H-Ras Activation Promotes Cytoplasmic Accumulation and Phosphoinositide 3-OH Kinase Association of ß-Catenin in Epidermal Keratinocytes

Correspondence to: Amparo Cano, Instituto de Investigaciones Biomédicas, CSIC-UAM, Arturo Duperier, 4, 28029 Madrid, Spain. Tel:34-91-585-4597 Fax:34-91-585-4587 E-mail:acano{at}iib.uam.es.

	Abstract

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The mechanisms underlying downregulation of the cadherin/catenin complexes and ß-catenin signaling during tumor progression are not fully understood. We have analyzed the effect of oncogenic H-Ras on E-cadherin/catenin complex formation/stabilization and ß-catenin distribution in epidermal keratinocytes. Microinjection or stable expression of V12Ras into keratinocytes promotes the loss of E-cadherin and -catenin and relocalization of ß-catenin to the cytoplasm and nucleus. Moreover, these effects are dependent on PI3K (phosphoinositide 3-OH kinase) activity. Interestingly, a strong association of p85 and p110 subunits of PI3K with ß-catenin is induced in V12Ras-expressing keratinocytes, and in vitro binding assays show a direct interaction between ß-catenin and p85. Overexpression of either V12Ras or constitutively active p110 induces metabolic stabilization of ß-catenin and promotes its accumulation in cytoplasmic and nuclear pools. In addition, the interaction of ß-catenin with the adenomatous polyposis coli protein is blocked in V12Ras and p110 transformants though no changes in glycogen synthase kinase 3 ß activity could be detected. Nevertheless, in V12Ras transformants the in vivo phosphorylation of ß-catenin in Ser residues is strongly decreased. These results indicate that H-Ras activation induces the relocalization and cytoplasmic stabilization of ß-catenin by a mechanism involving its interaction with PI3K.

Key Words: H-Ras, E-cadherin, ß-catenin, adenomatous polyposis coli, phosphoinositide 3-OH, kinase

	Introduction

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

CELL–cell adhesion mediated by the calcium-dependent cadherin receptors is fundamental for the differentiation and integrity of most adult tissues. Among the different members of the cadherin superfamily, the epithelial E-cadherin plays a pivotal role in the acquisition and maintenance of embryonic and adult epithelia (Takeichi 1991 ; Gumbiner 1996 ). E-cadherin is organized in adhesion complexes at the lateral membranes of neighboring cells. The receptor associates with cytoplasmic proteins of the catenin family, -, ß-, and -catenin (identical to plakoglobin), which in turn mediate the interaction of the complexes with the cortical actin microfilament network (Kemler 1993 ; Aberle et al. 1996 ). ß-catenin and plakoglobin directly bind the cytoplasmic domain of E-cadherin, whereas -catenin interacts with the other two catenins establishing the link with the actin microfilaments (Hinck et al. 1994 ; Nagafuchi et al. 1994 ; Jou et al. 1995 ; Knudsen et al. 1995 ; Rimm et al. 1995 ). An additional catenin, p120cas, has been described in some E-cadherin/catenin complexes but apparently with a weak interaction with -catenin (Reynolds et al. 1994 ; Daniel and Reynolds 1995 ).

Recent studies have clearly established that ß-catenin has an important signaling activity besides its role in the cadherin-mediated adhesion complexes. ß-catenin is homologous to the armadillo protein of Drosophila, and together with other members constitute the arm protein family (Peifer et al. 1992 , Peifer et al. 1994 ). Armadillo/ß-catenin are downstream effectors of the Wingless/Wnt signaling pathway (for review see Gumbiner 1995 ; Miller and Moon 1996 ; Willert and Nusse 1998 ). Their activity is mediated by the pool of soluble molecules and appears to be independent of their role in adhesive complexes (Orsulic and Peifer 1996 ).

In normal resting cells, the cytoplasmic ß-catenin levels are very low and are regulated by interaction with the adenomatous polyposis coli (APC)¹ product and by the upstream effectors of the Wnt signaling pathway, glycogen synthetase kinase 3ß (GSK3ß) and axin (Munemitsu et al. 1995 ; Rubinfeld et al. 1996 ; Yost et al. 1996 ; Ikeda et al. 1998 ; Sakanaka et al. 1998 ). These proteins probably direct the proteolytic degradation of ß-catenin by the ubiquitin-proteasome pathway (Aberle et al. 1997 ; Orford et al. 1997 ). Wnt signaling inhibits the activity of GSK3ß (Cook et al. 1996 ) and leads to the stabilization of cytoplasmic hypophosphorylated ß-catenin, which is able to interact with lymphocyte enhancer factor 1/T-cell factor (Lef-1/Tcf) transcription factors and the complex can act as a transcriptional coactivator in the nucleus (Behrens et al. 1996 ; Huber et al. 1996 ; Molenaar et al. 1996 ; Papkoff et al. 1996 ). Other studies have also reported that ß-catenin can be translocated to the nucleus independent of its interaction with Lef-1/Tcf transcription factors (Fagotto et al. 1998 ; Prieve and Waterman 1999 ).

It has been recently shown that activation of ß-catenin signaling occurs in intestinal and mammary cells after activation of the integrin-linked kinase, independent of Wnt activation but also involving downregulation of GSK3ß activity (Novak et al. 1998 ; Delcommenne et al. 1998 ). Significantly, the interaction of ß-catenin and APC is disturbed in colon carcinoma and melanoma cell lines with mutations in the interacting regions of either molecule (Korinek et al. 1997 ; Morin et al. 1997 ; Rubinfeld et al. 1997 ). Mutations in the serine/threonine residues susceptible of phosphorylation and interaction with APC in the ß-catenin gene have also been found in a variety of human carcinomas (Miyoshi et al. 1998 ; Palacios and Gamallo 1998 ; Voeller et al. 1998 ), in some cases associated with extensive nuclear localization of ß-catenin (Palacios and Gamallo 1998 ). These observations have fostered an increasing interest in the role of ß-catenin in tumor progression regarding the possibility of its functioning as an oncogene (Peifer 1997 ).

Oncogenic transformation frequently results in alterations of the epithelial properties, including loss of polarized morphology, less organized cell junctions, and increased migration of transformed epithelial cells (Vleminckx et al. 1991 ; Behrens et al. 1993 ; Kinch et al. 1995 ; Zhong et al. 1997 ). In some reports, changes in the E-cadherin/catenin complexes were associated to a decreased interaction of the complexes with the cytoskeleton and an increase in tyrosine phosphorylation of ß-catenin and/or association with p120cas (Behrens et al. 1993 ; Kinch et al. 1995 ).

Recently, Ras activation has been shown to induce the destabilization of E-cadherin/catenin complexes in MDCK cells by mechanisms involving both phosphoinositide 3-OH kinase (PI3K) and mitogen-activated protein kinase (MAPK) effector pathways (Potempa and Ridley 1998 ). Ras activation is a frequent genetic alteration in human and experimental tumors (Barbacid 1987 ), but it is presently unknown whether it is involved in ß-catenin signaling during tumor progression. The experimental model of mouse skin carcinogenesis offers a unique system to investigate this important issue as Harvey-Ras (H-Ras) activation is a frequent genetic event at the initiation stage (Brown et al. 1986 ; Quintanilla et al. 1986 ). Further alterations in the ras locus, leading to an increase in the dosage of activated H-Ras, accumulate during progression of papillomas to invasive carcinomas (Bianchi et al. 1990 ; Bremner and Balmain 1990 ). Downregulation of E-cadherin expression also occurs at this stage during mouse skin tumor progression (Navarro et al. 1991 ) and alterations in the integrity of the E-cadherin–mediated cell–cell adhesion have been found in high risk progressing papillomas (Cano et al. 1996 ).

To get further insights into the role of Ras activation in tumor development, we have investigated the effects of activated H-Ras on the organization of E-cadherin/catenin complexes and on ß-catenin localization in mouse epidermal keratinocytes. Here we show that activated H-Ras alters the distribution of ß-catenin in epidermal keratinocytes in the membrane-bound and cytoplasmic/nuclear pools in a PI3K-dependent manner. Our results indicate that Ras signaling interferes with the ß-catenin–APC interaction and promotes the interaction of soluble ß-catenin with PI3K and the metabolic stabilization of cytoplasmic ß-catenin pools.

	Materials and Methods

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

Cells and Retroviral Infections
Mouse Pam212 keratinocytes, an immortalized cell line spontaneously derived from a primary keratinocyte culture (Yuspa et al. 1980 ) and GP+E 86 cells producing retroviruses that express either V12H-Ras or the catalytic subunit of PI3K targeted to the plasma membrane (p110CAAX) were grown in DME supplemented with 10% FCS (GIBCO BRL), 100 µg/ml ampicillin, 32 µg/ml gentamicin, and 100 µg/ml amphotericin B (Sigma Chemical Co.). Cells were grown at 37°C in a humidified 5% CO₂ atmosphere. Retroviruses encoding V12H-Ras with a neomycin resistance marker or controls with the neomycin resistance marker alone have been previously described (Rodriguez-Viciana et al. 1997 ). Retrovirus encoding p110CAAX was generated by subcloning the BamHI insert from pSG5-p110CAAX into pLXSP3. pLXSP3 was a gift from A. Sewing (Imperial Cancer Research Fund, London, UK) and was generated by ligating the HindIII-XbaI fragment of pBabe puro, containing the puromycin resistance gene, into pLXSN. Infective retroviruses were obtained by growing GP+E 86 cells to confluence and collecting the culture medium. Supernatants were filtered through 0.45-mm pores and frozen as aliquots in the presence of polybrene. Retrovirus-containing supernatants were added to subconfluent cultures of Pam212 cells and replaced 16 h later with fresh medium. Pools of infected cells were obtained after selection with 400 µg/ml G418 (Calbiochem-Novabiochem Co.) or 1.5 µg/ml puromycin (Boehringer Mannheim) for 7 d, during which time all control noninfected cells died. More than 200 colonies were pooled from each infection.

Antibodies
The following antibodies were used: rat monoclonal anti-mouse E-cadherin (ECCD-2; a gift from Dr. M. Takeichi, Kyoto University, Kyoto, Japan); mouse monoclonal anti–ß-catenin, mouse monoclonal anti–-catenin, mouse monoclonal anti-GSK3ß, and mouse antiphosphotyrosine (PY20) (Transduction Laboratories); mouse monoclonal anti–c-H-Ras (Ab-1) and mouse monoclonal anti-pan Ras recognizing the normal and activated forms of H-Ras (Oncogene Science, Inc.); mouse monoclonal anti–6-His (CLONTECH Laboratories); rabbit anti–GSK3ß-P-Ser⁹ antiserum (Chemicon International Inc.; provided by Dr. F. Wandosell, Centro de Biología Molecular, Madrid, Spain); rabbit polyclonal anti-GST (Sigma Chemical Co.); rabbit antipeptide antiserum anti–-catenin (VB1) and rabbit antipeptide antiserum anti–ß-catenin (VB2) (Braga et al. 1995 ); rabbit polyclonal anti-APC (N-15) (Santa Cruz Biotechnology, Inc.); rabbit polyclonal anti–PI3 kinase p85 and anti–PI3 kinase p110 (Upstate Biotechnology); and mouse monoclonal anti–ß-tubulin (Amersham). Secondary antibodies included: BODIPY-conjugated goat anti–rat IgG, anti–mouse IgG and anti–rabbit IgG (Molecular Probes Inc.); AMCA-conjugated rabbit anti–rat IgG, Cy5-conjugated donkey anti–rabbit IgG (Jackson ImmunoResearch Laboratories) and peroxidase-conjugated sheep anti–rat IgG, anti–mouse IgG and anti–rabbit IgG (Amersham).

Recombinant Proteins and Microinjection
Recombinant constitutively active Ras (V12Ras), dominant negative Ras (N17Ras), C3 transferase and dominant negative Rac (N17Rac) were prepared as glutathione-S-transferase (GST) fusion proteins in Escherichia coli, purified using glutathione-Sepharose beads, thrombin cleaved, dialyzed, and concentrated as described (Ridley et al. 1992 ). The activity of each batch of recombinant proteins was tested in fibroblasts and keratinocytes as described (Braga et al. 1997 ). Recombinant GST–ß-catenin fusion protein was generated by isolation of full-length human ß-catenin cDNA from plasmid pQE32 (a gift of Dr. J. Behrens) by SmaI-SalI digestion and ligation into pGEX-5X-2 plasmid (Pharmacia Biotech). Recombinant His-p85 wt fusion protein was produced in COS cells as described (Rodriguez-Viciana et al. 1997 ) and purified with His-Trap columns (Pharmacia Biotech) following the instructions of the manufacturer. Confluent patches of keratinocytes were injected essentially as described (Braga et al. 1997 ) and visualized by mixing the recombinant proteins with dextran conjugated to Texas red (mol wt 10,000; Sigma Chem-ical Co.).

Immunostaining
After microinjection, cells were fixed in either cold methanol or 3.7% buffered formaldehyde for 5 min at 4°C and rinsed in PBS. Staining with the different antibodies was performed as described (Lozano and Cano 1998 ). In extraction experiments, cells grown on coverslips were treated with NT buffer (50 mM Tris, pH 7.4, 100 mM NaCl, 5 mM MgCl₂, 5 mM Ca₂Cl, 1% NP-40, 1% Triton X-100) for 15 min on ice before fixation and staining. Preparations were viewed either by confocal microscopy or in an Axiophot photomicroscope (Carl Zeiss). Confocal images were obtained using a laser scanner (MRC 1024; BioRad) attached to a Nikon microscope (Optiphot 2). Pictures were processed using the Adobe Photoshop 4.0 software (Adobe Systems, Inc.).

Preparation of Cell Extracts
Whole cell extracts were obtained from F-25 flasks of 80–90% confluent cells. For total protein extracts, cells were washed twice in cold HMF-Ca buffer (10 mM Hepes, pH 7.4, 100 mM NaCl, 10 mM Ca₂Cl) and extracted in 1 ml of S buffer (50 mM Tris, pH 7.4, 100 mM NaCl, 5 mM MgCl₂, 5 mM Ca₂Cl, 2% SDS) containing protease and phosphatase inhibitors (2 mM PMSF, 20 µg/ml aprotinin, 1 mM N-ethylmaleimide, 1 mM sodium orthovanadate, 2 mM hydrogen peroxide) for 5 min at room temperature under continuous agitation. Soluble and insoluble fractions were obtained as previously described (Lozano and Cano 1998 ) using the NT buffer containing the inhibitors described above.

Immunoprecipitation and Western Blotting
Immunoprecipitations of soluble fractions were carried out with different antibodies as previously described (Lozano and Cano 1998 ) and analyzed in 7.5% or 12% SDS-PAGE gels. In P-Tyr immunoprecipitations, controls were performed by adding 5 mM P-Tyr or P-Ser (Sigma Chemical Co.) to soluble fractions. Immunoblotting of the different fractions and immunoprecipitates was performed by transferring the gels to Immobilon P membranes (Millipore Corp.), incubation with the appropriate antibodies, and development with an enhanced chemiluminescent kit (Amersham).

Pulse–Chase Analysis of ß-Catenin
Cells were grown in F-25 flasks to 80% confluence in normal growth medium, washed three times in HMF-Ca buffer, and pulse-labeled for 1 h in 1 ml of methionine- and glutamine-free minimal essential medium (GIBCO BRL) supplemented with 4 mM glutamine, 10% FCS and 100 µCi [³⁵S]methionine-cysteine (trans-label; Amersham; 1,000 Ci/mmol). Labeled cells were rinsed three times in normal growth medium containing an excess of cold methionine (0.15 mg/ml), chased in this medium for the indicated times, and the soluble extracts subjected to ß-catenin immunoprecipitation. The labeled immunoprecipitates were resolved in 7.5% SDS-PAGE gels, transferred to Immobilon P membranes, and exposed to autoradiography. Bands corresponding to ß-catenin were identified by immunoblotting. ³⁵S-labeled ß-catenin detected at the different experimental points was quantified by scanning and digitalization of the autoradiograms with Adobe Photoshop 4.0 and integration with NIH Image 1.62f software. The integrated density obtained at the different times was normalized to that obtained at time 0 h in each experiment.

In Vivo Phosphorylation and Phosphoamino Acid Analysis of ß-Catenin
Metabolic labeling of keratinocytes with [³²P]orthophosphate was performed as previously described (Perez-Moreno et al. 1998 ) with slight modifications. 20 h after plating the cells, monolayers were labeled in media without phosphate supplemented with 500 µCi/ml of [³²P]orthophosphate (acid-free, 5 µCi/ml; Du Pont Company; NEN Life Science Products) for 4 h at 37°C in a CO₂ incubator. After labeling, cells were washed twice with PBS and lysed with NT buffer, containing a cocktail of phosphatase (1 mM sodium orthovanadate, 50 mM sodium fluoride, and 2 mM hydrogen peroxide) and protease inhibitors for 30 min at 4°C with gentle rotation. Extracts were prepared as described, immunoprecipitated with anti–ß-catenin antibodies (Transduction Laboratories), and resolved on 7.5% SDS-PAGE gels. Protease and phosphatase inhibitors were maintained during all the immunoprecipitation procedures. Total [³²P]phosphate labeling was detected by autoradiography, and the total ß-catenin protein was determined in the same gel by immunoblotting. ³²P-labeled and total ß-catenin were quantified by scanning and digitalization of the autoradiograms and blots as described.

Phosphoamino acids were analyzed based on the method of Boyle et al. 1991 with minor modifications. ³²P-labeled phosphorylated ß-catenin bands were excised from membranes and hydrolyzed with 6 N HCl at 110°C for 2 h. The hydrolysates were lyophilized using a speed-vac concentrator and resuspended in 10 µl of pH 1.9 buffer (2.2% formic acid, 7.8% acetic acid, pH 1.9) containing 2 µg each of cold phosphoamino acid standards. The samples were spotted onto thin-layer cellulose plates (5716; Merck) and amino acid separation was performed on an apparatus (HTLE-7000; CBS Scientific Co.) running at 1,500 V for 45 min in the first dimension with the pH 1.9 buffer. The second dimension thin layer chromatography was carried out in a mixture of n-buthanol/acetic acid/H₂O (100:22:50). The individual amino acids were identified by comparison with the internal standards detected by ninhydrin staining. The position of ³²P-labeled phosphoamino acids were determined by autoradiography.

GSK3ß Activity
Activity of GSK3ß was tested in the absence and presence of 50 mM lithium chloride in crude cell extracts prepared following the procedure recently described (Ryves et al. 1998 ) and using the specific phosphopeptide GSM (RRRPASVPPSPSLSRHSSHQRR, where S indicates a phosphoserine introduced during synthesis) (a gift of Dr. A.J. Harwood, MRC Laboratory for Molecular Cell Biology, London, UK). The difference between the activity obtained in the absence and presence of lithium chloride was represented as the specific GSK3ß activity.

Pull-down and In Vitro Protein Binding Assays
Pull-down assays were performed using soluble extracts obtained in NT buffer after preclearing with glutathione-Sepharose 4B (Pharmacia Biotech). 200 µl of the precleared extracts were incubated with 100 µl of purified GST–ß-catenin fusion protein (0.2 µg/µl) for 2 h at 4°C. For in vitro protein binding assays, 200 ng of both GST–ß-catenin and His-p85 wt were mixed in 500 µl of immunoprecipitation buffer and incubated 1 h at 4°C. In all cases, interacting ß-catenin–GST complexes were collected by addition of glutathione-Sepharose 4B, washed twice with immunoprecipitation buffer, and finally resuspended in Laemmli sample buffer. Complexes were analyzed in 7.5% SDS-PAGE gels and immunoblotted with the indicated antibodies.

Reporter Gene Assay
Nearly subconfluent cells were transfected in duplicate in P-60 dishes with 4 µg of the pRSV-LacZ containing a ß-galactosidase reporter gene and 4 µg of either pTOPFLASH or pFOPFLASH containing multimerized wild-type or mutated Lef-1/Tcf binding sites, respectively, and a luciferase reporter gene (Korinek et al. 1997 ) (a gift of Dr. H. Clevers, University Hospital, Utrecht, The Netherlands). Transfection was performed with lipofectamine plus (GIBCO BRL). Luciferase and ß-galactosidase activities were measured 24 h after transfection.

	Results

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

Microinjection of Keratinocytes with Dominant Active H-Ras Induces Loss of E-Cadherin and -Catenin and Relocalization of ß-Catenin to the Cytoplasm
To analyze short-term effects of activated H-Ras on the E-cadherin/catenin complexes, we chose the murine epidermal keratinocyte cell line Pam212, obtained after spontaneous immortalization of a primary keratinocyte cell culture (Yuspa et al. 1980 ). This cell line maintains all the epidermal characteristics of keratinocytes, expresses a normal H-Ras protooncogene, and is nontumorigenic when injected into athymic nude mice (Missero et al. 1991 ; Sanchez-Prieto et al. 1995 ). The dominant active form of H-Ras (V12Ras; 0.5 µg/µl) protein was microinjected in confluent Pam212 keratinocytes showing stable cell–cell contacts, and the cells were fixed and stained for different proteins after 1–24 h of incubation. As shown in Figure 1, Figure 2 Figure 3 Figure 4 h after microinjection E-cadherin (Figure 1 b) and -catenin (Figure 1 d) were completely absent from the cell–cell contacts established between microinjected cells. At the same time, V12Ras induced a strong cytoplasmic staining of endogenous ß-catenin (Figure 1f and Figure h). In addition, a diffuse nuclear labeling for ß-catenin could be detected in some of the microinjected cells (Figure 1 h). Microinjection of Pam212 cells with a dominant negative H-Ras protein, N17Ras induced no alterations in the adhesion complexes or ß-catenin localization (Figure 1j and Figure k). Our data indicate the specificity of V12Ras effects and are in agreement with previous data using anti–Ras antibodies in human keratinocytes (Braga, V.M.M., M. Betson, and N. Lamarche-Vane, manuscript submitted for publication). 16 h after V12Ras microinjection in Pam212 cells, E-cadherin and -catenin remained absent from the cell–cell contacts and ß-catenin was still faintly detected in the cytoplasm (data not shown), indicating that dominant active H-Ras induces dismantling of E-cadherin/catenin complexes and cytoplasmic accumulation of ß-catenin in mouse epidermal keratinocytes.

View larger version (66K): [in this window] [in a new window]   Figure 1. Microinjection of V12Ras in Pam212 keratinocytes induces dismantling of E-cadherin/catenin complexes and the cytoplasmic relocalization of ß-catenin. Confluent patches of Pam212 cells were microinjected with V12Ras (0.5 µg/µl) (a–h) or N17Ras (0.5 µg/µl) (i–k), and after 2–4 h fixed in 3.7% formaldehyde. Cells were stained for E-cadherin (b and j), -catenin (d), and ß-catenin (f, h, and k). Microinjected cells were identified by coinjection of dextran–Texas red (a, c, e, g, and i). Cells in c–f were fixed after 2 h of microinjection and the rest of cells after 4 h of microinjection. V12Ras microinjection induces a strong cytoplasmic staining and occasional nuclear localization of ß-catenin, whereas E-cadherin and -catenin disappear from cell–cell contacts on microinjected and adjacent cells. Images in a–h were obtained by confocal laser microscopy and those in i–k in an Axiophot microscope. Bars, 10 µm.

View larger version (40K): [in this window] [in a new window]   Figure 2. Inhibition of PI3K activity prevents E-cadherin/catenin complexes disassembly induced by V12Ras. (a) Confluent patches of Pam212 cells were preincubated with the PI3K inhibitor wortmannin (200 nM) for 30 min, microinjected with V12Ras (0.5 µg/µl), and after 3 h, fixed in methanol. Cells were stained for E-cadherin, and microinjected cells were identified by coinjection of dextran–Texas red. (b) Control PamNeo (top, Neo) or PamV12Ras (middle and bottom, Ras) cells were extracted in NT buffer for 15 min on ice, fixed in 3.7% formaldehyde, and stained for E-cadherin (left) or ß-catenin, using mouse mAb (right). PamV12Ras cells showed in the bottom were preincubated with the PI3K inhibitor wortmannin (Ras+W) for 1 h before NT buffer extraction. The nuclear staining detected with ß-catenin is background staining because of nonspecific binding of the BODIPY-conjugated anti–mouse IgG observed after detergent extraction. Both E-cadherin and ß-catenin are redistributed to the detergent soluble fraction in V12Ras-expressing cells and this solubilization is blocked after inhibition of PI3K activity in those cells. Images were obtained in an Axiophot microscope. Bars, 10 µm.

View larger version (150K): [in this window] [in a new window]   Figure 3. Biochemical analysis of the components and distribution of E-cadherin/catenin complexes in control Neo and Ras keratinocytes. (a) Soluble (S) and insoluble (I) fractions obtained in NT buffer from PamNeomycin (Neo)- and PamV12Ras (Ras)-transduced cells were immunoblotted for E-cadherin, -catenin (mouse monoclonal), ß-catenin (mouse monoclonal), and ß-tubulin. (b) Total cell extracts obtained in S buffer from PamNeomycin (Neo) and PamV12Ras (Ras) cells were immunoblotted for E-cadherin, -catenin, ß-catenin, ß-tubulin, and p21ras. (c) Soluble extracts obtained in NT buffer from PamNeomycin (Neo) and PamV12Ras (Ras) cells were immunoprecipitated with anti–E-cadherin antibodies (ECCD-2) (left) or with antiphosphotyrosine antibodies (PY20) (right) and subjected to immunoblotting for E-cadherin, -catenin, and ß-catenin. Bands detected in the P-Tyr immunocomplexes were specifically competed by an excess of P-Tyr but not by P-Ser.

View larger version (30K): [in this window] [in a new window]   Figure 4. Interaction of phosphoinositide 3-OH kinase with ß-catenin in vivo and in vitro. (a) In vivo interactions. Soluble extracts from PamNeomycin (Neo) and PamV12Ras (Ras) cells were immunoprecipitated with anti-p85 serum (top), anti-p110 serum (middle), or anti–ß-catenin antibody (mouse monoclonal) (bottom) and subjected to immunoblotting for ß-catenin and p85 as indicated. (b) Pull-down assays. Recombinant GST–ß-catenin fusion protein (200 ng) was incubated with soluble extracts from PamNeomycin (Neo) and PamV12Ras (Ras) cells, and the complexes were immunoblotted for E-cadherin (top) and p85 (middle). As an internal control the complexes were also immunoblotted for ß-catenin (bottom). (c) In vitro interaction of ß-catenin and p85. 200 ng of recombinant His-p85 wt fusion protein was incubated in the presence or absence of 200 ng of recombinant GST–ß-catenin fusion protein in immunoprecipitation buffer. Complexes were affinity-purified with glutathione-4B-Sepharose beads (AP:GST) (middle and right lanes) and detection of ß-catenin and p85 wt was performed by immunoblotting with anti-GST (GST) (top) and anti–6-His (His) antibodies (bottom), respectively. As an internal control, the presence of His-p85 wt in the precipitation buffer was tested before the addition of GST–ß-catenin (left lanes).

The possible participation of Rho and Rac in the dissociation of E-cadherin complexes induced by V12Ras in confluent mouse keratinocytes was also investigated. However, inhibition of endogenous Rho or Rac affected primarily the adhesion to substratum, resulting in the detachment of the cells from the dish within 2 h without affecting cell–cell contacts (data not shown), in contrast to our previous studies in human keratinocytes (Braga et al. 1997 ). These results might reflect a modulation on the response of cadherin receptors to inhibition of small GTPases because of the cellular context (Braga et al. 1999 ) and/or to specific effects of the extracellular matrix (Sander et al. 1998 ).

Destabilization of E-Cadherin/Catenin Complexes Induced by V12Ras Depends on PI3K and Is Independent of ß-Catenin Tyrosine Phosphorylation
Previous studies have implicated PI3K and MAPK activities in dismantling E-cadherin/catenin complexes induced by activated V12Ras in other systems (Potempa and Ridley 1998 ; Sander et al. 1998 ). In murine keratinocytes, the involvement of PI3K in the destabilization of E-cadherin/catenin complexes induced by activated H-Ras was confirmed by microinjection analysis in the presence of specific inhibitors. Preincubation of Pam212 cells during 30 min with the PI3K inhibitor wortmannin at 200 nM, blocked the effect of V12Ras on the adherens junctions (Figure 2 a).

To further investigate the effect of activated Ras and the involvement of PI3K in the destabilization of the E-cadherin/catenin complexes, we generated stable transfectants of Pam212 cells expressing H-V12Ras by retroviral transduction. Cells were pooled from three independent infection assays, which showed similar results. The solubility of E-cadherin/catenin complexes in control PamNeo (Neo)- and V12Ras-overexpressing (Ras) cells was first analyzed by immunostaining after detergent extraction of the cells. As showed in Figure 2 b, E-cadherin and ß-catenin were preserved at cell–cell contacts of control Neo cells after treatment with NT buffer (Figure 2 b, Neo). Both proteins were removed from cell–cell contacts by the detergent treatment in Ras cells (Figure 2 b, Ras), indicating that H-Ras activation promotes solubilization of the cadherin complexes. This solubilization was prevented by preincubation of Ras cells with wortmannin during 1 h (Figure 2 b, Ras+W), further supporting the involvement of PI3K activity in H-Ras–induced destabilization of the adhesion complexes.

Immunoblotting analysis of the distribution of the different components of the E-cadherin/catenin complexes into the detergent-soluble (S) and insoluble (I) fractions of control neomycin (Neo)- and V12Ras (Ras)-transduced cells is shown in Figure 3 a. E-cadherin and ß-catenin were found in both the soluble and insoluble fractions in Neo cells, whereas in Ras-expressing cells, most of the E-cadherin and ß-catenin and an increased proportion of -catenin were detected in the soluble fraction. Quantification of the data obtained in three independent experiments indicated that 8% and 11% of E-cadherin and ß-catenin, respectively, were detected in the insoluble fractions of Ras cells. In contrast, in control Neo cells, 39% of E-cadherin and 29% of ß-catenin were associated to the insoluble fraction. In addition, the distribution in soluble and insoluble fractions of a control protein, ß-tubulin, was not disturbed upon V12Ras overexpression (Figure 3 a). These results confirm that the components of the E-cadherin complexes were weakly associated to the actin cytoskeleton in the Ras-expressing cells.

Immunoblot analysis of total protein extracts of Neo and Ras cells showed that the level of p21 protein increased about 10-fold in PamV12Ras cells (Figure 3 b). Total protein levels of E-cadherin and -catenin decreased in V12Ras-overexpressing cells (Ras) as compared with control cells (Neo), but no changes in ß-catenin levels were observed (Figure 3 b). On the other hand, soluble E-cadherin of either Neo and Ras keratinocytes was able to associate in a similar manner to the - and ß-catenin components (Figure 3 c, left). Immunoprecipitation of tyrosine-phosphorylated proteins in the soluble fraction of Pam212 keratinocytes showed a similar degree of ß-catenin tyrosine phosphorylation in both Neo and Ras cells (Figure 3 c, right) and the absence of tyrosine phosphorylation in E-cadherin and -catenin in both cell lines. These results indicated that stable expression of dominant active H-Ras decreases the total levels of E-cadherin and -catenin without affecting the level of ß-catenin and, more significantly, induces the redistribution of the different components to a more soluble cytoplasmic pool.

Interaction of ß-Catenin with PI3K Is Strongly Induced in Ras-transformed Keratinocytes
To get further insights into the H-Ras–induced cytoplasmic relocalization of ß-catenin, we analyzed the participation of PI3K. Cell extracts obtained from control (Neo) and PamV12Ras (Ras)-transduced cells were immunoprecipitated with antibodies against the regulatory subunit of PI3K (p85), and the presence of ß-catenin was analyzed by immunoblotting. As shown in Figure 4 a, ß-catenin was detected in the p85 immunocomplexes from control Neo cells, but a significant increase of associated ß-catenin was detected in the immunocomplexes of Ras cells. However, the level of total (data not shown) and immunoprecipitated p85 (Figure 4 a) was similar in both cell types. The reverse experiment, immunoprecipitation with anti–ß-catenin antibodies and immunoblotting with anti-p85 (Figure 4 a), also showed an increase in ß-catenin/p85 association in Ras cells. In addition, the strong association of ß-catenin with the PI3K complex in Ras cells was also detected when the p110 catalytic subunit was immunoprecipitated (Figure 4 a). Interestingly, the interaction of p110 with its regulatory subunit, p85, was also significantly increased in Ras cells.

The interaction of ß-catenin with PI3K was confirmed in pull-down experiments with recombinant GST–ß-catenin. As shown in Figure 4 b, an excess of recombinant GST–ß-catenin interacts similarly with endogenous p85 derived from protein extracts of Neo and Ras cells. These results suggest that endogenous p85, from either control or V12Ras cells has the same ability to associate with recombinant ß-catenin. The quantitative differences found in the in vivo ß-catenin–p85 interaction might reflect different properties of endogenous ß-catenin in control and Ras-expressing cells. GST–ß-catenin recombinant protein also showed a strong interaction with E-cadherin and -catenin in the pull-down assays (Figure 4 b, and data not shown), indicating the functionality of the protein in in vitro interactions. A direct interaction of ß-catenin with the regulatory subunit of PI3K, p85, was further demonstrated in in vitro binding assays using recombinant GST–ß-catenin and His-p85 wt fusion proteins (Figure 4 c). Taken together, these results indicate the ability of ß-catenin to associate with PI3K in Pam212 keratinocytes. This interaction is significantly increased in V12Ras-overexpressing cells, where both the regulatory and catalytic subunits of PI3K form part of this novel ß-catenin complex.

Activated H-Ras Blocks the Interaction of ß-Catenin with APC and Decreases ß-Catenin–P-Ser Content
The above results prompted us to examine the interaction of ß-catenin with other known partners in Neo versus Ras cells. Because of the relevance of the ß-catenin–APC interaction in the regulation of cytoplasmic ß-catenin levels, we investigated whether activated H-Ras could influence such interaction. High levels of soluble ß-catenin coprecipitated with APC in control Neo cells (Figure 5 a, IP: APC, lane Neo), whereas very low levels of ß-catenin were detected in the APC immunocomplexes of PamV12Ras cells (Figure 5 a, IP: APC, Ras lane), even though the level of APC was similar in both cell types (Figure 5 a, lysates). On the other hand, similar levels of GSK3ß protein were detected in whole cell extracts from control Neo and Ras cells (Figure 5 b, lysates), but no stable association of ß-catenin with GSK3ß was found in either cell line (Figure 5 b, IP ß-catenin or GSK3ß).

View larger version (36K): [in this window] [in a new window]   Figure 5. Stable expression of V12Ras in Pam212 keratinocytes inhibits ß-catenin–APC interaction, but does not induce stable interaction of ß-catenin with GSK3ß or affect GSK3ß activity. (a) Soluble extracts from PamNeo (Neo) and PamV12Ras (Ras) cells were immunoprecipitated with anti-APC antibodies and subjected to immunoblotting for ß-catenin (bottom, IP: APC). As a control of the APC level, the extracts were immunoblotted with anti-APC antibodies (top, lysates). (b) Soluble extracts from PamNeo (Neo) and PamV12Ras (Ras) cells were immunoprecipitated with anti–ß-catenin (mouse mAb) (middle, IP: ß-catenin) or anti-GSK3ß (bottom, IP: GSK3ß) and subjected to immunoblotting for ß-catenin, GSK3ß, and P-Ser9GSK3ß, as indicated. As a control, total cell extracts from Neo and Ras cells (top, lysates) were also included in the immunoblottings. (c) GSK3ß activity was assayed in crude cell extracts of control PamNeo (Neo) and PamV12Ras cells from three independent infections (Ras1, Ras2, and Ras3) in the presence and absence of 50 mM lithium chloride using the specific peptide GSM as substrate. The specific activity is represented as the percentage of the difference between the values obtained in the absence and presence of lithium chloride in each cell line. Samples were analyzed in duplicate, and the results show the average value and SD. (d) Lef-1/Tcf–dependent transcriptional activity was measured in control PamNeo (Neo) and PamV12Ras (Ras) cells using pTOPFLASH (Top) and pFOPFLASH (Fop) reporter vectors containing multimerized wild-type (Top) or mutated (Fop) Lef-1/Tcf binding sites. Assays were performed in duplicate samples, and the results show the average value and SD.

To investigate whether the disturbed interaction of ß-catenin with APC induced by activated H-Ras was due to inhibition of GSK3ß, we analyzed its activity in crude cell extracts from control PamNeo and PamV12Ras cells. Ras-transformed cells from three independent infection assays (Ras1, 2, and 3) showed a level of GSK3ß activity sensitive to lithium chloride similar or slightly higher to that of control cells (Figure 5 c). In addition, endogenous phosphorylation of GSK3ß at Ser9 in Ras-expressing cells was slightly higher than in control Neo cells (Figure 5 b). These results indicate that the overall activity of GSK3ß in Pam212 cells was not significantly decreased by overexpression of activated H-Ras. Nevertheless, a slight increase of about twofold in basal Lef-1/Tcf–dependent transcriptional activity was observed in Ras-transformed cells (Figure 5 d), suggesting a weak activation of ß-catenin signaling in these cells.

To further analyze the status of ß-catenin in control and Ras-transformed keratinocytes, we performed in vivo phosphorylation analysis on both cell types after 4 h of metabolic labeling. The level of ß-catenin phosphorylation in PamV12Ras cells resulting from two independent infections, Ras1 and Ras2, was significantly lower than that of parental Pam212 cells (Figure 6 a). Quantitive analysis of the phosphorylated and total immunoprecipitated ß-catenin indicated that the ratio of [³²P]ß-catenin in Ras1 and Ras2 keratinocytes was 6% and 17% relative to that of the parental cells. In addition, the phosphoamino acid analysis of immunoprecipitated ß-catenin showed that P-Ser was the major phosphorylated amino acid, and, as expected, the relative P-Ser content of ß-catenin in Ras-transduced cells was much lower than that of parental cells (Figure 6 b). The P-Tyr content of ß-catenin could not be detected in the phosphoamino acid analysis, probably because of the lower stability of P-Tyr residues to acid hydrolysis (Duclos et al. 1991 ) or to a low level of P-Tyr labeling in the 4-h pulse, in contrast to the steady state levels detected in the immunoprecipitation analysis (Figure 3 c). These results indicate that activated H-Ras induces cytoplasmic accumulation of hypophosphorylated ß-catenin and inhibits its interaction with APC in keratinocytes, through a mechanism apparently independent of stable interactions with or reduced activity of GSK3ß.

View larger version (64K): [in this window] [in a new window]   Figure 6. In vivo phosphorylation of ß-catenin is strongly decreased in V12Ras-overexpressing keratinocytes and mainly affects the P-Ser content. (a) ß-catenin was immunoprecipitated from 32P-metabolically labeled Pam212 (P) and PamV12Ras cells from two independent infection assays (Ras1 and Ras2), resolved on polyacrylamide gel and subjected to autoradiography (top) and immunoblotting of the same gel for ß-catenin (bottom). The 32P-ratio of ß-catenin in the different cell lines was quantitated by densitometric scanning of the bands present in the autoradiogram and immunoblotting. (b) Phosphoamino acid analysis of ß-catenin. 32P–ß-catenin bands from Pam and Ras2 (Ras) cells were excised from the membranes and processed as described in Materials and Methods (top). Migration of standard amino acids, identified by ninhydrin staining, is indicated at the bottom and by the ovals (top). The TLC plates were simultaneously autoradiographed for 21 d. Only 32P-Ser could be detected, and it was strongly reduced in Ras cells.

Overexpression of Constitutively Active PI3K Is Sufficient to Stabilize Cytoplasmic ß-Catenin
To get additional information on the involvement of PI3K in the stabilization of cytoplasmic ß-catenin, Pam212 cells overexpressing the membrane-bound form of p110 subunit of PI3K (p110CAAX) and puromycin-resistant control cells were generated by retroviral transduction. Pam-p110 cells from two independent infections (p110S1 and p110S2) behaved similarly to PamV12Ras cells with respect to ß-catenin and APC content. Thus, no changes in the total level of both proteins (Figure 7 a, lysates) and a strong reduction in the level of ß-catenin–APC interaction (Figure 7 a, bottom, IP: APC) were observed in p110 cells, when compared with control puromycin-resistant (Puro) cells.

View larger version (94K): [in this window] [in a new window]   Figure 7. Expression of constitutively active PI3K inhibits ß-catenin–APC interaction and induces cytoplasmic and nuclear accumulation of ß-catenin. (a) Soluble extracts from control PamPuromycin (Puro)- and p110CAAX-overexpressing cells from two independent infections (p110S1 and p110S2) were immunoprecipitated with anti-APC antibodies and subjected to immunoblotting for ß-catenin (bottom, IP: APC). As control of the APC and ß-catenin levels, the extracts were also immunoblotted with anti-APC (top, lysates) and anti–ß-catenin (middle, lysates) antibodies. (b) Stable overexpression of V12Ras and p110CAAX induces cytoplasmic and nuclear accumulation of microinjected GST–ß-catenin. Confluent patches of PamV12Ras (Ras), Pamp110CAAX (p110) and Pam212 (Pam) cells were microinjected with GST–ß-catenin protein (1 µg/µl) and after 4 h fixed in cold methanol. Cells were stained for ß-catenin (mouse mAb) and E-cadherin, as indicated. Microinjected cells were identified by coinjection of dextran–Texas red. Note the cytoplasmic and nuclear staining of ß-catenin in Ras and p110 microinjected cells, whereas the staining of E-cadherin remained at the cell–cell contacts. Images were obtained in an Axiophot microscope. Bars, 10 µm.

The effect of p110 expression on ß-catenin localization was further investigated by microinjection of recombinant GST–ß-catenin fusion protein. 4 h after microinjection, a strong cytoplasmic and nuclear accumulation of ß-catenin was observed in PamV12Ras (Ras) and Pamp110 (p110) cells (Figure 7 b). In both cell types, ß-catenin staining was also detected at the cell–cell contacts of the microinjected cells. In contrast, ß-catenin staining was exclusively detected at the cell–cell contacts after microinjection of the GST–ß-catenin fusion protein in the parental Pam212 (Pam) cells (Figure 7 b), possibly because of its quick degradation or incorporation into junctions. In Ras and p110 microinjected cells staining with anti–GST antibodies showed localization of the exogenous protein at the membrane, cytoplasm, and nucleus but only at the membrane junctions in Pam cells (data not shown). On the other hand, staining of E-cadherin at the cell–cell contacts was not modified in p110 cells (Figure 7 b), indicating that PI3K activity alone is not sufficient to disrupt cell–cell adhesion in mouse keratinocytes.

The stabilization of endogenous ß-catenin in cells overexpressing either V12Ras or p110-CAAX was confirmed by pulse–chase experiments. As can be observed in Figure 8 a, ß-catenin was quickly degraded in both control puromycin (Puro)- and neomycin (Neo)-transduced cells. In contrast, the metabolic stability of endogenous ß-catenin was significantly increased in V12Ras (Ras)- and p110CAAX (p110)-overexpressing cells (Figure 8 a). Quantification of the autoradiograms shown in Figure 8 a indicated a half-life for ß-catenin of ~1 h in control Pam cells, and of >4 h in V12Ras- and p110CAAX-overexpressing cells (Figure 8 b). These results demonstrate that the stability of cytoplasmic ß-catenin is increased by the expression of V12Ras and constitutively active PI3K in Pam212 keratinocytes.

View larger version (33K): [in this window] [in a new window]   Figure 8. Increased metabolic stability of ß-catenin in Ras- and p110CAAX-overexpressing keratinocytes. (a) Control (Neo and Puro), PamV12Ras (Ras), and Pamp110CAAX (p110) cells were pulse-labeled for 1 h with [35S]methionine/cysteine and chased at the indicated times. Labeled ß-catenin was detected by immunoprecipitation and processed as described in Materials and Methods. (b) The integrated density of the ß-catenin–labeled bands at each chase time was normalized to that obtained at chase time 0 in each cell line. Assays were performed in two independent experiments for each cell type, and the results show the average value and SD. See the increased stability of ß-catenin in Ras- and p110-overexpressing cells as compared with control Neo and Puro cells.

	Discussion

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

Alterations in the expression or function of the E-cadherin/catenin adhesion system occur frequently in a wide variety of human carcinomas (for review see Takeichi 1993 ; Birchmeier and Behrens 1994 ). Indeed, a causal role for the loss of E-cadherin has been recently demonstrated during the transition from adenoma to invasive carcinoma (Perl et al. 1998 ). The molecular mechanisms underlying the loss of expression or functionality of individual components of the cadherin/catenin complexes in tumorigenesis are still poorly understood. The implication of ß-catenin in the Wnt signaling pathway has opened new avenues in the study of the modulation of the cadherin–adhesion complexes during tumor progression (Peifer 1997 ; Pennisi 1998 ). However, it is still largely unknown if other signaling pathways frequently activated in tumor cells and, more specifically, H-Ras activation can influence the signaling activity of ß-catenin. Our results indicate that activation of H-Ras induces the dismantling of E-cadherin/catenin complexes and the stabilization of hypophosphorylated cytoplasmic ß-catenin through signaling pathway(s) involving PI3K that lead to the inhibition of ß-catenin–APC interaction and to a stable interaction of ß-catenin with PI3K complex. In addition, activation of PI3K is sufficient to promote the stabilization of cytoplasmic ß-catenin and its nuclear translocation.

H-Ras expression in mouse epidermal keratinocytes induced a decrease in the total levels of E-cadherin and -catenin without significantly affecting the levels of ß-catenin, as previously described in intestinal and mammary cells (Novak et al. 1998 ). In addition, in V12Ras-expressing keratinocytes, most of the E-cadherin and associated ß-catenin are found in the detergent soluble fraction, indicating a weak interaction of the E-cadherin/catenin complexes with the cytoskeleton in those cells. We suggest that activation of H-Ras can affect the E-cadherin/catenin complexes in epidermal keratinocytes via signaling mechanisms different from those leading to increased P-Tyr, in contrast to previous reports using other cell types (Kinch et al. 1995 ). Despite the biochemical effects on cadherin complexes induced by activated H-Ras in mouse keratinocytes, no significant differences could be observed in the morphological phenotype of the parental Pam212, control PamNeo, and PamV12Ras cells when growing at medium high density. These results differ from those previously reported after Ras transformation of MDCK cells (Behrens et al. 1989 ; Vleminckx et al. 1991 ) or mammary MCF10A cells (Kinch et al. 1995 ; Zhong et al. 1997 ), where a more epitheloid or fibroblastic phenotype was sometimes observed. These differences may be related to the level of activated H-Ras expression obtained in the different studies or may be specific of the cell system analyzed. In this sense, it is worth mentioning that tyrosine phosphorylation of catenins plays a positive role in the stratification process in differentiated keratinocytes (Calautti et al. 1998 ). In spite of those differences, our results indicate that even in situations where a full phenotypic transformation is not observed, activated H-Ras is able to significantly modify the E-cadherin/catenin complexes as in the murine Pam212 epidermal keratinocytes. Thus, the modification of the adhesion complexes might be an early event driven by H-Ras transformation.

Our microinjection studies are in agreement with those showing that V12Ras leads to the loss of E-cadherin and ß-catenin from cell–cell contacts in MDCK cells, dependent on both PI3K and MAPK activities (Potempa and Ridley 1998 ). However, no cytoplasmic localization of ß-catenin was observed and the -catenin status was not analyzed in this study. These differences can be due to different fixation and permeabilization procedures or to the cell systems analyzed.

In addition to the involvement of PI3K in the Ras-dependent destabilization of cadherin complexes and relocalization of ß-catenin, our results provide evidence for a strong association of cytoplasmic ß-catenin with PI3K both in vivo and in vitro. In vitro binding studies clearly show a direct interaction between ß-catenin and p85, (Figure 4 c), suggesting that the in vivo interactions might be mediated by the regulatory subunit of PI3K. In fact, p85 is able to interact with endogenous ß-catenin in control Pam212 cells, and this interaction is significantly increased in V12Ras-overexpressing cells. Interestingly, concomitant with the increased association with the regulatory subunit, association of the catalytic subunit of PI3K with ß-catenin is strongly induced in PamV12Ras (Figure 4 a). These observations suggest that the PI3K heterodimer is involved in the stabilization of cytoplasmic ß-catenin induced by activated H-Ras in keratinocytes.

The involvement of PI3K in the Ras-induced ß-catenin stabilization is further supported by analysis of Pam212 keratinocytes overexpressing the membrane-bound catalytic subunit of PI3K (Pamp110 cells). In these cells as well as in PamV12Ras cells, microinjected recombinant ß-catenin is stabilized in the cytoplasm and translocated to the nucleus after 4 h of microinjection. In contrast, the exogenous catenin is apparently degraded or incorporated into junctions in control cells (Figure 7 b). Furthermore, the pulse–chase analysis demonstrates that expression of V12Ras or p110CAAX significantly reduced the turnover of endogenous ß-catenin. These results indicate that constitutive activation of PI3K is sufficient for stabilization of ß-catenin and its translocation to the nucleus, although not for disruption of cell–cell junctions. One interesting possibility is that other pathways activated by V12Ras, like MAPK, are required for initial dismantling of adhesion complexes, and that cytoplasmic ß-catenin is then stabilized because of its interaction with activated PI3K. This is now being investigated in further detail.

Here, we provide evidence to support that H-Ras-induced stabilization of ß-catenin occurs through interference with its APC interaction and decrease in the levels of serine phosphorylation. The ability of ß-catenin to associate with APC is significantly reduced in keratinocytes stably expressing V12Ras. However, in contrast to previous reports, our present results indicate that the stabilization of hypophosphorylated cytoplasmic ß-catenin induced by activated H-Ras might occur by mechanism(s) independent of stable interaction with GSK3ß or significant alterations in the total GSK3ß activity (Delcommenne et al. 1998 ). Inhibition of additional kinase(s) or activation of phosphatase(s) may be involved in the dephosphorylation of ß-catenin upon Ras activation. In this sense, it has been reported that ß-catenin can also be phosphorylated by diacylglycerol-independent protein kinase C isoforms (Orford et al. 1997 ), and that its stability is modulated by PP2A phosphatase (Seeling et al. 1999 ). In Ras-expressing mouse keratinocytes ß-catenin might transiently interact with distinct cytoplasmic partners for its translocation to the nucleus. Interestingly, in our Ras-expressing keratinocytes only a slight increment in Lef-1/Tcf–dependent transcriptional activity is observed, suggesting that additional factors are needed to fully induce ß-catenin transcriptional activation (see Prieve and Waterman 1999 ).

Regarding the mechanism(s) leading to ß-catenin stabilization, it is not known whether interaction with PI3K can modulate its association to APC or directly contribute to its stabilization in the cytoplasm. Interestingly, ß-catenin–APC interaction is also blocked in p110CAAX-overexpressing keratinocytes (Figure 7 a), but similar levels of total GSK3ß activity have been observed in controls, PI3K and V12Ras transformants (Espada, J., and A. Cano, unpublished results). We speculate that p85 (and/or p110) might compete with other ß-catenin partners, such as APC or E-cadherin, rendering the molecule inaccessible for the ubiquitin-proteasome degradation. On the other hand, PI3K activation by H-Ras can further increase the ß-catenin–PI3K interaction. The possibility of a recruitment of ß-catenin into vesicles through PI3K interaction cannot be discarded, although it is not supported from the immunofluorescent staining (Figure 1 and Figure 7 b).

In summary, our results show a direct effect of H-Ras activation on the stabilization of ß-catenin cytoplasmic pools in epidermal keratinocytes. This effect is mediated by the PI3K effector and involves a novel ß-catenin–PI3K complex and the inhibition of ß-catenin–APC interaction. Together with recent data from other groups (Delcommenne et al. 1998 ; Potempa and Ridley 1998 ; Sander et al. 1998 ), our results highlight the role of PI3K as a main regulator of different signaling pathways impinging on the modulation of the E-cadherin–mediated adhesion and ß-catenin signaling. They also indicate that H-Ras activation can induce ß-catenin signaling and, thus, can contribute to the present knowledge on the molecular mechanisms of cancer development.

	Acknowledgements

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

We thank Drs. M. Takeichi, A. Hall (MRC Laboratory for Molecular Cell Biology, London, UK), J. Behrens, F. Wandosell, H. Clevers, and A. Harwood for providing reagents and cells. We also thank Dr. M. Quintanilla (Instituto de Investigaciones Biomedicas, CSIC-UAM, Madrid, Spain), M.A. Nieto (Instituto Cajal, CSIC-UAM, Madrid, Spain), A. Hall, and A. Harwood for critical reading of the manuscript, and to C. Bailón (Instituto Cajal, CSIC-UAM, Madrid, Spain) for helpful assistance in the confocal analysis.

This work was supported by grants to A. Cano from the Spanish Commision Interministerial de Ciencia y Tecnología (SAF95-0818 and SAF98-0085-C03-01) and Comunidad Autónoma de Madrid (08.1/020/1997). V.M.M. Braga is supported by the Cancer Research Campaign, UK. J. Espada is a recipient of a fellowship from the Spanish Ministry of Education and Culture, M. Perez-Moreno was funded by the Mexican Consejo Nacional de Ciencia y Tecnología during the realization of this work.

Submitted: 18 February 1999
Revised: 2 August 1999
Accepted: 3 August 1999

1.used in this paper: APC, adenomatous polyposis coli; GST, glutathione-S-transferase; GSK3ß, glycogen synthase kinase 3ß; H-Ras, Harvey-Ras; Lef-1/Tcf, lymphocyte enhancer factor 1/T cell factor; MAPK, mitogen-activated protein kinase; PI3K, phosphoinositide 3-OH kinase; PP2A, protein phosphatase 2A

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