Collective cell migration is involved in development, wound healing and metastasis. In the Drosophila ovary, border cells (BC) form a small cluster that migrates collectively through the egg chamber. To achieve directed motility, the BC cluster coordinates the formation of protrusions in its leader cell and contractility at the rear. Restricting protrusions to leader cells requires the actin and plasma membrane linker Moesin. Herein, we show that the Ste20-like kinase Misshapen phosphorylates Moesin in vitro and in BC. Depletion of Misshapen disrupts protrusion restriction, thereby allowing other cells within the cluster to protrude. In addition, we show that Misshapen is critical to generate contractile forces both at the rear of the cluster and at the base of protrusions. Together, our results indicate that Misshapen is a key regulator of BC migration as it coordinates two independent pathways that restrict protrusion formation to the leader cells and induces contractile forces.
Collective cell migration plays crucial roles during morphogenesis, wound healing, and metastasis1,2,3,4. Border cell (BC) migration in the Drosophila egg chamber has emerged as a powerful model to study the collective migration of small cluster of tightly attached cells. BCs are somatic cells that detach from the follicular epithelium, form a small cluster of 6–10 cells and migrate between the giant nurse cells. Their migration is guided towards the oocyte, as it secretes ligands that activate receptor tyrosine kinases (RTK) on the cluster. These ligands target PVR (the sole PDGF-receptor and VEGF-receptor in Drosophila) and the EGF-receptor, which in turn activate the small GTPase Rac, thereby leading to the formation of actin-based protrusions5. The activation of the Myosin II regulatory light chain by the Rho-kinase Rok induces actomyosin contractility, which generates the traction and propulsive forces required for promoting BC motility6,7.
Single cell migration studies have shown that a well-tuned coordination between protrusion dynamics at the front and contractility at the back is necessary for efficient cell migration8. A similar coordination may also control BC migration, as Myosin II activity is concentrated at the back and at the front of the cluster, while protrusion formation is largely limited to a single front leader cell. This coordination requires communication between the cells of the cluster6,9. Moreover, we previously found that the small GTPase Rab11, which is part of the endosomal recycling machinery, and the actin-binding and membrane-binding protein Moesin are required for this cell–cell communication10. In Rab11 or Moesin loss-of-function conditions, multiple cells of the cluster form protrusions due to deregulated Rac activity. This coordination defect causes stalled migration due to opposing pulling forces. While the Rac activity restricting mechanism requires Rab11 and Moesin activity, the exact molecular pathway that achieves this restriction is unclear. The distribution of active Moesin at the periphery of the cluster suggests that it organizes a supracellular actin structure that unifies the cortices of the BCs. As Moesin increases cortical stiffness11, it is possible that its cortical activation prevents protrusion formation by increasing cortical stiffness throughout the cluster periphery12.
Since Moesin is crucial for the coordination of BC migration, we sought to understand its regulation. Activation of Moesin requires the phosphorylation of a conserved Thr residue within its actin-binding C-terminal ERM Association Domain (CERMAD, Thr556 in Drosophila)13. Here, we identifies Misshapen (Msn), a Ser/Thr kinase, as the direct activator of Moesin in BCs. While Msn was previously shown to be involved in BC migration, its mechanism of action was not defined14. We found that, through Moesin, Msn regulates protrusion restriction and cortical stiffness. Unexpectedly, we demonstrates that Msn is required for normal actomyosin contractility in a Moesin-independent manner. Overall, our findings show that Msn coordinates both protrusion formation and cortical contractility to promote the collective cell migration of BCs.
Msn is a Moesin kinase required for BC migration
We have previously shown that the mechanism that restricts Rac activation and protrusion formation to the leader cell of the BC cluster requires Moesin phosphorylation on Thr55610. To identify the Moesin kinase operating in BCs, we performed a targeted RNAi screen and scored candidates for migration defects (Fig. 1a and Supplementary Fig. 1a). Since most of the known kinases that activate the mammalian orthologs of Moesin (ERM proteins; Ezrin, Radixin, Moesin) belong to the Ste20 family, we used the c306-Gal4 driver to specifically deplete Ste20-like kinases in BCs. Of the 11 kinases tested, Msn and Tao depletion completely blocked BC migration while Pak3 and Hpo depletion partially affected BC migration. Surprisingly, depletion of Slik, the only Moesin kinase presently identified in flies15,16, had no effect on BC migration (Fig. 1a).
To determine if one of these kinases activates Moesin in BCs, we measured the level of total Moesin and phospho-Moesin (pMoe) by immunofluorescence upon the depletion of candidate kinases. We found that only one of the two msn-RNAi constructs (RNAi #1) marginally reduced the total level of Moesin, while the other RNAis had no effect (Supplementary Fig. 1b). However, both RNAis against msn induced a strong reduction of pMoe levels at the cluster periphery (Supplementary Fig. 1b, c). While depletion of Tao resulted in a minor decrease of pMoe staining, depletion of Pak3 and Slik did not significantly affect pMoe levels (Fig. 1c). Overall, this demonstrates that Msn is essential for the normal phosphorylation of Moesin in BCs.
Next, we determined if Msn could directly phosphorylate Moesin. For this, we incubated immunoprecipitated Msn-HA from Drosophila S2 cells with the Moesin CERMAD domain produced in bacteria. While wild-type Msn was found to phosphorylate the CERMAD domain of Moesin, two different kinase-inactive Msn proteins17,18 showed no activity towards Moesin (Fig. 1d and Supplementary Fig. 6), indicating that Msn directly regulates Moesin. More specifically, Msn directly phosphorylates the T556 residue of the CERMAD domain of Moesin, since a CERMAD where the Thr is mutated to an Ala is not phosphorylated by Msn in vitro (Supplementary Figs. 2a and 6).
To determine if the catalytic activity of Msn is required for BC migration, we performed rescue experiments in an Msn-depleted background. Using an RNAi-insensitive form of Msn, we found that expression of wild-type Msn (HA-msn) rescues BC migration, confirming that BC migration defects are due to Msn depletion. Next, we expressed an RNAi-insensitive and catalytically inactive mutant form of Msn (HA-msnD160N). To control that both HA-Msn and HA-MsnD160N are expressed at the same level, we checked their expression by Western Blot (Supplementary Figs. 2c and 7). We found that HA-MsnD160N was unable to rescue the phenotype associated with Msn depletion, demonstrating that the kinase activity of Msn is required for the migration of BCs (Fig. 1e). Using the same strategy, we found that the kinase activity of Msn is necessary for Moesin phosphorylation in vivo (Supplementary Fig. 2b).
We previously found that Moesin phosphorylation is restricted to the periphery of the BC cluster (Fig. 1f)10. To determine if Msn co-localizes with its substrate at this periphery, we used an enhancer-trap line that expresses Msn::YFP under the control of the endogenous msn promoter19. We found that Msn and Moesin co-localized in specific regions of the peripheral cortex of the cluster (Fig. 1f, arrows). Altogether, these data show that Msn phosphorylates Moesin to promote BC migration.
We previously showed that the small GTPase Rab11 is necessary for Moesin phosphorylation at the periphery of the cluster10. In addition to localizing at the cortex of the cluster, Msn is present on cytoplasmic punctae (Fig. 1g, i), suggesting that it is actively transported through vesicular trafficking. To test if Rab11 regulates the localization of Msn, we probed Msn localization in BCs expressing a dominant negative form of Rab11 (Rab11S25N). In wild type BCs, Msn accumulates at the cluster periphery (BC/NC (nurse cell) interface, Fig. 1g–e). Upon expression of Rab11S25N, Msn is redistributed to the BC/BC interface (Fig. 1g–e), and its vesicular distribution is reduced (Fig. 1i). Rab11 interacts with the exocyst subunit Sec15 to form vesicles destined to the plasma membrane20,21,22. Interestingly, we found that Msn co-localizes with both Rab11 and Sec15 on vesicular structures (Supplementary Fig. 3a, b). These results suggest that Rab11 promotes the phosphorylation of Moesin10 by regulating the vesicular transport of Msn to the cluster periphery.
Msn is required for BC protrusion restriction and detachment
To characterize the role of Msn in BC migration, we analyzed time-lapse microscopy recordings of egg chambers incubated at 25 oC. At this temperature, which we used for every subsequent experiment, the depletion of Msn is partial, allowing for the observation of the various processes affected by Msn-depletion. Live imaging of BCs expressing LifeAct::GFP probe, shows that control clusters detach from the follicular epithelium, are motile and usually form a single prominent protrusion in the front cell (Fig. 2a–f). BCs depleted for Msn are able to form distinct clusters, but are less motile overall (Fig. 2a–c and Supplementary Movies 1 and 2).Importantly, they extend several prominent protrusions (Fig. 2d, e and Supplementary Movie 2) but remain attached to the follicle cells (Fig. 2d, f and Supplementary Movie 2). Based on these observations, Msn appears to be involved in the final step of BC detachment from the follicular epithelium and in the restriction of protrusions to the leader cell.
To determine how Msn restricts protrusion formation to the leader cell and promotes BC detachment, we analyzed the impact of its depletion on different parameters associated with protrusion formation and actomyosin contractility. To do this, we first performed detailed protrusion analyses. We generated 3D reconstructions and z-projections of both control and Msn-depleted clusters expressing the actin probe LifeAct::GFP (Fig. 3a and Supplementary Movies 3 and 4). This analysis revealed that control clusters form a single large forward protrusion, while also forming small protrusions in non-leader cells (side protrusions, Fig. 3b). Msn-depletion lead to an increase in the total number of detected protrusions per cluster (Fig. 3b) but also to a change in protrusion morphology. Importantly, in control clusters, leader cell protrusions measure approximately three times the length of side protrusions. Msn-depletion promotes a reduction of this length ratio (Fig. 3c and Supplementary Movies 2–4). Hence, while in control clusters, long protrusions (>9 μm) are restricted to leader cells and point in the direction of the migration, long protrusion are formed by multiple BCs and point in different directions when Msn is depleted (Fig. 3d). These observations demonstrate that Msn restricts long protrusions to the leader cell.
Overall, our results suggest that Msn regulates the previously described Moesin-mediated cell–cell communication mechanism that controls protrusion restriction10. As this mechanism restricts high Rac activity to the front cell, we probed Rac activity in control and Msn-depleted clusters using a specific intra-molecular FRET biosensor9,23. We observed that Rac activity is restricted to leader cell in control clusters, leading to a polarization of the Rac activity in the direction of migration. We found that after Msn depletion, Rac activity is dysregulated and is no longer polarized (Fig. 3e, f).
These results show that Msn regulates cell–cell communication to restrict Rac activation and protrusion formation to the leader cell, possibly through the phosphorylation of Moesin.
Msn regulates cortical stiffness across the BC cluster
As Moesin increases cortical stiffness in its active state11, we wanted to test if Msn depletion could alter cortical stability in BC clusters. Since membrane curvature is a direct hallmark of cortical stiffness and architecture24, we performed a dynamic curvature analysis of migrating clusters (Fig. 4a). To allow visual analysis of curvature overtime, we constructed curvature heatmaps as kymographs (Fig. 4b). These kymographs reveal that the shape of the cortex of control clusters alternates between highly convex and highly concave curvatures (negative/positive/negative, NPN). This curvature NPN pattern indicates the presence of a protrusion. We found that NPN patterns are mostly restricted to the front of control clusters, while rare and transient NPN patterns are observed at their periphery (Fig. 4b, c). After depletion of Msn the number of NPN patterns increases. Furthermore, NPN patterns are more persistent and not restricted to the front of the cluster (Fig. 4b, c). This increase of the number of NPN patterns is consistent with reduced cortical stiffness. Interestingly, analysis of fixed Msn-depleted clusters reveals a decrease of sphericity compared to control clusters (Fig. 4d). As sphericity is another hallmark of stiffness15, these results suggest that maintenance of cortical stiffness at the BC cluster periphery requires Msn.
Next, we investigated if Msn regulates the dynamics of cortical deformation by analyzing strong positive curvatures (>80o) on curvature maps. Automated detection of such curvatures revealed that control clusters have highly dynamic curvature deformation at the front of migration. In contrast, Msn depletion reduces the frequency of positive curvatures (Fig. 4e, f) and increases their lifetime (Fig. 4g), suggesting that Msn controls cortical deformation dynamics. Furthermore, this increased positive curvature lifetime corresponds to the static protrusions observed in time-lapse recordings of Msn-depleted clusters (Fig. 2d and Supplementary Movie 2).
Altogether, these results show that Msn regulates protrusion dynamics, in addition to overall cortical stiffness around the cluster.
Msn regulates the spatial organization of actomyosin
The detachment defect (Fig. 2d, f and Supplementary Movie 2) and the reduced dynamics of cortical deformation induced by Msn depletion (Fig. 4e, g) prompted us to determine if Msn might also regulate actin-mediated contractility. First, we used immunofluorescence to analyze the localization of the active, phosphorylated form of the regulatory light chain of Myosin-II (pMLC2). Previous work showed that pMLC2 is enriched at the rear of the cluster to promote detachment from the epithelium and at the front to promote protrusion contractility6. Our results show that Msn depletion does not alter the amount of pMLC2 present at the front or back of cluster (Fig. 5a, b), but affects the actomyosin organization in specific cortical domains (Fig. 5c–f).
Indeed, analysis of pMLC2 distribution revealed that it accumulates symmetrically at the base of the front protrusion and that this accumulation requires Msn (Fig. 5e, f). Furthermore, Myosin II is known to form transient foci at the cluster periphery (Fig. 5c, black arrows), which are necessary for cluster contraction7,25. We found that these foci are absent in Msn-depleted clusters (Fig. 5d). Finally, Msn-depleted clusters present an asymmetrical pMLC2 distribution along the axis of migration (Fig. 5d, red arrows). This abnormal actomyosin distribution may be at the root of cluster elongation by inefficiently spreading the contraction forces normally required for contractility26.
Interestingly, we found that Msn localizes to cortical actin-rich structures (Supplementary Fig. 2a, b), including at the base and the tip of protrusions where it may regulate Myosin II activity (Supplementary Fig. 2a, c, d). This specific association with protrusions suggests that, in addition to potentially generating cortical stiffness via Moesin activation, Msn could also regulate protrusion retraction. Interestingly, a similar phenotype has been observed for Myosin II-depleted BC clusters7 To test if the dysregulation of Myosin II affects the morphology of protrusions, we quantified the distance from the nuclei to the tip of the protrusion and found an elongation of both front and side protrusions after Msn depletion (Fig. 5g).
Overall, our data demonstrate that Msn is required for the spatial organization of actomyosin and for protrusion contractility.
Msn coordinates contractility across the BC cluster
The detachment defect and the actomyosin disorganization observed after Msn depletion (Fig. 2d, f and Supplementary Movie 2) prompted us to characterize the role of Msn in regulating contractility across the entire cluster. To assess the impact of Myosin-II dysregulation on contractility, we performed a morphodynamic analysis by mapping the extension and retraction dynamics of migrating clusters (Fig. 6a)27. Similar to the curvature analyses, we used color-coded kymographs to represent extensions and retractions (morphodynamic maps, MDMs) (Fig. 6b). These MDMs reveal that the front of control clusters protrude with brief moments of contraction, while retraction events occurs at the back, suggesting that extension and contraction events are coordinated across the cluster (Fig. 6b–e). Interestingly, after Msn depletion, extension, and retraction coordination is impaired. Indeed, Msn-depleted cluster MDMs reveal that at certain time points, the entire periphery of the cluster extend (Fig. 6b, red arrows), indicating that Msn is required to coordinate the cortical movements during BC migration. Quantification of extension and retraction velocities from the entire periphery of the cluster, shows that Msn depletion reduces these velocities as well as their mean variation (Fig. 6b–f), reflecting a global loss of the cluster periphery dynamics.
These observations are consistent with our previous results showing a loss of protrusion restriction after Msn depletion. It also strengthens our data showing that Msn controls cortical deformation. Overall, our findings suggest that Msn coordinates contractility in BC clusters through the spatial regulation of Myosin-II activity.
Msn regulates protrusion restriction and BC contractility independently
To determine if Msn regulates both protrusion restriction and actomyosin contractility through Moesin activation, we expressed a constitutively active form of Moesin (MoeT556D) in Msn-depleted BCs. We found that the expression of MoeT556D rescued the Msn depletion-induced protrusion restriction defects, as shown by z-projections (Fig. 7a) and by the analysis of protrusions number and distribution (Fig. 7b, Supplementary Fig. 3a, b and Supplementary Movie 5). Furthermore, curvature analysis revealed that MoeT556D expression inhibits the ectopic deformations induced by Msn depletion (Supplementary Fig. 3c–e). These findings demonstrates that Msn regulates protrusion restriction and cortical stiffness through the activation of Moesin.
However, MoeT556D expression rescued neither cluster detachment nor protrusion size, which are associated with contractility (Fig. 7a, c–e and Supplementary Movie 5). To verify that excessive activation of Moesin did not induce contractility defects per se, we expressed MoeT556D in a control background and observed no detachment defects (Supplementary Fig. 5c). To confirm that Moesin activation is not necessary for the Msn-dependent cluster contractility, we analyzed MDMs of clusters expressing MoeT556D. These MDMs show that activity of Moesin is not sufficient to restore the contractility defect caused by Msn depletion (Fig. 7f–h). In addition, MoeT556D is unable to restore BC migration due to the strong Msn depletion-induced detachment defect (Fig. 7i–k). From these experiments, we concluded that active Moesin is sufficient to restrict protrusion formation and cortical deformation but is unable to promote contractility, suggesting that Msn acts through another pathway to regulate contractility.
As actomyosin contractility can be induced by the phosphorylation of MLC2 mediated by Rok (the Rock ortholog in Drosophila), we tested if increasing Myosin II activity is sufficient to restore contractility in Msn-depleted BCs. Thus, we expressed the catalytic domain of Rok (RokCAT) and found that it rescues the Msn depletion-induced global contractility defect (detachment, protrusion length, the contraction, and extension velocities defects) (Fig. 7a, c–h and Supplementary Movie 6). Interestingly, RokCAT expression does not restore protrusion restriction (Fig. 7a, b and Supplementary Fig. 3a, b and Supplementary Movie 6), suggesting that this mechanism depends on Moesin activation but not on actomyosin contractility. To verify that excessive activation of Rok does not induce protrusion restriction defects per se, we expressed RokCAT in a control background and observed no defaults (Supplementary Fig. 5c, d).
Curvature analysis revealed that expression of RokCAT in Msn-depleted clusters restores the dynamic deformation of the cortex at the front and enhances dynamic deformations at the side of the clusters (Supplementary Fig. 4d, e). This suggests that Myosin II-mediated contractility controls the dynamics of cortex deformation, but is unable to restrict protrusion formation. This complementary analysis demonstrates that Msn controls protrusion restriction through Moesin activation and contractility through a Myosin II-dependent pathway (Fig. 8a, b).
The Ste20-like kinase MSn has been previously involved in different morphogenic events in Drosophila, including cell migration. Early work described the involvement of Msn in photoreceptor cell morphology and cytoskeletal dynamics28. Later, Msn was found to be involved in axon targeting and growth cone motility29, nuclear migration in the eye30, dorsal closure17,29, elongation of the egg chamber through the migration of epithelial follicle cells19,31, and in BC migration14.
Here, we found that Msn acts on Moesin to restrict protrusion formation and regulates Myosin II to promote contractility during BC migration. Previous work using msn loss-of-function mutants, found a complete block of BC migration attributed to an abnormal E-Cadherin distribution14. By using the UAS-Gal4 system to deplete Msn, we were able to analyze the function of Msn in BCs in greater details. Indeed, this methodology allows for selective RNAi expression in the BC cluster. It also allows for depletion modulation by incubating flies at various temperature. Similarly to the effect of msn mutants, severe depletion of Msn (29°C) incurs a complete block of BC migration14, while lesser depletions (25°C) allowed for partial migration. On note, in the latter condition, we observed abnormally distributed E-Cadherin, but to the difference of msn mutant14, we do not observe a reduction of the number of BCs per cluster. Nevertheless, our data suggests that it is not the prime cause of impaired migration, since distinct aspects of msn RNAi expression-induced migration defects are rescued via MoesinT556D or RokCat expression. Hence, while our findings do not exclude a downstream Msn activity on E-Cadherin, they strongly suggest that it is not its primary target.
Previous work in mammals showed that different kinases are able to phosphorylate ERM proteins32. In Drosophila however, Slik was so far the sole kinase known to act on Moe. Phosphorylation of Moesin by Slik occurs in the tip tracheal cells33 and Slik was shown to be necessary for wing disc morphogenesis15,16 by regulating epithelial integrity in vivo. Moreover, Slik-dependent phosphorylation of Moesin is necessary to regulate cortical stiffness during cytokinesis11,34. More recently, Slik has been described to act on Moesin to maintain polarity and cortical stiffness during asymmetric cell division35.
Surprisingly, we found that Slik depletion has no impact on the phosphorylation of Moesin in BCs. This prompted us to perform a candidate RNAi screen to identify the Moesin kinase acting in BCs. As different kinases of the Ste20-like family act on ERMs in mammals32, we screened among these for abnormal BC migration. Among the few kinases we identified as involved in BC migration, we found that Msn is required for Moesin phosphorylation in vivo and can phosphorylate Moesin in vitro.
Other Ste20-like kinases seem to play important functions during BC migration, including Pak3, Hpo, and Tao. While both the Hippo pathway36,37,38 and Pak339 have already been shown to be involved in BC migration, the function of Tao is unknown.
Our previous work showed that Moesin is a key regulator of BC migration through its role in a cell–cell communication mechanism restricting protrusion formation to the leader cell10. As expected for a Moesin kinase, clusters depleted for Msn display large ectopic protrusions in follower cells due to the loss of cell–cell communication.
The mechanism by which Moesin and Msn inhibit the formation of large protrusions in follower cells is still unclear. Moesin regulates cortical stiffness, in accordance with a function of Msn in Moesin activation. When we analyzed the effect of Msn depletion, we found a reduction of sphericity and curvature, two morphological parameters associated with stiffness24. Prior work in MDCK cells showed that actin supracellular structures lead to cortical stiffness and inhibition of protrusion formation40. Hence, we are hypothesizing that Msn and Moesin inhibit protrusion formation by ensuring a continuous cortical stiffness across the different cells of the cluster.
Our previous work on Rab11 showed that it is involved both in the regulation of the polarization of the activity of guidance RTKs PVR and EGFR during BC migration and in the phosphorylation of Moesin10,41. The effect on Moesin seemed epistatic, as the expression of an active form of Moesin was able to rescue the effect of dominant negative Rab1110.
Interestingly, after Rab11-dominant negative expression, Msn relocalized from the cluster periphery to cellular interface inside the cluster. Surprisingly, despite being present on these interface, Moesin is not phosphorylated following Rab11-dominant negative expression10. Moesin exists in a closed and an open conformation. Previous work demonstrated that ERM proteins bind to Phosphatidylinositol 4,5-bisphosphate (Ptd(4,5)P2). Upon binding, ERMs partially change conformation and become accessible to phosphorylation by the kinase LOK, one of the Slik orthologs in mammals. Lok acts as a wedge to pry open and subsequently phosphorylate ERM proteins42. Msn lacks this wedge domain found in LOK and thus, may require a co-factor to efficiently phosphorylate Moesin at cellular interface inside the cluster. Alternatively, Ptd(4,5)P2 might be enriched at the periphery of the cluster.
In addition to its direct action on Moesin, Msn is also required to induce actomyosin contractility. Msn depletion induces detachment defects, elongated protrusions and a general lack of apparent contractility. While expression of active Moesin in Msn-depleted clusters rescues parameters associated with protrusion restriction and cortical stiffness, it does not influence those associated with contractility. On the other hand, expression of the Rok catalytic domain in Msn-depleted clusters rescues overall contractility, while not impacting protrusion restriction to leader cells.
Future work is required to determine the mechanism by which Msn affects contractility, in particular to identify its target in this pathway. While we found that Msn is involved in the spatial organization of Myosin II activity, it seems unlikely that it is involved in its direct activation, as Msn depletion does not affect total pSqh levels. Observation made by others suggest that a precise distribution of the actomyosin cytoskeleton at the multicellular level is important for its processivity and efficient cell retraction26. Our observation that Msn depletion leads to a disorganized actomyosin cytoskeleton at both the base of protrusions and the periphery of the cluster suggests that Msn is necessary to ensure Myosin II processivity and global cell contractility.
To migrate, cells need to form extensions at the front and to contract at the back. These two events are coordinated both in individually migrating cells and in collectively migrating cell clusters. Few molecular mechanisms are known that coordinate these two processes, in particular during collective migration. Recent work demonstrated that a mechanism similar to planar cell polarity acts simultaneously to control the formation of protrusions and promote contractility in the follicle epithelium surrounding the Drosophila egg chamber43,44. However, during the migration of follicular epithelium cells there is no hierarchy between the different migratory cells. Rather, in BC clusters the important difference rests in the cell behaviors of leader cells producing dynamic protrusions and follower cells contracting their trailing edge. Our work demonstrates that a single kinase is able to control protrusion formation and global contractility simultaneously. We propose that the supracellular actin structure regulated by Msn and Moesin serves to coordinate extension and retraction events. In this process, E-cadherin-bases cell–cell junctions might help to connect the actin structure of individual cells and thereby helping the mechanical transfer of information, in accordance to recent findings by others45.
The relevance of this observation to other collective migration systems, in particular in higher eukaryotes, is still to be determined. Interestingly though, recent studies have identified a function for Msn orthologs in various collective cell migrations. For example in Zebrafish, Msn1 was shown to act on actomyosin contractility during dorsal closure in vivo46. In mammals, the ortholog MAP4K4 regulates the endothelial sprouting and protrusion formation in angiogenesis assays and in vivo neovascularization by regulating the dynamics of focal adhesions through Moesin phosphorylation47. Together with our findings, these studies suggest that Msn might be a central regulator of various types of collective migrations.
To identify Ste20-like kinases involved in BC migration, the UAS-RNAi transgenic lines listed in Supplementary Fig. 1 were driven by c306-Gal4;UAS-LifeAct::GFP at 29 °C for 48 h. At least two independent RNAi lines (from the Vienna Drosophila RNAi Center and/or the Bloomington TRiP Stock Collection) were used for each gene. Other stocks used were msn::YFP/TM6 (DGRC #115454, gift from Sally Horne-Badovinac, University of Chicago19,48), UAS-Rab11S25N (gift from Marcos Gonzalez-Gaitan, University of Geneva49), UAS-RacFRET/TM3 (bl#31431, gift from Denise J. Montell, UCSB), UAS-Sec15::mCherry (gift from Christian Bökel, TU Dresden50). The following stocks were acquired from the Bloomington Stock Collection UAS-MoesinT559D::Myc (bl#8630), UAS-RokCAT (bl#6669), UAS-Lifeact::GFP (bl#35544), UAS-LifeAct::Ruby (bl#35545) and UAS-eGFP (bl#6658). The two msn RNAi lines used were msnjf03219 from the Bloomington TRiP collection (RNAi #1, bl#28791) and msnKK108948 from the Vienna Drosophila RNAi Center (RNAi #2, v101517). As control, we used an RNAi against mCherry (bl#35785). All the crosses with the msn RNAi (except for the Ste20-like kinases screen done at 29 °C) were done at 25 °C and maintained at that temperature until dissection. Transgenic flies overexpressing the RNAi-insensitive variants of msn were generated by Bestgene Inc., by injecting a pUAS-attB plasmid containing a modified HA-msn sequence (see below).
Heat-shock experiments, mRNA extraction, and QPCR analysis
Female were heat-shocked at 37 °C for 1 h and then incubated at 30 °C for 72 h and directly dissected for mRNA extraction using RNeasy Mini kit (Quiagen).
Msn kinase dead mutants and RNAi insensitive mutant
pA-HA-msn vector: Msn was subcloned from pOT2-msn (clone LD34191, gift from Vincent Archambault, IRIC, Montreal) into the pAHW gateway vector generating the pA-HA-msn vector. Those were used for in vitro kinase assays. First, we have created pDNR-msn using the following primers:
We have created the K61R and the D160N using QuickChange mutagenesis on the pDNR-msn plasmid and we have inserted it into the pAHW plasmid as below. To mutagenize the pDNR-msn sequence, we have used the following primers:
For the K51R mutation:
For the D160N mutation:
HA-msn-RNAi insensitive: We have generated the HA-msn-RNAi insensitive (wild type and kinase dead mutants) from the pA-HA-msn plasmid. The RNAi-insensitive mutants contain silent, point mutations in the regions targeted by both RNAi lines (from 2483 to 2945 bp for RNAi #1 and from 2279 to 2428 bp for RNAi #2). We have ordered the insensitive sequences to gBloc, Integrated DNA Technologies (IDT). Those mutated regions, were used to replace the corresponding msn region using standard cloning methods.
UAS-HA-msn-RNAi insensitive: We have sublconed HA-msn (wilt type and kinase dead mutants) from pA-HA-msn plasmid into the pUAS-AttB-Mek plasmids (from Marc Therrien’s laboratory). Those constructs were used to generate UAS-HA-msn-RNAi insensitive flies for rescues experiments.
Ste20 like kinase screen: Ste20-like kinase were depleted as described in the “Drosophila genetics” section of the “Methods”. Females were maintained at 29 °C and fed with yeast for 48 h prior to dissection. Egg chambers were dissected from adult young female in PBS 1X and fixed 20 min in 4% paraformaldehyde 4% diluted in PBS. Egg chamber were stained and mounted using standard immunofluorescence protocol41. BC migration was quantified at stage 10 of egg chamber development using an inverted microscope (Leica DM IRB). The Migration Index (M.I.) was calculated with the following formula:
n(100%) corresponds to the number of egg chambers where the cluster reached the oocyte, n(75%), the number of chambers where the cluster migrated to 75% of the final distance, etc. We also considered in our quantification, clusters that split and where three or more cells did not migrate whereas the rest of the cluster reached to the oocyte. We gave a 0.5 coefficient to these clusters in our migration index, since approximately half the cells only completed migration. A M.I. of 1 means 100% of the cluster has completed migration, whereas a value of 0 means that none of the clusters in the examined egg chambers migrated. A value of 0.5 could be obtained by various combinations of migration defects, including all the egg chambers displaying 50% migration or half of the chambers displaying a 100% migration and half of the chambers where the clusters did not migrate. The Completion Index (C.I.) corresponds to the number of egg chambers where the migration was completed (n(100%)) divided by the total number of egg chambers (n(total)):
Live Imaging and Rac FRET analysis
Living egg chambers were prepared for real-time imaging using the protocol developed by Denise Montell laboratory9 and imaged on a spinning-disk confocal (Zeiss) equipped with the camera AxioCam 506 Mono from Zeiss and a ×20/0.8 PlanApochromat objective. FRET imaging of live BCs was acquired on an Zeiss LSM880 inverted confocal microscope (Zeiss) equipped with a ×40/1.3 PlanApochromat oil immersion objective. Both CFP and YPF were captured simultaneously with independent PMT detectors. One image every 3 min were acquired. FRET images were generated from the CFP and YFP images using a homemade macro for ImageJ (gift from Damien Ramel, Université Paul Sabatier Toulouse III). Briefly, a Gaussian smooth filter was first applied to both channels. Then, the YFP image was used to create a binary mask with background set to zero. This mask is applied to the original smoothed CFP and YFP to remove the background signal. The final image ratio was generated by dividing the YFP signal by that of CFP with the «divide» function of ImageJ. The FRET ratio was calculated in the entire BC cluster or specifically at the leading edge and at the back of the cluster by measuring the average intensity of FRET and CFP using the Region measurements tool of ImageJ. For quantification, we used five different stacks and compare the means.
Morphodynamics and curvature analysis
Morphodynamics and curvature maps were generated using the open source ADAPT plugin, created and published by David J. Barry et al.27. The analyses were done on a single plane from confocal movies using a spinning-disk confocal (Zeiss) equipped with the camera AxioCam 506 Mono from Zeiss and a ×20/0.8 PlanApochromat objective. One image every 3 min were acquired. Three different planes were recorded. From these, we choose the plane with the best signal to noise ratio to perform the analysis. All velocity values are directly measured by the plugin and plotted in GraphPad Prism. For visual representation, raw map images (in.tif format) were stretched to optimize visualization. To detect membrane deformation events, we used the curvature map from the same ADAPT plugin. We applied a threshold in order to render the images into a binary of two population of curvatures, strong positive (>80°) in black and the rest in white. The “particle analysis” tool from ImageJ was used to automatically assess the number of deformation events at the front and at the side of the cluster. For control conditions, time zero corresponds to the moment when the cluster visibly detached from the epithelium. As Msn-depleted BCs rarely detach, the time zero corresponds to the moment when the cluster is formed and rounded.
Measurements of cluster velocity and mean square displacement
Automated cell tracking clusters were performed by using the “Cell tracker” plugin in ImageJ. Velocities were calculated using Ibidi’s Chemotaxis tool (http://ibidi.com/software/chemotaxis_and_migration_tool/). Mean square displacements were calculated using an homemade MSD plugin of Excel developed by R. Gorelik and A. Gautreau51.
Measurement of cluster sphericity, protrusion distribution, number, and length
3D reconstructions, representations, cluster sphericity, and protrusion length measurements were performed in Imaris (Bitplane) from 3D volume reconstructions of LifeAct::GFP and DAPI, both acquired with the Airyscan detector of a Zeiss LSM880 confocal. Sphericity was measured in the statistical analysis module of Imaris. Protrusion lengths of fixed samples were determined by measuring the distance between the center of the nucleus (DAPI) and the tip of the protrusions (LifeAct::GFP) for each protruding cell. Six measurements were performed at different positions of each protrusions and the mean was plotted in GraphPad PRISM. For protrusion number quantifications on fixed samples, a circle was drawn around the cell body. Any actin extension longer than 4 μm beyond this circle was defined as a protrusion. Extension longer than 9 μm was defined as “main protrusion”. For distribution analysis, each protrusion defined as previously was aligned on a radar map divided into eight different sectors of 45° each with the leading edge set at zero degrees and the trailing edge at 180°. The length and the width of the arrow represent the amount of protrusions in a given direction. Analysis and quantification were done with ImageJ and representations with Excel. For protrusion number quantification on live samples, we quantify the number of protrusions per cluster at each time point of 5 h movies. Any protrusions larger than 4 μm were automatically detected using ADAPT plugin of ImageJ and LifeAct::GFP as a marker. Analysis and quantification were done with ImageJ and representations with GraphPad PRISM.
Quantitative analysis of pMoe and total Moesin intensity
Images from fixed tissues were acquired using an LSM 700 microscope (Zeiss) equipped with a ×63/1.4 Plan Apochromat DIC oil immersion objective. Quantifications of pMoe or total Moesin fluorescence intensities were performed at the periphery of clusters as described in ref. 41. Briefly, the mean of three z-stacks were used for quantification. To normalize for varying staining between egg chambers, peripheral signals were divided by the intensity measured on nurse cell membranes.
Quantitative analysis of pMLC2 intensity
Images from fixed tissues were acquired using an LSM 700 microscope (Zeiss) equipped with a ×63/1.4 Plan Apochromat DIC oil immersion objective. Quantifications of pMLC2 fluorescence intensities at the back, the front, and the side of the cluster were performed as previously described6.
For more precise analysis of pMLC2 localization and for the line scan analysis, we acquired images from fixed tissues with the Airyscan detector of a Zeiss LSM880 confocal equipped with a ×63/1.4 Plan Apochromat oil immersion objective. Line scans were performed on the Zen Blue software and plotted in GraphPad Prism. Specific line scan were chosen according to the base of the protrusion. The protrusion bases were determined manually by its neck shape (opposite negative curvature shapes). The signal were normalized to the maximal signal of pSqh intensity.
Tissue staining and antibodies
Egg chambers were dissected from adult young female in PBS 1X and incubated for 20 min in 4% paraformaldehyde diluted in PBS. Egg chambers were stained using standard immunofluorescence protocol41. The following antibodies were used at the indicated dilutions: rabbit polyclonal anti-phospho-Ezrin (Thr567)/Radixin (Thr564)/Moesin (Thr558) at 1:100 (Cell Signaling Technology, #3141), rabbit polyclonal anti-phospho-Myosin Light Chain 2 (Ser19) at 1:100 (Cell Signaling Technology, #3671). The chicken polyclonal anti-Moesin was generated for this study (with Immune BioSolutions) and used at a 1:100 dilution. Goat anti-rabbit conjugated to Alexa Fluor 555 (Cell Signaling Technology #4413) and Goat anti-chicken conjugated to Alexa Fluor 555 (Invitrogen #A21437) were used as secondary antibodies at 1:250. Alexa Fluor 555-labeled Phalloidin (Invitrogen, #A34055) was used at 1:250 to visualize F-actin and DAPI (Sigma-Aldrich, #D9542) was used to stain DNA at 1:10,000. Egg chambers were mounted in VectaShield (Biolynx, #H-1000). Images were processed using Zen software from Zeiss, using only the “level” functions.
Kinase assay and immunoprecipitation
For immunoprecipitation of HA-Msn (WT, K61R, D160N), S2 cells (Thermo Fisher #R69007)were washed with cold phosphate-buffered saline (PBS) and lysed in RIPA (20 mM Tris pH 8, 137 mM NaCl, 1% NP-40, 0.1% SDS, 0.5% sodium deoxycholate). Cell lysates were incubated with anti-HA antibodies for 2 h at 4 °C, followed by a 1 h incubation at 4 °C with protein A–Sepharose CL-4B beads (GE Healthcare) and washed with lysis buffer (three times) then with the kinase buffer (one time).
Immunoprecipitated HA-Msn (WT, K61R, D160N) were incubated with 1 μg of purified Moesin CERMAD domain in a kinase buffer (25 mM Tris pH 7.4, 10 mM MgCl2, 5 mM β-glycerophosphate) with 5 μCi of [γ-32P] ATP for a total of 10 min at 30 °C. Samples were then separated by SDS–PAGE and radioactive 32P incorporation was revealed using a PhosphorImager. Reactions were analyzed by autoradiography, Western blots, and Coomassie (total protein).
Statistical analyses for two unpaired data sets were performed using unpaired Student’s t-test (Figs. 1h, 2a, 3b, c, f, 4d, f, g, 5b, f, and Fig. 6f). For more than two unpaired data sets we used one-way ANOVA test coupled with Bonferroni correction methods (Figs. 1c, 7d, e, g, h, i, k, Supplementary Figs. 1b, c, 2b, and 4a, b, e). For paired experiments we used two ways ANOVA test (Figs. 2c, e and 6e).
The criterion for all the statistical significance was p < 0.05. In figures, mean values were quoted ± s.e.m. Student’s t-test and one-way ANOVA/Bonferroni tests were performed using GraphPad Prism. Two ways ANOVA tests were performed using SigmaStat software.
All data are available upon reasonable request to the corresponding author.
Friedl, P. & Gilmour, D. Collective cell migration in morphogenesis, regeneration and cancer. Nat. Rev. Mol. Cell Biol. 10, 445–457 (2009).
Mayor, R. & Etienne-Manneville, S. The front and rear of collective cell migration. Nat. Rev. Mol. Cell Biol. 17, 97–109 (2016).
Haeger, A., Wolf, K., Zegers, M. M. & Friedl, P. Collective cell migration: guidance principles and hierarchies. Trends Cell Biol. 25, 556–566 (2015).
Scarpa, E. & Mayor, R. Collective cell migration in development. J. Cell Biol. 212, 143–155 (2016).
Fernandez-Espartero, C. H. et al. GTP exchange factor Vav regulates guided cell migration by coupling guidance receptor signalling to local Rac activation. J. Cell Sci. 126, 2285–2293 (2013).
Majumder, P., Aranjuez, G., Amick, J. & McDonald, J. A. Par-1 controls myosin-II activity through myosin phosphatase to regulate border cell migration. Curr. Biol. 22, 363–372 (2012).
Aranjuez, G., Burtscher, A., Sawant, K., Majumder, P. & McDonald, J. A. Dynamic myosin activation promotes collective morphology and migration by locally balancing oppositional forces from surrounding tissue. Mol. Biol. Cell 27, 1898–1910 (2016).
Ridley, A. J. et al. Cell migration: integrating signals from front to back. Science 302, 1704–1709 (2003).
Wang, X., He, L., Wu, Y. I., Hahn, K. M. & Montell, D. J. Light-mediated activation reveals a key role for Rac in collective guidance of cell movement in vivo. Nat. Cell Biol. 12, 591–597 (2010).
Ramel, D., Wang, X., Laflamme, C., Montell, D. J. & Emery, G. Rab11 regulates cell-cell communication during collective cell movements. Nat. Cell Biol. 15, 317–324 (2013).
Kunda, P., Pelling, A. E., Liu, T. & Baum, B. Moesin controls cortical rigidity, cell rounding, and spindle morphogenesis during mitosis. Curr. Biol. 18, 91–101 (2008).
Coscoy, S. et al. Molecular analysis of microscopic ezrin dynamics by two-photon FRAP. Proc. Natl Acad. Sci. USA 99, 12813–12818 (2002).
Karagiosis, S. A. & Ready, D. F. Moesin contributes an essential structural role in Drosophila photoreceptor morphogenesis. Development 131, 725–732 (2004).
Cobreros-Reguera, L. et al. The Ste20 kinase misshapen is essential for the invasive behaviour of ovarian epithelial cells in Drosophila. EMBO Rep. 11, 943–949 (2010).
Hipfner, D. R. & Cohen, S. M. The Drosophila sterile-20 kinase slik controls cell proliferation and apoptosis during imaginal disc development. PLoS Biol. 1, E35 (2003).
Hipfner, D. R., Keller, N. & Cohen, S. M. Slik Sterile-20 kinase regulates Moesin activity to promote epithelial integrity during tissue growth. Genes Dev. 18, 2243–2248 (2004).
Su, Y. C., Treisman, J. E. & Skolnik, E. Y. The Drosophila Ste20-related kinase misshapen is required for embryonic dorsal closure and acts through a JNK MAPK module on an evolutionarily conserved signaling pathway. Genes Dev. 12, 2371–2380 (1998).
Li, Q. et al. The conserved misshapen-warts-Yorkie pathway acts in enteroblasts to regulate intestinal stem cells in Drosophila. Dev. Cell 31, 291–304 (2014).
Lewellyn, L., Cetera, M. & Horne-Badovinac, S. Misshapen decreases integrin levels to promote epithelial motility and planar polarity in Drosophila. J. Cell Biol. 200, 721–729 (2013).
Zhang, X. M., Ellis, S., Sriratana, A., Mitchell, C. A. & Rowe, T. Sec15 is an effector for the Rab11 GTPase in mammalian cells. J. Biol. Chem. 279, 43027–43034 (2004).
Wu, S., Mehta, S. Q., Pichaud, F., Bellen, H. J. & Quiocho, F. A. Sec15 interacts with Rab11 via a novel domain and affects Rab11 localization in vivo. Nat. Struct. Mol. Biol. 12, 879–885 (2005).
Laflamme, C. et al. Evi5 promotes collective cell migration through its Rab-GAP activity. J. Cell Biol. 198, 57–67 (2012).
Itoh, R. E. et al. Activation of rac and cdc42 video imaged by fluorescent resonance energy transfer-based single-molecule probes in the membrane of living cells. Mol. Cell Biol. 22, 6582–6591 (2002).
Diz-Munoz, A., Fletcher, D. A. & Weiner, O. D. Use the force: membrane tension as an organizer of cell shape and motility. Trends Cell Biol. 23, 47–53 (2013).
Combedazou, A. et al. Myosin II governs collective cell migration behaviour downstream of guidance receptor signalling. J. Cell Sci. 130, 97–103 (2017).
Elliott, H. et al. Myosin II controls cellular branching morphogenesis and migration in three dimensions by minimizing cell-surface curvature. Nat. Cell Biol. 17, 137–147 (2015).
Barry, D. J., Durkin, C. H., Abella, J. V. & Way, M. Open source software for quantification of cell migration, protrusions, and fluorescence intensities. J. Cell Biol. 209, 163–180 (2015).
Treisman, J. E., Ito, N. & Rubin, G. M. misshapen encodes a protein kinase involved in cell shape control in Drosophila. Gene 186, 119–125 (1997).
Su, Y. C., Maurel-Zaffran, C., Treisman, J. E. & Skolnik, E. Y. The Ste20 kinase misshapen regulates both photoreceptor axon targeting and dorsal closure, acting downstream of distinct signals. Mol. Cell Biol. 20, 4736–4744 (2000).
Houalla, T., Hien Vuong, D., Ruan, W., Suter, B. & Rao, Y. The Ste20-like kinase misshapen functions together with Bicaudal-D and dynein in driving nuclear migration in the developing drosophila eye. Mech. Dev. 122, 97–108 (2005).
Horne-Badovinac, S., Hill, J., Gerlach, G. 2nd, Menegas, W. & Bilder, D. A screen for round egg mutants in Drosophila identifies tricornered, furry, and misshapen as regulators of egg chamber elongation. G3 (Bethesda) 2, 371–378 (2012).
Clucas, J. & Valderrama, F. ERM proteins in cancer progression. J. Cell Sci. 127, 267–275 (2014).
Ukken, F. P., Aprill, I., JayaNandanan, N. & Leptin, M. Slik and the receptor tyrosine kinase Breathless mediate localized activation of Moesin in terminal tracheal cells. PLoS One 9, e103323 (2014).
Carreno, S. et al. Moesin and its activating kinase Slik are required for cortical stability and microtubule organization in mitotic cells. J. Cell Biol. 180, 739–746 (2008).
Abeysundara, N., Simmonds, A. J. & Hughes, S. C. Moesin is involved in polarity maintenance and cortical remodeling during asymmetric cell division. Mol. Biol. Cell 29, 419–434 (2018).
Lucas, E. P. et al. The Hippo pathway polarizes the actin cytoskeleton during collective migration of Drosophila border cells. J. Cell Biol. 201, 875–885 (2013).
Chang, Y. C. et al. Rap1 negatively regulates the hippo pathway to polarize directional protrusions in collective cell migration. Cell Rep. 22, 2160–2175 (2018).
Lin, T. H., Yeh, T. H., Wang, T. W. & Yu, J. Y. The Hippo pathway controls border cell migration through distinct mechanisms in outer border cells and polar cells of the Drosophila ovary. Genetics 198, 1087–1099 (2014).
Felix, M., Chayengia, M., Ghosh, R., Sharma, A. & Prasad, M. Pak3 regulates apical-basal polarity in migrating border cells during Drosophila oogenesis. Development 142, 3692–3703 (2015).
Reffay, M. et al. Interplay of RhoA and mechanical forces in collective cell migration driven by leader cells. Nat. Cell Biol. 16, 217–223 (2014).
Assaker, G., Ramel, D., Wculek, S. K., Gonzalez-Gaitan, M. & Emery, G. Spatial restriction of receptor tyrosine kinase activity through a polarized endocytic cycle controls border cell migration. Proc. Natl Acad. Sci. USA 107, 22558–22563 (2010).
Pelaseyed, T. et al. Ezrin activation by LOK phosphorylation involves a PIP2-dependent wedge mechanism. Elife 6, https://doi.org/10.7554/eLife.22759 (2017).
Barlan, K., Cetera, M. & Horne-Badovinac, S. Fat2 and Lar define a basally localized planar signaling system controlling collective cell migration. Dev. Cell 40, 467–477 e465 (2017).
Mao, Q., Lavalou, J. & Lecuit, T. Fat2 and Lar Dance a Pas de Deux during collective cell migration. Dev. Cell 40, 425–426 (2017).
Cai, D. et al. Mechanical feedback through E-cadherin promotes direction sensing during collective cell migration. Cell 157, 1146–1159 (2014).
Koppen, M., Fernandez, B. G., Carvalho, L., Jacinto, A. & Heisenberg, C. P. Coordinated cell-shape changes control epithelial movement in zebrafish and Drosophila. Development 133, 2671–2681 (2006).
Vitorino, P. et al. MAP4K4 regulates integrin-FERM binding to control endothelial cell motility. Nature 519, 425–430 (2015).
Rees, J. S. et al. In vivo analysis of proteomes and interactomes using Parallel Affinity Capture (iPAC) coupled to mass spectrometry. Mol. Cell Proteom. 10, M110 002386 (2011).
Emery, G. et al. Asymmetric Rab 11 endosomes regulate delta recycling and specify cell fate in the Drosophila nervous system. Cell 122, 763–773 (2005).
Michel, M., Raabe, I., Kupinski, A. P., Perez-Palencia, R. & Bokel, C. Local BMP receptor activation at adherens junctions in the Drosophila germline stem cell niche. Nat. Commun. 2, 415 (2011).
Gorelik, R. & Gautreau, A. Quantitative and unbiased analysis of directional persistence in cell migration. Nat. Protoc. 9, 1931–1943 (2014).
We thank the Bloomington Stock Collection and the Vienna Drosophila RNAi Center for fly stocks. We thank N. Iannantuono for critical reading of the manuscript and C. Charbonneau for technical assistance and helpful discussions. This work was supported by grants from the Canadian Institute for Health Research (CIHR) to G.E. (MOP-148560), P.P.R. (MOP-142374), and to S.C. (MOP-133683) and from the Natural Sciences and Engineering Research Council of Canada (G.E., P.P.R., and S.C.). P.P.R. is scholar of the Fonds de la Recherche du Québec–Santé (FRQS). C.P. and C.Z. received fellowships from the FRQS.
The authors declare no competing interests.
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Plutoni, C., Keil, S., Zeledon, C. et al. Misshapen coordinates protrusion restriction and actomyosin contractility during collective cell migration. Nat Commun 10, 3940 (2019). https://doi.org/10.1038/s41467-019-11963-7