key: cord-0055346-iy1jl21s
authors: Sun, Yue; Liang, Yuzhen; Li, Zhengming; Xia, Ning
title: Liraglutide Promotes Osteoblastic Differentiation in MC3T3-E1 Cells by ERK5 Pathway
date: 2020-12-09
journal: Int J Endocrinol
DOI: 10.1155/2020/8821077
sha: 48ecd84e35ab4d3354466e8432e9aa09c8d65001
doc_id: 55346
cord_uid: iy1jl21s

Liraglutide is a glucagon-like peptide-1 analogue widely used in the treatment of type 2 diabetes mellitus. However, the effects of liraglutide on osteoblast proliferation and differentiation in MC3T3-E1 cells have not been fully elucidated. In the present study, the promoting effects of liraglutide were investigated in MC3T3-E1 cells. The results indicated that cell viability was affected following the treatment of the cells with different concentrations of liraglutide (0, 10, 100, and 1000 nM) at different time periods of culture (24, 48, and 72 h). Moreover, the activity levels of alkaline phosphatase and the number of mineralized nodules in MC3T3-E1 cells were significantly increased following treatment with 100 nM liraglutide. The mRNA and protein levels of Col-1, OPG, and OCN in MC3T3-E1 cells were also markedly increased following 100 nM liraglutide treatment compared with those of the control group. The expression levels of the ERK5 signaling pathway key proteins (MEK5, p-ERK5, ERK5, and NUR77) were increased following liraglutide treatment in MC3T3-E1 cells, and the gene expression levels of the ERK5 signaling pathway were also elevated. Moreover, the ERK5 inhibitor XMD8-92 significantly decreased the expression levels of p-ERK5 and NUR77 as well as the proliferation of osteoblasts. However, these changes could be rescued by liraglutide to some extent. Therefore, these results revealed that liraglutide may promote osteoblastic differentiation and proliferation in MC3T3-E1 cells via the activation of the ERK5 signaling pathway.

Osteoporosis is the most common metabolic bone disease associated with high risk of fracture, which is characterized by reduced bone strength [1] . Due to the fact that the early symptoms of this disease are not obvious, patients are often diagnosed following fractures. Once diagnosed, the patient may succumb to the disease from disability or complications [2] . erefore, osteoporosis is also considered a silent disease. e continuous increase of the global aging population has rendered osteoporosis a public health problem. It is estimated that, in 2040, >300 million adults worldwide will be suffering from high-risk fracture [3] . In addition to physical discomfort, osteoporosis imposes a higher socioeconomic burden on families and health care systems. e direct medical cost associated with osteoporosis treatment in the United States is expected to reach 25.3 billion U.S. dollars per year by 2025 [4] . erefore, it is imperative to identify treatment options and preventative strategies for osteoporosis.

Glucagon-like peptide-1 (GLP-1) is a glucagon-like gene encoded by intestinal L cells, which can be released into the blood after consumption of a meal. It can rapidly stimulate the secretion of insulin by pancreatic islet cells to inhibit the secretion of glucagon [5] . It is well known that GLP-1 mediates its biological effects mainly through the GLP-1 receptor (GLP-1R), which is a transmembrane protein.

Following activation by its ligand, the levels of cyclic adenosine phosphate and calcium ions in the cells of the pancreas are increased, triggering glucose-dependent insulin secretion [6] . Moreover, GLP-1R is widely distributed in a number of tissues, such as the digestive tract, endocrine system, lung, kidney, heart, and brain [7, 8] . Recent studies have reported that GLP-1R can be detected both in human and mouse osteoblasts, indicating that GLP-1 exerts a positive role in bone formation [9] [10] [11] . Certain experimental trials have illustrated that GLP-1 analogues play an important role in the proliferation and differentiation of osteoblasts, while increasing the gene expression levels of RUNX2, alkaline phosphatase, collagen-1, and osteocalcin in MC3T3 cells [12, 13] . GLP-1R agonists can promote bone anabolism in diabetic animal models [14] . Sun et al. [15] further demonstrated the positive effect of GLP-1 in ovariectomized animal models without diabetes. In addition, a previous study has shown that when GLP-1R is knocked out, the mice are more likely to develop fractures causing a bone mass decrease and an increase in the osteoclast number [16] . According to this evidence, GLP-1R agonists can improve bone formation and microarchitecture.

Liraglutide is a peptide, which exhibits high homology (97%) with the amino acid sequence of human intestinal GLP-1. As one of the GLP-1R agonists, it exerts beneficial effects in bone metabolism as determined by in vitro and in vivo studies and by clinical trials [17] [18] [19] . Although certain studies have demonstrated several types of signaling pathways that have been associated with bone metabolism, the potential mechanism of liraglutide in the proliferation and differentiation of osteoblasts remains unknown. In particular, the ERK5 signaling pathway has been a focus of investigation in recent years, and its role in bone metabolism and liraglutide-mediated effects has been rarely studied. e present study was performed to evaluate the effects of liraglutide on MC3T3-E1 cells and to identify the possible molecular mechanisms involved.

e mouse preosteoblastic MC3T3-E1 cell line was purchased from the Chinese Academy of Sciences Cell Bank. e cells were cultured in MEM-ALPHA medium (Biological Industries; cat. no. 01-042-1A) with 10% FBS (Biological Industries; cat. no. 04-001-1A) and 1% penicillin-streptomycin at 37°C, in the presence of 5% CO 2 in a humidified incubator. e substrate was cultured in an incubator containing 5% CO 2 at 37°C. When the cells reached 80-90% confluence, 0.25% trypsin-EDTA (Beyotime Institute of Biotechnology; cat. no. C0201) was used for digestion and subculture. e cells in the logarithmic growth stage were selected for the following experiments.

Assay. MC3T3-E1 cells were cultured in 96-well plates with 4 × 10 3 cells/well densities. After 24 h of cell culture, the cells were cultured with different concentrations of liraglutide (0, 10, 100, or 1,000 nM) for 24, 48, and 72 h. Cell viability assay was measured using the cell counting kit-8 (CCK-8, Dojindo Molecular Technologies, Inc.). e wavelength of absorbance was 450 nm.

e medium of the cells was collected and centrifuged at 1,500 rpm for 10 min at 4°C, and the supernatants were harvested. Based on the manufacturer's protocols, the ALP activity was assessed by the ALP assay kit (Nanjing Jiancheng Bioengineering Institute). e absorbance was determined by a microplate reader at 520 nm.

e cells were cultured at different concentrations of liraglutide (0, 10, 100, and 1,000 mM) for 14 days. Subsequently, the cells were gently washed twice with PBS and fixed in 4% paraformaldehyde solution for 15 min. Alizarin red S staining solution was added to the cells, and the samples were incubated for 30 min. Finally, the samples were washed again with PBS and allowed to dry naturally. e calcium nodules were observed and imaged under the microscope.

Total RNA of MC3T3-E1 cells was extracted using the TRIzol reagent, and it was reverse transcribed via a PrimeScript RT reagent kit with the gDNA Eraser (Takara Bio, Inc.) according to the manufacturer's protocol. Based on the instructions of the SYBR Premix Ex Taq II Reverse Transcriptase (Takara Bio, Inc.), the cDNA was used as a template and tested with the 7500 real-time PCR system (Applied Biosystems; ermo Fisher Scientific, Inc.). e PCR was performed using the following conditions: initial denaturation at 95°C for 30 sec, followed by 40 cycles of the two-step PCR (denaturation at 95°C for 5 sec and annealing at 60°C for 34 sec) and denaturation at 95°C for 15 sec, annealing at 60°C for 1 min, and redenaturation at 95°C for 15 sec. e mRNA expression levels were analyzed using the 2 −ΔΔCq method. Table 1 indicates the primer sequences of the genes examined.

e cells were washed three times with PBS solution. e proteins were extracted from the cells using RIPA buffer (Beyotime Institute of Biotechnology) for 30 min on ice and subsequently centrifuged at 140,000 G/ min for 10 min to collect the supernatant. e concentration of the proteins was assessed using the BCA assay (Beyotime Institute of Biotechnology). Subsequently, the proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and electrotransferred on polyvinylidene difluoride membranes. e membranes were blocked using 5% skimmed milk with TBST for 1 h at room temperature. e membranes were incubated overnight at 4°C with OPG (Abcam; cat. no. ab9986), COL11A1 (Abcam; cat. no. ab64883), OCN (Abcam; cat. no. ab93876), MEK5 (Abcam; cat. no. ab210748), ERK5 (Abcam; cat. no. ab40809), p-ERK5 (Santa Cruz Biotechnology, In.; cat. no. 135760), NUR77 (Abcam; cat. no. ab109180), and β-actin (Cell Signaling Technology, Inc.; cat. no. 4970). TBST was used to wash the membranes three times for 10 min each time. Finally, the membranes were incubated overnight at 4°C with secondary antibody, washed three times with TBST, and exposed to high-sig ECL western blotting substrate (Tanon Science and Technology Co., Ltd.) to detect the quantities of the proteins. e gray value of each image was analyzed and semiquantified using Image J software, and β-actin was used to standardize the original quantitative data.

Each experiment was repeated three times. SPSS 22.0 was used for statistical analysis, and the data were expressed as mean ± standard deviation. Statistical analysis was conducted by Student's t test and the one-way ANOVA, followed by the post hoc method. P < 0.05 was considered to indicate a statistically significant difference.

Cells. In order to examine the ability of liraglutide to affect the proliferation of MC3T3-E1 cells, the cells were exposed to different doses of this peptide at different time points. e results indicated that, following 24, 48, and 72 h of cell culture, 100 nM liraglutide promoted MC3T3-E1 cell proliferation (P < 0.01). Moreover, at the 48 h time point, the cell viability was increased following treatment of the cells with several concentrations of liraglutide (P < 0.01). e maximum effect was noted at 48 h compared to the 24 and 72 h time points ( Figure 1 ). erefore, the dose of 100 nM liraglutide and the 48 h culture point were selected for subsequent experiments.

Cells. ALP plays an important role in the early differentiation of osteoblasts. erefore, various doses of liraglutide were used to treat MC3T3-E1 cells, and ALP activity was subsequently detected. Different concentrations of liraglutide could increase the ALP activity compared with that of the control group ( Figure 2 ; P < 0.01). Notably, 100 nM liraglutide exhibited significantly higher effects among other groups (P < 0.01).

Cells. Bone mineralization is a crucial process of bone formation. MC3T3-E1 cells were induced by osteogenic differentiation for 14 days, and Alizarin red staining was performed to reflect the mineralization ability. e results indicated that liraglutide was a positive stimulating factor for the osteogenic mineralization of MC3T3-E1 cells (Figure 3 ).

Increases the mRNA Expression Levels of Col-1, OPG, and OCN in MC3T3-E1 Cells. Following the culture of the cells for 48 h, total RNA was extracted and RT-qPCR assay was performed to detect changes in the expression levels of genes associated with bone formation following exposure to different concentrations of liraglutide. e mRNA levels of Col-1, OPG, and OCN cells were significantly increased in MC3T3-E1 following intervention with 100 nM liraglutide compared with those of the control group (P < 0.01) (Figure 4) . ese findings demonstrated that liraglutide exhibited a positive effect on osteogenesis.

e effects of liraglutide were investigated on the protein expression levels of Col-1, OPG, and OCN in MC3T3-E1 cells following incubation for 48 h. e results indicated that the liraglutide groups exhibited increased protein expression levels of Col-1, OPG, and OCN compared with those of the control group at varying degrees (P < 0.01) ( Figure 5 ).

Activates the ERK5 Signaling Pathway in MC3T3-E1 Cells. To assess whether liraglutide stimulates the ERK5 signaling pathway, the expression levels of several key molecules involved in this pathway were investigated in MC3T3-E1 cells. Figure 6 indicates that 100 nM liraglutide induces the phosphorylation of ERK5. Moreover, the expression levels of its upstream and downstream molecules were also altered following the treatment of the cells with liraglutide (P < 0.01).

To further assess the role of ERK5 in liraglutide-treated MC3T3-E1 cells, 10 μM MXMD8-92 (ERK inhibitor) was added to the cells and incubated in the presence of 100 nM liraglutide. e XMD8-92-treated group led to a significant downregulation of the protein levels of p-ERK5 compared with those of the control group, indicating the inhibition of the ERK5 signaling pathway (Figure 7) . Furthermore, the protein levels of NUR77 were highly expressed in the liraglutide group, whereas they were downregulated in the XMD8-92 group compared with those of the control group (P < 0.05). e combined treatment of XMD8-92 with liraglutide resulted in an increase in the protein levels compared with those of the XMD8-92 group (P < 0.05). In addition, the protein levels of MEK5 were not significantly influenced by XMD8-92 treatment, suggesting that MEK5 was the upstream regulator of the ERK5 signaling pathway (Figure 8 ). Moreover, liraglutide at 100 nM increased the protein expression levels of Col-1, OPG, and OCN compared with those of the control cells ( Figure 9 ). Similar effects were noted in the XMD8-92 and XMD8-92 + liraglutide groups ( Figure 9 ; P < 0.05). Notably, the single XMD8-92 treatment group inhibited the osteogenic activities of MC3T3-E1 cells. However, following liraglutide treatment, the protein expression levels of Col-1, OPG, and OCN were increased (P < 0.05). Figure 10 represents the expression levels of three specific biomarkers, and the results illustrated that XMD8-92 had a negative impact on bone formation (P < 0.01). However, this inhibitory effect could be improved to some extent by treatment of the cells with the appropriate dose of liraglutide. As a result, the inhibition of the ERK5 signaling pathway by XMD8-92 notably weakened the activity of MC3T3-E1 cells. Liraglutide could relieve this inhibitory effect to some extent.

Previous studies have confirmed that osteoblasts are involved in the formation of bone tissue cells and that they play a key role in bone metabolism, proliferation, differentiation, and calcification [20] . erefore, the present study aimed to examine the effects of specific compounds and peptides on osteoblast proliferation and differentiation and to assess their therapeutic effects and associated mechanisms of action. Liraglutide is a novel antidiabetic agent, which is also effective in the treatment of osteoporosis. Accumulating studies have shown that liraglutide exerts a therapeutic role in clinical practice. e therapeutic effect of liraglutide has been confirmed by in vitro studies and clinical trials. Several studies have focused on the investigation of traditional bone proliferation signaling pathways. e studies that have examined the ERK5 signaling pathway are limited. erefore, the investigation of the interaction between liraglutide and the ERK5 signaling pathway with regard to the prevention of osteoporosis is of particular significance. Moreover, the role of liraglutide requires further assessment by experimental studies. e present study examined the effects of liraglutide on MC3T3-E1 cells in vitro. e viability of MC3T3-E1 cells was assessed following treatment with different concentrations of liraglutide, and the data indicated that 100 nM of peptide treatment increased cell proliferation, which were consistent with the results reported in previous studies [21] . Moreover, it was also discovered that this effect was mediated, at least partly, via the activation of the ERK5 pathway.

ALP is a zinc-containing glycoprotein produced by osteocytes and is one of the important indicators that can reflect the maturation of osteoblasts. is biomarker exhibits high specificity in reflecting the activity of osteocytes and bone formation [22, 23] . In the present study, the data indicated that MC3T3-E1 cells treated with 100 nM liraglutide exhibited higher ALP activity levels compared to those of the control group. In addition, liraglutide promoted the formation of calcified nodules in MC3T3-E1 cells. ese outcomes indicated that liraglutide may accelerate cellular differentiation in MC3T3-E1 cells.

Despite the positive role of ALP in osteoblast differentiation, OCN and Col-1 are also vital osteogenic factors, involved in the regulation of bone formation [24, 25] . ese International Journal of Endocrinology two biomarkers participate in osteoblastic differentiation [23] , whereas OCN and Col-1 are expressed in the late stages of mature osteoblasts [26] [27] [28] . In addition, OPG is mainly produced by osteoblasts and is increased with cell differentiation and maturation [29] . Previous studies have verified that OPG can prevent osteoclastogenesis by binding to RANKL and inhibiting its binding to the receptor RANK [30, 31] . In the present study, MC3T3-E1 cells were crucial role in accelerating osteoblastic differentiation in MC3T3-E1 cells by inducing the expression of OCN, Col-1, and OPG. e ERK5 signaling pathway is a newly discovered member of the MAPK family, which is involved in cell proliferation, differentiation, and apoptosis [32] . A previous study indicated that MEK5 is also an important member of the MAPK family of enzymes and that it could regulate the expression of ERK5 [33] . An additional study by Maria et al. [34] revealed that MEK5 participated in the osteoblast differentiation and osteogenic processes. Moreover, Zhao et al. [35] demonstrated that the activation of MER5/ERK5 was required for MC3T3-E1 cell differentiation and mineralization. Furthermore, in vivo assays demonstrated that ERK5 could relieve osteoblast apoptosis and increase osteoblast viability in an ovariectomized rat model [36] . In the present study, the ERK5 signaling pathway inhibitor XMD8-92 was used to confirm the role of ERK5 in MC3T3-E1 cell proliferation and differentiation. e results indicated that XMD8-92 decreased the expression levels of the markers of bone formation at all stages, indicating that the ERK5 signaling pathway was involved in the osteogenic process. Furthermore, the simultaneous incubation of MC3T3-E1 cells with XMD8-92 and liraglutide indicated that the expression levels of OCN, Col-1, OPG, MEK5, p-ERK5, and NUR77 were increased compared with those noted following a single treatment of the cells with XMD8-92. erefore, this evidence illustrated that liraglutide could activate the ERK5 signaling pathway and that it was able to rescue the inhibitory effects of XMD8-92 on MC3T3-E1 cells.

In the current study, the protective effects of liraglutide were verified on MC3T3-E1 cells by stimulation of the ERK5 signaling pathway. However, it is not known whether additional factors are involved in the interaction between liraglutide and the ERK5 signaling pathway, and further studies are required to investigate this hypothesis.

In summary, the present study indicated that liraglutide promoted osteoblastic differentiation in MC3T3-E1 cells via the ERK5 signaling pathway. Liraglutide may be used as a potential agent for the prevention and treatment of osteoporosis.

e data used to support the findings of this study are available from the corresponding author upon request.

e authors declare that they have no conflicts of interest.

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