Activation of JNK signaling links lgl mutations to disruption of the cell polarity and epithelial organization in Drosophila imaginal discs

Dear Editor, Identification of Drosophila melanogaster as a model organism for cancer research has facilitated the exploration of human tumor malignancy. In Drosophila, loss-of-function mutations in the neoplastic tumor suppressor genes (nTSGs) lethal(2)giant larvae (lgl), discs large (dlg) or scribble (scrib) cause a malignant tumor-like phenotype characteristic of disrupted cell polarity and overgrowth in epithelial tissues such as imaginal discs 1. Genetic studies have shown that the three nTSGs regulate the epithelial polarity and cell proliferation in Drosophila development through a common genetic pathway 2. However, the underlying regulatory mechanisms are largely unknown. Early on it was postulated that overgrowth is the secondary consequence of defective apicobasal polarity in nTSG-deficient epithelial cells 1. The coupling of the polarity to proliferation control may be mediated through signaling pathways. Indeed, two laboratories recently reported that the c-Jun N-terminal kinase (JNK) signaling activity is essential in both tumor growth and invasion induced by nTSG−/− clones expressing RasV12, the oncogenic form of Ras 3, 4. In RasV12, nTSG−/− clonal tumors, however, the genetic evidence for the causal relationship between loss of cell polarity and activation of JNK signaling appears to be less substantial. To better understand how JNK signaling contributes to the tumorigenesis induced by nTSG mutations, we used lgl homozygous mutant flies as an alternative to dissect the function of the JNK signaling pathway in each of the tumor phenotypes. First, we tested if the germ-line mutations in lgl can cause JNK activation during Drosophila development. For this purpose, we generated fly lines trans-heterozygous for lgl4/Df(2L)net62 or lgl4/lgl1 (hereafter referred to as lgl flies) in the presence of an enhancer trap line, pucE69-lacZ. As expression of pucE69-lacZ is considered as an indicator of JNK signaling activation in Drosophila 5, we thereby assessed the activity of JNK signaling pathway in lgl imaginal discs by monitoring β-galactosidase expression. As shown in Figure 1A, localized expression of puckered (puc) in stalk cells and some peripodial membrane cells was observed in the wild-type wing disc at the late third instar larvae (Figure 1A-i), whereas the ectopic activation of JNK pathway was evident in nearly all the cells in lgl imaginal discs at the same stage, including wing, eye-antennal, leg and haltere discs (Figure 1A-ii and iv; data not shown). Clearly, loss of lgl alone can activate JNK signaling in the developing discs, suggesting a role of JNK activity in lgl mutation-induced tumorigenesis similar to that in the development of RasV12, nTSG−/− clonal tumors. To analyze the potential function of JNK signaling in lgl tumor development, we next inhibited JNK activation in lgl flies by expressing a dominant-negative form of Drosophila JNK (Basket, Bsk), BskDN, using the UAS/GAL4 system 6. The flies homozygous for lgl show a typical growth pattern throughout larval development. Instead of pupating on day 5 after egg laying (AEL), lgl flies continued to grow for up to 10 additional days and finally died as giant larvae (Supplementary information, Table S1). During this extended larval period, lgl imaginal discs become overgrown (Supplementary information, Figure S1). In our experiments, 32B-Gal4-driven expression of UAS-bskDN in lgl flies resulted in phenotypic reversion of the tumor-like overgrowth as characterized by “rescued” size of the mutant discs, absence of the giant larvae and recurrence of pupariation (Supplementary information, Table S1 and Figure S1). Likewise, inhibiting JNK can largely suppress the invasion-like behavior of lgl tumorous discs, as indicated by the absence of a fusion between the adjacent mutant discs expressing BskDN under the control of 32B-Gal4 (Supplementary information, Figure S1). Taken together, the results of our study revealed that JNK activation is required for both tumor growth and invasion of lgl imaginal discs, which is reminiscent of the observations in RasV12, nTSG−/− clonal tumors. The Drosophila imaginal disc is comprised of a monolayer of elongated and polarized epithelial cells, forming a flat and folded disc (Figure 1B-i). Loss of lgl usually disrupts both epithelial polarity and tissue organization in the disc, showing a solid amorphous mass piled up with rounded, multilayered cells with defective apicobasal polarity (Figure 1B-ii). Thus, lgl discs can provide a good system for studying the causal link between polarity disruption and the JNK signaling pathway in tumor development. As described above, we found that the ectopic JNK activity is essential for overgrowth and invasion of lgl tumorous discs. Further examination of the rescued discs, however, revealed a partial restoration of the epithelial disorganization observed in lgl-deficient discs as well. JNK inhibition, on the whole, can bring back the overall shape of lgl discs close to the wild type (Figure 1B-i-iii). Remarkably, in lgl discs expressing BskDN under the control of 32B-Gal4, phalloidin staining showed the presence of a partially folded epithelial sheet in which the F-actin was apically accumulated in the monolayered cells with columnar morphology (inset in Figure 1B-iii). The F-actin localization pattern in the rescued discs suggests a role of JNK activation in disruption of epithelial polarity triggered by loss of lgl. This prompted us to further investigate how the apicobasal polarity in lgl discs expressing BskDN is restored by examining the subcellular localization of selected epithelial polarity proteins in the disc cells. Consistently, we observed a proper distribution of a series of the polarity proteins such as Armadillo (Arm, zonula adherens protein), Dlg (septate junction protein), aPKC (apical protein) and Fasciclin3 (Fas3, basolateral protein) along the apicobasal axis in epithelial cells of the rescued discs (Figure 1B-iv-ix). The restoration in tissue architecture and epithelial polarity was also obtained by expression of another dominant-negative allele of JNK (bskK53R), bskRNAi or the JNK-specific phosphatase Puc in lgl discs under the control of 32B, 69B or eyeless Gal4, respectively (data not shown), albeit to a lesser extent. Collectively, these data provide evidence that JNK signaling activated by loss of lgl mediates disruption of the epithelial polarity and tissue organization in the mutant discs in addition to promoting tumor growth. We further characterized the role of JNK activation in disrupting the epithelial polarity in lgl imaginal discs by expressing BskDN in a temporally and spatially regulated manner, based on the FLP-out system 7. When ectopic expression of BskDN was induced as early as 16 h AEL, we detected a clear restoration in both epithelial polarity and organization, as shown by the presence of polarized epithelial monolayers in the discs (Figure 1C-i). Moreover, the expression pattern of BskDN and the restored area match well in those rescued discs (Figure 1C-i, v-xi). To explore whether activated JNK signaling in lgl flies functions in a time-dependent manner during development, we performed a kinetic assay through suppressing JNK activities in nearly the whole tissue of lgl wing disc at different developmental stages. Interestingly, we found that the later the BskDN expression was induced, the lesser the epithelial organization in lgl wing discs was restored (Figure 1C-i-iv), suggesting a temporally regulated action of JNK signaling in the pathological process. Altogether, these findings suggest that loss of lgl induces activation of JNK signaling at early stage of the development to mediate locally the disruption of epithelial polarity and tissue organization, and that the duration of JNK activation is closely correlated with phenotypic severity. It is known that JNK signaling mediates a number of cellular and developmental processes through activating an evolutionarily conserved pathway. To address whether the canonical JNK pathway is responsible for the disruption of cell polarity and epithelial organization observed in lgl-deficient discs, we first targeted Hemipterous (Hep), the Drosophila JNK kinase for inactivation by introducing hepr75, a strong hypomorphic allele into lgl flies 8. Examination of the imaginal discs from hepr75/Y; lgl4/DF(2L)net62 larvae revealed a weaker restoration in apicobasal polarity of disc cells and disc morphology, compared with that in lgl discs expressing BskDN (Figure 1D-iii and vii; data not shown). We also investigated whether JNK-mediated effects in the polarity disruption and epithelial disorganization require AP-1 transcription factors. We found that inactivation of dFos by expressing either dominant-negative forms of the gene or an RNAi transgene can phenocopy the suppressive effects conferred by JNK inhibition (Figure 1D-iv and viii; data not shown). On the basis of these observations, we argue that an activated Hep-JNK-AP-1 pathway is involved in mediating lgl mutation-induced tumorigenesis regarding the loss of epithelial polarity and disruption of tissue organization (Figure 1E). This study showed that JNK signaling is an essential mediator of many tumorous phenotypes observed in lgl-deficient imaginal discs. In particular, we present evidence that activation of the JNK signaling pathway is causally linked to the disruption of apicobasal polarity and epithelial organization in the mutant tissues. It has been established that JNK could function as an either positive or a negative regulator in cancer development, depending on the tumor cell type, specific genetic setting or tumorigenic stage involved 9. Although JNK regulation of a number of biological processes such as morphogenesis, cell proliferation, migration, adhesion and apoptosis is implicated in human tumor malignancy, the exact role of JNK signaling in tumorigenesis is not yet fully understood. Given that defects in cell polarity are frequently seen in human malignant tumors 10, our finding in the Drosophila model that loss of lgl activates the JNK pathway to mediate the disruption of cell polarity and epithelial organization may suggest an evolutionarily conserved mechanism, thereby providing new insights into the involvement of JNK signaling in human cancer development. (Supplementary information is linked to the online version of the paper on the Cell Research website.) We thank Michel Sémériva (IBDML, France), Fumio Matsuzaki (RIKEN CDB, Japan), Michael J Galko (UT MD Anderson Cancer Center, USA), Enrique Martín-Blanco (Instituto de Biologia Molecular de Barcelona, Spain), Dirk Bohmann (University of Rochester, USA), Kyung-Ok Cho (Baylor College of Medicine, USA), the Bloomington Drosophila Stock Center, NIG-FLY (Japan), and the Developmental Studies Hybridoma Bank for providing fly strains and antibodies. We also thank Wenjuan Xiang and Wentian Gu in ML's Lab for the technical assistance. This work was supported by National Natural Science Foundation of China (30470890), National Basic Research Program of China (2007CB914504, 2007CB947301), the Shanghai Pujiang Program (05PJ14075) and Shanghai Leading Academic Discipline Project (B205).