Focal adhesion kinase regulates the phosphorylation protein tyrosine phosphatase-α at Tyr789 in breast cancer cells

Introduction

Protein tyrosine kinases (PTK) and protein tyrosine phosphatases (PTP) regulate tyrosine phosphorylation, which is an important cellular mechanism that regulates intracellular signaling pathways to control a number of cellular activities, including proliferation, growth and differentiation (1). Focal adhesion kinase (FAK), a non-receptor binding to tyrosine kinase, functions as a scaffold and coordinating center, which may regulate focal adhesion formation and disassembly. This has been demonstrated in a previous study, which investigated actin fiber stress and cytoskeletal organization (2). The most important site for the regulation of FAK phosphorylation is Tyr397. This mediates one key intramolecular regulatory interaction between the protein 4.1, ezrin, radixin, moesin (FERM) and kinase domains of FAK (3,4). In the integrin signaling pathway, FAK-Tyr397, accompanied by auto-phosphorylation reconstructs the Src family kinases (SFK)/FAK composite, which leads to further phosphorylation and maximal activation of FAK (2).

The important role of SFK in activating FAK has been demonstrated by the decreasing levels of FAK auto-phosphorylation following knock out of the Src, Fyn and Yes gene of SFKs in fibroblasts or by shielding the PTP gene in response to integrin engagement (5,6). In terms of the molecular mechanisms, evidence suggests that the FERM domain is responsible for FAK auto-inhibition by interacting with the kinase domain. The FERM domain was observed to switch from binding to the kinase domain to binding with heterologous protein or lipid partners, which led to FAK-Tyr397 auto-phosphorylation (3,6,7).

PTPα may also regulate the levels of FAK phosphorylation and a previous study suggested that PTPα and other PTP family members may catalyze the dephosphorylation of Src-Tyr527 by its own activity (8–10). During the mitotic process, phosphorylated Src-Tyr527 is able to activate the expression of Src, the regulation of which is mediated by PTPα (11). However, it has also been suggested that PTPα-mediated Src activation during mitosis was dependent on PP2A-mediated dephosphorylation of Ser204 in the juxtamembrane region of PTPα rather than Tyr789 (12). Therefore, the role of Src-Try789 phosphorylated by PTPα requires further investigation.

In our previous study, a novel splicing mutant, FAK-Del33, was identified in breast and thyroid cancer by sequencing (13). The mutation frequency of The FAK-De133 gene was found to be 14.2% (3/21) in breast carcinoma; in addition, when this gene was introduced into normal breast cell lines, it was reported to promote cell migration and invasion (13). This may be caused by FAK-Tyr397 hyperphosphorylation and enhancement of FAK-Src in downstream signaling pathways.

The present study investigated changes in the levels of amino acid phosphorylation in the signaling pathway of breast cancer cells and the activity of Src by western blot analysis. A novel pathway, in which the FAK-Del33 protein may activate c-Src through PTPα phosphorylation at the Tyr789 site, was identified. This was the first study, to the best of our knowledge, to demonstrate the effect of PTPα phosphorylation in a FAK mutant.

Materials and methods

Cell lines

The MDA-MB-468 and MDA-MB-435s cell lines were isolated from a breast cancer patient and melanoma derived cells (MDA-MB-435s) were obtained from American Type Culture Collection (Manassas, VA, USA) and cultured according to the manufacturer’s instructions. The HEK293T cell line was also obtained from American Type Culture Collection. The FAK-Del33 mutant cells were obtained from breast cancer mutation cells lacking exon 33 for FAK and were stored at the Department of Clinical Laboratory of Shanghai Ruijin Hospital (Shanghai, China).

Construction and identification of the expression system

The FAK-Del33 mutant cell suspension was harvested after 48 h in culture and the nucleic acids were then extracted using phenol-chloroform extraction technology. In brief, 500 μl phenol:chloroform:isoamyl alcohol (25:24:1) was added to the cell suspension and it was vortexed for ~20 sec, then centrifuged at 16,000 x g for 5 min at room temperature. The supernatant was transferred to a fresh tube and ethanol precipitation was performed by adding cold 95% ethanol, incubating for 1 h at −20°C, centrifuging at 16,000 × g for 15 min, decanting the supernatant, adding 80% ethanol and repeating the centrifugation. Polymerase chain reaction (PCR) was performed to amplify the FAK-Del33 gene, using the following primers: forward 5′-TCA GAA ACA GAT GAT TTT GCT GAG AT T ATA GAT GA-3′ and reverse 5′-AGC AAA ATC ATC TGT TTC TGA CAC AGA GA-3′. Furthermore, BamHI and NotI restriction sites were introduced at the 5′ and 3′ ends, respectively. The purified PCR fragment was inserted into multiple cloning sites in pCDNA3.1 (+). Construction of the expression plasmids used in the present study are shown in Fig. 1A.

Figure 1 Schematic diagram of FAK and FAK-Del33 (A) FAK-Del33 mutation involved deletion of exon33 of FAT. (B) PTPα analysis revealed five mutation patterns of FAK compared with FAK-Del33. (C) Model of c-Src activation in cells with FAK-Del33. FAK, focal adhesion kinase; FAK-Del33, FAK with exon 33 deletion; FAT, focal adhesion kinase targeting domain; PTPα, protein tyrosine phosphatase-α; FERM, protein 4.1, ezrin, radixin, moesin.

Retroviral expression system

The pGIPZ lentiviral vector-based expression system (Open Biosystems, Inc., Victoria, Australia) was used to clone and express the FAT-wild-type (Wt) and FAK-del33 (exon 33 of FAK deletion) genes in the cells, according to the manufacturers instructions, which packaged the lentivirus and infected the HEK293T cells to culture and amplify the virus.

Wound-healing assay

A wound-healing assay was performed to detect changes in the motility and migration of the MDA-MB-468 and MDA-MB-435s cell lines. The FAK-Del33 mutant was used as a positive control. Cells, which were infected with the recombinant virus and empty vector were used as a negative control.

The cells were seeded (3×105) into 60 mm2 plates and cultured for 12 h at 37°C. A vertical scratch was made using a p20 pipette tip in the middle of the plate to remove cells from this area. Following this, the cells were washed three times using phosphate-buffered saline (PBS) and cultured in serum-free medium. Images of the wound-healing distance were captured for each cell line at 0, 6, 12 and 24 h using an inverted microscope (IX73; Olympus Corp., Tokyo, Japan).

Migration assay

The cells (3×105) were cultured in 60 mm2 plates containing Transwell filters with an 8 μm pore size (Corning, Inc., New York, NY, USA) coated with 10 μg/ml fibronectin for 12 h. The culture medium (Dulbecco’s modified Eagle’s medium) was designed with a serum-free upper layer containing 0.1% bovine serum albumin (BSA) and a lower layer containing 20% fetal bovine serum (Gibco-BRL, Gaithersburg, MD, USA) in different chambers. After 24 h, the bottom of the filter was stained with Giemsa (Sangon Biotech Co., Ltd, Shanghai, China) to calculate the efficiency of the cell migration.

Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and western blot analysis

The FAK-Del33 mutant and FAK-Wt cell suspensions were harvested and centrifuged at 1,000 × g for 10 min (Thermo Fisher Scientific, Waltham, MA, USA). The supernatant was discarded and the pellet was resuspended in lysis buffer [20 mM Tris (pH 7.5), 150 mM NaCl, 1% Triton X-100; Beyotime Institiute of Technology, Jiangsu, China], containing 1% protease inhibitor cocktail (Sigma-Aldrich, St Louis, MO, USA), 25 mM NaF (Sigma-Aldrich) and 1 mM Na3VO4 (Sigma-Aldrich).

The mixture was freeze-thawed four times at −80°C prior to centrifuging at 10,000 × g for 30 min at 4°C (Thermo Fisher Scientific). The supernatant containing FAK-Del33 protein was collected and analyzed using 8% SDS-PAGE. The FAK-Wt breast cancer cells were used for comparison. Following SDS-PAGE, the proteins were transferred onto a polyvinylidene difluoride membrane (Millipore, Billerica, MA, USA).

The membrane was blocked using 5% BSA in Tris-HCl buffered saline containing 0.05% Tween-20 for 2 h at 25°C. The membrane was then incubated with the following primary monoclonal antibodies at 4°C overnight (1:1,000): Mouse anti-PTPα, rabbit anti-phospho-PTPα (Tyr789), rabbit anti-Src, rabbit anti-phospho-Src (Tyr527); rabbit anti-non-phospho-Src (Tyr527); rabbit anti-phospho-Src (tyr416) and rabbit anti-PTP1B, followed by incubation at room temperature for 2 h with anti-rabbit or anti-mouse immunoglobulin G secondary antibodies. All antibodies were purchased from Cell Signaling Technology, Inc. (Beverly, MA, USA). GADPH levels were used as an internal standard. The protein bands were detected using enhanced chemiluminescence (Bestbio, Shanghai, China). The Wt breast cancer cells were used as a negative control.

siRNA-induced apoptosis

The following siRNA sequences were used to target: PTPα forward 5′-GCU GGG AGC CAU UCC AAU UdTdT-3′ and reverse primers PTPα 5′GCU AGG AGC UAU UCC GAU U dTdT-3′, PTP1B 5′-AAU ACA GUG CGA CAG CUA GAA dTdT-3′ and control siRNA 5′-AAU UAA CCU UAC CGA GGG UCG dTdT-3′ (14). All the siRNA duplexes were synthesized by GenePharma, Inc. (Shanghai, China) using 2′-ACE protection chemistry. The Stemfect™ RNA Transfection kit (Stemgent, Cambridge, MA, USA) was used to transfect the siRNA into the cells. Fig. 1B shows the amino acid positions in the FAK protein.

Statistical analysis

Statistical analysis was performed using SPSS 17.0 software (SPSS, Inc., Chicago, IL, USA). Differences between the two groups were evaluated using a one-way analysis of variance. A χ2 test was used to calculate the significance of detection rates between the two groups. P<0.05 was considered to indicate a statistically significant difference.

Results

Wound-healing and migration assay

The healing rate of the FAK-Del33 mutant was faster than that of MDA-MB-468 and MDA-MB-435s cells. Following infection with a lentivirus contaning the FAK-Del33 gene, the healing efficiency of the MDA-MB-468 and MDA-MB-435s cells was higher compared with those observed in the cells containing the empty vector. The FAK-Del33 protein may regulate cell growth. The results obtained from the migration assays supported the hypothesis that this protein also regulates cell motility and migration (Fig. 2).

Figure 2 Analysis of images of cellular activity following infection with a lentivirus containing the FAK-Del33 gene. (A) Wound healing assay in the MDA-MB-468 cells. (B) Migration assay in the MDA-MB-435s cells. FAK, focal adhesion kinase; FAK-Del33; FAK with exon-33 deletion.

Western blot analysis

The main autophosphorylation of FAK, Src-Tyr397, was overexpressed in the FAK-Del33 mutant compared with the FAK-Wt cells. The results revealed ~60–80% of the Src-Tyr530 was dephosphorylated in the MDA-MB-468 and MDA-MB-435s cells compared with the FAK-Del mutant cells. The phosphorylation levels of Src-Tyr419 were 1.90-3.07-fold higher in the FAK-Del33 mutant compared with the FAK-Wt cells (Fig. 3).

Figure 3 Changes in the phosphorylation levels of Src-pTyr530 and Src-Tyr419, between FAK-Wt and FAK-Del33 cells. (A) Western blot analysis of the MDA-MB-468 cells. (B) Western blot analysis of the MDA-MB-435s cells. (C) Quantification of the phosphorylation levels at specific protein sites in the MDA-MB-468 cells. (D) Quantification of phosphorylation levels at specific protein sites in the MDA-MB-435s cells. FAK, focal adhesion kinase; Wt, wild-type; FAK-Del33, FAK with exon-33 deletion; N.C, normal control.

Significant differences were observed in the phosphorylation levels of PTPα-Tyr789 between the FAK-Del33 mutant and the FAK-Wt cells (Fig. 4A) and an association between phosphorylated PTPα-Tyr789 and dephosphorylated Src-Tyr530 was identified in the FAK-Del33 mutant cells (Fig. 4B).

Figure 4 Association between the phosphorylation of Y789 and the activation of PTPα between FAK-Wt and FAK-Del33 cells. (A) Comparison of western blot analysis between the MDA-MB-468 and MDA-MB-435s cells. (B) Quantification of the levels of phosphorylation at specific protein sites in the MDA-MB-468 and MDA-MB-435s cells. (C) Western blot analysis of the effect of Grb2 on PTPα phosphorylation PTPα. (D) Mutational analysis of amino acid sites following transfection of FAK-Del33, Y397F, K454R, Δ375 plasmids into MDA-MB-468 cells. PTPα, protein tyrosine phosphatase-α; FAK, focal adhesion kinase; FAK-Del33, FAK with exon 33 deletion; Wt, wild-type; N.C, normal control.

To assess the interference of Grb2 in the phosphorylation of PTPα-Tyr789, which was bound to the PTPα carboxyl terminus, western blot analysis was performed. The endogenous Grb2 antibody was obtained from lysates of the MDA-MB-468 cells by immunoprecipitation and its effects in the FAK-Del33 mutant cells were examined (Fig. 4C). The results demonstrated that PTPα-Tyr789 exhibited the same level of phosphorylation and was not associated with the Grb2 antibody, suggesting that Grb2 is not involved in the dephosphorylation of Src-Tyr530.

Mutational analysis of amino acids

A total of three amino acid sites were selected for mutational analysis; Y397F (autophosphorylation site), K454R (ATP-binding site) and Δ375 (deletion of FERM domain). As shown in Fig. 4D, all three FAK mutations in FAK-Del33 background failed to induce PTPα-Tyr789 phosphorylation; this therefore indicated that the ability of the FAK-Del33 protein to induce PTPα-Tyr789 phosphorylation was dependent on Tyr397, K454R and the FERM domain.

RNAi in the FAK-Del33 mutant

The Src gene sites of Tyr530 dephosphorylation and Tyr419 phosphorylation changed significantly in the FAK-Del33 mutant. Following transfection of cells with PTPα siRNA, the expression efficiency of these two Src genes were reduced significantly. In addition, PTPα siRNA reduced the phosphorylation levels of Src-Tyr397 (Fig. 5), which was a feedback effect of the regulation of Src activation. However, these effects were not observed in the PTP1B siRNA. In addition, wound-healing and migration analyses revealed that the PTPα siRNA had an effect on the efficiency of cell migration and growth of the MDA-MB-468 cells Therefore, PTPα siRNA inhibited the FAK-Del33-mediated action on tumorigenesis.

Figure 5 Western blot analysis of Src protein phosphorylation in response to siRNA interference at different sites. siRNA, small interfering RNA; N.C, negative control; PTP, protein tyrosine phosphatase; FAK, focal adhesion kinase; FAK-Del33, FAK with exon-33 deletion.

A schematic diagram of a model of c-Src activation in cells with the FAK-Del33 mutation is shown in Fig. 1C, in which the deletion of exon 33 may be important in the regulation of Tyr789 phosphorylation. The identification of differences in protein binding sites and the exact role of the FAK mutant in PTPα regulation are important areas for future investigation.

Discussion

According to previous studies, PTPα acts as an upstream activator in the modulation of FAK phosphorylation (13,14). The present study demonstrated a novel pathway, that the FAK-Del33 mutation regulated PTPα-Tyr789 phosphorylation, leading to Src-Tyr530 dephosphorylation. Previous studies involving PTPα-deficient fibroblasts revealed that the phosphorylation of FAK, particularly at the Tyr397 auto-phosphorylation site can be identified in PTPα-deficient fibroblasts and restored by reintroducing active, but not inactive, PTPα. It was suggested that PTPα is required for maximal integrin-stimulated Src-PTK activity as an upstream regulator of FAK-Tyr397 phosphorylation (15,16). The overexpression of PTPα has also been observed by increasing the tyrosine phosphorylation of FAK (17).

However, previous studies have demonstrated that FAK is required for PTPα phosphorylation and that the phos-phorylation of PTPα may be a consequence of, rather than a prerequisite for, FAK-Src-PTK activation (16,18). In mouse embryonic fibroblasts, it has been observed that PTPα was phosphorylated in response to integrin stimulation and required SFKs (Src or Fyn/Yes), FAK and an intact cytoskeleton. This suggested that the phosphorylation of PTPα-Tyr789 is mediated by the active SFK/FAK complex (18,19). The present study confirmed this hypothesis and, to the best of our knowledge, was the first to demonstrate the phosphorylation of PTPα-Tyr789 by an upstream activator, leading to Src activation. The majority (~20%) of Tyr789 phosphorylation is bound to Grb2 in NIH3T3 cells (19), however, this was not observed in >20% of the endogenous PTPα-Tyr789 in the present study, suggesting that free PTPα-Tyr789 displaces the pTyr530 binding to the Src SH2 domain for Tyr530 dephosphorylation. However, other studies have demonstrated that the dephosphorylation of pTyr530 also occurs in the Tyr789-independent activation of Src under certain circumstances and in other cell types (18,20). Therefore, the role of tyrosine phosphorylation of PTPα in Src activation remains to be elucidated.

Previous studies have demonstrated that PTPα dephosphorylates Tyr419 and Tyr530 at Src (8,11,21,22), leading to Src kinase activation. This indicates that Tyr789 leads to substrate specificity, not overall catalytic activity and is important in overexpressing the FAK-Del33 protein in breast cancer cells.

In conclusion, the present study revealed an unanticipated role for the FAK-Del33 protein in the regulation of PTPα phosphorylation, which is important in Src-Tyr530 dephosphorylation and, consequently, in enhancing cell migration and invasion.

Acknowledgments

This project was funded by Shanghai Committee of Science and Technology, China (grant no. 15ZR1426800). It was also funded by the National Natural Science Foundation of China under the grant 81071745.

References