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Article |
ß4 integrin activates a Shp2–Src signaling pathway that sustains HGF-induced anchorage-independent growth
Correspondence to Livio Trusolino: livio.trusolino{at}ircc.it
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Despite being a cell–matrix adhesion molecule, ß4 integrin can prompt the multiplication of neoplastic cells dislodged from their substrates (anchorage-independent growth). However, the molecular events underlying this atypical behavior remain partly unexplored. We found that activation of the Met receptor for hepatocyte growth factor results in the tyrosine phosphorylation of ß4, which is instrumental for integrin-mediated recruitment of the tyrosine phosphatase Shp2. Shp2 binding to ß4 enhances the activation of Src, which, in turn, phosphorylates the multiadaptor Gab1 predominantly on consensus sites for Grb2 association, leading to privileged stimulation of the Ras–extracellular signal-regulated kinase (ERK) cascade. This signaling axis can be inhibited by small interfering RNA–mediated ß4 depletion, by a ß4 mutant unable to bind Shp2, and by pharmacological and genetic inhibition of Shp2 or Src. Preservation of the ß4 docking sites for Shp2 as well as the integrity of Shp2, Src, or ERK activity are required for the ß4-mediated induction of anchorage-independent growth. These results unravel a novel pathway whereby ß4 directs tyrosine kinase–based signals toward adhesion-unrelated outcomes.
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Introduction |
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A few modes of action have been proposed to explain this feature. In some instances, carcinoma cells may secrete abundant quantities of laminin-5, which can ligate ß4 and sustain the expansion of nonadherent colonies through activation of a Rac–nuclear factor 
B antiapoptotic pathway (Zahir et al., 2003). Alternatively, the expression of ß4 is accompanied by the translational up-regulation of VEGF, which can act as a survival factor favoring colony formation (Lipscomb et al., 2005). Finally, we have recently demonstrated that ß4 can promote anchorage-independent growth in response to activation of the Met receptor for hepatocyte growth factor (HGF; Bertotti et al., 2005). This activity does not rely on laminin engagement, as it is retained by a ß4 truncated variant devoid of most of the extracellular domain and requires Met-dependent tyrosine phosphorylation of the ß4 cytoplasmic domain. However, the signaling pathway regulating this laminin-independent activity remains to be elucidated. Using biochemical, pharmacological, and genetic approaches, we found that the Met-mediated phosphorylation of ß4 initiates a previously unexplored transduction pathway that involves Shp2 recruitment, Src activation, and Gab1 phosphorylation and ultimately leads to dedicated stimulation of the MAPK/extracellular signal-regulated kinase (ERK) cascade. These results substantiate the crucial role of ß4 in epithelial tumorigenesis and describe a novel integrin-dependent signaling pathway that could be exploited by growth factor receptors for the implementation of oncogenic responses.
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Results |
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To begin to explore new signaling circuits potentially controlled by ß4 activity, we performed a progressive tyrosine/phenylalanine mutagenesis along the ß4 tail and mapped three tyrosines (Tyr1257, Tyr1440, and Tyr1494) that, when sequentially mutated into phenylalanines, cause a gradual reduction in ß4 phosphotyrosine content up to complete abrogation (Bertotti et al., 2005). Interestingly, an in silico analysis of the sequences surrounding these tyrosines revealed common structural features (Fig. 1 A): Tyr1257 and Tyr1494 are both located within immune T cell inhibitory motifs that have been characterized as canonical binding regions for protein and lipid phosphatases, including the SH2-containing tyrosine phosphatase Shp2; similarly, Tyr1440 is embedded in a degenerated consensus for Shp2. Based on these observations, we hypothesized that Tyr1257, Tyr1440, and Tyr1494 might be collectively involved in central signaling functions whose trait of union is multiple binding for Shp2.
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Shp2S), double (ß4-Shp2D), or triple (ß4-Shp2T) phenylalanine substitutions of the three critical tyrosines, with the consequent progressive reduction of ß4 tyrosine phosphorylation levels (Fig. 1, B and D); and (4) wild-type ß4 alone or wild-type Met alone as negative controls.
First, we examined direct interaction in vitro between ß4 and Shp2 in far-Western analysis using a GST fusion protein of the Shp2 N-terminal SH2-containing domain (GST-Shp2). This probe recognized ß4 immunoprecipitates when the integrin was fully phosphorylated by activated Met but not when Met-dependent phosphorylation was inhibited (Fig. 1 B). Association between GST-Shp2 and ß4 was gradually weaker when using the single and double ß4 mutants and was totally prevented upon expression of the ß4 triple mutant (Fig. 1 B), indicating that all of the putative consensus sites for Shp2 are involved in this interaction. Notably, the efficacy of Shp2 binding paralleled the extent of ß4 phosphorylation, suggesting that the tyrosines involved in Shp2 recruitment contain the bulk of the integrin substrate capacity for Met (Fig. 1 B). Tyrosine phosphorylation of ß4 as well as Shp2 binding could not be observed in the absence of transfected Met (Fig. 1 B). Similarly, the transfection of Met alone was ineffective because COS-7 cells do not express endogenous 
6ß4 (Niessen et al., 1997). When Tyr1257 and Tyr1494 were mutated into phenylalanines, the overall phosphotyrosine content of ß4 partially decreased, and ß4–Shp2 interaction was less efficient; however, the complete abolition of ß4 phosphorylation and Shp2 association was obtained only upon the phenylalanine permutation of Tyr1440 (Fig. 1 B). Thus, in principle, Tyr1440 could autonomously account for all of the observed binding events. To rule out this possibility, we repeated the far-Western experiment using a ß4 mutant bearing a single phenylalanine substitution of Tyr1440 (ß4-Y1440F). In COS-7 cells overexpressing Met and ß4-Y1440F, the tyrosine phosphorylation of ß4 and interaction between ß4 and Shp2 were reduced but not abolished (Fig. 1 C). This indicates that Tyr1440 is necessary but not sufficient for Shp2 association and that Tyr1257 and Tyr1494 display a residual binding activity for the phosphatase.
Next, we analyzed association in vivo by coimmunoprecipitation experiments in COS-7 cells overexpressing Shp2 and the various forms of Met and ß4. Met has been reported to associate with both Shp2 (Fixman et al., 1996) and ß4 (Trusolino et al., 2001). Therefore, it may act as a bridging molecule between the integrin and the phosphatase. To exclude this possibility and assess a direct interaction between ß4 and Shp2, we exploited a Met variant (MetD) that retains full catalytic activity (therefore, it is still able to phosphorylate ß4) but contains phenylalanine substitutions of Tyr1349 and Tyr1356, which represent the docking residues for several signal transducers, including Shp2 (Ponzetto et al., 1994; Fixman et al., 1996; Furge et al., 2000). This mutant was validated for its inability to bind Shp2 (Fig. 1 D) and for its capacity to phosphorylate ß4 (Fig. 1 E) upon transient transfection in COS-7 cells. Under these conditions, Shp2 could be efficiently recovered in ß4 immunoprecipitates. Conversely, the interaction was abolished in the absence of ß4 phosphorylation or in the presence of the ß4 triple mutant displaying complete substitution of the critical tyrosines and was progressively diminished in the single and double mutants (Fig. 1 E). Again, the efficiency of the ß4–Shp2 interaction paralleled the extent of ß4 phosphorylation; no tyrosine phosphorylation of ß4 nor association with Shp2 could be detected when ß4 or Met were transfected individually (Fig. 1 E).
Finally, we assessed whether tyrosine-phosphorylated ß4 can also recruit Shp2 in cells expressing endogenous proteins. Accordingly, we set up coimmunoprecipitation experiments in GTL16 cells, which express a constitutively active form of Met, and in FG2 cells, in which Met phosphorylation is inducible by HGF. Indeed, the association of Shp2 with ß4 could be detected basally in GTL16 (Fig. 1 F) and only after ligand stimulation in FG2 cells (Fig. 1 G). The binding between tyrosine-phosphorylated ß4 and Shp2 is specific, as no coimmunoprecipitation of Shp2 was observed with antibodies against an unrelated myc antigen (Fig. 1, F and G). As expected, ß4 tyrosine phosphorylation was constitutive in GTL16 cells and was induced by HGF in FG2 cells (Fig. 1, F and G).
Association between ß4 and Shp2 leads to increased phosphorylation of Gab1 through a Src-dependent mechanism
Translocation of Shp2 at the plasma membrane is essential for its function (Neel et al., 2003); therefore, the interaction of Shp2 with the intracellular domain of ß4 is likely to stimulate Shp2-dependent transduction pathways. One of the best-documented activities of Shp2 relies on its ability to stimulate Src catalysis by controlling Csk recruitment (Ren et al., 2004; Zhang et al., 2004). This notion, together with the established observation that Src can promote anchorage-independent growth when aberrantly activated (Yeatman, 2004), prompted us to investigate whether the signaling contribution of ß4 to this process could entail the stimulation of Src.
To explore this subject, we examined the activation of Src in MDA-MB-435 breast carcinoma cells, which do express Met but are devoid of ß4, and their counterpart cells stably transfected with a human ß4 cDNA (MDA-MB-435–ß4 cells; Fig. 2 A).
Under basal conditions, Src enzymatic function was already higher in ß4 cells compared with mock cells, possibly as a result of residual Met-based ß4 signaling or to adhesion-triggered Src stimulation as previously demonstrated (Dans et al., 2001; Gagnoux-Palacios et al., 2003). This priming favored the further activation of Src in response to HGF; indeed, ligand stimulation led to a rapid boost of Src activity in ß4 cells, whereas the HGF-dependent activation of Src in mock cells displayed slower kinetics and weaker intensity (Fig. 2 B). To evaluate whether the stronger and accelerated activation of Src in ß4-expressing cells is caused by the integrin ability to bind Shp2, we generated MDA-MB-435 transfectants expressing the ß4 triple variant that is unable to bind Shp2 (hereafter referred to as ß4Shp2). This mutant was exposed at the cell surface as efficiently as wild-type ß4 together with the endogenous 6 subunit (Fig. 2 A). In line with our hypothesis, disruption of the association between ß4 and Shp2 almost abolished the HGF-dependent activation of Src (Fig. 2 B). Interestingly, the ß4Shp2 mutant affected the stimulation of Src more potently than the simple absence of ß4, suggesting that this variant could not only behave as a signaling-dead molecule but also as a dominant repressor of other endogenous ß4 signaling partners. Accordingly, ß4 has been shown to impinge on signals emanating from the Ron tyrosine kinase receptor (Santoro et al., 2003), the EGF receptor (Mainiero et al., 1996; Rabinovitz et al., 1999), Erb-B2 (Gambaletta et al., 2000; Guo et al., 2006), and tetraspanins (Yang et al., 2004).
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Shp2 mutant led to a less efficient phosphorylation of Gab1 compared with cells expressing wild-type ß4 (Fig. 2 C). Likewise, stimulation with increasing amounts of HGF produced a weak dose-dependent curve of Gab1 phosphorylation in mock cells. Conversely, Gab1 phosphorylation in ß4 cells reached a plateau at a very low concentration of ligand, and the overall phosphorylation levels were more robust than in mock transfectants (Fig. 2 D). Again, the response of ß4Shp2 cells was similar or even lower than that showed by mock cells (Fig. 2 D).
In a complementary approach, we abated ß4 levels by lentiviral delivery of siRNA in MDA-MB-231 breast carcinoma cells, which endogenously synthesize both Met and the integrin (Fig. 2 E). We then reestablished ß4 expression in ß4-deficient cells using a siRNA-resistant variant that lacks most of the extracellular portion, including the siRNA target region, but retains the ability to transduce Met-dependent responses (ß4extra; Trusolino et al., 2001; Bertotti et al., 2005). In addition to wild-type ß4extra, which displays an intact cytoplasmic domain, we also expressed a ß4extra mutant with phenylalanine substitutions of the tyrosines involved in Shp2 binding (Fig. 2 E). In all cases, Met expression was unaffected (Fig. 2 E). Consistent with that observed in MDA-MB-435 cells, ß4 knockdown in MDA- MB-231 resulted in the reduced HGF-dependent phosphorylation of Gab1, whereas the rescue of ß4 expression was accompanied by the restoration of higher Gab1 phosphorylation levels in the presence of a signaling-competent cytoplasmic portion but not when Shp2 recruitment was abolished (Fig. 2 F).
If Shp2 and Src specifically contribute to Gab1 phosphotyrosine content in a ß4-dependent manner, the attenuation of Shp2 and/or Src activity should affect the HGF-triggered phosphorylation of Gab1 only in cells expressing ß4. In fact, Shp2 inhibition by expression of a catalytically inactive dominant interfering isoform (Shp2DN) resulted in the decreased phosphorylation of Gab1 in MDA-MB-435–ß4 cells but not in mock cells (Fig. 2 G). Similar results were obtained when mock and ß4 cells were treated with the Src pharmacological inhibitor PP2 (Fig. 2 H) or upon transfection of a kinase-dead variant of Src (SrcDN; Fig. 2 I).
ß4-dependent activation of Src leads to the selective association of Gab1 with Grb2
Gab1 is a scaffolding adaptor that associates with a variety of signal transducers after phosphorylation on multiple sites (Gu and Neel, 2003). We wondered whether the Src-dependent increase of Gab1 phosphorylation in ß4 cells leads to a generic, quantitative enhancement of the overall Gab1 phosphotyrosine content or to a selective, qualitative phosphorylation of defined tyrosine residues with consequent specific binding to a given transducer.
To investigate this issue, we overexpressed Gab1 in the various MDA-MB-435 transfectants and assessed the ability of Gab1 to form supramolecular complexes with a representative panel of SH2-containing signaling molecules, including Grb2, Shc, PI3K, and Shp2 itself. Among these signaling effectors, Grb2 appeared to bind Gab1 more efficiently in ß4 versus mock cells after HGF stimulation (Fig. 3 A).
This binding was reduced in cells expressing the ß4Shp2 mutant (Fig. 3 B); similarly, the PP2-mediated inhibition of Src, which decreases HGF-induced Gab1 phosphorylation only in ß4 cells, impaired the association of Grb2 with Gab1 in the presence but not in the absence of ß4 (Fig. 3 B).
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Shp2 mutant, and treatment with PP2 impaired Gab1–Grb2 association in ß4 transfectants but not in mock cells (Fig. 3 C). Together, these results indicate that the Shp2-mediated activation of Src in ß4 cells leads to the dedicated phosphorylation of Gab1 on tyrosine residues specifically responsible for Grb2 binding, a preferential association that can be abrogated by uncoupling ß4 from Shp2 or by hindering Src function. Privileged interaction between Gab1 and Grb2 in ß4 cells results in the increased stimulation of Ras-dependent effectors: indeed, the amplitude and persistence of ERK/MAPK activation after HGF stimulation were higher in ß4 compared with mock and ß4Shp2 transfectants (Fig. 3 D).
Shp2 and Src are required to promote ß4-mediated anchorage-independent growth
To verify whether the aforementioned signaling pathway is in fact responsible for the ability of ß4 to promote anchorage-independent growth, we performed soft agar assays on several different MDA-MB-435 transfectants (Figs. 2 E and 4 A).
As expected, the ectopic expression of ß4 considerably enhanced the basal and HGF-stimulated formation of suspended colonies compared with mock cells both in absolute numbers (Fig. 4 B, graph) and in size (Fig. 4 B, images). Analogous results were obtained upon transfection of the ß4extra variant, further validating the role of this nonadhesive mutant as an efficient substitute of wild-type ß4 in HGF-driven responses and confirming the notion that the Met-dependent signaling activity of ß4 does not require laminin ligation (Fig. 4 B; Trusolino et al., 2001; Bertotti et al., 2005). In contrast, expression of the ß4Shp2 signaling-dead mutant was less effective, indicating that the interaction between ß4 and Shp2 is critical for this process (Fig. 4 B). Transfection of dominant-negative isoforms of Shp2 or Src in ß4-expressing cells (Fig. 4 B) as well as treatment of ß4 cells with the Src inhibitor PP2 or with the ERK inhibitor PD98059 (Fig. 4 C) potently impaired HGF-dependent clonogenic activity in soft agar. Together, these results reinforce the observation that Shp2, Src, and ERKs are central downstream transducers of ß4-driven anchorage-independent growth.
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extra siRNA-resistant variant displaying a wild-type intracellular domain but not upon expression of the Shp2 mutant (Fig. 5).
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Discussion |
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In this study, we show that the ß4 integrin conspires with the tyrosine kinase Met for efficient execution of anchorage-independent growth by channeling Met signals toward activation of the Ras-ERK oncogenic cascade. This function relies on Met-triggered phosphorylation of the ß4 cytoplasmic domain and on the ensuing recruitment of the tyrosine phosphatase Shp2 to the integrin tail. ß4–Shp2 association results in the stimulation of Src, which, in turn, favors a more efficient phosphorylation of the Gab1 multiadaptor protein, mainly on tyrosines involved in Grb2 binding. Ultimately, privileged interaction between Gab1 and Grb2 leads to dedicated stimulation of the MAPK–ERK pathway.
Structural aspects of ß4–Shp2 interaction
Association between ß4 and Shp2 depends on the integrity of three tyrosines along the ß4 cytoplasmic domain (Tyr1257, Tyr1440, and Tyr1494) that are inserted in canonical or degenerated motifs for the SH2 domain of Shp2 and, consequently, could act as docking sites for the phosphatase when phosphorylated. However, based on the crystal structure of a fragment of the ß4 intracellular portion encompassing the first pair of type III fibronectin-like (FNIII) repeats (de Pereda et al., 1999), interaction between Shp2 and Tyr1257 appears to be more complicated because this tyrosine is part of the hydrophobic core of the second repeat (Fig. 1 A). Thus, it may not be easily accessible for phosphorylation because of conformational constraints.
This information is in disagreement with our findings and with a previous study showing the phosphorylation of Tyr1257 in response to the antibody-mediated ligation of ß4 (Shaw, 2001). A possible explanation for this discrepancy is that although the aromatic ring of Tyr1257 is in fact involved in hydrophobic interactions with other residues and is not accessible to the solvent, the side chain is not completely buried in the FNIII core so that the OH group reaches the solvent-accessible surface of the protein. This kind of spatial organization seems to be permissive for phosphorylation; for example, the human Vaccinia H1-related phosphatase is phosphorylated by ZAP-70 at Tyr138 despite that only the OH group of the amino acid is partially exposed to the solvent (Alonso et al., 2003). Moreover, physical association with Met could affect the structural organization of ß4 and induce a more relaxed conformation of the FNIII repeat, facilitating recognition by the kinase and transfer of the phosphate group.
In any case, our observation that the phenylalanine permutation of Tyr1257 results in reduction of the overall ß4 phosphotyrosine content and in a less efficient association with Shp2 does not exclude the possibility that Tyr1257 is not a direct phosphorylation site, but it is necessary for the phosphorylation of other residues that, in turn, could be involved in Shp2 recruitment. This hypothesis is in agreement with the general notion that bindings between SH2 domains and the corresponding ligand motifs hardly occur in rigid structural environments such as the FNIII fold.
A novel signaling pathway connecting ß4 integrin to ERK activation: biochemical and biological insights
The importance of the signaling axis explored here in ß4-mediated anchorage-independent growth is underscored by the observations that a ß4 mutant unable to bind Shp2 cannot sustain this process and that interference with Shp2, Src, or ERK impairs the biological activity of wild-type ß4. Interestingly, Shp2 is known to act downstream from Met when physically associated with Gab1 to sustain the prolonged stimulation of ERKs (Maroun et al., 2000). However, the signaling intermediates propagating this activity remain elusive (Gu and Neel, 2003). Our findings confirm the crucial role of Shp2 as a positive regulator of Ras-dependent signals in response to HGF and provide an alternative pathway as well as several additional molecular actors that connect Met function to the enhancement of ERK activity.
The unorthodox observation that ß4 contributes to the malignant phenotype by acting as a biochemical selector of tumorigenic signaling pathways unveils an unforeseen function that transcends the activity of ß4 as an integrin and assimilates it to classical signal relay adapters endowed with oncogenic potential. Something similar has been described for ß1A integrin, the most widely expressed spliced isoform of ß1 integrins: in this case, interaction between ß1A and the insulin-like growth factor-I tyrosine kinase receptor results in integrin-mediated recruitment of the downstream effector IRS1, which inhibits cell adhesion and stimulates insulin-like growth factor–dependent cellular proliferation and tumor growth (Goel et al., 2004).
Most of the signaling effectors along the transduction pathway discussed in this study are involved in human malignancies in vivo: Met, ß4, and Src are often overexpressed (and coexpressed) in a vast number of human carcinomas (Mercurio and Rabinovitz, 2001; Trusolino and Comoglio, 2002; Ishizawar and Parsons, 2004), and Shp2 gain of function mutations have been described in some solid tumors and in various forms of leukemia (Bentires-Alj et al., 2004). Gab2, a close homologue of Gab1, is amplified and overexpressed in a fraction of human breast tumors and collaborates with the ErbB2 oncogene for activation of a Shp2–ERK pathway that drives mammary carcinogenesis (Bentires-Alj et al., 2006). Intriguingly, ß4 has recently been shown to cooperate with ErbB2 in breast cancer onset (Guo et al., 2006). Finally, constitutively active Src transcriptionally up-regulates HGF in breast carcinoma cells, generating an autocrine loop that promotes cancer progression (Wojcik et al., 2006). Altogether, these findings suggest not only a functional role in vivo but also a cooperative effect and a potential epistatic relationship for these signals.
Finally, it is worth noting that the tyrosines involved in Shp2 binding represent biochemical hotspots for ß4 signaling capacity also with respect to other transduction pathways: Tyr1257 is necessary for ß4 phosphorylation in response to laminin ligation (Shaw, 2001), Tyr1440 is responsible for SH2-mediated interaction with the Grb2 upstream effector Shc (Dans et al., 2001), and Tyr1494 is involved in the adhesion-driven stimulation of PI3K (Shaw, 2001). It will be interesting to analyze whether these additional transducers can complement or substitute for the signaling axis identified in this study for fostering ß4-mediated anchorage-independent growth and possibly tumorigenesis.
Met and ß4 in cancer onset and progression
Accumulating evidence suggests that the aptitude of a neoplasm to disseminate at distant sites is already preordained by the protein repertoire that progenitor cells express relatively early in tumorigenesis. This indicates that the phenotype acquired en route by an evolving tumor cell can confer not only a selective advantage for cell replication (a condition necessary for formation of the primary tumor mass) but also, later during neoplastic progression, the tendency to metastasize (Bernards and Weinberg, 2002).
This line of thinking fits nicely with our findings on the role of ß4 and Met in tumor evolution. We and others have demonstrated that both molecules, individually or in combination, are able to enhance the motility and survival of cancer cells as a prelude for neoplastic invasion and metastasis (Mercurio and Rabinovitz, 2001; Trusolino and Comoglio, 2002). Here, we show that the same molecules can also cooperate for anchorage-independent growth, which is the experimental and phenotypic hallmark of primary tumorigenesis. Together, these data allow us to draw a linear flowchart along which ß4 and Met are causally involved first in the derailment of cell accretion and later in the promotion of metastatic spread.
This dual activity of ß4 and Met on epithelial cells is paralleled by their common ability to induce a peculiar phase of the angiogenic process in endothelial cells. Specifically, both the inhibition of ß4 signaling by an intracellularly truncated ß4 mutant (Nikolopoulos et al., 2004) and the inhibition of Met function by a decoy receptor (Michieli et al., 2004) prevent branching of medium- and small-size vessels into microvessels during intratumor vascularization, suggesting that both molecules are selectively involved in the onset of the invasive step of pathological angiogenesis. At present, we do not know whether this vascular phenocopy is supported by a functional collaboration between ß4 and Met. However, all of these observations highlight the versatility of the ß4–Met system in promoting the various and sequential aspects of neoplastic progression.
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Materials and methods |
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Shp2 construct containing phenylalanine mutations of Y1257, Y1440, and Y1494 was generated by PCR amplification of the BssHII–NotI fragment of a ß4 template already containing the Y1257F and Y1494F substitutions (obtained from L.M. Shaw, Harvard Medical School). To create the ß4 siRNA expression vector, oligonucleotides used by Chung et al. (2004) were annealed and ligated into pSUPER between the BglII and HindIII sites. BamHI- and XhoI-digested inserts were then subcloned into the pRLL5 lentiviral vector. A scrambled ß4 oligonucleotide was used as a control. The constructs encoding for wild-type Met, kinase-inactive Met, wild-type ß4, ß4-1440F, and ß4extra have been described previously (Trusolino et al., 2001). The ß4 cDNA used in this study corresponds to PubMed accession no. AAC51632 and matches with the sequence originally cloned by Suzuki and Naitoh (1990).
Cell culture, transfection, and viral infection
COS-7, MDA-MB-435, and MDA-MB-231 cells were cultured in DME supplemented with 10% FBS (Invitrogen). The expression of exogenous proteins was obtained with LipofectAMINE- or LipofectAMINE 2000 (Invitrogen)–mediated transfection according to the manufacturer's protocol or with retroviral or lentiviral infection. Viral hybrid vectors were produced by the transient transfection of 293T cells. Viral supernatants were filtered through a 0.22-µm filter, and infections were performed in the presence of 4 µg/ml polybrene (Sigma-Aldrich).
Biochemical methods
For immunoprecipitations, 5 x 106 cells were lysed for 20 min at 4°C with 1 ml of a buffer containing 50 mM Hepes, pH 7.4, 5 mM EDTA, 2 mM EGTA, 150 mM NaCl, 10% glycerol, and 1% Triton X-100 in the presence of protease and phosphatase inhibitors. For ß4–Shp2 coimmunoprecipitations in FG2 cells, 1% Brij58 was used instead of Triton X-100. Extracts were clarified at 12,000 rpm for 15 min, normalized with the BCA Protein Assay Reagent kit (Pierce Chemical Co.), and incubated with different mAbs for 2 h at 4°C. Immune complexes were collected with either protein G– or protein A–Sepharose, washed in lysis buffer in the presence of 1 M LiCl, and eluted. Total cellular proteins were extracted by solubilizing the cells in boiling SDS buffer (50 mM Tris-HCl, pH 7.5, 150 mM NaCl, and 1% SDS). Extracts were electrophoresed on SDS-polyacrylamide gels and transferred onto nitrocellulose membranes (Hybond; GE Healthcare). Nitrocellulose-bound antibodies were detected by the ECL system (GE Healthcare). Unless otherwise indicated, cells were stimulated with 50 ng/ml HGF for 30 min. PP2 was generally used at a 10-µM concentration and applied to cells for 30 min. In experiments aimed at analyzing the association of Gab1 with signal transducers and the HGF-dependent activation of ERKs, mock cells and cells expressing wild-type ß4 or ß4Shp2 were transiently transfected with a Gab1 cDNA.
For far-Western analysis, membranes were blocked for 1 h in TBS, 0.1% Tween-20, 5% BSA, and 3 µm glutathione and were incubated for 3 h with 1 µg/ml GST fusion protein previously adsorbed to 3 µM glutathione in 0.5% BSA. Filters were subsequently decorated with anti-GST antibody.
Src kinase assays were performed on Src immunoprecipitates using a commercial kit (Upstate Biotechnology) based on the phosphorylation of a specific substrate peptide (KVEKIGEGTYGVVYK) using the transfer of the 
-phosphate of -[32P]ATP by Src. The phosphorylated substrate was then separated from the residual -[32P]ATP using phosphocellulose paper and quantified with a scintillation counter.
Soft agar assay
3,000 cells were resuspended in complete medium containing 0.5% Seaplaque agar. Cells were seeded in 24-well plates containing a 1% agar underlay and supplemented twice a week with complete medium. In some experiments, MDA-MB-435–ß4 cells were treated twice a week with 5 µM PP2 or 10 µM PD98059. Colonies were stained by the incorporation of tetrazolium salts 2 (for MDA-MB-435) or 3 wk (for MDA-MB-231) after seeding. Colonies were coded and scored in a blinded fashion by a second observer. Colony numbers were obtained using a phase-contrast light microscope (DMIL; Leica) fitted with a 32-grid eyepiece at a total magnification of 20x. Images were captured with ImageReady software (Adobe) using a microscope (DMIL; Leica) and a 20 x 0.30 objective (Leica) equipped with a digital camera (DFC320; Leica).
Statistical and densitometric analysis
Results are means ± SEM. Comparisons were made using the two-tailed t test. P-values <0.05 were considered to be statistically significant. Blot images were captured using a molecular imager (ChemiDoc XRS; Bio-Rad Laboratories). Densitometric analysis was performed with analysis software (Quantity One 1-D; Bio-Rad Laboratories) installed on the imager. Images were arranged and labeled using Illustrator (Adobe).
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Acknowledgments |
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This work was supported by an Associazione Italiana per la Ricerca sul Cancro grant to P.M. Cornoglio and a Ministero dell'Istruzione dell'Università e della Ricerca (PRIN 2004) grant to L. Trusolino.
Submitted: 17 May 2006
Accepted: 15 November 2006
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References |
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