Electrical stimuli improve osteogenic differentiation mediated by aniline pentamer and PLGA nanocomposites

Abstract

Electrical stimulation may improve the proliferation of animal cells. In the present study, osteoblasts were cultured on electroactive aniline pentamer (AP)/poly(lactic-co-glycolic acid) (PLGA) copolymer composites, on which electric pulse was imposed. The combination of polymer and electric pulse enhanced the osteogenic differentiation of the osteoblasts, characterized by the upregulated expression of bone morphogenetic protein (BMP)-2, collagen I and osteonectin and the phosphorylation of Samd4, in contrast to polymer or electrical pulse alone. This action occurred in a polymer content-dependent manner. Therefore, the action of the electric pulse, assisted by the electroactive polymer implant, may be promising in the expedition of injured bone repair.

Introduction

Electric field pulse may improve the proliferation and differentiation of osteoblasts and the rehabilitation of injured bones. In the treatment of various bone injuries, electrical stimuli promote callusogenesis and play an important role in the regulation of the adhesion, proliferation and differentiation of osteoblasts (1–3). Even very small electrical stimuli may trigger DNA synthesis and cell division, which is attributed to the bioelectrical nature of cells (4).

Bone repair materials have been found to interact with osteoblasts and promote cell proliferation and osteogenic differentiation (5–7). Currently, there is increasing interest in conducting polymers with unique chemical and physical properties. Several conducting polymers have been used to create biosensors, neural probes, drug release regulators, initiators and auto-oxidants (8–10). Conducting polymers are also preferred for biomedical applications, due to their beneficial bone-healing properties (11–13). Wong et al(11) confirmed that conducting polymers effectively control the shape and growth of mammalian cells. Polyanilines (PAs) are a class of conducting polymers which appear promising, due to their stability and easy synthesis. Aniline oligomer composited with aliphatic polyester possesses conductive and biodegradable-biocompatible properties. The use of aniline oligomer/aliphatic polyester composites appears promising in the enhancement of the effect of electric pulse on the expedition of injured bone healing by multiple mechanisms.

In the present study, external electric pulse was imposed on osteoblasts, which were cultured on nanocomposites created from aniline oligomers and poly(lactic-co-glycolic acid) (PLGA) blends. We investigated the adhesion, proliferation and differentiation of osteoblasts under the action of conducting polymers in combination with electrical stimuli.

Materials and methods

Preparation and characterization of AP/PLGA nanocomposites

Preparations of aniline pentamer (AP) and its chemical structures have been previously described (12,13). AP and PLGA were dissolved in chloroform to form a 0.06 g/ml solution. First they were mixed together and then stirred and sonicated. Solid nanocomposites were obtained by precipitation in anhydrous alcohol and were dried in vacuum for 48 h. The nanocomposites were characterized as previously described (12,13).

Cell seeding

The nanocomposites and other materials were dissolved in chloroform (0.1 g/ml) to form a 10 wt% solution. The solution (0.5 ml) was dropped onto a 15-mm Fisherbrand coverslip (treated with 2% dimethyldichlorosilane/chloroform solution, then dried at 180°C for 4 h prior to use) and evaporated in vacuum for 48 h at room temperature to form a thin film. Prior to use, the coverslips were sterilized by UV illumination for 40 min.

Rat osteoblasts were freshly isolated in the laboratory as previously described (2) and seeded with a density of 5.0×10⁴ cells/well (1 ml medium per well) in 6-well plates (Corninng Costar) containing the coated coverslips. Cells were cultured in DMEM (Gibco, Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (Gibco), 1.0×10⁵ U/l penicillin (Sigma-Aldrich, St. Louis, MO, USA) and 100 mg/l streptomycin (Sigma-Aldrich), at 37°C, in a humidified incubator with 5% CO₂.

Electrical stimuli

The electrical stimuli were initiated 24 h after cell seeding. Each well of the 6-well plate had a pair of platinum electrodes (anode and cathode) placed in the cover. Function signal generator (TFG6030 DDS Function Signal Generator, China) supplied the electrical stimuli with a voltage of 2 V and a frequency of 100 Hz for 1 h per day. The stimulus parameters were detected by a Rigol DS1022C Digital Oscilloscope (Rigol, Guangdong, China). The experiments included five groups: AP/PLGA-stimulated (0.1, 1 and 5% AP), AP/PLGA-unstimulated and PLGA-stimulated.

Detections

Following electrical stimulation, the methyl thiazolyl tetrazolium (MTT; Sigma-Aldrich) method was used to assess cell viability (14). The absorbance was measured at 492 nm with a fully-automatic Microplate Reader (Biotek, Seattle, WA, USA).

The osteogenesis-associated genes, including collagen I, bone morphogenetic protein (BMP)-2 and osteonectin, were detected by quantitative real-time polymerase chain reaction (qPCR) (15). The RNA extraction kit and reverse transcription reagents were purchased from Promega (Madison, WI, USA); the qPCR kit was purchased from Stratagene (La Jolla, CA, USA). Primers were designed based on GenBank reference sequences and were verified by BLAST. Primer sequences are listed in Table I. The qPCR amplification program included predenaturation at 95°C for 2 min, denaturation at 95°C for 10 sec, annealing at 54°C for 20 sec and extension at 72°C for 10 sec. Data analysis was performed using MxPro software equipped with Real-Time PCR Amplifier (Stratagene). GAPDH was used as the internal control.

Table I.

Gene primer sequences.

Gene	Primer sequences
BMP-2	F: 5′-GCAAGGTGTCTCCA-3′
	R: 5′-CGCTGTTTGTGTTTC-3′
Collagen I	F: 5′-TCGCTCACCACCTTCTC-3′
	R: 5′-TAACCACTGCTCCACTCT-3′
Osteonectin	F: 5′-CGAAGAGGAAGTAGTG-3′
	R: 5′-GAAGTGGCAGGAGGA-3′
GAPDH	F: 5′-GATGGTGAAGGTCGGA-3′
	R: 5′-GTGGAGGTCAATGAAT-3′

BMP-2, bone morphogenetic protein-2; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.

Cells were lysed in ice-cold radioimmunoprecipitation assay lysis buffer (Beyotime, Nanjing, China) for 15 min. Proteins were separated on 10% SDS-PAGE gels and electroblotted onto a polyvinylidene fluoride (PDVF) film. The PDVF film was incubated overnight at 4°C with anti-BMP-2, anti-Smad4, anti-collagen I, anti-osteonectin and anti-GAPDH monoclonal antibodies (Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA), diluted 5,000 times with phosphate-buffered saline (PBS) containing 1% bovine serum albumin and rinsed 4 times by 0.01 M PBS, for 5 min each time. Color was developed using the Western Blotting DAB Testing kit (Beyotime). X-ray film exposure was performed, followed by scanning and analyzing.

Origin 7.5 software was used for data processing and statistical analysis. Comparisons between groups were conducted with one-way ANOVA and Dunn’s ad hoc test. Pearson’s correlation coefficient was used to analyze the correlation between AP content and cell viability. P<0.05 was considered to indicate a statistically significant difference.

Results

Preparation and characterization

UV-visible spectroscopy and cyclic voltammetry verified that the AP/PLGA nano-composites were successfully prepared and conductive. The conductivity of AP/PLGA nanocomposites was significantly decreased compared to pure AP (data not shown).

Cell viability

All AP/PLGA nanocomposites in combination with electrical stimuli resulted in significantly higher cell viability compared to 1% AP/PLGA alone. The stimuli were effective in improving cell proliferation. Under electrical stimulation, 5 and 1% AP/PLGA nanocomposites resulted in significantly higher cell viability compared to 0.5% AP/PLGA and PLGA. The ability of the stimuli to improve cell proliferation increased in proportion to the content of AP; however, there was no statistically significantly correlation (Pearson’s correlation coefficients: 0.79, 0.93 and 0.89; Sig.: 0.22, 0.06 and 0.11, respectively) (Table II).

Table II.

Cell viability of osteoblasts cultured on different materials (mean ± standard deviation, n=6).

	Cell viability (%)
Group	Day 1	Day 3	Day 7
5% AP/PLGA with stimuli	15.34a±1.33	57.51a±4.57	79.63a±5.17
1% AP/PLGA with stimuli	14.60a±0.85	50.14b±8.37	75.63b±6.17
0.5% AP/PLGA with stimuli	11.25b±1.14	43.21c±3.71	71.25c±6.73
PLGA with stimuli	10.15b,c±0.53	42.14c, d±5.43	68.28c±5.27
1% AP/PLGA alone	9.45c±0.64	41.67d±4.37b	63.77d±6.23

^a–dDunn’s ad hoc test demonstrates that cell viability decreases in order in each time point;

^aP<0.05, compared to ^b–d,

^bP<0.05, compared to ^c and ^d,

^cP<0.05, compared to ^d.

AP, aniline pentamer; PLGA, poly(lactic-co-glycolic acid).

Molecular expressions

Fig. 1 shows the expression of BMP-2, collagen I and osteonectin. The mRNA levels under electrical stimulation were significantly higher than those without stimulation. Under stimulation, the mRNA levels increased in proportion to the content of AP.

Figure 1.

(A) BMP-2, (B) collagen I and (C) osteonectin mRNA content of osteoblasts detected by qPCR in 7 days. Bars: 1, 1% aniline pentamer (AP)/poly(lactic-co-glycolic acid) (PLGA) alone; 2, PLGA with stimuli; 3, 0.5% AP/PLGA with stimuli; 4, 1% AP/PLGA with stimuli; and 5, 5% AP/PLGA with stimuli. ^&P<0.05 when compared to 4; ^#P<0.05 when compared to 2 and 3; ^*P<0.05 when compared to 2, 3, 4 and 5. n=3.

Fig. 2 shows the results of the western blot analysis of BMP-2, phospho-Smad4, collagen I and osteonectin. Their grayscales are listed in Table III. The protein levels under electrical stimulation were higher than those without stimulation. Under stimulation, the protein levels increased in proportion to the content of AP.

Figure 2.

Western blot analysis. Lanes: 1, 1% aniline pentamer (AP)/poly-(lactic-co-glycolic acid) (PLGA) alone; 2, PLGA with stimuli; 3, 0.5% AP/PLGA with stimuli; 4, 0.5% AP/PLGA with stimuli; 5, 1 and 5% AP/PLGA with stimuli.

Table III.

Grayscales vs. GAPDH as detected by western blot analysis in 7 days (mean ± standard deviation, n=3).

	1% AP/PLGA alone	PLGA with stimuli	0.5% AP/PLGA with stimuli	1% AP/PLGA with stimuli	5% AP/PLGA with stimuli
BMP-2	9.83±0.87	39.31±3.17	54.46±3.22	66.57±4.37	71.35±2.14
Phospho-Smad4	14.25±3.27	21.13±1.42	30.27±2.17	87.35±3.24	93.28±3.11
Collagen I	35.69±1.17	64.21±3.75	86.69±4.57	91.57±3.61	95.45±4.51
Osteonectin	25.89±4.79	53.74±3.57	79.00±3.97	94.23±3.19	92.36±3.26
GAPDH	100.1±6.31	99.25±3.29	101.1±3.47	100.4±3.11	100.3±2.59

AP, aniline pentamer; PLGA, poly(lactic-co-glycolic acid).

Discussion

The electric field and APs alone may improve the proliferation and osteogenic differentiation of osteoblasts. In the present study, rat-derived osteoblasts were cultured on AP/PLGA nano-composite films, simultaneously exposed to electrical stimuli. The electrical stimulation combined with the AP implants significantly improved the proliferation and osteogenic differentiation of osteoblasts, compared to when each agent was used individually.

Various cell functions involve complicated signal transduction (16). The chemical signals are the main form of information transmission between cells; however, the intraand intercellular electrical signal transduction is an important contributing factor to cell behavior. Electric fields may directly promote the proliferation of osteoblasts. Two mechanisms may be involved in electric fields acting on osteoblasts. A previous study by de Barros Filho et al(2) reported that magnetic fields may directly promote DNA and protein synthesis in rat cells. Blank and Goodman (16) reported that pulsed electric fields may act directly on osteoblast DNA, affecting gene expression, thereby promoting the proliferation of osteoblasts. The electrical stimulation of osteoblasts may also be mediated by calcium ions or cAMP. There is evidence supporting this hypothesis. Normally, the gap junctional intercellular communication (GJIC), which is responsible for the transport of calcium ions or cAMP, is inhibited during normal tissue regeneration and cell proliferation; electric fields may inhibit the function of GJIC, thereby promoting cell proliferation (18).

Only cells that adhere to materials are able to migrate, differentiate and proliferate and the presence of a scaffold is necessary for tissue engineering and osteogenesis. APs exhibit higher solubility and conductivity. Therefore, in the present study, AP and PLGA were composited to produce electroactive biodegradable polymer nanocomposites, which appear promising for research or medical applications, including tissue engineering and regeneration of bone, cartilage or other tissues. As a result, electrical stimuli combined with AP/PLGA nanocomposite implants led to more positive outcomes compared to when used alone.

BMPs, particularly BMP-2, may induce mesenchymal stem cell differentiation into cartilage and bone, namely promote bone formation, by inducing formation and promoting proliferation of osteoblasts (19). Smad4 is a key signal involved in BMP expression, which promotes osteo-differentiation and -formation. Osteonectin, a non-collagenous matrix protein abundantly found in bone matrix, plays an important role in the process of mineralization by promoting mineral deposition in collagen (20). Osteonectin may promote extracellular matrix synthesis and increase the rate of bone matrix deposition (21). Collagen I is the scaffold for calcium deposition and cell adhesion. Collagen fibers comprise ∼95% of the organic matter of the bone matrix and collagen I in particular comprises ∼90%. Collagen I expression is initiated in the cell proliferation phase and reaches its peak in the matrix synthesis phase. In the proliferation phase, osteoblasts increase in number to form multilayers of cells, merge and secrete collagen I in order to mineralize and achieve the formation of bone nodules. Thereupon, BMP-2, Smad4, collagen I and osteonectin play important roles in the osteogenic process (22).

In the present study, qPCR and western blot analysis demonstrated that the expression of BMP-2, Smad4, collagen I and osteonectin was more upregulated by the combination of electrical stimuli and AP/PLGA, compared to each agent used alone, indicating that the combination may integrate and amplify the effects of the individual constituents.

In conclusion, AP and PLGA were successfully blended to create electroactive biodegradable nanocomposite AP/PLGA. The electrical stimuli, combined with the nanocomposites, may upregulate the expression levels of BMP-2, Smad4, collagen I and osteonectin and promote proliferation of rat-derived osteoblasts, compared to when each agent was used individually. The electroactive biodegradable nanocomposite AP/PLGA bears the potential for bone tissue engineering under electrical stimulation.