Evaluation of the protective effects of curcuminoid (curcumin and bisdemethoxycurcumin)-loaded liposomes against bone turnover in a cell-based model of osteoarthritis
Received 27 November 2014
Accepted for publication 27 January 2015
Published 20 April 2015 Volume 2015:9 Pages 2285—2300
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Prof. Dr. Wei Duan
Chih-Chang Yeh,1,2 Yu-Han Su,3 Yu-Jhe Lin,3 Pin-Jyun Chen,3 Chung-Sheng Shi,1 Cheng-Nan Chen,3,* Hsin-I Chang3,*
1Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan, Republic of China; 2Orthopaedic Department, Chiayi Branch, Taichung Veterans General Hospital, Chiayi, Taiwan, Republic of China; 3Department of Biochemical Science and Technology, National Chiayi University, Chiayi, Taiwan, Republic of China
*These authors contributed equally to this work
Abstract: Curcumin (Cur) and bisdemethoxycurcumin (BDMC), extracted from Curcuma longa, are poorly water-soluble polyphenol compounds that have shown anti-inflammatory potential for the treatment of osteoarthritis. To increase cellular uptake of Cur and BDMC in bone tissue, soybean phosphatidylcholines were used for liposome formulation. In this study, curcuminoid (Cur and BDMC)-loaded liposomes were characterized in terms of particle size, encapsulation efficiency, liposome stability, and cellular uptake. The results show that there is about 70% entrapment efficiency of Cur and BDMC in liposomes and that particle sizes are stable after liposome formation. Both types of liposome can inhibit macrophage inflammation and osteoclast differential activities. In comparison with free drugs (Cur and BDMC), curcuminoid-loaded liposomes were less cytotoxic and expressed high cellular uptake of the drugs. Of note is that Cur-loaded liposomes can prevent liposome-dependent inhibition of osteoblast differentiation and mineralization, but BDMC-loaded liposomes could not. With interleukin (IL)-1β stimulation, curcuminoid-loaded liposomes can successfully downregulate the expression of inflammatory markers on osteoblasts, and show a high osteoprotegerin (OPG)/receptor activator of nuclear factor κB ligand (RANKL) ratio to prevent osteoclastogenesis. In the present study, we demonstrated that Cur and BDMC can be successfully encapsulated in liposomes and can reduce osteoclast activity and maintain osteoblast functions. Therefore, curcuminoid-loaded liposomes may slow osteoarthritis progression.
Keywords: liposome, osteoarthritis, curcuminoid, OPG/RANKL ratio, bone turnover
Bone turnover is a continuous process of bone resorption and formation for the purpose of maintaining normal bone mass. Bone turnover involves the old bone resorption by osteoclasts and new bone formation by osteoblasts.1–3 Osteoclasts, bone-resorbing multinucleated cells, are generated from hematopoietic monocyte/macrophage precursor cells through differentiation processes.4 Differentiated and matured osteoclasts are characterized by high expression of tartrate-resistant acid phosphatase (TRAP) and cathepsin K. TRAP is a metallophosphoesterase participating in osteoclast-mediated bone turnover.5 Cathepsin K is an essential cysteine proteinase in collagenous bone matrix degradation. Cathepsin K can efficiently activate TRAP through proteolytic processing and these two proteins colocalize in osteoclasts to increase bone resorptive activity.6 Bone formation involves the proliferation, differentiation, and mineralization of osteoblasts. Active osteoblasts produce bone formation markers which are expressed during different phases of osteoblast development.7 Bone formation markers include collagen I, alkaline phosphatase (ALP), osteocalcin, osteopontin, and other molecules.8–10 During the bone loss process, high concentrations of matrix metalloproteinases (MMPs) (involved in the initial destruction of collagen) and a high ratio of receptor activator of nuclear factor κB ligand (RANKL)/osteoprotegerin (OPG) are observed.11,12 RANKL, a member of the tumor necrosis factor (TNF) family, can activate nuclear factor-κβ ligand (NF-κB) through RANK–RANKL specific binding to stimulate the survival, differentiation, and activation of osteoclasts.13 OPG, a membrane-bound TNF-related factor, works as a decoy receptor for RANKL and therefore the binding of OPG to RANKL prevents RANK activation and subsequent osteoclastogenesis.14,15 The RANKL/OPG ratio is an index of osteoclastogenic stimulus.16
Osteoarthritis (OA) is a progressive bone disease characterized by degeneration of articular cartilage, synovial inflammation, and changes in periarticular and subchondral bone. Recently, OA has been often discussed when talking about bone turnover.17 In the early stages of OA, bone turnover rate and subchondral bone loss are elevated. OA that involves a number of inflammatory cytokines, chemokines, and other mediators such as interleukin (IL)-1β, IL-6, IL-11, IL-17 and TNF-α, can induce bone loss by increasing RANKL expression and decreasing OPG production on osteoblasts and stromal cells.18,19 A 50% decrease in cartilage pathology score, based on the gold-standard Mankin score, was reported on extensive inhibition of bone resorption, implicating the importance of osteoclast function and bone turnover in the pathogenesis of OA.20 Therefore, bone turnover is likely to play a pivotal role in the pathogenesis of OA.
Curcuminoids are yellow, lipid-soluble polyphenols extracted from the rhizome of turmeric (Curcuma longa). Curcuminoids consist of three principal active components: curcumin (Cur), demethoxycurcumin (DMC), and bisdemethoxycurcumin (BDMC).21 Curcuminoids have been shown to suppress oxidative stress and inflammatory markers in diabetic patients and induce apoptotic cell death of a wide variety of tumor cells.22–26 In 2009, Funk et al and Bharti et al reported that Cur is an attractive agent to chronic inflammatory diseases like neurodegenerative diseases, cardiovascular diseases, rheumatoid arthritis, and other arthritic diseases.27,28 Although some studies have reported that Cur inhibits RANKL activation in osteoclast precursors and suppresses osteoclastogenesis,29,30 it is interesting to note that the functions and mechanisms of curcuminoid in regulating bone turnover have not fully been investigated.31 In addition, light sensitivity, low water solubility, and poor oral bioavailability restrict the therapeutic value of curcuminoids. Based on recorded data, Cur and DMC are less stable than BDMC.32 To overcome the problems related to curcuminoid solubility, stability, and bioavailability, many nanocarriers have been attempted, including liposomes, polymeric nanoparticles, biodegradable microspheres, cyclodextrin, and hydrogels.33–35 Liposomes are artificially prepared vesicles made of phospholipid bilayers.35 Several techniques, such as the Bangham method, the detergent depletion method, the ether/ethanol injection method, reverse-phase evaporation, and the emulsion method, have been reported for preparing liposomes with high entrapment efficiency, narrow particle size distribution, and long-term stability.35,36 Previous studies have demonstrated that Cur encapsulation in liposomes can improve the drug bioactivities.37,38 In this study, we used liposomes encapsulating Cur and BDMC individually with nanoparticle sizes to improve the drug solubility and bioavailability and then investigate their therapeutic approach in an in vitro model of OA.
Materials and methods
Cell culture and reagents
Cur was purchased from Alfa Aesar (Heysham, England). BDMC was obtained from TCI, Japan. Soybean phosphatidylcholine (SPC) (Phospholipon 90G) were purchased from American Lecithin Company (Germany). Alkaline Phosphatase Colorimetric Assay kit, Trichrome Stain (Masson) kit, Acid Phosphatase Leukocyte Kit, and all chemicals of reagent grade were purchased from Sigma-Aldrich Co. (St Louis, MO, USA). All cell culture materials were purchased from Thermo Fisher Scientific (Waltham, MA, USA) and all solvents used were of analytical grade (J.T. Baker, USA). Cytokines were from Prospec. Mouse osteoblast-like cells (7F2) and macrophages (RAW264.7) were obtained from the Food Industry Research and Development Institute (Taiwan). Cell lines 7F2 and RAW264.7 were cultured in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% v/v fetal bovine serum (FBS), 100 units/mL penicillin, and 100 μg/mL of streptomycin. Cells were maintained at 37°C with 5% CO2 in a humidified incubator.
Liposomes loading with Cur or BDMC were prepared using the modified thin-film hydration method.39 Phospholipids were dissolved in chloroform and mixed with a range of molar ratios of cholesterol to lipid (30:70, 1:2, 40:60, 45:55). Cur or BDMC (2 mM) dissolved in ethanol was added into the phospholipid solution in a round-bottom flask. The solvent was evaporated with a rotary evaporator at 45°C and vacuum dried to form a dry lipid film. The lipid film was then hydrated with distilled water. The hydrated solution was downsized by sequence passing through 400 nm, 200 nm, and 100 nm polycarbonate membranes using an extruder (Avanti Mini Extruder; Alabama, USA) to obtain uniformly sized liposomes. Empty liposomes were prepared using the same protocol without Cur or BDMC.
The particle size distribution of liposomes was determined using a dynamic light scattering instrument (LB-550; HORIBA Ltd., Kyoto, Japan). Liposomal dispersions were diluted with double-distilled water to ensure the light scattering intensity in the instrument’s sensitivity range. The particle stability of the Cur- or BDMC-loaded liposomes (Cur-Lip and BDMC-Lip) was evaluated after storage at 4°C for 14 days and incubation with DMEM containing 10% bovine serum albumin at 37°C for 7 days. The measurements were performed in triplicate.
Cell viability and proliferation assay
7F2 osteoblast-like cells were seeded at a density of 104 cells/well in 24-well plates for cell viability and proliferation studies. Cell medium was replaced with the medium containing test samples (empty liposomes, Cur-Lip, and BDMC-Lip) at various concentrations. After 1, 4, 7, and 14 days of incubation at 37°C, the cell supernatants were removed and 200 μL MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide) reagent (100 μg/mL) was added to each well for another 4 hours’ incubation. To dissolve formazan crystals, 100 μL dimethyl sulfoxide (DMSO) was added to each well and the absorbance was measured at 570 nm using an enzyme-linked immunosorbent assay (ELISA) reader (Tecan Trading AG, Tecan, Switzerland). All experiments were performed in quadruplicate, and the relative cell viability (%) was expressed as a percentage relative to the untreated control cells.
After liposome formulation, the samples were spun down at 100,000 g for 30 minutes by Beckman ultracentrifuge. After centrifugation, the pellets were separated from the supernatant containing non-entrapped Cur or BDMC. The pellet was re-dissolved with ethanol and then the amount of Cur or BDMC in liposomes was measured by an ELISA reader at 427 or 419 nm. The encapsulation efficiency (EE) was calculated using the following equation:
For Cur, the sensitivity is 0.1 μg/mL and the linear range is 0.5–5 μg/mL. For BDMC, the sensitivity is 0.1 μg/mL and the linear range is 0.5–5 μg/mL.
Fluorescence spectroscopy method for intracellular uptake of liposomes
In order to study intracellular uptake of liposomes, 1 μL of 1,1′-dioctadecyl-3,3,3′,3′-tetramethylindocarbocyanine (DiI) (10 mg/mL in ethanol) was added to the phospholipid solution. Then, DiI-labeled liposomes were prepared as described in the section “Liposome formulation”. 7F2 cells were plated at a density of 2×104 cells/dish in 6 cm dishes, and replaced with medium containing DiI-labeled liposomes after 24 hours. Thereafter, the cells were incubated with liposomes for a range of durations (0.5–8 hours), and fixed with 0.05% paraformaldehyde for 30 minutes. Samples were washed three times with phosphate-buffered saline (PBS), and stained with 5 μg/mL 4′,6-diamidino-2-phenylindole (DAPI) for 5 minutes. After several washings with PBS, samples were imaged using a fluorescence microscope (Eclipse Ti-E; Nikon Instruments, Tokyo, Japan) with a charge-coupled device camera system (SPOT RT3; Diagnostic Instruments, Sterling Heights, MI, USA). To analyze liposome fluorescence in 7F2 cells, fluorescence intensity was measured in over 100 individual cells, using 20× images obtained with equal acquisition parameters and Image J software (National Institutes of Health, MD, USA). 7F2 cells in the control group were cultured in medium containing DiI (DiI solution was added on the top of the medium without the mixing) for 24 hours.
RAW 234.7 cells (5×105 cells/well) were plated in 24-well plates and incubated for 24 hours. The cells were stimulated with lipopolysaccharide (LPS) (500 ng/mL) for 24 hours and treated with curcuminoid-loaded liposomes (Cur-Lip and BDMC-Lip) at a concentration of 7–140 μM. The nitric oxide (NO) released from the macrophages in the medium was assessed by measuring nitrite concentration. Samples (100 μL) of the culture media were incubated with 100 μL of Griess reagent at room temperature for 15 minutes in 96-well microplates. The absorbance at 550 nm was measured using an ELISA reader. Standard calibration curves were prepared using sodium nitrite to quantify nitrite expression from cells (the sensitivity is 2.5 μM and the linear range is 20–100 μM).
Osteoclast differentiation assay
RAW 234.7 cells were cultured in 96-well plates at a density of 2,000 cells per well and incubated for 24 hours. The growth medium contained 50 ng/mL RANKL and 10 ng/mL LPS, and cells were treated with 70 μM Cur-Lip or BDMC-Lip. The medium was replaced every 3 days. After 5 days’ incubation, the samples were fixed with 10% w/v formaldehyde solution for 1 minute. Then, cells were stained with TRAP kit reagents as described in the manufacturer’s instructions (Sigma-Aldrich Co.). The cells containing three or more nuclei were marked as TRAP-positive and the percentage of multinucleated cells in each sample was counted.
TRAP activity was determined by para-Nitropheny Phosphate (pNPP) according to the microplate assay method of Park et al with the following modifications.40 Cells were fixed with 10% w/v formaldehyde for 1 minute and then with an equal mixture of acetone and formalin for another minute. After they were completely dry, cells were incubated with 100 μL phosphate substrate solution (3.7 mM pNPP and 10 mM sodium tartrate in 50 mM citrate butter, pH 4.6) at 37°C for 10 minutes. Then, the enzyme reaction was stopped by the addition of 100 μL 0.1 N sodium hydroxide solution and the absorbance of the resulting yellow-colored product was measured by an ELISA reader at a wavelength of 405 nm.
Cellular alkaline phosphatase activity
7F2 osteoblast-like cells were cultured at a density of 104 cells/well in 24-well plates in DMEM containing 10% FBS, 5 mM β-glycerol phosphate (β-GP), and 50 μg/mL ascorbic acid with or without 70 μM Cur-Lip or BDMC-Lip and incubated for 1, 4, 7, and 14 days at 37°C in a 5% CO2 atmosphere. The supernatants were removed and washed with PBS. Then, 1% v/v Triton solution was added to each well followed by incubation at 37°C for 10 minutes. After incubation, cell lysates were analyzed for alkaline phosphatase (ALP) using p-nitrophenyl phosphate (PNPP) as a substrate and diethanolamine buffer. PNPP solution (200 mL) was added into each well of the 96-well plate. The plate was incubated at room temperature for 30 minutes or until sufficient color developed. The stop solution (50 μL/well) was added to stop reaction and the absorbance was measured using an ELISA reader at a wavelength of 405 nm (the sensitivity is 0.02 mM and the linear range is 0.02–20 mM).
Mineralization of the extracellular matrix
7F2 osteoblast-like cells were seeded at a density of 104 cells/well in 1 mL medium containing 10% FBS, 5 mM β-GP, and 50 μg/mL ascorbic acid and incubated for 7, 14, and 21 days. Cur-Lip and BDMC-Lip (70 μM) were added to the growth medium. The samples were washed with PBS, fixed with 75% v/v ethanol, and dried at room temperature. After complete drying, the fixed cells were stained with 1% Alizarin Red S (200 μL) for an hour. The images of cell morphology were taken with a microscope (Nikon TI-E) and charge-coupled device camera system (SPOT RT3). Four hundred microliters of 10% w/v cetylpyridinium chloride solution was added to each well followed by shaking for 10 minutes to dissolve calcium. Finally, the absorbance was measured with an ELISA reader at a wavelength of 560 nm. Each experiment was done in triplicate (the sensitivity is 0.25 mM and the linear range is 0.25–2 mM).
Quantitative real-time polymerase chain reaction
Cells were seeded at a density of 2×105 cells in 6 cm dishes and incubated for 24 hours. RAW264.7 cells were treated with 70 μM Cur-Lip or BDMC-Lip in the solutions of RANKL (50 ng/mL) and LPS (10 ng/mL) for 5 days. 7F2 cells were using 5 mM β-GP, and 50 μg/mL ascorbic acid to induce osteoblast mineralization, and stimulated inflammatory responses with IL-1β (10 ng/mL).
After treatment, total RNA was extracted using the TRIzol reagent (RiboZol™; AMRESCO, OH, USA) following the protocol in the manufacturer’s instructions. For reverse transcription, 1 μg of the total RNA was converted to first-strand cDNA using a reverse transcription kit (Promega Corporation, Fitchburg, WI, USA). The resulting cDNA (equivalent to 20 ng) was used in a StepOnePlus™ Real-Time PCR System using Fast Start DNA Master-PLUS SYBR Green I (Thermo Fisher Scientific). The designed primers are shown in Table 1; all primers used nucleotide sequences present in the PrimerBank database. Each sample was corrected using the mean cycle threshold (CT) value for GAPDH. Relative gene expression was analyzed using the ΔCT method and expressed as fold change (2−ΔCCT).
Table 1 Sequences of primers used in real-time polymerase chain reaction experiment
The experiments were repeated at least twice with similar results, and the values were expressed as means ± standard deviations. Data analysis was performed by paired t-test using the commercial software MINITAB. Differences were considered to be statistically significant at P<0.05.
In vitro characterization of liposomes
The effect of lipid composition on particle sizes and stability of liposomes formulated from different ratios of SPC and cholesterol was monitored at 4°C for a period of 2 weeks (Figure 1A). The mean size of liposomes is an important requisite that can influence the drug carrier’s biological effectiveness.41 In order to produce smaller liposomes, extrusion through polycarbonate filters was carried out after hydration. Without extrusion, the mean diameter of liposomes was greater than 900 nm and the standard deviation was around 200 nm, showing the presence of large vesicles with a very large size distribution (Table 2). The extrusion procedure provided small multilamellar vesicles with mean diameters ranging from 95–120 nm. This procedure also allowed the formation of liposome suspensions with a very narrow size distribution having a standard deviation value less than 10 nm. At 4°C, these liposome systems displayed similar stability profiles over a 2-week period. In contrast, these liposomes are more stable than vesicles without extrusion (data not shown). Three formulations of liposomes were prepared in this study: empty liposomes, Cur-Lip, and BDMC-Lip. The stability of liposomes in vivo can be affected by interactions with lipoproteins and other proteins in the blood. The stability tests of liposomes in DMEM containing 10% bovine serum albumin showed less than 10% change in the particle size distribution in the three types of liposomal formulations (Figure 1B). As reported in Table 2, the curcuminoids showed high entrapment efficiency due to their lipophilic nature. After extrusion, the entrapment efficiency was decreased, possibly due to particle size reduction. Therefore, Cur-Lip and BDMC-Lip achieved maximum encapsulation efficiencies of 69.5% and 71.4% after extrusion.
Table 2 Encapsulation parameters of the liposomal formulations
Effect of liposomal formulations on cell viability, delivery efficiency, and NO production
The in vitro cytotoxic potential of liposomes formulated with various lipid compositions was assessed in mouse osteoblastic cell line 7F2, using the MTT assay. Lipid compositions in a range of molar ratios of cholesterol to SPC (30:70, 1:2, 40:60, and 45:55) resulted in slightly higher viability loss than SPC only (Figure 2A). Therefore, cholesterol was omitted in favor of SPC in liposomal preparation. Next, a dose–response study of the curcuminoid-loaded liposomes evaluated cell viability of 7F2 osteoblastic cells with MTT. As a whole, the viability loss is dose-related. When the curcuminoid concentration in liposomes was increased to 140 μM, a significant viability loss was noted (Figure 2B). Furthermore, Cur-Lip and BDMC-Lip showed less cytotoxicity than free drugs in DMSO (70 μM) (Figure 2C).
To study the cellular uptake of curcuminoid-loaded liposomes, DiI-loaded liposomes (red fluorescence) and DAPI-stained cells (blue fluorescence) were used to evaluate the delivery efficiency of liposomes. Cells were harvested at different time intervals and cellular uptake was observed by fluorescence microscopy (Figure 3A). The results showed that the uptake processes were started at 30 minutes after exposure and reached their maximum after 2 hours (Figure 3B).
The anti-inflammatory activity of curcuminoid-loaded liposomes in LPS-stimulated RAW264.7 macrophages was investigated by assessing the inhibition of NO. The amount of nitrite measured by the Griess reagent correlated directly to the NO production by RAW264.7 macrophages. When LPS-stimulated RAW264.7 macrophages were incubated with empty and curcuminoid-loaded liposomes, NO production in LPS-stimulated RAW264.7 macrophages was significantly decreased (Figure 4A). Curcuminoid-loaded liposomes inhibited NO production in a dose-dependent manner (in a range of 7–70 μM) (Figure 4B), but there was no significant difference in the reduction of NO production between Cur-Lip and BDMC-Lip.
Inhibitory effects of curcuminoid-loaded liposomes on osteoclast differentiation in RAW264.7 macrophages
To examine the potential of curcuminoid-loaded liposomes in osteoclast differentiation, RAW264.7 macrophages were incubated in the osteoclastogenic medium containing 10 ng/mL LPS and 50 ng/mL RANKL for 5 days, which led to a profound differentiation of the monocytic–macrophagic cell line into multinucleated TRAP-positive cells. The percentage of differentiated osteoclasts was significantly increased with the addition of LPS and RANKL, and the differentiated cells were larger than normal. The cells treated with Cur-Lip or BDMC-Lip showed reductions in cell size and the percentage of multinucleation (Figure 5A). In addition, when RAW264.7 macrophages were toward osteoclast differentiation and maturation, osteoclasts would express high TRAP activity for removing mineralized deposition. Therefore, osteoclast differentiation can be evaluated by measuring TRAP activity. As shown in Figure 5B, RAW264.7 macrophages with the treatment of LPS and RANKL presented higher TRAP activity. On the other hand, Cur-Lip and BDMC-Lip significantly reduced the TRAP activity, and that is roughly equivalent to control. With a view to finding out whether or not Cur-Lip and BDMC-Lip caused the suppression of osteoclastogenic differentiation due to altering cathepsin K and TRAP expression, RAW264.7 macrophages were assayed for the gene expression of cathepsin K and TRAP, which were previously known to be able to regulate osteoclast differentiation. All liposomal formulations revealed significant inhibition on RANKL-induced cathepsin K and TRAP gene expression (Figure 5C and D). Therefore, Cur-Lip and BDMC-Lip can inhibit RANKL-induced osteoclast differentiation and resorption activity (TRAP activity) through the suppression of cathepsin K and TRAP expression.
Effect on 7F2 osteoblasts of curcuminoid-loaded liposomes
The effect of curcuminoid-loaded liposomes on osteoblast proliferation was measured using the MTT assay (Figure 6A). The exposure of 7F2 osteoblastic cells to liposomes decreased cell number by approximately 10% after 7 days’ incubation, as compared with cells in mineralizing medium (MM) (50 μg/mL ascorbic acid and 5 mM β-GP). Furthermore, curcuminoid-loaded liposomes showed no marked inhibition on cell proliferation in a time-dependent manner.
Figure 6B presents the ALP activity of 7F2 osteoblastic cells in MM with or without the addition of liposomes (empty liposomes, Cur-Lip, and BDMC-Lip) after the number of days indicated. As expected, ALP activity was constantly increased with culture time in control and MM, but this increase was significantly blunted by liposome treatment. Therefore, empty and curcuminoid-loaded liposomes showed significant inhibition of ALP activity. It is worth noting that cells cultured in the medium containing Cur-Lip expressed higher levels of ALP activity than those with empty liposomes or BDMC-Lip.
The effects of curcuminoid-loaded liposomes on osteoblast mineralization was investigated after 7, 14, and 21 days of incubation using Alizarin Red S staining, which identifies calcium content within the bone matrix. Increased mineralization relative to controls was observed in cultures with MM, but mineral deposition was reduced in all groups of liposome-treated osteoblasts (Figure 6C and D). Under microscope observation, the numbers of mineralized nodules (red) were clearly lower on 7F2 osteoblastic cells treated with empty liposomes and BDMC-Lip on incubation day 21 (Figure 6C), but Cur-Lip still revealed high mineralized nodule formation. Similar patterns were observed in ALP activity.
OPG and RANKL are key factors in regulating bone metabolism; the ratio of OPG/RANKL is considered to better reflect environmental signals in OA patients than the levels of each of these factors individually, in which a high ratio level is indicative of bone formation promotion while a low level favors bone resorption.42 Our results indicated that Cur-Lip and BDMC-Lip increased the OPG/RANKL ratio significantly in 7F2 osteoblastic cells (Figure 6E). In contrast, the relative ratio of OPG/RANKL was lower in MM with or without the addition of empty liposomes than in control. Therefore, Cur-Lip can inhibit osteoclast differentiation through the increase of OPG/RANKL ratio, and retain osteoblast differentiation functions better than BDMC-Lip.
Curcuminoid-loaded liposomes protective osteoblast when stimulated with il-1β
7F2 osteoblastic cells responded to IL-1β stimulation by upregulated expression of proinflammatory mediators, cyclooxygenase 2 (COX-2) and MMP-3 (Figure 7A and B). Cells treated with empty or curcuminoid-loaded liposomes can suppress IL-1β-induced COX-2 and MMP-3 production (Figure 7C and D). This inhibitory effect was not significantly different between empty and curcuminoid-loaded liposomes at a concentration of 70 μM. These data revealed a tendency toward decrease in COX-2 and MMP-3 mRNA levels with respect to basal expression, suggesting that liposomal formulations can suppress IL-1β-induced inflammatory responses on 7F2 osteoblastic cells. To study the influence of curcuminoid-loaded liposomes on osteoclastogenesis-regulatory biomarkers on 7F2 osteoblastic cells, we further examined the mRNA expression of OPG and RANKL. As shown in Figure 7E, inflammatory responses reduced the OPG/RANKL ratio in 7F2 osteoblastic cells, indicative of a possible increase in bone remodeling/resorption capacity. With the addition of liposomes, OPG/RANKL ratios were expressed highly in 7F2 osteoblastic cells in the presence of IL-1β stimulation (Figure 7E). Of note, only Cur-Lip expressed a high OPG/RANKL ratio in the absence of IL-1β stimulation (Figure 6E). Therefore, these findings support that curcuminoid-loaded liposomes can downregulate IL-1β-induced MMP-3 and COX-2 expression and suppress osteoclastogenesis through the increase of the OPG/RANKL ratio.
In recent years, several novel delivery systems including polymeric implantable delivery systems have been proposed to improve drug bioavailability.34–37 In this study, we optimized liposomal formulation by using SPC (Phospholipon 90G) and cholesterol to develop liposomal delivery systems of curcuminoids, because soy phospholipids have been successfully used to improve the poor solubility and consequently low bioavailability of Cur.38,39 According to the literature, SPC liposomes can successfully increase the bioavailability of Cur in a rat model system, and liposomes composed with SPC showed better entrapment efficiency than other lipids.42 Our results have also shown high entrapment efficiencies of Cur and BDMC (>70%) and significant stability over 14 days. In cytotoxicity study, the concentration of Cur or BDMC in DMSO (70 μM) used to treat cells was twofold lower than the concentration added into liposomes (140 μM). However, 7F2 osteoblasts treated with Cur-Lip or BDMC-Lip showed a sixfold higher survival rate than those treated with Cur or BDMC in DMSO. Moreover, SPC liposomes displayed 20-fold (P<0.001) higher intracellular accumulations than the free drug on 7F2 osteoblastic cells. As a result of this, liposome formulation could reduce cytotoxicity and increase cellular uptake of curcuminoids.
The results of Tocharus et al indicated that Cur, DMC, and BDMC can all inhibit NO production in LPS-activated HAPI microglial cells.22 In addition, Cur was found to be the most active metabolite of curcuminoid in suppressing activation of TNF-induced NF-κB (Cur > DMC > BDMC).32 Recently, Jung et al showed that Cur had strong NO inhibitory potential through the inhibition of JNK, p38, and NF-κB signaling pathways.43 Although the ability of curcuminoids to inhibit the inflammatory response and suppress the osteoclastogenesis is established, how these responses are modulated by curcuminoid-loaded liposomes is not known. Our results indicate that Cur- and BDMC-loaded liposomes can inhibit NO production in RAW264.7 macrophages and prevent osteoclast differentiation through the downregulation of cathepsin K and TRAP expression. We also found that Cur-Lip and BDMC-Lip presented high OPG/RANKL ratios in IL-1β-induced 7F2 osteoblastic cells. The high level of OPG/RANKL ratio indicated the favorite of OPG-RANKL interaction and the prevention of its binding to RANK with a consequent decrease in osteoclast activation. Therefore, the inhibitory role of curcuminoid-loaded liposomes on RANKL-induced osteoclastogenesis was further confirmed.
Bone formation involves the proliferation, differentiation, and mineralization of osteoblasts. 7F2 osteoblastic cells normally begin to differentiate at day 4, and the heightening of ALP activity is present as a marker of the earlier period of cell differentiation. Figure 6B shows that ALP activities were clearly lower in 7F2 osteoblastic cells that had been treated with empty or curcuminoid-loaded liposomes. Furthermore, we monitored the mineralization of 7F2 osteoblastic cells by Alizarin Red S staining. Figure 6C and D shows that empty and curcuminoid-loaded liposomes inhibited the mineralization of 7F2 osteoblastic cells in a time-dependent fashion. In previous studies, Cur has been reported to inhibit the differentiation and mineralization of human or rat osteoblasts.31,44 The concentration (70 μM) of curcuminoid we loaded in liposomes was sevenfold higher than that of Cur (5–10 μM) used in studies of the inhibition of osteoblast proliferation and differentiation.44,45 Although Cur-Lip suppressed osteoblast differentiation and mineralization, there were only minor effects on cell proliferation. This difference may be due to the varieties of cell types or the reduction of curcuminoid toxicity by liposome encapsulation. Further, we found that Cur-Lip exhibited relatively higher levels of ALP activity and mineralization in 7F2 osteoblastic cells than empty liposomes and BDMC-Lip. This finding has not been reported previously. It is unclear why liposomes suppressed osteoblast differentiation and mineralization. Zhang et al mentioned that lecithin (as phosphatidylcholine) can induce adipocyte differentiation in both 3T3-L1 and primary preadipocytes and that is consistent with our data presented in Figure S1.46 Furthermore, Diascro et al demonstrated that a high fatty acid content in rabbit serum induced adipocyte-like differentiation in human and rat osteoblastic cells.47 Therefore, liposomes (lipid vesicles) can initiate the switch from osteoblasts to adipocyte-like cells. Interestingly, Cur-Lip maintained osteoblast differentiation activity, whereas a reduction in activity was observed by the addition of empty liposomes and BDMC-Lip. Since Cur can inhibit adipocyte-like differentiation through the dephosphorylation of mitogen-activated protein kinase (MAPK) (ERK, JNK, and p38) phosphorylation, we propose that Cur-Lip can prevent lipid-induced inhibition of osteoblast differentiation but not BDMC-Lip.48
IL-1β is a very potent inflammatory inducer. Our study showed that empty and curcuminoid-loaded liposomes can successfully downregulate IL-1β-induced COX-2 and MMP-3 expression in 7F2 osteoblasts and showed a high ratio of OPG/RANKL in the presence of IL-1β stimulation. However, empty liposomes and BDMC-Lip displayed a minor effect on the OPG/RANKL ratio in 7F2 osteoblasts in the absence of IL-1β stimulation. These results are in agreement with the findings of Mathy-Hartert et al49 who showed that Cur can inhibit IL-1β-induced COX-2 and MMP-3 expression in human osteoblasts, and Guo et al50 who reported that BDMC can inhibit LPS-induced COX-2 expression. Furthermore, Treede et al demonstrated that phosphaticholines can inhibit TNF-α-induced proinflammatory genes and NF-κB activation in Caco-2 cells.51 Therefore, empty liposomes can inhibit LPS-stimulated NO production and IL-1β-induced COX-2 and MMP-3 expression because of the phosphaticholine content. To date, Cur-Lip can prevent bone loss more effectively than BDMC-Lip by increasing the ratio of OPG/RANKL and preventing lipid-induced inhibition of osteoblast differentiation. In the clinical study of Belcaro et al, Meriva, a curcumin–phosphatidylcholine complex, was proven to decrease joint pain and improve joint function in 50 OA patients.52 Therefore, curcuminoid-loaded liposomes may have a promising effect against subchondral bone turnover and slow the progression of OA.
This work was supported by research grants from the National Science Council (Taiwan) (NSC 102-2320-B-415-001, NSC 102-2320-B-367-001, and MOST 103-2320-B-367-001-MY2) and Veterans Affairs Commission, Executive Yuan (Taiwan) (RVHCY101001, RVHCY102001, and RVHCY103005).
The authors report no conflicts of interest in this work.
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