Nanostructured Graphene Surfaces Promote Different Stages of Bone Cell Differentiation
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KeywordsCarbon nanowalls Graphene films Bone cell Cell differentiation Plasma nanoscience
Horizontally and vertically oriented carbon nanowalls (CNWs) have diverse influences on cell behavior.
The graphene-based topographies are nontoxic and support cell adhesion and growth.
Early cell differentiation was observed on the hybrid graphene layer surfaces. Later cell differentiation was stimulated by the CNW films.
The synergy between the CNWs and differentiation medium provides enhanced mineralization.
The use of nanomaterials for biological control has been a recurring topic of study over the past decades [1, 2, 3, 4, 5, 6, 7]. In addition to conventional chemical stimulus strategies, nanomaterials possess reduced-scale features that provide physical control over bacteria and cells [3, 4, 5, 6, 7, 8]. Designed nanofeatures are capable of directing and applying forces to cells in order to trigger the activation and/or suppression of genes involved in a number of cellular processes, such as cell adhesion, proliferation, and differentiation (a process where cells become another cell type) [1, 9, 10, 11, 12]. Therefore, the use of nanomaterials presents an interesting opportunity to control the fate of cells for the development of biomedical technologies, such as cell therapies and tissue engineering.
Graphene has attracted considerable attention in the biomedical field owing to its unique and specific properties [12, 13, 14, 15, 16]. The chemistry of carbon is well known, which makes graphene a useful material for molecular attachment and functionalization. The potential toxicity of graphene and its derivatives (e.g., a solution of graphene nanoplatelets) has been investigated to determine their capabilities for applications in biomedicine [17, 18, 19, 20]. For each nanostructure and variations on functionalization and concentration, different results were obtained. Studies on the interactions of graphene coatings/films with cells, using cell-based assays conducted in vitro, have also been reported. Glass and silicon coated with graphene films showed noncytotoxic responses and have been demonstrated to allow the proliferation of diverse types of cells [12, 21, 22, 23, 24, 25, 26].
Recent reports have described the use of graphene-based nanostructures to control the differentiation of neural cells [17, 27]. Glass coated with single-layer graphene, in combination with growth factors and proteins, was used to enhance the differentiation of human neural stem cells into neurons . Another study showed that reduced graphene oxide films could support the proliferation of neural stem cells and enhance their specific differentiation . The effects of graphene films on cellular responses were also investigated using human osteoblasts (Saos-2 bone-like cells) and mesenchymal stem cells (MSCs) for bone regeneration applications . Results showed that graphene films presented no cytotoxic effects on these cell types and were supportive of both cell adhesion and proliferation . Interestingly, although the use of graphene films did not influence the overall proliferation rate of MSCs, it did promote their differentiation into the bone pathway more efficiently than did differentiation factors alone . The origin of the enhanced bone differentiation of cells on graphene films was also explored [21, 22, 23]. It was found that graphene adsorbed osteogenic inducers that promote the differentiation of the cells into bone-forming cells while suppressing the differentiation of cells toward the adipogenic lineage (fatty tissue). These studies provide evidence of the impact of graphene on bone tissue engineering and its applications.
In addition to the chemical interaction between graphene and biological molecules, some of these reports mentioned the presence of topographical features on the graphene surface, such as wrinkles and ripples, as being a contributing factor in the cellular interactions [18, 21, 23, 25, 29, 30]. Despite the potential impact of these topographical nanofeatures in carbon-based materials, their intentional use to control cellular behavior has been poorly explored. The few examples include the use of vertically aligned carbon nanotubes and carbon nanowalls (CNWs) [31, 32]. However, to the authors’ best knowledge, no published study has been specifically designed to compare the effects of graphene-based topographies containing nanoscaled features (e.g., CNWs) with those of horizontally oriented graphene on the control of the cellular response.
Among graphene-based materials, CNWs possess a unique morphology, being composed of few-layer graphene sheets oriented vertically on a substrate, which gives them an inherently high aspect ratio [33, 34, 35]. The nanowalls have the advantages of carbon’s ability to bind biologically important molecules, specific properties of graphene-like materials, and the ability to provide topographical cues at the cellular level. The vertical nature and inherent topological effects are of particular importance as platforms for cellular attachment and for control of cells via mechanical stress. CNWs can be produced by a simple, reproducible, technologically sustainable, and unique plasma process [36, 37, 38]. This plasma-enhanced chemical vapor deposition (PECVD) technique has demonstrated improved control over the CNW structures at relatively low temperatures, and it is also possible to fabricate films with horizontal and vertical CNWs of a similar thickness and size and therefore similar (nontopological) properties [32, 36, 39]. Furthermore, this PECVD process allows chemical-free transfer of the CNW films onto the desired substrates, thereby reducing the risk of contamination with hazardous chemicals, which is of great importance when considering biological interactions .
In this study, we investigated the ability of different graphene-like films produced by the PECVD system to control the differentiation of Saos-2 cells into bone-like cells in vitro. The CNW films were compared with horizontally oriented graphene sheets that were produced using the same PECVD method with the same composition. This ensured similarity of the chemical properties on both surfaces, with the nanotopography being the only difference between them. The impact of defined graphene-surface nanotopography on cellular processes (including cell adhesion, proliferation, and differentiation stages) was examined using quantitative cell-based assays with the Saos-2 cell line, which is a human bone cell line that is known to differentiate in vitro when provided with specific culture medium supplements.
3.1 Growth and Chemical-Free Transfer of the Graphene Nanostructures
The growth of the graphene nanostructures was carried out in a radio-frequency (RF) inductively coupled plasma CVD system, as described in previous reports [35, 36, 37, 38, 40]. A piece of copper foil (99.95%, Alfa Aesar) of 4 × 4 cm2 dimensions was used as the growth substrate and placed on a stage in the plasma chamber. First, a gas mixture of 10 sccm argon (Ar) and 20 sccm hydrogen (H2) was fed into the chamber, and a pressure of 1.5 Pa was set. The plasma was then produced using 750 W from an RF power supply and a matching network. The copper foil was treated for 3 min with the H2–Ar mixture, following which methane was fed into the chamber for 6 min. The density of the graphene nanowalls was controlled by varying the H2 flow rate supplied during deposition. For this work, a high H2 content (80 sccm) was used to produce fewer and thinner CNWs, whereas a lower H2 content (20 sccm) generated denser and thicker CNWs on the copper foil. No external substrate heating was used; however, the substrate temperature reaches ~ 250 °C owing to plasma heating effects . Next, all produced CNW films were decoupled from the copper foil using deionized water. The foil was placed in the water and sink while the graphene film was left floating on the water surface. Subsequently, the films were transferred onto Thermanox™ coverslips for biological characterization. These substrates (made by Nunc and purchased from Thermo Fisher Scientific, Australia) are made from a hydrophilic polyester film with very low oxygen content and are highly resistant to solvents. Uncoated Thermanox™ coverslips were used as the experimental control. Therefore, by simply controlling the H2 content, the same production and transfer processes yielded two different topographies. The first comprised a dense CNW surface, and the second consisted of thin CNWs oriented horizontally with very few standing CNW sheets [hereafter named as hybrid graphene layers (HGLs)].
3.2 Material Characterization
The topography of the graphene nanostructures was studied by field-emission scanning electron microscopy (FE-SEM), and images were obtained with a Zeiss Auriga microscope operated with 5 keV electron beam energy and an InLens secondary electron detector. Raman spectroscopy was carried out on the graphene nanostructures, using a Renishaw inVia spectrometer with laser excitation at 514 nm (Ar laser) and a probing spot size of ~ 1 µm2. The hydrophobicity of the samples and of the uncoated coverslip control was determined using contact angle measurement at room temperature, where a high-resolution optical camera and free image analysis software (ImageJ) were used to obtain the photographs and angles between a water droplet and the samples.
3.3 Sample Sterilization
All graphene films on Thermanox™ coverslips produced for the cell-based assays were sterilized in 70% ethanol overnight and then rinsed with phosphate-buffered saline (PBS) the following day. All cell culture procedures after this substrate sterilization procedure were conducted in a biohazard hood, using aseptic techniques.
3.4 Cell Adhesion and Proliferation
Cell adhesion and cell proliferation assays were conducted on the graphene films as well as on uncoated Thermanox™ coverslips and tissue culture polystyrene (TCPS) as controls. The cell adhesion studies were run over 24 and 48 h to examine the early adhesion and spreading behavior of cells, which were examined by light microscopy using phalloidin staining and also by SEM. The cell proliferation assay was conducted over 7 days to track the growth kinetics of the cells. All cell-based assays were conducted using a human bone-derived cell line (Saos-2), which is recognized to have the capacity to differentiate into mature bone-like cells that produce alkaline phosphatase (ALP) and a bone-like mineralized matrix when cultured under the appropriate mineralizing/differentiating (osteogenic) conditions [41, 42]. The Saos-2 cells were routinely grown in Dulbecco’s modified Eagle’s medium (DMEM)/nutrient mixture F-12 supplemented with 100 U mL−1 penicillin, 100 µg mL−1 streptomycin, 20 mM l-glutamine (all from Gibco, Australia), and 10% fetal bovine serum (FBS; Bovagen, Australia). For all cell adhesion and cell proliferation assays, triplicate samples of each graphene sample and control surfaces were placed in individual wells of a 24-well TCPS plate (Corning, Australia). Saos-2 cells were then seeded onto each surface at a concentration of 3 × 104 cells mL−1 (1 mL of cell suspension per well). The plates were maintained in an incubator at 37 °C in a humidified atmosphere containing 5% CO2 until the predetermined time points for each assay.
3.4.1 Cell Adhesion Study
The cell adhesion study was designed to monitor the early adhesion and spreading behavior of cells on the test surfaces to 24 and 48 h time points, and samples were evaluated using either phalloidin staining to identify the actin filaments of the cell cytoskeleton or SEM to probe the cell–material interactions at higher magnifications. Samples for phalloidin staining were transferred to the wells of a fresh TCPS plate and fixed in 4% formol saline for 30 min at room temperature. The cells were then permeabilized in 0.1% Triton X-100/PBS for 5 min at room temperature, blocked in 1% BSA/PBS for 60 min, and then stained with a 1/40 dilution of Alexa Fluor 647 phalloidin (Thermo Fisher Scientific, Australia) for 30 min at room temperature in the dark. Finally, the substrates were washed twice with PBS and the adherent cells were visualized under a fluorescence microscope with a TRITC filter (Nikon IIi) and images were captured with a digital camera. Samples for SEM were washed in PBS and fixed with 10% paraformaldehyde for 30 min at room temperature and then washed in PBS before dehydration. The samples were dehydrated using a series of ethanol solutions (increasing from 30 to 100% and repeating the last step) for 10 min at each step. Then, the samples were soaked in hexamethyldisilazane (Sigma, USA) for 2 min at room temperature and allowed to dry overnight in a desiccator. Finally, the samples were mounted on SEM stubs, coated with 10 nm gold film, and placed in a desiccator until viewed by SEM (same as for sample characterization).
3.4.2 Cell Proliferation Assay
The cell proliferation assay was designed to measure the growth of cells over a 7-day period at the predetermined time points of days 1, 3, and 7. One extra sample of each type of the graphene and control surfaces was included for cell staining and imaging on day 7 to check the morphology of cells on each substrate. At each of the three time points, one plate was removed and samples were transferred to the wells of a fresh TCPS plate for MTT assay to measure the viability/number of adherent cells on each graphene sample. An MTT assay is a colorimetric assay used to measure cell viability, in which the yellow-colored 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) is converted into dark-blue water-insoluble formazan crystals by the activity of mitochondrial dehydrogenases in living cells. After transferring samples to fresh plates, 10 µL of Thiazolyl Blue Tetrazolium Bromide reagent (MTT; Sigma #M5655) at a final concentration of 0.5 mg mL−1 in fresh serum-free medium was added to each well of the plates, which were then returned to the incubator for 4 h. After the incubation in MTT, the medium in each well was replaced with 1 mL of dimethyl sulfoxide, and the plates were shaken for 10 min to dissolve the formazan product. A 100-µL sample was then taken from each well and transferred to the wells of a 96-well plate for spectrophotometric determination at 595 nm using a plate reader (SpectraMax, Molecular Devices, USA). At day 7, the extra samples included for cell morphology examination were rinsed in PBS, and the adherent cells were fixed in 4% formol saline for 30 min at room temperature. After rinsing in PBS and staining with 0.4% trypan blue for 15 min at room temperature, the cells were rinsed in PBS and inverted onto a glass microscope slide in glycerol:PBS (1:1). Samples were viewed using both phase contrast and fluorescence microscopes set on FITC wavelength, as the Thermanox™ material is autofluorescent at FITC wavelength, allowing darkly stained cells adhered to the opaque substrates to be visualized and imaged.
3.5 Differentiation/Mineralization Assays
This experiment was designed to test the ability of the graphene films to support the differentiation of bone cells, with evidence of mineralization over a longer time period. Cell-based assays using Saos-2 cells were used to assess cell differentiation by measuring the cellular production of the ALP enzyme and calcium over a 25-day time period in culture. For the differentiation assay, each of the Thermanox™ coverslips coated with a graphene film was placed into an individual well of a 12-well TCPS culture plate. Thermanox™ coverslips without graphene films and TCPS wells with no substrates were also included as assay controls. Saos-2 cells were seeded onto the substrates and controls at a concentration of 5 × 104 cells cm−2 in standard Saos-2 culture medium, and the plates were then placed in a 37 °C incubator supplied with 5% CO2 in humidified air for 72 h to allow cell attachment and growth. After 72 h, the culture medium was removed and replaced with either (1) standard culture medium (DMEM/F12 containing 10% FBS) as an undifferentiated control culture regime, or (2) a differentiation/osteogenic-specific culture medium containing additives specifically known to promote cell maturation/differentiation along the osteogenic/bone lineage (DMEM/F12 containing 10% FBS, 100 U mL−1 penicillin, 100 µg mL−1 streptomycin, and 20 mM l-glutamine and supplemented with 1.5 mg mL−1 β-glycerophosphate, 40 ng mL−1 dexamethasone, and 20 µg mL−1 ascorbic acid). These two culture regimes were continued in both series of plates for the rest of the 25-day assay period, with the medium replenished every 3–4 days. On day 25, samples maintained on these culture regimes were assayed for the ALP and calcium contents in adherent cells (as described in Sects. 2.5.1, 2.5.2 below).
An extra complete set of samples and controls was established to run in parallel with the differentiation assay so that the growth of the Saos-2 cells on each graphene-coated substrate at day 25 could be evaluated by standard MTT assay (as described in Sect. 2.4.2). This enabled the differentiation/mineralization data (ALP and calcium) to be adjusted according to the number of cells attached to each test substrate and TCPS control at day 25.
3.5.1 Alkaline Phosphatase Assay
ALP is a by-product enzyme of active bone formation, which means its level increases when the bone matrix is being formed. Induction of ALP can thus be used to predict bone formation in vitro as well as to measure early-stage cell differentiation . ALP production was measured in cells attached to the graphene surfaces and controls at 25 days, using a quantitative assay based on p-nitrophenyl phosphate (p-NPP; Sigma #N-1891). In brief, 500 µL of p-NPP at a concentration of 1.0 mg mL−1 in 0.1 M glycine buffer was added to each well containing a Thermanox™ coverslip, and the plate was shaken at 37 °C for 60 min. Then, the reaction was neutralized by the addition of 500 µL of 1 M NaOH per well. The sample sets were compared against a standard curve prepared from a 10 µmol mL−1 stock solution of p-NPP diluted in 0.1 M glycine buffer to create eight p-NPP standards ranging from dilutions of 1/5–1/640. The optical density of the wells containing test samples and standards was determined spectrophotometrically at 405 nm using the Spectramax plate reader. The results were normalized to take into account the number of cells present (cell density) on each surface, as determined by the MTT assay conducted in parallel with the differentiation assay over 25 days.
3.5.2 Calcium Assay
The calcium produced by bone cells as they differentiated/matured was used to identify mineral production by the cells attached to the test substrates after 25 days in culture. A calcium-sensitive dye, Arsenazo III, was used in this quantitative assay. The Thermanox™ coverslips coated with graphene films were individually transferred to the wells of culture plates, and 500 µL of 0.6 M HCl was added to each well. The plates were then shaken overnight at room temperature to permeabilize the cells and release the calcium. On the next day, the reaction was neutralized by the addition of 100 µL of 3 M NaOH per well. A 20-µL aliquot was then taken from each well and mixed with 200 µL of Arsenazo III reagent (Sigma #11090) at a concentration of 0.15 mg mL−1. The dye forms a complex with the calcium, resulting in a color change. The optical density of the test sample and standard wells was determined spectrophotometrically at 595 nm using the Spectramax plate reader. The sample sets were compared against a standard curve, which was prepared from a 1 mg mL−1 CaCl2 stock solution diluted in H2O to create eight CaCl2 standards ranging from dilutions of 1/100 to 0 µg mL−1. The results were normalized to take into account the number of cells present (cell density) on each surface, as determined by the MTT assay conducted in parallel with the differentiation assay over the 25-day period.
3.6 Statistical Analysis
Unless otherwise specified, the biological assays were performed in triplicates. The data are reported as the mean ± standard deviation, where the statistical significance of differences (p < 0.05) was determined with Student’s t test.
4 Results and Discussion
4.1 Surface Morphology of Graphene Surfaces
The HGL surfaces were created using the same process as used for the CNWs, to maintain the chemical composition; however, a lower relative concentration of methane was used. This approach yielded similar nanostructures prior to the transfer, made of thinner vertically aligned walls that collapsed onto the substrate during the transfer process (Figs. S1 and S2), leaving the few-layered graphene sheets (10 nm thick, 1 µm2 of area) lying horizontally on the substrate surface (Fig. 1b). However, these horizontal graphene sheets do not collapse in a uniform and completely flat manner, as can be seen in Fig. 1b where some of the sheets have edges raised from the surface that appear brighter in the image (owing to charging effects) and show some of the sheet boundaries. Nanostructures presenting a similar thickness and crystalline structure have been produced by the same process and extensively characterized by van der Laan and by Pineda et al. [36, 37, 38, 40, 45, 46, 47]. It should be noted that techniques have been developed to produce horizontally oriented CNWs by blinding the electromagnetic field of the plasma process, which follows a different growth mechanism .
These horizontally aligned, texturized surfaces were used to compare with the CNW surfaces, as they provided both a reduced graphene surface area (with only one plane available) and fewer topographical features for biological interactions while retaining the interactivity with the complex chemical system of the culture medium. These topographical differences were used to discriminate the influence of the mechanical anchoring of the cells from the purely chemical influence of the presence of graphene.
4.2 Surface Composition of Graphene Surfaces
The G peak (graphitic peak) was narrow for both graphene samples, whereas the D peak (defect peak), related to the predominance of graphene edges on the surface, was slightly higher for the CNW films owing to the edges of the vertically aligned graphene sheets. These results showed a higher intensity ratio between the D and G peaks (ID/IG) on the CNW samples (1.85) than on the HGL samples (ID/IG of 1.61), which was in agreement with the literature on graphene and CNWs [20, 21, 22, 39, 49]. However, the use of a more defectuous graphene film is justified in order to be able to compare both nanotopographies grown by the same technique. Importantly, although the concentration of methane used for the deposition influenced the morphology of the graphene films, the samples nevertheless retained a very similar composition.
4.3 Adhesion and Proliferation of Saos-2 on the Graphene Surfaces
The proliferation assay, combined with the early adhesion test and the contact angle measurement (Figs. 3–5 and S3), showed a certain degree of similarity of the cellular response on the studied surfaces. This similarity may rely on a combination of the different surface chemistries, topographies, and protein adsorption patterns. Although more wettable surfaces, like CNWs and Thermanox™, are expected to provide better cell attachment, their chemistry and topography may be playing combined roles to provide similar results [51, 52, 53, 54]. Graphene-coated surfaces have been reported to allow a high adsorption of serum proteins (due to π-electron interaction), which contain extracellular matrix proteins (e.g., albumin, fibronectin, vitronectin); this may explain the cellular behavior on the graphene-coated samples and suggests a similar profile of protein adsorption [21, 23]. Although the difference in the wettability of each surface is also expected to affect cell attachment, their different topographies combined with the protein adsorption may be working synergistically to promote a similar cellular response . This hypothesis of the mechanism involved remains to be tested.
4.4 Differentiation/Mineralization Assays of Saos-2 on the Graphene Surfaces
This outcome indicated that the cells on the HGL surfaces were in an earlier stage of the differentiation process and were more inclined toward proliferation compared with their counterparts on the CNW surfaces that were more actively differentiating. The higher levels of ALP produced by cells on the HGL surfaces revealed that the cells were in a less-differentiated state. This may be explained by the ability of graphene to adsorb important molecules known to induce cell proliferation, as shown by Lee et al. . In the mentioned study, graphene was shown to preconcentrate dexamethasone and β-glycerophosphate (usual osteogenic growth factors), which was attributed to the π–π interaction between the aromatic moieties of the molecules and the graphene plane . Similarly, other graphene-based topographical features (grids) presented highly accelerated differentiation that was also attributed to their ability to adsorb chemical inducers . Furthermore, our results of a synergistic association of graphene and growth factors yielded higher differentiation, in accordance with previous reports . Notably, the aforementioned effects for the HGL samples could be further enhanced on the CNW samples owing to their higher surface area and edge reactivity, where more chemical inducers could be adsorbed onto the vertical basal planes or could react to the chemical terminations of the CNW edges.
However, the randomly distributed nano-to-micro-vertical nanowalls on the CNW samples are a distinct topography (Fig. 1a) with noticeable disorder (Fig. 2) that stimulates cell differentiation, resulting in higher calcium production. It should be noted that the stimulated cell differentiation was solely related to the graphene morphology, as our graphene transfer process eliminated any chemical contamination. These results reinforce the ability of graphene-based nanotopographies to control the cell differentiation process by serving as anchoring points for cells.
The calcium release results were consistent with the ALP production by the cells, as the higher production of the enzyme on the HGL samples indicates that the cells had started the differentiation process but did not proceed with mineralization, producing less calcium overall. On the CNW surfaces, the topographical cues enhanced calcium production, showing that the cells were in a later stage of differentiation, and the production of ALP was therefore reduced (as identified in the enzyme assay).
The data from our adhesion and proliferation studies showed that cultured human bone cells could attach to and grow on both CNW and HGL nanostructures. Furthermore, the adhesion and proliferation outcomes were within approximately 75% of the level that occurred on the control Thermanox™ surface, a material specifically engineered to promote these cellular processes. Cells also spread on both the HGL and CNW surfaces, with some subtle but evident differences between the two surfaces in that aspect of cell behavior. Differentiation data showed that the cells were significantly affected by the topographical cues of the underlying graphene surfaces. The HGL surface maintained cells in a less-advanced differentiation state (as determined by ALP data), whereas the CNWs promoted the later stage of the cell differentiation process, as marked by the cellular mineral production (demonstrated by the calcium data). In conclusion, we have shown that graphene-coated surfaces are biocompatible and that the topography of the graphene coating can have a profound influence on the long-term behavior of cells, in particular the cellular differentiation and mineralization process involved in the generation of new bone (osteogenesis). The optimization of these designed topographical features based on graphene-coated surfaces using PECVD may lead to improved outcomes in tissue engineering.
This work was partially supported by the Australian Research Council (DP160103116) and CSIRO’s OCE Science Leadership Scheme. F. F. Borghi acknowledges the scholarship support from the National Council for Science and Technology Development (CNPq—Brasil).
FFB and TvdL have carried out the production and physicochemical characterization of the graphene surfaces. Along with SK and KO, these results were organized and interpreted. FFB, PAB, and MDME designed and executed the biological assays. All authors participated in the confection of the manuscript by expertise input on the data analysis and interpretation.
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