The cellular basis of bioadhesion of the freshwater polyp Hydra
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The freshwater cnidarian Hydra temporarily binds itself to numerous natural substrates encountered underwater, such as stones, leafs, etc. This adhesion is mediated by secreted material from specialized ectodermal modified cells at the aboral end of the animal. The means by which Hydra polyps attach to surface remain unresolved, despite the fact that Hydra is a classic model in developmental and stem cell biology.
Here, we present novel observations on the attachment mechanism of Hydra using high pressure transmission electron microscopy, scanning electron microscopy, atomic force microscopy, super-resolution microscopy, and enzyme histochemistry. We analyzed the morphology of ectodermal basal disc cells, studied the secreted material, and its adhesive nature. By electron microscopy we identified four morphologically distinct secretory granules occurring in a single cell type. All the secretory granules contained glycans with different distribution patterns among the granule types. Footprints of the polyps were visualized under dry conditions by atomic force microscopy and found to consist of a meshwork with nanopores occurring in the interstices. Two antibodies AE03 and 3G11, previously used in cell differentiation studies, labelled both, basal disc cells and footprints. Our data suggest that the adhesive components of Hydra are produced, stored and delivered by a single cell type. Video microscopy analysis corroborates a role of muscle contractions for the detachment process.
We clearly demonstrated that bioadhesion of Hydra relies on the secreted material. Our data suggest that glycans and/or glycoproteins represent an important fraction of the secreted material. Detachment seems to be initiated by mechanical forces by muscular contractions. Taken together, our study represents the characterization of an unique temporary adhesive system not known in aquatic organisms from other metazoan phyla.
KeywordsHydra Basal disc Biological adhesion Adhesion
Aquatic organisms, freshwater and marine, have evolved a myriad of effective solutions for underwater adhesion. Cases range from microscopic organisms, such as bacteria, through much larger and complex marine algae, invertebrates, and vertebrates. Examples include the permanent attachments of sessile mussels  and barnacles [2, 3], the temporary attachment of starfish and flatworms during locomotion [4, 5], the construction of protective shelters by sandcastle worms , and the defence against predators by the Cuverian tubules of sea cucumbers . All these bioadhesives were adapted by natural selection for specific roles in the organism’s life style. Likewise, the way they attach are also remarkably complex and involve a large range of interactions and components with different functions [8, 9]. Generally, these multicomponent adhesives are composed of protein, carbohydrates, and inorganic components. The amount of each component is highly variable in different organisms. For instance, in sea stars 21 % are proteins, 8 % carbohydrates, and 40 % inorganic material . On the contrary, in barnacles 90 % of the adhesive is made out of proteins with the remainder being 1 % carbohydrates, 1 % lipids, and 4 % inorganic material . Mussels have one of the best studied bioadhesive systems [12, 13]. These marine molluscs routinely stick to all kinds of surfaces underwater using their so-called byssus. This structure consists of a protein complex secreted as a fluid that spreads spontaneously and exhibits strong reversible interfacial bonding and tunable cross-linking. Similarly, the sabelariid polychaete sandcastle worm Phragmatopoma californica [6, 14] secretes microdroplets of adhesive to build a tube-like burrow from sand grains and other particles. Alternatively, the marine flatworm Macrostomum lignano, possesses a duo-gland adhesive system in the tail plate  that allows it to adhere and release from the substrate multiple times within seconds. The different characteristics of all these adhesives are often derived from the physico-chemical properties of the adhesive proteins, and in particular, from their post-translational modifications (PTM), such as hydroxylation, phosphorylation, and glycosylation [15, 16]. Some organisms contain glycans associated with the adhesive proteins, but it is unknown whether they are covalently attached to the proteins [10, 17].
Hydra is a classical model organism in axial pattern, regeneration, and stem cell biology [22, 23, 24, 25, 26]. In contrast to the existing detailed information about differentiation and regeneration of the ectodermal basal disc cells, only few studies have addressed Hydra’s astonishing attachment ability. The ultrastructure of ectodermal basal disc cells was studied by Chaet  and Philpott et al.  who provided a first description of Hydra’s secretory granules. They placed these granules in three categories, two of them representing the same type of granule in different stages of matureness, while the third granule is of a different type. Further, Davis  proposed that basal disc cells produce, by themselves or jointly with other cells, at least six types of granules, and a seventh one that originates from the neighbouring digestive cells. The only constituent identified inside the basal disc cells is the presence of hyaluronic acid as seen after an Alcian Blue [28, 29] and PAS staining . At the ultrastructural level, granules between 0.5 and 1.5 μm in diameter are known to be peroxidase positive . The mode of action and the components of the secreted adhesives are not understood. Enlarged cytoplasmic protrusions which were named as filopodia were observed during Hydra attachment by Pan et al. .
In this study, our goal was to characterize the cellular components responsible for Hydra’s underwater adhesion. Light-and electron microscopic techniques were utilised for a comprehensive description of basal disc morphology of free and attached polyps. Additionally, morphology and adhesiveness of the secreted material (footprint) was analysed using atomic force microscopy. To investigate the components involved in adhesion, we first used energy electron loss spectroscopy to identify nitrogen and phosphorus atom distribution. Second, the periodic acid-Schiff reaction was carried out to verify the presence of glycans, and diamino benzidine was used to attest peroxidase activity. The localisation of two antigens labelled by two antibodies was confirmed to be present in the footprints. Finally, we showed that lipids most probably do not play a role in Hydra adhesion. We suggest that detachment is driven by muscular activity. After investigating all these components, we paved the way for Hydra as a model organism for bioadhesion research using molecular approaches . It provides the basis for our current efforts to uncover the biochemical basis of the glue of Hydra.
Basal disc cell morphology and secretion of adhesive granules
The detachment process was recorded with video microscopy (Additional file 1). In the beginning, the full basal disc was attached. The polyp started the detachment from the outer rim towards the center of the basal disc. When the detachment got closer to the center, Hydra suddenly detached the last cells. A footprint was left behind which was transparent underwater (Additional file 1). Phalloidin staining revealed the actin filament distribution in the basal disc (Additional file 2). Within the ectodermal layer the myonemes were radially distributed (Additional file 2: Figure S2 a and b). From the radial myonemes a branch of myonemes goes perpendicularly towards the apical side of ectodermal basal disc cells (Additional file 2: Figure S2 c). This distribution of myonemes was corroborated by transmission electron microscopy experiments (Additional file 3: Figure S3 a). Within the endodermal layer they were circular (Additional file 2 Figure S2 a and b). Based on these observations, we propose that muscle contractions of the two cell layers (ectoderm and endoderm) of the basal disc were involved in the detachment of the animals.
The air dried footprints were easily located using phase contrast and could be precisely positioned beneath the AFM cantilever. Care was taken to select a scan site near to the rim of the footprints and to avoid regions that were too thick to image. When visualized through AFM, the footprints of Hydra were found to be a meshwork with nanopores occurring in the interstices of the deposited material (Fig. 5a). The secreted material seems homogeneous, traces of individual secretory granules cannot be detected. Several pores of about 0.5–1 μm where present at the surface of the footprint whose diameter correlated to the one of the protruded cytoplasmic extensions. The adhesion profile (Fig. 5b) showed that adhesive forces were higher in the deeper (thinner) areas of the footprint, reaching up to 66.4 nN. In summary, the AFM results corroborate the adhesive nature of the secreted material.
Chemistry of granules
Diamino benzidine treated polyps allowed to visualize peroxidase activity in the basal disc of Hydra (Fig. 6e and f). The reaction was stronger close to where exocytosis takes place. The peroxidase reaction was associated with HSGI (Fig. 6g and h), but not for all the granules. Peroxidase activity was also detected at the level of cytoplasmic components surrounding HSGII.
Based on information from other model organisms, in which lipids played an important role in adhesion [33, 34], the occurrence of lipids was investigated in the present study using Nile Red on Hydra whole mounts. When exposing stained specimens to both blue (450–500 nm) and green (550 nm) exciting light, dispersed droplets of lipids measuring between 1 and 1.8 μm were visible in basal disc cells (Additional file 5), but apparently not associated to secretory granules. Lipid droplets were also not observed in the footprints (data not shown). Therefore, these results support a view that lipids do not play a critical role in the adhesion process of Hydra.
Electron energy loss spectroscopy (EELS) and electron spectroscopic imaging (ESI) experiments allowed to determine the distribution of nitrogen and phosphorus on high-pressure freezing ultrathin resin sections from cryofixed specimens. Among the secretory granules, high contents of N atoms were found in HSGI and II (Additional file 6), demonstrating their protein nature. P atoms were observed in HSGI and II (Additional file 6) although at a lower density when compared to N atoms. In summary, EELS and ESI showed the presence of proteins and potentially post-translationally modified by phosphorylation, in some granules of basal disc.
In organisms well-known for their capacity to adhere temporarily, such as free living flatworms  and sea stars  the adhesive mechanism relies on a duo-gland system where two or more secretory cell types collaborate in a way that allows attachment and detachment by using adhesive and de-adhesive components. The number of cell types are variable, free living flatworms enclose one adhesive and one de-adhesive cell, while sea stars have two adhesive and one de-adhesive cell type. Some parasitic flatworms possess two different glands producing dissimilar adhesive components, while cells producing de-adhesive constituents are absent . In contrast, substrate detachment in Hydra is mediated by differentiated epithelia muscle cells of the ectoderm of basal disc. EM observations on secretory granules morphology in these cells [28, 29] with additional information on the molecules present. We have identified four morphologically distinct secretory granules (HSGs) as a major component of the basal disc cells that could be involved in adhesion although it remains unclear to which degree each granule type contributes to the adhesion process. We classified the HSGII as a mature granule derived from the HSGI, because these two granules share biochemical features, they are the only ones of protein nature, and contain phosphor. We also observed possible transition stages from HSGI to HSGII. Another feature is that HSGI is never seen close to the most-apical side of the cell. However, we have no direct proof for granule maturation. Therefore, this process must be further addressed in order to understand granule development.
The component that is actually labeled by the antibodies was not precisely identified. However, super-resolution microscopy experiments (Fig. 7d and h) showed that both antibodies stained granular structures that are eventually secreted and become a constituent of the secreted material. The footprint of Hydra is a meshwork of quite homogenous strands. The starfish and sea cucumber footprint have a similar meshwork morphology [7, 39], but contain globular nanostructures which are absent in Hydra. In the case of Hydra, all HSG have spherical morphology before release and are not recognizable in the footprint. The contents of the granules seem to have merged or fused into larger aggregates forming the strands. In the footprints of sea cucumber , adhesive forces of 17nN were measured under dry conditions, and for the rootlets of the English ivy  298 nN. Our measurements of Hydra footprints showed an adhesion force as high as 66 nN. Measurements in natural Hydra living conditions (i.e., under freshwater) would be necessary for a better understanding of its footprint adhesion forces. Yet, despite repeated attempts, the topographical visualization of the footprints under native conditions in culture medium was not possible, due to the transparent nature of the footprints. New technical developments would be needed to provide an appropriate contrast for identifying the footprint underwater.
Glycans are considered important components for temporary adhesives, e.g., in cephalopods, gastropods, and echinoderms [10, 17, 41, 42, 43]. Permanent glues seems to be generally composed mainly of protein. Glycans have not been considered as an important moiety, though reported from mussels, stalked and acorn barnacles, sandcastle worms, and caddisfly larva [2, 11, 44, 45]. Although previous reports showed alcian blue staining of basal disc cells of other Hydra species [28, 29], our alcian blue experiments performed at pH-value 2.5, staining was negative for H. magnipapillata. In Hydra, EM cytochemistry showed that glycans occur in all the HSG, with differential distributions (the present study). The presence of phosphor (P) in HSGI and II raises the question about possible protein phosphorylation of the Hydra adhesive. Phosphorus in the form of phosphate group may indeed be involved in phosphorylation, a PTM which confer additional functionalities to proteins, including adhesive proteins . Phosphoproteins have been identified in a number of aquatic adhesives, e.g., in adults and larvae of barnacles [3, 34], in the caddisfly larvae , in mussels , in sandcastle worms , in sea cucumbers , and in kelp spores . Although, covalently attached phosphate groups are usually present at substoichiometric levels (less than 5 % of the protein is modified) in intracellular proteins [50, 51], their proportion is usually much higher in extracellular structural proteins such as adhesive proteins. For instance, in Pc3 an adhesive protein from the sandcastle worm, up to 90 mol% (residues per 100 residues) of the serine residues are modified by phosphorylation . The P concentration observed within HSGII (Additional file 6) is lower than that of N (Additional file 6). Both, glycosylation and phosphorylation, could be important in the adhesion process of Hydra.
Peroxidase activity in the basal disc of Hydra [52, 53] has been used as an important biochemical marker for tracking the reappearance of basal disc cells during polyp regeneration . The Hydra genome  encodes five isoforms of putative peroxidases. Their functional significance for the animal is still under debate [55, 56], but most likely they play several roles. The obtained results are similar to the ones described earlier for other Hydra species . Although peroxidase-like enzymes are highly concentrated in basal disc cells, it is not the adhesive per se, and its role in Hydra’s adhesion remains to be elucidated. The peroxidase-like enzyme could catalyse the crosslinking of other components to post-draw the secreted adhesive as it occurs in the freshwater caddisfly silk . Furthermore, it is well known that peroxidase-like enzymes possess antimicrobial features , and can function to either foster beneficial relationships or control pathogenesis. During the attachment process, the basal disc secretes a protein-rich adhesive material which might serves as a nutrient source for bacteria and the peroxidase may have a protective role, reducing bacterial biodegradation over the time protein needs for curing. The combination of both functions, i.e., curing and antimicrobial, may occur in Hydra adhesion, though the functional significance of this is yet to be examined.
In various organisms, detachment from temporary adhesion is controlled by additional secretory products, enzymes, or by creating forces. However, the detachment processes are largely not well understood. The observations on Hydra presented here support the hypothesis that its detachment is mechanically induced (Additional files 1 and 2). If chemical detachment were the case, the basal disc would detach at once, and individual basal disc cells would not be seen detaching individually. When detachment is necessary, myonemes within both ectoderm (radial myoneme) and endoderm (circular myoneme) composing the basal disc contract, leading to an expansion of both radial and circular myonemes. This retracts the attached cells from the surface that in combination with the longitudinal myonemes contracting the vacuoles of water which expels water into the footprint meshwork would pull the polyp off the cured adhesive.
This study showed that cnidarian Hydra polyps secrete elaborate adhesive composites underwater (freshwater) to temporarily anchor themselves to substrate surfaces. The adhesive system used by Hydra exhibits unique features among metazoans. Glue based adhesion is the main component of the system: basal disc cells release their adhesive vesicles whose contents would have the ability to spread over the surface, displace water, and create a proper environment for curing the secreted glue. Projecting structures were observed, but the way they functions is enigmatic. The adhesive components of Hydra are produced, stored and delivered by a single cell type, the ectodermal basal disc cells. Our results revealed that the secretory granules contained glycans and phosphorus, which are important components in other bioadhesive systems. A Peroxidase-like enzyme was associated with secretory granules and could play a role in Hydra adhesion. This work was intended to offer a first overview of the Hydra adhesive system. The characteristics presented here provide a basis for an ongoing project aimed at unravelling the molecular components of Hydra’ glue.
Hydra magnipapillata strain 105 was used for all the experiments carried out in this study in compliance with animal welfare laws and policies (Austrian Law for animal experiments, TVG 2012, §1). Permanent mass cultures were bred and kept at 18 °C in growth chambers, and day/night light cycle at the Institute of Zoology, University of Innsbruck. Hydra cultures were fed five times per week with freshly hatched Artemia nauplii as previously described . Under these conditions, animals remained asexual and reproduced by budding. We selected animals that had at least one bud. Animals were starved for 24 h before experiments. Before fixation, animals were relaxed in 2 % urethane in culture medium for 2 min.
For bright field or differential interference contrast visualization, processed samples were examined with a Leica DM5000. Images were taken with a Leica DFC495 digital camera and a Leica LAS software.
Footprint: To collect Hydra’s footprints, polyps were placed onto glass slides and allowed attach for 30 min. After this period, polyps were gently detached with the help of a glass pipet. Glass slides bearing footprints were rinsed three times with Hydra culture medium before staining. Fresh footprints were stained using a 0.05 % solution (in culture medium) of Crystal Violet, and rinsed in culture medium.
Squeezing preparations: Living polyps were anesthetized in a 2:1 mixture of 2 % Urethane and culture medium, transferred in a drop onto a slide and slightly squeezed under a coverslip. The specimens were observed with interference contrast under the same microscopy as mentioned above.
Histology: Adult Hydra polyps were fixed in Carnoy’s fixative (ethanol, chloroform, glacial acetic acid, 6 + 3 + 1 respectively), Bouin’s fluid (saturated picric acid, 36 % formaldehyde, and glacial acid, 15 + 3 + 1 respectively), 4 % paraformaldehyde (PFA) in 0.1 M Phosphate Buffer (PBS)) and/or in Flemmings fixative (1 % chromium (VI) oxide, 2 % osmium tetroxide and glacial acetic acid, 15 + 4 + 1 respectively), dehydrated and embedded into paraplast or in Technovit 7100 resin. Paraplast sections (7 μm) and resin sections (3 μm) were produced with a Reichert Autocut 2030 (Reichert, Austria) and stained with hematoxylin and eosin (HE), periodic acid Schiff (PAS), or alcian blue (AB) pH 2.5.
Enzymehistochemistry: For peroxidase activity, Hydra polyps were fixed with 4 % PFA in 0.1 M PBS, stained with diamino benzidine (DAB + CHROMOGEN, Dako) post fixed either with 2.5 % glutaraldehyde or 1 % osmium tetroxide, dehydrated and embedded in PolyBed 812 resin. Semi thin sections (350 nm to 500 nm) were cut with a Leica ultra-microtome UCT (Leica, Austria) and stained according to Richardson et al. .
Lipid staining: PFA fixed polyps were stained with the fluorescence Nile Red method as whole mounts for lipid detection following method used by Gohad et al. . Negative controls were performed by exposing specimens to ETOH washes. Whole mounts were visualized under a Leica SP5 II confocal laser scanning microscope.
Two antibodies labelling basal disc cells were used: AE03 [35, 36], and 3G11  were kindly provided by the corresponding authors. The antibody staining method was slightly modified from the original protocols. Experiments were performed on whole mount, macerated cells and footprints. Samples were mounted in Vectashield (Vector), and visualized with a Leica DM5000, or a Leica SP5 II confocal scanning microscope. For super resolution microscopy, macerated cells samples were mounted in Mowiol and examined with a Leica TCS SP8 gSTED microscope system. Obtained super-resolution images were deconvoluted using the Huygens software from Scientific Volume Imaging implemented in the TCS SP8.
Whole mount preparation: For AE03 labelling, whole polyps were fixed in Zamboni’s fixative (2 % PFA, 0.2 % picric acid in 0.1 M PBS pH 7.2). For 3G11 labelling, whole polyps were fixed in 4 % PFA. Both fixations were done at 4 °C overnight. The following steps were applied to both antibodies: After three washes with PBS, the polyps were permeabilized with 0.5 % Triton in PBS for 30 min, and incubated with 0.5 % Triton, 1 % bovine serum albumin (BSA, w/v) in PBS with primary antibody (dilutions = AE03 1:5, and 3G11 1:1000) overnight at 4 °C. After this period, polyps were washed three times in PBS, and incubated for 2 h with fluorescein isotthiocyanate-conjugated (FITC) antimouse lgG (Dako) secondary antibody (1:200). Polyps were washed again three times in PBS and mounted.
Macerated cells: Basal discs (from approx. 150 polyps) were excised and incubated in 200 μl maceration medium (acetic acid, glycerol, and distilled water, 1:1:7) for 2 h at 30 °C. Basal discs were then mechanically disrupted by shearing them through the opening (roughly 1 mm diameter) of a pipette. The same amount of fixative, either Zamboni or PFA, were added to the medium containing cells and gently mixed. 50 μl of the sample were spread onto gelatine-coated slides and allowed dry for 20 min at RT. Steps for antibody staining were as for whole mount. Differences were a Triton concentration of 0.1 %, and an incubation time for the secondary antibody of 4 h. Slides were additionally counterstained with the DNA-specific fluorochrome, Hoechst 33342 (Life Technologies; 1 μg/ml). Samples examined with super-resolution microscopy were incubated with antimouse abberior STAR 488 (Abberior) secondary antibody diluted 1:100.
Footprint: Secreted material was collected on glass slides as described for light microscopy purposes. Immunofluorescence staining with AE03 and 3G11 was carried out as described above.
We tried to elucidate the subcellular binding of AE03 and 3G11, but several different immunogold approaches failed: i) post-embedded immunogold on both, cryo and chemically fixed material , ii) post-embedded immunogold on thawed cryosections according Tokuyasu , and iii) pre-embedded with horseradish labelled streptavidin conjugated antibodies.
Configuration of actin filaments in the basal disc were detected by phalloidin staining. Experiments were performed using amputated basal discs. Animals were let to attach to a glass slide for approximately 1 h and were then amputated. Basal discs were fixed with 4 % PFA for 1 h at room temperature, then washed three times for 10 min in PBS- 0.5 % Triton, and then incubated in Alexa 488 phalloidin (Invitrogen) in a concentration of 1:400 for 1 h at RT in the dark. Afterwards, they were washed three times for 10 min with PBS. Samples were mounted in Vectashield (Vector), and visualized with a Leica SP5 II confocal scanning microscope.
Scanning electron microscopy
Hydra polyps were fixed in 4 % PFA for 24 h. They were dehydrated in graded ETOH, dried by the critical point method (with CO2 as transition fluid), mounted on aluminium stubs, coated with gold in a sputter coater, and observed with a JEOL JSM-6100 scanning electron microscope.
Transmission electron microscopy
Conventional chemical fixation and cryofixation were performed basically as described by Holstein et al. . Chemical fixation: Hydra polyps were allowed to attach on a dialysis membrane, relaxed in 2 % urethane for 3 min and immediately fixed with a combined 2.5 % glutaraldehyde and 1 % osmium tetroxide fixative, dehydrated in a graded acetone series and embedded in Polybed 812 resin.
High pressure freezing (HPF) and freeze substitution
Basal discs were dissected and frozen with a HPM-010 (HPF apparatus from BAL-TEC, Baltzers, Liechtenstein), freeze substituted with acetone containing osmium tetroxide and uranyl acetate, and embedded into PolyBed 812 as previously described . Thick sections (350 nm) and ultrathin sections (70 nm) were cut with a Leica ultra-microtome UCT (Leica, Austria), mounted on copper grids and stained with uranyl acetate and lead citrate and examined with a Zeiss Libra 120 energy filter transmission electron microscope using zero loss electrons. Images were taken with a TRS 2048 high speed camera (Tröndle, Germany) and visualized through Olympus SiS iTEM 5.0 software.
Cytochemical detection of PAS-positive 1–2 vicinal diols was carried out according to Thiery . Sections from cryofixed samples were mounted on gold grids, exposed to periodic acid, thiocarbohydrazide, and silver proteinate. Negative control included omission of periodic acid treatment.
Peroxidase activity was detected in Hydra polyps fixed with 4 % PFA in 0.1 M PBS. They were stained with diamino benzidine (DAB + CHROMOGEN, Dako), and post fixation with 2.5 % glutaraldehyde/1 % osmium tetroxide, dehydration and embedding into Polybed 812. Images were taken without any further section post-staining. Controls included the inhibition of peroxidase activity by incubating samples in 3 % hydrogen peroxide for 20 min.
Electron energy loss spectroscopy (EELS) and electron spectroscopic imaging (ESI) were performed on ultrathin sections in order to detect element distribution in structures rich in nitrogen (N) and phosphorus (P) within the basal disc cells. The EELS charts and ESI images were collected using the software iTEM 5.0©. Distribution of N and P was measured according to a three-window power law difference ESI model with an energy slit width of 15 eV. Here, two background images and one image at the ionization edge of the appropriate element, K edge 397 eV for N and L2,3 edge at 129 eV for P were taken. Maximum element distribution was finally mix mapped with an inverted high contrast image taken at 250 eV.
The window-one was placed at 382 eV, the window-two at 350 eV, and window-three at 410 eV. The difference of the three windows coincide with the onset of the N –K ionization edge at 397 eV. The background image was set with the subtraction model obtained from the EELS analyses default, which ensures that only the energy loss from the ion under examination is mapped. Likewise, for constructing the distribution map of P, the window-one was placed at 121 eV, window-two at 110, and window-three at 153 eV. The energy-loss contribution of three windows coincide with the onset of P –L2,3 ionization edge of 129 eV.
Atomic force microscopy
Footprints from Hydra were collected on glass slides. The samples were let dry at room temperature and analyzed with Atomic Force Microscopy (AFM- Peak Force Tapping™, PFT). Data collection was achieved by applying controlled, low forces on the tip of the cantilever during imaging, which allows a direct comparison between the morphology and the adhesive properties at the nanometer (nm) scale. With the PFT method, an adhesion profile can be obtained by evaluating one force-distance curve for each pixel of the obtained image. Thereof, the adhesion force is defined as the maximum force needed to pull off the cantilever tip. The probe (silicon tip on silicon nitride cantilever—SNL, Bruker, Santa Barbara, CA, USA, k¼0.12 N/m) was calibrated on a stiff surface prior to the experiment for the measurements of the mechanical properties, in order to quantify the tip sample force.
AB, alcian blue; EELS, electron energy loss spectroscopy; EM, electron microscopy; ER, endoplasmic reticulum; ESI, electron spectroscopic imaging; HPF, high pressure freezing; HSG I-IV, Hydra secretory granule one to four; PAS, periodic acid Schiff
The authors are most grateful to Karin Gutleben and Thi Chinh Ngo for excellent assistance for high pressure freezing/freeze substitution, and atomic force microscopy, respectively. We are indebted to Marina P. Samoylovich, Yoshitaka Kobayakawa, and Alexander V. Klimovich for kindly providing the antibodies used in this study. We also thank Martin Offterdinger for support during SP8 experiments.
MR was supported by Marie-Curie FP7-PEOPLE-2013-IEF 626525 fellowship, and COST Action TD0906. The project was also supported by Austrian Science Fund (FWF) grant 25404-B25.
Availability of data and material
The datasets supporting the conclusions of this article are included within the article and its additional files.
MR and PLa conceived the study, performed experiments and wrote the paper. PLe performed and supervised AFM experiments. PF contributed to electron microscopy. MWH contributed to cryo-based electron microscopy and (immune) cytochemistry. WS performed histological and ultrastructural experiments. BH contributed on light microscopy, and cell macerations and Hydra biology. All authors have read and approved the manuscript.
The authors declare that they have no competing interests.
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