Of all live births with congenital anomalies, approximately one-third exhibit deformities of the head and face. Most craniofacial disorders are associated with defects in a migratory stem and progenitor cell population, which is designated the neural crest (NC). Musculocontractural Ehlers–Danlos syndrome (MCEDS) is a heritable connective tissue disorder with distinct craniofacial features; this syndrome comprises multiple congenital malformations that are caused by dysfunction of dermatan sulfate (DS) biosynthetic enzymes, including DS epimerase-1 (DS-epi1; also known as DSE). Studies in mice have extended our understanding of DS-epi1 in connective tissue maintenance; however, its role in fetal development is not understood. We demonstrate that DS-epi1 is important for the generation of isolated iduronic acid residues in chondroitin sulfate (CS)/DS proteoglycans in early Xenopus embryos. The knockdown of DS-epi1 does not affect the formation of early NC progenitors; however, it impairs the correct activation of transcription factors involved in the epithelial–mesenchymal transition (EMT) and reduces the extent of NC cell migration, which leads to a decrease in NC-derived craniofacial skeleton, melanocytes and dorsal fin structures. Transplantation experiments demonstrate a tissue-autonomous role for DS-epi1 in cranial NC cell migration in vivo. Cranial NC explant and single-cell cultures indicate a requirement of DS-epi1 in cell adhesion, spreading and extension of polarized cell processes on fibronectin. Thus, our work indicates a functional link between DS and NC cell migration. We conclude that NC defects in the EMT and cell migration might account for the craniofacial anomalies and other congenital malformations in MCEDS, which might facilitate the diagnosis and development of therapies for this distressing condition. Moreover, the presented correlations between human DS-epi1 expression and gene sets of mesenchymal character, invasion and metastasis in neuroblastoma and malignant melanoma suggest an association between DS and NC-derived cancers.
The musculocontractural type of Ehlers–Danlos syndrome (MCEDS) is characterized by distinct craniofacial features, multisystem congenital malformations and progressive fragility of connective tissues (Zhang et al., 2010; Kosho, 2016). This rare intractable disorder is caused by recessive loss-of-function mutations in genes that encode dermatan sulfate (DS) biosynthetic enzymes, including dermatan 4-O-sulfotransferase 1 (CHST14) and DS epimerase-1 (DS-epi1). Glycosaminoglycans (GAGs), such as DS, chondroitin sulfate (CS) and heparan sulfate (HS), are side chains of repeating disaccharides, which are covalently attached to distinct core proteins in the Golgi complex to form cell surface and extracellular matrix proteoglycans (PGs) (Iozzo and Schaefer, 2015). DS is formed from CS by the partial conversion of glucuronic acid (GlcA) into iduronic acid (IdoA) (Trowbridge and Gallo, 2002; Thelin et al., 2013). The content of IdoA is variable and ranges from one IdoA residue per chain to nearly 100% IdoA; thus, the name CS/DS is assigned to describe the hybrid nature of the chain. DS-epi1 and DS-epi2, which are encoded by Dse and Dse-like (Dsel), respectively, mediate the epimerization of a carboxyl group at C5 to form IdoA in CS/DS (Maccarana et al., 2006; Pacheco et al., 2009b). Dse-knockout mice have connective tissue fragility attributed to a CS/DS alteration of decorin, which results in impaired assembly of collagen fibrils (Maccarana et al., 2009; Gustafsson et al., 2014), and a series of malformations whose cause is not understood. In contrast, the loss of Dsel results in normal offspring (Bartolini et al., 2012). Double-knockout mice die around birth and completely lack IdoA in their CS/DS chains, which indicates that DS-epi1 and DS-epi2 are the only epimerases in DS biosynthesis (Stachtea et al., 2015). DS-epi1, which was originally referred to as squamous cell carcinoma antigen recognized by cytotoxic T lymphocytes 2 (SART2) (Nakao et al., 2000; Maccarana et al., 2006), is overexpressed in all tumors and functionally linked to the tumorigenic properties of esophagus squamous cell carcinoma that involve cell migration (Thelin et al., 2012). Nevertheless, it is not clear how a modified CS/DS chain leads to developmental abnormalities and malignancy.
To investigate the function of IdoA in CS/DS chains at the cellular level, we searched for an appropriate model system. Craniofacial anomalies constitute a high proportion of congenital malformations and are mainly caused by neural crest (NC) development defects (Gorlin et al., 1990). Interestingly, the craniofacial features in MCEDS (Müller et al., 2013; Syx et al., 2015; Kosho, 2016) are reminiscent of NC-associated disorders, such as Treacher Collins syndrome, Nager syndrome and Miller syndrome (Trainor and Andrews, 2013), which indicates that the NC might be a suitable model system for MCEDS. The NC comprises a population of multipotent and highly migratory cells that form at the border between the neural and epidermal ectoderm in the vertebrate embryo (Mayor and Theveneau, 2013; Simões-Costa and Bronner, 2015). Research predominately in Xenopus and the chick embryo has demonstrated that signaling molecules secreted from the surrounding ectoderm and the underlying mesoderm, including bone morphogenetic proteins, Wnts and fibroblast growth factors (FGFs), orchestrate a combinatorial expression of transcription factors that drive NC specification and morphogenesis. NC cells undergo an epithelial–mesenchymal transition (EMT), migrate along restricted pathways through the embryo and contribute to nearly every organ system in the body, including the craniofacial skeleton, melanocytes, endocrine cells and the peripheral nervous system. Developmental disturbances in the NC, which are collectively referred to as neurocristopathies, encompass defects in NC specification, migration and differentiation, and include tumors of NC lineages, such as neuroblastoma and melanoma (Zhang et al., 2014). EMT and cell migration are hallmarks of both NC development and cancer metastasis (Powell et al., 2013).
As a result of their large embryo size and external development, Xenopus is a favorable experimental system. Here, we demonstrate that DS-epi1 accounts for most DS biosynthesis in the early Xenopus embryo. In loss-of-function assays, DS-epi1 is required for the correct regulation of neural-plate-border- and NC-specific transcription factors. Moreover, DS-epi1 has an intrinsic role in NC cell migration and is indispensable for the cell adhesion, spreading and formation of polarized cell structures on fibronectin. Human DSE expression correlates with genetic markers of EMT, invasion and metastasis in both neuroblastoma and melanoma, which suggests a potential role of DS-epi1 in NC-derived cancers. A model is proposed, in which CS/DS PGs mediate the adherence of NC cells to fibronectin during cell migration.
Dse and Dsel are expressed in the early Xenopus embryo
We have previously demonstrated that intra-blastocoelic injection of purified DS, but not CS, stimulates posterior development, mesoderm formation and neuronal differentiation in an FGF-dependent manner (Hou et al., 2007). Enzymatic degradation of endogenous DS yielded opposite results, which suggests an important role of this GAG in early Xenopus embryos. To better understand the biosynthesis and function of DS, we focused on DS-epi1 and DS-epi2. Using a BLAST search in Xenbase for each gene, we identified two Xenopus laevis homeologs that differ in the derived amino acid sequences by 6% between DS-epi1.S and DS-epi1.L (Fig. S1), and 4% between DS-epi2.S and DS-epi2.L (Fig. S2), and also have well-conserved orthologs in other vertebrates. DS-epi1 and DS-epi2 share a cleavable signal peptide followed by an epimerase domain with 49% identity and two transmembrane domains (Fig. 1A). At the C-terminus, DS-epi2 contains a conserved sulfotransferase-like domain.
RT-PCR demonstrated that Dse expression was initiated in late gastrula embryos (Fig. 1B). Dsel was maternally expressed, and abundant zygotic transcripts were identified from the early tailbud stage onwards. DS epimerase activity represents the sum of DS-epi1 and DS-epi2 contributions (Maccarana et al., 2006). In Xenopus, there was a minute maternal level of epimerase activity and an onset of zygotic activity at the late gastrula stage, with a subsequent constant increase until at least stage 45 (Fig. 1C). Whole-mount in situ hybridization of stage 17 embryos indicated Dse expression in the epidermis, notochord and pre-migratory NC that overlapped with Snail2 expression in the cranial neural crest (CNC) (Fig. 1D-E′). Quantitative real-time PCR (qPCR) analysis confirmed Dse but not Dsel mRNA in isolated c-Myc+ CNC explants from stage 18 embryos (Fig. 1F). At stage 30, Dse and Dsel expression coincided with migrating Twist+ CNC cells in the mandibular, hyoid and branchial arches (Fig. 1G-I′).
DS-epi1 is the main contributor to early DS biosynthesis and is required for NC-derived structures
To investigate the relative contribution of DS-epi1 and DS-epi2 to epimerase activity in the embryo, we used morpholino oligonucleotides (MOs) against Dse and Dsel (Fig. 2A). Following microinjection into the animal pole of embryos (hereafter called animal injection), Dse- and Dsel-MOs blocked 89% and 12% of the endogenous DS epimerase activity, respectively, at stage 25 (Fig. 2B). The Dse-MO substantially suppressed the epimerase activity induced by injected Dse mRNA at stage 12, whereas a standard control MO and a Dsel-MO had no effect (Fig. 2C). In contrast, the Dse-MO did not block the epimerase activity of the injected Dse* mRNA, which contains seven point mutations in the MO target sequence; this finding demonstrates the specificity of the Dse-MO knockdown. The data suggest that DS-epi1 is the main contributor to DS biosynthesis in the early Xenopus embryo.
Animal injection of Dse-MO caused a decreased number of melanocytes, a reduction of head and eye structures, a lack of dorsal fin tissue and a kinked shortened tail in stage 40 embryos (Fig. 2E). Both the control-MO and Dse-5MM-MO, which contains five base mismatches with the Dse target mRNA, had no effect (Fig. 2D,F). Histological analysis at stage 38 indicated that Dse-morphant tadpoles had a hypoplastic notochord and somite structures that were dorsally abutting above the neural tube (Fig. 2G,H). Moreover, Dse knockdown led to a reduction in the mandibular, hyoid and branchial cartilage in the head at stage 45 (Fig. 2I-K). Interestingly, defects in melanocyte, craniofacial skeleton and dorsal fin formation are characteristic of deficient NC formation (Tucker, 1986; Sadaghiani and Thiébaud, 1987; Tucker and Slack, 2004), which suggests that DS-epi1 is required for NC development. Animal injection of Dse mRNA had no apparent effect on embryonic development at stage 40 and did not affect the formation or migration of Twist+ CNC cells at stages 16 and 26, respectively (Fig. S3).
Isolated IdoA residues are present in CS/DS PGs in early embryos
To investigate the PG expression and GAG composition in Xenopus embryos, we microinjected [35S]sulfate into the blastocoel at stage 9 and analyzed the purified PGs at stage 22 after chemical and lyase treatment to degrade distinct GAG chains (Fig. 3). Nitrous acid at low pH was used to degrade HS (Shively and Conrad, 1976), and chondroitinases that are specific for DS (denoted Chase B) or both CS and DS (denoted Chase ABC) were used to degrade the DS or CS/DS chains, respectively. The size separation of the split products indicated that 56% of the total radioactivity corresponded to CS/DS PGs (Fig. 3A). SDS-PAGE analysis demonstrated two broad bands that were resistant to nitrous acid treatment and compatible with being biglycan (Bgn, 200-300 kDa, Moreno et al., 2005) and versican (Vcan, ∼1000 kDa) (Fig. 3B). Both bands disappeared following Chase ABC digestion and decreased following Chase B digestion to 71% (Bgn) and 65% (Vcan). We have previously demonstrated that CS/DS chains are present in Xenopus overexpressing Bgn (Hou et al., 2007). In post-neurula embryos, both Bgn (Fig. 3C,C′) and Vcan (Casini et al., 2008) are expressed in the trunk NC. Chase B treatment demonstrated IdoA in the high molecular mass fractions of control-MO- but not Dse-MO-injected embryos (Fig. 3D,E), which underscores the crucial role of DS-epi1 in DS biosynthesis. The Chase-B-degraded products primarily moved to fractions of 10-20 kDa, which indicates that IdoA is predominately a rare and isolated structure that is surrounded by long stretches of GlcA. We conclude that embryos at the early tailbud stage synthesize high molecular mass CS/DS PGs, such as Bgn and Vcan, with only few IdoA residues per chain.
Biosynthesis of DS is not regulated by feedback
We subsequently investigated whether the presence of IdoA in CS/DS PGs affects the gene expression of DS epimerases. qPCR analysis indicated no changes in the Dse and Dsel mRNA levels in stage 18 CNC explants of the Dse-MO- compared with the Dse-5MM-MO-injected control embryos (Fig. S4). This result argues against feedback regulation of IdoA in CS/DS biosynthesis at the transcriptional level.
DS-epi1 regulates the expression of neural plate border and cranial neural crest markers
Animal injection of Dse-MO did not affect the extent of the Sox2+ neural plate or Cytokeratin+ epidermis (Fig. S5A,B); however, it expanded the expression domains of the neural plate border markers Pax3 and Msx3 into the ventral ectoderm at stage 15 (Fig. 4B,C,E,F). DS-epi1 knockdown had no substantial effect on the Sox9 expression in the pre-migratory CNC (Fig. 4H,I); however, it reduced the levels of both the Foxd3 and Twist markers (Fig. 4K,L,N,P) and concomitantly expanded the c-Myc expression in these cells (Fig. 4R,T). The Dse-5MM-MO had no effect (Fig. 4A,D,G,J,M,Q), and the co-injection of Dse* mRNA and Dse-MO reverted the reduction of Twist and the expansion of the c-Myc expression (Fig. 4O,S,P,T), which supports the specificity of the phenotypes. Thus, DS-epi1 is not involved in the early dorsoventral ectoderm patterning; however, it controls the expression of neural-plate-border- and distinct CNC-specific transcription factors in neurula embryos.
DS-epi1 is important for cranial neural crest cell migration
At the late neurula stage, Twist and Snail2 demarcate the mandibular, hyoid and branchial segments at the onset of CNC migration (Fig. 5A,D). DS-epi1 knockdown disturbed the segregation of CNC segments and shortened the early cell migration streams (Fig. 5B,C,E,G). In tailbud embryos, Twist and Sox9 label migrated CNC cells around the eye vesicle (mandibular stream), and in the hyoid and branchial arches (Fig. 5H; Fig. S5D). Dse-MO restricted the ventral migration of the CNC cells (Fig. 5I,M; Fig. S5E,I) and decreased the Rax and Sox9 expression in the eye and lens placode, respectively (Fig. S5C,E). The Dse-morphant migration defects were rescued by the co-injection of Dse* mRNA (Fig. 5F,G,J,M; Fig. S5F,I). Moreover, the injection of the human pcDNA3/CTAP-DSE expression plasmid restored normal CNC cell migration in the Dse-morphant embryos (Fig. 5K; Fig. S5G), whereas the catalytically inactive pcDNA3/CTAP-DSE (H205A) construct had no effect (Fig. 5L,M; Fig. S5H,I). Western blot analysis confirmed that pcDNA3/CTAP-DSE and pcDNA3/CTAP-DSE (H205A) (Pacheco et al., 2009a) in injected Xenopus embryos produced equal amounts of protein (Fig. 5N).
A TUNEL assay demonstrated that the Dse-MO had no detectable effect on apoptosis at the neurula or early tailbud stage; however, it induced cell death in advanced tailbud embryos (Fig. S6). The data indicate a distinct role of DS-epi1 in CNC cell migration.
DS-epi1 has a tissue-autonomous role in cranial NC cell adhesion and migration
To investigate where the CS/DS chains affect cell migration, we performed transplantation experiments with green fluorescent protein (GFP) as a lineage tracer. First, we homotypically grafted CNC explants from embryos that were co-injected with a morpholino oligonucleotide and GFP mRNA into uninjected sibling hosts at stage 17 (Fig. 6A). Cells from the control-MO-injected CNC grafts migrated ventrally and formed well-orchestrated mandibular, hyoid and branchial streams (Fig. 6B). In contrast, the migration of the Dse-MO-injected CNC cells was disturbed and only a few labeled cells reached their correct destination (Fig. 6C). When GFP+ CNC cells were transplanted into control- and Dse-morphant host embryos (Fig. 6A′), their cell migration was normal (Fig. 6D,E). These findings suggest that DS-epi1 is needed in the CNC graft, but apparently not in surrounding tissue, which indicates a tissue-autonomous function of CS/DS PGs in CNC cell migration.
The adhesive extracellular matrix (ECM) glycoprotein fibronectin is ubiquitously distributed along NC migration pathways in the Xenopus embryo (Davidson et al., 2004). CNC undergoes cell migration on immobilized fibronectin substrates in vitro and exhibits a similar stream formation as demonstrated in vivo (Sadaghiani and Thiébaud, 1987; Alfandari et al., 2003). To further analyze the role of DS-epi1 in cell migratory behavior, we cultured CNC explants on fibronectin-coated plates (Fig. 6F). At 2 h after plating, one side of the uninjected CNC explants had expanded, and cells had spread on the substrate and migrated as a cohesive sheet (Fig. 6G). After 4 h, distinct segments started to form that were reminiscent of the mandibular, hyoid and branchial streams (Fig. 6G′). In contrast, the Dse-MO-injected CNC cells acquired a round morphology after 30 min, and did not subsequently spread or migrate (Fig. 6H,H′ and data not shown). To visualize the cytoskeleton, we performed phalloidin staining ∼5 h after plating, when cells typically started to individually migrate. The cells of Dse-5MM-MO-injected CNC explants exhibited F-actin+ stress fibers throughout the cytoplasm, in addition to lamellipodia and filopodia at their leading edges (Fig. 6I). Dse-morphant cells only formed cortical networks of stress fibers below the membrane (Fig. 6J). The degree of cell spreading and percentage of cells that formed polarized protrusions were similar between the Dse-5MM-MO-injected and uninjected CNC explants, whereas the Dse-morphant cells had a 60% smaller surface and no protrusions (Fig. 6L,M). Importantly, Dse* mRNA restored the normal cell size and shape in the Dse-MO-injected CNC explants (Fig. 6K-M), which suggests that DS-epi1 is required for cells to spread and form polarized cell protrusions.
To investigate cell–matrix adhesion, dissociated single GFP+ CNC cells were cultured for 45 min on fibronectin, and the percentage of the adherent cells was quantified (Fig. 6N). Approximately 90% of the Dse-MO-injected CNC cells lost adherence to fibronectin compared with the uninjected cells, whereas Dse-5MM-MO had no significant effect. As previously reported (Alfandari et al., 2003), CNC cells failed to attach to bovine serum albumin (BSA)-coated substrates. The observed defects were not a result of apoptosis because fluorescence-activated cell sorting (FACS) indicated that 2 h after the extraction, the CNC cells from the Dse-MO-injected embryos had >95% cell viability, which was comparable to that of the uninjected cells (Fig. S7A-C′). Moreover, the Dse-morphant CNC cells exhibited a normal cell cycle progression (Fig. S7D-F). At more than 4 h after the extraction, the Dse-MO-injected CNC cells did not have a lower survival rate compared with the uninjected controls (data not shown). Thus, our data on CNC cells indicate that IdoA in CS/DS is essential for cell adhesion and migration on fibronectin.
Candidate CS/DS PGs in CNC cells
Based on the tissue-autonomous role of IdoA in CS/DS, we propose that DS-epi1 knockdown affects PGs that are synthesized in the CNC. The integrin α5β1 heterodimer (encoded by the Itga5 and Itgb1 genes), members of the syndecan (Sdc) family, Bgn, Vcan and CD44 have been presented as CS or CS/DS PGs, some of which have functions in cell adhesion (Thelin et al., 2013). In CNC explants of stage 18 embryos, qPCR indicated abundant mRNA levels of Itga5, Itgb1 and Sdc4, whereas Sdc1, Sdc3, Bgn, Vcan and CD44 were not expressed or were only expressed at very low levels (Fig. 7A). We did not identify changes in the Itga5, Itgb1 or Sdc4 mRNA levels in the Dse-morphant compared with the Dse-5MM-MO-injected control CNC cells (Fig. 7B). Moreover, western blot analysis demonstrated similar levels of integrin β1 protein in the DS-epi1+ and DS-epi1-deficient NC- and epidermis-enriched explants (Fig. 7C), which suggests that reduced IdoA levels do not alter the expression of integrins. In some mammalian cell types, it has been reported that the α5 and β1 integrin subunits (Veiga et al., 1997; Franco et al., 2009) and Sdc4 (Shworak et al., 1994; Deepa et al., 2004; Holmborn et al., 2012) are hybrid PGs that carry both CS and HS chains; however, it is not known whether they contain CS/DS chains. To investigate whether migratory CNC cells also synthesize IdoA in CS/DS chains, we isolated CNC explants at stage 18 and cultivated the cells in vitro in [35S]-containing medium for 24 h to label the PGs. Chase B degraded 47% of the labeled CS/DS PGs, which covered a wide range of molecular mass of over 18 kDa (Fig. 7D), and the size distribution of the degraded products indicated that isolated IdoA moieties are present in the native chains. The molecular mass of the IdoA-containing PGs is compatible with integrin α5β1 subunits (120-150 kDa) (Alfandari et al., 2003) and Sdc4 (40-250 kDa) (Gopal et al., 2010). However, we could not identify CS, CS/DS and HS chains on endogenous integrin α5 and β1 in Xenopus CNC tissue, as well as explants enriched in epidermis and neural crest (Fig. S8A,B). Moreover, we demonstrated that HS, but not CS and CS/DS, chains in Flag-tagged Sdc4 were produced in the mRNA-injected explants (Fig. S8C). In summary, integrin α5β1 and Sdc4 are expressed in CNC cells and do not appear to be decorated with CS or CS/DS chains in Xenopus embryos. These findings suggest that other not yet identified CS/DS PGs might mediate the DS-epi1-dependent CNC cell adhesion on fibronectin.
DSE expression in NC-derived cancers
The involvement of DS-epi1 in NC migration in Xenopus embryos prompted us to investigate a potential link between DSE expression and tumorigenic properties in two human NC-derived cancers (Fig. S9). Gene set enrichment analysis of the expression datasets from both neuroblastoma and metastatic melanoma (n=498 and 44, respectively) demonstrated that DSE expression correlated with genes associated with EMT, mesenchymal and invasive phenotypes, as well as genes involved in metastasis. These findings indicate a potential role of DS-epi1 in NC-tumor development, which warrants further investigation.
This study demonstrates, for the first time, an essential function of IdoA in early embryonic development and cell migration in vivo. The spatio-temporal expression of Dse in the Xenopus embryo suggested a role of DS-epi1 in ectoderm and NC development. The blockage of epimerase activity and IdoA biosynthesis upon the knockdown of DS-epi1 did not affect the allocation of neural and epidermal fates or the formation of NC progenitors. However, DS-epi1 deficiency altered the expression of neural-plate-border- and NC-specific transcription factors and decreased the extent of NC cell migration, which led to defects in craniofacial skeleton, melanocyte and dorsal fin formation. The functional links between DS-epi1 and EMT and between DS-epi1 cell adhesion on fibronectin, as established in this study for normal NC development, might have implications for neurocristopathies and cancer.
Our study demonstrates that, in Xenopus embryos, DS-epi1 is important for the formation of isolated IdoA moieties interspersed with unmodified GlcA residues. This result is noteworthy because previous findings in Dse-null mice (Maccarana et al., 2009) and a human patient with Dse loss-of-function (Müller et al., 2013) have suggested that DS-epi1 is mainly responsible for the biosynthesis of IdoA blocks. The amount and arrangement of IdoA residues in CS/DS chains depends on the protein core, tissue type and signaling status (Trowbridge and Gallo, 2002; Thelin et al., 2013). Our work comprises the first investigation to demonstrate in vivo that isolated IdoA residues change the biological properties of CS/DS PGs. Even a single IdoA is thought to render the CS/DS chain more flexible, which increases its ability to interact with growth factors and matrix components. For example, CS/DS chains isolated from embryonic pig brains contain sequences with a single IdoA residue that interacts with the growth factor pleiotrophin (Bao et al., 2005).
We note that despite the misregulation of NC-specific transcription factors, NC cells are formed in DS-epi1-deficient embryos. This finding is exemplified by the expression of Twist, which is initially reduced likely because of the concomitant downregulation of Foxd3 expression (Sasai et al., 2001), but is subsequently restored in CNC cells at the post-neurula stage, possibly as a result of Wnt/β-catenin signaling, which induces NC cell fate and maintains Twist expression during migration (Chang and Hemmati-Brivanlou, 1998; Borchers et al., 2001). The downregulation of Twist and Foxd3 expression in DS-epi1-morphant neurula embryos supports a function of DS-epi1 in EMT. Twist is a repressor of E-cadherin in Xenopus NC cells (Barriga et al., 2013). Low Twist and high E-cadherin cause a loss of polarized protrusions and a failure of cell–cell dissociation (Scarpa et al., 2015). Foxd3 promotes the EMT by modulating cell–cell adhesion in the chick embryo (Cheung et al., 2005; Fairchild et al., 2014). EMT inhibition might also explain the impaired segregation and reduced ventral migration of CNC cell streams following the knockdown of DS-epi-1.
A human esophagus squamous cell carcinoma cell line with short hairpin RNA (shRNA)-mediated DS-epi1 loss-of-function (Thelin et al., 2012) and cultured aortic smooth muscle cells from Dse−/− mice (Bartolini et al., 2013) both have a reduced level of plasma membrane protrusions and an abnormal actin cytoskeleton, which changes their migration properties similar to the findings in CNC cells. Interestingly, DS-epi1 deficiency in these in vitro wound scratch and invasion assays leads to a larger cell size and increased speed, but decreased directionality, of cell migration. In comparison, DS-epi1 morphant CNC cells had a smaller cell size and did not migrate in vitro because of a failure in cell adhesion to fibronectin. These discrepancies might be a result of the different cell types and matrix components.
In loss-of-function experiments, DS-epi1 is not required for CNC cell survival at the neurula and early tailbud stage. However, the reduced cell anchorage of DS-epi1 morphant CNC cells might account for the increased apoptosis in advanced tailbud stage embryos. A positive role of DS-epi1 in the maintenance of CNC cells might be mediated by integrins, which convey survival signals in the CNC (Goh et al., 1997).
We suggest a model in which DS-epi1 converts selected GlcA residues into isolated IdoA on CS/DS PGs in Xenopus CNC cells (Fig. 8). Following interaction with fibronectin, CS/DS PGs lead to the rearrangement of the actin cytoskeleton and facilitate CNC cell adhesion and migration. In support of this model, we demonstrated in Xenopus CNC that (1) DS-epi1 is expressed and synthesizes IdoA on CS/DS-PGs, (2) DS-epi1 has a tissue-autonomous role in cell migration, and (3) DS-epi1 is required for the cells to adhere, spread and extend polarized cell processes on fibronectin. The integrin α5β1 heterodimer (Alfandari et al., 2003) and Sdc4 (Woods et al., 2000; Matthews et al., 2008) bind to distinct domains of fibronectin and are required for NC cell adhesion and migration. The interaction of GAG chains with fibronectin is crucial for the functions of integrin α5β1 in cell migration (Shworak et al., 1994) and Sdc4 in the proper organization of the actin cytoskeleton and cell adhesion (Gopal et al., 2010). Although co-expressed with Dse in the CNC at the onset of cell migration, Itga5, Itgb1 and Sdc4 mRNAs and the integrin β1 protein level are not altered in DS-epi1-deficient embryos. We did not identify CS or CS/DS chains in endogenous integrin α5β1, and overexpressed Flag–Sdc4 contained HS, but not CS chains, which indicates that the expression and GAG status of this integrin and Sdc4 are not affected by DS-epi1 in Xenopus embryos. A previous finding that purified DS binds to fibronectin (Saito and Munakata, 2007) supports a direct interaction between CS/DS PGs and this extracellular matrix component. Other mechanisms might exist to explain the role of IdoA in cell adhesion and migration. For example, CS/DS PGs might stimulate the cell surface localization of adhesion proteins or cooperate with fibronectin to activate integrins; these processes remain to be investigated.
MCEDS is the first disorder that has been discovered to specifically affect the biosynthesis of DS (Kosho et al., 2016). A defect in NC cells might contribute to the craniofacial phenotype in this condition. The features of MCEDS include hypoplasia of the jaw, high and/or cleft palate, midface skeletal anomaly, down-slanting palpedral fissues and malformed ears (Müller et al., 2013; Syx et al., 2015). These craniofacial anomalies also occur in congenital defects caused by a reduced amount or abnormal migration of NC cells into the first (mandibular) and second (hyoid) pharyngeal arch in Treacher Collins syndrome, Nager syndrome and Miller syndrome (Trainor and Andrews, 2013), which suggests a conserved role of DS in human NC development. The knockdown of DS-epi1 in Xenopus embryos phenocopies the craniofacial defects in humans. Our study in the Xenopus model suggests that an insufficient amount of NC cells migrating to their destinations might be a result of (1) a defect in the EMT, (2) an inability of NC cells to adhere to fibronectin, and (3) cell death as a consequence of anchorage loss of NC cells. Thus, our study suggests that MCEDS might add to the list of neurocristopathies. The identification of NC cells as a target of DS deficiency might help explain the other clinical criteria of MCEDS (Kosho, 2016). For example, it remains to be investigated whether the congenital heart defects in patients could be caused by an insufficient contribution of NC cells to the cardiac septum and valve formation, and whether recurrent subcutaneous infections in patients might reflect a compromised immune defense as a result of a reduced ability of NC cells to contribute to the thymus. In view of the multitude of cell types and tissues that NC cells give rise to (Le Douarin and Dupin, 2012), additional, new manifestations, e.g. in inner organs, might be identified that improve the diagnosis and etiology-based therapy of this currently intractable disorder.
Neurocristopathies also encompass NC-derived cancers, including neuroblastoma and malignant melanoma. Neuroblastoma is the most common solid cancer in the first year of life and is a leading cause of death in children with cancer. Malignant melanoma is the most aggressive skin cancer and the second most common cancer in individuals under the age of 50. Our study indicates that in NC-derived neuroblastoma and melanoma, DSE expression is correlated with gene sets for various migratory properties of cancer cells, including EMT, invasion and metastasis. During tumor progression, carcinoma cells acquire mesenchymal gene expression patterns, which results in migratory and invasive properties that enable the cells to disseminate through the body to produce metastatic tumors in distinct organs (Thiery et al., 2009; Tsai and Yang, 2013). Because of the heterogeneity of tumors (which have both epithelial and mesenchymal cells), it has been difficult to investigate the EMT in cancer development in vivo (Tsuji et al., 2009). Our Xenopus NC model has established a functional link between DS-epi1 and cell migration. The correlation between DS-epi1 expression and EMT in NC-derived cancers suggests a possible involvement of DS in metastatic diseases that remains to be investigated.
The demonstration that DS is important for cell migration in vivo might shed light on other processes that are dependent on both DS (Syx et al., 2015) and fibronectin (Muro et al., 2003; Castelletti et al., 2008), such as skin wound healing and kidney function. These processes might also involve a functional link between DS and fibronectin in cell adhesion, as proposed in the present study.
MATERIALS AND METHODS
Constructs and microinjection
A full-length cDNA clone of X. laevis Dse.S in pCS105 (ID: XL487g09ex) that contained 251 nucleotides of the 5′ untranslated region (UTR), the open reading frame (ORF) and 680 nucleotides of the 3′UTR was obtained from the Osada/Taira NBRP Xenopus ANE library (Osada et al., 2003) and completely sequenced (GenBank accession number KU877109). To obtain pCS2-Dse*, the ORF of Dse.S was point-mutated by performing PCR and subcloned into pCS2, which resulted in seven nucleotide mismatches in the Dse-MO target sequence in positions −2, −1, +6, +9, +12, +15 and +18 relative to the translation start site. A full-length cDNA clone of X. laevis Dsel.L with 93 nucleotides of the 5′UTR, the ORF and 22 nucleotides of the 3′UTR (GenBank accession number KU877110) was generated by RT-PCR and subcloned into the pCR-XL-TOPO vector (Thermo Fisher Scientific), using total RNA from the head of stage 28 embryos and primers based on a corresponding Xenbase sequence entry.
Sense RNAs for microinjection were synthesized using the mMessage Machine kit (Ambion). cDNA plasmids were linearized and transcribed as follows: pCS105-Dse (BstX1, Sp6), pCS2-Dse* (NotI, Sp6), pCS2-nLacZ, (NotI, Sp6), pCS2-Flag-Sdc4 (NotI, Sp6; Muñoz et al., 2006) and pCMT-eGFP (NotI, Sp6; a kind gift from Eric Bellefroid, Université Libre de Bruxelles, Belgium). The Dse-MO (5′-GCTCCCCGAGTGTGAGTCCTCATTG-3′), Dse-5MM-MO (5′-GCTaCCCcAGTcTGAGTaCTaATTG-3′; lowercase letters represent mismatches), Dsel-MO (5′-ATGGTCCATTAGGAGAATAGTCAGT-3′) and standard control-MO (5′-CCTCTTACCTCAGTTACAATTTATA-3′) were obtained from Gene Tools LLC. Unless otherwise stated, mRNAs, DNAs and MOs were injected into the animal pole of all blastomeres at the two- or four-cell stage. A total of 45 ng MOs was injected per embryo. For single injections, a quarter of the MO amount with 125 pg nlacZ mRNA as a lineage tracer was used.
Embryo manipulations and histological staining
All Xenopus laevis experiments reported in this study were approved by the Lund/Malmö regional ethical committee (M140-14). The embryos were prepared, cultured and analyzed by Red-Gal staining, whole-mount in situ hybridization and TUNEL assay as described previously (Pera et al., 2015). For histological staining, embryos were fixed in Bouin's solution, dehydrated, embedded in paraffin, sectioned at 10 μm, dewaxed and stained with hematoxylin and eosin. For cartilage staining, tadpoles were fixed in MEMFA (0.1 M MOPS, 2 mM EGTA, 1 mM MgSO4, 3.7% formaldehyde, pH 7.4), dehydrated, and stained in Alcian Blue solution; the facial skeleton was dissected after rehydration in 80% glycerol in 2% KOH.
Preparation of explants and transplantation
Explants enriched in neural crest and epidermis were prepared by removing the chorion membrane with forceps, hemi-sectioning stage 18 embryos, and cutting off the neural epithelium and yolk with a surgical blade (Swann-Morton 10, REF 0301) on 1% agarose plates in MBS.
CNC explants from the embryos injected into the animal hemisphere with eGFP mRNA at stage 17 were dissected and homotypically grafted into host embryos as previously described (Borchers et al., 2000) with the following modifications: the dissection and grafting of the CNC explants were performed on 1% agarose in MBS. At ∼30 min after grafting, the embryo was transferred to a clean dish filled with 0.1× MBS and incubated at 17°C. At stage 26, the migration pattern of the transplanted CNC cells was monitored with a fluorescence stereomicroscope (Leica MZFLIII) and documented with a digital camera (Nikon DS-Fi1c).
CNC migration and adhesion assays
Substrates, including human plasma fibronectin (Millipore) and BSA (Sigma), were diluted at 10 µg/ml in PBS and coated on plastic at 4°C overnight. The migration assay with CNC explants on fibronectin-coated plastic dishes was performed as previously described (DeSimone et al., 2005). For the adhesion assay, fluorescently labeled CNC explants from the embryos injected into the animal hemisphere with eGFP mRNA were incubated in Ca2+- and Mg2+-free MBS for 1 h at 12°C to dissociate the cells (Alfandari et al., 2003). The single CNC cells were subsequently plated in 96-well plates coated with fibronectin or BSA and allowed to attach for 45 min at room temperature. Photographs were taken with a fluorescence microscope shortly before and after gently pipetting the medium up and down, and the attached cells were counted.
CNC explants were plated on fibronectin-coated cover glass slides (100 µg/ml). Following 5 h of culture, the explants were fixed in 4% formaldehyde in PBS for 1 h and blocked for 1 h in PBS with 1% BSA. The explants were incubated for 20 min with phalloidin–Alexa-Fluor-488 (1:100 in PBS, Life Technologies, A12379). Cover slides were mounted with Fluorescent Mounting Medium (Dako) that contained 4′,6-diamidino-2-phenylindole (DAPI), and the staining was monitored with a Zeiss LSM 780 confocal microscope.
RT-PCR and qPCR analysis
Total RNA was extracted with TRIzol® reagent (Ambion-Life Technologies). cDNA synthesis was performed using Reverse Transcriptase AMV (Roche) for whole embryos and SuperScript® II Reverse Transcriptase (Invitrogen Life Technologies) for CNC explants. RT-PCR was performed as previously reported (Hou et al., 2007). qPCR was performed on ten CNC explants per sample using the Fast SYBR® Green Master Mix (Ambion Life Technologies) and the StepOne™ Real-Time PCR System (Life Technologies). The relative expression was evaluated using the ΔCt method with the housekeeping gene eEF1A1 as the control. The primers are listed in Tables S1 and S2.
Embryos (n=250 to investigate the activity at different stages; n=50 to investigate the effect of morpholinos) were lysed in 1 ml PBS, 1% Triton X-100, 1 mM DTT, 1 mM EDTA and protease inhibitors (Complete Mini; Roche, 04693124001). Cleared supernatant was exchanged with dialysis buffer (20 mM MES, pH 5.5 at 37°C, 10% glycerol, 0.5 mM EDTA, 0.1% Triton X-100, 1 mM PMSF and 1 mM DTT) using PD10 columns (GE Healthcare). The protein content was measured by performing a Bradford assay (Bio-Rad), using bovine serum albumin (BSA) as the standard. Equal amounts of protein were assayed in a final 100 µl reaction buffer that was composed of dialysis buffer as previously described, which contained 2 mM MnCl2, 0.5% NP-40, 100 µg BSA and 30,000 dpm of the labeled chondroitin substrate ([5-3H]defructosylated, K4 prepared as previously described; Hannesson et al., 1996). Incubations were conducted for 20 h at 37°C, and the released tritium was quantified as previously described (Pacheco et al., 2009a). During the assay, it was determined that the inhibitory components in the lysates varied in the embryos of different developmental stages. To remove these inhibitions and to increase the sensitivity of the assay, in particular during the early stages, the lysates were enriched in epimerase activity by purification on Red-Sepharose gel (Pacheco et al., 2009a; Gustafsson et al., 2014). A total of 2 mg of lysates in 1 ml 60 mM MES pH 6.5 and 100 mM NaCl were prepared and batch-incubated overnight at 4°C with 30 µl Red-Sepharose gel (GE Healthcare). The gel was washed with incubation buffer, and the epimerases were eluted with 200 µl dialysis buffer, 2 M NaCl and 1 mg/ml BSA as the carrier. The samples were desalted on membranes by using dialysis buffer, and 50 µl of the preparation was subsequently assayed.
Proteoglycans were treated for 2 h at 37°C with 10 mIU chondroitinase ABC (Sigma) in 20 µl ammonium acetate pH 8.0 or 5 mIU chondroitinase B (R&D Systems) in 20 µl 50 mM Tris-HCl pH 7.5, 50 mM NaCl, 4 mM CaCl2 or a mixture of 2 mIU each of heparinases I, II and III in 20 μl 40 mM sodium acetate, pH 7.0, and 2 mM calcium acetate (heparinases were prepared in-house, purified from E.coli, stably singularly transfected with the pET-15b vector that contained heparinase I or vector pET-19b that contained heparinase II or III, a kind gift from Jian Liu, University of North Carolina, NC).
Metabolic labeling of proteoglycans and GAG analysis
[35S]sulfate (Perkin-Elmer; 600 nCi in 25 nl/embryo) was injected into the blastocoel of stage 9 embryos, and PGs were purified at stage 22. The PGs were extracted in 4 M guanidine, 50 mM sodium acetate, pH 5.8, 0.1% Triton X-100, 1 mM EDTA, 10 mM N-ethylmaleimide and protease inhibitors. The extraction buffer was exchanged to 6 M urea, pH 5.5, 0.1% Triton X-100, 1 mM EDTA, 0.2 M NaCl and protease inhibitors, and the PGs were anion-exchange purified using a DE52 gel. The purified labeled PGs, desalted with water, were treated with lyases as described above. The samples were subsequently deaminated in nitrous acid at pH 1.5 to degrade heparan sulfate (Shively and Conrad, 1976).
Proteoglycan labeling using dissociated cells of ten isolated CNC explants, which was adapted in consideration of the low number of available cells, was performed by changing the culture medium with a fresh medium that contained 2 mCi [35S]sulfate/ml and 10 µM sodium sulfate, and cultivating the cells for 24 h at 17°C. The culture medium was removed, and the cells were washed and solubilized with the urea-containing buffer as described above, followed by anion-exchange purification and HS degradation as described above. The CS/DS PGs were re-isolated by anion-exchange purification and desalted. Lyase treatment was performed as described above.
The control and lyase-treated, labeled PGs were analyzed by SDS-PAGE as previously described (Pacheco et al., 2009b); alternatively, they were applied to a size-permeation Superose 6 column (GE Healthcare) and run in the urea-containing buffer as previously described, and the eluted fractions were counted by β-scintillation.
Immunoblotting of DS-epi1
Ten embryos were lysed in modified Barth solution (MBS) (88 mM NaCl, 1 mM KCl, 0.7 mM CaCl2, 1 mM MgSO4, 2.5 mM NaHCO3, 5 mM HEPES, pH 7.4), 1% Triton X-100, 5 mM EDTA and proteinase inhibitors for 30 min on ice and centrifuged at 10,000 g for 30 min at 4°C. The protein content was measured using the Bradford method (Bio-Rad), with BSA as the standard. Equal protein amounts were separated on 8% SDS-PAGE, and immunoblotting was performed using an immunopurified anti-DS-epi1 antibody (1 μg/ml) (Pacheco et al., 2009a).
Immunoprecipitation of integrin α5
Twenty CNC explants from stage 18 embryos were incubated in Ca2+- and Mg2+-free MBS for 1 h at 12°C, and the dissociated cells were labeled with 500 μl of a 2 mg/ml sulfo-NHS-LC-biotin solution (Pierce, 21335) for 20 min at 15°C. After three washes with 100 mM of a glycine solution, the cells were lysed in MBS, 1% Triton X-100, 5 mM EDTA and proteinase inhibitors. Following centrifugation at 12,000 g for 30 min at 4°C, immunoprecipitation was performed overnight with 10 μg of anti-Intα5 antibody (P8D4, a kind gift from Dominique Alfandari, University of Massachusetts, MA) loaded on Protein A/G agarose beads (Invitrogen, 20423). The beads were washed three times in Tris-buffered saline (TBS) that contained 1% Triton X-100 and once in TBS, treated with lyases and ultimately eluted in 2× non-reducing Laemmli Buffer. Proteins were separated by 8% SDS-PAGE, transferred onto nitrocellulose and detected with horseradish peroxide (HRP)-conjugated streptavidin (Invitrogen, 1:75,000).
Immunoblotting of integrin β1 and Flag-Sdc4
Cleared lysates from the epidermis-enriched explants of 12 uninjected embryos were lysed in MBS, 1% Triton X-100, 5 mM EDTA and proteinase inhibitors for 30 min on ice, centrifuged at 10,000 g for 30 min at 4°C and dialyzed with 10 mM sodium acetate pH 7.0. The protein content was measured using the Bradford method (Bio-Rad), with BSA as a standard. Equal protein amounts were treated with lyases as described above.
Epidermal explant lysates from embryos injected into the animal hemisphere with Flag–Sdc4 mRNA and uninjected controls were diluted 1:3 in 9 M urea, pH 5.5, 1 mM EDTA, 0.1% Triton X-100, 0.2M NaCl and protease inhibitors, and were anion-exchange purified using 20 μl of DE52 gel. The released proteoglycans in 2 M ammonium bicarbonate, 0.05% Triton and BSA, which was added as a carrier, were diluted 1:10 in water and lyophilized. Equal parts of the resuspended PGs were treated with lyases. Then, equal protein amounts were separated by 8% SDS-PAGE, and immunoblotting was performed using a monoclonal anti-Intβ1 antibody (8C8, 1:140, DSHB) and HRP-conjugated anti-Flag antibody (1:1000, Sigma, A8592).
Fluorescence-activated cell sorting
To assess cell viability, dissociated cells from 20 CNC explants were incubated with 10 μg of propidium iodide (PI) and analyzed ∼2 h after extraction by performing FACS, with BD FACSCalibur™ and BD cellQuest™ pro software for acquisition. Analyses were performed with Flojow version X. To monitor the cell cycle, dissociated CNC cells were fixed with ethanol at 4°C overnight. The cells were subsequently washed and incubated with 10 μg of RNase A for 15 min. Prior to the analyses, the cells were incubated with 10 μg PI.
Gene expression analyses
Two publically available datasets, which comprised 498 neuroblastoma tumors (Wang et al., 2014) and 44 metastatic melanomas (Bogunovic et al., 2009), respectively, were obtained from the NCBI GEO website (http://www.ncbi.nlm.nih.gov/geo/; accession numbers GSE62564 and GSE19234, respectively). Ranked gene lists of the correlations between all genes and DSE expression were produced using Pearson correlations. A gene set enrichment analysis (GSEA; Subramanian et al., 2005) was subsequently performed on the ranked gene lists using the c2.v5 curated gene set collection available from the Molecular Signatures Database (MsigDB; broad.mit.edu/gsea/msigdb).
We thank Drs D. Alfandari, E. Bellefroid, R. Harland, J. Larraín, J. Liu and G. Schlosser and the Japanese National Bio-Resource Project (Xenopus) for reagents, as well as Drs Eric Théveneau, John Couchman, Yingyu Sun and Xiaolong Fan for discussion and comments regarding the manuscript. We are especially grateful to Dr Benny Pacheco and Franziska Wetzel for cloning pCS2-Dse* and pCR-XL-TOPO-Dsel.L, respectively, Christian Holmgren, Ignacio Prusén, Niklas Ortenlöf, Petter Karlsson and Magnus Moding for technical assistance, and Teona Roschupkina for help with the cell sorting.
The authors declare no competing or financial interests.
N.G., M.M. and E.M.P. designed the research; N.G., M.M. and I.S. performed the experiments; N.G., M.M., K.v.S. and I.S. analyzed the data; A.M. contributed to the discussion; and N.G., M.M., K.v.S. and E.M.P. wrote the manuscript.
This work was financially supported by the Vetenskapsrådet (Swedish Research Council) [grant numbers 2009-4951 to E.M.P. and 2012-2631 to A.M.]; the Barncancerfonden (Swedish Childhood Cancer Foundation) [grant numbers PROJ11/101 to E.M.P. and NBCNSPDHEL12/012 to N.G.]; and the Cancerfonden (Swedish Cancer Foundation) [grant number 140530 to M.M.].
Supplementary information available online at http://dmm.biologists.org/lookup/suppl/doi:10.1242/dmm.024661/-/DC1
- Received January 12, 2016.
- Accepted April 18, 2016.
- © 2016. Published by The Company of Biologists Ltd
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.