Icariin ameliorates dexamethasone‑induced bone deterioration in an experimental mouse model via activation of microRNA‑186 inhibition of cathepsin K.

The present study aimed to investigate bone deterioration in glucocorticoid‑induced osteoporosis (GIOP) mice, and the anti‑osteoporosis effect and underlying molecular mechanism of icariin. Dexamethasone (DSM) treatment was demonstrated to facilitate the induction of hypercalciuria in GIOP mice. Icariin treatment reversed the dexamethasone (DXM)‑induced disequilibrium of calcium homeostasis and bone resorption, and increased serum alkaline phosphatase, tartrate resistant acid phosphatase, osteocalcin and deoxypyridinoline. Haematoxylin and eosin staining revealed an increase in disconnections and separation in the trabecular bone network of the tibial proximal metaphysis, in the GIOP group. Icariin treatment reversed the DXM‑induced trabecular deleterious effects, and stimulated bone remodeling in GIOP mice. Furthermore, the results demonstrated that the mRNA and protein expression of cathepsin K were significantly increased in GIOP mice, compared with the control group. Icariin treatment may suppress the expression of cathepsin K in the tibia of GIOP mice. The levels of microRNA (miR)‑186 were markedly reduced in the tibia of GIOP mice compared with control group; however, this was inhibited by icariin treatment. Bioinformatics analysis demonstrated that miR‑186 regulates cathepsin K via binding to the upstream 3'‑untranslated region. Furthermore, transfection with miR‑186 mimics resulted in inhibition of cathepsin K expression, whereas miR‑186 inhibitors facilitated cathepsin K expression in osteoclasts. In conclusion, the present study demonstrated the protective effects of icariin against bone deteriorations in the experimental GIOP mice, and the underlying mechanism was mediated, at least partially, via activation of miR‑186‑mediated suppression of cathepsin K. These results provide evidence to support the use of icariin as a therapeutic approach in the management of glucocorticoid‑induced bone loss, and the disequilibrium of calcium homeostasis.

Introduction

Gluco<span class="Gene">corticoid-induced osteoporosis (GIOP) is a severe complication of prolonged systemic glucocorticoid use. GIOP-mediated bone loss, and the associated risk of fracture, is a relatively common disorder and the most prevalent type of secondary osteoporosis (1). It is believed that glucocorticoids may cause rapid bone loss, reduced bone formation and increased bone resorption, in vitro and in vivo (2,3). The therapeutic use of low doses of oral glucocorticoids and mild endogenous hypercortisolism may also be associated with bone loss (4). However, patients treated with glucocorticoids are not often evaluated and treated for this problem. Therefore, the exploration of a novel and effective adjuvant therapy is required.

<span class="Chemical">Icariin has been iden<span class="Chemical">tified as a flavonoid isolated from Herba Epimedii (Epimedium brevicornum), which is the most commonly used Chinese herbal medicine in the treatment of sexual dysfunction and osteoporosis (5,6). The anti-osteoporotic role of icariin has been verified in ovariectomized rats (7,8) and glucocorticoid-induced osteoporotic rats (9). A 24-month randomized double-blind placebo-controlled clinical trial indicated that an Epimedium-derived phytoestrogen flavonoid preparation containing 60 mg icariin, 15 mg daidzien and 3 mg genistein was able to limit bone loss in late postmenopausal women (10). Notably, molecular mechanism studies have suggested that icariin may induce osteoblast proliferation, differentiation and mineralization via estrogen receptor-mediated extracellular-signal related kinase and c-Jun N-terminal kinase signal activation (11), and may regulate the osteogenic differentiation of bone mesenchymal stem cells in a mitogen activated protein kinase-dependent manner (12). Furthermore, icariin, as an inhibitor of cathepsin K, suppresses cartilage and bone degradation in mice with collagen-induced arthritis (13). Previous study has indicated that cathepsin K serves an important role in the pathogenesis of rheumatoid arthritis (14). Cathepsin K is expressed by osteoclasts during bone resorption, and serves as the major collagenase responsible for organic bone matrix degradation during the bone remodeling process (15). Excessive cathepsin K is a key element in the pathogenesis of postmenopausal osteoporosis and other skeletal disorders; therefore, cathepsin K may be a valuable target in the development of novel therapeutic intervention strategies (16). The expression of cathepsin K and the effects of icariin in GIOP animal models remains largely unknown.

MicroRNAs (miRNAs) are a class of small noncoding (18–25 nucleo<span class="Chemical">tides), endogenous RNA molecules that regulate the translation of messenger RNAs (mRNAs) by attaching to the target 3′-untranslated region (3′-UTR) of mRNAs (17,18). The key roles of miRNAs involve regulation of cell proliferation, differentiation and apoptosis of several cell types, including osteoblasts and osteoclasts (19,20). A growing number of studies have demonstrated pathogenic alterations in various tissues that may be linked to abnormal miRNA expression, including the regulation of bone development (21,22). The present study hypothesized that a miRNA mechanism may be involved in icariin-mediated inhibition of secondary osteoporosis in mice, by targeting cathepsin K. This study aimed to improve the understanding of the anti-osteoporotic action and underlying molecular mechanism of icarrin, which may facilitate the treatment of secondary osteoporotic patients.

Materials and methods

Animal treatment

All procedures were evaluated and approved by the ethics committee of the Henan University of Tradi<span class="Chemical">tional Chinese Medicine (Henan, China). A total of 48 male C57BL/6J <span class="Species">mice (age, 8 weeks; weight, 20±2 g) were obtained from Slac Laboratory Animal (Shanghai, China; www.slaccas.com) and were allowed to acclimate to the environment for 1 week. The mice were given free access to food and tap water and were caged individually under controlled temperature (23±2°C) and humidity (55±5%) with an artificial 12-h light/dark cycle. The mice were randomly divided into four groups: Vehicle group (n=12) were injected with normal saline; dexamethasone (DXM), where mice were injected intramuscularly with 5 mg/kg body weight DXM three times weekly, for 12 weeks (n=12); low dose icariin GIOP, mice received oral icariin at a dose of 10 mg/kg/day for 12 weeks (Icariin + L, n=12) combined with DXM; high dose icariin GIOP, mice received oral icariin at a dose of 100 mg/kg/day, for 12 weeks combined with DXM (Icariin + H, n=12).

Cell culture

<span class="Species">Human <span class="Disease">embryonic kidney HEK293T cells [cat. no. CRL-11268; American Type Culture Collection (ATCC), Manassas, VA, USA] were maintained in Dulbecco's modified Eagle's medium (DMEM; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% (v/v) fetal bovine serum (FBS; Sigma-Aldrich; Merck Millipore, Darmstadt, Germany), 100 U/ml penicillin, and 100 mg/ml streptomycin, in a 5% CO2 atmosphere at 37°C.

Serum and urine chemistries

<span class="Species">Mice were placed in metabolic cages for 24 h to collect and re<span class="Gene">corded the volume of urine at week 12. Blood were collected after the animals were sacrificed at week 12 by intraperitoneal injection of sodium pentobarbital (2%; 200 mg/kg; cat. no. P3761; Sigma-Aldrich; Merck Millipore). The concentrations of calcium (Ca, absorbance was measured at 490 nm) and creatinine (Cr, absorbance was measured at 630 nm) in serum and urine were measured by standard colorimetric methods, using a microplate reader (BioTek Instruments, Winooski, VT, USA). The urinary Ca level was corrected against the urinary Cr concentration. Serum levels of alkaline phosphatase (ALP, cat. no. P0321; Beyotime Institute of Biotechnology, Haimen, China), tartrate resistant acid phosphatase (TRAP, cat. no. P0332; Beyotime Institute of Biotechnology), osteocalcin (OCN, cat. no. 60–1305; Immutopics, Inc., San Clemente, CA, USA) and deoxypyridinoline (DPD, cat. no. Ek-M20919; EK-Bioscience, Biotechnology Co., Ltd., Shanghai, China) were detected using mouse bioactive ELISA assays and measured using a SpectraMax M5 ELISA plate reader (Molecular Devices, LLC, Sunnyvale, CA, USA).

Osteoclast formation in RAW264.7 cells

<span class="CellLine">RAW264.7 cells (cat. no. <span class="Chemical">TIB 71; ATCC) were cultured in α-MEM + 10% FBS (Sigma-Aldrich; Merck Millipore) and were plated in 6-well dishes at 1×105 cells/well and were grown for 5 days with RANKL (20 ng/ml, cat. no. 462-TR; R&D Systems, Minneapolis, MN, USA) induction of osteoclastogenesis, as previously described (23).

Caspase-3 activity assay

Osteoclast (5×104) lysates were prepared in 2 ml of lysis buffer, containing 25 mM HEPES, pH 7.5, 5 mM <span class="Chemical">EDTA and 1 mM EGTA (all from Sigma-Aldrich; Merck Millipore), 5 mM MgCl2 and 10 mM sucrose (both from Thermo Fisher Scien<span class="Chemical">tific, Inc.), 5 mM dithiothreitol (DTT), 1% 3-[-(3-chloramidopropyl) dimethylammonio]-1-propanesulfonic acid (CHAPS), protease inhibitor cocktail (10 µl/ml), and 1 mM PMSF (all from Sigma-Aldrich; Merck Millipore). After 30 min incubation at 0°C, cell lysates were centrifuged at 12,000 × g for 15 min at 4°C, and the supernatants were collected. The activity of caspase-3 was determined using the caspase-3 activity assay kit (cat. no. C1116; Beyotime Institute of Biotechnology), according to the manufacturer's instructions. Release of p-nitroaniline was measured at a wavelength of 405 nm using a SpectraMax M5 ELISA plate reader, according to the manufacturer's instructions.

Quantification of apoptosis by flow cytometry

Quan<span class="Chemical">tita<span class="Chemical">tive assessment of apoptotic osteoclasts (5×104) was performed by terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labeling (TUNEL) method, which examines DNA-strand breaks during apoptosis, using an ApoAlert™ DNA Fragmentation Assay kit (BD Biosciences, Franklin Lakes, NJ, USA). Cells were trypsinized, fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100 in 0.1% sodium citrate. The cells were washed with PBS three times and subsequently incubated with the reaction mixture for 60 min at 37°C. Cells were immediately analyzed using a FACScan flow cytometer equipped with the CellQuest version 5.1 (BD Biosciences).

Bone histomorphology

The <span class="Disease">tibias were collected after the animals were sacrificed and were decalcified in 0.5 M <span class="Chemical">EDTA (pH=8.0) and embedded in paraffin by standard histological procedures. Sections (5 µm) were cut and stained with hematoxylin & eosin and safranin O, and were visualized under a Leica DM 2500 microscope (Leica Microsystems GmbH, Wetzlar, Germany). The trabecular bone microarchitecture of the proximal metaphysis of the tibia was measured using a SkyScan 1076 microtomography scanner (Bruker Corporation, Ettlingen, Germany), with a slice thickness of 22 µm. Bone morphometric parameters, including volumetric bone mineral density (BMD), bone volume over total volume (BV/TV), trabecula number (Tb.N), trabecula thickness (Tb.Th) and trabecula separation (Tb.Sp) were measured, as previously described (24). Femurs were placed in a 3-point bending configuration on an Instron Microtester 5848 system (Instron, Norwood, MA USA), to measure maximum load and stiffness, as previously described (25).

Transfection of miRNA-186 mimics and inhibitor

The <span class="Chemical">6-carboxyfluorescein-conjugated 2′-OMe-oligonucleo<span class="Chemical">tides were chemically synthesized and purified by high-performance liquid chromatography (GenePharma Co., Ltd., Shanghai, China). The 2′-OMe-miRNA (miR)-186 mimic was composed of RNA duplexes with the following sequence: 5′-CAAAGAAUUCUCCUUUUGGGCU-3′. The 2′-OMe-miR-1271 inhibitor sequence was: 5′-AGCCCAAAAGGAGAAUUCUUUG-3′, and the 2′-Ome-scramble sequence was: 5′-CUUGGUCAAGUCGCGAUCCGUA-3′. Osteoclasts (1×105) were transfected using Lipofectamine 2000™ (Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA), at a final concentration of 100 nM. The culture medium was changed 24 h post transfection. Cells were harvested for analysis after 48 h.

Luciferase reporter gene activity assay

The 3′-UTR of the <span class="Gene">cathepsin K gene containing the predicated target site for <span class="Gene">miR-186 was synthesized by GenePharma. The fragment was inserted into the multiple cloning site in the pMIR-REPORT luciferase miRNA expression reporter vector (Ambion; Thermo Fisher Scientific, Inc.). HEK293T cells (5×104; cat. no. CRL-11268; ATCC) were co-transfected with luciferase reporters containing cathepsin K 3′-UTR and miR-186 mimics using Lipofectamine 2000. The cell lysates were harvested following 48 h transfection, and the luciferase activity was measured using a dual luciferase reporter assay kit (cat. no. RG027; Beyotime Institute of Biotechnology) according to manufacturer's instructions.

Reverse transcription-quantitative PCR (RT-qPCR.)

The <span class="Disease">tibias were crushed in liquid <span class="Chemical">nitrogen and RNA extraction was performed using TRIzol® according to the manufacturer's instructions (Invitrogen; Thermo Fisher Scientific, Inc.). Synthesis of cDNA was performed by reverse transcription of 2 µg total RNA, using Moloney murine leukemia virus reverse transcriptase (Invitrogen; Thermo Fisher Scientific, Inc.), with oligo (dT)15 primers (Fermentas; Thermo Fisher Scientific, Inc., Pittsburgh, PA, USA), according to the manufacturer's instructions. The first strand cDNAs served as the template for the qPCR and were performed using an ABI 7300 thermocycler (Applied Biosytems; Thermo Fisher Scientific, Inc.). GAPDH served as an internal control to determine the relative expression of the target genes. The reaction conditions were set according to the kit protocol. The level of miR-186 was quantified using a mirVana qRT-PCR miRNA Detection kit (Ambion; Thermo Fisher Scientific, Inc.) and SYBR-Green (cat. no. D7260; Beyotime Institute of Biotechnology). Following the cycling reactions were used: 95°C for 10 min, followed by 40 cycles of 95°C for 15 sec, 58°C for 30 sec, and 72°C for 30 sec. U6 served as the internal control. The quantitation cycle (Cq) method (26) was used to determine relative expression levels. The PCR primers (Sangon Biotech, Co., Ltd., Shanghai, China) used in the present study were as follows: forward, 5′-CCAGGGCGTACGGAGGCCATT-3′ and reverse, 5′-GACCAAATTACGGCGTAGCCTC-3′ for ALP; forward, 5′-AGCATAAGGGTCCAAGTCCAA-3′ and reverse, 5′-TACCAAAAGCGGCGTAGTTA-3′ for TRAP; forward, 5′-AGGCGGAGGTCGATGCCCCG-3′ and reverse, 5′-CACGATGATGTCACCCTCGATGT-3′ for cathepsin K, forward, 5′-ACCGTGAGTTGTCCGTAGCATC-3′ and reverse, 5′-CGTAAGGGTCCGATACATCTC-3′ for osteoprotegerin (OPG); forward, 5′-CGTAGGTAGCCGGGTAGGATC-3′ and reverse, 5′-GCGTGGGAGCCTGATGCTCA-3′ for receptor activator of nuclear factor-κB ligand (RANKL); forward, 5′-GGCAGGTGCTTCAGAACTGG-3′ and reverse, 5′-GTGGTGGCAGGTAGGTATGG-3′ for Runt-related transcription factor 2 (Runx2); forward, 5′-TGAGCTGGAACGTCACGTGC-3′ and reverse, 5′-AAGAGGAGGCCAGCCAGACA-3′ for osterix; forward, 5′-CTCAGGGTTTCAGTGGTT-3′ and reverse, 5′-TTTCCACGAGCACCCATC-3′ for collagen type 1, α1 chain (Col1α1); and forward, 5′-ACAGGGGAGGTGATAGCATT-3′ and reverse, 5′-GACCAAAAGCCTTCATACATCTC-3′ for GAPDH.

Western blot analysis

The <span class="Disease">tibias were homogenized and extracted in NP-40 buffer, followed by 5–10 min boiling and centrifuga<span class="Chemical">tion (12,000 × g for 15 min at 4°C) to obtain the supernatant. Samples containing 50 µg protein were separated by 10% SDS-PAGE and transferred onto nitrocellulose membranes (Bio-Rad Laboratories, Inc., Hercules, CA, USA). The membranes were incubated at room temperature for 4 h with primary cathepsin K antibodies (1:500; R&D Systems). The blots were washed 3 times with TBS with Tween-20 (TBST), and incubated with donkey anti-goat immunoglobulin G (IgG; cat. no. OARA01784) and donkey anti-mouse IgG secondary antibodies (cat. no. OARA01848) at room temperature for 2 h, conjugated to IRDye 800CW Infrared Dye (LI-COR Biosciences, Lincoln, NE, USA), diluted 1:10,000. The membranes were washed 3 times with TBST. Blots were visualized using the Odyssey Infrared Imaging System (LI-COR Biosciences) and normalized to β-actin expression, to correct for unequal loading, using a mouse monoclonal anti-β-actin antibody (cat. no. AP0060; Bioworld Technology, Inc., St. Louis Park, MN, USA).

Statistical analysis

Data are presented as the mean ± standard devia<span class="Chemical">tion for each group. All statistical analyses were performed using PRISM version 4.0 (GraphPad Software, Inc., La Jolla, CA, USA). Inter-group differences were analyzed by one-way analysis of variance, followed by a post hoc Tukey's honest significant difference test for multiple comparisons. P<0.05 was considered to indicate a statistically significant difference.

Results

Effects of icariin on physiological and biochemical properties

Administra<span class="Chemical">tion of <span class="Chemical">DXM significantly downregulated the serum Ca level, compared with the control group, and icariin treatment did not recover these levels in GIOP mice (Fig. 1A). In contrast, DXM exposure markedly increased the level of urine Ca; however, high dose icariin-treatment reversed this upregulation in GIOP mice (Fig. 1B). ELISA analysis of bone formation and resorption markers indicated that DXM induced high bone turnover in mice, as evidenced by a significant increase in serum ALP (Fig. 1C), TRAP (Fig. 1D) OCN (Fig. 1E) and urinary DPD/Cr (Fig. 1F) levels. However, mice in the high dose icariin + H group demonstrated decreased serum ALP, TRAP and OCN and urinary DPD/Cr.

Figure 1.

Effects of icariin on physiological and biochemical parameters. (A) Serum and (B) urine Ca were measured by standard colorimetric methods. Serum levels of (C) ALP, (D) TRAP, (E) OCN and (F) urine levels of DPD were detected by ELISA. Data are expressed as mean ± standard deviation (n=12/group). *P<0.05, **P<0.01 and ***P<0.001 vs. DXM group. Ca, calcium; Cr, creatinine; ALP, alkaline phosphatase; TRAP, tartrate resistant acid phosphatase; OCN, osteocalcin; DPD, deoxypyridinoline; DXM, dexamethasone; L, low dose; H, high dose; U, units.

Effects of icariin on bone microarchitecture and biomechanical parameters

<span class="Disease">BMD decreased by 27.73 and 42.59% at weeks 6 and 12, respn>ectively, following administration of DXM (P<0.001), whereas administration with high-dose icariin (100 mg/kg) significantly restored the DXM-induced reduction in BMD in GIOP mice (Fig. 2A). A gross decrease in bone mass was observed following 12 weeks of DXM administration, which was inhibited when icariin was co-administered (Fig. 2B). Furthermore, structural parameters of the trabecular bone network in the tibial proximal metaphysis were measured. The results demonstrated that DXM-treated mice demonstrated significant decreases in trabecular BV/TV, Tb.N and Tb.Th, and increases in Tb.Sp, compared with the control group (Fig. 2C). Notably, icariin treatment in GIOP mice reversed the DXM-induced bone microarchitectural deteriorations. Bone biomechanical parameters, including maximum load and stiffness, decreased by 61.24 and 45.83% respectively, following DXM treatment. Mice in the icarrin + H group demonstrated significantly restoration of the DXM-induced biomechanical alterations in the tibial proximal metaphysis (Fig. 2D).

Figure 2.

Effects of icariin on bone microarchitecture and biomechanical parameters. (A) Volumetric BMD was measured by micro-CT. (B) Hematoxylin and eosin staining of the trabecular bone zone below the growth plate of the tibial proximal metaphysis (magnification, ×50). (C) BV/TV, Tb.N, Tb.Th and Tb.Sp were assessed by micro-CT. (D) Maximum load and stiffness were assessed by micro-force testing. Data are expressed as mean ± standard deviation (n=12/group). *P<0.05, **P<0.01 and ***P<0.001 vs. DXM group. BMD, bone mineral density; BV/TV, bone volume over total volume; Tb.N, trabecula number; Tb.Th, trabecula thickness; Tb.Sp, trabecula separation; DXM, dexamethasone; L, low dose; H, high dose; N, Newtons; CT, computed tomography.

Effects of icariin on the mRNA expression of key regulators in bone metabolism

<span class="Disease">ALP and <span class="Gene">TRAP mRNA were significantly increased in the DXM group, compared with the control group (Fig. 3A and B); however, these were reduced by high-dose icariin co-administration. Furthermore, expression of the bone formation-associated genes Runx2, osterix and Col1α1 were decreased with DXM administration compared with the vehicle group, and this was prevented by high dose icariin treatment in DXM-induced GIOP mice (Fig. 3C). To further investigate the molecular mechanism underlying DXM-induced inhibition of bone formation and promotion of bone resorption, RT-qPCR was used to assess the osteoclastogenesis-associated genes RANKL and OPG, which are produced by the osteoblast. The results indicated that DXM significantly elevated the expression of RANKL, and significantly reduced the RANKL/OPG ratio. However, these alterations in RANKL expression and the RANKL/OPG ratio were reversed by icariin co-administration (Fig. 3D).

Figure 3.

Effects of icariin on the mRNA expression of key regulators in bone metabolism. The mRNA expression of (A) ALP and (B) TRAP were measured by reverse transcription-quantitative polymerase chain reaction. The mRNA expression of (C) Runx2, Osterix and Col1a1, and (D) OPG and RANKL were measured by RT-qPCR. Data are expressed as mean ± standard deviation (n=/group). *P<0.05, **P<0.01 and ***P<0.001 vs. DXM group. ALP, alkaline phosphatase; TRAP, tartrate resistant acid phosphatase; Runx2, runt related transcription factor 2; Col1α1, collage type 1 α 1 chain; OPG, osteoprotegerin; RANKL, receptor activator of nuclear factor κB ligand; DXM, dexamethasone; L, low dose; H, high dose.

Effects of icariin on cathepsin K and miR-186 expression

<span class="Gene">Cathepsin K mRNA and protein <span class="Species">expression levels were significantly upregulated in DXM-treated mice, compared with the control group (Fig. 4A and B). However, these were reversed when icariin was co-administered in GIOP mice. Furthermore, the tibial levels of miR-186 were suppressed in GIOP mice compared with the control group; however, these levels were increased in icariin-supplemented GIOP mice (Fig. 4C). Notably, Spearman's rank correlation analysis indicated that the expression levels of cathepsin K protein and miR-186 were inversely correlated in DXM and icariin + H group mice (Fig. 4D). To further investigate the effect of cathepsin K on cartilaginous degeneration, safranin O staining was performed to observe the upper epiphyseal cartilage in the proximal tibias. The thickness of cartilage adjacent to the epiphyseal plate was reduced in the proximal tibia of the DXM mice, suggesting that DXM induces a delayed formation of new cartilage on the upper epiphyseal plate. However, the thickness of newly formed cartilage of the GIOP mice was improved by high concentrations of icariin (Fig. 4E).

Figure 4.

Effects of icariin on cathepsin K and miR-186 expression. The (A) mRNA and (B) protein expression levels of cathepsin K and (C) miR-186 were measured in the tibias. (D) Spearman's rank correlation analysis between the expression levels of cathepsin K protein and miR-186 were inversely correlated in DXM and icariin + H group mice. (E) Adjacent cartilage was visualized by Safranin O staining of the proximal metaphysis of the tibia (magnification, ×50). Data are expressed as mean ± standard deviation (n=12/group). ***P<0.001 vs. DXM group. DXM, dexamethasone; L, low dose; H, high dose; miR, microRNA.

Cathepsin K is a direct target of miR-186 in osteoclasts

The target prediction tools TargetScan, PicTar and microRNA.org were used to iden<span class="Chemical">tify potential target genes of miR-186; the results indicated that miR-186 may regulate cathepsin K (Fig. 5A). To investigate whether miR-186 may directly regulate cathepsin K expression, a luciferase reporter construct containing the 3′-UTR of cathepsin K was used. The wild-type and mutant cathepsin K luciferase expression vectors were transfected alongside an miR-186 mimic into HEK293T, and the level of luciferase enzyme activity was measured. Overexpression of miR-186 suppressed the luciferase activity of the reporter gene; however, a mutation in the miRNA binding site abolished the luciferase activity repression, confirming that the cathepsin K 3′-UTR contains a seed site for miR-186 (Fig. 5B).

Figure 5.

Cathepsin K is a direct target of miR-186 in osteoclasts. (A) Schematic representation of the putative miR-186 binding site in the cathepsin K 3′-UTR and (B) luciferase activity assay. (C) The protein expression of cathepsin K was measured by western blotting in osteoclasts transfected with an miR-186 mimic or inhibitor for 48 h. (D) Caspase-3 activity assay and (E) TUNEL staining were performed following osteoclast transfection with miR-186 mimics or inhibitor for 48 h. Data are expressed as mean ± standard deviation (n=12/group). *P<0.05 vs. DXM group. 3′-UTR, 3′-untranslated region; miR, microRNA; TUNEL, triphosphate nick-end labeling; Ctsk, cathepsin K; mut, mutant.

Transfec<span class="Chemical">tion with an <span class="Gene">miR-186 mimic decreased the levels of cathepsin K in osteoclasts, whereas transfection with miR-186 inhibitor increased these levels. However, cathepsin K protein expression was reduced when icariin was administered alongside the miR-186 inhibitor (Fig. 5C). In addition, apoptotic features induced by transfection with miR-186 mimic or inhibitor were assessed. The results demonstrated that caspase-3 activity was significantly increased in the miR-186 mimic group compared with the control group. In contrast, osteoclasts transfected with an miR-186 inhibitor suppressed caspase-3 activity, and this downregulation of caspase-3 was reversed when icariin was co-administered with the miR-186 inhibitor (Fig. 5D). TUNEL staining indicated that transfection with the miR-186 mimic induced cell apoptosis, whereas the miR-186 inhibitor suppressed cell apoptosis, and icariin treatment reversed the suppression of cell apoptosis in miR-186 inhibitor-treated osteoclasts (Fig. 5E).

Discussion

The present study revealed that <span class="Gene">cathepsin K is upregulated in GIOP <span class="Species">mice, and this is characterized by a reduction in bone volume and strength, accompanied with a high bone turnover, as evidenced by a significant increase in bone formation and resorption markers. Furthermore, when the expression of cathepsin K was blocked by icariin, the bone abnormalities were normalized. Notably, the protective effects of icariin against bone deteriorations in GIOP mice involved activation of miR-186, which serves to suppress cathepsin K.

It has previously been suggested that gluco<span class="Gene">corticoid treatment may influence bone remodeling and calcium homeostasis (27). Recent studies have indicated that DXM-exposure exhibits the typical features of GIOP in rabbits or mice, evidenced by the alterations in the basic bone microarchitecture and biomechanical parameters (2,28). A study investigating the pharmacological mechanisms of icariin revealed multiple targets in bone metabolism, and cathepsin K was identified as the critical node in the associated signaling networks (13). Growing evidence has suggested that cathepsin K inhibition may specifically block bone resorption without interfering with other pathways (16,29,30). In a randomized trial, the cathepsin K inhibitor odanacatib demonstrated an ability to decrease bone resorption, maintain bone formation and increase areal and volumetric BMD and increase estimated bone strength, in the hip and spine (31). Icariin has been identified as an inhibitor of cathepsin K and may suppress cartilage and bone degradation in mice with collagen-induced arthritis (13). In vivo, icariin has demonstrated significant anti-osteoporosis effects in ovariectomized rats and mice, glucocorticoid-induced rats and OPG knockout mice (7,8). However, in vitro studies have indicated that icariin may reduce TRAP activity and increase osteogenic differentiation, calcium deposition and mineralized nodule formation in induced bone marrow stromal and RAW264.7 cells (32,33). The present study revealed that high concentrations of icariin inhibits DXM-induced high bone turnover and cathepsin K upregulation in GIOP mice.

Several miRNAs have been associated with gluco<span class="Gene">corticoid-induced osteogenic differentiation and bone deterioration (34). Specifically, miR-29a ameliorates glucocorticoid-induced suppression of osteoblast differentiation by regulating β-catenin acetylation (35), and miR-29a overexpression may represent an alternative strategy for alleviating glucocorticoid-induced bone deterioration (36). Furthermore, miR-216a reverses DXM suppression of osteogenesis, promotes osteoblast differentiation and enhances bone formation by regulating the c-Casitas B-lineage lymphoma-mediated phosphoinositide 3-kinase/protein kinase B pathway (37). The results of the present study suggested that icariin prevents DXM-induced bone loss by inhibiting activated cathepsin K and increasing miR-186 levels. Notably, the expression levels of cathepsin K protein and miR-186 were inversely correlated in DXM and icariin + H group mice, and bioinformatics analysis suggested that miR-186 may regulate cathepsin K via binding to a seed region in the 3′-UTR of cathepsin K. These results suggested that miR-186 and cathepsin K serve a role in icariin-mediated protection against DXM-induced bone deterioration.

In conclusion, the present study demonstrated that <span class="Chemical">icariin may significantly ameliorate <span class="Disease">bone deterioration in GIOP mice, and the underlying mechanism may be mediated, at least partially, via activation of miR-186 and subsequent suppression of cathepsin K. These results may facilitate understanding of the underlying molecular mechanisms in DXM-induced osteoporosis, and may provide evidence to support the use of icariin as a therapeutic approach in the management of glucocorticoid-induced bone loss, and the disequilibrium of calcium homeostasis.