Study of Cell Behaviors on Anodized TiO2 Nanotube Arrays with Coexisting Multi-Size Diameters
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It has been revealed that the different morphologies of anodized TiO2 nanotubes, especially nanotube diameters, triggered different cell behaviors. However, the influence of TiO2 nanotubes with coexisting multi-size diameters on cell behaviors is seldom reported. In this work, coexisting four-diameter TiO2 nanotube samples, namely, one single substrate with the integration of four different nanotube diameters (60, 150, 250, and 350 nm), were prepared by repeated anodization. The boundaries between two different diameter regions show well-organized structure without obvious difference in height. The adhesion behaviors of MC3T3-E1 cells on the coexisting four-diameter TiO2 nanotube arrays were investigated. The results exhibit a significant difference of cell density between smaller diameters (60 and 150 nm) and larger diameters (250 and 350 nm) within 24 h incubation with the coexistence of different diameters, which is totally different from that on the single-diameter TiO2 nanotube arrays. The coexistence of four different diameters does not change greatly the cell morphologies compared with the single-diameter nanotubes. The findings in this work are expected to offer further understanding of the interaction between cells and materials.
KeywordsCoexisting multi-size TiO2 nanotubes Repeated anodization MC3T3-E1 cells Cell adhesion behaviors Cell-material interaction
Numerous studies of novel biomaterials have been revealed to control cell behaviors and direct cell fate, which indicates that material surface properties have profound influence on cell behaviors. However, the complete understanding of the cell-material interaction is still far from clear [1, 2]. A variety of material surface morphologies have been designed to investigate the communication between cells and material surfaces [1, 3, 4]. Recently, TiO2 nanotube arrays prepared by anodization have attracted extensive research interests in the medical applications due to their physiochemical properties, such as, high specific surface area, hollow interior structures, super hydrophilicity, interconnected interval among nanotubes, controllable microstructure size, and excellent biocompatibility [5, 6, 7, 8, 9, 10, 11]. To date, highly ordered and controlled-structure TiO2 nanotube arrays with different structures have been prepared by anodization process, and their effects on cell behaviors have been extensively studied [12, 13, 14, 15, 16]. The results of these studies showed that TiO2 nanotube arrays substantially enhanced cell adhesion, propagation, differentiation, and mineralization [17, 18, 19, 20, 21, 22, 23, 24].
However, many controversies were aroused over the influence of TiO2 nanotube arrays on cell behaviors. Schmuki et al. studied the effect of TiO2 nanotubes with diameters of 15, 20, 30, 50, 70, and 100 nm on rat mesenchymal stem cell behaviors and reported that 15 nm was the optimal length scale of nanotubes for cell adhesion, propagation, mobility, and differentiation. Meanwhile, the cell adhesion and propagation rate decreased with the increase of nanotube diameters [17, 18]. Jin et al. investigated the influence of TiO2 nanotubes with diameters of 30, 50, 70, and 100 nm annealed 2 h on cell behaviors of MC3T3-E1 osteoblasts and hBMSCs, and it was observed that the 30-nm nanotubes could remarkably improve the adhesion of MC3T3-E1 and hBMSCs without obvious differentiation. Also, apparent cell elongation and the highest alkaline phosphatase activity were achieved on 70- and 100-nm nanotubes. The results suggested that the MC3T3-E1 had better osteogenic abilities on 70- and 100-nm nanotubes compared with that on 30-nm nanotubes, and the 70- and 100-nm nanotubes promoted the differentiation of hBMSCs into osteoblasts [19, 20]. Zhang et al. implanted TiO2 nanotube arrays with diameters of 30, 70, and 100 nm into mini pigs and revealed that 70-nm nanotubes were the optimum scale for bone conduction and integration . Moreover, our previous research investigated the cell behaviors of MC3T3-E1 on large-diameter TiO2 nanotube (150–470 nm). The highest cell elongation (nearly 10:1), the lowest cell number, and the peak of ALP activity were observed on TiO2 nanotubes with 470-nm diameter, and the lowest cell elongation and highest cell number were achieved on TiO2 nanotubes with 150-nm diameter [26, 27]. We notice that these studies mentioned above were carried out using uniform-diameter TiO2 nanotube arrays on the single sample. When the cells were cultured on the uniform-diameter TiO2 nanotube arrays, they adhered on this sample without other choices. It is necessary to investigate the cell behavior expression on TiO2 nanotube arrays with coexisting multi-size diameters. As we all know, few studies refer to the cell responses to the coexisting multi-size nanostructures.
In the present paper, TiO2 nanotube arrays with four different diameters ranging from 60 to 350 nm on the same piece of substrate were prepared by repeated anodization. And then MC3T3-E1 cells were cultured on these samples with coexisting four-diameter TiO2 nanotube arrays, and the superiority of cell adhesion was observed. Here we report an apparent inclination of cell adhesion on coexisting different diameters. Our research will be expected to provide inspirations and references for further studies on cell behaviors at initial stage of culture on coexisting multi-size nanostructures.
2 Materials and Methods
2.1 Fabrication of Coexisting Four-diameter TiO2 Nanotube Arrays
2.2 Characterization of Surface Topography
A field emission scanning electron microscope (FE-SEM, Quanta 250 FEG, FEI) was utilized to observe the surface morphology and to measure the diameters of coexisting four-diameter TiO2 nanotube arrays.
2.3 Contact Angle Measurement
As per the request of contact angle measurement, an optical contact angle measuring device (OCA20, Dataphysics) was utilized to determine water contact angles of the surface of each region of coexisting four-diameter TiO2 nanotube arrays.
2.4 Cell Culture
MC3T3-E1 mouse osteoblasts (ATCC CRL-2594, the cell bank of Chinese Academy of Science) were used in this work. Each 1-ml original cells was mixed with 6-ml alpha minimum essential medium (α-MEM, Gibco) in the presence of 10 vol% fetal bovine serum (FBS, Gibco) and 1 vol% penicillin–streptomycin–neomycin antibiotic mixture (PSN, Gibco). Then the cell suspension was plated in a cell culture flask (430639, Corning Incorporated) and incubated at 37 °C in a humidified atmosphere of 5 vol% CO2 environment. After 4-day culture, the concentration of MC3T3-E1 cells reached ~3 × 105 cells mL−1. A dilution process was carried out to set the concentration to 5000 cells ml−1. The cells in the form of cell suspension (4 mL per well) were seeded onto the experimental samples, which were placed on a 6-well polystyrene plate, and incubated at 37 °C in a humidified atmosphere of 5 vol% CO2 environment for 2, 6, 12, and 24 h to observe the cell morphology and count the number of viable cells attached at different incubation time. The concentration of the cell seeded onto the specimen substrate was 2 × 104 cells per well.
2.5 Cell Morphology Via SEM
After 2, 6, 12, and 24 h of incubation, the adhered cells on experimental samples were washed with 1 × PBS and fixed with 2.5 % w/v glutaraldehyde (Sinopharm Chemical Reagent Co., Ltd) in 1 × PBS for 4 h. Then, the samples were washed with 1 × PBS and then dehydrated in a gradient series of ethanol (20, 50, 70, 80, 85, 90, 95, and 100 vol%) for 3 min. A critical point dryer (EM CPD300, Leica) was utilized to dry the cells on samples. Finally, the samples with cells were sputter coated with gold by a sputter coater (EMSCD050, Leica) and then were observed via a field emission scanning electron microscope (FE-SEM, Quanta 250 FEG, FEI).
2.6 Fluorescence Observation
In order to observe the distribution of viable cells and count the number of viable cells on the coexisting four-diameter TiO2 nanotube arrays, a fluorescein diacetate (FDA, MP Biomedicals) staining was conducted. After the 2, 6, 12, and 24 h incubation process, respectively, the samples with attached cells were washed with PBS. Each 5 mg FDA stock was dissolved in 1 ml acetone and mixed with PBS (10 μL/10 mL). After being incubated in the solution for 30 s and washed again with 1 × PBS, all samples were inverted onto coverslips, visualized, and photographed via a fluorescence microscope (Scope.A1, ZEISS) with a green filter. The fluorescence effect was excited by blue laser.
In order to count the cells adhered on different regions of coexisting four-diameter TiO2 nanotube arrays, we established a rectangle coordinate system to cover the whole sample. Each fluorescence picture was taken at the intercross point of the gridding. The software Image Pro Plus, which is specialized in fluorescent cell counting, was applied to calculate the number of viable cells in each picture as the cell density at the intercross point. The distribution of cell density on the whole coexisting four-diameter sample can be expressed by heat map. Fluorescent images of the osteoblast cells cultured 2, 6, 12, and 24 h on coexisting four-diameter TiO2 nanotube arrays were taken.
2.7 Statistical Analysis
All experiments were carried out with 4 replicates. SPSS (IBM) was utilized to conduct the statistical significance analysis. The statistical differences were compared by one-way ANOVA analysis and defined as p < 0.05. All data were shown as means ± standard errors.
3 Results and Discussion
3.1 Morphology of Coexisting Four-diameter TiO2 Nanotube Arrays
3.2 Cell Morphology
3.3 Cell Distribution and Counting
The results of the cell density as a function of incubation time reveal that there is a significant difference between 60-nm and larger diameter nanotube (250 and 350 nm), and a significant difference also exists between 150-nm and larger diameter nanotube (250 and 350 nm). However, there is no difference between 250 and 350 nm in the 24 h of incubation, and no difference appears between 60 and 150 nm except 6 h incubation. In this work, the cell suspension covered the whole samples at the very earliest stage of cell suspension ejecting onto the samples, and the cell distribution on the whole samples should have been even without the effect of the special structure of the used sample on cell behaviors. However, the result from fluorescence testing and cell counting (in Figs. 5, 6, 7) shows that the difference of cell density on the regions with different diameters is significant. In our previous study, the MC3T3-E1 cells were cultured on the several groups of single-diameter TiO2 nanotube samples with 150–470 nm in diameter, and there was no significant difference of cell density among these single-diameter TiO2 nanotube samples at the same incubation time , which is totally different from the results in this work. It is concluded that the smaller diameter (less than 150 nm in this work) nanotubes attracted a far greater cell adhesion than larger nanotubes (more than 250 nm in this work) under the coexistence situation of different nanotube diameters. It can be speculated that coexistence of different diameter TiO2 nanotubes can promote the cell adhesion on the small diameter TiO2 nanotubes at the early stage of cell adhesion, and the smaller diameter nanotubes scramble the chances of cell adhesion from bigger diameter nanotubes. We believe that the phenomenon is attributed to the distinct surface physicochemical properties caused by different diameters.
Water contact angle of the surface of each region of coexisting four-diameter TiO2 nanotube arrays
Contact angle (°)
60 nm (15 V)
7 ± 1
150 nm (40 V)
4 ± 1
250 nm (80 V)
3 ± 1
350 nm (120 V)
3 ± 1
The coexisting four-diameter TiO2 nanotube arrays were fabricated via a repeated anodization process at different voltages. The boundaries between two different diameter regions of coexisting four-diameter TiO2 nanotube arrays are regular, and there is no obvious difference in height between two different diameter regions. The cell adhesion behaviors of MC3T3-E1 on each region of coexisting four-diameter TiO2 nanotube were investigated. The combination of four different diameters does not bring any changes in cell morphologies compared with the single-diameter TiO2 nanotubes. The significant difference of cells density exists between the smaller nanotubes (60 and 150 nm) and the larger ones (250 and 350 nm) at 2, 6, 12, and 24 h of incubation, which indicates smaller diameter TiO2 nanotubes offer the better triggering structure for cells adhesion than the larger diameter nanotubes under the coexistence situation of different diameter. A further study is needed to investigate the advantage of the smaller diameter nanotubes compared with the larger diameter nanotube. This discovery is expected to give further cognition of cell–material interaction.
This work was supported by the National Natural Science Foundation of China (No. 51401126, No. 51271117) and Shanghai Committee of Science and Technology, China (No. 14441901800).
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