Anti-proliferative effects of Salacia reticulata leaves hot-water extract on interleukin-1β-activated cells derived from the synovium of rheumatoid arthritis model mice
© Sekiguchi et al; licensee BioMed Central Ltd. 2012
Received: 1 December 2011
Accepted: 9 March 2012
Published: 26 April 2012
Salacia reticulata (SR) is a plant native to Sri Lanka. In ayurvedic medicine, SR bark preparations, taken orally, are considered effective in the treatment of rheumatism and diabetes. We investigated the ability of SR leaves (SRL) to inhibit in vitro the interleukin-1β (IL-1β)-activated proliferation of synoviocyte-like cells derived from rheumatoid arthritis model mice.
Inflammatory synovial tissues were harvested from type II collagen antibody-induced arthritic mice. From these tissues, a synoviocyte-like cell line was established and named MTS-C H7. To determine whether SRL can suppress cell proliferation and gene expression in MTS-C H7 cells, fractionation of the SRL hot-water extract was performed by high-performance liquid chromatography (HPLC), liquid-liquid extraction, sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE), and protease digestion.
The 50% inhibitory concentration of the SRL hot-water extract against MTS-C H7 cells proliferation was ~850 μg/mL. Treatment with a low dose (25 μg dry matter per millilitre) of the extract inhibited IL-1β-induced cell proliferation and suppressed the expression of the matrix metalloproteinase (MMP) genes in MTS-C H7 cells. Various polyphenolic fractions obtained from HPLC and the fractions from liquid-liquid extraction did not affect cell proliferation. Only the residual water sample from liquid-liquid extraction significantly affected cell proliferation and the expression of MMP genes. The results of SDS-PAGE and protease digestion experiment showed that low molecular weight proteins present in SRL inhibited the IL-1β-activated cell proliferation.
We surmised that the residual water fraction of the SRL extract was involved in the inhibition of IL-1β-activated cell proliferation and regulation of mRNA expression in MTS-C H7 cells. In addition, we believe that the active ingredients in the extract are low molecular weight proteins.
Salacia reticulata (SR) is a plant native to Sri Lanka. In traditional Sri Lankan medicine, called ‘Ayurveda’, the roots and stems of SR are used for the prevention of rheumatism and diabetes [1, 2]. For example, the roots and stems of SR are known to contain unique compounds such as salacinol, kotalanol, and mangiferin [3–5]. In a previous study with a murine disease model, SR leaves (SRL) ameliorated the symptoms of rheumatoid arthritis (RA) .
Although the aetiology of RA is not yet fully understood, classical studies have suggested that autoantibody production, inflammatory cell infiltration, and tumour-like proliferation of synovial ‘pannus’ are involved in the pathogenesis of RA [7, 8]. Recent research on the roles of fibroblast-like synoviocytes in the pannus has gained recognition . The pannus releases several proinflammatory mediators and matrix metalloproteinases . RA treatment is currently based mainly on the administration of anti-inflammatory drugs and anti-rheumatic drugs .
In this study, we investigated the potential of SRL as a prophylactic or therapeutic agent for RA.
Preparation of samples
SRL were sun-dried. After removing the damaged leaves, the dried intact leaves were pulverized in a food mill and filtered through a 150-μm mesh sieve to obtain the powder. The powder was boiled in pure distilled water, and the extract solution was centrifuged for 20 min at 2190 × g to remove the pellet. The supernatant was filtered through a 0.20-μm filter membrane and dried using a freeze dryer. We purchased commercial agents prepared from stems of SR, such as mangiferin (Sigma-Aldrich Co., USA), triptotriterpenic acid B (AApin Chemicals Abingdon, UK), and (−)-epicatechin (Sigma-Aldrich Co., USA). These agents were dissolved in ethanol. All samples were stored at −20°C until use.
Collagen antibody-induced arthritic (CAIA) mice were generated using DBA/1 J mice as reported previously . Synovial tissues were obtained from the knee joints of these mice. The inflammatory synovial tissues were minced and stirred with type IV collagenase (Sigma-Aldrich Co., USA) in serum-free DMEM/F12 medium at 37°C for 3 h in an incubator shaker. The synovial tissue lysate was then filtered through a 40-μm nylon mesh, washed extensively, and seeded at 1 cell/well in 96-well microplates. The cells were cultured in DMEM/F12 supplemented with 10% FBS and benzylpenicillin potassium (100 units/mL) at 37°C/5% CO2. The inflammatory synovial tissue has been reported that the gene of Synoviolin is over-expressed . Therefore, the cell named MTS-C H7 of high-expressed genes of Synoviolin was established. The study was performed in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals and the Institutional Animal Care and Use Committee of Josai University, Saitama, Japan.
Cell viability assay
MTS-C H7 cells were plated in 96-well microplates at a density of 5 × 103/well. After 3 h, the SRL extract was added and cultured for 24 h. After incubattion, 10 μL of the cell proliferation reagent WST-1 (Roche Diagnostics, USA) was added and incubated for 30 min. Cell proliferation was measured at 450 nm by using a spectrophotometer.
Cell proliferation assay
MTS-C H7 cells were plated on 96-well microplates at a density of 5 × 103/well. After 3 h, mouse IL-1β or other samples were added and cultured for 24 h. The cell proliferation assay was performed as describe above.
The HPLC system consisted of an LC-Organizer, L-6200 Intelligent pump, L-4200H UV–VIS Detector, and ELITE LaChrom Column Oven L-2350 (HITACHI, Japan). Separation was carried out on a Wakosil-II 5C18AR column (250 mm × 4.6 mm, 5 μm). HPLC conditions were performed according to the reference . All samples were evaporated and dried, dissolved in ethanol. All samples were stored at −20°C until use.
Liquid-liquid distribution assay
The SRL extract was separated by hexane, diethyl ether, ethyl acetate, and n-butanol. The up layers and residual water fraction were collected. These samples were evaporated and dried, dissolved in ethanol or ultrapure water. All samples were stored at −20°C until use.
RNA extraction and reverse transcription (RT)-PCR
MTS-C H7 cells were cultured at approximately 2 × 105/dish. After 24 h, mouse IL-1β and other samples were added and cultured for 24 h. RNA was extracted using the TRIzol reagent according to the manufacturer’s instructions. The term of genes expression has been reported previously .
SDS-PAGE was used to determine the molecular weight and purity of the protein isolated from SRL. The samples were run on a MULTIGEL Mini 15/25 (COSMO BIO, Tokyo, Japan) gradient gel with the SDS-PAGE buffer (0.1% SDS, 0.05 M Tris, 0.05 M tricine). After electrophoresis, the gel was fixed with ultrapure water for 15 min and stained with GelCode Blue Safe Protein Stain (Thermo Fisher Scientific K.K., Waltham, USA) for 1 h.
Protease digestion assay
SRL extract was mixed with CPaseY incubated at 25°C from 0 to 60 min. MTS-C H7 cells were plated in 96-well microplates at a density of 5 × 103/well. After 3 h, SRL + CPaseY and IL-1β were added and cultured for 24 h. The cell proliferation assay using samples were performed as describe above.
The results are expressed as the mean and standard deviation (SD) of three independent experiments. Statistical analysis was carried out with Stat-Mate III Version 3.18 (ATMS Co., Ltd., Japan). Data distributions were compared using the Analysis of variance.
Cytotoxic effect of SRL on MTS-C H7 cells
Effect of SRL on MTS-C H7 cell proliferation induced by inflammatory mediators
Effects of reference compounds present in the stems of SR on cell proliferation
HPLC analysis of the SRL hot-water extract
Effects of various HPLC fractions of the SRL extract on cell proliferation
As shown in Figure 4B, Cell proliferation in the presence of IL-1β did not change when F1, F2, or F3 were added to the culture. These results show that none of the HPLC polyphenolic fractions of the SRL extract suppressed the IL-1β-induced cell proliferation.
Effects of various liquid-liquid distribution fractions of the SRL extract on cell proliferation
Effect of residual water from the SRL hot-water extract on gene expression results
As shown in Figure 5B, SRL extract and residual water samples were significant decrease in the mRNA levels for MMP-3 and MMP-13. These results show the possibility that the active ingredients in the residual water fraction decrease the activation of gene expression by IL-1β.
Characterization of the active ingredients as peptides
Discussion and Conclusions
RA treatments often cause severe adverse effects depending on the patient’s sensitivity or the drug dosage [15–17]. Traditional herbal therapy for RA takes advantage of using extracts of plants [18, 19]. However, herbal medicines have been reported to cause fewer adverse effects [20, 21].
The present study contributes to elucidating the effect of the SRL extract and residual water fraction sample on IL-1β-activated cell proliferation and gene expression against MTS-C H7 cells. The amount of protein in SRL extract (100 mg dry matter/ml) was confirmed by Lowry method to be 0.52 mg/mL . Moreover, SDS-PAGE analysis confirmed that SRL contains low molecular weight proteins (≤3 kDa).
In conclusion, we investigated whether the SRL can affect the functions of IL-1β-activated MTS-C H7 cells. Our results show that the active ingredients might be 3 kDa peptides. Moreover, it is well known that salacinol and kotalanol are similar in structure. Salacinol was reported to be in n-butanol fraction . The active ingredients did not appear to be catechins, salacinol, kotalanol, or mangiferin.
SRL appears to have potential as a functional food or herbal medicine for RA. In order to identify the sequence of these peptides, the future, we need to consider how to purify the peptides.
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