Role of TGF‑β1 expressed in bone marrow‑derived mesenchymal stem cells in promoting bone formation in a rabbit femoral defect model.

Bone defects represent a major clinical and socioeconomic problem without suitable treatment options. Previous studies have shown that transforming growth factor β1 (TGF‑β1) is important in the development of various diseases. The present study aimed to investigate the therapeutic potential of rabbit bone marrow‑derived mesenchymal stem cells (BMSCs) expressing TGF‑β1 in the treatment of rabbit femoral defects. First, rabbit BMSCs were identified and cultured. TGF‑β1 was then stably overexpressed in the rabbit BMSCs by lentivirus transfection, which was expressed at a high level in the femoral defects treated with TGF‑β1‑overexpressing BMSCs, compared with PBS‑treated controls. In addition, the TGF‑β1‑overexpressing BMSCs promoted new bone formation in the rabbit femoral defect model, and increased the expression of bone‑related markers at week 2 and week 6. Therefore, the study demonstrated that BMSCs overexpressing TGF‑β1 may provide a novel therapeutic option for femoral defects.

Introduction

Bone defects are caused by several clinical conditions, including cancer, trauma, congenital malformation, and infection (1). The costs of medical treatment, together with the loss of income of those with these musculoskeletal diseases, in the United States of America are estimated to be $849,000,000,000, which is ~7.7% of the gross domestic product from 2002 to 2004 (1). In addition, suitable treatment options that promote bone healing are still lacking (2). Although autograft is the gold standard for the treatment of bone defects at present, this approach has two major drawbacks, namely the limited number of donor sites and the occurrence of donor site morbidity (3). Furthermore, bone regenerative ability can also be limited with increase in age (4) and by certain conditions, including arthritis and osteoporosis (5,6). Therefore, those patients who require bone grafts the most may not have the autologous stem cells required for autografting. Therefore, transplantation of allogeneic stem cells is an attractive option for engineering bone tissue.

Previous studies have shown that tissues can be regenerated through tissue engineering approaches (7), and osteogenic differentiation and bone regeneration can be achieved with stem cells (8). Bone marrow-derived mesenchymal stem cells (BMSCs) were first separated in the 1970s, and are the source of several mesenchymal tissues, including fat, bone, and cartilage (9,10). BMSCs are a type of multipotent mesenchymal stem cell found in bone marrow. They have a high capacity for self-renewal and the potential to differentiate into various cell types, and have long been considered a valuable source of cells for bone tissue engineering (11-14). Therefore, BMSCs have been identified as an important source of osteogenic cells for bone tissue engineering.

Transforming growth factor β1 (TGF-β1) belongs to the TGF-β superfamily of proteins, which regulate cell growth and differentiation. The TGF-β family includes activins, inhibins, Müllerian inhibitory substance, and bone morphogenetic proteins. Early studies showed that TGF-β is important in inflammation, tissue repair, and embryonic development (15,16). Subsequent studies have shown that TGF-β is also crucial in cell growth, differentiation and immune function (17,18). TGF-β1 as a signal molecule is important in bone regeneration, and the importance of TGF-β1 in the migration, growth and differentiation of BMSCs has been established (19). However, the effects of TGF-β1 in combination with BMSCs on bone repair remain to be fully elucidated.

The present study showed that bone formation was highest in femoral defects treated with TGF-β1-overexpressing BMSCs of all the experimental groups, and that the combination of BMSCs and TGF-β1 may be a potential novel therapeutic option for femoral defects.

Materials and methods

Experimental animals and generation of the femoral defect model

A total of 42 New Zealand white rabbits (male), weighing 2.0-2.5 kg each, aged 2-3 months, were purchased from the Experimental Animal Center at Guangzhou University of Chinese Medicine (Guangzhou, China). All animal experiments were performed in accordance with the policies and principles in the Guide for Care and Use of Laboratory Animals (20). In addition, rabbits were housed as previously described (20). A rabbit femoral bone defect model was generated using a custom-made distraction support, as previously reported (21). Briefly, the rabbit was anesthetized with sodium pentobarbital (25 mg/kg) and xylazine (8 mg/kg). A 2-mm Kirschner wire was used to penetrate the double bone cortex (~20 mm), and was fixed with a tension bracket 200 mm from the skin. The rectus femoris from the vastus lateralis muscle was then bluntly separated, and the medial rectus muscle was opened, and a 14-mm defect in length was generated in the femur.

Femoral samples were collected from the rabbits, which were randomly divided into three experimental groups of 14 rabbits each: Control group (phosphate-buffered saline, PBS), BMSC group, and BMSC+TGF-β1 group. An osteotomy was generated (1.4 cm in length), and the speed and quality of new bone formation was then observed and assessed. The established rabbit femoral defect models were then treated with PBS, BMSCs, or TGF-β1-overexpressing BMSCs for 2 or 6 weeks. The study was approved by the Animal Care and Use Committee of Guangzhou University of Chinese Medicine.

Isolation, culture and verification of rabbit BMSCs

The BMSCs were obtained from the rabbit tibiae and femora. Density gradient centrifugation (800 × g, 5 min, 22°C) and adherent screening were used to isolate BMSCs, as previous described (10). The tibiae and femora were flushed with Low glucose-Dulbecco's modified Eagle's medium (L-DMEM) (Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA), and the BMSCs were cultured in L-DMEM supplemented with 10% fetal bovine serum (Invitrogen; Thermo Fisher Scientific, Inc.) and 1% penicillin-streptomycin, and incubated with 5% CO2 at 37°C. BMSCs from the third passage were used for all experiments in the present study.

Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) analysis

Total RNA was isolated from rabbit BMSCs using TRIzol reagent (cat. no. 15596026, Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA) according to the manufacturer's protocol. The TGF-β1 RT reaction was performed with the TaqMan RNA Reverse Transcription kit (cat. no. 4366596; Applied Biosystems; Thermo Fisher Scientific, Inc.) according to the manufacturer's protocol. cDNA was reverse-transcribed from 2 µg total RNA using a Reverse Transcription kit (Takara, Biochemical, Tokyo, Japan). cDNA was then amplified using SYBR GREEN PCR Master mix (cat. no. 638320, Takara Biotechnology Co., Ltd., Dalian, China) according to the manufacturer's protocols and analyzed with an ABI7500 Real-time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc.). Following the reaction, the Cq value was obtained, and the results were analyzed using the 2−ΔΔCq method (22). The expression of TGF-β1 was normalized to the expression of glyceraldehyde 3-phosphate dehydrogenase (GAPDH). All data are presented as the mean ± standard deviation of three independent experiments. The qPCR cycling conditions were as follows: Pre-denaturing at 95°C for 10 min, followed by 40 cycles of denaturing at 95°C for 10 sec, annealing at 58°C for 20 sec, and extension at 72°C for 10 sec. The specific PCR primers used were as follows: GAPDH, forward 5′-ATG TCG TGG AGT CTA CTG GC-3; and reverse 5′-TGA CCT TGC CCA CAG CCT TG-3′; TGF-β1, forward 5′-CAG CAA CAA TTC CTG GCG ATA-3′ and reverse 5′-AAG GCG AAA GCC CTC AAT TT-3′.

Western blot analysis

Proteins were extracted from the rabbit BMSCs with radio-immunoprecipitation assay buffer (cat. no. R0278; Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) containing Protease Inhibitor Cocktail (Thermo Fisher Scientific, Inc.). The total protein concentration was determined using the protein assay kit (Qcbio Science Technologies Co., Ltd., Shanghai, China). Total proteins (30 µg) were separated by electrophoresis with 10% SDS-PAGE and transferred onto a polyvinylidene fluoride (EMD Millipore) membrane. The membrane was blocked with 5% skim milk and incubated with the respective primary antibodies at 4°C overnight. The membrane was washed and incubated with horseradish peroxidase (HRP)-conjugated secondary antibody (1:5,000; cat. no. 115-035-003; Jackson ImmunoResearch Laboratories, Inc., West Grove, PA, USA) the following day at room temperature for 2 h, and the blots were analyzed by enhanced chemiluminescence (ECL) using the ECL substrate kit (Amersham; GE Healthcare Life Sciences, Chalfont, UK). The primary antibodies used were as follows: Anti-TGF-β1 (1:1,000; cat. no. ab66043; Abcam, Cambridge, UK) and anti-GAPDH (cat. no. FL-335, an internal loading control, 1:2,000; Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA).

Enzyme-linked immunosorbent assay (ELISA)

The culture supernatant was harvested from rabbit BMSCs transfected with the TGF-β1 construct or from non-transfected BMSCs, which served as the negative control (NC). The activity of alkaline phosphatase (ALP) in the culture medium was detected using the ELISA kit (R&D Systems, Inc., Minneapolis, MN, USA) according to the manufacturer's protocol. A 96-well plate was coated with a monoclonal anti-ALP antibody (1:1,000 dilution; SAB2500128; Sigma-Aldrich; Merck KGaA) for 1 h at room temperature, which was then detected with a HRP-conjugated secondary antibody (1:30,000 dilution; A0545; Sigma-Aldrich; Merck KGaA) for 1 h at room temperature. The absorbance at 450 nm was determined using a microtiter plate reader (Multiskan Go microplate reader, Thermo Fisher Scientific, Inc.).

Masson's staining

Masson's staining was performed to observe the histopathology of the rabbit femoral defects. The treated rabbit femoral defects were washed twice with Dulbecco's-PBS, fixed with cold methanol for 10 min at 4°C, washed twice with sterile water, and then stained with the Masson stain kit (Diagnostic BioSystems, Pleasanton, CA, USA). The stained samples were observed and images were captured under a light microscope.

Alizarin red staining

The cells were stained with Alizarin Red S to detect calcium deposition (23). The BMSCs were washed three times with PBS and then fixed with 70% ethanol for 1 h at 4°C. Following fixation, the cells were washed with water and stained with 0.2% Alizarin red (Sigma-Aldrich; Merck KGaA) in 2% ethanol for 15 min, and then washed three times with water, and dried at 37°C.

Transmission electron microscopy (TEM)

The samples were prepared and analyzed as previously described (24). Briefly, the samples were fixed and sectioned to 60 nm using an MTXL RMC ultramicrotome (Boeckeler Instruments Inc., Tucson, AZ, USA), and stained with 1% toluidine blue. The sections were observed using a Morgagni 268 TEM (FEI Company, Eindhoven, The Netherlands) at 80 kV. Images were captured using MegaView III CCD using iTEM-SIS software (Olympus, Soft Imaging System GmbH, Münster, Germany).

X-ray microtomography

The rabbit femoral defect model was established and treated with PBS, BMSCs, or TGF-β1-overexpressing BMSCs for 2 and 6 weeks. The rabbits were anesthetized with xylazine (5 mg/kg) and ketamine (25 mg/kg). An X-ray source was then used to irradiate the right forelimb of the rabbits. X-ray irradiation (MI-201, Shimadzu Corporation, Kyoto, Japan) was used to detect the right ulna, radius, and surrounding soft tissues.

Statistical analysis

All data are presented as the mean ± standard deviation. The statistical analysis was performed using SPSS 13.0 (SPSS, Inc., Chicago, IL, USA), and statistical significance was assessed using Student's t-test or one-way analysis of variance (ANOVA) test followed by a Student-Newman-Keuls post hoc test. P<0.05 was considered to indicate a statistically significant difference.

Results

Characterization of rabbit BMSCs

The rabbit BMSCs were cultured, and the first and third passages were observed. As shown in Fig. 1A and B, the cultured BMSCs exhibited a round shape at passage 1 (Fig. 1A) and spindle-shaped morphology at passage 3 (Fig. 1B). Flow cytometry was performed to characterize BMSC surface markers; 88.3% of the BMSCs were CD29-positive and 87.6% of the BMSCs were CD44-positive, whereas <6.75% of the BMSCs were CD34-positive (Fig. 1C).

Figure 1

Identification of rabbit BMSCs. Rabbit BMSCs were cultured and amplified in vitro, and images of the morphology of the (A) first passage and (B) third passage of rabbit BMSCs were captured under a light microscope. (C) Surface markers of BMSCs were determined by flow cytometry. Scale bar=100 µm. BMSCs, bone marrow-derived mesenchymal stem cells.

TGF-β1 is stably overexpressed in rabbit BMSCs and improves osteogenesis

To evaluate whether TGF-β1 was overexpressed in the BMSCs, RT-qPCR analysis was performed and the results indicated that the mRNA expression of TGF-β1 was high in the BMSCs transfected with TGF-β1, compared with that in the NC BMSCs (Fig. 2A). This was consistent with the results of western blot analysis (Fig. 2B). In addition, the ELISA results showed that the activity of ALP was higher in the BMSCs transfected with TGF-β1 than in the NC BMSCs (Fig. 2C). Furthermore, TGF-β1 improved the osteogenesis of the BMSCs (Fig. 2D).

Figure 2

Overexpression of TGF-β1 in rabbit BMSCs. (A) mRNA levels of TGF-β1 in rabbit BMSCs were quantified using reverse transcription-quantitative polymerase chain reaction. (B) Protein expression of TGF-β1 in BMSCs measured using western blot analysis. (C) Activity of ALP in the culture medium of TGF-β1-overexpressing BMSCs measured using ELISA. (D) Alizarin red staining of BMSCs at week 1 and week 2 post-culture. **P<0.01, ***P<0.001 vs. NC. Scale bar=200 µm. BMSCs, bone marrow-derived mesenchymal stem cells; TGF-β1, transforming growth factor-β1; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; ALP, alkaline phosphatase; NC, negative control.

Expression of TGF-β1 is high in newly formed bone of femoral defects treated with TGF-β1-overexpressing BMSCs

New bone ultrastructure of the rabbit femoral defect models was determined using electron microscopy. The femoral defects treated with TGF-β1-overexpressing BMSCs exhibited improved bone formation (Fig. 3), whereas in the control groups, there were numerous collagen fiber bundles arranged in a single direction and fewer new osteoids.

Figure 3

New bone ultrastructure under electron microscope. New bone ultrastructure of the femoral defects treated with PBS, BMSCs, or TGF-β1-overexpressing BMSCs (BMSC+TGF-β1) for 2 and 6 weeks. Scale bar=10 µm. BMSCs, bone marrow-derived mesenchymal stem cells; PBS, phosphate-buffered saline; TGF-β1, transforming growth factor-β1.

Treatment with TGF-β1-overexpressing BMSCs promotes new bone formation in femoral defects

As shown in Table I, it was found that the maximum torque, failure angle, failure energy, and torsional rigidity were significantly increased in the femoral defects treated with the TGF-β1-overexpressing BMSCs, compared with those in the PBS- and BMSC-treated control groups. In the BMSC- and TGF-β1-overexpressing BMSC-treated groups, the bone surface was smooth, the trabecular bone was relatively dense, and calcification was more complete and closer to that in the normal bone surface (Fig. 4). X-ray analysis further demonstrated that the alignment of the majority of femurs was well-maintained 2 weeks following surgery, and the implants were in a stable position in the TGF-β1-overexpressing BMSC group. However, a number of implants in the control group had partially collapsed. In all three groups, a cartilaginous callus had formed and surrounded the majority of the implant, although gaps were visible. At 6 weeks post-surgery, the cartilaginous callus began to take shape and was remodeled into a thin cortical lamellar bone, with the presence of gaps disappearing in all three groups. However, the remodeled cortical lamellar bone was closer to the natural bone in the femoral defects treated with TGF-β1-expressing BMSCs than in that in the control group (Fig. 5).

Table I

Biomechanical indices of rabbit femoral defects.

Group	Maximum torque (Nm)	Failure angle (radian)	Failure energy (Nm × angle)	Torsional rigidity (Nm/angle)
A	0.205±0.035	3.136±0.112	3.215±0.165	0.021±0.005
B	0.403±0.059a	5.232±0.106a	4.136±0.325a	0.027±0.003
C	0.457±0.048b	5.243±0.162b	4.225±0.568a	0.045±0.006b
D	0.402±0.065	5.163±0.157	4.207±0.149	0.033±0.002
E	0.654±0.074c	5.373±0.168	6.355±0.186d	0.052±0.004c
F	0.698±0.046d	7.454±0.194d	7.526±0.512e	0.068±0.005d

Rabbit femoral defect models were established and treated for 2 weeks with (A) PBS, (B) BMSCs or (C) transforming growth factor-β1-expressing BMSCs, and for 6 weeks with (D) PBS, (E) BMSCs or (F) transforming growth factor-β1-expressing BMSCs.

P<0.05 and

P 0.01, vs. group A;

P<0.05,

P<0.01 and

P<0.00, vs. group D. BMSCs, bone marrow-derived mesenchymal stem cells; PBS, phosphate-buffered saline.

Figure 4

Histopathology of femoral defects treated with TGF-β1-overexpressing BMSCs. Trichrome staining of femoral defects treated with PBS, BMSCs, or TGF-β1-overexpressing BMSCs for 2 and 6 weeks. Scale bar=50 µm. BMSCs, bone marrow-derived mesenchymal stem cells; PBS, phosphate-buffered saline; TGF-β1, transforming growth factor-β1.

Figure 5

X-ray imaging of external fixator and callus. X-ray imaging of femoral defects treated with PBS, BMSCs, or TGF-β1-overexpressing BMSCs at week 2 and week 6. BMSCs, bone marrow-derived mesenchymal stem cells; PBS, phosphate-buffered saline; TGF-β1, transforming growth factor-β1.

TGF-β1-overexpressing BMSC treatment increases bone-related markers in the rabbit femoral defect model

To determine whether TGF-β1-overexpressing BMSCs increase bone formation, bone-related markers, including SATB homeobox 2 (Satb2), Runt-related transcription factor 2 (Runx2) and osteocalcin (OCN), were quantified using RT-qPCR and western blot analyses. As shown in Fig. 6A and B, compared with the PBS-treated control group, significant increases were detected in these three markers following treatment with TGF-β1-overexpressing BMSCs at weeks 2 and 6.

Figure 6

Expression of bone-related markers in TGF-β1-overexpressing BMSCs treated femoral defects. (A) mRNA levels of Satb2, Runx2, and OCN in femoral defects treated with PBS, BMSCs, or TGF-β1-overexpressing BMSCs at week 2 and week 6, quantified by reverse transcription-quantitative polymerase chain reaction analysis (*P<0.05; **P<0.01). (B) Protein expression of Satb2, Runx2, and OCN in femoral defects treated with PBS, BMSCs, or TGF-β1-overexpressing BMSCs at week 2 and week 6, measured by western blot analysis (*P<0.05; **P<0.01; ***P<0.001). BMSCs, bone marrow-derived mesenchymal stem cells; PBS, phosphate-buffered saline; TGF-β1, transforming growth factor-β1; Satb2, SATB homeobox 2; Runx2, Runt-related transcription factor 2; OCN, osteocalcin; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

Discussion

Distraction osteogenesis is an effective novel method for treating bone defects. However, clinical problems associated with this method, including the long treatment cycle, remain. Therefore, a large number of studies have been performed to accelerate the ossification and shorten the treatment process using various methods. Studies have shown that combining growth factors with distraction osteogenesis can effectively shorten the duration of treatment (25,26). However, the delivery of growth factors into the defective region remains challenging. In addition, the cost of growth factor treatment is prohibitive for the majority of patients. Therefore, the development of novel strategies that are effective and convenient is critical.

Mesenchymal stem cells (MSCs) are the progenitor cells of connective tissues, including adipose tissue, cartilage and bone (27). BMSCs are a type of pluripotent MSC. Under specific induction conditions, BMSCs can differentiate into various cell types, including bone cells. Therefore, BMSCs offer potential for treating musculoskeletal injuries and disorders. In addition, BMSCs can be readily separated and cultured, with high proliferation capacity and weak immunogenicity, making them ideal for tissue engineering (28).

TGF-β1 is one of the most important cytokines in the bone matrix (29). Previous studies have shown that it is involved in a variety of biological processes, including development, apoptosis, proliferation, inflammation, bone formation, differentiation and tumor growth. TGF-β1 can be activated by dissociation from latency-associated peptide, when tissue is injured or remolded (30,31). TGF-β then rapidly recruits perivascular MSCs to the bone surface for osteoblast differentiation and new bone formation (32). Therefore, TGF-β has significant effects on bone homeostasis during remodeling by recruiting MSCs.

In the present study, TGF-β1 was stably overexpressed in rabbit BMSCs to evaluate the effects of TGF-β1 in combination with BMSCs on new bone formation in a rabbit femoral defect model. The results showed that TGF-β1 was expressed at a high level in the new bone of the femoral defects treated with TGF-β1-overexpressing BMSCs, and that the combination of BMSCs and TGF-β1 significantly promoted the formation of new bone. In the femoral defects treated with TGF-β1-overexpressing BMSCs, the bone surface was smooth, the trabecular bone was relatively dense, and the calcification was more complete and closer to that of the normal bone surface. In addition, in this TGF-β1-overexpressing BMSC group, the remodeled cortical lamellar bone was closer to natural bone than that of the control group, and the cartilaginous callus began to take shape and was remodeled into thin cortical lamellar bone. Therefore, the results suggested that TGF-β1, in combination with BMSCs, promoted new bone formation in the rabbit femoral defect model. Previous studies have shown that TGF-β is important in the repair of BMSC-mediated subchondral osteoarthritis (33), as the bone matrix releases and activates TGF-β, and the active TGF-β recruits MSCs to the bone resorption pit (34). Therefore, TGF-β signaling is crucial in the formation of new bone by BMSCs.