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Induction of apoptosis of human primary osteoclasts treated with extracts from the medicinal plant Emblica officinalis

BMC Complementary and Alternative Medicine volume 8, Article number: 59 (2008) Cite this article

Abstract

Background

Osteoclasts (OCs) are involved in rheumatoid arthritis and in several pathologies associated with bone loss. Recent results support the concept that some medicinal plants and derived natural products are of great interest for developing therapeutic strategies against bone disorders, including rheumatoid arthritis and osteoporosis. In this study we determined whether extracts of Emblica officinalis fruits display activity of possible interest for the treatment of rheumatoid arthritis and osteoporosis by activating programmed cell death of human primary osteoclasts.

Methods

The effects of extracts from Emblica officinalis on differentiation and survival of human primary OCs cultures obtained from peripheral blood were determined by tartrate-acid resistant acid phosphatase (TRAP)-positivity and colorimetric MTT assay. The effects of Emblica officinalis extracts on induction of OCs apoptosis were studied using TUNEL and immunocytochemical analysis of FAS receptor expression. Finally, in vitro effects of Emblica officinalis extracts on NF-kB transcription factor activity were determined by gel shift experiments.

Results

Extracts of Emblica officinalis were able to induce programmed cell death of mature OCs, without altering, at the concentrations employed in our study, the process of osteoclastogenesis. Emblica officinalis increased the expression levels of Fas, a critical member of the apoptotic pathway. Gel shift experiments demonstrated that Emblica officinalis extracts act by interfering with NF-kB activity, a transcription factor involved in osteoclast biology. The data obtained demonstrate that Emblica officinalis extracts selectively compete with the binding of transcription factor NF-kB to its specific target DNA sequences. This effect might explain the observed effects of Emblica officinalis on the expression levels of interleukin-6, a NF-kB specific target gene.

Conclusion

Induction of apoptosis of osteoclasts could be an important strategy both in interfering with rheumatoid arthritis complications of the bone skeleton leading to joint destruction, and preventing and reducing osteoporosis. Accordingly, we suggest the application of Emblica officinalis extracts as an alternative tool for therapy applied to bone diseases.

Peer Review reports

Background

Osteoclasts (OCs) are multinucleated cells of hematopoietic origin and are the primary bone resorbing cells [1–4]. There is increasing evidence that OCs play a crucial role in bone loss in rheumatoid arthritis [5–9], as recently reported by Ochi et al. [5] and reviewed by several authors, including Schett [6], Haynes [7], Tremoulet and Albani [8], Boyce et al. [9], Sato and Takayanagi [10] and Teitelbaum [11]. Abundant osteoclasts are found within the synovial tissue at sites adjacent to bone, creating resorption pits and local bone destruction followed by degradation of the bone matrix and calcium solubilization [6]. The basis of this behavior is that the synovial tissue of inflamed joints harbor high concentrations of monocytes/macrophages, which are osteoclast precursors, as well as cells that provide the specific molecular signals that drive osteoclast formation [6]. For instance, human rheumatoid synovial lymphocytes and fibroblasts promote osteoclastogenic activity by activating the receptor activator of NF-kB ligand (RANKL). The cytokines involved in this process are well known and have been the object of several studies [12, 13], pointing out that TNFα, and IL-7 are involved in OCs differentiation [13]. Osteoclasts thus represent a link between joint inflammation and structural damage [6]. Hence, therapeutic approaches inhibiting osteoclastogenesis have been proposed by several authors for rheumatoid arthritis therapy [14–20].

These drugs are also expected to be of interest in the therapy of other pathologies associated with bone loss, such as osteoporosis [21–23] and bone metastasis [24–27], as inhibition of bone resorption, aimed at preventing further bone loss, is based on the efficient targeting of OCs function [21–27]. In conclusion, several therapeutic approaches are based on inhibition of osteoclast-dependent bone resorption through inhibition of OCs differentiation or stimulation of OCs apoptosis.

Recent results support the concept that some medicinal plants and natural products derived from them are of great interest for developing therapeutic strategies against bone disorders, including rheumatoid arthritis and osteoporosis [28–33]. Yin J. et al. demonstrated that water extracts of Dioscorea spongiosa stimulate osteoblasts proliferation, exhibiting at the same time a potent inhibitory activity on osteoclastogenesis [34]. Fruit extracts of Psoralea corylifolia [35] and Cnidium monnieri [36] have been shown to exhibit osteoblastic proliferation stimulating activity in osteoblast-like UMR106 cells in vitro. Several plant extracts inhibiting OCs differentiation also display strong anti-inflammatory properties [34–36].

Emblica officinalis is certainly a medicinal plant of interest [37–45]. It has played an important medicinal role for centuries in the Indian system of medicine. Fruits of E. officinalis are used for the treatment of a number of diseases, such as dyslipidemia [37] and atherosclerosis [38], as hepatoprotective [39], antibacterial [40] and anti-inflammatory agent [41]. In many cases, E. officinalis has been shown to be a potent free radical scavenging agent thereby preventing carcinogenesis and mutagenesis [42].

In this study we investigated whether extracts of Emblica officinalis fruits display effects of possible interest for the treatment of rheumatoid arthritis and osteoporosis, by activating programmed cell death of human primary osteoclasts. The effects of E. officinalis on human osteoclasts obtained from peripheral blood mononuclear cells [46, 47] were analyzed by determining the proportion of apoptotic OCs. The effects of Emblica officinalis extracts were studied also on NF-kB/DNA interactions by electrophoretic mobility shift assay [48], given the possible involvement of the NF-kB transcription factor on the maintenance of the differentiation program of osteoclasts [49–51]. The effects of Emblica officinalis extracts on the expression of NF-kB dependent genes were also determined.

Methods

Culture of human primary osteoclasts

Human OCs were prepared as reported by Mitsuzaki et al. [52] with slight modifications. Peripheral blood was collected from healthy normal volunteers after informed consent. Mononuclear cells (PBMCs) were prepared from diluted peripheral blood (1:2 in Hanks Balanced Salt Solution), which was layered over Histopaque 1077 (Sigma, St. Louis, MO, USA) solution, centrifuged (400 g), washed and suspended in D-MEM/10% FCS. 3 × 106 PBMCs/cm2 were plated in 24-well plates or in chamber slides and allowed to settled for 2 hours. Wells were then rinsed to remove non-adherent cells. Monocytes were maintained at 37°C, in 5% CO2, in medium supplemented with 10% FCS and cultured for 14 days in the presence of human M-CSF (25 ng/ml), RANKL (30 ng/ml) and 10-7 M PHT. Culture media were replenished with fresh media every 3–4 days. Cells were used for the described experiments when mature multinuclear cells were predominant in the cultures.

Tartrate-resistant acid phosphatase (TRAP) staining

TRAP staining of the cells was performed as reported by Villanova et al. [53]. Cells were fixed in 3% para-formaldehyde with 0.1 M cacodilic buffer, pH 7.2 (0.1 M Sodium cacodilate, 0.0025% CaCl2) for 15 min, extensively washed in the same buffer, and stained for TRAP (Acid Phosphatase Kit n. 386 – Sigma, St. Louis, MO, USA). After washing with distilled water and drying, mature TRAP positive multinucleated cells containing more than three nuclei were considered as osteoclasts.

Plant extracts

The dried fruits of Emblica officinalis were extracted with absolute ethanol and the yield was 9.33%. The chemical composition has been determined by GC/MS and was reported elsewhere [54, 55].

Electrophoretic mobility shift assay (EMSA)

Electrophoretic mobility shift assay (EMSA) was performed by using double stranded 32P-labelled oligonucleotides as target DNA [51]. Binding reactions were set up as described elsewhere in binding buffer (10% glycerol, 0.05% NP-40, 10 mM Tris-HCl pH 7.5, 50 mM NaCl, 0.5 mM DTT, 10 mM MgCl2), in the presence of poly(dI:dC).poly(dI:dC) (Pharmacia, Uppsala, Sweden), 2 μg of crude nuclear extracts and 0.25 ng of labelled oligonucleotide, in a total volume of 20 μl [28]. After 30 min binding at room temperature, samples were electrophoresed at constant voltage (200 V for 1 hr) through a low ionic strength (0.25 × TBE buffer) (1 × TBE = 0.089 M Tris-borate, 0.002 M EDTA) on 6% polyacrylamide gels until the tracking dye (bromophenol blue) reached the end of a 16 cm slab. Gels were dried and exposed for autoradiography with intensifying screens at -80°C. In these experiments, DNA/protein complexes migrate through the gel with slower efficiency. In studies on the inhibitors of protein/DNA interactions, the addition of the reagents was as follows: (a) poly(dI:dC).poly(dI:dC); (b) labelled oligonucleotides mimicking the binding sites for transcription factors to be analyzed; (c) plant extracts; (d) binding buffer; (e) nuclear factors. The nucleotide sequences of double-stranded target DNA utilized in these experiments were 5'-CGC TGG GGA CTT TCC ACG G-3' (sense strand, HIV-NF-kB binding site), and 5'-CTG ATT TCC CCG AAA TGA CGG-3' (sense strand, STAT-3 binding site).

Measurement of apoptosis

After 14 days of cell culture and 2–3 days of incubations with E. officinalis extracts, the cells were rinsed twice with PBS solution and fixed for 25 min in 4% paraformaldehyde at room temperature. Apoptotic cells were detected by the DeadEnd Colorimetric Apoptosis Detection System (Promega) according to the manufacturer's instructions. Measurement of apoptosis was calculated as a percentage of apoptotic nuclei (dark brown nuclei) versus total nuclei of multinucleated TRAP positive cells, evaluated in three independent measurements. A dark brown DAB signal indicates positive staining, while shades of blue-green to greenish tan indicate a nonreactive cell [46, 47].

Immunocytochemistry analysis

Immunocytochemistry analysis was performed employing the streptavidin-biotin method using Ultraystain Polyvalent-HRP Immunostaining Kit. OCs grown in multichamber slides were fixed in 100% cold methanol, and permeabilized with (v/v) Triton X-100 (Sigma) in TBS (Tris-buffered saline). Cells were incubated in 3% H2O2 and blocked with Super Block reagent (Ultraystain Polyvalent-HRP Immunostaining Kit). After the reaction with the primary antibodies, rabbit polyclonal antibodies of human origin (Santa Cruz Biotech) against MMP9, FAS receptor, IL-6, and NF-kB (2 mg/ml) were used accordingly to the manufacturer's protocols, at 1:500 (MMP9), 1:100 (FAS receptor), 1:800 (IL-6) and 1:800 (NF-kB) dilutions. Incubation was carried out at 4°C for 16 hr. Cells were then incubated at room temperature with anti-polyvalent Biotinylated Antibody (Ultraystain Polyvalent-HRP Immunostaining Kit). After rinsing in TBS, Streptavidin HRP (Ultraystain Polyvalent-HRP Immunostaining Kit) was applied, followed by the addition of Substrate-chromogen mix (AEC Cromogeno kit). After washing, cells were mounted in glycerol/TBS 9:1 and observed using a Leitz microscope [46, 47].

Cytotoxicity studies

The cytoxicity analysis was determined on in vitro cultured human OCs. PBMCs were plated in 96-well plates and, after 14 days, OCs were incubated with E. officinalis plant extracts for 3 days. Determinations of viable cells were performed after colorimetric assay with MTT (thiazolyl blue). The assay, based on the conversion of the yellow tetrazolium salt MTT to purple formazan crystals by metabolically active cells [56], provides a quantitative determination of viable cells. After 72 hr of treatments in triplicate, 200 μL of MTT was added to each well of cells, and the plate was incubated for 2 hr at 37°. The medium was removed, and the MTT crystals were solubilized with 50% DMF. Spectrophotometric absorbance of each sample was then measured at 570 nm.

Statistical analysis

Data are presented as the mean ± SEM from at least three independent experiments. Statistical analysis was performed by one-way analysis of variance followed by the Student's t-test. A P value < 0.005 was considered statistically significant.

Results

Effects of Emblica officinalis extracts on differentiation and viability of human primary osteoclasts

Human primary osteoclasts were obtained from peripheral blood and cultured in complete D-MEM plus MCSF, PTH and RANKL for 14 days. OCs differentiation was tested by tartrate-acid resistant acid phosphatase (TRAP)-positivity (Fig. 1) and metalloproteinase-9 (MMP-9) expression (data not shown). In order to test the effect of E. officinalis extracts on osteoclast differentiation, mature OCs (Fig. 1A) or monocytes during the two weeks of induction (Fig. 1B) were exposed to 0.5, 5, 50 μg/ml of plant extracts. The conditions used for these experiments correspond to the concentrations of E. officinalis extracts leading to 50% of inhibition (IC50 value) of cell growth, previously analyzed in different cell lines [55]. As reported in Figure 1, the presence of comparable levels of TRAP-positive cells cultured both in presence and in absence of E. officinalis extracts did not affect the process of osteoclastogenesis, at the concentrations employed. Quantitative data from three independent experiments are presented in the lower sides of Figure 1, demonstrating that treatment of the cultures with E. officinalis extracts does not have inhibitory effects on the development of TRAP-positive OCs. Cytotoxic effects of E. officinalis extracts were then analyzed. Human primary OCs were treated with increasing amount of E. officinalis extracts (0.5–500 μg/ml) for 72 hours and the viability of the cells was examined by the colorimetric MTT assay [56]. As shown in Figure 2, 0.5, 5 and 50 μg/ml of E. officinalis extracts did not cause any cytotoxic effect on the total cell population (1–5% of which is constituted by OCs). Only E. officinalis extracts used at 500 μg/ml were found to induce a slight but not significant decrease of viability.

Figure 1
figure 1

TRAP staining analysis of human primary osteoclasts obtained after 14 days of culture in presence of 0.5, 5, and 50 μg/ml of Emblica officinalis extracts, as indicated (A); the same percentage of multinucleated TRAP-positive cells was obtained when mature osteoclasts were grown for 60 hours with the same amount of Emblica officinalis extracts (B). Cells were photographed at the 20 × magnification. In the lower part of the panel data from five determinations are presented (average ± SD).

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Figure 2
figure 2

Effect of different concentrations (0.5–500 μg/ml) of Emblica officinalis extract on cell survival of human primary osteoclast obtained by MTT colorimetric assay. Results are expressed as the percentage of surviving cells and are the average ± SD of three independent experiments. The viability of controls only treated with vehicle (H2O) has been set as 100%.

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Emblica officinalis extracts induce apoptosis of osteoclasts

In a previous study we demonstrated that in different cell lines (K562, B-lymphoid Raji, T-lymphoid Jurkat and HEL cells) E. officinalis extracts retain an antiproliferative effect [55]. In the present paper we investigated osteoclasts in terms of apoptosis. To this aim, TUNEL test was performed on OCs after exposure, up to 60 hours, to 0.5, 5, and 50 μg/ml of E. officinalis extracts. As shown in the representative experiment reported in Figure 3 (panels A and B), a low but significant level of apoptosis (20%) was induced by 0.5 μg/ml of extract; at 5 and 50 μg/ml, a dramatic increase (respectively 50% and 98%) in TUNEL-positive nuclei was observed. Table 1 reports summary data from three independent experiments, confirming the observation that 5 and 50 μg/ml of E. officinalis extracts consistently induce high levels of apoptosis of osteoclasts. Times of exposure shorter than 60 hours were also tested (24 and 48 hours) without obtaining significant differences from untreated cells (data not shown). These results were confirmed by immunocytochemical analysis of FAS receptor, a well known apoptosis-related protein [57], whose expression increased, as shown in Figure 3C, in OCs treated with E. officinalis extracts at all the concentrations used. When extracts from different medicinal plants, such as Satureja montana and Satureia hortensis were employed, no OCs apoptosis was induced (data not shown).

Figure 3
figure 3

A, B. Detection of apoptosis by TUNEL assay in human primary osteoclasts. The presence of apoptotic OCs after treatment with 0.5, 5, 50 μg/ml of Emblica officinalis extract for 60 hours is shown in panel A. Brown color reaction indicates cells that underwent apoptosis. Quantitative results of the experiment shown in panel A are depicted in panel B (the data reported represent the average ± SD of six independent determinations). C. Immunocytochemical analysis of FAS receptor expression levels in human primary osteoclasts subjected to the same experimental conditions reported in panel A. (-): control cells. Cells were photographed at the 20 × magnification.

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Table 1 Apoptotic osteoclasts following treatment with E. officinalis extracts
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In vitro effects of Emblica officinalis extracts on NF-kB transcription factor activity

The ability of E. officinalis extracts to interfere with NF-kB binding to DNA was investigated, given that the transcription factor NF-kB plays a critical role in OCs activities by regulating the expression of a large number of OCs specific genes [48–50]. E. officinalis extracts were incubated in presence of 5 μg of nuclear extracts from K562 cells with an oligonucleotide containing a cis element of the LTR of HIV-1 representing the DNA binding site for NF-kB. DNA-protein interactions were then analyzed by EMSA [51]. As reported in Figure 4, a dose dependent effect was observed, indicating the ability of E. officinalis extracts to completely inhibit NF-kB interaction with its cis element, when used at 100, 50, and 25 μg/reaction. On the contrary, 100 μg of E. officinalis extracts were not able to abolish the DNA-protein interactions of the transcription factor STAT-3 with its cis element (right side of Fig. 4) indicating a selectivity of the effects of E. officinalis extracts for NF-kB/DNA interactions. The sensitivity of NF-kB/DNA interactions to E. officinalis extracts was demonstrated to be related to the type of plant extracts and not to the extracting buffers, since no inhibitory effects were observed (a) with the extracting buffer and (b) other extracts from medicinal plants, such as Oroxylum indicum, Cuscuta reflexa, Paederia foetida, Hygrophilla auriculata, Ocimum sanctum (data not shown and Lampronti et al.) [57].

Figure 4
figure 4

Analysis by electrophoretic mobility shift assay of the effects of Emblica officinalis extracts on NF-kB DNA binding activity. Nuclear extracts from the K562 cell line were incubated with 32P-labelled oligonucleotides (*) NF-kB and STAT-3, in the presence of different amounts (100, 50, 25, 12.5, 6, 3, 1.5, 1 μg) of Emblica officinalis extracts. Protein/DNA complexes and free probe are indicated by arrows.

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In order to determine whether E. officinalis extracts affect NF-kB dependent biological activity in OCs, we have evaluated the effects of the plant extracts on the expression of IL-6, a target gene of NF-kB transcription factors [58, 59]. Immunocytochemical analysis, reported in Figure 5, clearly shows a significant decrease of IL-6 levels in OCs treated with 5–50 μg/ml of E. officinalis extracts after comparison to control untreated cells.

Figure 5
figure 5

Different expression of IL-6 in human primary osteoclasts analyzed by immunocytochemistry with specific antibody after incubation for 60 hours in the absence (-), or in the presence of 0.5, 5 and 50 μg/ml of Emblica officinalis extracts. Cells were photographed at the 20 × magnification.

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Discussion

The present study suggests the employment of primary cultures of human osteoclasts as a tool to test the potential interest of extracts of Emblica officinalis fruits in the experimental therapy of human pathologies associated with bone loss, including osteoarthritis and osteoporosis. The possible use of natural products, including plant extracts and nutriaceuticals, is under debate. A systematic review of the scientific evidence supporting the hypothesis that nutrition can improve the symptoms of declared osteoarthritis has been recently published [60]. In addition, the possible use of medicinal plant extracts or single products derived from them for preventing or treating experimentally rheumatoid arthritis has been reported [31–33]. In this respect, one of the best example is Turmeric, derived from the plant Curcuma longa, a gold-colored spice commonly used in the Indian subcontinent in Ayurvedic medicine as a treatment for inflammatory disorders, including arthritis. On the basis of this traditional usage, dietary supplements containing turmeric rhizome and curcuminoid-containing turmeric extracts are used in the western world for arthritis treatment and prevention [31].

Emblica officinalis is reported to have antitumor activity [42, 45, 54] together with beneficial effects in gynecological, hepatic, respiratory and skin [43, 44] disorders. However, the biological activity of Emblica officinalis extracts of possible interest for treatment of arthritis and osteoporosis have not yet been reported. To verify this effect in vitro different experimental approaches should be used in parallel, including analysis of possible positive effects on osteoblastogenesis and negative effects on osteoclastogenesis. In fact, increase of bone formation, leading to anti-osteoporotic and anti-osteoarthritis activity, could be obtained by induction of osteoblast activity, inhibition of osteoclast bone resorption, or both of these effects. In previous studies [34–36] osteoblast-like UMR106 cells, derived from a rat osteogenic sarcoma, were used to screen drugs and plant extracts for stimulation of bone formation.

The aim of our study was to determine the activity of E. officinalis extracts on osteoclasts, using primary OCs of human origin isolated from peripheral blood and incubated for different length of time and with different amounts of E. officinalis extracts. The analysis of cellular viability and apoptosis demonstrates that these plant extracts do not have any cytotoxic effect, even at a concentration of 500 μg/ml, still inducing significant level of apoptosis. This effect was confirmed by the finding of increasing levels of FAS receptor after treatment with both high and low concentrations of E. officinalis extracts. Hence, we conclude that E. officinalis extracts are strong inducers of the apoptotic pathway of primary human osteoclasts.

Since the transcription factor NF-kB has been reported to be important for the expression of several osteoclast-specific genes, we verified whether E. officinalis extracts were able to inhibit the biological activity of this factor. An electrophoretic mobility shift assay demonstrated that NF-kB/DNA complexes are inhibited after incubation of nuclear DNA-binding proteins with increasing amounts of E. officinalis extracts. Accordingly, when the analysis was carried on cultured OCs, high levels of inhibition of IL-6, a NF-kB modulated protein were found, further demonstrating that NF-kB dependent biological functions are impaired following treatment with E. officinalis extracts. On the basis of this experimental evidence we propose that the pro-apoptotic action of E. officinalis extracts on osteoclasts could be mediated, at least in part, by interfering with NF-kB activity.

Interestingly, the effects on human OCs of E. officinalis extracts are similar to those reported for other inhibitors of NF-kB functions, such as biphenylcarboxylic acid butanediol ester (ABD56) [61] and genistein [62]. In addition the effects of E. officinalis extracts are almost over imposable to those of a decoy double-stranded oligonucleotide mimicking NF-kB binding sites [46]. Similarly to this decoy oligonucleotide, E. officinalis extracts, at the concentrations employed, induce OCs apoptosis without inhibiting osteoclastogenesis. An effect of E. officinalis at higher concentrations cannot be excluded; however, at these levels a certain cytotoxicity (see Figure 2) renders difficult the discrimination between a possible inhibitory effect on OCs differentiation and an overall antiproliferative activity.

Finally, we like to point out that our results are based on an in vitro approach, and specificity in vivo of the effects here described should be carefully determined, since the transcription factor NF-kB is also important for other cellular systems, including macrophages, that when exposed to the extracts may overwhelm the effects on osteoclasts. In this respect, several in vivo systems suitable for testing inducers of OCs apoptosis are now available [63–65].

Conclusion

The data here reported on the effects of E. officinalis extracts on mature human osteoclasts suggest the possible use of this medicinal plant as a therapeutic tools against different forms of arthritis and osteoporosis, improving the activity of already employed drugs. In addition, E. officinalis extracts could be analyzed to identify single compounds responsible for the biological activity identified.

Abbreviations

OCs:

osteoclasts

TRAP:

tartrate-resistant acid phosphatase

NF-kB:

nuclear factor kappa-B

RANKL:

receptor activator of NF-kB ligand

PBMCs:

peripheral blood mononuclear cells

PTH:

parathyroid hormone

MCSF:

macrophage colony-stimulating factor

MTT:

3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide.

References

  1. Szekanecz Z, Koch AE: Macrophages and their products in rheumatoid arthritis. Curr Opin Rheumatol. 2007, 19: 289-95. 10.1097/BOR.0b013e32805e87ae.

    Article  PubMed  Google Scholar 

  2. Hadjidakis DJ, Androulakis II: Bone remodeling. Ann N Y Acad Sci. 2006, 1092: 385-96. 10.1196/annals.1365.035.

    CAS  Article  PubMed  Google Scholar 

  3. Giuliani N, Morandi F, Tagliaferri S, Rizzoli V: Targeting pathways mediating bone disease. Curr Pharm Biotechnol. 2006, 7: 423-9. 10.2174/138920106779116955.

    CAS  Article  PubMed  Google Scholar 

  4. Blair HC, Zaidi M: Osteoclastic differentiation and function regulated by old and new pathways. Rev Endocr Metab Disord. 2006, 7: 23-32. 10.1007/s11154-006-9010-4.

    CAS  Article  PubMed  Google Scholar 

  5. Ochi S, Shinohara M, Sato K, Gober HJ, Koga T, Kodama T, Takai T, Miyasaka N, Takayanagi H: Pathological role of osteoclast costimulation in arthritis-induced bone loss. Proc Natl Acad Sci USA. 2007, 104: 11394-11399. 10.1073/pnas.0701971104.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  6. Schett G: Cells of the synovium in rheumatoid arthritis. Osteoclasts. Arthritis Res Ther. 2007, 9: 203-10.1186/ar2110.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Haynes DR: Emerging and future therapies for the treatment of bone loss associated with chronic inflammation. Inflammopharmacology. 2006, 14: 193-7. 10.1007/s10787-006-0006-1.

    CAS  Article  PubMed  Google Scholar 

  8. Tremoulet AH, Albani S: Novel therapies for rheumatoid arthritis. Expert Opin Investig Drugs. 2006, 15: 1427-41. 10.1517/13543784.15.11.1427.

    CAS  Article  PubMed  Google Scholar 

  9. Boyce BF, Schwarz EM, Xing L: Osteoclast precursors: cytokine-stimulated immunomodulators of inflammatory bone disease. Curr Opin Rheumatol. 2006, 18: 427-32. 10.1097/01.bor.0000231913.32364.32.

    CAS  Article  PubMed  Google Scholar 

  10. Sato K, Takayanagi H: Osteoclasts, rheumatoid arthritis, and osteoimmunology. Curr Opin Rheumatol. 2006, 18: 419-26. 10.1097/01.bor.0000231912.24740.a5.

    CAS  Article  PubMed  Google Scholar 

  11. Teitelbaum SL: Osteoclasts; culprits in inflammatory osteolysis. Arthritis Res Ther. 2006, 8: 201-10.1186/ar1857.

    Article  PubMed  Google Scholar 

  12. Kim KW, Cho ML, Lee SH, Oh HJ, Kang CM, Ju JH, Min SY, Cho YG, Park SH, Kim HY: Human rheumatoid synovial fibroblasts promote osteoclastogenic activity by activating RANKL via TLR-2 and TLR-4 activation. Immunol Lett. 2007, 110: 54-64. 10.1016/j.imlet.2007.03.004.

    CAS  Article  PubMed  Google Scholar 

  13. Colucci S, Brunetti G, Cantatore FP, Oranger A, Mori G, Quarta L, Cirulli N, Mancini L, Corrado A, Grassi FR, Grano M: Lymphocytes and synovial fluid fibroblasts support osteoclastogenesis through RANKL, TNFalpha, and IL-7 in an in vitro model derived from human psoriatic arthritis. J Pathol. 2007, 212: 47-55. 10.1002/path.2153.

    CAS  Article  PubMed  Google Scholar 

  14. Tanishima S, Kishimoto Y, Fukata S, Mizumura H, Hagino H, Teshima R: Minodronic acid influences receptor activator of nuclear factor kB ligand expression and suppresses bone resorption by osteoclasts in rats with collagen-induced arthritis. Mod Rheumatol. 2007, 17: 198-205. 10.1007/s10165-007-0566-y.

    CAS  Article  PubMed  Google Scholar 

  15. Kitahara K, Kawai S: Cyclosporine and tacrolimus for the treatment of rheumatoid arthritis. Curr Opin Rheumatol. 2007, 19: 238-45. 10.1097/BOR.0b013e328099af80.

    CAS  Article  PubMed  Google Scholar 

  16. Gillespie MT: Impact of cytokines and T lymphocytes upon osteoclast differentiation and function. Arthritis Res Ther. 2007, 9: 103-10.1186/ar2141.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Suematsu A, Tajiri Y, Nakashima T, Taka J, Ochi S, Oda H, Nakamura K, Tanaka S, Takayanagi H: Scientific basis for the efficacy of combined use of antirheumatic drugs against bone destruction in rheumatoid arthritis. Mod Rheumatol. 2007, 17: 17-23. 10.1007/s10165-006-0531-1.

    CAS  Article  PubMed  Google Scholar 

  18. Shu G, Yamamoto K, Nagashima M: Differences in osteoclast formation between proximal and distal tibial osteoporosis in rats with adjuvant arthritis: inhibitory effects of bisphosphonates on osteoclasts. Mod Rheumatol. 2006, 16: 343-9. 10.1007/s10165-006-0515-1.

    CAS  Article  PubMed  Google Scholar 

  19. Haynes DR: Emerging and future therapies for the treatment of bone loss associated with chronic inflammation. Inflammopharmacology. 2006, 14: 193-7. 10.1007/s10787-006-0006-1.

    CAS  Article  PubMed  Google Scholar 

  20. Verdrengh M, Carlsten H, Ohlsson C, Tarkowski A: Addition of bisphosphonate to antibiotic and anti-inflammatory treatment reduces bone resorption in experimental Staphylococcus aureus-induced arthritis. J Orthop Res. 2007, 25: 304-10. 10.1002/jor.20317.

    CAS  Article  PubMed  Google Scholar 

  21. Croom KF, Scott LJ: Intravenous ibandronate: in the treatment of osteoporosis. Drugs. 2006, 66: 1593-601. 10.2165/00003495-200666120-00005.

    CAS  Article  PubMed  Google Scholar 

  22. Chapurlat RD, Delmas PD: Drug insight: Bisphosphonates for postmenopausal osteoporosis. Nat Clin Pract Endocrinol Metab. 2006, 2: 211-9. 10.1038/ncpendmet0121.

    CAS  Article  PubMed  Google Scholar 

  23. Manette C, Collette J, Sarlet N, Tancredi A, Zegels B, Reginster JY: Comprehensive therapy in osteoporosis using a single drug: from ADFR to strontium ranelate. Curr Med Chem. 2006, 13: 1585-90. 10.2174/092986706777442057.

    CAS  Article  PubMed  Google Scholar 

  24. Cicek M, Oursler MJ: Breast cancer bone metastasis and current small therapeutics. Cancer Metastasis Rev. 2006, 25: 635-44. 10.1007/s10555-006-9035-x.

    CAS  Article  PubMed  Google Scholar 

  25. Lipton A: Future treatment of bone metastases. Clin Cancer Res. 2006, 12 (20 Pt 2): 6305s-6308s. 10.1158/1078-0432.CCR-06-1157.

    CAS  Article  PubMed  Google Scholar 

  26. Bagi CM: Targeting of therapeutic agents to bone to treat metastatic cancer. Adv Drug Deliv Rev. 2005, 57: 995-1010. 10.1016/j.addr.2004.12.014.

    CAS  Article  PubMed  Google Scholar 

  27. Kanakis I, Kousidou OCh, Karamanos NK: In vitro and in vivo antiresorptive effects of bisphosphonates in metastatic bone disease. In Vivo. 2005, 19: 311-8.

    CAS  PubMed  Google Scholar 

  28. Putnam SE, Scutt AM, Bicknell K, Priestley CM, Williamson EM: Natural products as alternative treatments for metabolic bone disorders and for maintenance of bone health. Phytother Res. 2007, 21: 99-112. 10.1002/ptr.2030.

    Article  PubMed  Google Scholar 

  29. New SA: Intake of fruit and vegetables: implications for bone health. Proc Nutr Soc. 2003, 62: 889-99.

    PubMed  Google Scholar 

  30. Hidaka S, Okamoto Y, Yamada Y, Kon Y, Kimura TA: Japanese herbal medicine, Chujo-to, has a beneficial effect on osteoporosis in rats. Phytother Res. 1999, 13: 14-9. 10.1002/(SICI)1099-1573(199902)13:1<14::AID-PTR375>3.0.CO;2-V.

    CAS  Article  PubMed  Google Scholar 

  31. Funk JL, Oyarzo JN, Frye JB, Chen G, Lantz RC, Jolad SD, Solyom AM, Timmermann BN: Turmeric extracts containing curcuminoids prevent experimental rheumatoid arthritis. J Nat Prod. 2006, 69: 351-5. 10.1021/np050327j.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  32. Ramprasath VR, Shanthi P, Sachdanandam P: Curative effect of Semecarpus anacardium Linn. nut milk extract against adjuvant arthritis – with special reference to bone metabolism. Chem Biol Interact. 2006, 160: 183-92. 10.1016/j.cbi.2005.11.009.

    CAS  Article  PubMed  Google Scholar 

  33. Sohail MT, Chaudhry MI, Usman MK, Mian T, Ishaq MN: Efficacy and tolerance of atrisin in degenerative and inflammatory joint disorders. Phytother Res. 2005, 19: 365-8. 10.1002/ptr.1680.

    CAS  Article  PubMed  Google Scholar 

  34. Yin J, Tezuka Y, Kouda K, Le Tran Q, Miyahara T, Chen Y, Kadota S: Antiosteporotic activity of the water extract of Dioscorea spongiosa . Biol Pharm Bull. 2004, 27: 583-586. 10.1248/bpb.27.583.

    CAS  Article  PubMed  Google Scholar 

  35. Wang D, Li F, Jiang Z: Osteoblastic proliferation stimulating activity of Psoralea corylifollia extracts and two of its flavonoids. Planta Med. 2001, 67: 748-749.

    CAS  Article  PubMed  Google Scholar 

  36. Meng F, Xiong Z, Sun Y, Li F: Coumarins from Cidium monnieri (L.) and their proliferation stimulating activity on osteoblast-like UMR106 cells. Pharmazie. 2004, 59: 643-645.

    CAS  PubMed  Google Scholar 

  37. Anila L, Vijayalakshmi NR: Flavonoids from Emblica officinalis and Mangifera indica, effectiveness for dyslipidemia. J Ethnopharmacol. 2002, 79: 81-87. 10.1016/S0378-8741(01)00361-0.

    CAS  Article  PubMed  Google Scholar 

  38. Thakur CP, Mandal K: Effect of Emblica officinalis on cholesterol-induced atherosclerosis in rabbits Indian. J Med Res. 1984, 79: 142-146.

    CAS  Google Scholar 

  39. Bhattacharya A, Kumar M, Ghosal S, Bhattacharya SK: Effect of bioactive tannoid principles of Emblica officinalis on iron-indued hepatic toxicity in rats. Phytomedicine. 2000, 7: 173-175.

    CAS  Article  PubMed  Google Scholar 

  40. Ahmad I, Mehmood Z, Mohammad F: Screening of some Indian medicinal plants for their antimicrobial properties. J Ethnopharmacol. 1998, 62: 183-93. 10.1016/S0378-8741(98)00055-5.

    CAS  Article  PubMed  Google Scholar 

  41. Asmawi MZ, Kankaanranta H, Moilanen E, Vapaatalo H: Anti-inflammatory activities of Emblica officinalis Gaertn leaf extracts. J Pharm Pharmacol. 1993, 45: 581-584.

    CAS  Article  PubMed  Google Scholar 

  42. Jeena KJ, Kuttan G, Kuttan R: Antitumor activity of Emblica officinalis. J of Ethnoph. 2001, 75: 65-69. 10.1016/S0378-8741(00)00378-0.

    Article  Google Scholar 

  43. Sancheti G, Jindal A, Kumari R, Goyal PK: Chemopreventive action of Emblica officinalis on skin carcinogenesis in mice. Asian Pac J Cancer Prev. 2005, 6: 197-201.

    PubMed  Google Scholar 

  44. Sultana S, Ahmad S, Khan N, Jahangir T: Effect of Emblica officinalis (Gaertn) on CCl4 induced hepatic toxicity and DNA synthesis in Wistar rats. Indian J Exp Biol. 2005, 43: 430-6.

    PubMed  Google Scholar 

  45. Scartezzini P, Antognoni F, Raggi MA, Poli F, Sabbioni C: Vitamin C content and antioxidant activity of the fruit and of the Ayurvedic preparation of Emblica officinalis Gaertn. J Ethnopharmacology. 2006, 104: 113-8. 10.1016/j.jep.2005.08.065.

    CAS  Article  PubMed  Google Scholar 

  46. Penolazzi L, Lambertini E, Borgatti M, Piva R, Cozzani M, Giovannini I, Naccari R, Siciliani G, Gambari R: Decoy oligodeoxynucleotides targeting NF-kappaB transcription factors: induction of apoptosis in human primary osteoclasts. Biochem Pharmacol. 2003, 66: 1189-98. 10.1016/S0006-2952(03)00470-2.

    CAS  Article  PubMed  Google Scholar 

  47. Piva R, Penolazzi L, Lambertini E, Giordano S, Gambari R: Induction of apoptosis of human primary osteoclasts treated with a transcription factor decoy mimicking a promoter region of estrogen receptor alpha. Apoptosis. 2005, 10: 1079-94. 10.1007/s10495-005-0618-8.

    CAS  Article  PubMed  Google Scholar 

  48. Borgatti M, Lampronti I, Romanelli A, Pedone C, Saviano M, Bianchi N, Mischiati C, Gambari R: Transcription factor decoy molecules based on a peptide nucleic acid (PNA)-DNA chimera mimicking Sp1 binding sites. J Biol Chem. 2003, 278: 7500-9. 10.1074/jbc.M206780200.

    CAS  Article  PubMed  Google Scholar 

  49. Piva R, Penolazzi L, Zennaro M, Bianchini E, Magri E, Borgatti M, Lampronti I, Lambertini E, Tavanti E, Gambari R: Induction of apoptosis of osteoclasts by targeting transcription factors with decoy molecules. Ann N Y Acad Sci. 2006, 1091: 509-16. 10.1196/annals.1378.092.

    CAS  Article  PubMed  Google Scholar 

  50. Park BK, Zhang H, Zeng Q, Dai J, Keller ET, Giordano T, Gu K, Shah V, Pei L, Zarbo RJ, McCauley L, Shi S, Chen S, Wang CY: NF-kappaB in breast cancer cells promotes osteolytic bone metastasis by inducing osteoclastogenesis via GM-CSF. Nat Med. 2007, 13: 62-9. 10.1038/nm1519.

    CAS  Article  PubMed  Google Scholar 

  51. Yamashita T, Yao Z, Li F, Zhang Q, Badell IR, Schwarz EM, Takeshita S, Wagner EF, Noda M, Matsuo K, Xing L, Boyce BF: NF-{kappa}B p50 and p52 Regulate Receptor Activator of NF-{kappa}B Ligand (RANKL) and Tumor Necrosis Factor-induced Osteoclast Precursor Differentiation by Activating c-Fos and NFATc1. J Biol Chem. 2007, 282: 18245-53. 10.1074/jbc.M610701200.

    CAS  Article  PubMed  Google Scholar 

  52. Matsuzaki K, Katayama K, Takahashi Y, Nakamura I, Udagawa N, Tsurukai T, Nishinakamura R, Toyama Y, Yabe Y, Hori M, Takahashi N, Suda T: Human osteoclast-like cells are formed from peripheral blood mononuclear cells in a coculture with SaOS-2 cells transfected with the parathyroid hormone (PTH)/PTH-related protein receptor gene. Endocrinology. 1999, 140: 925-32. 10.1210/en.140.2.925.

    CAS  Article  PubMed  Google Scholar 

  53. Villanova I, Townsend PA, Uhlmann E, Knolle J, Peyman A, Amling M, Baron R, Horton MA, Teti A: Oligodeoxynucleotide targeted to the alphav gene inhibits alphav integrin synthesis, impairs osteoclast function, and activates intracellular signals to apoptosis. J Bone Miner Res. 1999, 14: 1867-79. 10.1359/jbmr.1999.14.11.1867.

    CAS  Article  PubMed  Google Scholar 

  54. Khan MTH, Lampronti I, Martello D, Bianchi N, Jabbar S, Choudhuri SMK, Datta BK, Gambari R: Identification of pyrogallol as an antiproliferative compound present in extracts from the medicinal plant Emblica Officinalis: effects on in vitro cell growth of human tumor cell lines. Int J Oncol. 2002, 20: 187-192.

    Google Scholar 

  55. Lampronti I, Martello D, Bianchi N, Borgatti M, Lambertini E, Piva R, Jabbar S, Shahabuddin Kabir Choudhuri M, Tareq Hassan Khan M, Gambari R: In vitro antiproliferative effects on human tumor cell lines of extracts from the Bangladeshi medicinal plant Aegle marmelos Correa. Phytomedicine. 2003, 10: 300-308. 10.1078/094471103322004794.

    CAS  Article  PubMed  Google Scholar 

  56. Denizot F, Lang RJ: Rapid colorimetric assay for cell growth and survival. Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability. Immunol Meth. 1986, 22: 271-277. 10.1016/0022-1759(86)90368-6.

    Article  Google Scholar 

  57. Lampronti I, Khan MTH, Borgatti M, Bianchi N, Gambari R: Inhibitory effects of Bangladeshi medicinal plant extracts on interaction teween transcription factors and target DNA sequences. Evidence-based Complementary and Alternative Medicine. 2007

    Google Scholar 

  58. Pritts T, Hungness E, Wang Q, Robb B, Hershko D, Hasselgren PO: Mucosal and enterocyte IL-6 production during sepsis and endotoxemia – role of transcription factors and regulation by the stress response. Am J Surg. 2002, 183: 372-83. 10.1016/S0002-9610(02)00812-7.

    CAS  Article  PubMed  Google Scholar 

  59. Domingo-Domenech J, Oliva C, Rovira A, Codony-Servat J, Bosch M, Filella X, Montagut C, Tapia M, Campas C, Dang L, Rolfe M, Ross JS, Gascon P, Albanell J, Mellado B: Interleukin 6, a nuclear factor-kappaB target, predicts resistance to docetaxel in hormone-independent prostate cancer and nuclear factor-kappaB inhibition by PS-1145 enhances docetaxel antitumor activity. Clin Cancer Res. 2006, 12: 5578-86. 10.1158/1078-0432.CCR-05-2767.

    CAS  Article  PubMed  Google Scholar 

  60. Ameye LG, Chee WS: Osteoarthritis and nutrition. From nutraceuticals to functional foods: a systematic review of the scientific evidence. Arthritis Res Ther. 2006, 8: R127-10.1186/ar2016.

    Article  PubMed  PubMed Central  Google Scholar 

  61. Idris A, Mrak E, Greig I, Guidobono F, Ralston SH, van't Hof R: ABD56 causes osteoclast apoptosis by inhibiting the NFkappaB and ERK pathways. Biochem Biophys Res Commun. 2008, 371: 94-8. 10.1016/j.bbrc.2008.04.014.

    CAS  Article  PubMed  Google Scholar 

  62. Uchiyama S, Yamaguchi M: Genistein and zinc synergistically stimulate apoptotic cell death and suppress RANKL signaling-related gene expression in osteoclastic cells. J Cell Biochem. 2007, 101: 529-42. 10.1002/jcb.21208.

    CAS  Article  PubMed  Google Scholar 

  63. Do SH, Lee JW, Jeong WI, Chung JY, Park SJ, Hong IH, Jeon SK, Lee IS, Jeong KS: Bone-protecting effect of Rubus coreanus by dual regulation of osteoblasts and osteoclasts. Menopause. 2008, 15: 676-83.

    Article  PubMed  Google Scholar 

  64. Faloni AP, Sasso-Cerri E, Katchburian E, Cerri PS: Decrease in the number and apoptosis of alveolar bone osteoclasts in estrogen-treated rats. J Periodontal Res. 2007, 42: 193-201. 10.1111/j.1600-0765.2006.00932.x.

    CAS  Article  PubMed  Google Scholar 

  65. Penolazzi L, Magri E, Lambertini E, Bianchini E, Piva R, Gambari R: "In vivo" local transfection of a cis element decoy mimicking an estrogen receptor alpha gene promoter region induces apoptosis of osteoclasts following application of orthodontic forces to rat teeth. Apoptosis. 2006, 11: 1653-6. 10.1007/s10495-006-8763-2.

    CAS  Article  PubMed  Google Scholar 

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Acknowledgements

R.G. is funded by CIB (Consorzio Interuniversitario di Biotecnologie, Italy), AIRC (Associazione Italiana Ricerca sul Cancro), AVTL (Associazione Veneta per la Lotta alla Talassemia, Italy), SPINNER e PRIITT (EU, Obiettivo 2), Fondazione Cassa di Risparmio di Padova e Rovigo, STAMINA Project of Ferrara University and UE ITHANET Project. We would like to thank Dr. Amanda J. Neville (Department of Experimental and Diagnostic Medicine, Section of Medical Genetics) for her contribution in revising the text.

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Authors and Affiliations

  1. BioPharmaNet, ER-GenTech, Department of Biochemistry and Molecular Biology, Ferrara University, Ferrara, Italy

    Letizia Penolazzi, Ilaria Lampronti, Monica Borgatti, Margherita Zennaro, Roberta Piva & Roberto Gambari

  2. Department of Pharmacology, Institute of Medical Biology, University of Tromso, Tromso, Norway

    Mahmud Tareq Hassan Khan

  3. H.E.J. Research Institute of Chemistry, International Center for Chemical Sciences, University of Karachi, Karachi, Pakistan

    Mahmud Tareq Hassan Khan

  4. Biotechnology Center, Ferrara University, Ferrara, Italy

    Roberto Gambari

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  1. Letizia Penolazzi
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  2. Ilaria Lampronti
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  3. Monica Borgatti
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  4. Mahmud Tareq Hassan Khan
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  5. Margherita Zennaro
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  6. Roberta Piva
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  7. Roberto Gambari
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Correspondence to Roberto Gambari.

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The authors declare that they have no competing interests.

Authors' contributions

LP developed the culture of osteoclasts from the peripheral blood; IL characterized the E. officinalis extracts with respect to effects of cell growth; MB performed gel shift experiments using nuclear factors and oligonucleotides mimicking the NF-kB binding sites; MTHK isolated the the E. officinalis extracts; RP designed the experiments with the osteoclasts cultures; RG wrote the paper and coordinated the experiments. All authors read and approved the final manuscript.

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Penolazzi, L., Lampronti, I., Borgatti, M. et al. Induction of apoptosis of human primary osteoclasts treated with extracts from the medicinal plant Emblica officinalis . BMC Complement Altern Med 8, 59 (2008). https://doi.org/10.1186/1472-6882-8-59

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Keywords

  • Plant Extract
  • Electrophoretic Mobility Shift Assay
  • Human Osteoclast
  • Turmeric Extract
  • Proliferation Stimulate Activity

BMC Complementary Medicine and Therapies

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