Osteocyte-derived exosomes induced by mechanical strain promote human periodontal ligament stem cell proliferation and osteogenic differentiation in an inflammatory environment via the miR-181b-5p/PTEN/AKT signaling pathway

doi:10.21203/rs.3.rs-21278/v1

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Osteocyte-derived exosomes induced by mechanical strain promote human periodontal ligament stem cell proliferation and osteogenic differentiation in an inflammatory environment via the miR-181b-5p/PTEN/AKT signaling pathway

https://doi.org/10.21203/rs.3.rs-21278/v1

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published 17 Jul, 2020

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Background: The oral cavity is a complex environment in which periodontal tissue is constantly stimulated by external microorganisms and mechanical forces. Proper mechanical force helps maintain periodontal tissue homeostasis and improper inflammatory response can break the balance. Periodontal ligament (PDL) cells plays crucial roles in responding these challenges and maintaining the homeostasis of periodontal tissue. However, the mechanisms underlying PDL cell property changes induced by inflammatory and mechanical force microenvironments are still unclear. Recent studies have shown that exosomes function as a mean of cell-cell and cell-matrix communication in biological processes.

Methods: Human periodontal ligament stem cells (HPDLSCs) were tested by the CCK8 assay, EdU, alizarin red and ALP staining to evaluate the functions of exosomes induced by mechanical strain. MicroRNA sequencing was used to find the discrepancy miRNA in exosomes. In addition, RT-PCR, FISH, luciferase reporter assay and western blotting assay were used to investigated the mechanism of miR-181b-5p regulating proliferation and osteogenic differentiation through the PTEN/AKT pathway.

Results: In this study, the exosomes secreted by MLO-Y4 cells exposed to mechanical strain (Exosome-MS) contributed to human periodontal ligament stem cell (HPDLSC) proliferation and osteogenic differentiation. High-throughput miRNA sequencing showed that miR181b-5p was upregulated in Exosome-MS compared to the exosomes derived from MLO-Y4 cells lacking MS. The luciferase reporter assay demonstrated that miR-181b-5p may target Phosphatase tension homolog deletion (PTEN). In addition, PTEN was negatively regulated by overexpressing miR-181b-5p. PCR and western blot analyses verified that miR‐181b-5p enhanced the protein kinase B (AKT) activity and improved downstream factor transcription. Furthermore, miR-181b-5p effectively ameliorated the inhibition of HPDLSC proliferation and osteogenesis induced by inflammation.

Conclusions: This study concluded that exosomes induced by mechanical strain promote HPDLSC proliferation and osteogenic differentiation via the miR-181b-5p/PTEN/AKT signaling pathway, suggesting a potential mechanism for maintaining periodontal homeostasis.

Stem Cell & Developmental Cell Biology

human periodontal ligament stem cells

mechanical strain

exosomes

miR-181b-5p

AKT signaling pathway

The periodontium consists of the gingiva, periodontal ligament (PDL), root cementum and alveolar bone. The PDL plays a crucial role in periodontium homeostasis, repair, and nutrition [1, 2]. PDL fibers distribute the force to alveolar bone during the chewing movement, and PDL cells turn mechanical signals into biochemical signals that regulate various osteogenic-related pathways for periodontal tissue remodeling [3].

PDLSCs are adult stem cells and were first isolated from human PDL tissue [4]. These cells exhibit potential for self-renewal and multidirectional differentiation, which may be associated with mechanical loading from mastication or occlusion. PDLSCs subjected to static mechanical strain (SMS) show an increased proliferation rate and differentiation ability [5].

PDLSCs require a specific microenvironment to maintain their own undifferentiated and self-renewing state. This microenvironment is also known as the stem cell niche, and its activity depends on the interaction between cells[6]. Exosomes have been shown to function as a mean of intercellular communication in the body. Exosomes from PDLSCs promote bone regeneration and revascularization [7], and exosomes released in mechanical environments contribute to the maintenance of periodontal immune/inflammatory homeostasis [8]. Osteocytes are also mechanically sensitive cells and can secrete multiple biologically active factors to regulate bone remodeling. A previous study suggested that bone cells produce exosomes containing selective miRNAs that may be transferred to other organs [9].

Periodontitis is a bacteria-initiated inflammatory disease that causes periodontal soft and hard tissue loss and is the main cause of tooth loss in adults. The presence of a chronic inflammatory environment for a long duration changes the epigenetic characteristics of cells and reduces the regeneration capacity of periodontal tissue [5]. PDLSCs are important for the restoration of periodontal tissuesas they are the main source of cells that form new attachments between periodontal tissues and root surfaces after periodontitis treatment [10–12]. Enhancing the regeneration capacity of HPDLSCs during an inflammatory challenge is one of the goals of treating periodontitis.

In this study, we present in vitro results demonstrating that exposure of MLO-Y4 cells to MS-derived exosomes could promote HPDLSC proliferation and osteoblastic differentiation in an inflammatory environment. Moreover, we show that miR-181b-5p-mediated activation of the PTEN/PI3K/AKT axis is the key factor for this effect.

Cell culture

Human PDLSCs were isolated from extracted premolars and impacted third molars where obtained from systemically healthy adults for orthodontic purpose (18–25 years of age) with written informed consent and, and was under approved guidelines set by the Ethics Committee of Tianjin Medical University Stomatological Hospital. Primary cells were cultured as previously reported [13]. All HPDLSCs used in this study were at passage 3–5.

Murine osteocyte-like (MLO-Y4) cells were cultured in α-MEM containing 5% fetal bovine serum and 5% calf serum with penicillin-strepomycin in flasks precoated with rat tail collagen type I.

Characterization of HPDLSCs

HPDLSC surface markers were analyzed by flow cytometry. HPDLSCs (P4) were trypsinized and adjusted to 5 × 10⁶ cells/mL, and 1 µg of antibody (CD45, CD146, CD90 and CD73; eBioscience, San Jose, CA, USA) was added to 200 µl of cell suspension. The samples were incubated at 4 °C in the dark for 2 h and centrifuged at 800 r/min for 5 min. The supernatant was discarded, and the cell pellet was washed twice with PBS and resuspended in 200 µl of PBS for flow cytometry analysis (Beckman Coulter, CA, USA).

Mechanical strain loading on MLO-Y4 cells

FBS was centrifuged at 4000 × g for 15 min and then at 100,000 × g for 70 min to sediment and concentrate EVs followed by filtration through a 0.22 µm filter membrane for exosome-depleted FBS preparation. Cells were exposed to mechanical strain (MS) by the Flexcell Tension Plus system (FX-4000T, Flexcell International, Burlington, NC). MLO-Y4 cells were seeded into 6-well Bioflex plates (Flexcell International, Burlington, NC) at a density of 1 × 10⁵ cells/well and incubated for 24 h. The cells were then replaced with culture medium containing 10% exosome-depleted FBS. The experimental group was subjected to cyclic stretch with 8% shape variable at a frequency of 0.1 Hz for 30 min and the cell culture supernatant was collected after 24 h. The same operation was performed again in the next 3 days. The supernatant from the control groups was collected every 24 h for 3 days.

Exosomes isolation, purification and identification from MLO-Y4 cell culture supernatants

Briefly, cell culture supernatants were centrifuged at 300 × g for 15 min to remove cells, filtered through a 0.22 µm filter membrane to remove cellular debris, and ultracentrifuged at 100,000 × g for 70 min. The isolated pure exosomes were collected and stored at − 80 °C for future use.

Nanoparticle tracking analysis (NTA), transmission electron microscopy (TEM), and western blotting were used to identify the collected particles. Absolute size distribution of exosomes was directly tracked by the NanoSight NS 300 system (NanoSight Technology, Malvern, UK). The collected exosomes were adjusted to 10⁶/ml. Under 450 nm laser irradiation, the camera recorded for 1 min at 25 frames/second, and this process was repeated 3 times. According to the Brownian motion of exosomes, the Einstein equation was used to calculate the concentration and hydrodynamic diameter of the exosomes.

The morphology and diameter of exosomes were investigated using TEM (Hitachi HT7700 TEM, Tokyo, Japan). The exosome sample (10 µl) was placed on a copper net with a pore size of 2 nm followed by incubation at room temperature for 2 min. Filter paper was used to drain the liquid from the side of the filter. The sample was then negatively stained with 2% phosphotungstic acid solution (pH 7.0) for 1 min and then submitted to TEM for observations.

In addition, the exosomal surface-specific proteins CD63, CD81 and Alix were detected by western blot.

Cell viability and proliferation assay

Cell proliferation was measured using the Cell Counting Kit-8 (Dojindo, Japan) according to the manufacturer instruction. HPDLSCs were cultured in a 96-well plate (2 × 10⁴ cells/well) and subjected to the following treatments: PBS, Porphyromonasgingivalis lipopolysaccharide (Pg.LPS) (San Diego, CA, USA) (1 µg/mL), LPS + exosomes from normally cultured cells (Exosome); exosomes from MS-treated cells (Exosome-MS), and combination of LPS + Exo-MS. The OD value was recorded from day 0 to day 4 of culture. The absorbance was measured using a microplate reader (Bio-Tek, USA) at a wavelength of 450 nm.

5-Ethynyl-2'-deoxyuridine (EdU) staining

DNA replication activity was evaluated by EdU apollo 567 in vitro kit (Solarbio, Beijing, China) to further confirm the HPDLSC proliferation rate according to the manufacturer’s instructions. HPDLSCs were plated into a glass-bottom plate at a density of 1 × 10⁵ cells and treated by working solution for 24 h. Cell culture medium of all groups was replaced with the mixture and incubated at 37 °C for 2 h. After incubation, cells were fixed with 4% paraformaldehyde at 4 °C for 30 min and then washed three times with PBS. Cells were permeabilized with 0.1% Triton X-100 for 2 min on ice and washed twice with PBS. Nuclei were stained with DAPI (Sigma, USA). Images were captured with a confocal fluorescence microscope.

Osteogenic differentiation assay

HPDLSCs in different groups (2 × 10⁵ cells/well) were cultured in 6-well plates containing osteogenic differentiation medium (Cyagen, Suzhou, China). The medium was refreshed every 3 days until the 21st day. Cells were fixed with 4% paraformaldehyde. Mineralized nodules were observed by staining with a 1% Alizarin red solution (Cyagen, Suzhou, China). The activity of alkaline phosphatase (ALP) was analyzed using an Alkaline Phosphatase Staining Kit (MKbio, Shanghai, China). Staining images were acquired using an inverted microscope, and ImageJ was used to analyze the images.

High-throughput miRNA sequencing

The high-throughput sequencing service and subsequent bioinformatics analysis were provided by BGI Biotech (Shenzhen, China). Briefly, miRNA was purified from exosome total RNA using the TaqMan ABC miRNA Purification Kit (Thermo Scientific, USA) following the manufacturer's instructions. RNA libraries were generated and sequencing was performed using BGISEQ-500. The differential expressed miRNA was identified by BGI with the value of log2-Ratio > 1 and Q value < 0.001. Gene ontology and KEGG pathway analyses were based on NCBI.

miRNA fluorescence in situ hybridization (FISH)

The subcellular localization of miRNA was determined by FISH, which was conducted as previously reported [14]. The FAM-5’-CCCACCGACAGCAATGAATGT-3’ probe was synthesized from the sequence of miR-181b-5p. In situ hybridization was conducted according to the instructions of the FISH Detection Kit (QIAGEN, Germany) followed by counterstain with DAPI. Images were acquired with a confocal fluorescence microscope.

Transient transfection

HPDLSCs were seeded into 6-well plates (5 × 10⁵ per well) and incubated for 24 h. Cells were either left untreated or transiently transfected with miR-181b‐5p mimics, mimics NC, inhibitors and inhibitors NC (Ribobio, Guangzhou, China) using Lipofectamine 2000 (Invitrogen, USA) according to the manufacturer’s instructions. Briefly, miR‐181b‐5p mimics (50 nM), mimics NC (50 nM), inhibitors (100 nM), and inhibitors NC (100 nM) were separately mixed with diluted Lipofectamine 2000 at room temperature for 20 min. The mixtures were then cultured with cells for 48 h. The following sequences were used: miR‐181b‐5p mimics NC sense 5’-UUC UCC GAA CGU GUC ACG UTT-3’ and antisense 5’-ACG UGA CAC GUU CGG AGA ATT-3’’ miR‐181b‐5p inhibitor 5’-ACCCACCGACAGCAAUGAAUGUU-3’; and miR-181b-5p inhibitor NC 5’-CAG UAC UUU UGU GUA GUA CAA-3’.

Luciferase reporter assay

TargetScan, microT, PITA and miRanda were used to predict the potential miR-181b-5p-binding site in the 3' untranslated region (3'-UTR) of the wild and mutant PTEN gene. HPDLSCs were seeded into 24-well plates (1 × 10⁵ per well) for the luciferase reporter assays, and cells in each well were cotransfected with a pmir-GLO Dual-Luciferase miRNA Target Expression Vector (containing a wild-type or mutant PTEN 3'UTR; Promega, USA) and miR-181b-5p mimics, mimics-NC, inhibitor or inhibitor-NC using the Attractene Transfection Reagent Kit (Invitrogen, USA). The luciferase activity was assayed using a Dual Luciferase Reporter Assay Kit (Promega, USA) 24 h posttransfection according to the manufacturer's instructions.

Biotin-coupled miRNA capture

Because PTEN plays an important role in regulating cell proliferation and is one of the miR-181b-5p target genes, a pull-down assay was performed to investigate whether miR-181b-5p directly binds to PTEN. Briefly, HPDLSCs were transfected with biotinylated miRNA mimics or nonsense control (NC) (GenePharma, Shanghai, China), and cells were collected at 48 h after transfection. The biotin-conjugated RNA complex was pulled down using streptavidin-coated magnetic beads (Pierce Biotechnology, USA). The bound mRNA was purified using a RNeasy Mini Kit (QIAGEN, Germany). The enrichment of PTEN mRNA was evaluated by Real-Time PCR analysis.

Western blotting assay and antibodies

Cells were lysed using RIPA buffer to obtain total protein, and exosomal protein was extracted using a ProteoPrep® Total Extraction Sample Kit (Sigma-Aldrich, USA) following the manufacturer’s protocol. Protein concentration was measured using a BCA Protein Assay Kit (Thermo Fisher Scientific, USA). Equivalent amounts of proteins were then electrophoresed on SDS-PAGE and transferred onto PVDF membranes. Membranes were blocked using 5% BCA for 2 h at room temperature and incubated with primary antibodies at 4 °C overnight. After three PBST washes, membranes were incubated with secondary antibodies at 37 °C for 1 h. ECL solution was then prepared, and the bands on the membranes were scanned and imaged in a dark room. The results were quantified using ImageJ. GAPDH was used as an internal control.

Real-time reverse transcriptase polymerase chain reaction

Total RNA was extracted from the cells using TRIzol reagent (Invitrogen, USA). The concentration and purity of the RNA were measured using a NanoDrop One Microvolume UV-Vis Spectrophotometer (Thermo Fisher Scientific, USA) according to the manufacturer's instruction. The Prime Script RT Reagent Kit (TaKaRa, Japan) was used for reverse transcription according to the manufacturer's instructions. The SYBR Premix Ex Taq II Kit (TaKaRa, Japan) was used for real-time PCR analysis using the Roche Light Cycler 480 sequence detection system (Roche Diagnostics, Switzerland). GAPDH or U6 + miR16 was used as an internal control.

Statistical analysis

All data were presented as the means ± standard deviation (SD). The data of each group were tested for homogeneity, and the results were analyzed by one-way analysis of variance and minimum significant difference test (Fisher’s least significant difference [LSD]). P < 0.05 was considered as statistically significant. All statistical analyses were performed using SPSS 23.0 (IBM Corp., USA).

Characterization of HPDLSCs

HPDLSCs exhibited typical long spindle-shaped morphology and were arranged in a vortex observed by inverted microscope (Fig. 1A). Flow cytometry analyses showed that these cells were highly positive for the mesenchymal stem cell-positive markers CD73, CD146 and CD90 (Fig. 1B-1D) but were negative for CD45 (Fig. 1E). These findings indicated that HPDLSCs were successfully isolated from periodontal ligament tissue.

Characterization of exosomes derived from MLO-Y4 culture supernatants

NTA, TEM, and western blotting were used to identify the purified exosomes. TEM showed that MLO-Y4-Exos exhibited a round morphology with a size ranging from 30 to 100 nm (Fig. 2A). Western blotting showed that MLO-Y4-Exos were positive for the characteristic exosomal surface markers including CD63, CD81 and Alix (Fig. 2B). The NTA measurements revealed that the size of these particles varied from 30 to 100 nm (Fig. 2C). The exosome particle size distribution intensity is shown in Fig. 2D. Therefore, these analyses confirmed that the MLO-Y4-derived particles collected in our experiments are exosomes.

Effects of Exosome-MS on the proliferation of HPDLSCs

To investigate the functional roles of exosomes derived from MLO-Y4 cells subjected to mechanical strain (Exosome-MS) on cell proliferation under normal or inflammatory conditions, HPDLSCs were treated with Pg.LPS or normal media for 12 h followed by coculture with Exosome or Exosome-MS treatments for a series of functional assays. From day 2, the CCK-8 results revealed that the cell proliferation rate in the Exosome-MS group increased compared to that in the control group (P < 0.05) and that THE LPS treatment markedly reduced the proliferative capability of cells (P < 0.05) (Fig. 3B). In addition, the LPS-induced downregulation of proliferation was rescued by Exosome-MS, whereas Exosome did not significantly differ from the control group. To confirm the ability of Exosome-MS to promote proliferation, an EdU assay was performed (Fig. 3C). The EdU assay result was the similar as that of the CCK-8 assay (Fig. 3D). These results indicated that exosomes produced by mechanically stimulated cells promote proliferation, even in an inflammatory environment, and reduce the inhibitory effects of inflammation but that exosomes produced from unstimulated cells do not have these effects.

Effects of Exosome-MS on osteogenic differentiation of HPDLSCs

HPDLSCs were cultured in osteogenic differentiation medium, and Alizarin red staining was used to evaluate the calcium nodule-forming ability. The Alizarin red staining results showed that the number of calcium nodules in the Exosome-MS group was significantly higher than that in the control group, and the staining in the Exosome-MS group was also more intense than that in the control group (Fig. 4B). There were fewer calcium nodules in the LPS and LPS + Exosome groups, and the numbers of calcium nodules in these groups were significantly different from that in the LPS + Exosome-MS group. The ALP staining results were the similar as the Alizarin red staining results(Fig. 4A). Thus, these findings suggested that Exosome-MS not only promotes proliferation but also promotes osteogenic differentiation of HPDLSCs even in an inflammatory environment.

Analysis of functional attributes connected to Exosome-MS changes in gene sets and signaling pathways

We explored the molecular biological mechanisms of Exosome-MS in promoting cell proliferation and osteogenic differentiation. miRNA-seq was performed to detect differential gene expression between Exosome-MS and Exosome. A total of 121 targets were upregulated and 85 targets were downregulated in Exosome-MS compared with Exosome, and the results were illustrated using a heat map (Fig. 5A and 5B). GO enrichment analysis suggested that the miRNAs in Exosome-MS play a key role in metabolic processes (Fig. 5C and 5D). KEGG pathway enrichment analysis was performed to evaluate the characteristics of exosome-mediated gene expression (Fig. 5E). Related genes were more abundant in environmental signal transduction and infectious diseases.

miR-181b-5p targets to PTEN

Among the differentially expressed microRNAs, miR-181b-5p was selected for further research. Recent studies have shown that miR-181b-5p plays an important role in regulating cell proliferation, apoptosis [15] and the immune inflammatory response [16]. miR-181b-5p expression was upregulated in Exosome-MS (Fig. 6A). FISH assays showed that miR-181b-5p was mainly located in the cytoplasm of HPDLSCs treated with exosomes and that the Exosome-MS group had a higher fluorescence intensity than the Exosome group (Fig. 6B).

We screened the PITA (http://genie.weizmann.ac.il) [17], DIANA microT (http://diana.imis.athena-innovation.gr/DianaTools/index.php?r=microT_CDS/index) [18], TargetScan (http://www.targetscan.org) [19] and miRnada (http://www.microrna.org) [20] databases to predict the target genes of miR-181b-5p. We obtained 157 crossover genes. Phosphatase tensin homolog deletion (PTEN) is closely related to cell growth and apoptosis [21]. The results showed that miR-181b-5p is predicted to interact with wild-type and mutant PTEN (Fig. 6D), and the luciferase assay also revealed that miR-181b-5p interacted with PTEN (Fig. 6G). PCR showed that overexpression of miR-181b-5p inhibited PTEN expression (Fig. 6E) and that suppression of miR-181b-5p upregulated PTEN expression (Fig. 6F). To detect whether miR-181b-5p directly binds to PTEN, miR-181b-5p was labeled with biotin, and the enrichment observed in the Biotin-miR-181b-5p group was 4.7-fold greater than that in the control group (Fig. 6H).

Exosomal miR-181b-5p regulates HPDLSC proliferation through the PTEN/AKT signaling pathway

The PI3K/Akt signaling pathway is one of the most important pathways for cell survival, cell growth, glucose metabolism and protein synthesis in host cells [22], and PTEN negatively regulates the PI3K/Akt pathway. To verify the mechanisms of exosomal miR-181b-5p promoting HPDLSC proliferation, real time-PCR was performed to investigate the related genes including PTEN, cyclin D1 (CCDN1), phosphoinositide-3-kinase regulatory subunit 1 (PI3KR1), phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PI3KCA) in the PTEN/PI3K/Akt signaling pathway. The results showed that CCDN1, PI3KR1, and PIK3CA were upregulated in the miR181b-5p mimics group but downregulated in the miR181b-5p inhibitor group. PTEN showed the opposite trend. In addition, western blotting was performed to further verify the AKT phosphorylation level. The results showed that miR181b-5p promoted PIP2 phosphorylation to PIP3 by inhibiting PTEN, thereby activating AKT and its downstream factors.

Exosomal-MS regulates HPDLSC osteogenic differentiation via miR-181b-5p

To verify the mechanisms of Exosome-MS in promoting HPDLSC osteogenic differentiation under inflammatory conditions, real time-PCR was performed to investigate related genes including bone morphogenetic protein-2 (BMP2) and RUNX family transcription factor 2 (Runx2). In addition, ALP and Alizarin red staining assays were performed after 21 days of induction. The results showed that addition of miR-181b-5p mimics to the LPS + Exosome group improved LPS inhibition of BMP2, Runx2, AKT1 and PI3KCA expression but that the miR-181b-5p inhibitor downregulated gene expression in the LPS + Exosome-MS group. These results demonstrated that Exosome-MS regulates osteogenic differentiation through miR-181b-5p.

Mechanical stimulation plays an essential role in regulating bone remodeling and maintaining bone homeostasis [23], and PDLSCs are indispensable in this process [24]. Therefore, exploring the cell niche changes of PDLSCs in a mechanical environment is beneficial to further understand the role of occlusal force in the reconstruction of periodontal tissues. In our study, MLO-Y4-Exos induced by MS promoted proliferation and osteogenic differentiation of HPDLSCs and rescued the inhibitory effects of LPS-induced inflammation, which were mediated by the miR-181b-5p/PTEN/AKT axis.

Previous studies have focused on the regulation of osteogenesis by periodontal ligament cells under mechanical force. It was reported that PDLSCs maintain bone homeostasis during tooth movement by regulating the balance between osteoblastic and osteoclastic process via the Wnt/β-catenin pathway [24]. Osteocytes are the most abundant cells in alveolar bone, but less attention has been paid to the response of bone cells exposed to mechanical forces and their effects on surrounding cells. In our study, exosomes derived from osteocytes stimulated by MS altered the PDLSC survival environment. Thus, the mechanical force promoted PDLSC proliferation and differentiation through indirect pathways mediated by exosomes. In addition, we investigated the mechanisms of exosomes in promoting proliferation and osteogenic differentiation. The present study showed that activation of the miR-181b-5p/PTEN/AKT pathway is vital to explain the above phenomena.

The proliferation effect of exosomes has also been demonstrated in previous studies. MSC exosomes increase PDL cell migration and proliferation through CD73-mediated adenosine receptor activation of pro-survival AKT and ERK signaling. Inhibition of AKT or ERK phosphorylation suppresses PDL cell migration and proliferation [25]. Recent studies have also reported that miRNAs are involved in the development of periodontal disease, especially the process of alveolar bone destruction [26–28]. In addition, mechanically sensitive miRNAs have been found in osteoblasts and have been shown regulate cell differentiation [29]. During bone formation, miRNA molecules are highly enriched in exosomes, and miRNAs play an important role as a "matrix" in bone development through the transfer of exosomes between cells. In the present study, miR-181b-5p was identified in Exosome-MS (Fig. 6A) and localized in the cytoplasm (Fig. 6B). Exosomal miRNAs are involved in a variety of cellular behaviors, including angiogenesis, stem cell proliferation and differentiation, the immune inflammatory response, and tumorigenesis [30–33]. The luciferase assay and biotin labeling demonstrated that miR-181b-5p interacts with PTEN (Fig. 6G and 6H). Overexpression of miR-181b‐5p inhibited PTEN and activated the AKT pathway and downstream factors in the present study (Fig. 7). Akt can be activated by small-magnitude mechanical stress [34], and it promotes cell survival by inhibiting apoptosis through inactivating apoptotic proteins [35]. Our results demonstrated that MS upregulates miR-181b-5p in exosomes and activates the AKT pathway by silencing PTEN.

Toll-like receptor-4 (TLR4) on the cell surface recognize Porphyromonas gingivalis lipopolysaccharide (Pg.LPS) [36], which activates downstream proinflammatory cytokine production and cell apoptosis, eventually causing alveolar bone damage [37]. Consistent with previous reports, BMP2 and Runx2 expression in PDLSCs was downregulated in the inflammatory environment [38]. Our results showed that overexpression of miR-181b-5p improves osteogenesis in HPDLSCs under inflammatory conditions (Fig. 8).

In conclusion, proper mechanical stimulation is beneficial to maintain stem cell properties in an inflammatory environment. The present results not only indicated that the miR-181b-5p/PTEN/AKT signaling pathway functions as a potentially novel mechanism for physiological mechanical force contributing to periodontal homeostasis through the intercellular communication of exosomes in periodontal tissue but also suggested the potential role of exosomes induced by mechanical force as therapeutic tools for periodontitis and periodontal regeneration.

PDL Periodontal ligament

HPDLSC Human periodontal ligment stem cell

P.g Porphyromonasgingivalis

PI3K Phosphatidylinositol-4,5-bisphosphate 3-kinase

Akt Protein kinase B

Runx2 Runt-related transcription factor 2

BMP2 Bone morphogenetic protein-2

PTEN Phosphate and tension homology deleted on chromsome

NTA Nanoparticle Tracking Analysis

FISH Fluorescence in situ hybridization

EdU 5-ethynyl-2’-deoxyuridine

LPS Lipopolysaccharide

TEM Transmission Electron Microscope

miRNA MicroRNA

CCDN1 Cyclin D1

PI3KR1 Phosphoinositide-3-kinase regulatory subunit 1

PI3KCA Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha

TLR4 Toll-like receptor-4

SD Standard Deviation

Acknowledgments

Not applicable.

Funding

This study was supported by the 13th 5-Year Comprehensive Investment and First-class Discipline Construction/Stomatology (No. 11601502/xk0126) and Tianjin Medical University Science Fund Project (No. 2016KYZM06).

Availability of data and material

The datasets during and/or analysed during the current study available from the corresponding author on reasonable request.

Author Contributions

M.-j. K. and Y.-L.W. spearheaded and supervised all of the experiments. M.-j.K. and P.-y. L. designed this project. P.-y. L., M.-j. K., P.-f. G., Y.-Y.Y. and F.-f. M. conducted experiments. P.-y.L., P.-f.G., and Z.-h.W. analyzed data. G.-j.T. provided materials. P.-y. L., M.-j.K. and P.-f.G. prepared the manuscript. L.S. provided great help in correcting the grammatical errors and language polishing for this article. All authors reviewed and approved the manuscript.

Ethics approval and consent to participate

Each patient signed an informed consent form for tissue sample donation. This study was approved by the Ethics Committee of Tianjin Medical University Stomatological Hospital (TMUhMEC20190929) and was conducted according to all current ethics guidelines.

Consent for publication

Not applicable.

Competing interests

The authors declare no conflict of interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Sup. Fig. 1 The effects of supernatants from MLO-Y4 cells stimulated by different mechanical forces on HPDLSC proliferation (*P < 0.05 and **P < 0.01).

Sup. Fig. 2 Upregulated miRNA levels in Exosome and Exosome-MS were analyzed using RT-qPCR. (*P < 0.05 and **P < 0.01)

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Osteocyte-derived exosomes induced by mechanical strain promote human periodontal ligament stem cell proliferation and osteogenic differentiation in an inflammatory environment via the miR-181b-5p/PTEN/AKT signaling pathway

Status:

Journal Publication

Version 1

Abstract

Figures

Introduction

Materials And Methods

Cell culture

Characterization of HPDLSCs

Mechanical strain loading on MLO-Y4 cells

Exosomes isolation, purification and identification from MLO-Y4 cell culture supernatants

Cell viability and proliferation assay

5-Ethynyl-2'-deoxyuridine (EdU) staining

Osteogenic differentiation assay

High-throughput miRNA sequencing

miRNA fluorescence in situ hybridization (FISH)

Transient transfection

Luciferase reporter assay

Biotin-coupled miRNA capture

Western blotting assay and antibodies

Real-time reverse transcriptase polymerase chain reaction

Statistical analysis

Results

Characterization of HPDLSCs

Characterization of exosomes derived from MLO-Y4 culture supernatants

Effects of Exosome-MS on the proliferation of HPDLSCs

Effects of Exosome-MS on osteogenic differentiation of HPDLSCs

Analysis of functional attributes connected to Exosome-MS changes in gene sets and signaling pathways

miR-181b-5p targets to PTEN

Exosomal miR-181b-5p regulates HPDLSC proliferation through the PTEN/AKT signaling pathway

Exosomal-MS regulates HPDLSC osteogenic differentiation via miR-181b-5p

Discussion

Conclusions

Abbreviations

Declarations

References

Supplemental Figures

Supplementary Files

Status:

Journal Publication

Version 1