Collective cell migration (CCM) is essential for organism development, wound healing, and metastatic transition, the primary cause of cancer-related death, and it involves cell–cell adhesion molecules of the cadherin family. Increased P-cadherin expression levels are correlated with tumor aggressiveness in carcinoma and aggressive sarcoma; however, how P-cadherin promotes tumor malignancy remains unknown. Here, using integrated cell biology and biophysical approaches, we determined that P-cadherin specifically induces polarization and CCM through an increase in the strength and anisotropy of mechanical forces. We show that this mechanical regulation is mediated by the P-cadherin/β-PIX/Cdc42 axis; P-cadherin specifically activates Cdc42 through β-PIX, which is specifically recruited at cell–cell contacts upon CCM. This mechanism of cell polarization and migration is absent in cells expressing E- or R-cadherin. Thus, we identify a specific role of P-cadherin through β-PIX–mediated Cdc42 activation in the regulation of cell polarity and force anisotropy that drives CCM.
Collective cell migration (CCM), the coordinated movement of cells connected by cell–cell adhesion, is a fundamental process in development, tissue repair, and tumor invasion and metastasis (Friedl and Gilmour, 2009; Rørth, 2009; Friedl et al., 2012). Both epithelial (carcinoma) and mesenchymal (sarcoma) cancer cells undergo CCM (Theveneau and Mayor, 2011). Cells within a moving collective group have two types of interactions: one with the substratum (which is often the ECM, but also other cells) and one with neighboring moving cells through cell–cell interactions. Two protein families typically mediate these interactions and the generation of mechanical forces: integrins (with the underlying ECM) and cadherin trans-dimers (at intercellular adhesion sites). Classic cadherins, a central component of cell–cell and adherens junction formation, are major drivers of CCM (Halbleib and Nelson, 2006). Mechanical coupling between migratory cells may result in the production of force-dependent signals by which the cells can influence their collective behavior (Trepat et al., 2009; Tambe et al., 2011; Mertz et al., 2012, 2013; Hirashima et al., 2013) and also force transmission to the ECM (Jasaitis et al., 2012; Mertz et al., 2013). Besides the physical forces per se, their orientation also influences CCM, because a broad variety of cell types migrate along the direction of maximal intercellular tension (Tambe et al., 2011).
The mechanotransduction pathways whereby cadherin-mediated cell–cell adhesion promotes CCM, and in particular the molecular mechanisms that couple mechanical forces to the correlated cell motion, remain largely to be elucidated. One major process during CCM is the coordination of migration, polarization, and rearrangement of cytoskeletal elements by cells that are moving collectively. Rho GTPases play a crucial role in this coordination (Weber et al., 2012; Das et al., 2015a). RhoA and RhoE activity modulation appears to be involved in decreasing cell contractility at cell–cell contacts, an event that is important for CCM (Hidalgo-Carcedo et al., 2011; Omelchenko and Hall, 2012) and for the formation and maintenance of the migration fingers observed in epithelial MDCK cells (Reffay et al., 2014). In vivo studies using border cells moving in the Drosophila melanogaster ovary—a well-studied model of CCM—or using neural crest cells have demonstrated that Rac1 is activated at the front of migrating cells and participates in CCM (Theveneau et al., 2010; Wang et al., 2010). Recently, positive feedback between E-cadherin and Rac1 signaling was shown to occur in border cell migration (Cai et al., 2014). Moreover, Cdc42 localizes at the astrocyte migrating front and controls polarity during the collective migration of fibroblasts and astrocytes (Cau and Hall, 2005; Osmani et al., 2006). However, it is not known how the cadherin-mediated response regulates Rho GTPase activity during CCM. We decided to tackle this problem by focusing on P-cadherin. Indeed, aberrant P-cadherin expression has been described in many tumor types, including carcinoma and aggressive sarcoma (Paredes et al., 2012; Thuault et al., 2013; van Roy, 2014). In these tumors, P-cadherin is expressed in invasive rather than in in situ lesions, showing that aberrant expression of P-cadherin could be a useful marker for the invasion capacity of tumor cells. Additionally, P-cadherin expression is associated with cell invasiveness (Thuault et al., 2013), and P-cadherin knockdown in MCF10A cells resulted in a reduction of cell migration directionality and persistence during wound healing (Ng et al., 2012).
In this study, to directly investigate the role of P-cadherin during migration, we used mesenchymal C2C12 myoblasts that do not express P-, E-, and R-cadherin and analyzed the impact of P-cadherin expression in a 2D migration assay upon removal of a physical barrier. Because N- and M-cadherin, the two cadherins expressed in C2C12 myoblasts, are downregulated upon P-cadherin expression (Thuault et al., 2013), P-cadherin becomes the main cadherin expressed in these cells. As controls, we generated C2C12 cells that express E- or R-cadherin. By measuring velocity, persistence, directionality, and polarity, we demonstrated that expression of P-cadherin, but not E- or R-cadherin, induces efficient CCM. Using micropatterned cell monolayer and traction forces and monolayer stress microscopy, we dynamically mapped—for the first time in migrating mesenchymal cells—the mechanical forces developed and demonstrated that P-cadherin has a major and specific role in the induction of intercellular and traction force anisotropy in the cell layer. We also found that P-cadherin specifically activates Cdc42 during CCM through the guanine nucleotide exchange factor (GEF) β-PIX and identified the P-cadherin/β-PIX/Cdc42 axis as crucial for P-cadherin–mediated CCM.
P-cadherin induces CCM
Because P-cadherin is up-regulated in aggressive tumors and associated with cell invasiveness, we investigated its role in cell migration by monitoring mouse C2C12 cells that express P-cadherin (C2C12 Pcad; Fig. 1 a) after removal of a physical barrier to provide free space into which confluent cells could migrate. As a control, C2C12 cells expressing only empty vector (C2C12 LZRS), E-cadherin (C2C12 Ecad), or R-cadherin (C2C12 Rcad) were used (Fig. 1 a). All cadherins were expressed at a similar level and reached the plasma membrane in a similar way (Fig. 1 b and Fig. S1, a and b). By combining time-lapse microscopy, cell tracking, and computational analysis, we characterized cell movements and cell–cell coordination in the sheet from 0 to 15 h after barrier removal (Fig. 1, c–i; and Fig. S1, c and d). Within the first 2 h, cells became progressively motile in the direction perpendicular to the free edges. The mean cell migration velocity and persistence were not significantly different in the four cell lines. Conversely, after 2–3 h, only P-cadherin expression, which induced a reorganization of the cell layer, increased the velocity and persistence of migration (Fig. 1, c and d; Fig. S1, c and d; and Video 1). Tracking the cells in the first three rows indicated directed movement in P-cadherin–expressing cells, whereas control cells (vector alone and E- or R-cadherin–expressing cells) tended to spread in all directions. Measuring the trajectory angle distribution revealed that P-cadherin expression increased the directionality of the movement of individual cells (Fig. 1 e). E- or R-cadherin expression in C2C12 cells also downregulated N- and M-cadherin as in P-cadherin expressing cells (Fig. 1 a and Fig. S1 a), but it did not promote cell layer reorganization (Fig. S1, c and d; and Video 2) and increase in velocity, persistence, and directionality observed upon P-cadherin expression (Fig. 1, c–e). These data demonstrate the specific effect of P-cadherin expression in CCM induction. P-cadherin–mediated CCM requires P-cadherin homotypic interaction because (a) isolated P-cadherin–expressing cells migrated randomly with a persistence similar to that of control cells (Fig. S2, a–e), and (b) calcium chelation by incubation with EGTA perturbed cadherin homophilic cell–cell adhesion and decreased persistence (Fig. S2, f and g). Conversely, mitomycin C treatment did not modify migration speed or persistence, thus excluding the involvement of cell proliferation (unpublished data). We also analyzed cell polarization by monitoring the position of the centrosome and the Golgi apparatus relative to the nucleus (Ridley et al., 2003; Yadav et al., 2009): P-cadherin expression, but not E- or R-cadherin expression, induced a marked orientation of the centrosome and Golgi in front of the nucleus and toward the protruding edges (Fig. 1, f and g). To map cell velocities within entire layers, we used particle image velocimetry (PIV) analysis, a technique that computes correlations between successive images (Petitjean et al., 2010) to visualize individual displacement fields across the cell sheet. P-cadherin expression oriented the velocity fields, and in these cells, the angle distribution was narrower than in control cells (Fig. 1 h). This analysis also confirmed a significant and specific increase in velocity after P-cadherin expression in the entire cell layer (Fig. 1 i).
These results indicate that P-cadherin expression specifically promotes efficient CCM by increasing cell velocity, directionality, and persistence toward the free space. Moreover, compared with E- and R-cadherin, P-cadherin expression efficiently and specifically promotes polarization of cells and cell movement.
P-cadherin expression modifies cellular and focal adhesion (FA) organization and turnover
We then analyzed the overall cellular and FA organization in the four cell lines. Immunostaining analysis of the actin cytoskeleton revealed the specific formation of large protrusions in the direction of migration by the first multicellular row of P-cadherin–expressing cells (Fig. 2, a and b). Moreover, cryptic lamellipodia, which are structures characteristic of cells that migrate collectively, were detected at the front edge of cells inside the multicellular layer (Fig. 2 c; Farooqui and Fenteany, 2005). EGTA addition to P-cadherin–expressing cells decreased the orientation of the protrusion in the direction of migration (Fig. S2, h–j). Immunostaining for paxillin, a marker of most adhesion sites (Zaidel-Bar et al., 2003), showed that P-cadherin expression was associated with a marked increase in the number of small nascent FA at the leading edge (within the first 10 µm from the cell edge) and with an important reorientation of mature FAs parallel to the direction of migration across the entire cell layer (Fig. 2, d–f). Moreover, monitoring FA dynamics with paxillin-GFP in migrating cells using time-lapse video microscopy (Fig. 2 g and Video 3) revealed that P-cadherin expression induced a dramatic increase in FA assembly and disassembly rates (Fig. 2 h).
Our results show that P-cadherin expression remodels the actin cytoskeleton with the formation of a large protrusion in the first cell row and of cryptic lamellipodia. It also remodels FAs, with the formation of many nascent FAs at the leading edge of the multicellular migrating row. Moreover, P-cadherin expression specifically promotes the polarization of the membrane protrusion and of FAs toward the direction of migration. These events appeared to be specific of P-cadherin, and not of E- or R-cadherin expression.
P-cadherin expression increases traction forces, intercellular stresses, and plithotaxis
During CCM, mechanical forces play a major role in monolayer expansion. Particularly, traction forces, which are exerted by cells on the underlying substrate, and intercellular stresses allow long-range cell guidance (Trepat et al., 2010; Tambe et al., 2011). Collectively migrating cells also migrate preferentially along the direction of maximum principal stress, a process called plithotaxis (Trepat and Fredberg, 2011).
Using a micropatterned cell monolayer and traction-force microscopy (Trepat et al., 2009), we investigated whether P-, E-, or R-cadherin expression influenced the traction forces. C2C12 cells on collagen-coated polyacrylamide gels assumed morphologies comparable to those on a more rigid culture substrate (i.e., glass or plastic; Fig. S3 a and Video 4), and P-cadherin expression similarly increased both the velocity and persistence of migration (Fig. S3, b and c). We measured traction forces along the x direction (Tx; i.e., parallel to the direction of migration) over 8 h within an advancing cell sheet cultured on a collagen-coated polyacrylamide gel. Tx values were higher in P- and E- than in R-cadherin–expressing and control cells in the first 40 µm behind the leading edge (Fig. 3, a and b; and Video 5). The mean Tx value from 0 to 40 µm was highest in P-cadherin–expressing cells (Fig. 3 c). In contrast, Ty values (i.e., traction forces perpendicular to the direction of migration) were significantly decreased after 40 µm in P-cadherin–expressing cells, whereas they were increased in control and E- and R-cadherin–expressing cells (Fig. 3 a). Thus the Tx/Ty ratio was significantly increased in P-cadherin compared with E- or R-cadherin–expressing and control cells, suggesting a polarization of cell movement in P-cadherin–expressing cells. Indeed, the analysis of traction-force orientation from 0 to 40 µm and from 60 to 140 µm from the leading multicellular row toward the center of the cell layer revealed that P-cadherin expression promoted traction-force reorientation in the entire cellular layer toward the direction of migration (Fig. 3 d).
Using micropatterned cell and monolayer stress microscopy, we measured local intercellular stress within the monolayer during cell migration (Tambe et al., 2011). This technique is based on the principle that, according to Newton’s laws, traction forces applied at the cell–gel interface must be balanced by intra- and intercellular forces (Trepat et al., 2009; Maruthamuthu et al., 2011). We measured σxx, the stress component in the direction of expansion of the monolayer. We refer to it interchangeably as monolayer stress or intercellular stress (Tambe et al., 2011). Similarly to persistence, monolayer stress increased monotonically with time and tended to reach a plateau, the magnitude of which was significantly higher for P-cadherin–expressing cells (Fig. 4, a–c; and Video 6). When local monolayer stress was represented as an ellipse with axes corresponding to local maximum and minimum stresses, P-cadherin expression increased stress anisotropy (Fig. 4 d). Moreover, the cell velocity vectors tended to orient with the orientation of the maximum principal stress, and this phenomenon was more pronounced in regions of high stress anisotropy (Fig. 4 e). This mechanism for collective cell guidance is called plithotaxis (Tambe et al., 2011; Trepat and Fredberg, 2011) and was observed exclusively after P-cadherin, but not E- or R-cadherin, expression in C2C12 cells.
These results show that P-cadherin expression increases the anisotropy and strength of traction forces and of intercellular stresses in the entire layer and also plithotaxis.
P-cadherin expression specifically activates Cdc42 to promote CCM
Because P-cadherin expression specifically promoted the polarization of many cell processes and structures (i.e., cell organelles, cell trajectories, intercellular stresses, traction forces, and FAs), we asked whether P-cadherin expression induced the activation of Cdc42, a major regulator of polarity (Etienne-Manneville and Hall, 2001; Zegers and Friedl, 2014). Global Cdc42 activation during migration after massive wounding was assessed using a pull-down assay. Cdc42 was specifically activated in P-cadherin–expressing cells, but not in E- or R-cadherin–expressing and control cells (Fig. 5 a). This P-cadherin–dependent Cdc42 activation required P-cadherin homotypic interactions and CCM, because the level of Cdc42 activation was not increased upon P-cadherin expression in isolated migrating (Fig. 5 b) and nonmigrating (Fig. 5 c) confluent cells. Using the Förster resonance energy transfer (FRET) biosensor Raichu-Cdc42 (Itoh et al., 2002), we mapped Cdc42 activity within migrating cells and detected elevated Cdc42 activity at the leading edge of migrating cells located at the multicellular leading row and inside the multicellular layer in cryptic lamellipodia (Fig. 5 d). Moreover, we measured global Rac1 activity and showed that P-cadherin expression increased Rac1 activity in a Cdc42-dependent manner (Fig. 5 e). In contrast, P-cadherin expression was not correlated with RhoA activation (Fig. 5 f) or with an overall increase in myosin light chain phosphorylation (Fig. 5 g).
To identify potential regulators of Cdc42 activation downstream of P-cadherin, we performed a proteomic analysis of molecules that were immunoprecipitated with P-cadherin and identified β-PIX (Table S1 and Fig. S4), a GEF involved in Cdc42 and Rac1 activation and CCM in vivo (Osmani et al., 2006; Omelchenko et al., 2014). β-PIX association with P-cadherin was confirmed by coimmunoprecipitation (Fig. 6 a). Knockdown of β-PIX using a specific shRNA (Fig. S5 b) impaired P-cadherin–induced Cdc42 activation during CCM (Fig. 6 b). Cdc42 activation in C2C12 Pcad β-PIX shRNA cells could be rescued by expression of shRNA-resistant wild-type β-PIX (β-PIXWT), but not by a β-PIX GEF dead mutant (β-PIXGD; Fig. S5 g). We then monitored the contribution of Cdc42 to P-cadherin–induced CCM by depleting Cdc42 using specific shRNA or in β-PIX–depleted cells (Fig. S5, a and b). In both cases, P-cadherin accumulation at cell–cell contacts was not affected (Fig. S5, e and f). As a control, we used C2C12 Pcad Luciferase shRNA cells, the migration behavior of which was indistinguishable from that of the parental C2C12 Pcad cells (Fig. S5, c and d). We found that Cdc42 was required for P-cadherin–induced CCM. Cdc42 or β-PIX depletion did not affect migration velocity but did impair the P-cadherin–dependent increase in migration persistence (Fig. 6 c), as did Cdc42 specific inhibition with the chemical inhibitor ML-141 (Fig. S5 c). β-PIX depletion in E- or R-cadherin–expressing cells did not decrease their migration velocity or persistence (Fig. 6 c). Moreover, expression of shRNA-resistant β-PIXWT, but not of β-PIXGD, in C2C12 Pcad β-PIX shRNA cells significantly rescued the decrease in migration persistence (Fig. S5 g). These data show the specific role of β-PIX in P-cadherin–expressing cells.
We also found that Cdc42 and β-PIX are required for P-cadherin–induced cell polarization (Fig. 6 d and Fig. S5 h; compare with Fig. 1 g). Tracking the cells in the first three rows (Fig. 6 e, and Fig. S5 I, and Video 7) and PIV analysis of the entire cell layer (Fig. 6 f and Fig. S5 j) showed that Cdc42 and β-PIX are required for P-cadherin–induced polarized migration. Finally, we demonstrated that Cdc42 and β-PIX are required for P-cadherin–induced membrane protrusion (Fig. 6 g), FA remodeling and orientation in the direction of the multicellular layer migration (Fig. 6, h–j; compare with Fig. 2, d–f), and FA dynamics (Fig. 6 k and Video 8). These results show that P-cadherin, but not E- or R-cadherin, activates Cdc42 in a β-PIX–dependent manner and that β-PIX and Cdc42 are required for P-cadherin–induced CCM.
β-PIX and Cdc42 are required for P-cadherin–induced mechanical force generation
We next investigated whether Cdc42 and β-PIX contribute to P-cadherin–induced intercellular stresses and traction-force generation. Inhibition of Cdc42 (by knockdown) or of β-PIX completely prevented P-cadherin–dependent increases of intercellular stresses (Fig. 7 a and Video 9), stress anisotropy (compare Fig. 7 b with Fig. 4 d), and plithotaxis (Fig. 7 c).
Moreover, Cdc42 inhibition prevented P-cadherin–dependent increase of the traction-force Tx/Ty ratio (Fig. 7 d and Video 10). Analysis of the traction-force orientation from 0 to 40 µm showed that Cdc42 knockdown impaired P-cadherin–induced traction-force reorientation toward the direction of migration (Fig. 7 e). Altogether, these data demonstrate that β-PIX and Cdc42 are required downstream of P-cadherin to increase monolayer stress and traction-force strength and anisotropy.
β-PIX is specifically recruited at P-cadherin–mediated cell–cell junctions (CCJs) during CCM
β-PIX could associate with P-cadherin and also with N-, E-, and R-cadherin (Fig. 8 a), but not with α-tubulin or Hsp90, two abundantly expressed proteins (Fig. S5 l). However, detailed analysis of β-PIX colocalization with these cadherins revealed that only P-cadherin recruited β-PIX at CCJs (Fig. 8, b–d). β-PIX recruitment at P-cadherin–mediated CCJs occurred only in collectively migrating cells and not in confluent nonmigrating cells and required P-cadherin homophilic interaction (Fig. 8 b).
These results show that although β-PIX can associate with P-, N-, E-, and R-cadherin, it is specifically recruited by P-cadherin at CCJs only during CCM.
P-cadherin is expressed in invasive carcinoma and sarcoma and is associated with poor prognosis (Paredes et al., 2012; Thuault et al., 2013). To analyze P-cadherin’s role in cell migration, we used a validated 2D system to investigate cell migration in response to the sudden removal of boundaries (Poujade et al., 2007; Trepat et al., 2009; Petitjean et al., 2010; Tambe et al., 2011; Ng et al., 2012). This in vitro system mimics the collective cell movement of tumor cells occurring as 2D monolayers migrating along tissue clefts (Alexander et al., 2013). It allows investigating questions concerning the complex process of CCM by combining mechanical force measurements and molecular imaging. C2C12 myoblasts are of mesenchymal origin, express only N- and M-cadherins, and form and maintain cell–cell contacts. However, they do not endogenously exhibit CCM as do MCF10A or MDCK epithelial cells. In contrast, upon P-cadherin expression, C2C12 cells adopt a very efficient CCM phenotype with features characteristic of a collective migration model. We show that P-cadherin expression is associated with an increase in cell velocity, persistence, directionality, and polarization. All the cells in a layer expressing P-cadherin exhibit a similar behavior and migrate in a coordinated, directional fashion in a cell–cell interaction–dependent manner. CCM induction in this mesenchymal cell model is specific to P-cadherin expression and is not observed upon expression of E- or R-cadherin. Moreover, N- and M-cadherin were similarly downregulated upon expression of P-, E-, or R-cadherin. This indicates that P-cadherin–induced CCM was not caused by the downregulation of these cadherins, thus further supporting a P-cadherin–specific role in CCM. A previous study demonstrated that P-cadherin knockdown in epithelial MCF10A cells perturbed directionality and persistence during CCM (Ng et al., 2012). Thus, P-cadherin is involved in CCM not only in mesenchymal cells but also in epithelial cells.
Importantly, we demonstrated that P-cadherin specifically increases intercellular forces, both intercellular stress and traction forces. Interestingly, P-cadherin expression was recently shown to be predictive of the level of intercellular tension in epithelial cells (Bazellières et al., 2015). Our study not only confirms this observation in mesenchymal cells by comparing P-, E-, and R-cadherin; it also demonstrates that P-cadherin specifically increases the anisotropy of intercellular stresses across CCJs and the alignment between cell velocities and the maximal principal stress direction. This mode of local cell guidance, called plithotaxis, enables the efficient translocation of the entire cell layer, because cells are aligned and migrate along the direction of the transmitted stress (Tambe et al., 2011). Although described mostly in epithelial cells and tumor cells (Friedl et al., 1995; Friedl and Gilmour, 2009), mesenchymal cells also exhibit CCM (Arboleda-Estudillo et al., 2010; Theveneau and Mayor, 2011). Nevertheless, it was unknown whether and how cadherins expressed in mesenchymal cells could have a mechanical role and how they could be involved in force transmission during CCM. We demonstrate here that P-cadherin specifically induces CCM and polarization through an increase in the strength and anisotropy of mechanical forces. The advancement of the P-cadherin–expressing cell sheet was achieved not in a cell proliferation–dependent process but through the development of traction forces that counterbalance intercellular forces (Maruthamuthu et al., 2011) and drive the movement of the cell layer. Our data showing that P-cadherin increases polarization and intercellular stress nicely confirm the predictive theory of soft active matter on force–velocity relationships in 1D and 2D living systems (Marchetti et al., 2013). This theory proposes that high polarization and high viscosity or stress would lead to rapid and cohesive expansion under high intercellular tension (fast-strong phenotype).
P-cadherin expression not only polarizes mechanical forces but also extensively remodels cells and polarizes them toward the migration direction. At the front, a large and polarized protrusion is generated; inside the multicellular layer, cells display a polarized organization and develop polarized cryptic lamellipodia, which help maintain a coordinated and efficient migration, as recently reported (Das et al., 2015b). P-cadherin–dependent induction of CCM in C2C12 cells is characterized by the formation or development of a multicellular leading row, as reported for other cell types (Khalil and Friedl, 2010). This is in contrast to the pluricellular migration fingers preceded by leader cells in MDCK cell layers (Poujade et al., 2007; Reffay et al., 2014). Interestingly, migration fingers are associated with the activity of RhoA (Reffay et al., 2014), a GTPase not activated in P-cadherin–mediated CCM of C2C12 cells (Fig. 5 f), suggesting that distinct molecular pathways control these two types of collective cell guidance.
In contrast, our data show that Cdc42 is specifically activated by P-cadherin, but not by E- or R-cadherin, during CCM and is required for P-cadherin–mediated polarized cell organization and CCM. Cdc42 activation during P-cadherin–mediated CCM is logical because (a) polarization of cells, trajectories, membrane protrusions, and FA is the obvious P-cadherin–mediated downstream effect, and (b) Cdc42 was previously shown to control polarity during the collective migration of fibroblasts and astrocytes (Cau and Hall, 2005; Osmani et al., 2006). The key finding is that for the first time we demonstrate a Cdc42 role in mechanical force control in general and more specifically in cadherin-dependent force generation. We show that Cdc42 controls both plithotaxis and traction-force polarization and generation to enable the efficient P-cadherin–mediated collective displacement of cells. Our identification of a P-cadherin–mediated/Cdc42-mediated polarity pathway as the major regulator of mechanical-force generation provides insight into the role of cell–cell contacts in directing cell migration. C-cadherin engagement (only when stress is applied) allows Xenopus laevis mesodermal cells to polarize and extend protrusions in the direction of migration (Weber et al., 2012). We confirmed this process here upon P-cadherin expression in C2C12 cells that generates a large and polarized protrusion at the front of the first row of migrating cells and cryptic lamellipodia at the front of migrating cells across the layer. Interestingly, substrate micropatterning was used to demonstrate that traction forces increase with the cell spreading area (Reinhart-King et al., 2003; Tan et al., 2003; Stricker et al., 2011). Moreover, FA polarization in the migration direction may enable force-vector orientation, resulting in an increased Tx/Ty ratio, thus making FA orientation an interesting predictive parameter of traction force across the entire cell. The generation of small FAs, as we observed upon P-cadherin expression, can also participate in increasing traction forces at the leading edge of migrating cells (Beningo et al., 2001). These morphological modifications (i.e., membrane protrusion and small FA formation) were lost in P-cadherin–expressing cells in which Cdc42 was inhibited. These modifications are characteristic of the activation of Rac1, a small G protein downstream of Cdc42 that we found to be activated upon P-cadherin expression.
Proteomic analysis of the molecules that are immunoprecipitated together with P-cadherin revealed the presence of the Cdc42 GEF β-PIX. It was previously reported that β-PIX directs CCM of anterior visceral endoderm cells in early mouse embryos (Omelchenko et al., 2014). Here, we provide data showing that β-PIX is crucial for P-cadherin–mediated plithotaxis, traction force orientation in the direction of migration, and their increase and thus CCM. Although β-PIX can associate with all tested cadherins (P-, E-, R-, and N-cadherin), we show that β-PIX is specifically required for P-cadherin–mediated CCM. β-PIX is activated and recruited at CCJ exclusively by P-cadherin, but not by N-, E-, or R-cadherin, and only during CCM. Future studies should determine whether the higher intercellular tension generated by P-cadherin during monolayer extension, identified in this study by comparing P-, E-, and R-cadherin (Fig. 4), and also in Bazellières et al. (2015) by comparing P- and E-cadherin, could be responsible for β-PIX recruitment to P-cadherin–mediated CCJs. Indeed, tension generated at cadherin adhesion sites is emerging as an important process in protein recruitment at CCJs (Buckley et al., 2014; Yao et al., 2014). Our data also suggest that Cdc42 is activated at the cell front, where P-cadherin is not engaged in CCJs. How β-PIX is activated there and whether an external stimulus is involved, as described during cell migration in fibrillar collagen environments (Kutys and Yamada, 2014), remain to be determined.
In conclusion, we demonstrated that P-cadherin, a protein upregulated in carcinomas and sarcomas, promotes CCM through an increase in the strength and anisotropy of physical forces (Fig. 9, a and b). Moreover, we identified Cdc42, activated by the GEF β-PIX, as a major regulator of intercellular stresses and traction-force polarization and generation in the induction of P-cadherin–dependent CCM. Our study brings important clues about a biological mechanism that links mechanical forces to the resulting cell movement.
Materials and methods
C2C12 mouse myoblasts expressing either the LZRS empty vector (from K. Johnson, University of Nebraska Medical Center, Omaha, NE; C2C12 LZRS), LZRS-MS-neo-hPcad plasmid (from K. Johnson; C2C12 Pcad), LZRS-MS-neo-Ecad plasmid (from A. Reynolds, Vanderbilt University Medical Center, Nashville, TN; C2C12 Ecad), or LZRS-MS-neo-hRcad (the plasmid pLZRS-Ms-Neo-R-cadherin was generated by cloning the mouse R-cadherin cDNA from K. Johnson between AfeI and SfiI sites in pLZRS-Ms-Neo; C2C12 Rcad) were generated as well as C2C12 Pcad, C2C12 Ecad, and C2C12 Rcad cell lines that stably express β-PIX shRNA using the retroviral vector pSIREN-RetroQ. The pSIREN-RetroQ vector, which targets the firefly luciferase (Luci shRNA), was used as a control. Cell lines were generated by infection with recombinant retroviruses produced by Phoenix cells transfected with the corresponding vectors. Infection was performed on exponentially growing C2C12 myoblasts (5 × 105 cells per 60-mm dish) by using 5 ml viral supernatant. Stably transfected cells were selected with 1 mg/ml G418, and different clones were isolated by limited dilution. Cdc42 knockdown was performed by transient infection of Cdc42 shRNA. Cells were analyzed 48–72 h after infection.
shRNA constructs were generated using the retroviral vector pSIREN-RetroQ according to the manufacturer’s protocol (BD Biosciences). To suppress endogenous Cdc42 expression, the annealed double-strand oligonucleotides 5′-GATCCGATTCCCATCGGAATATGTATTCAAGAGATACATATTCCGATGGGAATCTTTTTTACGCGTG-3′ (forward) and 5′-AATTCACGCGTAAAAAAGATTCCCATCGGAATATGTATCTCTTGAATACATATTCCGATGGGAATCG-3′ (reverse; for Cdc42 shRNA1) and 5′-GATCCGCTCACCACTGTCCAAAGACTTCAAGAGAGTCTTTGGACAGTGGTGAGCTTTTTTACGCGTG-3′ (forward) and 5′-AATTCACGCGTAAAAAAGCTCACCACTGTCCAAAGACTCTCTTGAAGTCTTTGGACAGTGGTGAGCG-3′ (reverse; for Cdc42 shRNA2) were inserted into the RNAi-Ready pSIREN-RetroQ vector (Clontech). Bold letters correspond to positions 246–263 or 469–486 of the mouse Cdc42 cDNA sequence (NCBI Reference Sequence accession no. NM_009861.3). To suppress endogenous β-PIX expression, the annealed double-strand oligonucleotides were used: 5′-GATCCGAGGAGTTCGCTGTGCGCAATTCAAGAGATTGCGCACAGCGAACTCCTCTTTTTTACGCGTG-3′ (forward) and 5′-AATTCACGCGTAAAAAAGAGGAGTTCGCTGTGCGCAATCTCTTGAATTGCGCACAGCGAACTCCTCG-3′ (reverse) for β-PIX shRNA1 and 5′-GATCCGGCAAAGACCATGTTCGCCATTCAAGAGATGGCGAACATGGTCTTTGCCTTTTTTACGCGTG-3′ (forward) and 5′-AATTCACGCGTAAAAAAGGCAAAGACCATGTTCGCCATCTCTTGAATGGCGAACATGGTCTTTGCCG-3′ (reverse) for β-PIX shRNA2. Bold letters correspond to position 1,961–1,978 or 3,867–3,884 of the mouse β-PIX (Arhgef7) cDNA sequence (NCBI Reference Sequence accession no. NM_017402.4). The siRNA constructs Luciferase shRNA was made by inserting the oligonucleotide 5′-GATCCGTGCGTTGCTAGTACCAACTTCAAGAGAGTTGGTACTAGCAACGCACTTTTTTGCTAGCGAATTC-3′. Bold letters correspond to oligonucleotide 1,310–1,328 of the Photinus pyralis (firefly) luciferase sequence (GenBank accession no. M15077.1).
For rescue experiments, the retroviral vector pMSCV-Hygro-GFP-β-PIXc-“shRNAresist” was generated as follows. Site-directed mutagenesis was performed using peGFP-L11–β-PIXc (from mouse origin; NCBI Reference Sequence accession no. NM_017402) as a template to introduce silent mutations in the sequence targeted by the β-PIXc shRNA: 5′-AGGAGTTCGCTGTGCGCAA-3′ in 5′-AGGAATTCGCTGTACGCAA-3′ (underlined letters are the mutated bases). The obtained GFP–β-PIXc shRNA-resistant sequence was then amplified by PCR and subcloned in pMSCV-Hygro (Clontech) between the XhoI and AgeI restriction sites. The retroviral vector pMSCV-Hygro-GFP-GEF-dead-β-PIXc LL-“shRNAresist” was obtained from the pMSCV-Hygro-GFP-β-PIXc-“shRNAresist” template by site-directed mutagenesis to generate the L238S and L239S mutations.
Antibodies and reagents
Mouse antibodies against P-cadherin (Invitrogen), M-cadherin (Charrasse et al., 2004), E-cadherin, pMLC (S19), and dipMLC (S19T18; Cell Signaling); R-cadherin (MRCD5; gift from Takeichi); Cdc42, Rac1, Paxillin, Hsp90, N-cadherin, and β- and p120 catenin (BD Biosciences); GIT1 (sc-9657; Santa Cruz); and β-actin, Pan-cadherin (from rabbit), FLAG (from rabbit), and myosin light chain (MLC) (Sigma-Aldrich) were used. Rabbit polyclonal antibodies against Pericentrin (Eurogentec) and α-tubulin (Sigma-Aldrich) were also used. Rabbit polyclonal antibodies were raised in-laboratory against the extracellular domain (aa 184–519) of human P-cadherin and against the SH3 domain of β-PIX (aa 1–65). F-actin was labeled with Alexa Fluor 405 or 546 phalloidin conjugates (Molecular Probes and Interchim), nuclei with Hoechst 33342 (Sigma-Aldrich), and Golgi using Alexa Fluor 488 lectin conjugates from Helix pomatia (Molecular Probes).
Primary antibodies were detected with Alexa Fluor 488– or 546–conjugated goat anti–mouse or anti–rabbit IgG (Molecular Probes). The Cdc42 inhibitor (ML-141; Tocris) was used at 20 µM. Cells were pretreated for 4 h before insert removal, and fresh medium with the drug was added before analysis.
Cells were plated in Ibidi Culture-Inserts (BioValley; 20,000 cells per chamber) until they reached the desired density level. The insert was removed to allow the cells to migrate into the cell-free areas. The cells were imaged using an Axiovert inverted microscope (Carl Zeiss) equipped with a motorized stage, as well as a heated and CO2-regulated incubator. Phase-contrast images were taken every 5–15 min overnight using a 10×/0.3 NA PH1 DIC1 objective and captured with a CCD MicroMax 1300 Y/HS camera (Roper Scientific) controlled with the MetaMorph 7.0 software.
Measurements of cell velocity, persistence, and directionality
Manual cell tracking and x/y cell position recording (of each cell at each time point) were performed using MetaMorph software. Individual cell mean speed, cell persistence, and cell directionality were calculated and illustrated using Ibidi’s Chemotaxis tool. Angles were plotted using Rose.net software.
Particle velocimetry analysis
The velocity field in monolayers was mapped via PIV analysis (available at http://folk.uio.no/jks/matpiv/index2.html; Poujade et al., 2007). Stacks of images were analyzed using the MatPIV toolbox (http://www.mn.uio.no/math/english/people/aca/jks/matpiv/) for MATLAB (MathWorks). We used an in-laboratory loop protocol in MATLAB to analyze sequential time frames for velocity and angle measurements (see dataset in the online supplemental material). Velocities were plotted in GraphPad Prism and angles in Rose.net software. The time between successive analyzed images was 5 or 10 min. The window size was set to 32 or 64 pixels, with no noticeable differences.
Preparation of polyacrylamide gels
In brief, polyacrylamide gels with a Young’s modulus of 12 kPa were prepared as previously described (Yeung et al., 2005; Kandow et al., 2007; Serra-Picamal et al., 2012) using a solution containing 19% acrylamide, 8% bis-acrylamide, 0.5% ammonium persulfate, 0.05% tetramethylethylenediamine, 0.64% of 200-nm-diameter red fluorescent carboxylate-modified beads, and 2 mg⋅ml−1 NH-acrylate. After polymerization, the gels were incubated overnight with 0.1 mg/ml collagen I.
Polydimethylsiloxane (PDMS) membrane fabrication
PDMS membranes were fabricated according to previously described procedures (Ostuni et al., 2000; Poujade et al., 2007; Serra-Picamal et al., 2012). SU8-50 masters containing rectangles of 300 × 2,500 µm were generated using conventional photolithography. Uncured PDMS was spin-coated onto the masters to a thickness lower than the height of the SU8 feature and cured for 2 h at 60°C. A thick border of PDMS was left at the edges of the membranes for handling purposes. The PDMS was then peeled off from the master and stored in ethanol at 4°C until use.
Cell monolayer patterning and time-lapse microscopy
To pattern the cells on top of the polyacrylamide gels, a PDMS membrane with a rectangular opening was deposited on top of the polyacrylamide gel. We then seeded 20,000 cells within the rectangle defined by the PDMS stencils; the cells were allowed to adhere and proliferate on the gel for a few hours. Before the time-lapse analysis, the PDMS membrane was carefully removed, enabling the cells to migrate toward the available substrate. The time-lapse imaging was performed using an automated inverted microscope (10× lens; Eclipse Ti; Nikon) equipped with thermal, CO2, and humidity control with MetaMorph (Universal Imaging) software. The recording started ∼30 min after removal of the PDMS membrane and lasted for 15 h. Images were obtained every 3 min over a period of 1–15 h.
Traction force microscopy
As cells migrate, they exert traction forces on the substrate. Traction forces are computed from the gel deformations induced by the cells at the interface with the gel substrate. These gel deformations are observed by imaging the displacements of fluorescent beads embedded in the gel. Beads displacements between any experimental time point and a reference image obtained after cell trypsinization are computed using custom-made particle imaging velocimetry software. To reduce systematic biases in subpixel resolution and peak-locking effects, we implemented an iterative process (up to four iterations) based on a continuous window shift technique (Serra-Picamal et al., 2012). Traction vectors Ti,j(t) within the field of interest are obtained from displacement vectors ui,j(t) for all time points t = 1,…, n and locations (i,j) of the M × N gel interface matrix. Traction field vectors Ti,j are computed by superimposing the equilibrium solution for a 3D linear-elastic gel substrate in the Fourier space (Trepat et al., 2009).
Monolayer stress microscopy
To compute maps of mechanical inter- and intracellular tension within the monolayer sheets, we used monolayer stress microscopy as previously described (Tambe et al., 2011). According to Newton’s law, traction forces applied at the cell–gel interface must be balanced by intra- and intercellular forces (Tambe et al., 2011, 2013; Serra-Picamal et al., 2012). In a 2D approximation, monolayer stress is fully captured by a tensor possessing two independent normal components (σxx and σyy) and two identical shear components (σxy and σyx; Tambe et al., 2011). At every pixel of the monolayer, these four components of the stress tensor define two particular directions of the plane, one in which the normal stress is maximum and one in which it is minimum. These directions, which are mutually orthogonal, are called principal stress orientations, and the stress values in each principal orientation are called maximum (σ11) and minimum (σ22) stress components. The mean normal stress is defined as σn = (σ11 + σ22)/2, and the maximum shear stress is defined as σs = (σ11 − σ22)/2. The spatial resolution and force precision of MSM are formally set by those in the original traction maps (Tambe et al., 2013).
The alignment angle between the major axis of the principal stress ellipse and the direction of the cellular motion was measured as described (Serra-Picamal et al., 2012). The maximum principal stress direction was obtained at each point by diagonalization of the stress tensor. These principal directions were compared with the directions of cell displacement obtained by PIV to obtain the angle between principal stress and cellular motion.
Gel electrophoresis and immunoblotting
Protein extracts (20–60 µg) prepared as described elsewhere (Thuault et al., 2013) were resolved on 10% or 15% polyacrylamide gels and transferred to Immobilon-FL membranes (Millipore). The membranes were incubated with indicated antibodies as described previously (Thuault et al., 2013). For protein detection and quantification, the Odyssey Infrared Imaging System (LI-COR Biosciences) was used. Immunoblots were quantified via densitometry using Odyssey version 3.0 and ImageJ (National Institutes of Health).
Cell lysates were obtained as described previously (Thuault et al., 2013). Polyclonal anti–β-PIX or P-cadherin antibodies or IgG (1 µg) were incubated with protein G (Dynabeads; Invitrogen) at RT for 30 min. After washing, 1 mg protein extract was added at RT for 1 h.
Cells were plated in Ibidi’s culture inserts on 12-mm-diameter coverslips until they reached the desired density level. 5–10 h after insert removal, the cells were fixed in 3.2% paraformaldehyde (in PBS) for 15 min, followed by a 2-min permeabilization with 0.1% Triton X-100 (in PBS) and saturation with 2% BSA (in PBS). The cells were incubated with primary and secondary antibodies in PBS containing 2% BSA.
Images were taken using a confocal SP5-SMD (Leica) with 40×/1.3 or 63×/1.4 oil HCX PL APO CS objectives (Leica) and captured with a hybrid detector (Leica HyD) controlled using C software. Colocalization data originating from multichannel fluorescence stacks were collected using a Leica SP5 microscope. For each stack, a single value of the Pearson’s coefficient (ranging from −1 to 1) was measured at the CCJ, imposing a threshold value (calculated based on the algorithms by Costes et al. ) for green and red channels using the colocalization analysis section of Imaris (Bitplane).
Cell surface biotinylation
Cells grown on 60-mm dishes were incubated in cold PBS for 5 min and then with 1 mg/ml sulfosuccinimidyl-2-(biotinamido)ethyl-dithioproprionate (sulfo-NHS-SS-biotin; Pierce Chemical Co.), followed by washing with sulfo-NHS-SS-biotin blocking reagent (50 mM NH4Cl in PBS containing 1 mM MgCl2 and 0.1 mM CaCl2) to quench free sulfo-NHS-SS-biotin, followed by several further washes in PBS. Cells were then scrapped and lysed as described in Thuault et al. (2013) before centrifugation to obtain a detergent-soluble supernatant. At this stage, an aliquot of 10 µl was kept (= total fraction), and the remainder was incubated with streptavidin beads to collect biotinylated proteins. Samples were then analyzed by SDS-PAGE and immunoblotting to identify cadherins using an anti–pan-cadherin antibody. Quantification of at least three independent experiments was performed using the Odyssey system (LI-COR Biosciences).
GTPase activity assays
For global GTPase activity measurements, we induced CCM by injuring a confluent monolayer using a device designed to perform multiple calibrated and reproducible injuries with a spiral scarificator (Turchi et al., 2002). After 6 h of migration, the cells were processed as described to measure Cdc42 and Rac1 activities (Meriane et al., 2002) and RhoA activity (Charrasse et al., 2002). Migrating isolated and confluent cells were also used.
Cdc42 activity measurement
To analyze local Cdc42 activity, we used FRET measurement with the Raïchu-Cdc42 biosensor (1,054×). More details about the probes are available at http://www.fret.lif.kyoto-u.ac.jp/e-phogemon/vector.htm. Cells transfected with the biosensor were plated in Ibidi inserts. After 24 h, the inserts were removed, and after an additional 5 h the cells were imaged using an inverted microscope (TE Eclipse; Nikon) equipped for a 37°C and 5% CO2 humidified atmosphere. The CFP and FRET mages were taken using a Nikon 100× PL APO VC 1.4 oil objective, an excitation filter and dichroic mirror for CFP, and an emission filter wheel containing the CFP emission wavelength filter and another filter for the YFP emission wavelength. Fluorescence was captured with an electron-multiplying CCD camera (C9100-13; Hamamatsu ImagEM) controlled using MetaMorph 7.0 software. A ratio image of FRET/CFP was created to represent FRET efficiency, which correlated with the activity of Cdc42. Pseudocolored ratio images were generated from images from CFP and FRET channels as described previously (Hodgson et al., 2006). Background values were calculated from a mean intensity value within a region of interest outside the cell and subtracted from the entire image. We create a binary mask based on the intensity threshold performed on the FRET image. We applied this mask to CFP and FRET images. Image ratios were calculated by pixel-wise divisions of the masked CFP and masked FRET images. ImageJ Fire LUT was applied to a fixed dynamic range of the 32-bit ratio image.
Cell polarity measurement
5–10 h after Ibidi insert removal, the cells were fixed, and the nuclei, centrosomes, and Golgi apparatus were stained. The cells in the first four rows were analyzed. Measurements of cell polarity toward a global monolayer direction (centrosomes located in front of the nucleus and behind the Golgi apparatus within the quadrant facing the wound) were scored as correctly oriented (Osmani et al., 2006).
FA quantification and orientation
Confocal images of paxillin staining were taken 6 h after removal of the Ibidi insert. The images were binarized to create a mask based on a manually selected threshold level that enabled the visualization of all FAs containing paxillin using an in-laboratory protocol with Cell Profiler software (dataset in supplemental material). The subareas 0–10 µm or 10–40 µm from the leading edge were scored manually using masks, and the FA surface area was measured from binarized images using ImageJ.
FA orientation was measured using ImageJ (dataset in supplemental material), and angle values were plotted using Rose.Net software. FA orientation was determined according to the monolayer migration direction as a reference axis.
Cells were transfected with the pBabe-paxillin-GFP vector (a gift from C. Albiges-Rizo, Université Joseph Fourier, Grenoble, France); after 24 h, the FAs were imaged during cell migration at 37°C using a confocal microscope (SP5-SMD) equipped with thermal, CO2, and humidity control. Images were taken using a 63×/1.4 oil HCX PL APO CS objective (Leica) and captured with a hybrid detector (Leica HyD) controlled using Leica LAS AF software. Images were taken every 5 s at 5 h after Ibidi insert removal and lasted for 10 to 15 min.
Confocal images of paxillin-GFP–expressing cells were binarized and thresholded using ImageJ. The rate of FA area gains and losses was quantified over 15 min, and mean values were normalized to the FA area in addition to the change in mean intensity. Ratio images were generated using the same procedure.
For experiments with n > 30, a Student’s t test was used to assess significant differences between two experimental conditions. For experiments with n < 30, the nonparametric Mann–Whitney U test was used. At least three independent experiments were performed.
Protein separation and identification by LC–MS/MS
C2C12 Pcad cells grown in light and heavy stable isotope labeling with amino acids in cell culture (SILAC) media for 1 wk were used to compare changes in specific P-cadherin interaction partners between control immunoprecipitation using an anti-FLAG antibody (heavy) and immunoprecipitation with a rabbit anti–P-cadherin antibody (light) of cell extracts obtained from confluent cells (IP1) or cells after 6 h of collective migration (IP2) using a device designed to perform multiple calibrated and reproducible injuries with a spiral scarificator (Turchi et al., 2002). 5 mg cell lysates obtained as described in Thuault et al. (2013) were incubated overnight at 4°C with antibody/cross-linked protein A beads, as indicated by the manufacturer (Abcam). After three washes with lysis buffer, beads were recovered by centrifugation and boiled in 15 µl DTT at 95°C for 5 min. Samples from heavy and light conditions were then mixed to obtain a final volume of 30 μl.
Proteins were separated on SDS-PAGE gels (12% polyacrylamide; Mini-Protean TGX Precast Gels; Bio-Rad) and stained with Page Blue Stain (Fermentas). Gel lanes were cut into several gel pieces and destained by three washes in 50% acetonitrile and 50 mM triethylammonium bicarbonate (TEABC). After protein reduction (with 10 mM dithiothreitol in 50 mM TEABC at 56°C for 45 min) and alkylation (55 mM iodoacetamide TEABC at RT for 30 min), proteins were in-gel digested using trypsin (1 µg/band; Gold; Promega). Digested products were dehydrated in a vacuum centrifuge and reduced to 3 µl. The generated peptides were analyzed online by nano-flow HPLC–nanoelectrospray ionization using an LTQ Orbitrap XL mass spectrometer (Thermo Fisher Scientific) coupled to an Ultimate 3000 HPLC (Thermo Fisher Scientific). Sample desalting and preconcentration were performed on-line on a Pepmap precolumn (0.3 × 10 mm; Dionex). A gradient consisting of 0–40% B for 60 min and 80% B for 15 min (A = 0.1% formic acid, 2% acetonitrile in water; B = 0.1% formic acid in acetonitrile) at 300 nL/min was used to elute peptides from the capillary reverse-phase column (0.075 × 150 mm, Acclaim Pepmap 100 C18; Thermo Fisher Scientific). Eluted peptides were electrosprayed online at a voltage of 2.2 kV into an LTQ Orbitrap XL mass spectrometer. A cycle of one full-scan mass spectrum (400–2,000 m/z) at a resolution of 60,000 (at 400 m/z), followed by five data-dependent MS/MS spectra was repeated continuously throughout the nanoLC separation. All MS/MS spectra were recorded using normalized collision energy (35%, activation Q 0.25, and activation time 30 ms) with an isolation window of 3 m/z. Data were acquired using Xcalibur software (version 2.0.7). For all full-scan measurements with the Orbitrap detector, a lock-mass ion from ambient air (m/ 445.120024) was used as an internal calibrator. Raw data analysis was performed using MaxQuant software (version 184.108.40.206). Peak lists from IP1 and IP2 were searched against the UniProt mouse database, 250 frequently observed contaminants, as well as the reversed sequences of all entries. Search parameters were the default parameters when using MaxQuant: the search precursor mass tolerance was set at 20 ppm and the main search (after recalibration) at 7 ppm. Enzyme specificity was set to trypsin, and a maximum of two missed cleavages were allowed. Carbamidomethylation was set as fixed cysteine modification and oxidation was set as variable methionine modification for searches. The false discovery rate was set at 0.01 for peptides and proteins and the minimal peptide length at 7. Quantification was also performed using standard parameters; we considered only proteins with at least two peptides identified/quantified, after elimination of reverse and contaminant entries. The statistical validity of the results and the determination of significant proteins were assessed using significance A, as defined using Perseus (version 220.127.116.11, standard parameters), on the logarithmized ratio (base 2). Identified proteins and peptides are included in the supplementary table. The graphic representation (Fig. S4) was generated using Perseus software.
Online supplemental material
Fig. S1 and Videos 1 and 2 show the migration of the four used cell lines and the quantification of cadherin expression levels. Fig. S2 shows that P-cadherin engagement is required for CCM and membrane protrusion polarization. Fig. S3 and Video 4 show C2C12 LZRS and C2C12 Pcad cell morphology and behavior on acrylamide gels. Videos 3 and 8 illustrate FA organization and dynamics. Fig. S4 shows the proteomic analysis. Videos 5, 6, 9, and 10 show the mechanical forces generated by parental and Cdc42 or β-PIX knockdown C2C12 LZRS and C2C12 Pcad cell lines. Video 7 shows the migration of C2C12 Pcad cells in which Cdc42 or β-PIX was knocked down. Fig. S5 shows Cdc42 and β-PIX shRNA efficiency and their effects on velocity, persistence, cadherin accumulation at CCJ, polarity, directionality, and FA number. Rescue experiments show the effect on Cdc42 activity and persistence of expressing β-PIXWT or β-PIX GD in silenced cells. Three datasets are provided for the MatPIV toolbox used to analyze sequential time frames for velocity and angle measurements, the method for FA detection using Cell Profiler software, and the ImageJ macro to measure FA orientation. Table S1 lists all the proteomic data. Additional data are available in the JCB DataViewer at http://dx.doi.org/10.1083/jcb.201505105.dv.
We thank Virginie Georget, Sylvain de Rossi, and Vicky Dialou from Montpellier Imaging, Halima Amnai and Edith Demettre from Montpellier Proteomic Facilities, Dimitris Liakopoulos for critical reading of the manuscript, and Corinne Albiges-Rizo, Albert Reynolds, and Keith Johnson for plasmids.
This work was supported by the Ligue Nationale contre le Cancer (“Equipe labellisée”) and the Institut National du Cancer. C. Gauthier-Rouvière was supported by Institut National de la Santé et de la Recherche Médicale, C. Plutoni by the Association pour la Recherche contre le Cancer, and M. Le Borgne-Rochet by the Ligue Nationale contre le Cancer, Spanish Ministry of Economy and Competitiveness (grant BFU2012-38146), the Generalitat de Catalunya (grant 2014-SGR-927), and the European Research Council (grant StG-242993 and CoG-616480).
The authors declare no competing financial interests.
collective cell migration
Förster resonance energy transfer
guanine nucleotide exchange factor
particle image velocimetry
stable isotope labeling with amino acids in cell culture