The Effect of Covalently Immobilized FGF-2 on Biphasic Calcium Phosphate Bone Substitute on Enhanced Biological Compatibility and Activity

Moon, Kyung-Suk; Choi, Eun-Joo; Oh, Seunghan; Kim, Sungtae

doi:https://doi.org/10.1155/2015/742192

BioMed Research International

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Abstract Introduction Materials and Methods Results and Discussion Conclusion Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2015 | Article ID 742192 | https://doi.org/10.1155/2015/742192

The Effect of Covalently Immobilized FGF-2 on Biphasic Calcium Phosphate Bone Substitute on Enhanced Biological Compatibility and Activity

Kyung-Suk Moon,¹Eun-Joo Choi,²Seunghan Oh,¹and Sungtae Kim³

Academic Editor: Joshua R. Mauney

Received26 Feb 2015

Revised13 Apr 2015

Accepted20 Apr 2015

Published07 Sept 2015

Abstract

The purpose of this research was to covalently graft fibroblast growth factor 2 (FGF-2) onto biphasic calcium phosphate (BCP) via a bifunctional cross-linker technique and to estimate the optimal dose of FGF-2 resulting in the best osteogenic differentiation of human mesenchymal stem cells (hMSCs). SEM observation revealed that the surface of the 100 ng FGF-2 coated BCP was completely covered with the nanoparticles expected to be from the silane coupling agent. XRD, FT-IR, and XPS analysis showed that silane treatment, bifunctional cross-linker coating, and FGF-2 covalent grafts were conducted successfully without deforming the crystalline structure of BCP. An MTT assay demonstrated that FGF-2 coated BCP had good biocompatibility, regardless of the concentration of FGF-2, after 24 or 48 h of incubation. An alkaline phosphatase (ALP) activity assay (14 days of incubation) and the ALP gene expression level of real-time PCR analysis (7 days of incubation) revealed that 50, 100, and 200 ng FGF-2 coated BCP induced the highest activities among all experimental groups and control group (). Thus, low concentrations of FGF-2 facilitated excellent osteogenesis and were effective at enhancing osteogenic potential. Also, the bifunctional cross-linker technique is expected to be a more feasible way to induce osteogenic differentiation while minimizing the risk of FGF-2 overdose.

1. Introduction

Fibroblast growth factors (FGFs) are known to play critical roles in bone development and early osteogenesis. FGF signaling regulates the expression of various genes related to bone formation and is involved in osteoprogenitor proliferation and differentiation into bone forming cells [1–4]. Among the FGF ligands, fibroblast growth factor-2 (FGF-2) is known to promote the attachment and proliferation of osteoblasts [5, 6]. Many researchers have used various substrates to use FGF-2 to promote osteogenesis in vitro and in vivo. These substrates include polymer scaffolds, cross-linked gels, and biodegradable hydrogels [1, 7–10].

The concentration of FGF-2 and the application method are thought to directly affect the osteogenesis of osteoblasts in vitro and in vivo after FGF-2 administration. Several reports documented various results regarding the effect of FGF-2 on osteogenic differentiation [11–14]. Most of these studies were mainly aimed at analyzing the synergic effect of FGF-2 and other compounds or growth factors on osteogenic differentiation. However, the administration type and the amount of FGF-2 influencing the osteogenesis of bone forming cells was not considered. In particular, systematic injections of low concentrations of FGF-2 are thought to expect the ambiguous effect of osteogenesis within a short period and cause the accumulated overdose of growth factor.

Recent studies on the use of FGF-2 in combination with biomaterials, such as biodegradable polymers and calcium phosphate ceramics, reported the promotion of sustained release of FGF-2 and the localized effect of the FGF-2/biomaterial composites [15–18]. However, physical entrapment and coprecipitation techniques used by previous researchers have a possibility of generating mechanical weakness between FGF-2 and the substrate [19, 20]. This may affect the release of FGF-2, which is dependent on the durability of the biomaterials. On the contrary, covalent grafts are expected to be suitable for creating a strong bond between low amounts of FGF-2 and the substrate, regardless of the type of biomaterial. Most studies related to FGF-2 coated hydroxyapatite have been used the technique of physical adsorption, entrapment and coprecipitation to immobilize FGF-2 on hydroxyapatite or calcium phosphate scaffold. However, only a few researches of the FGF-2 coated biomaterials via covalent bonding technique have been published [21].

Thus, the purpose of this study was to prepare and characterize FGF-2 coated biphasic calcium phosphate (BCP) via the bifunctional cross-link method, which is one of covalent bonding techniques. In addition, we sought to find the minimal concentration of FGF-2 that induces excellent osteogenic differentiation and no cytotoxicity in human mesenchymal stem cells (hMSCs).

2. Materials and Methods

2.1. FGF-2 Grafting Process

The biphasic calcium phosphate (BCP) granule (Osteon GBC0305,) was obtained from Dentium Corporation, Suwon, Korea, and FGF-2 was obtained from the Genoss Corporation, Suwon, Korea, respectively. BCP is a 70% hydroxyapatite (HAp) scaffold coated with 30% β-tricalcium phosphate (β-TCP) with a particle size of 0.3–0.5 μm. As previously reported [22], the procedure for preparing FGF-2 coated BCP (see Figure 1) includes the grafting of 3-aminopropyl triethoxysilane (APTES, Sigma, MO, USA) onto the BCP surface and the replacement of the terminal amine by a maleimide functional group that reacts with FGF-2 via a heterobifunctional cross-linker (N-Succinimidyl-3-maleimidopropionate: SMP, Sigma, MO, USA). Briefly, 1.0 g of BCP powder was silanized by 10 mM APTES dissolved in hexane (Sigma, MO, USA) for 2 h. The silanized BCP powder was substituted for maleimide groups by 2 mM SMP dissolved in anhydrous dimethylformamide (DMF, Sigma, MO, USA) for 2 h. Then, FGF-2 dissolved in anhydrous DMF was immobilized on BCP by stirring for 2 h. All experimental procedures were performed at 25°C to avoid the risk of FGF-2 denaturation.

2.2. Surface Analysis

The surface morphology of the BCP powder was observed by field emission scanning electron microscopy (FE-SEM; S4800, Hitachi/Horiba Co., Japan). In addition, X-ray diffractometer (X’Pert PRO MRD, PANalytical B.V., Netherlands) with Ni-filtered Cu-Kα ray, Fourier transform infrared spectroscopy (FT-IR; Nicolet, Thermo Co., WI, USA), and X-ray photoelectron spectroscopy (XPS, K-Alpha ESKA system; Thermo, USA) were used to analyze the changes in chemical composition of the BCP before and after FGF-2 immobilization. For XRD measurement, we fixed the glancing angle of the specimen at 5° against the incident beam, enabling the detection of XRD patterns to be at a depth of less than 5 μm from the top surface of the substrate.

2.3. hMSC Culture

We obtained human mesenchymal stem cells (hMSCs) from the Lonza Corporation (Poietics hMSCs, Switzerland). The cell growth media used in this study was composed of α-MEM (Invitrogen, CA, USA), 10% fetal bovine serum (FBS) (Invitrogen), and 1% penicillin-streptomycin (Invitrogen). The hMSCs were incubated at 37°C and 5% atmospheric CO₂. During the study, the hMSCs were passaged 4-5 times. After confluence, they were seeded onto BCP powder, placed in a 24-well plate (cell density of 10,000 cells per well), and were stored in a CO₂ incubator for a range of incubation times. Two days after hMSC seeding, osteogenic induction media consisting of 10 mM β-glycerol phosphate (Sigma, MO, USA), 150 μg/mL ascorbic acid (Sigma, MO, USA), and 10 nM dexamethasone (Sigma, MO, USA) was added to promote osteogenic differentiation. The osteogenic induction medium was changed every 2 days.

2.4. Cell Adhesion and Proliferation Test

To test the degree of cell adhesion at the beginning of the incubation time, fluorescein diacetate (FDA; Sigma, MO, USA) staining was conducted to visualize viable hMSCs adhered to the experimental specimen. At 24 and 48 h after plating, FDA staining was performed. The detailed procedure of FDA staining was previously reported [23]. The FDA stained specimens were viewed under an inverted fluorescence microscope (CKX41, Olympus Co., Japan). An MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay was conducted to investigate the proliferation of hMSCs cultured on various experimental specimens. 1 mL of MTT dye agent (Sigma, MO, USA) was added to each well. After 3 h of incubation, 1 mL of isopropanol (Sigma, MO, USA) was added to each well, and the 24-well plate was then shaken for 30 minutes. The absorbance of each solution was measured at 570 nm by a microplate ELISA reader (SpectraMax 250, Thermo Electron Co., USA).

2.5. Alkaline Phosphatase (ALP) Activity Assay

After 7 and 14 days of incubation, the experimental samples were rinsed with PBS solution, lysed by lysis buffer solution (25 mM Tris, pH 7.6, 150 mM NaCl, and 1% NP-40) and stored in ice for 30 min. Cell lysate (50 μL) was used for the ALP assay, and the rest of the cell lysate was used for the measurement of the total protein concentration (Bradford Protein Assay Kit, Bio-Rad Laboratories, USA). Cell lysate (50 μL) was mixed with 200 μL of paranitrophenylphosphate (p-NPP, Sigma, MO, USA), and the mixed solution was stored at 37°C for 30 min to activate the reaction. After 30 min, 50 μL of 3 N NaOH (Sigma, MO, USA) was added to the mixed solution to stop the reaction. The absorbance of the mixed solution was measured at 405 nm by a microplate ELISA reader (Spectra Max 250, Molecular Device, CA, USA). The level of ALP activity was normalized to the amounts of total protein in the cell lysates (units/mg protein).

2.6. Real-Time PCR Assay [23]

After 7 days of culture, total RNA of the cells cultured on samples was extracted by TRI agent (Invitrogen, USA), and then the extract was reverse-transcribed into cDNA by cDNA Synthesis Kit (SuperScript VILO; Invitrogen, USA). SYBR Green Dye-Based Gene Expression Assays (Invitrogen, USA) was used to perform real-time PCR (StepOne Real-Time PCR System, Applied Biosystems, USA) assay. The detailed information of PCR primer used in this study is listed in Table 1. cDNA samples (1 μL for total volume of 20 μL) were analyzed for interested genes and for house-keeping gene GAPDH. To quantify the gene expression level of each sample, cycle-threshold point was compared by analysis software assisted with real-time PCR. All levels of expression of experimental group were normalized by the level of expression of control group (hMSCs cultured on pure BCP without osteogenic induction media).

2.7. Data Analysis

The data of MTT assay and ALP activity assay were expressed as mean ± standard deviation and analyzed statistically by one-way ANOVA (SPSS 12.0; SPSS GmbH, Germany) and post hoc Duncan’s multiple range tests. The data of real-time PCR assay were analyzed statistically by paired -test. Differences were considered significant if values were less than 0.05.

3. Results and Discussion

3.1. Surface Characterization of FGF-2 Coated onto BCP

Figure 2 shows SEM images of BCP, silanized BCP, and 50 and 100 ng FGF-2 coated BCP, respectively. As shown in Figure 2, 10–20 nm nanoparticles were deposited on and partially covered the 50 ng FGF-2 coated BCP. However, they covered the whole surface of 100 ng FGF-2 coated BCP. Figure 3 indicates the XRD patterns and FT-IR spectra of the BCP, silanized BCP, and 100 ng FGF-2 coated BCP, respectively. As shown by the XRD patterns, the HAp and β-TCP crystalline structures were confirmed [24, 25], and there was no structural change after the silane treatment and the FGF-2 grafting process. In the FT-IR spectra, new peaks corresponding to the silane treatment of APTES were detected at 760, 2881, and 2931 cm⁻¹ in the FT-IR spectra of the silanized and FGF-2 coated BCP [26, 27]. These peaks are reported to result from the formation of SiO_3/2 (silsesquioxane) nanoparticles [28].

(a)

(b)

(c)

(d)

Figure 4 shows the XPS spectra of C1s and N1s for silanized BCP, bifunctional cross-linked BCP, and 100 ng FGF-2 coated BCP, respectively. From the C1s spectra, four peaks (lines 1, 2, 3, and 4) were detected from experimental specimens as shown in Figure 4. Lines 1 and 2 (detected at 289 and 288.3 eV, resp.) indicate the chemical structures of O=C-O and C=O. These peaks are thought to originate from maleimide (bifunctional cross-linker) and FGF-2. Line 3 (284.8 eV) represents the silanization of BCP via APTES treatment [29]. In the N1s XPS spectra, 3 peaks were detected on experimental samples. Line 1 (399.7–400.7 eV) shows the existence of maleimide, and line 2 (399.7–400.8 eV) is the portion of N-C=O originating from maleimide and FGF-2. Line 3 (398.9 eV) represents the chemical structures of C-NH₂ and C-O and is thought to originate from FGF-2.

From the results of SEM observation and FT-IR analysis, 10–20 nm SiO_3/2 nanoparticles were deposited on the whole surface of the 100 ng FGF-2 coated BCP. XRD and XPS analyses indicated that FGF-2 was coated onto the surface of the BCP through silanization and bifunctional cross-linking without causing structural deformation of the BCP. It is well known that there are free thiol groups on FGF2 existing outside and activating binding site [30–32]. Particularly, FGF-2 has four cysteine residues binding to the maleimide groups of bifunctional cross-linker used in this study. Thus, FGF-2 is expected be coated onto the surface of BCP on the basis of the complete silanization and bifunctional cross-linking of BCP surface.

3.2. Initial Attachment and Proliferation of hMSCs

In terms of biological assay testing, the effect of FGF-2 covalently coated BCP on the osteogenic differentiation of hMSCs, an experimental group performing 20 ng FGF-2 dosed to cell culture media every 2 days was added to evaluate the comparison of the previous results of the effect of FGF-2 injection to the culture media on the osteogenic differentiation of cells [5, 13] to the results of this study. The detailed information of control group and experimental groups are listed in Table 2.

Figure 5(a) displays the images of FDA-stained live hMSCs cultured on experimental specimens after 24 and 48 h of incubation. Unlike a cell culture dish, BCP powder did not provide a flat surface on which to culture the hMSCs. Because of this, it was difficult to count live hMSCs cultured on BCP powder. Thus, we simply confirmed from the images of the FDA-stained cells that there was no drastic reduction in the number of live hMSCs between the experimental groups regardless of the incubation time. Figure 5(b) indicates the results of the MTT assay from hMSCs cultured on experimental specimens. After 24 h of incubation, the reduction in MTT values was inversely proportional to the amount of FGF-2 grafted. In addition, the MTT value of the 400 ng FGF-2 coated BCP (400C) was significantly lower than that of the control group, the culture media containing 20 ng FGF-2 (20D), and the 10 ng FGF-2 coated BCP (10C) (). However, the MTT values showed that there was no significant difference between experimental groups after 48 h of incubation. According to the ISO 10993-5, if the relative MTT value of specimen is higher than 70%, the specimen has biocompatibility [33]. Thus, it was confirmed that all experimental specimens showed excellent biocompatibility after 24 and 48 hours of incubation and the proliferation of hMSCs was not affected by the amount of coated FGF-2 after 48 h of incubation.

(a)

(b)

3.3. Alkaline Phosphatase (ALP) Activity of hMSCs

Figure 6 illustrates the results of an ALP activity assay on hMSCs cultured on experimental specimens after 7 and 14 days of incubation. As shown in Figure 6(a), the ALP activity of the control group was significantly lower than that of any of the FGF-2 coated BCP groups. The activities of the 50, 100, 200, and 400 ng FGF-2 coated BCP groups (50C, 100C, 200C, and 400C) were significantly higher than that of the group in which 20 ng FGF-2 was added to the culture media (20D) (). Thus, it was confirmed that within a short incubation period, covalent grafting of FGF-2 caused higher osteogenic differentiation of hMSCs than when FGF-2 was added to the cell culture media. Figure 6(b) indicates the ALP activities of hMSCs after 14 days of incubation. As shown in Figure 6(b), 50, 100, and 200 ng FGF-2 coated BCP (50, 100C, and 200C) showed significantly higher values than other experimental groups and the control group (). Interestingly, the ALP activities of the 100 ng FGF-2 coated BCP groups showed the trend of the highest values among all experimental groups, even though there is no significant difference among 50, 100, and 200 ng FGF-2 coated BCP groups. In addition, the values of ALP activity have a tendency to be reduced on the condition of more than 100 ng FGF-2 coated BCP groups within this research. From the results of ALP activity, we could expect that covalent bonding of FGF-2 is more effective than addition of FGF-2 to culture media with regard to the osteogenic differentiation of hMSCs. However, the grafting of high concentrations of FGF-2 seemed to inhibit the ALP activity of hMSCs. With regard to the unique trend of ALP activity results, we are currently identifying the factor that prohibits the differentiation of hMSCs into osteoblasts when high concentrations of FGF-2 are coated onto BCP.

(a)

(b)

3.4. Real-Time Assay of hMSCs

To assess the osteogenic functionality of experimental specimens, real-time PCR analysis for alkaline phosphatase (ALP), osteocalcin (OCN), and osteopontin (OPN) expression after 7 days of incubation were performed (Figure 7). Expression of OCN and OPN genes was not significantly different between all experimental groups. However, three significant differences between experimental groups were detected from the expression results of ALP gene. Within all groups, the ALP expression value of the 10, 50, 100, 200, and 400 ng FGF-2 coated BCP groups (10C, 50C, 100C, 200C, and 400C) were significantly higher than that of control group. Within all experimental groups excepting control group, the ALP expression value of the 50, 100, 200, and 400 ng FGF-2 coated BCP groups (50C, 100C, 200C, and 400C) were significantly higher than that of the group in which 20 ng FGF-2 was added to the culture media (20D). In addition, within all FGF-2 coated BCP groups, the ALP expression value of the 50, 100, and 200 ng FGF-2 coated BCP groups (50C, 100C, and 200C) was significantly higher than that of the 10 ng FGF-2 coated BCP group (10C). Thus, real-time PCR results were mostly similar to the results of ALP activity assay. In terms of the behavior of OCN and OPN gene expression, ALP gene was already known to be the first expressed phenotypical marker of bone formation and followed by OPN and OCN gene [34, 35]. Thus, the results of real-time PCR assay after 7 days of incubation are supposed to be similar to the behavior of researches previously reported.

Alizarin red S assay was also conducted to evaluate the formation of bone nodule at the surface of BCP. However, alizarin red S solution stains calcium of both newly formed bone nodule and BCP substrate at the same time (data are not shown). Thus, ALP activity assay and real-time PCR analysis were performed to estimate the osteogenesis of experimental groups instead.

3.5. Anti-FGF-2 FITC Immunofluorescent Staining

To confirm that FGF-2 was successfully coated onto the BCP surface, we stained FGF-2 by using a FITC antibody labeling kit (Pierce, Thermo Scientific, Co., USA). FGF-2 was administrated to the surface of a cell culture dish and to BCP by injection and covalent bonding methods, respectively. Then, FITC antibody labeling was performed according to the instruction manual. For detecting FITC antibody-labeled FGF-2, a fluorescent inverted microscope (CKX-41, Olympus, Co., Japan) was used and FITC was visualized under 526 nm green light. Figure 7 illustrates the FITC immunofluorescence images of FGF-2 in cell culture media and coated onto the BCP surface. As shown in Figure 7, FGF-2 covalently coated onto the surface of a cell culture dish or onto BCP was detected clearly by FITC immunofluorescence labeling. In contrast, we could not detect FITC signal in cell culture media dosed with FGF-2 (see Figure 8).

4. Conclusion

Fibroblast growth factors are known to be involved in angiogenesis, embryonic development, and bone formation [36–38]. In addition, FGFs are closely related to interact with cell-surface associated reaction and play an important role in the proliferation and differentiation of various cells and tissues. Thus, FGF-2 seems to be related to the interaction between cell and matrix, and this interaction is more effective, if FGF-2 is located between cell and matrix instead of the continuous injection of FGF-2 into the culture media. From the surface characterization, we confirmed that FGF-2 was bonded covalently onto the surface of BCP by the bifunctional cross-linker technique, and 100 ng FGF-2 was enough to cover a whole BCP granule from the images of FE-SEM. The results of the biological assay revealed that high concentrations of FGF-2 reduced the initial attachment of hMSCs to the surface of BCP at the beginning of incubation, but hMSC proliferation was not affected by the amount of coated FGF-2 after 48 h of incubation. In addition, the results of ALP activity assay and the ALP gene expression level of real-time PCR analysis indicated that small amounts of FGF-2 were enough to promote the ALP activity of hMSCs compared to other experimental groups and the control group. Thus, covalent immobilization technique is expected to be useful for enhancing the osteogenesis of bone forming cells by low concentrated growth factors.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Authors’ Contribution

Kyung-Suk Moon and Eun-Joo Choi equally contributed to this study.

Acknowledgments

This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (NRF-2013R1A1A1008441).

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Copyright © 2015 Kyung-Suk Moon et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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