Inactivation of the tumor suppressor NF2/merlin underlies neurofibromatosis type 2 (NF2) and some sporadic tumors. Previous studies have established that merlin mediates contact inhibition of proliferation; however, the exact mechanisms remain obscure and multiple pathways have been implicated. We have previously reported that merlin inhibits Ras and Rac activity during contact inhibition, but how merlin regulates Ras activity has remained elusive. Here we demonstrate that merlin can directly interact with both Ras and p120RasGAP (also named RasGAP). While merlin does not increase the catalytic activity of RasGAP, the interactions with Ras and RasGAP may fine-tune Ras signaling. In vivo, loss of RasGAP in Schwann cells, unlike the loss of merlin, failed to promote tumorigenic growth in an orthotopic model. Therefore, modulation of Ras signaling through RasGAP likely contributes to, but is not sufficient to account for, merlin’s tumor suppressor activity. Our study provides new insight into the mechanisms of merlin-dependent Ras regulation and may have additional implications for merlin-dependent regulation of other small GTPases.
Neurofibromatosis type 2 (NF2) is a multiple tumor syndrome that results from loss-of-function mutations in the NF2 gene . The hallmark of NF2 is the development of bilateral vestibular schwannomas, although NF2 patients can develop other schwannomas, meningiomas, ependymomas, and astrocytomas . Biallelic NF2 inactivation also occurs in various sporadic tumors, especially in schwannomas, meningiomas, malignant mesothelioma, and ependymomas .
The NF2 gene encodes a 70-kDa protein called merlin that belongs to the ezrin, radixin, and moesin (ERM) protein family. Merlin and ERM proteins share a similar domain organization, containing an N-terminal FERM domain, a central α-helical domain and a C-terminal tail . However, merlin and ERM proteins appear to act antagonistically on cell proliferation and transformation . Merlin is long recognized as a critical mediator of contact inhibition of proliferation; its exact mechanisms remain unclear, although multiple pathways and mechanisms have been implicated, including regulation of Ras pathway activity .
Sustained activity of the Ras pathways, caused by mutations in Ras or/and its pathway components, promotes cellular transformation and drives tumorigenesis . Loss of merlin functions likewise results in cellular transformation and is associated with sustained activation of the Ras pathways [5, 6]. Conversely, overexpression of merlin can counteract Ras-induced transformation [7, 8], supporting the relevance of merlin-mediated regulation of the Ras pathways, which may occur at multiple levels (see later in “Discussion”). Whilst we have previously shown that merlin interferes with the activation of the small GTPases Ras and Rac , the exact mechanism by which merlin interferes with Ras activation remains largely unknown.
Ras cycles between an inactive GDP-bound and an active GTP-bound state . However, the spontaneous GTP-loading and the intrinsic Ras-GTP hydrolysis are very slow. Rather, the activity of Ras is directly controlled by guanine nucleotide exchange factors (GEFs) that catalyze the exchange of GDP for GTP, and by GTPase activating proteins (GAPs) that stimulate the GTPase activity . Several Ras GAPs exist in mammals, among which p120RasGAP (also named RasGAP, encoded by RASA1) and neurofibromin (encoded by NF1) are prototypic, coexisting in most cell types . In this study, we demonstrate that merlin can bind both Ras and RasGAP. Whereas merlin does not appear to directly regulate the catalytic activity of RasGAP, the interactions with Ras and RasGAP may fine-tune Ras signaling in space and time.
Nf2 −/− mouse Schwann cells exhibit elevated Ras activity and require Ras activity for focus formation
We used immortalized Nf2−/− and the matched Nf2+/+ mouse Schwann cells  (mSCs; Fig. S1a) to analyze Ras activity. Nf2−/− mSCs showed elevated Ras-GTP levels, regardless of cell density (Fig. 1a). This too was the case when the cells were under growth factor-starved condition or further stimulated with PDGF-BB (Fig. 1b), a growth factor contributing to Schwann cell survival and proliferation [11,12,13]. Loss of contact inhibition in Nf2−/− mSCs was evidenced by multiple foci formation in culture (see Fig. 1c). To investigate the contribution of Ras hyperactivity to Nf2 loss-induced focus formation, we constructed a Ras-inhibitory protein (Ras-i) consisting of EGFP, the Ras-binding domain (RBD) and the cysteine-rich domain (CRD) of Raf1, and the GAP-related domain (GRD) of NF1 (Fig. S1b). The RBD-CRD of Raf1 has been shown to be able to block endogenous Ras-GTP signaling , whereas NF1 GRD can potently promote Ras-GTP inactivation. The combination of both, we reasoned, should be capable of counteracting Ras hyperactivity. Indeed, introduction of Ras-i into Nf2−/− mSCs lowered Ras-GTP level as expected (Fig. S1c), reduced focus formation, and improved contact inhibition, although not as efficiently as the reconstitution of merlin (Fig. 1c). Of note, Ras-i was poorly expressed (Fig. 1d) and the expression was rapidly lost when the cells were further expanded (not shown). These data suggest that Ras activity is required for focus formation in Nf2−/− mSCs and suppression of Ras activity is likely an important part of merlin’s tumor suppressor functions.
The FERM domain of merlin can directly interact with Ras
Merlin and ERM proteins are regarded as physiological counter players [5, 15, 16]. We have previously shown that ezrin is actively involved in Ras activation by directly binding to both Ras and Son of Sevenless (SOS), a major Ras GEF [15, 16]. The F1 subdomain of FERM is an ubiquitin/Raf1-RBD-like domain  and the F1–F2 subdomains of ezrin FERM appear to mediate Ras binding [15, 18], suggesting that merlin may do likewise. Indeed, merlin FERM (amino acids [aa] 1–313), but not the α-helical-tail domains (aa 312–595), could pull down purified HRas 1–166 (Fig. 2a, b). In contrast to Ras effectors like Raf proteins , merlin did not show any preference for either GTP- or GDP-loaded Ras, and the binding was apparently very weak. Further truncation revealed that a part of merlin’s F1 subdomain (aa 1–73) was sufficient to bind Ras (Fig. S2). To test whether merlin can bind other Ras isoforms, we performed pulldown with nontagged full-length (FL) KRas4B overexpressed in 293 cells, the most abundant and essential Ras isoform [19, 20]. The results illustrated that merlin FERM can also bind KRas4B and that the isolated α-helical domain or the tail from merlin isoform 1 or 2 (iso1/2, see later) cannot (Fig. 2c). An attempt was made to test merlin’s binding to FL HRas and NRas under the same condition; however, both bound to glutathione sepharose nonspecifically (not shown). Nevertheless, because HRas 1–166 represents the highly conserved G-domain, almost identical in H-, K-, and NRas , the results suggest that merlin is likely able to bind all Ras isoforms directly.
Merlin interacts with Ras in vivo
Given the weak interaction between merlin and Ras, it is difficult to demonstrate the in vivo interaction by co-immunoprecipitation (Co-IP). We therefore employed a proximity biotinylation approach, mediated by the promiscuous biotin ligase BioID2 . Expression of BioID2-KRas4B versus BioID2 alone in 293 cells resulted in clearly increased biotinylation of endogenous merlin (Fig. S3a). Even when biotin concentration was reduced to 0.1 μM (a very low concentration for this type of assay) and BioID2-KRas4B was expressed much lower than endogenous Ras by reducing transfected DNA amounts, increased biotinylation of merlin was still detectable (Figs. 2d and S3b)—suggesting that KRas4B and merlin are at close proximity in vivo. Together with the in vitro binding data, the in vivo interaction between Ras and merlin could be inferred.
Merlin interacts with RasGAP
It has been shown that the GAP activity (toward Ras) from cell extracts was proportional to cell density in culture, suggesting that Ras GAPs may be involved in contact inhibition . We hypothesized that merlin may recruit a RasGAP to negatively regulate Ras, reminiscent of the Ras-activating complex formed by ezrin and SOS [15, 16]. Indeed, RasGAP could be co-immunoprecipitated with endogenous merlin from confluent RT4 cells (a rat schwannoma cell line; Fig. 3a), whereas neurofibromin was poorly extracted with the same lysis buffer and thus not detectable (not shown). Moreover, GST-merlin could efficiently pull down endogenous RasGAP from RT4 cell lysate (Fig. 3b), further supporting the interaction and leading us to focus on RasGAP in this work.
Merlin interacts with RasGAP predominantly at the plasma membrane
To validate merlin:RasGAP interaction and localize it within a cellular context, we attempted to stain the endogenous proteins, but failed to obtain confident signals. The bimolecular fluorescence complementation (BiFC) approach was then employed, using two complimentary fragments (Cerf and Cerl) of a split cerulean fluorophore [23, 24]. Coexpression of Cerf-merlin and Cerl-RasGAP resulted in reconstituted cerulean fluorescence; outperforming the background fluorescence signals from the control combinations (Fig. 3c), supporting the specificity of merlin:RasGAP interaction. The fluorescence was predominant at the plasma membrane, consistent with the reported subcellular localization of active merlin  and where Ras activity regulation should occur.
Both the FERM and the tail domains of merlin interact with RasGAP
Pulldown was performed using GST-merlin fragments, in order to define the domains mediating merlin:RasGAP interaction (Fig. 4a, b). Both the FERM domain and the α-helical-tail domains could pull down RasGAP independently, while the former was more efficient. Progressive truncation located two RasGAP-binding sites, one in the F1 subdomain and the other in the tail. The F3 subdomain, a PTB/PH-like domain , is unlikely involved in the binding, the deletion of which rather enhanced the binding. The first 18 amino acids (aa 1–18), unique to merlin and not present in ERMs, were unable to bind RasGAP on their own. For determining whether merlin can directly bind RasGAP, we used GST-tagged merlin fragments to pull down purified FL RasGAP in vitro (Fig. 4c), therein confirming that both the aa 1–73 fragment and the tail of merlin are able to bind RasGAP directly and independently.
The PH-C2 domains of RasGAP interact with merlin
Reciprocal GST pulldown revealed that, FL RasGAP, as well as the C-terminal fragment (C-term), could efficiently pull down merlin from cell lysates, whereas the N-terminal fragment and the GAP domain could not (Fig. 4d, e)—suggesting that the merlin-binding site is within the PH-C2 region. Of note, RasGAP’s binding to the nonphosphorylatable merlin S518A mutant (active) was much stronger than to the phospho-mimicking S518D mutant (inactive), likely due to a conformational effect . We further confirmed that the isolated PH-C2 fragment was indeed able to bind merlin (Fig. 4f). Moreover, both the PH and the C2 domains could independently bind merlin, suggesting multiple merlin contact sites within the PH-C2 region. Conversely, deletion of the PH-C2 domains from FL RasGAP essentially eliminated merlin binding.
Far-western blotting was performed to corroborate the pulldown results, by incubating purified merlin with GST-RasGAP fragments immobilized on a nitrocellulose membrane (Fig. S4a, b). Consistent with the GST pulldown data, all the PH domain-containing fragments showed strong interaction with merlin, whereas the GAP domain and the partial C2 domain (aa 606–648) did not exhibit any binding. Conversely, deletion of the PH domain greatly reduced merlin binding, whereas partial deletion of the C2 domain had no effect. Viewed together, these results support a direct binding between merlin and RasGAP, mediated primarily by the PH domain. Incidentally, C540Y, a capillary malformation-arteriovenous malformation patient-derived mutation within the PH domain , did not impair merlin binding, suggesting that C540 may not be directly involved in the binding. C540Y more likely impairs protein folding, as the protein yields were greatly reduced (see Ponceau staining of the 158–1047 fragments in Fig. S4b).
We further tested the importance of the PH domain for merlin binding in cotransfected Sc4 cells (a merlin-deficient line) and learned that merlin could be co-immunoprecipitated with either EGFP-RasGAP or EGFP-PH, but not with EGFP-RasGAP ΔPH (Fig. S4c); demonstrating that the PH domain determines the interaction with merlin in vivo.
Merlin isoform 2 also binds RasGAP
Merlin has two major isoforms, with the only difference at the C-terminus  (Fig. 2a). An interaction between the FERM and the tail in merlin iso1 renders a relatively closed conformation , whereas merlin iso2 has a relatively open conformation due to lack of such interaction . Of note, merlin’s α-helical domain may contribute more to the closed conformation [30, 31]; thus, the difference in the conformations between the isoforms is more likely localized. To compare their binding to RasGAP, we overexpressed their S518A mutants (to prevent a potential effect by phosphorylation) in 293 cells and performed GST pulldown—they bound similarly to RasGAP (Fig. S5a). As merlin’s binding to angiomotin and lipids induces conformation opening [26, 32], we also performed pulldown with merlin expressed in E. coli and different binding buffers (Fig. S5b). These results did reveal a more efficient binding to RasGAP by merlin iso2 under two buffer conditions, further supporting the conformational effect.
RasGAP may prefer to bind merlin rather than ERMs
In order to test whether RasGAP also binds ERMs, GST pulldown was performed with the lysate from 293 cells, which express all ERMs and merlin (Fig. S6). While unable to detect any binding to ezrin or moesin, we detected a weak binding to radixin, relatively less efficient than to merlin. Thus, RasGAP appears to prefer to bind merlin over ERMs, in line with the less conserved α-helical-tail domains between merlin and ERMs . Of note, ERMs have a more closed conformation than merlin iso1 , which can be opened by lipid binding and subsequent phosphorylation at T567/564/558, respectively . Given that the conformation states are unknown, further experiments using open conformation constructs with an identical epitope tag will help to draw a clearer conclusion.
NF2 patient-derived mutations impair merlin’s interaction with RasGAP in vivo
The nontruncating mutations identified in NF2 patients are mostly concentrated within the F1 subdomain and the tail of merlin . Two pathogenic mutations in the F1 subdomain—L64P and ΔF96—that most likely impair merlin folding [35, 36] were chosen and tested as to whether they impair the interaction with Ras or RasGAP. For in vitro binding, we chose to purify merlin aa 1–340 (wild type and the mutants), because FL merlin is difficult to purify from E. coli. Both mutants exhibited enhanced binding to Ras (Fig. S7a), whereas they bound to RasGAP similarly to the WT (Fig. S7b), suggesting that these mutation sites may not be directly involved in the binding.
Because the in vitro binding experiments may not reflect the in vivo situation in the context of FL merlin, BIFC experiments were performed to assess the mutations’ effect on merlin:RasGAP interaction (Fig. 5a). Both mutations caused markedly decreased BiFC efficiency, down to the negative control level (Cerf-merlin + Cerl-RasGAP ΔPH-C2). Although we cannot exclude an effect from different expression levels of the constructs (Fig. 5b), the BiFC signals from merlin mutants were predominantly displaced from the plasma membrane. Taken together, these mutations potentially impair a productive merlin:RasGAP interaction in different ways. First, the mutations may cause decreased expression and stability of merlin. Second, merlin mutants might form an ineffective interaction with RasGAP, away from the normal plasma membrane sites of activity.
RasGAP is constitutively active and merlin does not increase the GAP activity in vitro
The PH domain of RasGAP has been reported to bind the GAP domain and inhibit its activity . Merlin can directly bind to Ras and the PH-C2 domains of RasGAP, raising the possibility that merlin may increase RasGAP activity by releasing RasGAP from autoinhibition and/or facilitating Ras and the GAP domain interaction. Therefore the in vitro GAP activity was tested using purified merlin, Ras (preloaded with GTP), and RasGAP (FL and fragments; Figs. 6a, b and S8a). The amount of remaining Ras-GTP after GAP-stimulated hydrolysis, which negatively correlates with GAP activity, was determined by a GST-Raf1 RBD pulldown-based approach. Yet, the presence of merlin did not increase, but rather slightly interfered with GAP activity. Nevertheless, we noticed that RasGAP FL and the C-term were much more active than the isolated GAP domain, indicating that the PH-C2 part contributes to, rather than inhibits, GAP activity—agreeing with an earlier study showing that RasGAP FL is around ten times more active than the GAP domain alone .
In testing whether the PH domain is autoinhibitory, we purified RasGAP aa 158–1047 (for better yield than the FL) and the PH-deleted counterpart, and tested the in vitro GAP activity in the absence and presence of merlin FERM (in case merlin FL may not interact with RasGAP efficiently in vitro, because of a relatively closed conformation; Figs. 6a, c and S8b). As seen with merlin FL, merlin FERM likewise failed to increase the GAP activity of any included RasGAP fragment. Deletion of the PH domain essentially had no effect on the GAP activity, while the isolated GAP domain was less active than the C2-GAP-containing fragments. We therefore conclude that RasGAP is constitutively active, the PH domain does not confer autoinhibition, the C2 domain is required for full GAP activity, and merlin cannot increase the GAP activity in vitro.
Loss of merlin leads to more sustained activation of the downstream effectors in PDGF-BB signaling than loss of RasGAP
Although merlin appears unable to increase RasGAP activity in vitro, our previous data suggest that it can inhibit Ras activity in vivo (see Fig. 1a, b). Meanwhile, RasGAP is a well-known negative regulator of Ras. Indeed, there was elevated and prolonged Ras activation in confluent RasGAP-knockout (Rasa1−/−) mouse embryonic fibroblasts (MEFs)  following PDGF-BB stimulation (Fig. S8c). The phenotypes of merlin or RasGAP deficiency regarding Ras-GTP inactivation and tumorigenicity were further compared by generating Nf2+/+ mSCs derivatives with stable knockdown (KD) of merlin or RasGAP. We first analyzed PDGF-BB-induced Ras signaling in the cultures close to confluence (Fig. 6d). While the Ras-GTP dynamics varied between individual experiments, overall increased Ras-GTP levels in merlin-KD and RasGAP-KD mSCs were consistently observed. This too was the case for elevated expression of PDGFRβ and prolonged activation of Akt, MEK1/2, and Erk1/2 in merlin-KD mSCs—two prominent Ras effector pathways driving tumorigenesis ; Ras protein level also appeared to be elevated in merlin-KD mSCs, when normalized to the total protein level (Fig. S8d). By contrast, PDGFRβ signaling was terminated more rapidly in RasGAP-KD mSCs; although MEK1/2 and Erk1/2 were activated to a higher extent, they were deactivated similarly to the control cells. Thus, both merlin and RasGAP appear to suppress PDGF-BB-induced Ras signaling; however, loss of merlin leads to more sustained activation of the downstream effectors.
Loss of RasGAP is not sufficient to promote tumorigenic growth in an orthotopic model
RasGAP has been previously implicated in contact inhibition  and we observed that Rasa1−/− MEFs formed multiple foci after 2–3 weeks of culture (Fig. S9a), suggesting that RasGAP might be a relevant effector of merlin for contact inhibition.
Next, orthotopic transplantations were conducted to assess the in vivo tumorigenic potential of merlin-KD and RasGAP-KD mSCs. We first generated Nf2+/+ mSCs/Luc that stably express a luciferase to enable bioluminescence imaging, and established the derivatives with stable KD of merlin or RasGAP (Fig. S9b). The cells were transplanted into sciatic nerves of nude mice and tumor growth monitored weekly for a total of 3 weeks. While KD of merlin promoted tumor growth, KD of RasGAP did not (Figs. 7a, b and S9c).
Loss of merlin leads to more profound activation of MEK1/2–Erk1/2 in detachment-induced signaling than loss of RasGAP
Because anchorage-independent growth correlates with tumorigenicity [41, 42], it was prudent to analyze the signaling profiles of merlin-KD and RasGAP-KD cells under a detaching condition. Upon detachment, we expect that the Ras effector pathways to be uncoupled from Ras—this phenomenon is supposed to ensure that cells are unable to survive or proliferate in erroneous sites, a control mechanism lost in transformed cells . For detachment, the cells were treated with PBS/5 mM EDTA, resulting in transient activation of MEK1/2 and more sustained activation of Erk1/2 (Fig. 7c), a response likely contributing to transient protection of the cells from anoikis . Intriguingly, merlin-KD cells showed markedly increased MEK1/2–Erk1/2 activity, while the response of RasGAP-KD cells was comparable to that of control-KD cells. By contrast, detachment caused a rapid decrease of Akt activity in all tested cells. These results indicate that in addition to the merlin:RasGAP interaction upstream of Ras, merlin also targets the Ras effector pathways, particularly the MEK1/2–Erk1/2 branch—in the absence of merlin, the normal step to attenuate this pathway is lost, leading to an overactivation of MEK1/2 and Erk1/2.
Herein, we demonstrate that merlin directly interacts with both Ras and RasGAP. Merlin binds to RasGAP’s PH-C2 domains, whereas the PH and the C2 domains have been previously implicated in contact inhibition: only reconstitution of Rasa−/− MEFs with RasGAP FL—but not with either PH or partial C2 domain-deleted—restored contact inhibition . As PH domain deletion did not affect RasGAP’s catalytic activity in vitro, this rather indicates that loss of binding, e.g., toward merlin, may underlie the inability of PH-deleted RasGAP to restore contact inhibition. Moreover, we identified the C2 domain as an integral part of RasGAP’s catalytic unit, highlighting its importance for GAP activity.
That both merlin and RasGAP are required for proper Ras activity regulation, together with the identified interactions, points to a functional link between merlin and RasGAP. However, merlin appears not to directly regulate RasGAP’s catalytic activity. Given that the SH2-SH3-SH2 domains mediate RasGAP translocation from the cytoplasma to the plasma membrane through binding the consensus phosphotyrosine in various receptor tyrosine kinases (RTKs) , it is plausible that merlin acts in concert with activated RTKs to recruit RasGAP to fine-tune spatial-temporal Ras-GTP inactivation (Fig. 7d). Alternatively, merlin might recruit RasGAP independent of RTKs to suppress RTK-independent Ras activation and signaling. Note that merlin might not simultaneously bind to both Ras and RasGAP—these interactions might be highly transient and how they are regulated in vivo is not addressed in this study. The presence of merlin appears to modulate the signaling ability of Ras; however, the molecular details are still under investigation.
While RasGAP is a well-established negative regulator of Ras, our evidence does not support RasGAP as a prominent tumor suppressor. This is in agreement with genetic data that germline mutations of RASA1 in humans cause the capillary malformation-arteriovenous malformation syndrome and other related vascular anomalies, without clear evidence for tumor predisposition . Emerging evidence suggests that RasGAP is a weak tumor suppressor, whose loss contributes to tumor development in cooperation with additional factors [46,47,48].
An increasing body of literature suggests that merlin potentially suppresses Ras signaling at multiple levels, from RTKs to downstream. Merlin can suppress EGFR signaling during contact inhibition  and merlin loss leads to increased expression of multiple RTKs, including PDGFRβ . Merlin can interfere with the formation of the Ras-activating Grb2/SOS/ezrin complex  and may also interact with Grb2 [50, 51]. Merlin loss leads to increased Ras expression at transcription level, mediated by YAP activation . Downstream of Ras, overexpressed merlin can disrupt the B-Raf/Raf1/MLK3 complex formation by interacting with MLK3 ; merlin loss causes KSR1 overexpression and merlin may interact with KSR1 to interfere with KSR1:Raf1 interaction . Our work suggests that merlin also acts at the Ras level. Notably, a merlin:RasGAP complex upstream of Ras was discovered; in addition, merlin targets Ras effector pathways, particularly the MEK1/2–Erk1/2 branch.
Finally, it is worth noting that merlin is involved in multiple pathways apart from Ras regulation and that its tumor suppressor activity is most likely a collective effect. However, given the extraordinarily high prevalence of Ras pathway activation in human tumors, including Schwann cell-derived tumors, e.g., neurofibromas caused by loss of NF1 , regulation of Ras signaling very likely contributes significantly to merlin’s tumor suppressor activity.
Materials and methods
Sc4 is an immortalized Schwann cell line  established from Nf2Δex2/Δex3 mice by Marco Giovannini laboratory. RT4-D6P2T (RT4; subcloned from an ethylnitrosourea-induced rat schwannoma line ) was from European Collection of Authenticated Cell Cultures. RT4/Tet-NF2 (WT, S518A, or S518D) are derivatives of RT4, harboring doxycycline-inducible NF2 transgenes . Rasa1−/− and Rasa1+/+ MEFs  were from Christian Widmann, originally from Tony Pawson. 293 and 293T cells were from ATCC. The above-mentioned lines were grown in DMEM/10% FBS. Nf2+/+ (FH-912, genotype Nf2flox2/flox2) and Nf2−/− (FC-1801, genotype Nf2Δex2/Δex2) mSCs  were from Marco Giovannini. MSCs and the derivatives were grown in DMEM:F12-HAM (1:1) medium plus N2 supplement (Gibco), 2% FBS, 1 μM forskolin, and 10 ng/ml heregulin-β1 (recombinant EGF-like domain; PeproTech), on noncoated tissue culture plates. Or, plates were coated with 0.05 mg/ml poly-L-lysine (Sigma-Aldrich), air dried, and further coated with DMEM/10% FBS; the cells were grown in the above-mentioned medium omitting FBS. All cells were maintained in a humidified atmosphere with 5% CO2 at 37 °C.
Orthotopic transplantation and bioluminescence imaging
All animal experiments were approved by the Wistar Institutional Animal Care and Use Committee and performed in accordance with relevant institutional and national guidelines. Nf2+/+ mSCs were first transduced with lentiviruses carrying pLU-Tet-EF1aL-FFluc-mCherry (encoding firefly luciferase and mCherry, provided by the Wistar Institute Vector Core), and sorted by FACS. The established luciferase-expressing mSCs/Luc were further transduced with the KD lentiviruses and selected with puromycin. A total of 2 × 105 cells were transplanted into the sciatic nerve sheath (one side) of each NOD/SCID mouse (Jackson labs stock# 005557; male, 6–8 weeks of age; n = 8–9 per group) by intraneural injection. Tumor growth was monitored weekly for a total of 3 weeks by bioluminescence imaging on an IVIS-200 system, according to the manufacturer’s instructions (Xenogen, San Francisco, CA).
Statistical analyses were performed with GraphPad Prism 7.
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We thank Marco Giovannini, David Gutmann, Tony Pawson, Christian Widmann, Reza Ahmadian, Ion C. Cirstea, Christian Hoischen, Mitsu Ikura, and Addgene and the respective labs for providing cells and/or plasmids; Stephan Schacke for cloning GST-NF2 iso2 tail; Anne Gompf for FACS sorting; Karl-Heinz Gührs for mass-spec analysis; and Birgit Pavelka and Uta Papke for technical support.
This study was supported in part by grants from Deutsche Forschungsgemeinschaft (MO 1421/2-1 and MO 1421/5-1) and Deutsche Krebshilfe (612000) to HM, and from National Natural Science Foundation of China (81761138047) to HJ.
Conflict of interest
The authors declare no potential conflicts of interest.
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