- Research article
- Open Access
Structure and epitope distribution of heparan sulfate is disrupted in experimental lung hypoplasia: a glycobiological epigenetic cause for malformation?
BMC Developmental Biology volume 11, Article number: 38 (2011)
Heparan sulfate (HS) is present on the surface of virtually all mammalian cells and is a major component of the extracellular matrix (ECM), where it plays a pivotal role in cell-cell and cell-matrix cross-talk through its large interactome. Disruption of HS biosynthesis in mice results in neonatal death as a consequence of malformed lungs, indicating that HS is crucial for airway morphogenesis. Neonatal mortality (~50%) in newborns with congenital diaphragmatic hernia (CDH) is principally associated with lung hypoplasia and pulmonary hypertension. Given the importance of HS for lung morphogenesis, we investigated developmental changes in HS structure in normal and hypoplastic lungs using the nitrofen rat model of CDH and semi-synthetic bacteriophage ('phage) display antibodies, which identify distinct HS structures.
The pulmonary pattern of elaborated HS structures is developmentally regulated. For example, the HS4E4V epitope is highly expressed in sub-epithelial mesenchyme of E15.5 - E17.5 lungs and at a lower level in more distal mesenchyme. However, by E19.5, this epitope is expressed similarly throughout the lung mesenchyme.
We also reveal abnormalities in HS fine structure and spatiotemporal distribution of HS epitopes in hypoplastic CDH lungs. These changes involve structures recognised by key growth factors, FGF2 and FGF9. For example, the EV3C3V epitope, which was abnormally distributed in the mesenchyme of hypoplastic lungs, is recognised by FGF2.
The observed spatiotemporal changes in HS structure during normal lung development will likely reflect altered activities of many HS-binding proteins regulating lung morphogenesis. Abnormalities in HS structure and distribution in hypoplastic lungs can be expected to perturb HS:protein interactions, ECM microenvironments and crucial epithelial-mesenchyme communication, which may contribute to lung dysmorphogenesis. Indeed, a number of epitopes correlate with structures recognised by FGFs, suggesting a functional consequence of the observed changes in HS in these lungs. These results identify a novel, significant molecular defect in hypoplastic lungs and reveals HS as a potential contributor to hypoplastic lung development in CDH. Finally, these results afford the prospect that HS-mimetic therapeutics could repair defective signalling in hypoplastic lungs, improve lung growth, and reduce CDH mortality.
The majority of the extracellular proteins involved in regulating embryonic development interact with heparin/heparan sulfate (HS), and, moreover, require HS for their cellular activities . These include proteins required for lung morphogenesis [2, 3]. For example, not only are fibroblast growth factors (FGFs) essential for lung development [4–10], but they require HS for FGF receptor activation and subsequent signalling [11–13]. Due to its vast interactome and location at the cell surface and within the extracellular matrix (ECM), HS is ideally positioned to integrate biochemical regulators of lung development with mechanical stimuli required for normal lung growth [14, 15].
HS is a linear polysaccharide consisting of N-acetyl glucosamine-glucuronic acid disaccharide repeats. Chains are variably modified by N-deacetylation/N-sulfation of N-acetyl glucosamines, O-sulfation at various positions and conversion of glucuronic acid to its C-5 epimer, iduronic acid. These modifications do not occur at every potential site within a chain, resulting in a diverse range of HS chain structures displayed by a cell . Moreover, HS is post-synthetically remodelled by 6-O-endosulfatase enzymes, which selectively remove sulphate groups [16–18]. HS chains are usually attached to core proteins to form HS proteoglycans (HSPGs), which are expressed by most mammalian cells and represent a major component of the cell surface and ECM. Individual cells of a tissue display a variety of HS chains, which, in addition to being structurally complex and diverse, are dynamic, altering over time and with cellular physiology . Since interactions between HS and proteins are mediated by specific HS structures, changes in HS structure in vivo are likely to alter HS:protein binding events and related signalling. Characterising HS fine structure in vivo is, therefore, important as it equates to a view of HS function.
Obtaining structural information on native HS is challenging due to the non-template nature of HS biosynthesis (unlike proteins or nucleic acids). Tissue HS is typically analysed by extraction and purification. However, the inherent averaging of this approach limits the information to an overall assessment of the mixed population of HS structures present, and all spatial information is lost. In addition, due to the relative low immunogenicity of HS, only a limited number of HS specific monoclonal antibodies are available [19–21]. However, single chain variable fragment (scFv) antibodies generated by bacteriophage ('phage) display methodology [22, 23] allow specific classes of structures in HS to be probed in situ. We have demonstrated recently that these antibodies display distinct specificities for different HS structures in vitro and, therefore, the individual HS epitopes they recognise, though structurally complex, are unique . Limited analysis of one antibody shows that these probes are suitable to identify the diversity of HS in different cellular compartments of fetal lungs .
HS plays a fundamental role in airway morphogenesis. In Drosophila and mice, disrupted HS biosynthesis in vivo results in defective airway branching, which in the mouse, results in lethal neonatal respiratory insufficiency [26–29]. In addition, digestion of endogenous HS in cultured lung explants using heparitinases or inhibition of HS sulfation with sodium chlorate, disrupts branching [30, 31]. Further compelling evidence for a critical role of HS in lung disease is the association in humans and mice of mutations in the HSPG, glypican-3, with lung hypoplasia and congenital diaphragmatic hernia (CDH), known as Simpson-Golabi-Behmel syndrome [32–35]. It is, therefore, clear that HS is crucial for lung development and identifies HS as a potential contributor to pulmonary pathologies such as pulmonary hypoplasia in CDH .
CDH is characterised by a diaphragmatic defect, herniation of abdominal contents into the thoracic cavity and pulmonary hypoplasia. The high neonatal morbidity and mortality is largely attributed to severe respiratory insufficiency resulting from hypoplastic lung growth and pulmonary hypertension. Hitherto, most work exploring the pathogenesis of human birth defects has focussed on the identification of changes in gene expression and/or in protein levels. However, very few truly genetic causes of these defects have been identified. Since strong evidence supports a central role for HS as a master regulator of extracellular proteins controlling embryogenesis, we have investigated HS structure during development of the lung, and in the pathogenesis of CDH and pulmonary hypoplasia using HS specific 'phage display antibodies. We utilised the teratogen-induced rodent model of CDH, which uses nitrofen (2,4-dichlorophenyl-p-nitrophenyl ether) to induce congenital malformations in the offspring of treated pregnant dams with striking similarity to human CDH [36–38]. Here, we demonstrate that HS undergoes structural alterations during normal lung development and that there are pronounced abnormalities of HS structure and epitope distribution in hypoplastic lungs. Aberrations in epithelial basement membrane structure and composition were also identified in hypoplastic lungs, reflecting a specific abnormality in the ECM. The functional importance of these changes to HS structure during normal development and in hypoplastic lung is illustrated by our finding that a number of the HS epitopes are analogous to structures recognised by the critical morphogenetic growth factors, FGF2 and FGF9. Hence, these novel glycobiological defects may contribute to defective lung morphogenesis via altered interactions between HS and key signalling molecules such as FGFs. In addition, altered contacts between the ECM and cell surface are likely to interrupt mechanotransduction across a tissue, which is crucial for morphogenesis. HS may, therefore, play significant biochemical and biomechanical roles in the pathogenesis of pulmonary hypoplasia in CDH.
Seven HS 'phage display antibodies were chosen on the basis that they have been raised against HS/heparin from a variety of tissue sources and display distinct binding specificities, which we have characterised in depth . The data on antibody binding specificities and epitope structures are summarised in Table 1.
HS structure changes during normal rat lung development
One particular HS epitope recognised by HS4C3V was not identified in developing rat lungs of any age. The use of adult rat kidney as a positive control demonstrates that this structure is indeed absent from lung (Figure 1). The remaining six antibodies show distinct patterns of staining in fetal rat lungs, and the various lung compartments display different HS structures (additional files 1, 2, 3, 4, 5 and 6, summarised in Table 2). For example, in airway epithelium, HS structures recognised by EV3C3V, AO4B08V and HS3A8V are displayed, whereas the other three antibody epitopes are not. At E13.5, only the EV3C3V HS epitope is displayed by the epithelium, and at E15.5, the AO4B08V and HS3A8V HS epitopes are also present (Figure 2). The spatial localisation of these HS epitopes was shown to change during lung morphogenesis, indicating alterations in the structure of native HS chains during mammalian lung development (Figures 1 and 3 and additional files 1, 2, 3, 4, 5 and 6). For example, the HS epitope recognised by HS3A8V is displayed exclusively by epithelial basement membranes at E13.5 at a high level. At the early pseudoglandular period (E15.5), this structure is additionally displayed at a high level throughout the mesenchyme and by the airway epithelium. At the late pseudoglandular period (E17.5), mesenchymal expression of this epitope remains high; however, distribution of the structure becomes particularly concentrated around smaller developing airways and epithelial staining is no longer present. At canalicular (E19.5) and saccular (E21.5) fetal stages, HS3A8V epitope levels in the mesenchyme decrease and epitope distribution becomes more widespread (Figure 3 and Table 2). In contrast, the HS epitope identified by EW4G1V is not present in E13.5 rat lungs; however, at E15.5 it is detected in epithelial basement membranes and in the surrounding mesenchyme at a low level (Figure 3 and Table 2). At E17.5, levels of this HS epitope drastically increase, particularly in epithelial basement membranes, while epitope levels in the mesenchyme remain low and its distribution becomes concentrated around smaller distal airways. From E19.5 - E21.5, distribution of the EW4G1V epitope becomes more widespread throughout the mesenchyme (Figure 3 and Table 2).
In the pulmonary vasculature, HS3B7V shows a unique staining profile, specifically highlighting regions in the outer tunica media of arterial walls (Figure 4). This HS structure is absent from the inner medial layer, in contrast to the other five antibody epitopes, which were present and showed comparable vascular staining, highlighting the medial layer of both arteries and veins, predominantly the basal lamina surrounding smooth muscle cell layers (Figure 4).
HS structure is abnormal in hypoplastic lungs from nitrofen-induced CDH
Identification of HSPGs with the 3G10 antibody, which recognises the neo-epitope generated on all HSPGs following heparitinase digestion of the HS chains, indicated that there is no gross disruption in the overall spatial localisation of HSPGs in hypoplastic lungs. However, levels of HSPGs are reduced, particularly at E15.5 - E17.5 and in epithelial basement membranes (Figure 5A). Analysis of specific HS epitopes with 'phage display antibodies indicated an abnormality in the fine structure of HS in hypoplastic lungs, which was also more marked in lungs of earlier gestation (Figures 5, 6 and 7, summarised in Table 2). Levels of a number of HS epitopes are reduced (AO4B08V) or lost (HS3A8V, EV3C3V and EW4G1V) from the airway epithelium at E15.5 and E17.5 compared to normal lungs (Figure 5B and Table 2). Moreover, all of the HS structures analysed are displayed at a lower level by epithelial basement membranes. Although a number of HS structures are also shown to be reduced in hypoplastic lung mesenchyme (HS4E4V, HS3A8V and AO4B08V at E15.5 - E17.5) (Figure 5C and additional files 2, 3 and 4), HS structural alterations are more complex than a simple reduction or loss of epitopes. Levels of the HS epitope identified by EV3C3V are increased in hypoplastic lung mesenchyme, and in addition, the spatial distribution of this HS structure is abnormal (Figure 6 and Table 2). In E15.5 - E17.5 control lung mesenchyme, a gradient of EV3C3V epitope distribution is observed, with sub-epithelial areas adjacent to smaller, distal airways displaying high epitope levels and more proximal regions of the lung displaying a lower level of the structure. However, in nitrofen treated hypoplastic lungs, this gradient is not present and epitope distribution is more widespread throughout the entire lung mesenchyme (Figure 6 and Table 2). At E19.5 - E21.5, EV3C3V epitope levels and distribution are comparable to that observed in control lungs.
Pulmonary arteries of nitrofen-treated hypoplastic lungs have thickened vessel walls with increased smooth muscle content, contributing to the persistent pulmonary hypertension associated with CDH [39–41]. Although we confirmed marked thickening in arterial walls of nitrofen-treated lungs, no difference in HS or HSPG staining was observed. All HS antibodies highlighted the tunica media, with five predominantly staining the basal lamina surrounding the layers of smooth muscle and HS3B7V specifically highlighting an outer region of the arterial walls.
HS/HSPG staining identifies abnormalities in epithelial basement membranes
Abnormalities in epithelial basement membrane HSPG expression and HS structure were identified in hypoplastic lungs. Basement membranes appear thinner, and levels of both HSPGs (Figure 7A) and specific HS epitopes (Figure 7B and 7C) are reduced. In addition, staining with HS antibodies revealed discontinuities in basement membrane HS distribution, which are not observed with 3G10 immunohistochemistry.
To examine the general structure of epithelial basement membranes in hypoplastic lungs and evaluate whether abnormalities are HS/HSPG specific, hypoplastic rat lungs were probed with an antibody to laminin (Figure 7D), an integral component of basement membranes. Immunohistochemical detection of laminin indicated that epithelial basement membranes are indeed thinner; however, no discontinuities in laminin staining were observed (Figure 7D). The abnormally fine laminin staining of epithelial basement membranes was more pronounced in lungs at the pseudoglandular stages of development (E15.5 and E17.5), reminiscent of HS and HSPG basement membrane staining.
Functional analysis of HS epitopes using ELISA
To further our understanding of the functional consequences of abnormal HS structure identified in hypoplastic lungs, we analysed the specificities of the HS antibodies in competition ELISAs with FGF2 and FGF9, which are known to be involved in lung morphogenesis [4, 42–44]. The relative binding affinities of FGFs for HS epitopes were evaluated by determining IC50 values, defined as the concentration of FGF that inhibits antibody binding to HS by 50% (Figure 8). This allowed us to investigate possible overlap between antibody epitope structures and FGF binding sites in HS, to identify potential biological functions of the antibody epitopes.
FGF2 competed for all six antibody epitopes to varying extents (Figure 8A and 8B), whereas FGF9 only competed for two antibody epitopes, recognised by HS3B7V and HS3A8V (Figure 8C and 8D). The ability of FGF2 to compete for HS3B7V, HS4E4V and HS3A8V epitopes was similar, with IC50 values of 150 nM ± 2.8 nM, 130 nM ± 26 nM and 130 nM ± 1.9 nM. FGF2 also showed comparable competition for AO4B08V and EW4G1V epitopes, with IC50 values of 85 nM ± 4.2 nM and 94 nM ± 7.1 nM. Significant competition for the EV3C3V epitope structure in HS was achieved with FGF2, with an IC50 value of 9.3 nM ± 2 nM. In contrast to FGF2, FGF9 only competed with two antibodies, HS3B7V and HS3A8V, for HS binding, with IC50 values of 670 nM ± 18 nM and 1.8 μM ± 0.81 μm, respectively (Figure 8C and 8D).
Discussion and Conclusions
HS is a master regulator of morphogenesis and is essential for lung development. In the present study, we have demonstrated spatiotemporal alterations in HS structure and distribution during normal and hypoplastic lung development using HS specific 'phage display antibodies. Moreover, we show that a number of antibody epitopes are also structures recognised by FGFs, suggesting that abnormal distribution of these epitopes in hypoplastic CDH lungs may alter FGF binding, with functional consequences for morphogenesis.
HS structure in normal fetal rat lungs
A number of HS scFv antibodies have been used previously to analyse HS structures in adult human lungs . Only one of these antibodies used in the previous work is used in the present study (EV3C3V). In adult lungs, the EV3C3V HS epitope is identified in airway epithelial cells and their underlying basement membranes and in basement membranes surrounding smooth muscle cells of blood vessels . We also identified the EV3C3V epitope in epithelial and smooth muscle cell basement membranes at all developmental stages (Figures 2, 4, 6 and additional file 5) and in airway epithelial cells at E13.5 - E17.5 (Figure 2). This demonstrates a degree of conservation in HS structure between species.
We demonstrate that distinct cellular compartments of the lung display a variety of HS chains of different structure, which are modified during lung development, with temporal variation in both expression level and spatial localisation of HS epitopes identified by HS antibodies.
The epitope for one antibody, HS4C3V, was not identified in fetal lungs, however, it was present in kidney tissue (Figure 1) and has previously been detected in immunoblots of solubilised fetal lung extracts . This raises the possibility of cryptic binding sites for the antibodies in situ, and is an important consideration when interpreting immunohistochemical data, i.e., the absence of an epitope in situ does not necessarily mean it is not present in a tissue, rather, the epitope may be masked, for example, by endogenous proteins bound to HS. The antibodies, therefore, specifically highlight free binding structures in HS. Indeed, occupied, cryptic binding sites in HS in situ have been identified previously in growing mammary glands probed with FGF2 .
The antibody binding specificities (Table 1) suggests the nature of the observed changes in HS structure that occur in developing lungs. For example, the HS4E4V HS epitope is not found in E13.5 lungs, and at E15.5 - E17.5, the epitope is identified in the mesenchyme surrounding distal, but not proximal airways (Figure 1 and additional file 2). This can be explained by contrasting patterns of sulfation, e.g., highly sulfated HS modified with both 6-O- and 2-O-sulfates are located in the mesenchyme surrounding proximal airways, while less sulfated HS, modified by 6-O- or 2-O- sulfates is found in mesenchyme surrounding distal airways, where it offers optimal binding for HS4E4V . In contrast to HS4E4V, HS3A8V binds to more highly sulfated HS, particularly N-sulfated sequences (Table 1), and displays a wider epitope distribution throughout fetal lung mesenchyme (Figures 1 and 3). Hence, more highly sulfated HS in proximal mesenchyme may allow binding of HS3A8V, but not HS4E4V, while a more heterogeneous population of HS structures in distal mesenchyme, allows binding of both.
The localisation of specific HS structures within the developing lung and their importance for the coordination of branching morphogenesis has been hinted at in previous studies, e.g., expression of the epitope recognised by the HS specific monoclonal antibody, 10E4, was shown to alter rapidly with lung growth in vitro . In addition, blanket addition of heparin to lung cultures lacking endogenous sulfated GAGs after sodium chlorate treatment results in generalised epithelial expansion, indicating a global growth response, rather than defined branching . These data, together with ours, suggest that distinct HS structures are specifically displayed by the various lung cell types to direct localised signalling and spatiotemporally restricted morphogenetic cues, e.g., epithelial budding. In addition, modification of HS fine structure during development, together with alterations in HS microenvironment via dynamic HS:protein interactions, will influence crucial cell-cell and cell-matrix communication governing lung morphogenesis. HS structural dynamics are, therefore, likely to be an important regulator of fetal lung morphogenesis.
HS structure and epitope distribution are abnormal in hypoplastic CDH lungs
Using the nitrofen rat model of CDH, we investigated the potential role of HS in hypoplastic lung development, since HS has been shown to be crucial for normal lung morphogenesis. In addition, it has been shown previously that nitrofen-exposed rat lung explants respond abnormally to exogenous FGF1 and FGF2 and also heparin, suggesting a possible defect in the FGF:FGFR:HS signalling system [47, 48]. Notably, in humans, a mutation in the gene encoding the HSPG, glypican-3, features multiple congenital anomalies, including CDH [32–35].
Following analysis of HS fine structure and its developmental regulation during normal rat lung morphogenesis, HS structure and distribution was analysed in hypoplastic lungs from rats with nitrofen-induced CDH. In hypoplastic lungs, HSPG expression is reduced, and in addition, specific abnormalities in HS structure and spatial distribution were observed, which cannot simply be a consequence of an overall reduction in the level of HSPGs, since the level of some epitopes is increased, e.g., EV3C3V (Figure 6). As the overall distribution of HSPGs appears the same in control and hypoplastic lungs, abnormalities in the spatial distribution of specific epitopes is likely to reflect alterations in HS fine structure and irregular localisation of discrete HS structures displayed by the various lung cell types. In addition, the occupancy or availability of antibody binding sites may differ in hypoplastic lungs due to differences in protein binding events. It is of note that the molecular abnormalities highlighted in hypoplastic lungs are most striking at the pseudoglandular period of respiratory morphogenesis, when the lung is actively branching (E15.5 - E17.5) (Figures 5 and 6 and additional files 1, 2, 3, 4, 5 and 6). This supports previous work, suggesting that in CDH, lungs are intrinsically abnormal from early stages of organogenesis and that lung defects emerge in tandem alongside the hernia [49–51].
Abnormal HS structure has been shown to result in defective lung development in previous studies, e.g., in mice lacking HS biosynthetic enzymes, NDST-1 or C5-epimerase [27, 28]. In Drosophila, RNAi of HS 6-O-sulfotransferase (HS6ST) perturbs FGF signalling and disrupts primary branching of the tracheal system  and, similarly, a proportion of mutant Drosophila embryos lacking functional HS6ST develop tracheal branching defects . The generation of double mutants lacking functional 2-O-sulfotransferase (HS2ST) and HS6ST is completely lethal, with disrupted FGF signalling and a failure of tracheal precursor cells to migrate to form primary branches . In the mammalian lung, chemical inhibition of HS sulfation prevents FGF10 induced epithelial budding  and HS6ST1 deficient mice exhibit impaired alveolarisation . In contrast to previous studies where HS biosynthesis has been perturbed and effects on the lung sought, the present study investigates an established developmental malformation (pulmonary hypoplasia, CDH) to show for the first time that hypoplastic lungs feature substantial abnormalities of HS structure and epitope distribution. Moreover, previous studies in which HS has been disrupted, e.g., by deletion of genes encoding HS biosynthetic enzymes, have not characterised in any depth the actual effects on HS structure and epitope distribution in the malformed lung.
Changes in HS structure in the lung is likely to modify HS:protein interactions, since these rely on specific HS structures . This in turn, will affect various signalling systems, as HS:protein interactions have been shown to be functionally significant, regulating transport and effector functions of the protein ligand. For example, HS plays a key role in FGF signalling, which is fundamental for lung morphogenesis.
HS facilitates interactions between FGFs and FGFRs and is also required for sustained FGFR activation and subsequent cellular signalling [11–13]. Cells expressing FGFRs but lacking HSPGs are unresponsive to FGF unless heparin/HS is added [11, 12] and treatment of cells with sodium chlorate or heparinase blocks the biological activity of FGFs, an effect which can be restored by the addition of exogenous heparin . In an ex vivo model system of epithelial branching morphogenesis using mouse salivary gland, modification of FGF:HS binding affinities was shown to impact upon the morphogenetic effect of FGFs . FGF10 with a reduced affinity for HS (via single amino acid mutations in the heparin binding site), formed abnormal gradients due to altered transport properties, resulting in an induction of epithelial branching rather than elongation observed with wild type FGF10 . In contrast, reduced affinity of FGF10 for its receptor, FGFR2b, affected only the extent of the response, without altering the nature of the response.
Abnormal HS structure and distribution observed here in hypoplastic lungs can, therefore, be expected to contribute to defective lung morphogenesis via aberrant epithelial-mesenchymal signalling as a result of altered HS:protein interactions.
Competitive selectivity of FGFs and antibodies provides insight into structure:function relationships of epitopes and a functional consequence of abnormal HS in hypoplastic lungs
Competitive binding assays with FGFs and HS antibodies allowed us to demonstrate that antibodies recognise specific HS structures that are also recognised by key FGF morphogens, thereby revealing biological relevance of epitopes. Alterations in FGF bindings sites in the lung has previously been shown to have functional consequences for morphogenesis .
FGF2 is expressed in the developing lung and is important for lung morphogenesis [43, 44, 56]. The HS binding specificity of FGF2 is well characterised, requiring N-sulfated and 2-O-sulfated HS structures [57, 58] and at least a tetrasaccharide  for binding. In competitive binding assays, FGF2 competed with all six HS antibodies to varying extents. Of particular note is the effectiveness of FGF2 to compete with EV3C3V, which was significantly higher compared to competition with the other antibodies (Figure 8A and 8B). Previous characterisation of epitope structures reveals that EV3C3V binding structures are analogous to those recognised by FGF2. Both require N-sulfation and 2-O-sulfation for binding, with little sensitivity to the presence or absence of 6-O-sulfates (Table 1) [24, 57]. The other epitopes appear to overlap in part with structures recognised by FGF2, requiring a higher concentration of FGF2 to successfully compete with the antibodies. These structures may represent lower affinity binding sites for FGF2, which have been previously identified in HS .
Similarly, FGF9 is essential for normal lung development [4, 42, 61, 62]. In binding assays, FGF9 showed more selective competition than FGF2, competing only for the epitopes recognised by HS3B7V and HS3A8V (Figure 8C and 8D). Although the binding specificity of FGF9 is not as well characterised as that of FGF2, the competitive binding data for FGF9 illustrates the biological relevance of the observed variation in these epitopes in normal and hypoplastic prenatal lungs. FGF9 competes most effectively for HS3B7V epitopes, with an IC50 value almost three times lower than with HS3A8V (670 nM compared to 1.8 μM). We have previously shown that HS3B7V requires longer HS structures for significant binding (Table 1) , and this may also reflect the binding specificity of FGF9. As FGF9 has been shown to readily form homodimers in solution [63, 64], the requirement for longer HS structures for binding may not be that surprising.
Functional analysis of epitope structures enables us to suggest potential biological consequences of abnormal epitope distribution in developing lungs. In CDH hypoplastic lungs, the EV3C3V epitope was identified at a higher level compared to normal lungs, and in addition, was shown to be abnormally distributed in hypoplastic lung mesenchyme (Figure 6). This may indicate an increase in the number of EV3C3V epitopes and, therefore, structures recognised by FGF2, in the HS synthesised by the lung cells. Alternatively, the availability of these structures may be increased in the lung mesenchyme due to altered expression of proteins that bind this class of structures. Moreover, these lungs respond abnormally to FGF2 . Addition of FGF2 to nitrofen-treated lung explants results in increased lung area and formation of dilated, cystic airways, whereas FGF2 was shown to have minimal effect on the growth of control lung explants . Our data describing an increased number of available EV3C3V/FGF2 binding structures in the mesenchyme of hypoplastic lungs provides a possible explanation for this abnormal response to exogenous FGF2.
Epitopes analogous to structures recognised by FGF9, i.e., the HS3A8V and HS3B7V epitopes, were also abnormally expressed in nitrofen-treated lungs. Both epitopes were expressed at a reduced level in epithelial basement membranes and in addition, showed abnormal mesenchymal expression (Table 2 and additional files 1 and 3). The HS3B7V epitope was displayed at a low level in sub-epithelial mesenchymal compartments of E19.5 hypoplastic lungs, and this is a compartment which was not stained in normal lungs (Table 2 and additional file 1). The HS3A8V epitope was identified at a high level in sub-epithelial mesenchyme at E15.5 and E17.5 in normal lungs, however, in hypoplastic lungs, mesenchymal expression was reduced and the partitioning of HS3A8V staining in sub-epithelial and sub-mesothelial mesenchyme was not evident (Table 2 and additional file 3). Thus, these HS structures recognised by FGF9 are either synthesised at an abnormal frequency in HS chains, or the availability of these structures in HS chains is reduced in an irregular manner. FGF9 has been shown to be particularly important for mesenchymal growth and differentiation [4, 42, 62, 65] and mesenchymal-epithelial signalling through regulation of other morphogen expression levels . An abnormal distribution of HS structures able to bind FGF9 in the lung mesenchyme may, therefore, have a significant effect on FGF9 transport between cellular compartments and/or activity, including downstream effects on other morphogens regulated by FGF9, for example, SHH and FGF7 and FGF10 [42, 62]. Collectively, these data suggest that observed changes in HS structure in hypoplastic lungs is likely to result in altered interactions with critical regulatory proteins, such as FGFs, leading to irregular cell signalling and epithelial-mesenchymal cross-talk, which may ultimately contribute to defective lung morphogenesis.
Abnormal HS may help explain disrupted mechanobiology in hypoplastic lungs
The ECM facilitates communication between cellular and extracellular environments, including mechanotransduction [66–68]. Prenatal airway smooth muscle (ASM) exhibits periodic contractility resulting in rhythmic airway peristalsis, which moves lung liquid along the airways and induces a distending pressure in end buds, stretching the lung to promote growth [69–72]. Demonstrating a specific link between HS dependent signalling and airway contractility, FGF10 is synthesised by these ASM cells  and stimulates airway peristalsis . However, in hypoplastic lungs from the nitrofen CDH model, reduced FGF10 levels  accompany abnormal airway peristalsis [75, 76]. Given the large HS interactome, the structural changes in HS identified here provide a promising possible explanation for the mechanical abnormalities measured in hypoplastic lungs.
Epithelial basement membranes are abnormal in hypoplastic lungs
Basement membranes are specialised extracellular matrices underlying epithelial and endothelial cells  composed mainly of collagen IV, laminin, nidogen/entactin and proteoglycans including HSPGs, perlecan , agrin [79, 80] and collagen XVIII [81, 82]. HSPGs contribute to basement membrane assembly, structure and function: e.g., when grown in sodium chlorate, murine teratocarcinoma cells develop an incorrectly assembled basement membrane . In addition, heparin and HS influence associations between basement membrane components, laminin and collagen IV [84, 85]. HSPGs also regulate growth factor activity by controlling their transport through the matrix and sequestering them to form local reservoirs [86–89]. In the developing lung, basement membranes are pivotal for epithelial-mesenchymal cross talk and irregular assembly and structure of airway basement membranes is detrimental to lung morphogenesis [90, 91].
We have shown here that hypoplastic lungs exhibit abnormal epithelial basement membranes. Immunodetection of laminin, HSPGs and HS structures demonstrated an abnormally thinned basement membrane. Additionally, HS epitopes, but not HSPGs or laminin, were displayed discontinuously in hypoplastic lungs, suggesting abnormal localisation of HS epitopes and/or availability of binding sites in HS.
Current treatments for CDH primarily focus on postnatal management to address the consequences of pulmonary hypoplasia and hypertension, including strategies aimed at providing adequate tissue oxygenation via inhaled nitric oxide, high frequency oscillatory ventilation and extracorporeal membrane oxygenation (ECMO). However, CDH mortality has not been greatly improved. Results from the present work suggest that heparin/HS based therapeutics may be beneficial in ameliorating hypoplastic lung growth in CDH. Indeed, a number of glycotherapeutics are emerging for the repair of damaged tissue, e.g., skin and bone [92–96] and for the treatment of some cancers [97–99]. The morphogenetic effect of chemically modified heparins has previously been investigated in salivary gland branching morphogenesis . Using a similar rationale, investigating the effect of various engineered heparins on lung growth may help develop a class of HS structures able to ameliorate lung hypoplasia, reduce smooth muscle cell proliferation and increase vascular branching. With chemically modified heparins available, which possess low or zero anticoagulant activity , this is an exciting potential future therapeutic avenue.
Lung retrieval and induction of CDH
Timed-pregnant Sprague-Dawley rats (Charles River, UK) were gavage fed 100 mg nitrofen (2,4-dichloro-4'-nitrodiphenylether) (Zheijang Chemicals, Hangzhou, China) dissolved in olive oil on day 9.5 of gestation (vaginal plug positive, day 0) to induce left-sided CDH and pulmonary hypoplasia in newborn pups . Control animals received olive oil. Embryos and fetuses were harvested on embryonic day (E)13.5 (controls only), E15.5, E17.5, E19.5 and E21.5 of gestation by caesarean section under terminal anaesthesia (intraperitoneal sodium pentobarbitone). Lungs were dissected out and fixed in 4% (w/v) paraformaldehyde in phosphate buffered saline (PBS) (7.5 mM Na2HPO4, 2.8 mM NaH2PO4, 150 mM NaCl pH 7.4). Lungs were washed in PBS, cryoprotected with 20% (w/v) sucrose in PBS overnight and gelatine embedded. Gelatine blocks containing lung tissue were covered in Cryo-M-Bed (Bright, Huntington, UK) and snap frozen in cooled isopentane. Adult kidney was prepared in the same way. Tissue sections were cut at 8 μm on a cryostat, mounted onto chrome alum gel slides and stored at -40°C.
All animal procedures complied with the UK Animal (Scientific Procedures) Act 1986 and were conducted with UK Home Office approval, ref. PPL40/2293.
Slides were removed from - 40°C, allowed to thaw and rinsed in PBS. Sections were blocked in 10% (v/v) goat serum in PBS for 2 h at room temperature for all antibodies. Following immunohistochemistry, sections were mounted with fluorescent mounting medium. Scoring of staining was performed blind by two independent observers with images that were representative of at least three separate lung samples.
HS 'phage display scFv antibodies
HS antibodies were diluted 1/5 in 1% (v/v) goat serum in PBS and incubated with lung sections overnight at 4°C. Bound antibody was detected with rabbit VSV-G tag antibody (Abcam, Cambridge, UK), diluted 1/200 in 1% (v/v) goat serum in PBS, for 2 h at room temperature, followed by FITC conjugated goat anti-rabbit IgG (Sigma-Aldrich, Gillingham, UK), diluted 1/500 in the dark for 1 h. Controls were the omission of HS antibody or treatment of sections with heparitinase (EC 22.214.171.124) (IBEX Technologies Inc, Canada) overnight at 37°C (changing enzyme after 4 h), prior to antibody incubation, to remove HS epitopes.
HSPG specific antibody, 3G10
In order to reveal the 3G10 neo-epitope in tissue sections, endogenous HS was digested with heparitinase (EC 126.96.36.199) overnight at 37°C, replacing enzyme after 4 h. 3G10 antibody (Seikagaku/AMS Biotechnology, Oxon, UK) was diluted 1/200 in 1% (v/v) goat serum in PBS and incubated with lung sections overnight at 4°C. Bound antibody was detected using FITC conjugated goat anti-mouse IgG (Sigma-Aldrich, Gillingham, UK), incubated in the dark for 1 h. Controls were omission of 3G10 antibody or omission of heparitinase digestion to leave HS chains intact and the 3G10 neo-epitope unavailable.
Rabbit anti-laminin (Sigma-Aldrich, Gillingham, UK) was diluted 1/100 in 1% (v/v) goat serum in PBS and sections incubated overnight at 4°C. Bound antibody was detected with FITC conjugated goat anti-rabbit IgG, diluted 1/200 and incubated in the dark for 1 h.
FGF2 and FGF9 synthesis and purification
Full-length human recombinant FGF2 with an N-terminal hexahistidine tag was produced in E. coli exactly as described . FGF9 (Uniprot Accession: P31371; residues: 1-208) with a 6 × Histidine tag and a TEV cleavage site (26 amino acids, MKHHHHHHPMSDYDIPTTENLYFQGA) at the N-terminus was expressed in C41 E.coli cells using a modified pET-24b vector (pETM-11, kind gift from Dr Paul Elliott, University of Liverpool), which provides the sequences of the 6 × Histidine tag and the TEV cleavage site. Protein was produced in bacteria using an auto induction system . Cells were grown at 37°C, for 7 h in Terrific Broth, and FGF-9 production was induced at 22°C for 16 h. Cell pellets were lysed by sonication in Buffer A9 (0.3 M NaCl, 50 mM Tris, 1 mM DTT, pH7.4) with 0.2 mg/ml lysozyme (lysozyme, chicken egg white, Calbiochem, Nottingham, UK), 10 μg/ml DNase I (deoxyribonuclease I, from bovine pancreas, Sigma-Aldrich, Gillingham, UK), 1 tablet of protease inhibitor (complete EDTA-Free, Protease Inhibitor Cocktail Tablets, Roche, West Sussex, UK), 0.2% (v/v) Tween-20 and 5% (v/v) glycerol. The lysate was loaded onto 5 ml heparin agarose column (Affi-Gel Heparin Gel, Bio-rad, Hemel Hempstead, UK), which was washed with Buffer A9 until the absorbance returned to baseline. FGF-9 was eluted in Buffer B9 (50 mM Tris, 2 M NaCl, 1 mM DTT, pH 7.5). The eluate was diluted 4-fold with 50 mM Tris and applied to a 1 mL HiTrap column (GE Healthcare UK Ltd, Buckinghamshire, UK), and eluted with an imidazole gradeint (50 mM to 500 mM imidazole) in 0.5 M NaCl, 1 mM DTT, 50 mM Tris, pH7.5. Eluted protein was dialysed against 10 mM phosphate, pH 7.5, 1 mM DTT and then stored at -80°C.
Maxisorp 96-well microtitre plates were coated with 3 μg/ml streptavidin (Pierce Biotechnology, IL, USA) in 0.1 M Na2CO3/0.1 M NaHCO3 (pH 9.6) for 16 h at 4°C and then blocked with 1% (w/v) BSA in PBS with 0.05% (v/v) Tween-20 (PBST). Porcine mucosal HS (PMHS) was internally biotinylated with EZ-link NHS-LC-biotin (Pierce Biotechnology, IL, USA) as described previously  and plates coated with 100 μg/ml biotinylated PMHS for 2 h at room temperature and then washed with PBST. Fifteen μl of HS antibody was added to each well with 15 μl competitor FGF and incubated overnight at 4°C. Antibody dilutions were determined in a titre and were used at final concentrations of; HS3B7V 1/5, HS4E4V 1/2, HS3A8V 1/20, AO4B08V 1/5, EV3C3V 1/10 and EW4G1V 1/2. FGF2 (1.2 mg/ml) and FGF9 (2.2 mg/ml) in sodium phosphate buffer, pH 7.4 were diluted in 1% (w/v) BSA in PBST to the required concentrations. For a positive control, HS antibodies were added to wells alone, without FGF competitor and for a negative control, HS antibodies were added to wells lacking biotinylated HS. Plates were washed in PBST and bound HS antibody was detected with mouse anti-VSV-G IgG (clone P5D4) (Abcam, Cambridge, UK) diluted 1/2000 in 1% (w/v) BSA in PBST followed by HRP-conjugated sheep anti-mouse IgG (GE Healthcare UK Ltd, Buckinghamshire, UK) diluted 1/2000 in 1% (w/v) BSA in PBST. After a final wash in PBST, plates were developed with o-phenylenediamine (0.8 mg/mL) (AbD Serotec, Oxford, UK) containing 0.03% (v/v) hydrogen peroxide. The reaction was stopped with 0.5 M H2SO4 and absorbance read at 492 nm.
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This work was supported by the Human Frontiers Science Program, the Birth Defects Foundation, the Biotechnology and Biological Sciences Research Council (United Kingdom), the Cancer and Polio Research Fund and the North West Cancer Research Fund. ECJ is supported by an MRC New Investigator Award.
SMT carried out all the experimental work and wrote the manuscript. MGC carried out animal dissections and assisted in experimental work. RX synthesised and purified FGF2 and FGF9 proteins. THvK provided the phage display antibodies, gave advice on their application and contributed to experimental design of the study. JET, ECJ, DGF and PDL conceived of the study, participated in its design and coordination, obtained funding and edited the manuscript. All authors read and approved the final manuscript.
David G Fernig and Edwin C Jesudason contributed equally to this work.
Electronic supplementary material
Additional file 1: HS3B7V. Immunohistochemical staining of E13.5 - E21.5 normal lungs and E15.5 - E21.5 hypoplastic lungs with HS3B7V. The HS3B7V HS epitope is localised to the epithelial basement membrane in both control and hypoplastic lungs from E15.5. However, in hypoplastic lungs, expression of this HS structure is reduced and staining of epithelial basement membranes is irregular. In addition, in nitrofen E19.5 lungs, there is additional weak staining identified in sub-epithelial mesenchyme. As a negative control, endogenous HS was digested with heparitinase prior to antibody incubation. (aw) airway, (mes) mesenchyme, (ep) epithelium, (bm) basement membrane, (br) bronchus. (PDF 161 KB)
Additional file 2: HS4E4V. Immunohistochemical staining of E13.5 - E21.5 normal lungs and E15.5 - E21.5 hypoplastic lungs with HS4E4V. In normal lungs, the HS4E4V HS epitope is present in epithelial basement membranes and the surrounding mesenchyme, particularly in sub-epithelial areas adjacent to distal airways. In hypoplastic lungs, expression of this epitope is severely reduced, particularly in epithelial basement membranes and mesenchyme of E15.5 and E17.5 lungs. As a negative control, endogenous HS was digested with heparitinase prior to antibody incubation. (aw) airway, (oe) oesophagus, (mes) mesenchyme, (ep) epithelium, (bm) basement membrane, (br) bronchus. (PDF 167 KB)
Additional file 3: HS3A8V. Immunohistochemical staining of E13.5 - E21.5 normal lungs and E15.5 - E21.5 hypoplastic lungs with HS3A8V. In normal lungs, the HS epitope recognised by HS3A8V is restricted to epithelial basement membranes at E13.5. From E15.5, distribution of the epitope is more widespread and is present in epithelial basement membranes and throughout the mesenchyme, particularly in sub-epithelial mesenchyme. Epithelial cells also display this HS structure transiently at E15.5 and (more weakly) at E17.5. In hypoplastic lungs, mesenchymal expression of the HS3A8V epitope is reduced, particularly at E15.5 and E17.5, and epithelial staining observed in normal lungs is lost. Additionally, irregularities in epithelial basement membrane staining are observed. As a negative control, endogenous HS was digested with heparitinase prior to antibody incubation. (aw) airway, (mes) mesenchyme, (ep) epithelium, (bm) basement membrane, (br) bronchus. (PDF 182 KB)
Additional file 4: AO4B08V. Immunohistochemical staining of E13.5 - E21.5 normal lungs and E15.5 - E21.5 hypoplastic lungs with AO4B08V. Expression of the AO4B08V HS epitope increases during the course of normal lung development. At E13.5, it is only weakly expressed by epithelial basement membranes, and at E15.5, is additionally displayed at a low level in the mesenchyme and airway epithelium. From E17.5 - E21.5, levels of this epitope increases in basement membranes and throughout the mesenchyme. In hypoplastic lungs, however, expression of the AO4B08V epitope is reduced in the epithelium and underlying basement membranes, and in addition, basement membranes appear discontinuous. In lung mesenchyme, however, the AO4B08V epitope structure is displayed at a higher level compared to normal lungs. As a negative control, endogenous HS was digested with heparitinase prior to antibody incubation. (aw) airway, (mes) mesenchyme, (ep) epithelium, (bm) basement membrane, (br) bronchus. (PDF 170 KB)
Additional file 5: EV3C3V. Immunohistochemical staining of E13.5 - E21.5 normal lungs and E15.5 - E21.5 hypoplastic lungs with EV3C3V. In normal lungs, the EV3C3V epitope is displayed by the epithelium at E13.5 - E17.5 and in the underlying basement membranes at E13.5 - E21.5. A gradient of epitope expression is observed in the mesenchyme, with highest levels in sub-epithelial mesenchyme around smaller, distal airways and lower levels in sub-mesothelial mesenchyme. However, in hypoplastic lungs, this gradient of mesenchymal expression is lost, and the EV3C3V epitope is more extensively and evenly distributed throughout the entire mesenchyme. In addition, epithelial staining is lost from hypoplastic lungs and basement membrane staining is irregular. As a negative control, endogenous HS was digested with heparitinase prior to antibody incubation. (aw) airway, (mes) mesenchyme, (ep) epithelium, (bm) basement membrane, (br) bronchus. (PDF 178 KB)
Additional file 6: EW4G1V. Immunohistochemical staining of E13.5 - E21.5 normal lungs and E15.5 - E21.5 hypoplastic lungs with EW4G1V. In normal developing lungs, the HS structure identified by EW4G1V is absent at E13.5. From E15.5 onwards, however, it is present in all epithelial basement membranes and also at a low level in the mesenchyme, with increased levels at E21.5. This epitope is transiently expressed by the epithelium at E15.5. In hypoplastic lungs, levels of this epitope appear to be raised somewhat in the mesenchyme compared to normal lungs and simultaneously reduced in epithelial basement membranes. As a negative control, endogenous HS was digested with heparitinase prior to antibody incubation. (aw) airway, (mes) mesenchyme, (ep) epithelium, (bm) basement membrane, (br) bronchus. (PDF 161 KB)
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Thompson, S.M., Connell, M.G., van Kuppevelt, T.H. et al. Structure and epitope distribution of heparan sulfate is disrupted in experimental lung hypoplasia: a glycobiological epigenetic cause for malformation?. BMC Dev Biol 11, 38 (2011) doi:10.1186/1471-213X-11-38
- Congenital Diaphragmatic Hernia
- Congenital Diaphragmatic Hernia
- Pulmonary Hypoplasia
- Hypoplastic Lung
- Epithelial Basement Membrane