Alveolar bone is the thickened ridge of jaw bone that supports teeth. It is subject to constant occlusal force and pathogens invasion, and is therefore under active bone remodeling and immunomodulation. Alveolar bone holds a distinct niche from long bone considering their different developmental origin and postnatal remodeling pattern. However, a systematic explanation of alveolar bone at single-cell level is still lacking. Here, we construct a single-cell atlas of mouse mandibular alveolar bone through single-cell RNA sequencing (scRNA-seq). A more active immune microenvironment is identified in alveolar bone, with a higher proportion of mature immune cells than in long bone. Among all immune cell populations, the monocyte/macrophage subpopulation most actively interacts with mesenchymal stem cells (MSCs) subpopulation. Alveolar bone monocytes/macrophages express a higher level of Oncostatin M (Osm) compared to long bone, which promotes osteogenic differentiation and inhibits adipogenic differentiation of MSCs. In summary, our study reveals a unique immune microenvironment of alveolar bone, which may provide a more precise immune-modulatory target for therapeutic treatment of oral diseases.
Due to tooth-derived inflammatory response and occlusal stress stimuli, the metabolism and remodeling of alveolar bone are considered to be the most active among the entire skeletal system.1,2,3,4 Alveolar bones have a different developmental origin and ossification process compared with long bones and other bones.5 Craniofacial bone marrow mesenchymal stem cells (MSCs) show higher proliferation rate and osteogenic differentiation potential, but lower chondrogenic and adipogenic differentiation capability.6,7 Interestingly, alveolar bone is more resistant to bone loss and adipocytes accumulation than long bone in ovariectomized rodents.8,9 Alveolar bone contacts with the external microenvironment through the periodontal barrier, which exerts important regulatory effects on immune homeostasis of alveolar bone.10 Although accumulating evidence demonstrated unique physiological characteristics of alveolar bone, there is a lack of systematic description of alveolar bone cell heterogeneity and the difference from long bone.
Single-cell RNA sequencing (scRNA-seq) makes it be possible to analyze tissue heterogeneity at the level of individual cell and explore the contribution of different cell subtypes to physiological function and pathogenesis. Recently, two independent studies constructed complete single-cell atlas of long bone stromal cells with fluorescence-activated cell sorting (FACS).11,12 Baccin et al. further explored the spatial heterogeneity of bone marrow stromal cells with laser capture microdissection technique.13
Besides stromal cells, the skeletal system is also the largest reservoir of haematopoietic lineages, which contains haematopoietic stem cells, lymphoid/myeloid progenitors, and mature immune cells. These immune cells interact with bone marrow stromal cells, thereby regulating the homeostasis of skeletal system.14 The regulatory effect of macrophages on bone stromal cells has been confirmed.15,16 Mice depleted of macrophages showed an osteoporotic phenotype.17 In aged mice that received bone marrow macrophages transplantation from young mice, transplanted macrophage infiltration was observed at the fracture site and the healing of fracture was accelerated.18 Although previous scRNA-seq studies have constructed single-cell atlas of long bone marrow cells, study focusing on the regulation of immune cell populations on bone marrow stromal cells and bone homeostasis through scRNA-seq is still lacking.
In this study, we perform scRNA-seq on mouse mandibular alveolar bone and reveal that macrophages are the largest cell population that interacts with MSCs. Compared with long bone marrow (LBM), the proportion of activated macrophage subcluster in alveolar bone marrow (ABM) is higher, and this subcluster is the major group that secretes cytokine Oncostatin M (Osm). ABM macrophage-conditioned medium more effectively promotes osteogenic differentiation and inhibits adipogenic differentiation of MSCs through an Osm-dependent pathway.
Characterization of mandibular alveolar bone single-cell atlas
The mouse mandibular alveolar bones were dissected for enzymatic digestion and subjected to droplet-based scRNA-seq (Fig. 1a). A total number of 10 224 cells were obtained with 29 053 genes of each cell. We preprocessed the dataset with Seurat package. The median value of feature_RNA is between 1 000 and 2 000, and cells with mitochondrial gene expression higher than 25% are filtered out (Fig. S1a, b). After quality control, 2 000 genes with the most variable value from 29 053 genes were selected for subsequent analysis (Fig. S1c). Then the UMAP method was applied to reduce the dimensionality (Fig. S1c). Cells were divided into 12 subgroups based on classic cell surface markers (neutrophil—S100a8, myeloid progenitor—Mpo, macrophage—Csf1r, dendritic cell—Siglech, B cell—Cd79a, pro-B cell—Vpreb1, T cell—Cd3g, natural killer cell—Klrd1, megakaryocyte—Ms4a2, erythrocyte—Hbb-bt, hematopoietic stem and progenitor cell—Cd34, and mesenchymal cell—Col1a1) (Fig. 1c, d). The top 5 expressed genes expressed in each defined cell type were identified and compared (Fig. S1d).
Since non-immune cells (mesenchymal stromal cells) accounted for only 1.74% of all identified cells, these cells were divided into a small cluster for identification. They are divided into four subclusters (Fig. S2a), categorized as MSCs (Lepr+), osteoblasts (Bglap+), endothelial cells (Cdh5+), and neurological cells (Plp1+) (Fig. S2b, c). As expected, chondrocyte was not identified in alveolar bone stromal cells, which is different from that of long bone.
Identification of cell–cell interaction in alveolar bone microenvironment
Using CellPhoneDB2, a cell ligand/receptor pairing-based database,19 we identified a close interaction between the monocytes/macrophages and MSCs (Fig. 2a). To further identify the regulatory effects of macrophages on stromal cells, we plotted the essential cytokines that involved in macrophage-MSC crosstalk, including Tgfb,20 Osm,21 Lrp118, Igf122, and Bmps23 (Fig. 2b). We found that Osm/Osmr and Osm/Lifr pathways were the most significantly enriched in monocyte/macrophage-MSC crosstalk. Tgfb and Lrp1 related pathways also have a strong interaction with MSCs. However, the expression of Bmp2, Bmp4, and Igf1 in alveolar bone monocyte/macrophages was barely detectable (Fig. 2c), indicating a limited role of these pathways in regulating monocyte/macrophage-MSC crosstalk. The expression of corresponding receptors in different types of stromal cells was also shown. Bmpr1a and Mdk were mainly expressed in MSCs, while other receptors were widely expressed in various cell types (Fig. 2d).
Comparative analysis of the heterogeneity of monocytes/macrophages
To unveil the unique characteristics of alveolar bone-derived monocytes/macrophages, we retrieved published scRNA-seq datasets of immune organs (bone marrow, peripheral blood mononuclear cells, peritoneum, and spleen) for comparative analysis (Fig. 3a, Fig. S3a). The Csf1r-positive cell population was extracted and identified as monocyte/macrophage (Fig. S3b). The monocyte/macrophage population was divided into four subclusters (Fig. 3b). Clusters 0 and 1 expressed universal markers of monocytes/macrophages, such as Csf1r, Cd68, and Cd14 (Fig. 3c). For cluster 1, the polarized macrophage markers, such as Stat1, Il1b, and Ccr2, were highly expressed (Fig. 3c). For cluster 2, markers of alternatively activated macrophages, such as Mrc1 and Cd209f, were highly expressed.
Next, we performed GO enrichment analysis and found that cluster 0 was enriched in phagocytic functions and antigen presentation (Fig. 3d). Cluster 1 was related to cytokine secretion, bacterial and intracellular pathogen immune response. Characteristic features of alternatively polarized macrophages such as wound healing and regulation of blood vessel formation, were found in cluster 2. The biological functions of the cluster 3 were enriched in cell division, DNA replication, and cell proliferation-related pathways. In brief, cluster 3 was the main proliferative population of monocyte/macrophage, and clusters 0, 1, and 2 were mature monocyte/macrophage populations with different functions.
As monocytes/macrophages are highly plastic that can be polarized to different states depending on the tissue microenvironment,24,25 we compared the cell composition among monocytes/macrophages from different origins (Fig. 3e). ABM and LBM had the closest cell composition. Cluster 1 accounted for a high proportion of ABM, LBM, and peripheral blood mononuclear cells (PBMC). Interestingly, almost all the cells in PBMC were distributed in cluster 1 and most cells in peritoneum were enriched in cluster 2. Monocytes/macrophages in the spleen were evenly distributed in clusters 0, 1, and 2. Cluster 3 was almost exclusively distributed in bone marrow tissue.
Through flow cytometry analyses of ABM and LBM, we verified that the proportion of Cd86+ (a classical polarization marker) macrophages in ABM (~28%) was about twice that of LBM (~11%), while that of Cd206+ (alternatively polarization marker) macrophages in ABM was slightly lower (Fig. 3f, Fig. S4). Moreover, through the combined analysis of single-cell sequencing of immune cells in ABM and LBM, we found that the ratio of mature B cells and neutrophils is higher in ABM, and the proportion of pro-B cells and myeloid prog cells is higher in LBM (Fig. S5).
Based on the gene expression dynamics of monocytes/macrophages, we constructed a pseudotime developmental tree and determined two independent branch points (Fig. 4a). The 4 monocyte/macrophage subclusters scattered at different branches in the developmental tree (Fig. 4b). Cluster 3 had the lowest pseudotime value and was located at the initial position of the developmental tree, indicating a developmental origin for other subclusters. This observation was consistent with the GO enrichment of cluster 3 (as a proliferative population) (Fig. 3d). Cluster 0 and 1 located at two different branches, while cluster 2 distributed more extensively, partially overlapping with clusters 0 and 1.
The gene expression pattern across pseudotime showed that the expression curves of Cd68 and Csf1r were relatively smooth (Fig. 4c). The increase in the expression of Apoe and Adgre1 was accompanied by a decrease in the expression of Il1b and Stat1, but the expression of Mki67 and Pcna was only upregulated in cluster 3. As shown in Fig. 4d, genes with the most significant changes in the two branches were clustered.
Meanwhile, we found that the expression of Bmp2 and Igf1, which was barely detectable in ABM-derived monocytes/macrophages (Fig. 2c), was significantly increased in other sources of macrophages (in peritoneal macrophages) (Fig. S6a). The expression of several angiogenesis-related growth factors differed within subclusters (Fig. S6b). Vegfa and Pigf were highly expressed in cluster 1, and Vcam1 was mainly expressed in cluster 2, suggesting that monocytes/macrophages from different subclusters have different patterns of cytokine secretion.
Regulatory effect of monocytes/macrophages on MSCs
To compare the regulatory effects of ABM- and LBM-derived monocytes/macrophages on MSCs, we supplemented these two types of conditioned mediums into the MSCs culture, respectively (Fig. 5a). Both conditioned mediums promoted the proliferation of MSCs, and ABM-derived one induced a greater proliferation on day 5 (Fig. 5b). Although both conditioned mediums enhanced the colony-forming ability of MSCs, the effect of ABM was more significant (Fig. 5c, d). In addition, scratch assay showed that ABM-derived monocytes/macrophages conditioned medium more efficiently accelerated the migration of MSCs (Fig. 5e, f).
Next, we sought to compare their effect on differentiation of MSCs. Alkaline phosphatase (ALP) staining and Alizarin red (ARS) staining proved that both conditioned mediums promoted the osteogenic differentiation of MSCs (Fig. 5g–j). In addition, the expressions of osteogenesis-related genes (Osx, Runx2, Bglap, Col1a1) were significantly upregulated (Fig. 5k). As for adipogenic differentiation of MSCs, both macrophage-conditioned medium inhibited lipid droplet formation (Fig. 5l, m) and downregulated the expression of adipogenic-related genes (Pparg, Cebpa, Adipoq, Plin1) (Fig. 5n). Notably, the conditioned medium from ABM-derived monocytes/macrophages exhibited an enhanced effect in promoting osteogenic differentiation and inhibiting adipogenic differentiation of MSCs, which indicated a different immune-modulatory potential between alveolar bone and long bone.
Osm is highly expressed in ABM-derived monocytes/macrophages
Next, we explored the underlying mechanism by comparing the expression of previously reported 59 cytokines.26 Osm was identified as the most differently expressed cytokine between ABM and LBM monocyte/macrophage (Fig. 6a). We found that the expression of Osm in ABM-derived macrophage was significantly higher than other tissues (Fig. 6b, c). This observation was further confirmed by qRT-PCR analysis and enzyme-linked immunosorbent assay (ELISA) (Fig. 6d, e).
Osm is a regulatory cytokine considered to be secreted by the classically polarized macrophages.27,28 Among the four monocyte/macrophage subclusters, we found that Osm was mainly expressed in cluster 1 (Fig. 6f, g). Therefore, we supposed that the higher proportion of activated macrophages in ABM led to the increased expression of Osm, which subsequently regulate the osteogenic and adipogenic differentiation of MSCs.
The regulatory effect of monocytes/macrophages on MSCs is Osm-dependent
To test whether the effect of monocytes/macrophages conditioned medium on the osteogenic differentiation of MSCs was Osm-dependent, we added Osm neutralizing antibody to the conditioned medium. Osm antibody significantly weakened the ALP activity and ARS staining induced by macrophage-conditioned medium (Fig. 7a–d), and the expression of osteogenesis-related genes was also downregulated (Fig. 7e). Osm neutralization partially rescued the lipid droplet formation of MSCs under macrophage-conditioned medium (Fig. 7f, g), and increased the expression of adipogenesis-related genes (Fig. 7h). Notably, after Osm neutralization, ABM and LBM macrophage-conditioned medium showed similar osteogenic and adipogenic potential, suggesting the higher expression of Osm in ABM-derived monocytes/macrophages was a key factor that led to the different effects between the ABM and LBM.
The oral environment is resided with a complex microbial community, and periodontal microorganism can penetrate the periodontal barrier to alveolar bone.29 Therefore, the immune homeostasis of alveolar bone might be directly affected by microorganisms. Besides, alveolar bone is bearing mechanical loads, whose force is two times higher than that of long bones.30,31 A recent study showed that mechanical stimulation could promote the conversion of myeloid-derived monocytes into an activated status,32 suggesting that occlusal force might lead to the difference of the immune microenvironment between alveolar bone and long bone.
In this study, we constructed a single-cell atlas of the mouse mandibular alveolar bone by 10x scRNA-seq, and found that immune cells in the mouse mandibular microenvironment accounted for the majority of cell components. We conducted a cell-to-cell communication analysis and found that among various types of immune cells, monocyte/macrophage population had the most interactions with MSC population. Based on previous studies about the regulation of osteogenic differentiation by monocytes and macrophages,18,22,23,33,34 we analyzed several previously reported classic pathways for monocytes/macrophages to regulate MSCs, and found Tgfb, Osm, and Lrp1 were widely expressed in alveolar bone monocytes/macrophages. As for the expression of cytokine receptors in stromal cells, both Osmr and Lifr were expressed in MSCs and osteoblasts, while Osmr was also highly expressed in endothelial cells. Study has shown that Osm could also promote angiogenesis in vitro and in vivo.35 In addition, we found that in the monocyte/macrophage population, the expression of growth factors related to angiogenesis including Vegfa and Pigf was also higher. Therefore, we suppose that macrophages participate in the maintenance of bone homeostasis by regulating both osteogenesis and angiogenesis.
The monocyte/macrophages were divided into four main subclusters, and the proportions of each subcluster from different tissues were quite different. Compared with long bone, the proportion of the cluster 1 (classically polarized monocyte/macrophage) in the ABM was relatively higher. Interestingly, the proportion of cluster 2 (alternatively polarized monocyte/macrophage) was very low in both ABM and LBM. Monocytes/macrophages in bone marrow and peripheral blood are mainly derived from bone marrow HSCs, while monocytes/macrophages in peritoneum are generally considered as tissue-resident macrophages. The different tissue sources and microenvironment have significant effects on the state of monocyte/macrophages.33,36 In this study, we found that the monocyte/macrophage population in bone marrow microenvironment participates in the regulation of MSCs and bone homeostasis by expressing Tgfb, Osm, and Lrp1 rather than Bmps and Wnts.
Previous study revealed that monocyte/macrophage-conditioned medium could promote MSCs colony formation in vitro.18 In this study, we observed that ABM-derived monocyte/macrophage-conditioned medium more effectively promote the proliferation and migration of MSCs, meanwhile enhancing osteogenic differentiation and inhibiting adipogenic differentiation. Although the monocyte/macrophage population may lose part of the cell heterogeneity during in vitro culture, it can still reflect the different regulatory effects of monocyte/macrophage derived from alveolar bone compared to long bone. To explore the mechanism responsible for their different regulatory effects, we compared the expression of cytokines in ABM and LBM monocytes/macrophages through differential gene analysis. We found Osm is most significantly upregulated among the 59 cytokines.
Osm is a cytokine secreted by monocytes/macrophages, and has important regulatory role on bone homeostasis.37,38,39,40 Osm receptor knockout mice exhibit decreased bone remodeling activity.34 In a tibial defect model, Osm knockout led to a decrease in osteoblasts number and delayed bone healing.41 Moreover, Osm inhibited the adipogenic differentiation of MSCs.42 Osm knockout mice show increased adipose tissue accumulation in bone marrow with age.43 Therefore, we speculate that the higher expression of Osm secreted by monocyte/macrophage in ABM may regulate the fate commitment of MSCs, leading to different biological characteristics of alveolar bone and long bone. In addition, Osm has an indirect role on osteoclasts, because it is one of the most important cytokines that stimulates osteoblasts to secrete receptor activator of nuclear factor-kappa B ligand (RANKL).44 We, therefore, speculate that the high expression of Osm might induce more active osteoclasts in the alveolar bone to participating alveolar bone remodeling. Further study is expected to elucidate the role of Osm on osteoclast in ABM.
In summary, we constructed a single-cell atlas of mouse mandibular alveolar bone through 10x scRNA-seq, and verified the regulatory effect of monocytes/macrophages on MSCs. Our study reveals a unique immune microenvironment of alveolar bone, which might provide a more precise immune-modulatory target for therapeutic treatment of oral diseases.
Materials and methods
Single-cell RNA sequencing
Eight 12-week-old male C57BL/6J wild-type mice (Chengdu Dossy Experimental Animals CO.LTD) were combined to extract single-cell suspensions. Mandible was carefully dissected under a stereo microscope to obtain the mandibular alveolar bone tissue. Soft tissues and molars are removed. Jaw bone around the incisor and behind condyle was cut off. Subsequently, the obtained alveolar bone tissue was cut into small pieces (<1 mm3) and digested in 1 mg·mL−1 collagenase type I (Worthington) and 1 mg·mL−1 Dispase II (Sigma-Aldrich) at 37 °C for 1 h (200 r·min−1). The sample was then collected into a centrifuge tube through a 40-μm filter, and the supernatant was removed after centrifugation. 1 mL of ACK lysis buffer was added on ice for 5 min to lyse red blood cells, and the supernatant was removed by centrifugation.
The centrifuged cells were resuspended in 0.4% BSA PBS solution. Placenta blue stain was used to calculate the number of cells and cell viability on a hemocytometer, and the cell concentration was adjusted to 800–1 500 cells per μL. About 20 000 cells were loaded to capture 10 000 cells. cDNA library was constructed using Chromium single-cell v3.0 reagent, and sequenced on the Illumina Nova-seq system.
Preprocessing of scRNA-seq data
After obtaining the initial sequencing data, we compared them to the mouse genome mm10, and folded the UMI with Cellranger (version 3.1, 10x Genomics) software to obtain a single-cell gene expression matrix. Then we imported the expression matrix into the Seurat package (v 4.0) for further analysis. Genes expressed in less than three cells are deleted, mitochondrial genes >25%, and cells with genes <300 are filtered out. The FindVariableGenes function in the Seurat package is used to select variable genes, and then principal component analysis (PCA) was performed, and UMAP dimensionality reduction and visualization were performed based on PCA results. According to the specific genes of different subgroups, we annotated the cell types of different subclusters.
Cell–cell interaction analysis
CellPhoneDB2 is a Python-based analysis tool for calculating the interaction between ligands and receptors between different cell populations. So far, CellPhoneDB2 only supports the input of human genes. Therefore, we first mapped the mouse mgi_symbol to human hgnc_symbol through the BioMart package, and then used CellPhoneDB2 for cell–cell communication calculation and analysis. To reveal the strength of the specific pathways between macrophages and MSCs, we selected several common macrophage-MSC-related pathways for visualization, including Bmps, Wnts, Osm, Tgfb, and Lrp1.
To determine the differentiation trajectory of monocytes/macrophages, we used Monocle2 package to calculate the differentiation trajectory of these cells. After determining the pseudotime value arrangement and differentiation trajectory, we used the plot_genes_in_pseudotime function in the Monocle2 package to show the changes of classic macrophage marker genes in the differentiation trajectory. The clustered heatmap of the expression pattern of the hub genes (P < 1e–8) in branches 1 and 2 was displayed with the plot_pseudotime heatmap function.
Flow cytometry analysis
The mouse mandibular alveolar bone and femur were obtained according to the above manner. Then the alveolar bone and femur were cut into pieces, digested in 1 mg·mL−1 collagenase I, 1 mg·mL−1 dispase II at 37 °C for 30 min, centrifuged. After lysis of red blood cells on ice, the samples were passed through a 70-μm filter, centrifuged, and ready for staining. FITC anti-mouse Cd11b, PE-Cy7 anti-mouse Cd86, and APC anti-mouse Cd206 were purchased from BD Biosciences, and the permeabilization/fixation kit was purchased from eBioscience. All staining processes were performed in 100 μL PBS. For cell surface staining, after blocking the cell surface Fc receptors, the flow cytometry antibody was directly added to the cell suspension and stained on ice for 30 min. For intracellular antibody staining, the fixed cells were permeabilized and then stained with flow cytometry antibody for 30 min. The samples were then tested using flow cytometry (BD Biosciences), and the flow cytometry data were analyzed and visualized using Flowjo software.
Culture of bone marrow MSCs
To isolate MSCs, we separated the femur and tibia from C57BL/6J mice in PBS, the bone marrow was flushed out and transferred to α-MEM medium containing 10% FBS (Gibco) and 1% penicillin/streptomycin (Hyclone). After culturing in a petri dish with a diameter of 100 mm at 37 °C, a 5% CO2 constant temperature incubator for 48 h, the medium was changed to remove non-adherent cells.45 Afterward, the medium was changed every 3 days and digested when the confluence reached 80% for the next experiment.
Isolation of monocytes/macrophages
To isolate macrophages from long bone, we dissected the femur and tibia as described above and flush out the bone marrow to mix with the culture medium. For macrophages from ABM, we separated the alveolar bone as described above and then cut the alveolar bone into small pieces in the culture medium. After the bone pieces settled, the culture medium containing the bone marrow cells was transferred. To balance the number of primary cells extracted from mouse alveolar bone and femur, the mandibular alveolar bones of 10 mice were combined. Then the isolated cells were cultured with 10% FBS and 1% penicillin/streptomycin αMEM medium, and 50 ng·mL−1 M-CSF (R&D Systems) was added.46 The medium was changed three days later to remove non-adherent cells.
To obtain the monocyte/macrophage-conditioned medium, the medium was changed once every three days and the conditioned medium was collected, centrifuged at 1 500 × g for 10 min. The supernatant was stored for further use. For conditioned medium treatment, the conditioned medium collected from the ABM and LBM monocyte/macrophage directly mixed with the complete culture medium, osteogenic induction medium, and adipogenic induction medium at a ratio of 1:1. For wound healing analysis, 1% FBS αMEM medium was used to eliminate the influence of serum on cell migration.
Cell proliferation assay
The MSCs were seeded in a 96-well plate at a density of 5 000 cells per well, and the conditioned medium for alveolar bone and long bone was added as described above. After culturing for 1 d, 3 d, and 5 d, 10 μL of CCK8 (Dojindo Laboratories) reagent was added to each well and then placed in the incubator to continue incubating for 1 h, and the absorbance at 450 nm was measured with a microplate reader.
Colony formation test
MSCs were seeded in 6-well plate at a density of 500 cells per well. ABM and LBM-derived macrophage-conditioned medium was added as described above, and the medium was changed every 3 days. After 2 weeks of culture, cells were fixed with 4% paraformaldehyde solution and stained with 1% crystal violet solution. Colonies with more than 30 cells were included.
Scratch wound healing assay
MSCs were seeded in 6-well plate and cultured till 100% confluence, and the 10% FBS medium was replaced with 1% FBS medium for starvation culture 24 h before making scratches. A 20–200 μL pipette tip was applied to trace the center of the orifice along a ruler, leaving a uniform and straight scratch.47 Subsequently, the medium was replaced with 1% FBS medium and macrophage-conditioned medium. The wound closure was observed and pictures were taken at 0/24/72 h. ImageJ software was used to calculate the proportion of the healing area.
Osteogenic and adipogenic differentiation
MSCs derived from long bone marrow (femur and tibia) were used for all subsequent studies. For osteogenic induction, MSCs were seeded into a 24-well plate at a density of 2.5 × 105 per well. Ascorbic acid (50 μg·mL−1), β-glycerophosphate (5 mmol·L−1), and dexamethasone (100 nmol·L−1) were added to αMEM complete medium.48 Conditioned medium was added at a ratio of 1:1.
After 7 days of induction, ALP staining and ALP activity detection were performed. ALP staining was performed following the recommended protocol with ALP staining kit (Beyotime). After incubating for 15 min, a scanner (EPSON) was used to collect images. ALP activity was measured by ALP assay kit (Nanjing Jiancheng) according to the recommended protocol.49
ARS staining was performed 21 days after induction. 1% Alizarin Red Staining Solution (Solarbio) was used to stain the mineralized nodules. After fixing the cells for 15 min, the excess staining solution was washed off with PBS, and the stained image was obtained by scanning under the scanner. Subsequently, 10% cetylpyridinium chloride was used to dissolve the mineralization, and the absorbance was detected at 562 nm with a microplate reader (Thermo Fisher).50
For adipogenesis induction, MSCs were seeded into 24-well plates at a density of 2.5 × 105 per well. 3-isobutyl-1-methylxanthine (IBMX, 0.5 mmol·L−1), dexamethasone (1 μmol·L−1), and insulin (10 μg·mL−1) were added to the DMEM complete medium.51 The conditioned medium was added at a ratio of 1:1. After 21 days of induction, the cells were fixed with 4% paraformaldehyde solution, and then the intracellular lipid droplets were stained with 1% oil red O solution. The excess dye solution was washed away with PBS, and the images were taken with an inverted microscope. Then isopropanol was used to dissolve the Oil Red O dye, and the absorbance was measured at a wavelength of 520 nm using a microplate reader.
The total RNA was isolated with Trizol reagent (Invitrogen), and the absorbance A260/A280 was measured with Nanodrop 2000 to detect the concentration and purity. PrimeScript RT kit (TaKaRa Bio) was used to reverse transcription of RNA into cDNA and added to a PCR instrument (Bio-Rad) for real-time RT-PCR. Gapdh was used as an endogenous control, and the relative expression level of mRNA was calculated by the 2−ΔΔCt method. For adipogenesis-related genes, 34B4 was used as an endogenous control.
Osm levels in alveolar bone and long bone tissue were measured by a mouse Osm ELISA kit (Cusabio). Briefly, mouse alveolar bone and long bone were collected, cut into pieces, and weighed for the same weight (100 mg). the samples were diluted into 1 mL with buffer, frozen, and thawed three times in a −80 °C refrigerator. After centrifugation at 200 × g for 5 min, 100 μL of supernatant was added to a 96-well plate with high binding capacity and incubated for 2 h.
All values were expressed as mean ± SEM. Statistically significant differences were performed by two-tailed Student’s t test for comparison between two groups, one-way or two-way analysis of variance (ANOVA) followed by the Tukey’s post hoc test for multiple comparisons. P value < 0.05 was considered to be statistically significant.
Mouse alveolar bone scRNA-seq data could be downloaded from Sequence Read Archive (SRA) datasets (https://www.ncbi.nlm.nih.gov/sra/) via accession number PRJNA697839. All public scRNA-seq dataset used in the study, including long bone marrow cells (GSE109774), peritoneal macrophages (GSE139999), peripheral blood mononuclear cells (GSE108097), and spleen cells (GSE109774), can all be downloaded from the GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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We thank Menglin Yao and Tingting Guo from the Precision Medicine Center in West China Hospital of Sichuan University for technique assistance. This work was supported by grants from the National Natural Science Foundation of China (NSFC 81722014, 81970913), State Key Laboratory of Oral Diseases (SKLOD202008), and West China Hospital of Stomatology (RD-03-202010).
The authors declare no competing interests.
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Lin, W., Li, Q., Zhang, D. et al. Mapping the immune microenvironment for mandibular alveolar bone homeostasis at single-cell resolution. Bone Res 9, 17 (2021). https://doi.org/10.1038/s41413-021-00141-5
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