- Research article
- Open Access
Compression and tension variably alter Osteoprotegerin expression via miR-3198 in periodontal ligament cells
BMC Molecular and Cell Biologyvolume 20, Article number: 6 (2019)
Osteoclasts play a critical role in bone resorption due to orthodontic tooth movement (OTM). In OTM, a force is exerted on the tooth, creating compression of the periodontal ligament (PDL) on one side of the tooth, and tension on the other side. In response to these mechanical stresses, the balance of receptor activator of nuclear-factor kappa-B ligand (RANKL) and osteoprotegerin (OPG) shifts to stimulate osteoclastogenesis. However, the mechanism of OPG expression in PDL cells under different mechanical stresses remains unclear. We hypothesized that compression and tension induce different microRNA (miRNA) expression profiles, which account for the difference in OPG expression in PDL cells.
To study miRNA expression profiles resulting from OTM, compression force (2 g/cm2) or tension force (15% elongation) was applied to immortalized human PDL (HPL) cells for 24 h, and miRNA extracted. The miRNA expression in each sample was analyzed using a human miRNA microarray, and the changes of miRNA expression were confirmed by real-time RT-PCR. In addition, miR-3198 mimic and inhibitor were transfected into HPL cells, and OPG expression and production assessed.
We found that certain miRNAs were expressed differentially under compression and tension. For instance, we observed that miR-572, − 663, − 575, − 3679-5p, UL70-3p, and − 3198 were upregulated only by compression. Real-time RT-PCR confirmed that compression induced miR-3198 expression, but tension reduced it, in HPL cells. Consistent with previous reports, OPG expression was reduced by compression and induced by tension, though RANKL was induced by both compression and tension. OPG expression was upregulated by miR-3198 inhibitor, and was reduced by miR-3198 mimic, in HPL cells. We observed that miR-3198 inhibitor rescued the compression-mediated downregulation of OPG. On the other hand, miR-3198 mimic reduced OPG expression under tension. However, RANKL expression was not affected by miR-3198 inhibitor or mimic.
We conclude that miR-3198 is upregulated by compression and is downregulated by tension, suggesting that miR-3198 downregulates OPG expression in response to mechanical stress.
Orthodontic tooth movement (OTM) describes the orchestrated responses of periodontal tissues in response to physical force. During OTM, site-specific bone metabolisms take place simultaneously: osteoclastic bone resorption in the compression zone and osteoblastic bone formation in the tension zone of periodontal ligament (PDL) [1,2,3]. Osteoclastogenesis is primarily regulated by receptor activator of nuclear-factor kappa-B ligand (RANKL) . RANKL signaling is inhibited by osteoprotegerin (OPG), and the balance between RANKL and OPG contributes to the regulation of bone resorption . The relationship between the RANKL/OPG ratio and progression of OTM has been extensively studied. Compression induces RANKL expression [6,7,8,9] and reduces OPG expression [10, 11] in PDL cells, thereby increasing the RANKL/OPG ratio, and favoring RANKL-mediated osteoclastogenesis. Conversely, tension increases OPG expression in PDL cells both in vivo [12, 13] and in vitro [14,15,16,17], which in turn inhibits RANKL. However, the mechanism regulating OPG expression in PDL cells under different mechanical stresses remains unclear.
The relationship between mechano-sensing and microRNA (miRNA) expression has recently become clearer. It is now understood that miRNAs in vascular endothelial cells play an essential role in shear stress-regulated endothelial responses . Mechanical stretch regulates microRNA expression in C2C12 myoblasts . Furthermore, mechanical stress can induce expression of miRNAs that modulate the expression of osteogenic and bone resorption factors, thus effecting bone remodeling due to mechanical stresses . These studies suggest miRNAs might play a role in the regulation of differential OPG expression in PDL cells under compression and tension.
We hypothesized that compression and tension induce different miRNA expression profiles, resulting in differential OPG expression in PDL cells. To test this hypothesis, in the present study we used miRNA microarrays to examine miRNA expression profiles of cultured PDL cells under compression and tension. We identified several miRNAs that were differentially regulated during compression and tension, and, using target prediction databases, identified OPG as a potential target for the miRNA miR-3198. We found miR-3198 was upregulated by compression and downregulated by tension. Augmentation and attenuation of miR-3198 by a miRNA mimic and an inhibitor, respectively, revealed that OPG expression was downregulated by miR-3198.
Thus, we show here that compression and tension differentially regulate miRNA expression. Importantly, we found that miR-3198, which was induced by compression and reduced by tension, downregulates OPG expression in PDL cells.
miRNA expression is mediated by mechanical stress
We examined miRNA expression in human PDL (HPL) cells in three different groups (control, compression, and tension) using a microarray. The top 20 differentially expressed miRNAs between the control and compression groups, the control and tension groups, and the tension and compression groups were identified (Table 1). Some miRNAs, such as miR-1268, − 3648, −642b, and -135a, were upregulated in both the compression and tension groups compared with the control group. The data suggest these miRNAs are upregulated by any type of mechanical stress. miRNAs such as miR-572, − 663, − 575, − 3679-5p, UL70-3p, and − 3198 were upregulated in the compression group compared with both the control group and tension group, suggesting that these miRNAs are specifically upregulated by compression. miRNAs upregulated in the tension group relative to the control group included miR-376a. These results suggest that some miRNAs are upregulated in response to any type of mechanical stress, whilst other miRNAs are upregulated only in response to a specific type of mechanical stress.
miRNAs targeting OPG are regulated by mechanical stress
Since OPG expression is regulated by mechanical stress in OTM, we investigated whether miRNAs upregulated by mechanical stress were also miRNAs predicted to target OPG. miRNAs that target OPG were predicted by two databases (Table 2). miR-1207 was on neither list; therefore an miR-1207 mimic and inhibitor were used as negative controls. We identified miR-3198 on both of the lists, raising the possibility that compression-induced miR-3198 downregulates OPG expression.
Expression of miR-3198 and OPG was regulated differentially in compression and tension
Real-time RT-PCR analysis confirmed the effects of − 3198 due to mechanical stress. Compression induced miR-3198 expression in HPL cells, whereas tension reduced miR-3198 expression (Fig. 1a). These results were consistent with the miRNA array analysis. OPG expression was reduced by compression but was induced by tension (Fig. 1b). RANKL expression was increased by both compression and tension (Fig. 1c). Western blotting revealed that compression reduced OPG protein level in the cultured HPL cells (Fig. 1d and e). In addition, tension increased OPG protein level in the cultured HPL cells. These results suggest that miR-3198 downregulates OPG expression in response to mechanical stress.
miR-3198 gain-of-function and loss-of-function experiments
We further examined the relationship between miR-3198 and OPG expressions through gain- and loss-of-function experiments. We found that transfection of miR-3198 inhibitor in HPL cells reduced miR-3198 expression (Fig. 2a), whereas transfection of miR-3198 mimic upregulated miR-3198 expression (Fig. 2b). Similarly, OPG mRNA expression was induced by miR-3198 inhibitor (Fig. 2c) and reduced by miR-3198 mimic (Fig. 2d). RANKL mRNA expression was stable irrespective of the transfection of miR-3198 inhibitor or mimic. OPG protein levels were also increased by miR-3198 inhibitor (Fig. 2e) and decreased by miR-3198 mimic (Fig. 2f).
To clarify whether these phenomena were dependent on miR-3198 specifically, we examined the role of miR-1207, which was not predicted to target OPG. We found that the transfection of miR-1207 inhibitor reduced miR-1207 expression in HPL cells (Fig. 2g), and the transfection of miR-1207 mimic upregulated miR-1207 expression (Fig. 2h), consistent with the results of the miR-3198 inhibitor and mimic experiment. OPG and RANKL expression were stable regardless of the transfection of miR-1207 inhibitor or mimic (Fig. 2i and j).
These results suggest that mechanical stress-induced miR-3198 downregulates OPG expression in HPL cells.
miR-3198 regulates mechanical stress-mediated OPG expression
Finally, we examined the role of miR-3198 in the regulation of mechanical stress-mediated OPG expression. We found that OPG expression was reduced by compression, although transfection of miR-3198 inhibitor rescued the compression-mediated downregulation of OPG (Fig. 3a). In addition, there was no significant difference between the control and the compression + miR-3198 inhibitor groups, indicating that miR-3198 plays a role in the regulation of OPG expression under compression. RANKL mRNA expression was upregulated by compression, and it was stable irrespective of the transfection of miR-3198 inhibitor.
Conversely, we found that under tension, augmentation of miR-3198 expression by miR-3198 mimic reduced OPG expression (Fig. 3b). There was a significant difference in the OPG expression levels between the control and the tension + miR-3198 mimic (P = 0.03). RANKL mRNA expression was upregulated by tension, and it was stable irrespective of the transfection of miR-3198 mimic.
Consistent with results of real-time PCR, OPG quantification by ELISA revealed that compression reduced OPG protein levels (Fig. 3c), whereas miR-3198 inhibitor prevented the compression-mediated reduction of OPG. In addition, tension upregulated OPG production (Fig. 3d). Similarly, we found that miR-3198 mimic significantly reduced the tension-mediated increase in OPG production.
Western blotting for OPG also revealed that the miR-3198 inhibitor prevented the compression-mediated reduction of OPG (Fig. 3e and g). On the other hand, miR-3198 mimic significantly reduced the tension-mediated increase in OPG production (Fig. 3f and h). These results indicate that miR-3198 downregulates OPG expression in HPL cells under mechanical stress.
Osteoclastic bone resorption is tightly regulated by RANKL  in the periodontal ligament during OTM [7, 10]. Conversely, OPG, the decoy receptor to RANKL, inhibits osteoclastogenesis . The RANKL/OPG ratio increases at the compression zone of the PDL during OTM . In vitro experiments have revealed that compression increases the RANKL/OPG ratio in PDL cells [9, 22,23,24]. On the other hand, tension decreases RANKL/OPG ratio in PDL cells, mainly by the induction of OPG expression [14,15,16,17]. Generally, OPG expression in the PDL cells usually increases under tension and decreases under compression. Though our previous report  and this study revealed upregulation of RANKL by tension, induction of OPG by tension predominates over RANKL, resulting in a low RANKL/OPG ratio and inactive osteoclastogenesis.
In this study, we examined whether miRNAs are involved in site-specific changes in OPG expression during OTM. We found that miRNAs were differentially regulated by compression and tension. In particular, miR-3198 was upregulated by compression and downregulated by tension. Furthermore, we found that miR-3198 regulates OPG expression in response to mechanical stresses, which is consistent with phenomena observed in the PDL during OTM; namely, osteoclastic bone resorption in the compression zone and osteoblastic bone formation in the tension zone of the PDL . On the other hand, RANKL expression was not affected by miR-3198. Our present results indicate that tension-induced OPG expression is reduced by the overexpression of miR-3198 mimic, although we did find a significant difference in OPG expression between control and tension + miR-3198 mimic groups. Considering that miR-3198 plays a role in the regulation of OPG expression under different mechanical stresses, epigenetic regulation such as methylation of miR-3198 and mutation of miR-3198 would interfere the mechanical stress-mediated miR-3198 expression followed by the difference in OPG expression, which regulates the alveolar bone resorption during orthodontic tooth movement. Further studies will shed light on the importance of miR-3198 on the regulation of the alveolar bone metabolism during orthodontic tooth movement.
Regarding the relationship between OTM and miRNA, Chen et al. reported that miR-21 deficiency attenuated OTM via inhibition of alveolar bone resorption on both the compressive and tensile sides . In addition, Chang et al. reported the role of miRNA in tension force-induced bone formation . They concluded that miR-195-5p, miR-424-5p, miR-1297, miR-3607-5p, miR-145-5p, miR-4328, and miR-224-5p were core miRNAs of tension force-induced bone formation. Within these miRNA, no miRNAs were changed by mechanical stresses in our experiment, except miR-145. We presumed that the difference in observed miRNAs between Chang’s study and ours would be due to the different time points assessed (at 72 h in Chang’s paper, and at 24 h in ours). We wanted to explore the early response of PDL cells against mechanical stress via miRNA, and examined only at 24 h, the timing the other researchers tested at [27, 28]. Exploration of the time course change of each miRNA would be useful to clarify this. Liu et al. reported that miR-503-5p functions as a mechano-sensitive miRNA and inhibits bone marrow stromal cell osteogenic differentiation subjected to mechanical stretch and bone formation in OTM tension sides . Chen et al. reported that cyclic stretch decreased, and compression increased, the expression of miR-29 in PDL cells, which directly interacts with Col1a1, Col3a1 and Col5a1 . These studies reveal the relationship between mechanical stress-mediated miRNA expression and bone formation or tissue remodeling. However, the effects of miRNA on the RANKL/OPG ratio during OTM were unclear until now.
Regarding the regulation of OPG expression by miRNAs, miRs-21 [31, 32], − 145 , −146a , − 150 , and − 200  have been reported to regulate OPG expression. Among them, miRs-21, − 145, and − 200 were thought to be direct regulators of OPG expression in the databases of miRDB.org and microRNA.org. Therefore, we presumed that the refinement of candidate miRNAs using the available databases was a sufficiently accurate method to choose candidates.
We found that miR-3198 plays a role in the regulation of the mechanical stress-mediated OPG expression, although the reciprocal regulatory mechanism of miR-3198 by compression and tension remains unclear. Some mechanical stresses induce differential intracellular signaling systems, such as G-proteins, calcium signaling, MAPK signaling, and nitric oxide signaling . Further studies are needed to clarify the regulatory mechanism of miR-3198 by compression and tension. miR-3198 was identified in human tumor breast tissue , and is on 22q11.21 of the genome. It is important to confirm that miR-3198 downregulates OPG expression by mechanical stress in animal models. However, there is no orthologue of miR-3198 in mice or rats, which makes it difficult to conduct such experiments. Nevertheless, further confirmatory experiments are required.
In conclusion, we found that miRNAs were differentially regulated by compression and tension in PDL cells. Furthermore, miR-3198 downregulates OPG expression in PDL cells in response to mechanical stress.
Human immortalized periodontal ligament cell lines (HPL cells) were received from the University of Hiroshima, Hiroshima, Japan, where they were originally established . HPL cells were cultured in alpha modified Eagle’s medium (Wako Pure Chemical, Osaka, Japan) containing 10% fetal bovine serum (Thermo Fisher Scientific, Waltham, MA) and supplemented with penicillin (100 U/mL) and streptomycin (100 μg/mL). All cells were cultured at 37 °C in a 5% CO2 incubator.
Application of mechanical stress
Compressive force was applied to the HPL cells using a glass cylinder, as described elsewhere . Briefly, a glass cylinder was placed over a confluent cell layer in the well of a 6-well plate. HPL cells were subjected to 2 g/cm2 of compressive force for 24 h. Cyclical tensile force was applied to HPL cells with a Flexercell Strain-Unit (Flexcell Corp., Hillsborough, NC, USA), as described elsewhere . Briefly, PDL cells were pre-cultured in flexible-bottomed culture plates coated with type I collagen until confluent. The culture plates were then set on the rubber gasket of the Flexercell Strain Unit, and PDL cells were subjected to cyclical tensile force (15% elongation, 1 s stretch/1 s relaxation) for 24 h.
miRNA and RNA extraction
miRNA and RNA were extracted separately from HPL cells using the Nucleospin miRNA isolation kit (Macherey-Nagel, Düren, Germany), according to the manufacturer’s instructions.
miRNA array analysis
The quality of the extracted miRNAs was examined by an Agilent 2100 Bioanalyser (Agilent Technologies, Santa Clara, CA). RNA integrity numbers ranged from 8.7 to 9.5. miRNA expression in each sample was analyzed using a SurePrint G3 Human miRNA microarray 8 × 60 K miRBase 16.0 (Agilent Technologies), according to the manufacturer’s instructions.
Database analysis for miRNAs target prediction
Reverse transcription (RT) and real-time RT-PCR analysis
Isolated miRNA (2 μg each) were reverse-transcribed (RT) with the miScript II RT kit (Qiagen, Germantown, MD), according to the manufacturer’s instructions. After reverse transcription, cDNA samples were diluted 5× with TE buffer. Real-time RT-PCR was performed using the miScript SYBR green PCR kit (Qiagen). The following PCR primers were used for the detection of miRNA: miR-1207 (MIMAT0005871), miR-3198 (MIMAT0015083), and RNU6B. Fold change of miR-3198 expression relative to the control was calculated by the Δ-Δ Ct method with RNU6B as a reference gene. Isolated RNA (500 ng) was reverse-transcribed using the iScript cDNA-Supermix (Bio-Rad, Hercules, CA, USA), according to the manufacturer’s instruction. After reverse transcription, cDNA samples were diluted 5× with TE buffer. Real-time RT-PCR was performed using the SsoFast EvaGreen-Supermix (Bio-Rad). PCR primers used for the experiments were human OPG (forward, 5′-AAGGGCGCTACCTTGAGATAG-3′; reverse, 5′-GCAAACTGTATTTCGCTCTGGG-3′), human RANKL (forward, 5′-CGTTGGATCACAGCACATCAG-3′; reverse, 5′-GCTCCTCTTGGCCAGATCTAAC-3′), and human ribosomal protein S18 (RPS18) (forward, 5′-GATGGGCGGCGGAAAATAG-3′; reverse, 5′-GCGTGGATTCTGCATAATGGT-3′). Fold changes of OPG and RANKL expression relative to the control were calculated by the Δ-Δ Ct method with RPS18 as a reference gene.
miR-3198 gain-of-function and loss-of-function experiments
To observe the influence of miR-3198 on OPG expression, miR-3198 mimic (Qiagen) and miR-3198 inhibitor (Qiagen) were transfected into HPL cells using the TransIT-TKO® transfection reagent (Mirus Bio LLC, Madison, WI), according to the manufacturer’s instructions. miR-1207 mimic (Qiagen) and miR-1207 inhibitor (Qiagen) were used as the negative control. miR mimic and miR inhibitor were used at a final concentration of 50 nM (stock concentration, 20 μM), according to the manufacturer’s recommendation. The expression of miR-3198 was observed at 24 h after transfection. In some experiments, mechanical stress was applied to transfected HPL cells, beginning 12 h after transfection.
The concentration of OPG in the culture supernatant was measured using an OPG ELISA kit (Boster Biological Technology, Pleasanton, CA), according to the manufacturer’s instructions. Culture supernatants were diluted 5× prior to measurement.
Western blotting for OPG
Culture supernatants were subjected to electrophoresis on TGX Precast gels (BioRad), proteins were transferred to a PVDF membrane, which was blocked with PVDF Blocking Reagent (Toyobo Co. Ltd., Osaka, Japan), then incubated with a rabbit IgG anti-OPG antibody (GeneTex, Irvine, CA, USA). After thorough washing with 0.5% Tween-20 in PBS (PBS-T), the membrane was incubated with a horseradish peroxidase-conjugated anti-rabbit IgG antibody (R&D Systems, Inc., Minneapolis, MN, USA). Chemiluminescence was produced by using Luminata-Forte (EMD Millipore, Billerica, MA) and detected with LumiCube (Liponics, Tokyo, Japan).
All data are presented as mean ± SD. Comparisons between two groups were performed using Student’s t-test. Multiple comparisons were performed by using Tukey’s test. A P-value < 0.05 was considered statistically significant.
Enzyme-linked immunoSorbent assay
- HPL cells:
Human immortalized periodontal ligament cell lines
Orthodontic tooth movement
Receptor activator of NF-κB ligand
Reverse transcription polymerase chain reaction
Transforming growth factor beta
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We acknowledge Drs. Takashi Takata and Masae Kitagawa (University of Hiroshima, Hiroshima, Japan) for providing human immortalized periodontal ligament cell lines. We also acknowledge the Division of Oral Physiology, Tohoku University Graduate School of Dentistry, for their generous permission to use the Flexercell Strain-Unit. The authors acknowledge the Center of Research Instruments, Institute of Development, Aging and Cancer, Tohoku University, for generous permission to use the experimental instruments. Finally, the authors give their heartfelt appreciation to the experimental reagent companies and instrument companies for their various forms of support in the rehabilitation from the damage caused by the Tohoku earthquake on March 11, 2011.
This work was supported by Grants-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (JP23689081, JP25670841, JP15K11356, JP16H05552, and JP15K11376).
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