Dihydroartemisinin attenuates osteoarthritis by inhibiting abnormal bone remodeling and angiogenesis in subchondral bone
- Authors:
- Published online on: January 15, 2021 https://doi.org/10.3892/ijmm.2021.4855
- Article Number: 22
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Copyright: © Ma et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Osteoarthritis is the most common degenerative joint disease, causing pain and dysfunction in numerous joints (1). Due to its complex pathogenesis, there is currently no effective treatment for osteoarthritis (OA) (1). Therefore, a better understanding of the pathogenesis of OA would be of great significance to aid in its early prevention and treatment.
The subchondral bone is located below the articular cartilage, which plays a significant role in disease pathogenesis (2). Changes in the microstructure of the subchondral bone can be observed earlier than damage to the articular cartilage (3,4). Under physiological conditions, bone remodeling maintains bone tissue integrity through the coupling of osteoclast-mediated resorption and osteoblast-mediated formation of bone (5). Abnormal bone remodeling causes microstructural destruction of the subchondral bone, altering its mechanical properties (6). Additionally, articular cartilage does not withstand shear stress during joint movement, degenerating as a result (2,7). Increased subchondral bone remodeling is characterized by increased bone loss, decreased bone density, and deterioration of its microstructure, which leads to articular cartilage degeneration (8). Bone resorption due to osteoclasts has been demonstrated to significantly increase in anterior cruciate ligament transection (ACLT) and ovariectomized (OVX) models of OA. A reduction in articular cartilage degeneration can be observed when osteoclast-mediated bone resorption is inhibited using alendronate (9,10). In OVX mice, estrogen deficiency causes osteoclast-mediated bone resorption, increased subchondral bone remodeling, and deterioration of the subchondral bone microstructure, resulting in degeneration of the articular cartilage, which establishes an osteoporosis-associated OA mouse model induced by ovariectomy (9,11,12). These studies suggest that abnormal subchondral bone remodeling destroys subchondral bone microstructure, inducing degeneration of the articular cartilage.
Sclerostin, a potent inhibitor of the Wnt/β-catenin pathway, is secreted by osteocytes and inhibits osteoblast-mediated bone formation (13,14). As OA develops, concentrations of sclerostin in the subchondral bone gradually decrease, activating the Wnt/β-catenian pathway that promotes bone formation and accelerates cartilage degradation (15). Previous studies have suggested that mechanical stress leads to a decrease in sclerostin in subchondral bone, however, the mechanism by which sclerostin levels decline in the subchondral bone remains entirely unclear (16-18). LIF is secreted by osteoclasts and acts between bone resorption and formation as a regulator of bone remodelling (19). Studies on osteoporosis have demonstrated that osteoclasts oversecrete LIF, inhibiting the expression of sclerostin and, thus, promoting abnormal bone formation and mediating abnormal bone remodelling (20). Inhibition of osteoclastogenesis can reduce the secretion of LIF, thereby reducing abnormal bone remodeling in osteoporosis (20). However, the role of LIF in the abnormal remodeling of the subchondral bone during OA remains unclear.
Abnormal angiogenesis of the subchondral bone is an important pathological feature that leads to abnormal bone remodeling in OA (21). In a mouse model of OA established by ACLT and OVX, the vascular endothelial progenitor cell marker CD31 was significantly increased in the subchondral bone (12,22-24) and the expression of the catabolic factors, MMP-13 and VEGF were also significantly increased, resulting in the articular cartilage being severely damaged. Inhibition of the abnormal angiogenesis of the subchondral bone alleviates articular cartilage degeneration (22-24).
Artemisinin, a well-known antimalarial drug, is a sesquiterpene lactone isolated from Artemisia (25). Dihydroartemisinin (DHA) is a semisynthetic derivative of artemisinin that has fewer side effects (26). DHA reduces bone loss by inhibiting receptor activator of nuclear factor κB ligand (RANKL)-induced osteoclastogenesis in OVX mice and in a wear particle-induced mouse osteolysis model (27,28). In addition, DHA has been revealed to have an antiangiogenic effect (27,28). However, the role of DHA in the abnormal bone remodeling and angiogenesis of OA remains unclear. The aim of this study was to investigate the potential role of DHA in alleviating abnormal subchondral bone remodeling and angiogenesis in order to reduce articular cartilage degeneration in a mouse model of OA.
Materials and methods
Ethics statement
All procedures and protocols were approved by the Scientific Research Ethics Committee of the General Hospital of Ningxia Medical University (protocol no. 2016-147). All experiments were performed in accordance with the principles and guidelines of the National Institutes of Health Guide for Care and Use of Laboratory Animals.
Animals
A total of 120 female C57BL/6j mice (weight, 19-20 g), ten weeks old, were used in the present study. All mice were housed at a constant temperature (25°C), at 55% humidity on a 12-h light/dark cycle with free access to food and water. The mice were anesthetized with pentobarbital sodium salt (60 mg/kg) by intraperitoneal injection. The schematic of the experimental protocol is listed in Fig. 1.
Sixty mice were randomly divided into 3 groups: A sham-operated group (n=20), ACLT+vehicle group (n=20), and ACLT+DHA group (n=20). Surgery was performed on the right knees of each mouse as previously described (29). In the two ACLT groups, the right knee joint capsule was exposed using a medial parapatellar approach and then the anterior cruciate ligament was transected with micro-scissors, prior to closing the joint capsule and skin. The same procedure was performed in the sham-operated group with the exception of the transection of the ACL. The ACLT+DHA group was treated with DHA (product no. D7439; Sigma-Aldrich; Merck KGaA) by intraperitoneal injection (1 mg/kg/2 days) from the first post-operative day until sacrifice (Fig. 1A). Flow displacement rate of CO2 used for euthanasia was 30%. Mouse euthanasia was confirmed, including lack of pulse, breathing, corneal reflex, and response to firm toe pinch. DHA was prepared according to the literature (30), and the method was as follows: 25 mg of DHA was weighed in a precision electronic balance, and dissolved in 1 ml of prepared DMSO, and then diluted in 99 ml sterile PBS solution to prepare 1 mg/kg DHA. The sham and vehicle treatment groups were administered solvent as a vehicle, using the same dose, frequency and duration as the DHA group.
Sixty mice were randomly divided into 3 groups: A sham-operated group (n=20), OVX+vehicle group (n=20), and OVX+DHA group (n=20). According to the literature, the mice were operated from the abdominal cavity through the back to remove the bilateral ovaries (12,31). The same procedure was performed in the sham-operated group, except that the bilateral ovaries were only removed. The OVX+DHA group was treated with DHA from the first day after operation (1 mg/kg/2 days) until sacrifice (Fig. 1B). Ovietectomy was performed under anaesthesia. The mice were anesthetized with pentobarbital sodium salt (60 mg/kg) by intraperitoneal injection. The method of euthanasia and the configuration of DHA were the same as those of the ACLT mice. The sham operation and carrier groups used the same dose, frequency, and duration as the DHA group. Ten mice were separately euthanized at 4 or 8 weeks after surgery in each group by carbon dioxide inhalation, followed immediate harvesting of the right knees for subsequent analysis.
Histology
Harvested knees were fixed in 4% paraformaldehyde for 24 h at 4°C then decalcified in 10% EDTA (pH 7.4) for 3 weeks prior to embedding in paraffin. The medial compartment of the knee joints were cut into 4-µm-thick sections along the sagittal plane and stained with safranin O-fast green at 25°C in the laboratory. Deparaffinization of the slides was performed in xylene two times for 10 min, followed by hydration in 100% alcohol twice for 5 min, 95% alcohol for 2 min and 80% alcohol for 2 min. Hematoxylin was added to slides for 3 min prior to hydrating the slides gently in running water for 10 min. Slides were then stained with 0.2% Fast Green (product no. F7252; Sigma-Aldrich; Merck KGaA) for 3 min, and then subjected to 1% acetic acid for 5 sec, 0.1% Safranin O (product no. S8884; Sigma-Aldrich; Merck KGaA) for 3 min. Slides were hydrated in 95% alcohol for 5 sec, 100% alcohol twice for 15 sec, followed by 2 changes in xylene prior to cover-slipping the slides. Regions from three slides per mouse were imaged by light microscopy at a magnification of ×100 and three fields per region were randomly selected per slide. The Osteoarthritis Research Society International (OARSI)-modified Mankin score was used to perform a histopathological grade assessment of the cartilage.
Immunohistochemistry and immunofluorescence
Standard immunostaining was conducted in the present study. Sagittal sections that had been paraffin-embedded were incubated overnight at 4°C with primary antibodies against matrix metalloproteinase-13 (MMP-13) (1:100; product code ab39012; Abcam), vascular endothelial growth factor A (VEGFA) (1:100; product code ab52917; Abcam), leukemia inhibitory factor (LIF) (1:100; cat. no. AB-449-NA; R&D Systems, Inc.), sclerostin (1:50; product code ab63097; Abcam), β-catenin (1:100; cat. no. 51067-2-AP; ProteinTech Group, Inc.), RANKL (1:100; product code ab216484; Abcam) and CD31 (1:25; product code ab28364; Abcam). For immunohistochemical staining, sections were processed using a two-step IHC detection reagent (ZSGB-Bio; OriGene Technologies, Inc.). Briefly, sections were incubated with reaction enhancement solution (reagent 1) for 20 min at 37°C and then with enhanced enzyme-labeled goat anti-rabbit IgG polymer (reagent 2) for 40 min at 37°C. The sections were then developed using 3,3′-diaminobenzidine (DAB) (ZSGB-Bio; OriGene Technologies, Inc.), followed by counterstaining with hematoxylin (ZSGB-Bio; OriGene Technologies, Inc.). For immunofluorescence staining, sections were incubated with Alexa Fluor® 488 goat anti-rabbit secondary antibody (1:500; product code ab150077; Abcam) for 1 h at 37°C in the dark. Regions from three slides per mouse were imaged by fluorescence microscopy at a magnification of ×400 and three fields per region were randomly selected per slide. Image-Pro Plus 6.0 (Media Cybernetics, Inc.) was used to count chondrocytes within the entire tibial articular cartilage and all cells within the entire tibial subchondral bone which exhibited positive staining for each antibody.
Micro-computed tomography (CT) analysis
Harvested knee joints were dissected free of soft tissue, fixed overnight in 70% ethanol at 4°C and analyzed by micro-CT (SkyScan 1176; Bruker micro-CT) at a resolution of 9 µm/pixel. The micro-CT scans were acquired over an exposure time of 900 ms, a voltage of 50 kV and a current of 500 µA. Images were reconstructed by NRecon version 1.1.11 (Bruker micro-CT) and analyzed by CTAn, v1.15 (SkyScan1176 in vivo micro-CT; Bruker). A sagittal view of the entire medial compartment of the tibial subchondral bone was used for 3D histomorphometric analysis, with bone volume/tissue volume (BV/TV, %), trabecular separation (Tb.Sp), and BMD extracted for performing comparisons.
Statistical analysis
Data were analyzed using one-way and two-way factorial design analyses of the variations followed by Student-Newman-Keuls and Bonferroni post hoc tests. Data are presented as the means ± SD. For OARSI scores, data were analyzed using Kruskal-Wallis test followed by Dunn's test. P<0.05 was considered to indicate a statistically significant difference. GraphPad Prism 5 software (GraphPad Software, Inc.) was used for statistical analysis.
Results
DHA preserves articular cartilage in ACLT mice
Safranin O-fast green staining indicated that there was significant loss of proteoglycans, with OARSI scores increasing significantly in the ACLT+vehicle group relative to the sham-operated group at 4- and 8-weeks following surgery (Fig. 2A and D). Similarly, results of immunohistochemical staining demonstrated that the expression of MMP-13 (Fig. 2B and E) and VEGF (Fig. 2C and F) was significantly increased after 4 and 8 weeks. Administration of DHA resulted in retention of proteoglycans and OARSI scores that were improved in the ACLT+DHA group compared with the ACLT+vehicle group after 4 and 8 weeks (Fig. 2A and D). Aberrantly expressed MMP-13 (Fig. 2B and E) and VEGF (Fig. 2C and F) were recovered in the ACLT+DHA group compared with the ACLT+vehicle group at both 4- and 8-weeks following surgery.
DHA restores the microarchitecture of the subchondral bone in ACLT mice
Abnormal bone remodeling destroys the microstructure of subchondral bone which results in articular cartilage degeneration (21). It was investigated whether DHA was able to protect articular cartilage by preserving the microstructure of subchondral bone. The tibial subchondral bone structure of the tibia was analyzed by micro-CT. The results demonstrated that DHA improved the subchondral bone microstructure (Fig. 3A). BV/TV (Fig. 3B) and BMD (Fig. 3D) were significantly decreased in the ACLT+vehicle group compared with the sham-operated group at both 4- and 8-weeks but DHA abrogated these changes (ACLT+DHA group) relative to the ACLT+vehicle group 4-weeks after surgery (Fig. 3B and D). The Tb.Sp was significantly increased in the ACLT+vehicle group relative to the sham-operated group at both 4- and 8-weeks (Fig. 3C). DHA recovered these changes (ACLT+DHA group) compared with the ACLT+vehicle group 4-weeks after surgery (Fig. 3C). Collectively, these data indicated that systemic administration of DHA inhibited abnormal bone remodeling and restored the subchondral bone microstructure.
DHA inhibits abnormal bone remodeling in the subchondral bone in ACLT mice
Immunohistochemistry and immunofluorescence were performed to investigate whether systemic DHA was able to inhibit abnormal bone remodeling and angiogenesis in subchondral bone 4-weeks after surgery. RANKL-immunostained sections demonstrated a significant increase in the number of cells positive for RANKL in the ACLT+vehicle group relative to the sham-operated group (Fig. 4A and E). Administration of DHA significantly reduced this increased number relative to the ACLT+vehicle group (Fig. 4A and E). To investigate whether osteoclasts altered the expression of sclerostin in osteocytes, sclerostin expression was measured by immunohistochemistry. The results demonstrated a significant decrease in sclerostin expression in the ACLT+vehicle group relative to the sham-operated group (Fig. 4B and F). Treatment with DHA significantly increased sclerostin expression relative to the ACLT+vehicle group (Fig. 4B and F). The expression of β-catenin in osteoblasts was assessed by immunohistochemistry and a significant increase was observed in the ACLT+vehicle group compared with the sham-operated group (Fig. 4C and G). Administration of DHA significantly reduced β-catenin expression compared with the ACLT+vehicle group (Fig. 4C and G).
It was also investigated whether DHA inhibited the excessive expression of LIF, which is secreted by osteoclasts in the subchondral bone, using immunohistochemistry 4-weeks after surgery. The results demonstrated that a significant increase in LIF expression was observed in the ACLT+vehicle group compared with the sham-operated group (Fig. 4D and H). DHA significantly reduced this expression relative to the ACLT+vehicle group (Fig. 4D and H).
These results indicated that DHA inhibited the excessive expression of LIF secreted by osteoclasts in ACLT mice, thus reducing inhibition of sclerostin and preventing subchondral bone remodeling, thereby restoring the subchondral bone microstructure and inhibiting articular cartilage degeneration.
DHA inhibits abnormal angiogenesis in the subchondral bone in ACLT mice
Abnormal angiogenesis in the subchondral bone is a pathological feature of OA (32). An angiogenic marker, CD31-positive endothelial progenitor cells (33), was assessed using immunofluorescence. The results indicated that its number significantly increased in the ACLT+vehicle group relative to the sham-operated group (Fig. 5) and that the number was reduced in the ACLT+DHA group compared with the ACLT+vehicle group (Fig. 5).
DHA preserves the articular cartilage in OVX mice
Safranin O-fast green staining indicated that there was significant loss of proteoglycans, with OARSI scores significantly increasing in the OVX+vehicle group relative to the sham-operated group at 8-weeks following surgery (Fig. 6A and D), but not 4-weeks. Similarly, the results of the immunohistochemical staining demonstrated that the expression of MMP-13 (Fig. 6B and E) and VEGF (Fig. 6C and F) significantly increased after 8-weeks, but not 4-weeks. Administration of DHA resulted in retention of proteoglycans and OARSI scores that were improved in the OVX+DHA group compared with the OVX+vehicle group after 8-weeks (Fig. 6A and D). Aberrantly expressed MMP-13 (Fig. 6B and E) and VEGF (Fig. 6C and F) were recovered in the OVX+DHA group compared with the OVX+vehicle group at 8-weeks following surgery.
DHA restores the microarchitecture of the subchondral bone in OVX mice
Abnormal bone remodeling destroys the microstructure of the subchondral bone which results in articular cartilage degeneration (21). It was investigated whether DHA was able to protect the articular cartilage by preserving the microstructure of the subchondral bone. The tibial subchondral bone structure of the tibia was analyzed by micro-CT. The mouse OA model established by OVX, was established 8-weeks after surgery, but not 4-weeks. The OVX mice were also euthanized after 4 weeks but model establishment was not successful at that time-point. Therefore, the micro-CT result only contains 8-week results. The results demonstrated that DHA improved the subchondral bone microstructure (Fig. 7A). BV/TV (Fig. 7B) and BMD (Fig. 7D) significantly decreased in the OVX+vehicle group compared with the sham-operated group at 8-weeks, but DHA abrogated these changes (OVX+DHA group) relative to the OVX+vehicle group 8-weeks after surgery (Fig. 7B and D). The Tb.Sp significantly increased in the OVX+vehicle group relative to the sham-operated group at 8-weeks (Fig. 7C). DHA recovered these changes (OVX+DHA group) compared with the OVX+vehicle group 8-weeks after surgery (Fig. 7C). Collectively, these data indicated that systemic administration of DHA inhibited abnormal bone remodeling and restored subchondral bone microstructure.
DHA inhibits abnormal bone remodeling in subchondral bone in OVX mice
Immunohistochemistry and immunofluorescence were performed to investigate whether systemic DHA was able to inhibit abnormal bone remodeling and angiogenesis in the subchondral bone 8-weeks after surgery. RANKL-immunostained sections demonstrated a significant increase in the number of cells positive for RANKL in the OVX+vehicle group relative to the sham-operated group (Fig. 8A and E). Administration of DHA significantly reduced that increased number relative to the OVX+vehicle group (Fig. 8A and E). To investigate whether osteoclasts altered the expression of sclerostin in osteocytes, sclerostin expression was assessed by immunohistochemistry. The results demonstrated a significant decrease in sclerostin expression in the OVX+vehicle group relative to the sham-operated group (Fig. 8B and F). Treatment with DHA significantly increased sclerostin expression relative to the OVX+vehicle group (Fig. 8B and F). The expression of β-catenin in osteoblasts was assessed by immunohistochemistry and a significant increase was observed in the OVX+vehicle group compared with the sham-operated group (Fig. 8C and G). Administration of DHA significantly reduced β-catenin expression compared with the OVX+vehicle group (Fig. 8C and G).
It was investigated whether DHA inhibited excessive expression of LIF secreted by osteoclasts in the subchondral bone using immunohistochemistry 8-weeks after surgery. The results demonstrated that a significant increase in LIF expression was observed in the OVX+vehicle group compared with sham-operated group (Fig. 8D and H). DHA significantly reduced this expression relative to the OVX+vehicle group (Fig. 8D and H).
The results indicated that DHA inhibited excessive expression of LIF secreted by osteoclasts in OVX mice, thus reducing inhibition of sclerostin and preventing subchondral bone remodeling, thereby restoring the subchondral bone microstructure and inhibiting articular cartilage degeneration.
DHA inhibits abnormal angiogenesis in subchondral bone in OVX mice
Abnormal angiogenesis in subchondral bone is a pathological feature of OA (32). The number of CD31-positive endothelial progenitor cells were assessed using immunofluorescence. The results indicated that compared with the sham-operated group, their numbers significantly increased in the OVX+vehicle group (Fig. 9) and that compared with the OVX+vehicle group, their numbers were decreased in the OVX+DHA group (Fig. 9).
Discussion
OA is the most common degenerative joint disease and possesses a complex pathogenesis. Abnormal bone remodeling and angiogenesis in the subchondral bone destroys the subchondral bone microstructure and leads to articular cartilage degeneration (22,23). The present study revealed that DHA decreased the inhibition of sclerostin by reducing the LIF secretion of osteoclasts and, hence, attenuated aberrant bone remodeling and inhibited angiogenesis in subchondral bone, thereby preserving the subchondral bone microstructure and attenuating articular cartilage degeneration.
The microstructural integrity of the subchondral bone is especially important for the protection of articular cartilage (2). Studies have revealed that microstructural changes in subchondral bone may precede the degeneration in articular cartilage in OA (3,4). The integrity of the bone microstructure is maintained through the coupling of bone remodeling, which includes the temporal and spatial balance of bone resorption and formation. This in turn involves resorption of the bone matrix by osteoclasts, normally replaced by new bone matrix by osteoblasts (34). Abnormal bone remodeling can disrupt the homeostatic balance of the bone and destroy the integrity of the bone microstructure (35). At present, the mechanisms that balance bone resorption and formation resulting in bone remodeling remain unclear.
The most commonly used surgical method of inducing OA is ACLT. In this method, the ACL is transected with micro-scissors, which causes joint destabilization. The anterior drawer test with the joint flexed is used to confirm that transection of the ligament has occurred. The ACLT leads to the increase of joint mechanical stress. The increased load on the posterior tibial plateau leads to the destruction of cartilage and subchondral bone, which leads to OA (29,36). Osteoclasts are the sole cells that resorb bone matrix, through dissolution by the secretion of acids and proteases. RANKL is a key factor in osteoclastogenesis (37). The secretion of RANKL by osteoblast precursors following abnormal mechanical stimulation results in its binding to RANK on osteoclast precursors, inducing osteoclastogenesis that mediates bone resorption (22). The prevalence of OA in postmenopausal women is higher than that in men. Ovariectomy significantly reduced the production of estrogen in mice, resulting in increased bone resorption mediated by subchondral bone osteoclasts, resulting in increased subchondral bone loss and bone microstructure deterioration, thereby promoting articular cartilage degeneration and inducing osteoarthritis (31,38). Osteoporosis (OP) is characterized by increased bone loss, deterioration of bone microarchitecture and an increased risk of fragility fractures (39). The pathogenesis of OA has not been fully elucidated. OA is considered a whole-joint disease in which all components are involved, with the subchondral bone, which is located below the articular cartilage, playing a significant role in disease pathogenesis (40). In the subchondral bone of OA, osteoclast-mediated bone resorption increases bone loss, and its microstructure deteriorates, which leads to articular cartilage degeneration (41). Excessive bone resorption, which is a hallmark of postmenopausal OP, also occurs at the early stage in the development of OA (42). They both have increased bone remodeling, increased osteoclast-mediated bone resorption, and deterioration of bone microstructure in OVX mice. The present study demonstrated that the expression of RANKL significantly increased in the ACLT+vehicle and OVX+vehicle group compared with the sham-operated group. This indicates that RANKL-induced osteoclastogenesis is significantly enhanced in ACLT mice. Consistent with previous studies, the present results revealed that DHA reduced bone resorption by inhibiting RANKL-mediated osteoclastogenesis.
The Wnt/β-catenin signaling pathway is considered the most important pathway that regulates bone homeostasis (43). Activation of the Wnt/β-catenin pathway promotes differentiation of bone marrow mesenchymal stem cells into osteoblasts, promoting osteoblast proliferation and maturation, inhibiting osteoblast apoptosis, and thereby promoting osteoblast-mediated bone formation (44). Sclerostin, encoded by the SOST gene, is secreted by osteocytes and binds to LDL receptor-related protein (LRP) 5/6 (13,45). It is an antagonist of the Wnt/β-catenin signalling (13). Sclerostin inhibits osteoblast-mediated bone formation by binding to LRP5/6 on osteoblasts (45). Previous studies have revealed that SOST knockout (KO) mice and postmenopausal osteoporotic rats treated with sclerostin antibodies exhibited a significant increase in bone volume, bone formation, and the number of osteoblasts on the surface of their bones (46). As OA progresses, sclerostin expression significantly decreases, causing β-catenin expression to significantly increase in the subchondral bone leading to gradually worsening articular cartilage degeneration in humans (47). The present study demonstrated that compared with the sham-operated group, sclerostin expression in osteocytes significantly decreased and β-catenin expression in osteoblasts significantly increased in the subchondral bone in the ACLT+vehicle group. This indicated that decreased expression of sclerostin in the subchondral bone caused abnormal remodeling that destroyed its microstructural integrity in ACLT mice. After OVX, OP caused by oestrogen revealed an increase in bone remodeling, specifically osteoclast-mediated enhancement of bone resorption, and osteoblast-mediated bone formation was relatively weakened (9). In OVX-induced OP-related osteoarthritis, subchondral bone remodeling increases, characterized by increased bone loss, decreased bone mass, decreased bone density, and deteriorated bone microarchitecture (9,12,31). The present study also demonstrated that compared with the sham-operated group, sclerostin expression significantly decreased in osteocytes, and β-catenin expression also significantly increased in osteoblasts in the subchondral bone in the OVX+vehicle group. This indicated that the decreased expression of sclerostin in the subchondral bone of OP-induced mouse OA caused abnormal bone formation and abnormality of the subchondral bone remodeling, which destroyed the microstructural integrity of the subchondral bone.
LIF is a bone remodeling regulatory protein that is secreted by osteoclasts and binds to a receptor complex of glycoprotein 130 (gp130)/LIF receptor (LIFR) on osteocytes, which inhibits sclerostin (48,49). Thus, the inhibitory effect of sclerostin on Wnt/β-catenin in osteoblasts is reduced, promoting osteoblast-mediated bone formation in RANKL transgenic mice and OPG-KO mice compared with wild-type mice (20). Treatment of OPG-KO mice with anti-RANKL antibody, an anti-bone resorption agent, was revealed to suppress the expression of LIF and increase the expression of sclerostin, thereby reducing bone formation via inhibition of the Wnt/β-catenin pathway (20). Specific knockout of gp130 in osteocytes was revealed to increase the expression of sclerostin, and, thus, inhibit bone formation in mice (50). The aforementioned studies demonstrated that the osteoclast-derived factor LIF inhibited the expression of sclerostin in osteocytes and, hence, promoted bone formation. The present study demonstrated that the expression of LIF in osteoclasts significantly increased in the ACLT+vehicle group relative to the sham-operated group. We inhibited osteoclastogenesis by DHA which reduced the expression of the osteoclast-derived factor LIF, thereby increasing the expression of sclerostin that inhibits abnormal bone formation and remodeling of the subchondral bone. Sclerostin is an important factor in bone remodeling, and is affected by numerous factors (51,52). Previous studies have found that mechanical stimulation inhibit the expression of sclerostin (16-18). Studies on osteoporosis have revealed that osteoclasts oversecrete LIF and inhibit the expression of sclerostin (20); however, in the subchondral bone of OA, its mechanism is unclear. We first established a model of OA in mice with ACLT mechanical injury and it was revealed that LIF secreted by osteoclasts decreased the expression of sclerostin. However, the influence of the increased mechanical stress in the ACLT model cannot be completely eliminated. We then used the OVX-induced OP-related mouse OA model to further investigate the effect of LIF secreted by osteoclasts on sclerostin. The present study revealed a significant increase in the expression of LIF in osteoclasts in the OVX+vehicle group compared with that in the sham-operated group. After treatment with DHA, the expression of LIF in OVX+DHA group was significantly lower than that in OVX+vehicle group. This indicated that DHA inhibited osteoclastogenesis to reduce the expression of osteoclast-derived factor LIF, and, therefore, the expression of sclerostin was significantly increased. Compared with the OVX+vehicle group, DHA significantly decreased Tb.Sp and significantly increased BV/TV (%) and BMD in the subchondral bone of the OVX+DHA group. Similarly, the expression of MMP-13 and VEGF and the OARSI score in the articular cartilage were significantly decreased. This indicated that DHA reduced the expression of osteoclast-derived factor LIF by inhibiting osteoclastogenesis, thereby reducing the inhibition of bone sclerotin by LIF, reducing abnormal bone formation, inhibiting the increase of subchondral bone remodeling, and retaining the microstructure of the subchondral bone to slow the degeneration of articular cartilage.
Angiogenesis provides oxygen and nutrients for bone formation, which is associated with bone remodeling for bone homeostasis (50). However, abnormal angiogenesis is a key pathological feature of OA in the subchondral bone. Abnormal angiogenesis in subchondral bone increases with increased bone remodeling, which leads to abnormal bone formation (22,23). CD31, encoded by the platelet endothelial cell adhesion molecule (PECAM1) gene, is a specific marker of endothelial progenitor cells and is used to assess angiogenesis (32). The present study demonstrated that CD31-positive endothelial progenitor cells in the subchondral bone significantly increased in number in the ACLT+vehicle group. Previous studies have also revealed that DHA has anti-angiogenic effects (27,53,54). After treatment with DHA, CD31-positive staining significantly decreased in the ACLT+DHA group relative to the ACLT+vehicle group. Previous tudies have revealed that in the OA model of OVX rats, the expression of CD31 in the subchondral bone of the model group was significantly increased, and the microstructural destruction of the subchondral bone similarly with the expression of MMP-13 in the articular cartilage was increased, and the loss of proteoglycan was severe (9,12,55). The present study revealed a significant increase in the number of CD31-positively labeled endothelial progenitor cells in the subchondral bone of the OVX+vehicle group compared with sham-operated group. However, the role of DHA in OVX-induced abnormal angiogenesis of the subchondral bone in OP-associated OA remains unclear. The present experiments revealed that CD31 expression was significantly reduced in the OVX+DHA group compared with the OVX+vehicle group. These results indicated that DHA inhibited abnormal angiogenesis of subchondral bone and slowed abnormal bone remodeling.
DHA is an effective drug against malaria, and a semi-synthetic derivative of artemisinin with fewer side effects. It performs an important role in inhibiting inflammation, is anti-angiogenic, suppresses cancer and is anti-osteoclastogenic (26-28). DHA suppresses the expression of osteoclast marker genes, such as cathepsin K, calcitonin receptor and tartrate resistant acid phosphatase (TRACP); DHA also inhibits RANKL-induced osteoclast formation and bone resorption, thus reversing the ovariectomized bone loss in oestrogen deficient-induced osteoporosis of OVX mice (27). In addition, DHA effectively inhibited osteoclastogenesis and prevented breast cancer-induced osteolysis (28). Abnormal bone remodeling and angiogenesis in the subchondral bone destroys its microstructure and causes articular cartilage degeneration (22,23). The present study revealed that DHA reduced the expression of the osteoclast-derived factor LIF by inhibiting osteoclastogenesis, thereby reducing inhibition of sclerostin and thus suppressing abnormal subchondral bone remodeling. In addition, DHA inhibited angiogenesis resulting in less abnormal bone remodeling. Therefore, DHA attenuated articular cartilage degeneration by inhibiting abnormal bone remodeling and angiogenesis in OA mice.
In conclusion, DHA decreased the inhibition of sclerostin by reducing LIF secretion by osteoclasts and thus attenuated aberrant bone remodeling and inhibited angiogenesis in the subchondral bone, thereby preserving the subchondral bone microstructure and attenuating articular cartilage degeneration. Future studies are required to further verify the underlying mechanism of DHA decreasing the inhibition of sclerostin by reducing LIF secretion by osteoclasts, such as anti-LIF antibodies.
Funding
The present study was supported by the National Natural Science Foundation of China (grant nos. 81660373).
Availability of data and materials
The datasets used during the current study are available from the corresponding author on reasonable request.
Authors' contributions
QJ designed the experiment. LM, XZ, YL, JW and XY conducted the main experiments. LM analyzed the data, drafted the manuscript, and revised it. All the authors read and approved the final submitted manuscript.
Ethics approval and consent to participate
The experimental procedures were carried out in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals, and were approved by the Scientific Research Ethics Committee of the General Hospital of Ningxia Medical University (Yinchuan, China) (protocol no. 2016-147).
Patient consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Acknowledgments
Not applicable.
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