- Research article
- Open Access
The linkage between β1 integrin and the actin cytoskeleton is differentially regulated by tyrosine and serine/threonine phosphorylation of β1 integrin in normal and cancerous human breast cells
© Takahashi; licensee BioMed Central Ltd. 2001
- Received: 8 August 2001
- Accepted: 8 November 2001
- Published: 8 November 2001
Structural requirements for the β1 integrin functions in cell adhesion, spreading and signaling have been well documented mainly for fibroblasts. In this study, we examined the reason for the reduced surface expression of β1 integrin in human breast cancer MCF-7 cells compared to normal human breast epithelial (HBE) cells, both of which adhered to collagen type IV.
The β1 integrin immunoprecipitates from either HBE or MCF-7 cells involved α-actinin while actin coprecipitated with β1 integrin from HBE cells but not from MCF-7 cells. Immunoblotting using the anti-phosphotyrosine (PY) antibody indicated the phosphorylation of β1 integrin at least at tyrosine in both cells. Dephosphorylation of β1 integrin from HBE cells by protein tyrosine phosphatase (PTP), but not by protein serine/threonine phosphatase (PP), caused dissociation of actin from β1 integrin, although dephosphorylation of it from MCF-7 cells by either PTP or PP caused association of the two proteins. In MCF-7 cells β1 integrin coprecipitated doublet of proteins having the Ca2+/calmodulin-dependent protein kinase (CaMK) II activity that was susceptible to KN-62, a specific inhibitor of CaMKII.
The results suggest that β1 integrin is tyrosine phosphorylated and links with actin via α-actinin in HBE cells but prevented from linking with actin in MCF-7 cells by phosphorylation at both tyrosine and serine/threonine of β1 integrin which forms a complex with α-actinin and CaMKII. Thus the linkage formation of β1 integrin with actin may be differentially regulated by its tyrosine and serine/threonine phosphorylation in normal HBE cells and breast cancer MCF-7 cells.
- Actin Cytoskeleton
- Cytoplasmic Domain
- Protein Tyrosine Phosphatase
- Human Breast Epithelial Cell
- Human Breast Epithelial
The integrin family of surface receptors play a critical role in many cellular processes that include cell adhesion, cell spreading, and growth signaling [1–6]. Integrins interact extracellularly with the substratum such as collagens at specific sites called focal adhesions and intracellularly with many actin-binding proteins such as α-actinin, talin, and vinculin, thereby linking these proteins with the actin cytoskeleton. Links between cell surface receptor β integrins and the actin cytoskeleton are though to be established in more than one way. Integrin binds to talin , which also binds to vinculin [8–10], which in turn binds to α-actinin [11, 12], which then binds to actin. This constitutes a three-protein link between integrin and actin. In addition, talin can also bind actin directly [13, 14], so that talin may form a direct one-protein link between integrin and actin. Similarly, the actin-binding protein α-actinin binds to the β1 integrin subunit . While many isoforms of β1 integrin have been reported [16, 17], a short cytoplasmic domain of 47 amino acids of β1 integrin isoform A contains the three putative domains with the highest affinity for α-actinin . In addition, several amino acids and motifs within the cytoplasmic domain of the β subunit, which are potential phosphorylation sites, have been implicated in the integrin function. The β1 subunit contains a Val-Thr-Thr sequence and these two threonines appear to be important for adhesion of fibroblast cells , and adhesion and invasion of lymphoid cells . However, the relevance of phosphorylation of these amino acids within the cytoplasmic domain of β1 integrin in its function remains largely unclear.
Human breast cancer MCF-7 cells have many cellular properties characteristic to malignantly transformed cells; such as an enhanced growth ability in soft agar and poor cell adhesion to the substatum compared to their normal counterpart HBE cells . Poor cell adhesion of MCF-7 cells to the substratum is thought to be mainly caused by a low level of β1 integrin expression on the cell surface . This observation gave a clue to further understanding the relevance of β1 integrin function to cell adhesion, cell spreading, and anchorage-independent growth in cancerous cells. In this study, we examined why only a small population of β1 integrin present in MCF-7 cells is expressed on the cell surface compared to HBE cells, both of which adhere to collagen type IV. Immunoprecipitation and Western blot analysis revealed that intracellular linkage between β1 integrin and actin formed in HBE cells was lost in MCF-7 cells. The relevance of phosphorylation of β1 integrin to its linkage forming ability with actin was also examined in this study using PTP and PP.
The absence of coprecipitation of actin with β1 integrin in MCF-7 cells
α-Actinin-mediated interaction between β1 integrin and actin
Expression of the wild-type integrin β1A in both HBE and MCF-7 cells
The phosphorylation state of β1 integrin
Effects of dephosphorylation of β1 integrin on its link with actin
CaMKII binding to β1 integrin in MCF-7 cells
Immunoprecipitation and Western blotting revealed that actin coprecipitated with β1 integrin from quiescent HBE cells but not from MCF-7 cells. Coprecipitation of actin with β1 integrin but not with the control IgG precipitates from HBE cells indicates that association of β1 integrin with actin is not non-specific. Since actin expression in MCF-7 cells adhering to collagen IV was comparable with that in HBE cells, the result suggests that loss of linkage between β1 integrin and the actin cytoskeleton in MCF-7 cells may not be due to the absence of actin expression.
The β1 integrin subunit interacts by its cytoplasmic domain with many actin-binding proteins, such as α-actinin, talin, and vinculin, thereby forming a link between β1 integrin and the actin cytoskeleton [7–12]. Immunoprecipitation followed by Western blotting revealed that only α-actinin, but not talin or vinculin, coprecipitated with β1 integrin but not with the IgG precipitates from both HBE and MCF-7 cells. This indicates the specific association between α-actinin and β1 integrin in both HBE and MCF-7 cells. Whereas comparable amounts of α-actinin and vinculin are present in HBE and MCF-7 cells and slightly reduced level of talin is seen in MCF-7 cells, the result suggests that α-actinin, but not talin or vinculin, may predominantly mediate a one-protein link between β1 integrin and actin in both HBE and MCF-7 cells and that the loss of linkage between the two proteins in MCF-7 cells may be due to the absence of a link between β1 integrin-associated α-actinin and actin.
In spite of the fact that α-actinin may directly bind with actin , structural requirements for the functions of the cytoplasmic domain of β1 or β3 integrin in cell adhesion and cell spreading are strongly suggested by many investigations [19, 20, 22, 23]. In addition, there are several isoforms within the cytoplasmic domain of β1 integrin [16, 17]. These observations prompted us to examine which isoform of β1 integrin is expressed in MCF-7 cells. RT-PCR, using a set of primers corresponding to the sequences covering the cytoplasmic domain of β1 integrin isoform A, demonstrated that the same cDNA fragments in lengh were amplified from HBE and MCF-7 cells. Sequence analysis indicated that the cDNA fragments had the identical sequence and corresponded to sequences encoding the cytoplasmic domain of the wild-type β1A integrin. This suggests that both HBE and MCF-7 cells express the same wild-type β1 integrin and that the loss of linkage between β1 integrin and actin may not be due to the structural difference in the cytoplasmic domain of β1 integrin in MCF-7 cells from that in HBE cells.
The relevance of phosphorylation of the β subunit of integrin at threonine [19, 20] or tyrosine residue  to the integrin functions that include cell adhesion and invasion has been documented. Therefore we next examined the phosphorylation state of β1 integrin and its relation to the linkage formation with actin. Metabolic labeling of cells with [32P]orthophosphoric acid and Western blotting using the anti-PY antibody indicated that β1 integrin, but not α-actinin, in either HBE or MCF-7 cells was phosphorylated at least on a tyrosine residue and that there was no apparent difference in the phosphorylation state of β1 integrin between two cells. Therefore, the susceptibility of the linkage forming ability of β1 integrin with actin to PTP or PP was examined. Effects of the PTP treatment of the β1 immunoprecipitates from HBE and MCF-7 cells were contradictory; that is, coprecipitation of actin with β1 integrin from HBE cells was lost, while that of two proteins from MCF-7 cells was induced after incubation of the PTP-treated immunoprecipitates with the supernatant of the immunoprecipitates or with exogenous human platelet actin. As the reactivity of anti-PY antibody with β1 integrin from either HBE or MCF-7 cells was lost by PTP and exogenous actin coprecipitated with PTP-treated β1 integrin from MCF-7 cells, alterations in coprecipitation of actin with β1 integrin may be due to tyrosine dephosphorylation of β1 integrin and not other proteins involved in the immunoprecipitates or the supernatant of the immunoprecipitates. In addition, the result suggests that tyrosine phosphorylation is necessary for β1 integrin to link with actin in HBE cells but inhibitory for it in MCF-7 cells. Contrary to this, treatment of the β1 integrin immunoprecipitates with PP2A1 did not result in any alteration in coprecipitation of actin with β1 integrin from HBE cells but caused coprecipitation of the two proteins from MCF-7 cells. As PP2A1 did not affect tyrosine phosphorylation of β1 integrin from either HBE or MCF-7 cells and exogenous actin became coprecipitated with PP2A1-treated β1 integrin from MCF-7 cells as endogenous actin in the supernatant, the results suggested that PP2A1-induced coprecipitation of β1 integrin from MCF-7 cells with actin may be due to serine/threonine dephosphorylation of β1 integrin rather than other cellular proteins and that the ability of β1 integrin to link with actin in MCF-7 cells may be prevented by its serine/threonine phosphorylation. While it appears that phosphorylation at either tyrosine or serine/threonine is necessary for β1 integrin to link with actin and phosphorylation at both tyrosine and serine/threonine prevents β1 integrin from linking with actin, the linkage formation of β1 integrin with the actin cytoskeleton may be differentially regulated in MCF-7 cells as compared to HBE cells by tyrosine or serine/threonine phosphorylation of β1 integrin.
Finally we examined whether some protein kinases associate with β1 integrin in MCF-7 cells, using antibodies to several serine/threonine protein kinases. Among these, the anti-CaMKII antibody reacted with doublet of proteins with molecular mass of around 56 kDa which coprecipitated with β1 integrin from MCF-7 cells but not from HBE cells. As the antibody to CaMKII did not react with any protein in the control IgG precipitates from MCF-7 cells, association of the doublet of proteins with β1 integrin may be specific. The results demonstrating that the β1 integrin immunoprecipitates from MCF-7 cells had the kinase activity for a specific substrate peptide, Autocamtide II, under the conditions where calmodulin and inhibitor peptides of PKA and PKC were present and that this kinase activity was completely inhibited by 10 μM KN-62, a specific inhibitor of CaMKII [26–28], suggest that the doublet of proteins which associate with β1 integrin in MCF-7 cells may be CaMKII isoforms. Even though the reason for an elevated level of the kinase activity of the β1 immunoprecipitates from HBE cells by KN-62 is unknown at present, it is possible to assume that some unidentified protein kinases which are responsive to KN-62 may associate with β1 integrin in HBE cells. Coprecipitation of CaMKII with β1 integrin in MCF-7 cells does not imply their direct association. As direct association between CaMKII and α-actinin has been reported by yeast two-hybrid and biochemical assays , CaMKII in MCF-7 cells may bind to α-actinin, which may also bind to β1 integrin, forming a ternary complex with α-actinin and β1 integrin. Whether serine/threonine phosphorylation of β1 integrin in MCF-7 cells is regulated by the β1 integrin-associated CaMKII, or whether loss of intracellular linkage between β1 integrin and the actin cytoskeleton causes the reduced cell surface expression of β1 integrin, are areas for further investigation.
Intracellular linkage of β1 integrin with the actin cytoskeleton via α-actinin was formed in HBE cells which adhered to type IV collagen. However, this linkage was lost in adherent MCF-7 cells. The present results suggest that tyrosine phosphorylation may be required for β1 integrin to link with actin in HBE cells, but phosphorylation of β1 integrin at both tyrosine and serine/threonine residues in MCF-7 cells may cause dissociation of actin from it. Thus the linkage formation of β1 integrin with the actin cytoskeleton may be differentially regulated by its tyrosine and serine/threonine phosphorylation in normal HBE cells and breast cancer MCF-7 cells.
Cell culture and replating on collagen type IV
HBE cells obtained form Clonetics were maintained in serum-free defined medium MCDB 170  supplemented with 10 ng/ml EGF, 1.4 μM hydrocortisone, 5 μg/ml insulin, 0.1 mM ethanolamine, 0.1 mM phosphoethanolamine, and 25 μM prostaglandin E2  at 37° C in a humidified atmosphere of 95% air and 5% CO2. MCF-7 cells were maintained in 5% fetal bovine serum (FBS)-containing RPMI 1640 medium. Subconfluent culture of HBE or MCF-7 cells were harvested with 0.25% (w/v) trypsin-2.65 mM EDTA solution and the cells were replated on 60-mm collagen IV-coated dishes (Becton-Dickinson). HBE or MCF-7 cells were then growth arrested by incubation in an EGF-deprived medium for 3 days or in 0.1% FBS-containing medium for 2 days, respectively.
Immunoprecipitation and Western blot analysis
Cells adherent to collagen type IV were lysed in RIPA buffer (10 mM Tris-HCl, pH 7.4, 0.15 M NaCl, 1% sodium deoxycholate, 1% Triton X-100, 0.1% SDS, 1 mM phenylmethylsulfonyl fluoride (PMSF), and 1 mM sodium orthovanadate)  and sonicated briefly using an ultrasonic cell disruptor (Misonix Inc.). The cell lysates were incubated with the anti-integrin β1 monoclonal antibody (Life Technologies) or control IgG followed by Protein A-Sepharose (Amersham Pharmacia). The immunoprecipitates were washed three times with PB buffer (20 mM phosphate buffer, pH 8.6, 0.5% Nonidet P-40, and 0.1% SDS) and boiled for 2 min in lysis buffer (0.0625 M Tris-HCl, pH 6.8, 2% SDS, 10% glycerol, and 5% 2-mercaptoethanol). Whole cell lysates were prepared by homogenizing cells in 1% SDS in 20 mM Tris-HCl, pH 7.4, 1 mM PMSF and 1 mM sodium orthovanadate, and then boiling for 2 min, before sonicating briefly. The protein content was determined using a protein reagent kit (Pierce) with bovine serum albumin (BSA) as the standards. The immunoprecipitates or whole cell lysates were dissolved in SDS-polyacrylamide gel electrophoresis (PAGE) and after electrophoresis the samples were transferred onto membranes (Millipore). The blots were probed with anti-actin (ICN), anti-β1 integrin, anti-α-actinin (Upstate Biotechnology), anti-talin (Chemicon), anti-vinculin (Sigma), anti-phosphotyrosine (PY) (Upstate Biotechnology), or anti-CaMKII antibody (Santa Cruz Biotechnology). After incubation of the membrane with horseradish peroxidase-conjugated secondary antibodies (Amersham Pharmacia), the reactivity was visualized using an ECL kit (Amersham Pharmacia) and X-ray films (Fuji-film).
RT-PCR and direct sequencing
Total RNA was extracted from unstimulated cells which adhered to collagen IV, using TRIzol reagent and then digested with DNase I (Life Technologies). A one-step RT-PCR was carried out using an RT-PCR kit (CLONTECH) at the anealing temperature of 55°C. The primer set for the cytoplasmic domain of β1A integrin was 5'-TCCTATTTTAACATTACCAA-3' and 5'-ACTGTGACTATGGAAATTGC-3' . The PCR products were electrophoresed on 1.6% (w/v) agarose gels and the cDNA was extracted from the gel bands. The DNA sequence was confirmed for both forward and reverse strands of cDNA fragments using the set of PCR primers on an automated DNA sequencer (ABI PRISM 3100, Applied Biosystems).
Metabolic labeling of cells
Adherent cells to collagen IV-coated dish were labeled with 100 μCi/ml of [32P]orthophosphoric acid (Amersham Pharmacia) in phosphate-free medium for the last 24 h during incubation to arrest the cells. Immunoprecipitation of β1 integrin and SDS-PAGE of the immunoprecipitates were carried out as described above. After electrophoresis, gels were dried under vacuum and autoradiographed using X-ray films at -70°C for a weak.
Immunoprecipitation of β1 integrin was carried out as described above and the supernatant obtained by centrifugation of the immunoprecipitates with the Protein A-Sepharose beads was retained at room temperature. The β1 integrin immunoprecipitates were washed twice with PB buffer and once with phosphatase buffer (50 mM Tris-HCl, pH 7.0, 150 mM NaCl, and 0.1 mM EDTA). Then the immunoprecipitates were treated with or without 1.0 unit of PTP (LAR, Calbiochem) [31–33] for 10 min or 0.1 units of serine/threonine-specific PP (PP2A1, Calbiochem) [34–36] for 15 min in 100 μl of phosphatase buffer at 30°C. In some experiments, the phosphatase-treated immunoprecipitates were washed with RIPA buffer and incubated with the retained supernatant of the β1 immunoprecipitates that contained unbound actin or with 5 μg/ml human platelet actin (Cytoskeleton, Inc.) in RIPA buffer containing 0.2 mM CaCl2 for 30 min at room temperature.
Immunoprecipitation of β1 integrin was carried out as described above, and the β1 integrin immunoprecipitates were washed twice with PB buffer and once with 20 mM phosphate-buffered saline, pH 7.2. In vitro kinase assay for β1 integrin-associated CaMKII was carried out at 30°C for 10 min using [γ-32P]ATP (NEN Life Science Products) and a CaMKII assay kit (Upstate Biotechnology) that included specific substrate peptide Autocamtide II, calmodulin, and inhibitor peptides of PKA and PKC. In some experiments, the kinase assay was done in the presence of KN-62 (1-[N,O-Bis(5-isoquinolinesulfonyl)]-N-methyl-L-tyrosyl-4-phenylpiperazine) (Sigma), a specific inhibitor of CaMKII [26–28] at the indicated concentrations. The background kinase assay was carried out using the precipitates with the Protein A-Sepharose beads but without the antibody to β1 integrin. Radioactivity incorporated into the substrate peptide was determined with a liquid schintillation counter. After subtraction of the background, the activity was normalized to the amount of β1 integrin that was quantified by measurement of the band intensity of β1 integrin on SDS-PAGE gels using an image analyzer equipped with a digital camera (EDAS 290, Kodak).
I thank Katsuo Suzuki (Laboratory of Biochemistry, Kanagawa Cancer Center Research Institute) for technical help. This work was supported by a grant from the Ministry of Health, Labour and Welfare of Japan for the Second-Term Comprehensive 10-Year Strategy for Cancer Control.
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