelerated as a consequence of EGF ligand-binding [34, 36–43]. It is highly probable that the noted fluctuations in ILK expression in the WHCO3, WHCO5 and SNO cell lines are attributed to this receptor internalisation/recycling process where lowered EGF signalling occurs as a result of EGFR reduction at the plasma membrane. A direct consequence being reduced ILK activated due to reduced PI3K signalling.
Likewise, the receptors of TGFβ1 also undergo recycling both in the presence and absence of ligand activation . Although scarce, early reports suggest that internalised receptors are either rapidly replaced or recycled back to the cell membrane [45, 46]. More recently,  showed that in lung epithelial cells TGFβ1 receptors do indeed recycle and degrade in a clathrin-dependent approach, but in a manner that is not dependent on ligand stimulation. It is possible that ligand stimulation may be required in the case of HOSCCs and the noted fluctuations following TGFβ1 exposure may be explained by receptor recycling.
To determine whether growth factors induced a similar response in both ILK expression and activity in HOSCCs, ILK kinase assays were conducted in the presence of EGF and TGFβ1. Given that the greatest increase in ILK expression was noted following 24 hours growth factor exposure, cells were exposed to growth factors for a similar period of time. With the exception of the WHCO3 cell line which showed a marked increase in ILK kinase activity, the general trend was a decline in ILK kinase activity over the other cell lines following growth factor exposure (see figure 8D). This data is surprising since , have previously shown that a rapid stimulation of ILK activity by insulin and PDGF occurred in intestinal epithelial cells.
The substantial increase in ILK activity in the WHCO3 cell line could be attributed to decreased PTEN since TGFβ1 has been shown to downregulate PTEN mRNA in keratinocytes . In contrast, EGF and TGFβ1 may be stimulating PTEN activity in the WHCO1, WHCO6 and SNO cell lines. Due to the increased EGFR that have been reported with regards to the oesophageal SCC lines, one could also argue that the cell lines WHCO1, WHCO6, and SNO are at an upper limit of growth factor response. Thus, growth factor treatment of these cell lines would not elicit any further cellular responses, a consequence being that ILK would not be activated, accounting for the low levels of ILK kinase activity observed in these cell lines. This speculation is supported by the suggestion that in fibroblasts higher TGFβ1 concentrations results in inhibition of both cell migration and proliferation .
While the cellular expression of ILK in HOSCCs is comparable to that of other cell types, particularly noteworthy is that ILK expression in HOSCCs appears to be dependent on the receptor recycling of both the EGF and TGFβ1 receptors. EGF/TGFβ1 has been shown to result in a rapid, marked increase in ILK expression, and since it is known that EGFR overexpression occurs in these HOSCCs, it is plausible that a constitutive increase in ILK expression exists in these HOSCCs. A direct consequence of EGF/TGFβ1 stimulation of the ILK pathways could thus be decreased cellular adhesion due to impaired integrin-mediated signalling, or a stimulation of mitogenic pathways such as MAPK thereby promoting transformation.
Materials and methods
Five South African moderately differentiated human oesophageal squamous carcinoma cell lines WHCO1, WHCO3, WHCO5, WHCO6  and SNO  were obtained from the Cell Biology Laboratory, School of Molecular and Cell Biology, University of the Witwatersrand. Medium was removed and cells washed twice with pre-warmed (37°C) phosphate buffered saline (PBS). Cells were harvested using 0.05% (w/v) trypsin and 0.01% (w/v) EDTA. Cell lines were cultured in 10 cm Nunc™ tissue culture dishes with Dulbecco's Modified Eagles Medium (DMEM)/Hams F12 (3:1), supplemented with 10% Foetal Calf (or bovine) Serum (FCS or FBS). Cultures were maintained in a humid, 37°C incubator, 5% carbon dioxide (CO2) atmosphere.
ILK amplification by reverse transcription polymerase chain reaction (RT-PCR)
Cells were grown to 80% confluence in sterile 10 cm Nunc™ tissue culture dishes and total RNA isolated using TRIzol® solution (GibcoBRL). For reverse transcription, 2μg of total RNA was converted into cDNA by MMLV reverse transcriptase at 37°C for 1.5 hours in a 25μl RT reaction. Briefly, PCR amplification mixtures contained cDNA, ILK antisense primer (5'-CTCGAGCTACTTGTCCTGCATCTTCTCAAG-3'), sense primer (5'-GAATTCGTATGGACGACATTTTCACTCAGTGC-3') and Expand High FidelityPLUS Taq (Roche, SA). Thermal cycle conditions included denaturation at 95°C for 10 minutes, and 30 cycles between 95°C for 15 seconds, 50°C for 1 minute and a 2 minute extension step at 72°C, followed by a final elongation at 72°C for 10 minutes. RT-PCR products were visualised on 2% agarose gels following ethidium bromide (EtBr) staining.
Restriction Fragment Length Polymorphism (RFLP) analysis of amplified ILK cDNA
ILK RT-PCR products were purified using a QIAGEN® QIAquick Purification Kit. Thereafter, restriction digests were performed by the addition of Bam H1 and Hinc II restriction enzymes to purified ILK products, and incubated for 1.5 hours at 37°C. Subsequent digestions were cleared of protein by the addition of phenol/chloroform and centrifuged at 6000 rpm for 2 minutes and aqueous phase transferred to a sterile tube. Both 0.7 M EtOH and 3 M NaAc were added and allowed to precipitate DNA for 12 hours at -20°C. Samples were centrifuged at 6000 g for 20 minutes, the supernatant decanted, and the DNA pellet resuspended in dH2O. Products were visualised on 2% agarose gels following EtBr staining.
Polyclonal rabbit anti-ILK antibody (Zymed®, USA) and polyclonal horseradish peroxidase (HRP)-bound anti-rabbit secondary antibody (Separations, SA) antibodies were used for immunoprecipitation and immunoblotting procedures. Polyclonal rabbit anti-ILK antibody and a fluoroscine isothiocyanate (FITC)-conjugated anti-rabbit secondary antibody (Chappel, USA) were used for indirect immunofluorescence.
Cells grown to 80% confluency and seeded onto sterile glass coverslips were fixed with 4% paraformaldehyde and permeabilised in 0.25% Triton X-100. Exposure to anti-ILK (1:500) followed by incubation with an anti-rabbit Fluoroscine Isothiocyanate (FITC)-conjugated anti-rabbit antibody (1:1000) for ILK. Slides were viewed under a Zeiss LSM 410 confocal microscope (FITC excitation 490, emission 525).
Preparation of nuclear cell lysates
Nuclear extractions were performed utilising the CelLytic™ Nuclear™ Extraction Kit (Sigma, USA), which is based on a hypotonic buffer treatment followed by a high salt buffer release of nuclei.
Treatment of oesophageal carcinoma cell lines with EGF and TGFβ1
To examine growth factor effects on the WHCO1, WHCO3, WHCO5, WHCO6 and SNO HOSCC cell lines, cell cultures were first serum starved for a period of 16 hours. Cells were then treated with either 10 ng/ml EGF or TGFβ1 for a period of 0.5, 1, 3, 6 and 24 hours respectively. Experiments were repeated on three separate occasions.
Preparation of membrane cell lysates
Cell cultures were washed in PBS containing 20 mM phenyl-methyl-sulphonyl fluoride (PMSF)/Aprotinin (Trasylol® Bayer, SA) stock solution. The cell suspension was centrifuged at 1000 g for 2 minutes. The supernatant was decanted, and the cell pellet resuspended in an extraction buffer (containing 50 mM Tris, 150 mM NaCl, 1 mM CaCl2, 1 mM MgCl2 and 0.01% aprotinin pH 8.5) and incubated for 2 hours on ice. Thereafter, samples were centrifuged at 6000 g for 10 minutes. The resulting cell lysates were stored at -70°C. Total protein content was determined using the Bradford assay  using the protocol from .
Cell lysates (10 μg) were electrophoresed through 10% SDS-PAGE gels according to Laemmli, (1970), transferred to Nitrobind nitrocellulose transfer membrane (MSI, USA). Nitrocellulose membranes were blocked with a casein-based blocking buffer (BLOTTO), incubated in polyclonal anti-ILK antibody (1:1500), followed by incubation in HRP-bound secondary anti-rabbit antibody (1:2500). Detection was carried out with the Supersignal® West Pico Chemiluminescent kit. The experiment was performed on three separate occasions.
Cell lysates (100 μg) were incubated with 2 μg anti-ILK antibody for 12 hours at 4°C. The resulting immune complexes were incubated for 4 hours at 4°C with protein A sepharose (Sigma, SA). Immune complexes were captured by centrifugation and immunoprecipitated ILK resolved on 10% SDS-PAGE gels, transferred to nitrocellulose filter and probed with an anti-ILK antibody (1:1500). Detection was carried out with the Supersignal® West Pico Chemiluminescent kit (Pierce, USA).
ILK kinase activity
Immunoprecipitated ILK was incubated in a kinase reaction buffer (50 mM Hepes, 10 mM MnCl2 and 10 mM MgCl2 pH7), 10 μCi [γ-32P] ATP (Amersham, UK) and 10 μg myelin basic protein (MBP) (Sigma, USA) for 2 hours at 30°C with gentle agitation. The reaction was terminated by the addition of an equal volume of 2 × laemmli buffer and incubation at 95°C for 5 minutes. Phosphorylated MBP products were recovered by centrifugation at 6000 g for 10 minutes and resolved on 10% SDS-PAGE, following Coomassie Blue staining, destaining, and rinsing in dH2O and 10% ethanol respectively. Gels were subsequently dried on a slab gel drier SE1160 (Hoefer, San Francisco). Phosphorylated MBP was detected via autoradiography.
Densitometric analysis of the western blot and kinase assay x-ray plates were used for semi-quantitative comparison of ILK protein levels by using the area under the peak. Expression levels were represented as a percentage of the maximum per 10 μg of protein. In interpreting the growth factor data, we considered a 1.2 fold increase (equivalent to 20%), to be an appreciable increase in ILK expression levels. All subsequent fold increases are compared to an untreated control, unless otherwise stipulated.
This study was supported by a grant to RBV by the National Research Foundation (NRF) and the HE Griffin Cancer Trust.
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