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Introduction

Osteoporosis (OP) is a systemic skeletal disease characterized by decreased bone mass and microarchitectural deterioration in the bone tissue, which predisposes affected individuals to increased bone fragility and fracture risk (1). The diagnosis of OP is based on bone mineral density (BMD) measurement using dual-energy X-ray absorptiometry (DXA). According to the World Health Organization, a BMD T-score of <-2.5, as measured by DXA, is defined as OP (2). Approximately 50% of women experience at least one bone fracture following menopause worldwide in 2020; OP has become a significant public health problem and received considerable attention worldwide (3).

Type-2 diabetes mellitus (T2DM) has been hypothesized to cause decreased BMD (4). A large prospective study of post-menopausal women recruited into the Study of Osteoporotic Fractures confirmed that female patients with T2DM experienced higher fracture rates compared with that in female patients without T2DM (5). In addition, BMD decreased as diabetes progressed, suggesting that hyperglycemia is an important risk factor for OP (6).

Advanced glycation end products (AGEs) are a group of modified proteins and/or lipids with damaging potential, that are formed under hyperglycemic conditions (7). AGEs have been largely reported to be involved in the pathogenesis of T2DM and diabetic complications (7). In addition, increasing evidence indicates that AGEs play a role in aggravating bone fragility, as observed during the progression of classic diabetic complications (8,9). AGEs have been found to significantly inhibit osteoblast proliferation, differentiation and mineralization and induce osteoblast apoptosis (10,11). AGEs can affect osteoblast proliferation and function by modulating autophagy via the receptor of AGEs (RAGE) pathway, indicating that autophagy is involved in these processes (12). These observations suggest that the AGE/RAGE axis may play an important role in bone formation.

A recent study have revealed that another form of regulated cell death, ferroptosis, may be involved in the pathogenesis of OP (13). Ferroptosis (iron-dependent cell death) differs from apoptosis, autophagy, necrosis, necroptosis and pyroptosis, and is characterized by the accumulation of intracellular iron and lipid reactive oxygen species (14). The increase in osteoblast ferroptosis plays an important role in hormone-induced OP (15), and iron overload plays an important role in general OP and osteoblast function (16). In a rat model of T2DM-related OP (OP-T2DM), ferroptosis was observed in the bone tissue (17). However, none of the aforementioned studies directly studied the level and changes of ferroptosis in osteoblasts.

Therefore, the aim of the present study was to investigate the role of ferroptosis in AGE-regulated dysfunction of human osteoblasts. Ex vivo experiments using clinical samples from patients with OP and healthy individuals were performed. In addition, in vitro experiments using the hFOB1.19 osteoblast cell line, which was cultured in media containing AGEs and serum from healthy individuals or patients with OP and a normal fasting blood glucose (FBG) level and patients with OP and T2DM to observe cell differentiation, mineralization, apoptosis and ferroptosis, were also performed.

Materials and methods

Sample collection

The present study was approved by the Ethics Committee of the Nanjing Pukou District Central Hospital (Nanjing, China). Written informed consent was obtained from all participants. A total of 10 healthy individuals and 10 patients with OP (among which 4 were diagnosed with T2DM) were enrolled into the present study. Participants with a femoral neck and/or lumbar spine T score ≤-2.5 were considered to have OP, while a T score of >-1 was considered normal. Patients with malignancy, coronary heart disease or other severe diseases in the previous 5 years were excluded. Images of lumbar vertebra and femur, along with the BMD from healthy individuals and patients with OP, were obtained using DXA absorptiometry (Hologic, Inc.). Blood samples from the enrolled participants were centrifuged at 1,000 × g for 10 min at 4°C, and the serum was stored at −80°C.

Measurement of AGEs and FBG

All the participants fasted from 10:00 pm the previous night, and 10 ml venous blood was collected at ~9:00 am the next morning. The blood samples were centrifuged at 1,000 × g for 10 min at 4°C, and the serum was used to assess AGEs and FBG or stored at −80°C for subsequent experiments. The concentration of AGEs and FBG in the serum samples was measured using an AGE assay kit (cat no ab238539; Abcam) and a blood glucose kit (Glucose Oxidase Peroxidase Assay; cat no WD-0108 Shanghai Rongbai Biotechnology Co., Ltd.), following the manufacturer's instructions.

Preparation of AGEs

AGEs were prepared as previously described (18). Briefly, human serum albumin (15 mg/ml; Sigma-Aldrich; Merck KGaA) was incubated with 1 mM 3-deoxygluconaldeone in distilled water at 37°C for 14 days.

Cell culture and grouping

The human hFOB1.19 osteoblast cell line (American Type Culture Collection; ATCC) was cultured in medium containing 1:1 mixture of Ham's F12 medium and DMEM (both from Thermo Fisher Scientific, Inc.) with 2.5 mM L-glutamine (ATCC), supplemented with 10% FBS (Gibco; Thermo Fisher Scientific, Inc.), 100 U/ml penicillin, 100 U/ml streptomycin (Merck KGaA) and 0.3 mg/ml G418 (Merck KGaA). The cells were cultured at 37°C in a humidified incubator with 5% CO2.

The hFOB1.19 cells were divided into different groups: Blank (cultured in normal medium), AGEs (cultured in medium containing 50 pg/ml AGEs), control (cultured in medium containing 10% serum from healthy individuals), OP-normal (cultured in medium containing 10% serum from patients with OP and a normal FBG level), OP-T2DM (cultured in medium containing 10% serum from patients with OP and T2DM), AGEs + deferoxamine (DFO; cultured in medium containing 50 pg/ml AGE and 80 µM DFO), OP-T2DM + DFO (cultured in medium containing 10% serum from patients with OP and T2DM, and 80 µM DFO).

Cell counting kit (CCK)-8 assay

The hFOB1.19 cell line, in the logarithmic growth phase, were seeded into 96-well plates, at a density of 3×103 cells/well, with five replicate wells in each group. Following culture for 24 h in normal medium, the medium was replaced with new medium according to the aforementioned groups. Following culture for 0, 24, 48 and 72 h, 10 µl CCK-8 solution (Beyotime Institute of Biotechnology) was added to each well and the samples were incubated at 37°C in the dark for 2 h. The absorbance value of each well was measured at 450 nm using a microplate reader (Bio-Rad Laboratories, Inc.).

Alkaline phosphatase (ALP)

The ALP level in the hFOB1.19 cell lysate from each group was measured using a commercial ALP Assay kit (cat no ab83369; Abcam), following the manufacturer's instructions. Briefly, following culture in different media for 48 h, the cell supernatant was removed and the production of p-nitrophenyl phosphate was determined by measuring the absorbance at 405 nm using a microplate reader (Bio-Rad Laboratories, Inc.).

Alizarin red staining

The bone mineralization of the hFOB1.19 cells in each group was detected using Alizarin red staining (Merck KGaA), following the manufacturer's instructions. Briefly, the cells were stained with 2% Alizarin red (pH 4.2) for 10 min at room temperature, then washed with distilled water. The mineralized nodules were examined using phase-contrast microscopy after culturing for 21 days.

TUNEL staining

Cell apoptosis was evaluated using a TUNEL assay (TUNEL Assay kit-FITC; cat. no. ab66108; Abcam), according to the manufacturer's instructions. Briefly, following culture in different media for 48 h, the cells were trypsinized, washed with PBS and fixed in 1% paraformaldehyde at 4°C for 2 h. The cells were then incubated with DNA labeling solution for 60 min at 37°C, followed by the addition of PI/RNase A solution for 30 min. The images of the TUNEL-labeled cells from 3 random fields were captured using a fluorescent microscope (magnification, ×200; Evos FL Cell Imaging System; Thermo Fisher Scientific, Inc.).

Determination of iron level

The ferrous iron level in the cells was determined using a commercially available indicator (cat. no. P14312; Thermo Fisher Scientific, Inc.), as previously described (19). Briefly, following treatment, the cells were resuspended in normal medium, then Phen Green™ SK fluorescent iron chelator was added for 15 min. The fluorescence represented the release of free iron and was observed at the excitation/emission values of 490/520 nm using a fluorescence microscope (magnification ×200; Evos FL Cell Imaging System; Thermo Fisher Scientific, Inc.).

Malondialdehyde (MDA) and oxidized low density lipoprotein (oxLDL) assessment

The relative MDA and oxLDL levels in the hFOB1.19 cells were detected using a Lipid Peroxidation (cat. no. ab118970) and oxLDL (cat. no. ab242302) (both from Abcam) assay kits, respectively, according to the manufacturer's instructions.

Glutathione (GSH)/oxidized GSH (GSSG) assay

The relative GSH concentration in the cells was assessed using a GSH/GSSG Ratio Detection Assay kit (Fluorometric-Green; cat. no. ab138881; Abcam), according to the manufacturer's instructions. Briefly, the whole cell lysates were diluted at 1:80 for GSH analysis, and a series dilution of GSH and GSSG stock standards were prepared as standards. A one-step fluorimetric reaction was performed, with the assay buffer and probes, for 30 min at room temperature in the dark. Fluorescence intensity was monitored at the excitation/emission values of 490/520 nm. GSH was calculated from the standard curve. GSSG was determined using the following equation: GSSG=(total GSH-GSH)/2.

Western blot analysis

Following treatment, the cells were lysed in cold RIPA buffer (Beyotime Institute of Biotechnology). The protein lysates were then centrifuged at 12,000 × g for 10 min at 4°C and the supernatant was collected. Protein concentration was determined using a BCA assay kit (Beyotime Institute of Biotechnology). A total of 10 µg total protein was separated using 10–15% SDS-PAGE, then transferred onto PVDF membranes. The membranes were then blocked for 1 h at room temperature with 5% skimmed milk and subsequently incubated with the primary antibodies overnight at 4°C. Finally, the membranes were incubated with a HRP-conjugated secondary antibody (goat anti-rabbit IgG; cat no. ab6721; Abcam; 1:10,000) for 2 h at room temperature. The bands were detected using the ECL Advance reagent (Cytiva) and quantified using ImageJ software (version 1.8.0; National Institutes of Health). The following primary antibodies were used: GSH peroxidase (GPX4; ab125066; Abcam; 1:5,000), solute carrier family 7 member 11 (SLC7A11; ab175186; Abcam; 1:5,000), nuclear receptor coactivator 4 (NCOA4; ab86707; Abcam; 1:3,000), acyl-CoA synthetase long-chain family member 4 (ACSL4; ab15282; Abcam; 1:10,000), transferrin receptor (TFR1), divalent metal transporter 1 (DMT1; ab214039; Abcam; 1:1,000) and GAPDH (ab181602; Abcam; 1:1,000).

Statistical analysis

All the data are from 3 experiments and are presented as the mean ± SD. Comparisons between two groups were analyzed using an unpaired Student's t-test. Comparisons among multiple groups were evaluated using one-way ANOVA followed by Tukey's post hoc test. P<0.05 was considered to indicate a statistically significant difference. All statistical analysis was performed using SPSS software (version 11.5; SPSS, Inc.).

Results

Level of serum AGEs and FBG is increased in patients with OP

Fig. 1A shows the images of lumbar vertebra and femur in healthy individuals and patients with OP, which were collected during DXA absorptiometry. Compared with that in the healthy individuals, patients with OP exhibited a decreased BMD in both the lumbar vertebra and femur. Fig. 1B reveals the significantly lower BMD in patients with OP compared with that in the healthy individuals. Next, the level of AGE and FBG in the serum of the participants were measured. Patients with OP exhibited a significantly higher level of AGEs (Fig. 1C) and FBG (Fig. 1D). The correlation between BMD and AGEs, and between FBG and AGEs in patients with OP was analyzed and the results showed that in patients with OP, the higher the AGE level, the lower the BMD level, but the higher the FBG level (Fig. 1E and F, respectively). These results suggested that an increase in the concentration of AGEs and FBG may be associated with the decrease in BMD, and even contribute to OP.

Figure 1. Patients with OP exhibit an increased level of serum AGEs and FBG compared with that in healthy individuals. (A) Images of lumbar vertebra and femur in healthy individuals, patients with OP, and patients with osteopenia were collected using DXA absorptiometry. (B) The BMD of healthy individuals and patients with OS was measured using DXA absorptiometry. (C) AGE and (D) FBG serum levels in healthy individuals and patients with OP. Correlation between (E) BMD and AGEs, and (F) FBG and AGEs, in patients with OP. **P<0.01 and ***P<0.001. BMD, bone mineral density; AGEs, advanced glycation end products; FBG, fasting blood glucose; DXA, dual-energy X-ray absorptiometry; OP, osteoporosis.

AGEs and serum from patients with OP inhibit the proliferation, differentiation and mineralization of hFOB1.19 osteoblasts

To validate the aforementioned hypothesis in vitro, the hFOB1.19 osteoblast cell line was cultured in normal medium (blank), medium containing AGEs (AGEs), or media containing serum from healthy individuals (control), OP patients with a normal FBG level (OP-normal) and OP patients with T2DM (OP-T2DM). Cell proliferation, differentiation and mineralization were then assessed. The cells that were treated with AGE, and serum from patients with OP and T2DM exhibited significantly reduced cell proliferation ability 24 h post-treatment, compared with that in cells in the blank and control groups, respectively (Fig. 2A). Compared with that in serum from the healthy individuals, serum from patients with OP and a normal FBG level had significantly lower cell proliferation 48 h post-treatment (P<0.05). In addition, the serum from patients with OP and T2DM resulted in a relatively higher decrease in cell proliferation compared with that in serum from patients with OP and a normal FBG level (Fig. 2A). A similar result was found for ALP levels in the hFOB1.19 cells (Fig. 2B), in which ALP level was decreased by AGEs and serum from patients with OP (OP-Normal and OP-T2DM). Alizarin red staining was performed to determine the mineralization of osteoblasts. Compared with that in cells in the blank and control groups, cells in the AGE, OP-Normal and OP-T2DM groups exhibited a decrease in the number of mineralized nodules (Fig. 2C). These results suggested that AGEs and serum from patients with OP could inhibit the proliferation, differentiation and mineralization of hFOB1.19 osteoblasts. In addition, the effect of serum from patients with OP and T2DM was stronger compared with that of serum from patients with OP and a normal FBG level.

Figure 2. AGEs and serum from patients with OP inhibit the proliferation, differentiation and mineralization of hFOB1.19 osteoblasts. (A) A Cell Counting Kit-8 assay was used to detect cell proliferation. (B) The cellular ALP level of hFOB1.19 osteoblasts was measured using an ALP kit. (C) Alizarin red staining was performed to observe the formation of mineralized nodules. **P<0.01 and ***P<0.001 vs. Blank; #P<0.05, ##P<0.01 and ###P<0.001 vs. Control; ∆∆P<0.01 and ∆∆∆P<0.001 vs. OP-Normal. AGEs, advanced glycation end products; OP, osteoporosis; ALP, alkaline phosphatase; OD, optical density; T2DM, type-2 diabetes mellitus.

AGEs and serum from patients with OP induce ferroptosis in hFOB1.19 osteoblasts

Subsequently, changes in cell ferroptosis were investigated. TUNEL staining was used to observe cell apoptosis. As shown in Fig. 3A, the AGEs group had a higher percentage of apoptotic cells compared with that in the blank group. The OP-Normal and OP-T2DM groups also exhibited increased apoptosis compared with the control group. Next, cellular free iron levels were analyzed (Fig. 3B) and the results showed that AGEs and serum from patients with OP significantly increased the cellular free iron level of hFOB1.19 osteoblasts. The concentrations of MDA and oxLDL was also significantly increased by AGEs and serum from patients with OP (OP-Normal and OP-T2DM), compared with those in the blank and control groups, respectively (Fig. 3C and D). However, the opposite effect was caused by AGEs and serum from OP patients (OP-Normal and OP-T2DM) on GSH/GSSG level (Fig. 3E). Following the detection of the expression level of ferroptosis-associated proteins, it was found that AGEs and serum from patients with OP resulted in a decrease in the protein expression level of GPX4 and SLC7A11, but an increase in the protein expression level of NCOA4, ACSL4, TFR1 and DMT1 (Fig. 3F and G). The results revealed that AGEs and serum from patients with OP significantly increased ferroptosis in hFOB1.19 osteoblasts, and that the effect of the serum from patients with OP and T2DM was stronger compared with that from patients with OP and a normal FBG level.

Figure 3. AGEs and serum from patients with OP induces apoptosis and ferroptosis in hFOB1.19 osteoblasts. (A) Representative images and quantitative analysis of TUNEL staining in hFOB1.19 cells from different treatment groups. (B) Cellular free iron levels in hFOB1.19 osteoblasts in different treatment groups. The relative levels of (C) cellular MDA, (D) ox-LDL and (E) GSH/GSSG in hFOB1.19 osteoblasts in different treatment groups. (F and G) The expression levels of proteins associated with ferroptosis was measured using western blot analysis. **P<0.01 and ***P<0.001 vs. Blank; #P<0.05, ##P<0.01 and ###P<0.001 vs. Control; ∆P<0.05, ∆∆P<0.01 and ∆∆∆P<0.001 vs. OP-Normal. AGEs, advanced glycation end products; OP, osteoporosis; MDA, malondialdehyde; ox-LDL, oxidized low density lipoprotein; GSH/GSSG, glutathione/oxidized GSH; T2DM, type-2 diabetes mellitus; GPX4, GSH peroxidase; SLC7A11, solute carrier family 7 member 11; NCOA4, nuclear receptor coactivator 4; ACSL4, acyl-CoA synthetase long-chain family member 4; TFR1, transferrin receptor; DMT1, divalent metal transporter 1.

Ferroptosis inhibition reverses the effect of AGEs and serum from patients with OP and T2DM on hFOB1.19 osteoblasts

To determine the role of ferroptosis in the impairment of hFOB1.19osteoblast biological activities induced by AGEs and serum from patients with OP and T2DM, the ferroptosis inhibitor, DFO was added to the culture medium in the hFOB1.19 cells treated with AGEs and serum from patients with OP and T2DM (20). The CCK-8 and ALP assays, and Alizarin red staining results showed that the presence of DFO promoted cell proliferation, ALP production and mineralized nodule formation in the hFOB1.19 osteoblasts from the AGE and OP-T2DM groups (Fig. 4A-C). Cell apoptosis was measured using TUNEL staining, and the results showed that DFO decreased the number of apoptotic cells in the AGEs and OP-T2DM groups; however, the result was not significant (P>0.05), (Fig. 4D). By contrast, DFO significantly reduced cellular iron, MDA and oxLDL levels, and increased GSH/GSSG levels in the hFOB1.19 osteoblasts from the AGE and OP-T2DM groups (Fig. 4E-H), indicating a DFO-induced inhibition of ferroptosis.

Figure 4. Ferroptosis inhibitor, DFO, reverses the effect of AGEs and serum from patients with OP and T2DM on hFOB1.19 osteoblasts. (A) A Cell Counting Kit-8 assay was used to detect proliferation in hFOB1.19 cells in different treatment groups. (B) Cellular ALP level of hFOB1.19 osteoblasts was measured using a ALP kit in different treatment groups. (C) Alizarin red staining was used to observe the formation of mineralized nodules in different treatment groups. (D) Representative TUNEL staining and quantitative analysis for hFOB1.19 osteoblasts in different treatment groups. (E) The cellular free iron level inhFOB1.19 osteoblasts in different treatment groups. The relative level of cellular (F) MDA, (G) ox-LDL and (H) GSH/GSSG in hFOB1.19 osteoblasts in different treatment groups. **P<0.01 and ***P<0.001 vs. AGEs; #P<0.05 and ###P<0.001 vs. OP-T2DM. DFO, deferoxamine; AGEs, advanced glycation end products; OP, osteoporosis; T2DM, type-2 diabetes mellitus; ALP, alkaline phosphatase; MDA, malondialdehyde; ox-LDL, oxidized low density lipoprotein; GSH/GSSG, glutathione/oxidized GSH; OD, optical density.

Discussion

OP is a common debilitating bone disease characterized by loss of bone mass and degradation of bone architecture. The involvement of AGEs in OP, particularly diabetes-related OP has been previously reported (21–23). In the present study, the inhibitory effect of AGEs on osteoblast proliferation, differentiation and mineralization was demonstrated, and the role of ferroptosis in these effects was identified. The results suggested that therapeutically targeting AGEs and AGE-induced ferroptosis in osteoblasts may promote bone formation and even relieve OP.

Patients with T2DM are more susceptible to OP, and the formation and accumulation of AGEs have been reported to cause diabetes-related OP (24). Increased AGE production is observed in diabetic rats, and AGE levels are negatively correlated with BMD (25). Higher levels of serum AGEs are found in patients with OP and osteopenia compared with those in healthy women (26). Consistently, the results in the present study showed increased serum AGE levels in patients with OP and a negative correlation with BMD. Furthermore, a higher concentration of FBG was observed in patients with OP compared with that in healthy individuals, and a positive correlation between AGEs and FBG was observed in patients with OP. The results further confirmed the crucial role of AGEs and hyperglycemia in OP.

OP is also a disease caused by an imbalance between osteoclasts and osteoblasts. Osteoblasts can contribute to bone formation by secreting various proteins that guide the deposition of bone extracellular matrix, such as ALP, osteocalcin and osteopontin (27). The results from the present study showed that AGEs and serum from patients with OP, which showed a higher concentration of serum AGEs compared with that in healthy individuals, significantly inhibited hFOB1.19 osteoblast proliferation, differentiation and mineralization. Furthermore, the effect of serum from patients with OP and T2DM was markedly stronger compared with serum from patients with OP and a normal FBG level, demonstrating the detrimental effect of hyperglycemia on human bone formation. These results were in accordance with those of previous studies, which showed that hyperglycemia and AGEs suppressed osteoblast differentiation and mineralization, accompanied by an enhanced RAGE expression (28–30). It has been reported that AGEs are diverse compounds that are generated via a non-enzymatic reaction between reducing sugars and the amine residues on proteins, lipids and nucleic acids (9). Intra- and extracellular AGEs accumulate in an age-dependent manner in human tissue including cartilage, thus contributing to bone fragility in patients with diabetes (31). Therefore, the disruption of osteoblast function caused by serum from patients with OP and T2DM may also be attributed to the high production of AGEs.

To elucidate the mechanisms underlying the destructive effect of AGEs on bone function, ferroptosis was investigated, as it is a process that has been found to be involved in OP pathogenesis in recent years (13,15,17,32). The results from the present study showed that AGEs and serum from patients with OP triggered apoptosis, and increased the cellular level of free iron, MDA and oxLDL levels, and reduced GSH/GSSG level in hFOB1.19 osteoblasts. Furthermore, AGEs and serum from patients with OP resulted in a decrease in the protein expression levels of GPX4 and SLC7A11, but an increase in the protein expression levels of NCOA4, ACSL4, TFR1 and DMT1. The accumulation of intracellular iron and lipid peroxidates, such as MDA, oxLDL and GSH, which are normally synthesized by ACSL4 and dissipated by the antioxidant enzyme GPX4, is a key feature of ferroptosis (33). In addition, the downregulation of SLC7A11 ultimately leads to a suppression of GPX4 activity and ferroptosis activation. NCOA4 is an autophagy cargo receptor, TFR1 is a transferrin receptor and DMT1 transports metal ions across membranes in mammals; all are necessary for iron release into the cytoplasm (34). The potential association between AGEs level and iron overload has been suggested in previous studies (35,36). AGEs were also reported to enhance heme oxygenase-1 (HO-1) mRNA expression in endothelial cells (37) and inhibited Nrf2 activation in H9C2 cells (38). Nrf2 is a transcription factor that regulates iron metabolism genes in response to oxidative stress, and increased HO-1 activity has been shown to increase cellular iron levels (39). The Nrf2/HO-1 signaling pathway has been reported to increase the cellular iron levels and promote ferroptosis (13,40). The aforementioned studies have found an association between AGEs and ferroptosis; however, to the best of our knowledge, the present study was the first to demonstrate the effect of AGEs on ferroptosis. Subsequently, the ferroptosis inhibitor DFO was found to not only suppress ferroptosis, but also induce a recovery of hFOB1.19 osteoblast proliferation, differentiation and mineralization in the AGE, and OP-T2DM groups. However, DFO had no significant effect on apoptosis in the hFOB1.19 cells treated with AGE and serum from patients with OP and T2DM. This may be due to the specific inhibition of DFO on ferroptosis without affecting apoptosis. This was in line with our hypothesis, suggesting that AGEs may disrupt osteoblast function by inducing ferroptosis. Nevertheless, the present results remain to be validated using in vivo animal models, which will be performed in future research.

In conclusion, the results from the present study demonstrated the inhibitory effect of AGEs on bone formation in OP. AGEs significantly suppressed proliferation, differentiation and mineralization in hFOB1.19 osteoblasts. In addition, ferroptosis influenced the effects of AGEs. To the best of our knowledge, the present study was the first to uncover the mechanisms mediating the effect of AGEs on osteoblast function and demonstrated the role of osteoblast ferroptosis in bone formation. Therapies targeting AGEs and ferroptosis may be valuable in relieving OP.

Acknowledgements

Not applicable.

Funding

Funding: No funding was received.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author upon reasonable request.

Authors' contributions

WLu, WG and JJ contributed to the conception or design of the study and performed the experiments. WW, JJ, JY, WLi and YC contributed to data analysis and interpretation. WLu, WG and JJ drafted the manuscript and revised it critically for important intellectual content. All authors read and approved the final manuscript. WLu, WG and JJ confirm the authenticity of all the raw data.

Ethics approval and consent to participate

All the experiments were approved by the Ethics Committee of the Nanjing Pukou District Central Hospital (Jiangsu, China). Written informed consent was obtained from all participants.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References