- Open Access
Impaired autophagy triggered by HDAC9 in mesenchymal stem cells accelerates bone mass loss
Stem Cell Research & Therapy volume 11, Article number: 269 (2020)
Bone mass loss in aging is linked with imbalanced lineage differentiation of bone marrow mesenchymal stem cells (BMMSCs). Recent studies have proved that histone deacetylases (HDACs) are regarded as key regulators of bone remodeling. However, HDACs involve in regulating BMMSC bio-behaviors remain elusive. Here, we investigated the ability of HDAC9 on modulation of autophagy and its significance in lineage differentiation of BMMSCs.
The effects of HDAC9 on lineage differentiation of BMMSCs and autophagic signaling were assessed by various biochemical (western blot and ChIP assay), morphological (TEM and confocal microscopy), and micro-CT assays.
Sixteen-month mice manifested obvious bone mass loss and marrow fat increase, accompanied with decreased osteogenic differentiation and increased adipogenic differentiation of BMMSCs. Further, the expression of HDAC9 elevated in bone and BMMSCs. Importantly, HDAC9 inhibitors recovered the lineage differentiation abnormality of 16-month BMMSCs and reduced p53 expression. Mechanistically, we revealed that HDAC9 regulated the autophagy of BMMSCs by controlling H3K9 acetylation in the promoters of the autophagic genes, ATG7, BECN1, and LC3a/b, which subsequently affected their lineage differentiation. Finally, HDAC9 inhibition improved endogenous BMMSC properties and promoted the bone mass recovery of 16-month mice.
Our data demonstrate that HDAC9 is a key regulator in a variety of bone mass by regulating autophagic activity in BMMSCs and thus a potential target of age-related bone loss treatment.
Osteoporosis is a common aged-related disease and is characterized by decrease bone mass and bone mineral density, leading to bone fragility and a higher risk of fractures [1, 2]. The increasing incidence of fracture in senile osteoporosis has become a heavy burden on health care worldwide, especially in China, which has a growing aging population. Researchers have discovered several risk factors associated with osteoporosis, including genetic and epigenetic factors, hormone imbalance, and stem cell senescence [2,3,4].
Bone marrow mesenchymal stem cells (BMMSCs) are a group of cell residual in the bone marrow. They have self-renewal capacity and multilineage differentiation potential. There is considerable data showing that BMMSCs play crucial roles in maintaining bone remodeling, reparation, and regeneration [5, 6]. Importantly, the number of BMMSCs declines and their lineage commitment shifts from osteoblasts to adipocytes with aging [7, 8] leading to an imbalance between bone mass and bone marrow fat. This imbalance is considered to be a hallmark of aged-related bone loss disorder, osteoporosis.
During senescence, mesenchymal stem cells (MSCs) undergo epigenetic and transcriptional changes, including decreased expression of stemness genes, Oct4 and Nanog , and increased age-related genes, p16 and p53 [5, 10]. Some adverse factors that trigger MSC senescence have been identified, such as reactive oxygen species (ROS) accumulation, telomere shortening, and epigenetic effectors, including histone deacetylases (HDACs) and DNA methyltransferases (DNMTs) [11, 12]. However, the details of the epigenetic regulation network remain elusive and its roles in BMMSCs during aged-related bone loss remain to be established.
HDACs are important epigenetic regulators that control gene transcription by removing acetyl groups from lysine side chains in histones and other proteins [13, 14]. Mammalian HDACs are divided into four classes based on their structure and function. Class I HDACs consist of HDAC1–3 and HDAC8, while class II HDACs include HDAC4–7, HDAC9, and HDAC10. Class III HDACs, also known as named sirtuins (Sirt1–7), differ from the other HDACs, as they are dependent on nicotinamide adenine dinucleotide. Class IV HDAC has only one member, HDAC11. HDAC family members have been shown to be involved in a wide range of aging-associated diseases, including muscle atrophy, loss of physical activity, and neurodegenerative diseases [13, 15, 16]. Recent evidence indicates that HDACs are key regulators on bone remodeling. For example, HDAC3 and HDAC8 supported bone formation , while HDAC4, HDAC7, and HDAC9 promoted bone resorption [17,18,19]. However, whether and how HDACs regulate BMMSCs senescence remains unclear.
In this study, we report that HDAC9 plays an important role in maintaining the balance between osteogenesis and adipogenesis of BMMSCs during aged-related bone mass loss. Furthermore, we found that the downregulation of HDAC9 could partially reverse the differentiation of aging BMMSCs and bone loss by regulating autophagy both in vitro and in vivo. These results suggest that aged-related bone mass loss may be partially controlled by the HDAC9-meditated autophagy of BMMSCs.
All animal procedure, operations, and experiments were approved and performed, and experimental protocols were approved by the guidelines of the Animal Care Committee of the Fourth Military Medical University, Xi’an, Shaanxi, China. Two-month-old female C57BL/6J mice were purchased from the Animal Experimental Center of the Fourth Military Medical University. Sixteen-month-old female C57BL/6J mice were purchased from Changzhou Kaiwensi Laboratory Animal Center, Jiangsu, China. All mice were housed under specific pathogen-free conditions (22 °C, 50–55% humidity) on a 12-h light/12-h dark cycle with food and water easily accessible.
Micro-computed tomography analysis
The mouse femora at mid-diaphysis were scanned with the GE micro-CT system (GE, USA). X-ray source was set at 80 kV and 80 μA microfocus. Three-dimensional images were reconstructed, and data analysis was performed with GEHC MicroView analysis software. The relevant bone morphometric parameters, including trabecular bone mineral density (BMD), trabecular volume relative to total volume (BV/TV), and cortical bone thickness (Ct.Th), were measured.
Isolation and culture of C57B/L BMMSCs
Bone marrow-derived mesenchymal stem cells were harvested from the femora and tibiae of 2-month-old young C57BL/6J and 16-month-old aged C57BL/6J mice. Mice were sacrificed with cervical dislocation and sterilized with 75% alcohol. The femora and tibiae were separated, and attached muscle was stripped. After epiphyses were amputated and the bone marrow was exposed, primary BMMSCs were drawn out; cultured with basal medium containing α-MEM medium (Gibco, Grand Island, NY, USA), 20% FBS (Sijiqing, Hangzhou, China), 2 mM l-glutamine (Invitrogen, Carlsbad, CA), 100 U/mL penicillin, and 100 U/mL streptomycin (North China Pharmaceuticals Company, Shijiazhuang, China); and incubated at 5% CO2 at 37 °C. The medium was changed every 3 days. Cells were digested with 0.25% trypsin when confluence reached 90%. BMMSCs used for the majority of experiments were at passage 1 in this study.
Isolation and culture of C57B/L myoblasts
Muscles were harvested from the hind limbs of 2-month-old young C57BL/6J and 16-month-old aged C57BL/6J mice. Firstly, the excessive connective tissues and fat were separated from muscle in cold sterile PBS. Then, muscles were cut into small pieces and enzymatically digested with 400 IU/mL collagenase II (Worthington) at 37 °C for 1 h. The digested slurry was sequentially passed through a 70-μm and then 30-μm cell strainer (BD Falcon). The filtrate was centrifuged at 1000g, and the pellets were suspended in myoblast growth medium (Ham’s F-10 medium with 10% FBS) and incubated at 5% CO2 at 37 °C. Briefly, the cell suspension was seeded for 15–30 min to allow quick adherence of fibroblasts, thus leaving a purer population of myoblasts in the supernatant, which was then transferred to another dish for subculturing. Myoblasts were digested with 0.25% trypsin when confluence reached 80%.
Senescence-associated β-galactosidase staining
The femora were fixed in 4% paraformaldehyde, decalcified with 17% EDTA (pH 7.0), dehydrated with 30% sucrose, and embedded in OCT. Fifteen-micrometer-thick longitudinal sections were prepared and collected on slide for SAbetaGal staining. The β-galactosidase activity was assessed with a SAbetaGal staining kit (Cell Signaling). Briefly, the slices were washed twice with PBS and fixed with Fixative Solution of the SAbetaGal staining kit at room temperature for 10–15 min. Then, the samples were washed twice with PBS, covered with SAbetaGal staining solution, and incubated at 37 °C overnight. On the next day, the slides were washed with PBS three times and 80% glycerin was mounted on the samples. Then, coverslips were inverted onto slide and excess glycerin was removed. The SAbetaGal positive cells were observed under a microscope.
Osteogenic and adipogenic differentiation assays
Young and aged BMMSCs were seeded at the density of 4.2 × 104 cells/cm2 on 6-well or 12-well plastic plates and cultured with basal medium. When cell confluence reached 80%, cells were induced with osteogenic differentiation medium (100 nmol/L dexamethasone, 50 μg/mL ascorbic acid, and 5 mmol/L β-glycerophosphate) up to 1 week for western blot assay or 2 weeks for Alizarin Red staining assay, with the medium changed every 3 days. To assess osteogenic differentiation, cells were fixed with 4% paraformaldehyde and stained with 1% Alizarin Red. The expressions of Runx2 and ALP were detected by western blot.
Young and aged BMMSCs were cultured using the same method described above. When cell confluence reached 85%, cells were induced with adipogenic differentiation medium (0.5 mol/L 3-lisobutyl-1-methyxanthine, 200 μmol/L indomethacin, 1 μmol/L hydrocortisone, and 10 μg/mL insulin) up to 5 days for western blot or 7 days for Oil Red O staining, with the medium changed every 3 days. Lipid droplet formation in cells was detected by staining with Oil Red O solution. The expression of PPAR-γ was detected by western blot.
Oil Red O staining
For cell Oil Red O staining, the BMMSCs were fixed with 4% paraformaldehyde for 15 min at room temperature and then stained with Oil Red O staining for 15 min at room temperature. The stained cells were washed twice with PBS and then observed under microscope. The images were analyzed with Image Pro Plus software.
Alizarin Red staining
Alizarin Red staining was performed to determine mineralization after 14 days of osteogenic induction. BMMSCs were fixed with 60% isopropanol for 90 s and washed once with ddH2O. Then, the cells were stained with 1% Alizarin Red (Sigma Aldrich) for 3–5 min and washed twice with ddH2O. Quantitative parameters of the mineralized area were analyzed with Image J software.
Alcian blue staining
Alcian blue staining was carried out to detect the chondrocytes in growth plates of the femora. Firstly, the samples of decalcified femora were cut into 10 μm thick and mounted on slides. Then, samples were stained with 0.1% Alcian blue staining solution containing acetic acid for 20 min at room temperature. Then, slides were washed twice with ddH2O and the positive areas were observed under microscope.
For cell immunofluorescence staining, cells were seeded on 3.5 cm confocal dish at the density of 3 × 104. Cells were treated with or without the autophagy-flux inhibitor chloroquine (CQ) (50 μM) 3–5 h before staining. In sequence, cells were fixed with 4% paraformaldehyde at 4 °C for 10–15 min, washed with PBS, incubated with 0.5% Triton-100 at room temperature for 10 min, and blocked with PBS containing 1% BSA at room temperature for 40 min. Next, the samples were incubated with primary antibodies to LC3 (Cell Signaling Technology, 1274, 1:100), aggrecan (GeneTex, GTX54920, 1:100), collagen II (Abcam, ab34712, 1:100), OCN (Santa Cruz Biotechnology, sc-390877, 1:100), PPAR-γ (Abcam, 2435, 1:50), and TRAP (Santa Cruz Biotechnology, sc-30833, 1:100) overnight at 4 °C and subsequently incubated with fluorescent secondary antibodies, respectively. The positive cells were examined under a laser scanning confocal microscope (Olympus FluoViem FV 1000, Tokyo, Japan). Quantitative histomorphometric analysis was conducted with Image Pro Plus software.
Transmission electron microscopy analysis
Cells were harvested and fixed in 4% glutaraldehyde in 0.1 M PB (pH 7.4) for 24 h, followed by 1% osmic acid for 2 h. After fixation, cells underwent osmosis by acetone and 812 resins. Then, samples were embedded with Epon 812 and kept in a thermostatic drying oven for 4 h at 36 °C, 6 h at 45 °C, and 12 h at 60 °C. Afterwards, embedding blocks were successively cut into semithin sections (1–2 μm) and ultrathin sections (50–100 nm). Then, samples were stained with uranyl acetate and lead citrate. Finally, images were captured with a transmission electron microscope (FEI, USA) at an accelerating voltage of 80–120 kV.
Total RNA was extracted from BMMSCs, myoblasts, bone marrow, and muscle by RNAiso plus (TaKaRa, Japan) according to the manufacturer’s instruction. Then, the mRNA was reversely transcribed into cDNA by PrimescriptTM RT master mix (TaKaRa, RR036A). Real-time PCR was performed with SYBR Premix Ex TaqTMII (TaKaRa) and detected by CFX96 Trademark Real-time PCR detection system (Bio-Rad, USA). The primers used in real-time PCR were listed in the Supplementary Table 1.
Western blotting analysis
Total proteins were harvested from BMMSCs, bone marrow, and other organs with RIPA lysis buffer (Beyotime, China) and quantified by BCA assay. Next, the proteins were separated on sodium dodecyl sulfonate-polyacrylamide gels (SDS-PAGE), transferred to PVDF membranes (Millipore, Billerica, MA, USA), blocked in TBST containing 5% BSA, and incubated in first antibodies with Beclin1 (Cell Signaling, 3738, 1:1000), ATG7 (Cell Signaling Technology, 8558, 1:1000), LC3 (Cell Signaling Technology, 1274, 1:1000), p62 (Proteintech, 18420-1-AP, 1:1000), HDAC9 (Abcam, ab59718, 1:1000), H3K9ac (Abcam, ab10812, 1:1000), H3K18ac (Cell Signaling Technology, 9675, 1:1000), H4K16ac (Abcam, 13534, 1:1000), H3 (Cell Signaling Technology, 9715, 1:1000), p53 (Cell Signaling Technology, 2524, 1:1000), phospho-p53 Antibody (R&D systems, AF1043, 1:2500), Runx2 (Cell Signaling Technology, 2435, 1:1000), ALP (R&D systems, AF2910, 1:500), PPAR-γ (Abcam, 2435, 1:300), and GAPDH (Cwbiotech, CW0100, 1:4000), respectively. Then, the membranes incubated in secondary antibodies which coupled to peroxidase (Cwbiotech, China). Finally, the signals were detected by an enhanced chemiluminescence kit (7seapharmtech, China).
HDAC inhibitor TSA and NaB treatment
BMMSCs were cultured in the medium with Trichostatin A (TSA, sigma) at 50, 100, and 200 (nmol/L) or sodium butyrate (NaB, sigma) at 50, 100, 200, and 400 (μmol/L). To assess the effects of TSA or NaB on inhibition of HDACs in cells, HDAC1–11 were detected by qRT-PCR. The expressions of HDAC9 and acetylated H3k9 were detected by western blotting. To examine the effects of HDACs on BMMSC differentiation, the cells were treated with or without NaB or TSA at their effective concentrations selected above.
Small interfering RNA (siRNA) targeting mice BECN1 (Ribobio, China) or HDAC9 (Santa Cruz, USA) were transfected into cells at a final concentration of 50 nM using riboFECT™ CP (Ribobio, China). siNC (Ribobio, China) was used as negative controls. All steps were performed according to the instruction in the riboFECT™ CP kit. The following experiments were performed according to the experiment designed. In detail, siRNA silencing HDAC9 was transfected into BMMSCs to investigate the effects of HDAC9 on osteogenic and adipogenic differentiation of BMMSCs and binding to the promoter of autophagy-related genes. In addition, aged BMMSCs were co-transfected with siHDAC9 and siBECN1 to investigate the hypothetical HDAC9-autophagy axis which may regulate BMMSC lineage differentiation.
To confirm the interaction between HDAC9 and targeting genes, chromatin immunoprecipitation assays were performed according to the manufacturer’s protocol (Millipore, LSKMAGG02, USA). Antibodies against HDAC9 (Abcam, ab59718) and polyclonal anti-histone H3 (acetyl K9) (Abcam, ab10812) were incubated with randomly interrupted genome DNA samples. Normal rabbit IgG (Merck Millipore) was used as a negative control. Then, antibody-DNA complexes were captured by protein A/G magnetic beads. Finally, the precipitated DNA samples were detected by qRT-PCR, and the results were normalized to the input value. The primers designed according to the promoters of Atg7, BECN1, LC3a, and LC3b (Sangon biotech, China) are listed in Supplementary Table 2.
shHDAC9 virus injection in vivo
The shRNA sequences for targeting HDAC9 were as follows: forward sequence—5′-CCGGCTGGGCACAAAATTCTGAACACTCGAGTGTTCAGAATTTTGTGCCCAGTTTTTG-3′; reverse sequence—5′-AATTCAAAAACTGGGCACAAAATTCTGAACACTCGAGTGTTCAGAATTTTGTGCCCAG-3′. The shHDAC9 lentivirus was packaged by co-transfecting shHDAC9 lentiviral vector with two packaging systems (pMD2.G and psPAX2) in 293T cells which were purchased from China Center for Type Culture Collection (CCTCC, GDC187), and the medium containing virus was collected and concentrated 48 h later. Detailedly, the medium was centrifuged at 800 rpm and 4 °C for 10 mins, and the supernatant was filtered by a 0.45-μm filter. Then, the filtrate was mixed with Lenti-X (TaKaRa, 631,231) and kept at 4 °C overnight. The next day, the mixture was centrifuged for 40 min at 1500g and the precipitate was resuspended with PBS whose volume is 1/100 of collected medium. The final virus titer was more than 1 × 108/mL. To evaluate the effect of HDAC9 on bone mass/skeletal metabolism in senescence-induced bone loss, aged mice (n = 21) were randomly divided into three groups (7/each group), namely the control group, the shScr group, and the shHDAC9 group, respectively. Aged mice were anesthesized through intraperitoneal injection with 1% pentobarbital sodium and were administrated with 20 μL of lentivirus containing shHDAC9 or empty vector every 2 weeks for 1 month through intra-bone marrow injection in the distal femora. After a 1- or 2-month treatment, the mice from above three groups were sacrificed by cervical dislocation and the femora from each group were collected for micro-CT scanning, Oil Red O staining, and SAbetaGal staining. BMMSCs were harvested and cultured from the femora for lineage differentiation analysis and autophagy analysis as above methods.
The data were presented as the mean ± SD. Comparisons were made using t test and one-way ANOVA for experiments with more than two groups. All of the experiments were repeated more than three times, with representative experiments shown. The P values of less than 0.05 were considered significant.
HDAC9 level increased in BMMSCs and bone marrow during aged-related bone mass loss
Firstly, young mice (2-month-old) and aged mice (16-month-old) were compared. The micro-CT analysis showed that the aged mice presented typical aged-related bone mass loss, including decreased bone mineral density (BMD) and trabecular bone volume (BV/TV), whereas no cortical bone thickness difference was observed (Fig. 1a). Moreover, increased numbers of TRAP-positive osteoclasts and PPAR-γ-positive adipocytes and reduced expression of OCN were observed in the bone marrow of aged mice (Fig. 1b–d). Immunoblotting showed higher protein expression levels of senescence-related proteins p53 and p-p53, in aged mice compared with those in young mice (Fig. 1e). Given that HDACs have been implicated as key factors in the pathogenesis of age-related disorders and diseases, gene expressions of HDAC family members were measured in the bone marrow from young and aged mice. Only HDAC9 expression remarkedly increased, while HDAC5 and HDAC7 expression levels reduced in aged mice. Meanwhile, there was no significant difference in the expression levels of HDAC1–4, HDAC6, HDAC8, HDAC10, or HDAC11 in the bone marrow from young and aged mice (sFig. 1a).
To screen for changes in HDAC gene expression, BMMSCs were isolated from the femora of young and aged mice respectively and cultured in vitro. The senescence-associated proteins p53 and p-p53 were highly expressed in BMMSCs from aged mice compared to those from young mice (Fig. 1f). The aged BMMSCs possessed significantly impaired potential osteogenesis capacity and higher adipogenesis ability compared with young BMMSCs (Fig. 1g, h). RT-PCR result showed almost an approximately tenfold increase in the level of HDAC9 mRNA and significant decrease in the level of HDAC5 mRNA of aged BMMSCs. Expression levels of the other HDACs were not significantly different between the two groups of cells (sFig. 1b). Based on the increased HDAC9 expression both in the bone marrow and BMMSCs of aged mice, we focused on the potential roles of HDAC9 in aged-related bone mass loss. We analyzed the level of HDAC9 protein and key histone acetylation sites, including H3K9, H3K14. and H3K18 in young and aged BMMSCs by western blotting. Significantly increased expression of HDAC9 (Fig. 1i) and decreased level of H3K9 acetylation (Fig. 1j) were observed in BMMSCs from aged mice compared with those from young mice. However, no differences were found in the acetylation level of H3K18 or H4K16. In the light of the importance of communication between bone and muscle, skeletal muscle and myoblasts were examined in young and aged mice. The increased expression of p53, p-p53, and HDAC9 and decreased acetylation level of H3K9 in aged BMMSCs were also observed in muscles and myoblasts from aged mice (sFig. 2a-f).
Inhibition of HDAC9 rebalance lineage differentiation in aged BMMSCs
To assess the effect of HDAC9 on aged BMMSC differentiation, HDAC activity was inhibited in BMMSCs using the histone deacetylase inhibitors Trichostatin A (TSA), sodium butyrate (NaB), and HDAC9 siRNA (siHDAC9) during osteogenic and adipogenic differentiation. Firstly, BMMSCs were treated with different doses of TSA (50, 100, and 200 nmol/L) and NaB (50, 100, 200, and 400 μmol/L) to examine changes in H3K9 acetylation. Western blotting results showed that 100 nmol/L and 200 nmol/L of TSA (sFig. 3a), and 200 μmol/L and 400 μmol/L of NaB (sFig. 3b) effectively enhanced H3K9 acetylation level in BMMSCs. However, much apoptosis occurs in cells administrated with 200 nmol/L TSA and 400 μmol/L NaB, respectively. Hence, 100 nmol/L of TSA and 200 μmol/L of NaB were chosen as the working concentration. The results of Alizarin Red staining and western blotting analysis of osteogenic associated proteins showed that treatment with TSA or NaB significantly restored the osteogenic differentiation of aged BMMSCs (sFig. 3c). Oil Red O staining and western blotting analysis of adipogenic associated protein PPAR-γ displayed that TSA or NaB effectively inhibited the adipogenic differentiation of aged BMMSCs (sFig. 3d). Next, we used HDAC9 siRNA to specially inhibit HDAC9 expression in aged BMMSCs (sFig. 4). We found that HDAC9 inhibition promoted osteogenic differentiation and repressed adipogenic differentiation in aged BMMSCs (Fig. 2a, b) and reduced the expression of senescence-related proteins p53 and p-p53 (Fig. 2e). To explore whether the effect of HDAC9 on BMMSC differentiation is age dependent, HDAC9 was silenced by siRNA in young BMMSCs. These results showed that HDAC9 regulated lineage differentiation in young BMMSCs (Fig. 2c, d) and the expression of senescence-related proteins (Fig. 2f), but not as effective as in aged BMMSCs. Above all, these results indicated that inhibition of HDCA9 converted BMMSCs into a younger state, with partially restored lineage differentiation balance and reduced expression of senescence-related proteins. However, the underlying mechanism of how HDAC9 regulates the differentiation of aged BMMSCs remained unclear.
Autophagy decreased in BMMSCs derived from aged mice
Our previous study showed that autophagy is a key regulator of BMMSC differentiation in OVX-induced osteoporosis and aged-induced bone mass loss [20, 21]. To evaluate changes in autophagy activity in BMMSCs, the autophagy-flux inhibitor, chloroquine (CQ), was used to prevent autophagy-lysosome degradation during active autophagy . The transmission electron microscope (TEM) results showed that aged BMMSCs possessed fewer autophagosomes than young cells, especially when treated with CQ (sFig. 5a). Furthermore, immunofluorescence staining results showed that the number of LC3 (an autophagy marker)-positive cells significantly decreased in aged BMMSCs (Fig. 3a). Meanwhile, the expression levels of the autophagy-related proteins, ATG7, Beclin1, and LC3II/I, were reduced in aged BMMSCs (Fig. 3b). However, the expression level of p62, the substrate of selective autophagy, increased in aged BMMSCs (Fig. 3b). These data suggested impaired autophagic activity in aged cells.
HDAC9 impaired the differentiation of aged BMMSCs by regulating autophagy
As the role of histone deacetylases involved in autophagy has previously been explored [23, 24], we next investigated the role of HDAC9 in the epigenetic regulation of autophagy in BMMSCs. To confirm whether HDAC9 could regulate autophagy in aged BMMSCs, we silenced HDAC9 expression using HDAC9 siRNA. The results showed HDAC9 expression significantly decreased and H3K9 acetylation levels increased in aged BMMSCs transfected with HDAC9 siRNA (sFig. 6). Next, we found that HDAC9 siRNA treatment increased the number of LC3-positive cells (Fig. 3c) and autophagosomes (sFig. 5b) in aged BMMSCs. These effects of HDAC9 siRNA were amplified when aged cells were treated with CQ. In addition, the protein expression levels of ATG7, Beclin1, and LC3II/I were higher and protein expression levels of p62 were lower in BMMSCs treated with HDAC9 siRNA or CQ, compared with that in control cells (Fig. 3d). These results indicated that HDAC9 has a close relationship with autophagy.
To test the hypothesis that HDAC9 regulates autophagy by modulating the acetylation of H3K9 associated with autophagy-related genes, chromatin immunoprecipitation (ChIP) assays were performed in BMMSCs. ChIP analysis was performed using antibodies that individually recognize either acetylated H3K9 (H3K9ac) or HDAC9, and the primers were used to amplify the promoter regions of Atg7, BECN1, LC3a, and LC3b (Supplementary Table 2). First, the effect of HDAC9 binding to autophagy-related genes was examined in young and aged BMMSCs. ChIP results showed that the level of HDAC9 binding to the promoters of Atg7, BECN1, LC3a, and LC3b significantly increased in aged BMMSCs. In contrast, the level of H3K9ac binding to these promoters was significantly reduced in aged BMMSCs (Fig. 3e). To confirm that decreased H3K9 acetylation in the promoters of Atg7, BECN1, LC3a, and LC3b genes was dependent on HDAC9 expression, HDAC9 was knocked down by HDAC9 siRNA in aged BMMSCs. We found that HDAC9 binding to the promoters of these genes was blocked in aged BMMSCs transfected with an HDAC9 siRNA, and subsequently, the level of H3K9 acetylation at these promoters increased (Fig. 3f). Overall, these results indicated that HDAC9 regulates autophagy in BMMSCs by controlling the acetylation of H3K9 associated with autophagy-related genes.
Given that HDAC9 siRNA effectively improved aged BMMSC differentiation and that HDAC9 regulates autophagy, we next examined whether HDAC9 affect the differentiation of aged BMMSCs by regulating autophagy. We silenced HDAC9 and BECN1, a key gene in the regulation of autophagosome formation [25, 26], in aged BMMSCs (sFig. 7). The effect of HDAC9 siRNA on improving the osteogenic differentiation of aged BMMSCs was neutralized by silencing BECN1 expression (Fig. 4a). Conversely, Oil Red O staining and western blotting results showed that the adipogenic differentiation of aged BMMSCs increased when cells were co-transfected with both HDAC9 siRNA and BECN1 siRNA, compared with cells transfected with HDAC9 siRNA only (Fig. 4b). Collectively, these results showed that the HDAC9-induced imbalance in the differentiation of aged BMMSCs was partially attributed to impaired autophagy.
Inhibition of HDAC9 improved bone mass loss in aged mice
To determine whether HDAC9 functions in vivo, we used a lentivirus containing HDAC9 shRNA to inhibit HDAC9 expression in the bone marrow of aged mice with senile osteoporosis. Micro-CT analysis was performed to examine the bone mass of control mice, shHDAC9-treated mice, and shScr-treated mice. The results showed that improved bone mass (increased BMD, BV/TV) of aged mice was observed 4 weeks or 8 weeks after shHDAC9 treatment (Fig. 5a). Moreover, no further improvement of bone mass was detected 8 weeks compared with 4 weeks. The bone mass of all groups underwent slight decrease in the further 1 month. SAbetaGal and immunofluorescence staining of PPAR-γ showed that the number of senescence cells and adipocytes reduced and the number of OCN-positive cells increased in the bone marrow of aged mice after HDAC9 inhibition (Fig. 5b, c). Considering chondrocytes are important in bone formation, we detected the chondrocytes in growth plate after inhibition of HDAC9. The Alcian blue staining showed that inhibition of HDAC9 had no significant improvement on the thickness of growth plate (sFig. 8), but promoted the expression of aggrecan and collagen II in chondrocytes (Fig. 5d).
Then, primary BMMSCs from control, shHDAC9-treated, and shScr-treated mice were cultured and detected. Western blotting was used to detect H3K9 acetylation and the expression of senescence- and autophagic-associated proteins in BMMSCs. BMMSCs from shHDAC9-treated aged mice were shown to have increased H3K9 acetylation (Fig. 6a), decreased protein expression levels of p53 and p-p53 (Fig. 6b), and increased the number of LC3-positive cells and the expressions levels of ATG7 and Beclin1 (Fig. 6c, d). In addition, the osteogenic and adipogenic differentiation capacities of BMMSCs were evaluated. Alizarin Red staining and western blotting results showed that osteogenesis of BMMSCs significantly improved from shHDAC9-treated mice (Fig. 6e). Furthermore, Oil Red O staining and the expression of adipogenesis-associated protein PPAR-γ demonstrated shHDAC9-treated BMMSCs had a lower level of adipogenic differentiation than control cells (Fig. 6f). In summary, these data suggested that the inhibition of HDAC9 could improve BMMSC lineage differentiation imbalance and ameliorate bone mass loss in aged mice. Our results indicated that the inhibition of HDAC9 could alleviate aged-related bone mass loss in mice, which suggests its potential as a target in the clinical treatment of senile osteoporosis (Fig. 6g).
The effects of HDACs on bone formation, bone absorption, and regeneration have been studied over the last few decades. The conditional deletion of HDAC3 in osteochondral progenitors using Osx1-Cre or in osteoblasts using OCN-Cre leads to cortical and trabecular bone mass loss and increased marrow adiposity [27, 28]. Some studies have demonstrated reduced bone mass and increased bone resorption in HDAC4- , HDAC5- , HDAC7- , and HDAC9-deficient  mice. Conversely, HDAC6-deficient mice showed increased bone mineral density . Although various HDAC-deficient animal models have been established to investigate bone remodeling, the effects on aged-related bone mass loss and the associated mechanisms remain unclear.
In this study, of the HDAC family members detected, only HDAC9 increased and acetylation of H3K9 consequently decreased in the bone and muscle of aged mice compared with young mice. The same results were also observed in senescent BMMSCs. Our previous works found that HDAC9 expression significantly increased in human periodontal ligament stem cells (PDLSCs) under inflammatory microenvironment . Kofman et al. showed that HDAC9 expression increased in aging spermatogonial stem cells and then decreased when cells were exposed to the anti-aging drug, rapamycin , which is consistent with our findings. HDAC inhibitors have been proposed as promising anti-aging drugs. In this study, we found modulating HDAC9 expression in BMMSCs could regulate the levels of the senescence-related proteins p53 and p-p53. In addition, increased HDAC9 expression impaired the osteogenesis capacity of both aged BMMSCs and inflammatory PDLSCs . Meanwhile, increased HDAC9 expression facilitated adipogenic differentiation in BMMSCs. Inhibition of HDAC9 by siRNA transfection improved the lineage differentiation capacity and decreased the senescence of aged BMMSCs, whereas HDAC9 inhibition in young BMMSCs did not display as effective as in aged BMMSCs, possibly because the level of HDAC9 expression was relatively low in young BMMSCs. Interestingly, some studies reported that HDAC9 regulates the osteogenic differentiation of MSCs [33, 34]. Chen et al. showed that HDAC9 expression decreased in old mice and this was associated with bone aging , which contradicts our observations in aged mice. In our study, HDAC9 expression was compared in the bone marrow of 2-month-old and 16-moonth-old female mice. However, Chen et al. compared HDAC9 expression in MSCs from mice in their study which were designed less than 7-month-old as young mice and more than 7-month-old as old mice, with no details information of the sex. There are known to be sex differences in the pathogenesis and mechanisms of senile osteoporosis. Furthermore, the MSCs were performed for functional verification of HDAC9 which was different. Chen and colleagues used MSCs derived from human; however, the MSCs used were derived from mice in this study. These differences in observation time points and cell genus may be key factors leading to contrasting results.
Autophagy is a very important degradation system, playing a crucial role in maintaining cell homeostasis in response to cellular stress [35, 36]. Autophagy dysfunction is associated with several diseases, such as inflammation, cancer, neurodegeneration, and aging . Recent studies have indicated that autophagy is a key process in bone cell differentiation. It has been reported that autophagy can regulate osteoclast and chondrocyte differentiation  and protect BMMSCs from oxidative stress , which indicates that autophagy plays protective roles in maintaining bone homeostasis. Our previous study also showed that impaired autophagy triggers intracellular ROS-induced senescence in BMMSCs, which shifts cellular lineage commitment from osteoblasts to adipocytes, consequently leading to bone aging [20, 21]. This is consistent with the mainstream views that autophagy acts as a crucial stem cell fate regulator by controlling ROS associated with p16 and p21 [22, 39]. However, the upstream factors regulating autophagy in BMMSCs are still unclear and need to be further investigated.
Epigenetic modifications associated with the aging process have received our attention over the past few decades. Epigenetic regulations have been widely studied in somatic stem cells to help us understand its roles in governing self-renewal or lineage differentiation. Meanwhile, some studies have reported epigenetic modifications, including acetylation of H4K16 associated with ATG genes [24, 40], regulation of LC3 transcription by histone methyl-transferase (HMT) G9a [23, 41], and hypermethylation of the BECN1 promoter , which is involved in regulating the formation of autophagosomes. To date, very few studies have detected histone deacetylases in MSCs to explore whether changes in epigenetic modification are associated with autophagy during bone aging. Here, we demonstrated that increased HDAC9 expression impaired autophagy activity in aged BMMSCs. Furthermore, we found that HDAC9 directly interact with the promoter of autophagy-related genes, ATG7, BECN1, and LC3a/b, by ChIP analysis. Inhibition of HDAC9 expression in aged BMMSCs by siRNA transfection reduced HDAC9 binding to the promoters of Atg7, BECN1, LC3a, and LC3b, but increased the levels of acetylated H3H9 interaction in the promoter of autophagy-related genes. Thus, we speculated the increased expression of HDAC9 in aged BMMSCs is an important factor leading to autophagic degeneration and this finding may uncover a new mechanism for the regulation of aged-related bone mass loss by HDAC9. However, there are still some unanswered questions. For example, the animal model we used was aged female mice with postmenopausal osteoporosis, which may not have an identical pathogenesis to aged male mice. Therefore, further investigation is required to determine whether the mechanism identified in this study is also applicable to aged male mice. Furthermore, HDAC9 was found to affect bone resorption , which is a key factor in maintaining the balance of bone remodeling. We need to explore the HDAC9-mediated osteoclastogenesis in bone remodeling in more detail in future experiments and identify the regulatory networks operating between BMMSCs and osteoclasts.
Taken together, our study suggested a potential role and mechanism of HDAC9 in BMMSC lineage commitment by regulating autophagy activities. Knockdown HDAC9 improved endogenous BMMSC properties and promoted the bone mass recovery in aged mice. Our finding provided a potentially promising target for the prevention of osteoporosis and treatment of aged-related bone mass loss.
Availability of data and materials
All datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Bone marrow mesenchymal stem cells
Reactive oxygen species
Runt-related transcription factor 2
Peroxisome proliferator activated receptor gamma
Tartrate-resistant acid phosphatase
Microtubule associated protein 1 light chain 3
Ubiquitin-binding protein p62
Histone H3 lysine 9
Acetyl-histone H3 lysine 9
Histone H3 lysine 14
Histone H3 lysine 18
Tumor protein p53
Real-time polymerase chain reaction
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We thank Shiyu Liu, Chenghu Hu, and Bei Li for their intellectual suggestions and help on the project.
This work was supported by the National Key Research and Development Program of China (2017YFA0104800) and the National Natural Science Foundation of China (31601099, 31571532, 31870970, and 81970915).
Ethics approval and consent to participate
Mice were used according to federal guidelines and as approved by the Animal Ethical and Welfare Committee of the Fourth Military Medical University (approval number SCXK (Military) 2007-007).
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Additional file 1: sFig. 1
The expressions of HDACs family members in bone marrow and BMMSCs HDACs gene were examined in bone marrow (a) and BMMSCs (b) from young mice and aged mice by qRT-PCR. sFig. 2 The expressions of senescence associated proteins and HDAC9 in skeletal muscle and myoblasts. The expression of p53, HDAC9 and H3K9 acetylation, and HDAC9 in skeletal muscle (a-c) and myoblasts (d-f) were examined by western blotting and qRT-PCR from young mice and aged mice. sFig. 3 HDACs inhibitors promoted osteogenic differentiation and inhibited adipogenic differentiation in aged BMMSCs The expression of HDAC9 and H3K9 acetylation were detected in aged BMMSCs treatment with different dose of TSA (a) or NaB (b) by western blotting. Osteogenic differentiation (c) and adipogenic differentiation (d) were observed in aged BMMSCs treated with TSA or NaB. Scale bars = 100 μm. sFig. 4 The silence efficiency of HDAC9 siRNA HDAC9 and H3K9 acetylation were examined in aged BMMSCs after transfected with HDAC9 siRNA for 48 hours, 3 days and 7days by qRT-PCR (a, d) and western blotting (b, c, e). sFig. 5 HDAC9 siRNA restored the number of autophagosomes in aged BMMSCs Autophagosomes in young, aged BMMSCs (a) and aged BMMSCs transfected with HDAC9 siRNA (b) were detected by TEM. Scale bars = 1 μm. sFig. 6 HDAC9 siRNA decreased H3K9 acetylation in aged BMMSCs. The expression of HDAC9 and H3K9 acetylation were examined by western blotting in aged BMMSCs transfected with HDAC9 siRNA and those cells treated with CQ. sFig. 7 The silence efficiency of BECN1 siRNA Beclin1 was examined by western blotting in aged BMMSCs transfected with BECN1 siRNA 48 hours later. sFig. 8 No changes in growth plate thickness in aged mice were treated with HDAC9 shRNA lentivirus Alcian blue staining were performed to assess growth plate thickness.
Additional file 2: Supplementary Table 1
. Primer sequences for Real-Time PCR assay. Supplementary Table 2. Primer sequences for ChIP assay.
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Zhang, L., Qi, M., Chen, J. et al. Impaired autophagy triggered by HDAC9 in mesenchymal stem cells accelerates bone mass loss. Stem Cell Res Ther 11, 269 (2020). https://doi.org/10.1186/s13287-020-01785-6
- Bone mass loss
- Lineage differentiation