High glucose inhibits osteogenic differentiation and proliferation of MC3T3‑E1 cells by regulating P2X7.

Diabetes mellitus adversely affects human bones and increases the risk of developing osteoporosis. In the present study, treatment with 30 mmol/l glucose was used to establish a high glucose (HG) cell model in vitro. Plasmids were used to overexpress the P2X purinoceptor 7 (P2X7) gene. Brilliant blue G and (4‑benzoyl‑benzoyl)‑ATP were used as a P2X7 antagonist and agonist, respectively. Proliferation of osteogenic MC3T3‑E1 cells and alkaline phosphatase (ALP) activity were determined using MTT and colorimetric assays, respectively. Alizarin Red S was used to assess calcification of MC3T3‑E1 cells. Western blotting and reverse transcription‑quantitative PCR were performed to determine protein and mRNA expression levels. The results demonstrated that HG inhibited MC3T3‑E1 cell proliferation and P2X7 expression, reduced calcification, and downregulated the expression levels of ALP and osteocalcin (Ocn) in MC3T3‑E1 cells. Overexpression of P2X7 in HG conditions increased calcification and proliferation, and upregulated the levels of ALP and Ocn in MC3T3‑E1 cells. Inhibition of P2X7 downregulated the expressions of ALP and Ocn in MC3T3‑E1 cells under HG conditions. Therefore, the present results indicated that HG caused damage to osteogenic MC3T3‑E1 cells. Thus, P2X7 may be a regulatory factor that may be used to counteract the effects of HG on osteogenesis.

Introduction

As a metabolic disease characterized by hyperglycemia, diabetes mellitus (DM) results from deficient insulin secretion or insulin resistance. The American Diabetes Association indicates that chronic hyperglycemia causes dysfunction in a number of organs, including the eyes, kidneys, nerves, heart and blood vessels (1). It is reported that DM also adversely affects human bones and is related to an increased risk of developing osteoporosis (2). Osteoporosis is associated with fractures, which lead to morbidity and mortality, particularly in the developed countries (3,4). Children with type 1 diabetes (T1D) have a 5–21% loss of bone mass, and clinical surveys indicated that patients with DM have a high risk of suffering fractures, including hip, vertebral and tibia fractures, due to insufficient bone mineral density (BMD) (5–8). Lower BMD was reported to be caused by hyperglycemia in patients with T1D (9). High glucose (HG) and MC3T3-E1 cells have been used as an in vitro model to investigate the effects of DM on bone (10,11).

P2X purinoceptor 7 (P2X7) is a member of the P2X receptor family, a group of trimeric ligand-gated ion channels (12). The P2X receptors are assembled from seven possible subunits (P2X1-7) (13,14). Extracellular ATP activates P2X family receptors to regulate the passage of Na+, Ca2+ and other cations (15). P2X subunits share similar membrane topology: Intracellular N- and C-termini, two membrane-spanning domains, and an extracellular loop containing an ATP binding site (16,17). P2X7 is involved in various physiological and pathophysiological processes, including activation of the inflammasome and inflammatory factors (18), stimulation of metalloproteases (19), and the generation of reactive oxygen and nitrogen species (20). Previous studies reported that P2X7 may be a susceptibility gene in non-obese diabetic mice (21,22). P2X7 has also been reported to be involved in the development of diabetic complications; Portillo et al (23) found that P2X7 was involved in diabetic retinopathy. The part purinergic system reactivity of P2X7 was identified to be involved in the pathogenesis of diabetic nephropathy, and antagonizing the P2X7 receptor may alleviate kidney damage caused by diabetes (24). Wesselius et al (25) demonstrated that the aberrant function of P2X7 was associated with a low BMD and an increased risk of osteoporosis. P2X7 has been reported to regulate osteoblast activity by potentiating the Wnt/β-catenin pathway (26). Therefore, the aim of the present study was to investigate the effect of P2X7 on HG-induced pre-osteoblastic MC3T3-E1 cells.

Materials and methods

Cell culture

MC-3T3-E1 cells, derived from the bone of a newborn mouse, were purchased from The American Type Culture Collection. MC-3T3-E1 cells were cultured with αMEM (Gibco; Thermo Fisher Scientific, Inc.), supplemented with 10% FBS (Gibco; Thermo Fisher Scientific, Inc.), 100 u/ml penicillin and 100 µg/ml streptomycin (Gibco; Thermo Fisher Scientific, Inc.), in an incubator with 5% CO2 at 37°C. For the HG group, the dose of 30 mmol/l glucose was selected; since αMEM already contains 5.5 mmol/l D-glucose, the media was supplemented with 24.5 mmol/l D-glucose powder (Gibco; Thermo Fisher Scientific, Inc.) in order to generate the HG conditions. For the mannitol (Man) group, which acted as a control for osmotic pressure, an equal amount of mannitol, 24.5 mmol/l, was added to αMEM containing 5.5 mmol/l D-glucose. The cells were cultured for 48 h with 0, 1, 2, 5, 10, 20 µM Brilliant blue G (BBG; Shanghai Aladdin Bio-Chem Technology., Co., Ltd.).

Reagents

The P2X7 agonist (4-benzoyl-benzoyl)-ATP (BzATP) (27) was purchased from MedChemExpress. The P2X7 antagonist BBG (28) was obtained from Aladdin. Cells were stimulated with BzATP (300 µM) or BBG (10 µM) at a final concentration 300 or 10 µM for 2 h at room temperature. Application of PBS was used as the control.

Cell transfection

Cells were seeded in 35 mm plates 24 h prior to transfection experiments. Then, 50 nmol of P2X7 and mock (empty vector) plasmids were purchased from Cobioer Biosciences Co., Ltd. Lipofectamine® (Invitrogen; Thermo Fisher Scientific, Inc.) was diluted in Opti-MEM (Invitrogen; Thermo Fisher Scientific, Inc.). The plasmids and Lipofectamine® solution were added to tubes containing FBS-free αMEM. The mixed solution was added to the cells for 2 h, after which the medium was removed and replaced with fresh complete culture medium. The cells were cultured for a further 24 or 48 h.

Cell viability

MTT was used to determine the levels of cell viability. MTT was dissolved in PBS to a concentration of 5 mg/ml. The cells (5×103) were seeded in 96-well plates for 24 h in a 5% CO2 incubator at 37°C. After the cells were treated for 24 or 48 h, the culture medium was removed. MTT solution (5 mg/ml) was diluted to a concentration of 0.5 mg/ml with FBS-free αMEM. MTT working solution (200 µl) was added to each well and incubated for 2 h in a 5% CO2 incubator at 37°C. The MTT working solution was discarded, and 100 µl DMSO was added to each well for 10 min at 37°C. The absorbance was determined using a microplate reader at a wavelength of 570 nm.

Colorimetric assay for alkaline phosphatase (ALP)

After the cells had been treated with the reagents as aforementioned for 48 h, protein was extracted using cell lysis buffer (Thermo Fisher Scientific, Inc.) on ice, followed by centrifugation at 20,000 × g for 15 min at 4°C. The concentration of total protein was determined using the bicinchoninic acid (BCA) method. A nitrophenyl phosphate kit (Beijing Leagene Biotech Co., Ltd.) was used to determine ALP activity, according to the manufacturer's instructions. The absorbance was detected using a spectrophotometer at a wavelength of 405 nm.

Alizarin Red S assay

The cells (2×104 cells/cm2) were seeded in 6-well plates and treated for 48 h, as aforementioned. The cells were cultured using complete culture medium supplemented with vitamin C (50 µg/ml; Sigma-Aldrich; Merck KGaA) and β-phosphoglycerol (10 mmol/l; Sigma-Aldrich; Merck KGaA) for 20 days. After removing the medium, PBS was used to wash the cells three times. The cells were fixed using 0.05% glutaraldehyde in H2O for 10 min at room temperature and washed three times with PBS. Alizarin Red S solution (0.4%; Beijing Solarbio Science and Technology Co., Ltd.) was used to stain the cells for 5 min at room temperature. After washing with PBS, images of the cells were captured using a light microscope (magnification, ×200; Olympus Corporation).

Western blot analysis

Total protein was extracted from MC-3T3-E1 cells using cell lysis as aforementioned, and the concentration was determined using the BCA method. A protein ladder (Thermo Fisher Scientific, Inc.) and (20 µg/lane) protein samples were separated using 10% SDS-PAGE. The proteins were transferred to PVDF membranes, which were blocked with 5% BSA for 2 h at room temperature. The following primary antibodies were incubated with the membranes overnight at 4°C: P2X7 (cat. no. ab109054; 1:1,000; Abcam) and β-actin (cat. no. ab8227; 1:1,000; Abcam). The membranes were washed three times with TBS with 0.05% Tween-20 (TBST), incubated with a horseradish peroxidase-conjugated anti-rabbit secondary antibody (cat. no. ab7090; 1:1,000; Abcam) at room temperature for 2 h, and then washed three times with TBST. Protein bands were visualized using ECL (Thermo Fisher Scientific, Inc.). An E-gel imager (Thermo Fisher Scientific, Inc.) was used to capture images and ImageJ (version 1.8, National Institutes of Health) was used for densitometry analysis.

Reverse transcription-quantitative PCR (RT-qPCR)

Total RNA was extracted from MC-3T3-E1 cells using TRIzol (Invitrogen; Thermo Fisher Scientific, Inc.), followed by centrifugation for 10 min at 16,000 × g at 4°C. Total RNA was dissolved in ddH2O and a spectrophotometer was used to detect the RNA concentration at a wavelength of 260 nm. Total RNA was reverse transcribed using a cDNA reverse transcription kit (High-Capacity cDNA reverse transcription kit, Applied Biosystems; Thermo Fisher Scientific, Inc.) at 42°C for 15 min and 95°C for 3 min. RT-qPCR was conducted on ABI 7500 Real-time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc.) using SYBR green (Invitrogen; Thermo Fisher Scientific, Inc.). The following primers were used for qPCR: P2X7 forward, 5′-CTTCGGCGTGCGTTTTG-3′ and reverse, 5′-AGGACAGGGTGGATCCAATG-3′; ALP forward, 5′-CAGTGGTATTGTAGGTGCTGTG-3′ and reverse, 5′-TTTCTGCTTGAGGTTGAGGTTAC-3′; osteocalcin (Ocn) forward, 5′-GGCGTCCTGGAAGCCAATGTG-3′ and reverse, 5′-GACCAGGAGGACCAGGAAGTCCACGT-3′; and β-actin forward, 5′-AGCAGAGAATGGAAAGTCAAA-3′ and reverse, 5′-ATGCTGCTTACATGTCTCGAT-3′. The conditions of the qPCR were as follows: 95°C for 1 min, followed by 40 cycles of 95°C for 30 sec, 62°C for 60 sec and 72°C for 30 sec, with a final extension at 72°C for 90 sec. The relative mRNA expression levels were analyzed using the 2−ΔΔCq method (29).

Statistical analysis

Data are presented as the mean ± SD from three independent experiments and were analyzed using one-way ANOVA followed by Turkey's multiple comparison test. Data were analyzed using SPSS 21.0 (IBM Corp.). P<0.05 was considered to indicate a statistically significant difference.

Results

HG reduces MC-3T3-E1 proliferation and the expression of P2X

Stimulation with 30 and 50 mmol/l glucose significantly inhibited the proliferation of MC-3T3-E1 cells (Fig. 1A); therefore, the dose of 30 mmol/l glucose was selected as HG conditions to treat MC-3T3-E1 cells in the subsequent experiments. To control for the effect of osmotic pressure, Man was used as a control group (Fig. 1B). The osmotic pressure created by Man, that would be equivalent to the HG conditions, did not affect cell proliferation (Fig. 1B). Furthermore, HG was found to inhibit the expression of P2X7, both at the mRNA and the protein level (Fig. 1C-E).

Figure 1.

HG inhibits MC3T3-E1 cell proliferation and P2X7 expression. (A) MC3T3-E1 cells were cultured with medium containing 15, 30 or 50 mmol/l D-glucose for 24 or 48 h. Cell viability was then assessed by MTT assay. (B) MC3T3-E1 cells were cultured with medium containing 30 mmol/l D-glucose or 24.5 mmol/l Man for 24 or 48 h. MTT assay was then used to determine cell viability. (C) mRNA expression levels of P2X7 were determined by reverse transcription-quantitative PCR. (D) P2X7 protein expression levels were determined by western blot analysis. (E) Quantification of western blot analysis. Data are presented as the mean ± SD. *P<0.05 and **P<0.001 vs. Con group. HG, high glucose; P2X7, P2X purinoceptor 7; Man, mannitol; Con, control; OD, optical density.

HG inhibits calcification and the levels of ALP and Ocn in MC-3T3-E1 cells

Next, the present study investigated whether HG affected calcification, and the expression levels of ALP and Ocn. The results indicated that HG stimulation downregulated the mRNA expression levels of ALP and Ocn (Fig. 2F). In addition, the Alizarin Red S staining in the HG group was markedly lighter compared with the control group (Fig. 2G), which suggested that HG stimulation resulted in reduced calcification in MC-3T3-E1 cells.

Figure 2.

Effects of HG and P2X7 on calcification and the expression levels of ALP and Ocn in MC3T3-E1 cells. MC3T3-E1 cells were transfected with mock or P2X7-overexpressing plasmids, under normal or HG (30 mmol/l) conditions. (A) After 24 or 48 h of treatments, MTT assay was used to determine cell viability. (B) After treatments as indicated for 8 h, a nitrophenyl phosphate kit was used to determine ALP activity. (C) After treatments as indicated for 48 h, mRNA expression levels of P2X7 were determined by RT-qPCR. (D) After treatments for 48 h, P2X7 protein expression levels were determined by western blot analysis. (E) Quantification of the western blot analysis. (F) After treatments as indicated for 48 h, mRNA expression levels of ALP and Ocn were determined by RT-qPCR. (G) Alizarin Red S staining was used to assess calcification in the MC3T3-E1 cells. Data are presented as the mean ± SD. *P<0.05 and **P<0.001 vs. Con; ^P<0.05 and ^^P<0.001 vs. HG. HG, high glucose; P2X7, P2X purinoceptor 7; ALP, alkaline phosphatase; Ocn, osteocalcin; RT-qPCR, reverse transcription-quantitative PCR; Con, control.

Overexpression of P2X7 increases calcification, proliferation and the levels of ALP and Ocn expression in MC-3T3-E1 cells under HG conditions

First, successful P2X7 overexpression was confirmed, both at the mRNA and the protein level, in MC-3T3-E1 cells (Fig. 2C-E). Overexpression of P2X7 had no significant promotion effect on the cell proliferation of MC-3T3-E1 cells under HG conditions (Fig. 2A). In addition, P2X7 overexpression enhanced ALP activity and upregulated the expression of ALP, under both normal glucose or HG conditions (Fig. 2B and F). P2X7 overexpression also increased the mRNA expression levels of Ocn, under both normal glucose or HG conditions (Fig. 2F). The Alizarin Red S staining analysis revealed no difference between the P2X7 overexpression group and the control group; however, the HG+P2X7 group had a darker Alizarin Red S staining than the HG alone group (Fig. 2G), suggesting that P2X7 overexpression improved calcification in MC-3T3-E1 cells.

Inhibition of P2X7 reduces the levels of ALP and Ocn in MC-3T3-E1 cells under HG conditions

To investigate the effect of P2X7 on MC-3T3-E1 cells in HG conditions, the P2X7 antagonist BBG was used. The results demonstrated that 10 µM BBG had no significant effect on cell viability (Fig. 3A). BBG treatment (10 µM) inhibited the activity of ALP (Fig. 3B), the mRNA and protein expression of P2X7 (Fig. 3C-E), and the mRNA expression levels of ALP and Ocn (Fig. 3F). By contrast, overexpression of P2X7 partially reversed the effects of BBG on above the gene expression with or without HG treatment (Fig. 3C and F).

Figure 3.

BBG inhibits the expressions of P2X7, ALP and Ocn in MC3T3-E1 cells under HG conditions. BBG (10 µmol/l), P2X7 overexpression, mock or their combination were used to treat MC3T3-E1 cells for 48 h under normal or HG (30 mmol/l) conditions. (A) MTT was used to determine cell viability at different BBG concentrations. (B) A nitrophenyl phosphate kit was used to determine ALP activity. (C) mRNA expression levels of P2X7 were determined by RT-qPCR. (D) P2X7 protein expression levels were analyzed by western blot analysis. (E) Quantification of the western blot analysis. (F) mRNA expression levels of ALP and Ocn were determined by RT-qPCR. Data are presented as the mean ± SD. *P<0.05 vs. 0 µmol/l BBG; aP<0.05 and aaP<0.001 vs. Mock; bbP<0.001 vs. P2X7; cP<0.05 and ccP<0.001 vs. HG+Mock; dP<0.05 and ddP<0.001 vs. HG+P2X7; **P<0.001 vs. BBG10+Mock; ##P<0.001 vs. BBG10+HG+Mock. BBG, Brilliant blue G; P2X7, P2X purinoceptor 7; ALP, alkaline phosphatase; Ocn, osteocalcin; HG, high glucose; RT-qPCR, reverse transcription-quantitative PCR; Con, control; OD, density.

Activation of P2X7 increases the expression of ALP and Ocn in MC-3T3-E1 cells under HG conditions

To further investigate the role of P2X7, cells were treated with the P2X7 agonist BzATP. BzATP treatment promoted ALP activity (Fig. 4A) and upregulated the expression of ALP and Ocn (Fig. 4E). Overexpression of P2X7 increased the effects of BzATP (Fig. 4A-E). BzATP in combination with the overexpression of P2X7 promoted ALP activity and further upregulated the expression of ALP and Ocn in the HG group.

Figure 4.

BzATP promotes the expression of P2X7, ALP and Ocn in MC3T3-E1 cells under HG conditions. BzATP (300 µmol/l), P2X7 overexpression, mock or their combination were used to treat MC3T3-E1 cells for 48 h under normal or HG (30 mmol/l) conditions. (A) A nitrophenyl phosphate kit was used to determine ALP activity. (B) mRNA expression levels of P2X7 were determined by RT-qPCR. (C) P2X7 protein expression levels were determined by western blot analysis. (D) Quantification of the western blot analysis. (E) mRNA expression levels of ALP and Ocn were determined by RT-qPCR. Data are presented as the mean ± SD. aP<0.05 vs. Mock; ccP<0.001 vs. HG+Mock; **P<0.001 vs. BzATP+Mock; #P<0.05 and ##P<0.001 vs. BzATP+HG+Mock. BzATP, (4-benzoyl-benzoyl)-ATP; P2X7, P2X purinoceptor 7; ALP, alkaline phosphatase; Ocn, osteocalcin; HG, high glucose; RT-qPCR, reverse transcription-quantitative PCR; Con, control.

Discussion

The present study demonstrated that HG stimulation caused damage to osteogenic MC3T3-E1 cells, with the damage becoming more serious if glucose at a high concentration was used to treat MC3T3-E1 cells for an extended period of time. HG resulted in the reduced expression of P2X7 in osteogenic MC3T3-E1 cells.

ALP is a plasma membrane-bound glycoprotein (30). The mammalian ALP is a zinc-containing metalloenzyme encoded for by a multigene family. ALP is expressed in the placenta, intestine, liver, kidneys and bone (30). Romagnoli et al (31) reported that the expression of ALP in bones is useful in clinical practice. ALP can be used as a marker to assess osteoblast activity and decreased serum ALP activity reduces osteogenesis (32,33). In the present study, HG stimulation decreased the activity and expression of ALP, suggesting that HG reduced osteogenesis. Furthermore, HG inhibited the calcification of osteoblasts. However, overexpression of P2X7 in osteogenic MC3T3-E1 cells attenuated the effects of HG and promoted osteogenesis and calcification. A previous study has found that osteoblasts regulated glucose homeostasis, which is an aspect of energy metabolism, by conducting studies on an animal model and conducting cell biology experiments (34). Another previous study demonstrated that osteoblasts stimulate insulin secretion and that this function was regulated by Ocn, suggesting that osteoblasts act as endocrine cells (35). Genetic evidence from mice suggest that G-protein coupled receptor family (GPRC6A) is important for Ocn in regulating insulin secretion and expression (36). GPRC6A is a master regulator of complex endocrine networks and metabolic processes, including insulin, bone, liver metabolism and fat metabolism, and immune function (37). In the present study, HG stimulation decreased the expression of Ocn, with the overexpression of P2X7 in osteogenic MC3T3-E1 cells increasing Ocn expression under HG conditions, indicating that HG may attenuate the ability of osteoblasts to secrete insulin and that the overexpression of P2X7 may improve insulin secretion.

To further analyze the role of P2X7 in osteoblasts under HG conditions, BBG and BzATP were used to antagonize and activate P2X7 function, respectively. The present results demonstrated that overexpression of P2X7 promoted the differentiation of MC3T3-E1. BBG had no significant effect on cell viability, indicating that BBG had no obvious toxicity to cells. In addition, BBG and BzATP participated in the differentiation of osteoblast MC3T3-E1 by regulating the function of P2X7. In addition, the overexpression of P2X7 partially reversed the effects of BBG with or without HG treatment. Wu et al (38) used a hyperglycemic mice model to investigate the effect of HG on bone formation and bone resorption. Nicke et al (39) describe a novel P2X7 isoform with distinct functional properties that contributes to the diversity of P2X7 receptor signaling. In the present study, it was demonstrated that HG caused damage to osteogenic MC3T3-E1 cells and that the overexpression of P2X7 increased osteogenic differentiation and proliferation of MC3T3-E1 cells. It was also found that inhibiting P2X7 decreased osteogenesis under HG conditions. Therefore, the findings of the present study suggested that P2X7 may be a regulator of the action of HG on osteogenic MC3T3-E1 cells. Future studies will be required to provide a more in-depth validation experiments of P2X7 in osteoblasts under HG conditions.

In conclusion, the present study indicated that HG stimulation inhibited the proliferation and differentiation of osteoblasts by downregulating the expression of P2X7, and that activating P2X7 could significantly improve the function of osteoblasts under HG conditions. However, the role of P2X7 in insulin and glucose metabolism requires further investigation, since the present study did not examine the relationship between P2X7 and GPRC6A. In addition, the culture of cells in HG conditions could affect cell viability, which may also affect osteoblast differentiation.