Turmeric and curcumin suppress presenilin 1 protein expression in Jurkat cells

Introduction

Alzheimer's disease is a neurodegenerative disease caused by amyloid-β accumulation in brain cells combined with oxidative stress and inflammation (1,2). Neurotoxic amyloid-β is an approximately 4-kDa peptide generated via cleavage of the amyloid-β precursor protein (APP) by the γ-secretase proteolytic complex (3). Presenilin is the catalytic member of the γ-secretase complex, and mutations in presenilin are the major cause of early-onset familial Alzheimer's disease. Presenilin is involved in several biological functions, but is well known for its role in the generation of the amyloid-β peptide in Alzheimer's disease and is therefore thought to be an important drug target for this disorder. Thus, an increased understanding of Presenilin may help to improve the development of drugs for Alzheimer's disease and for other neurological diseases (4).

Certain herbs have been demonstrated to possess a multitude of beneficial activities, and herbal medications are currently being used for widespread clinical use in disease therapy, as herbs exhibit relatively mild bioavailability and low toxicity (5). As for Alzheimer's disease, polyphenols extracted from grape seeds have been found to inhibit amyloid-β aggregation, reduce amyloid-β production and protect against amyloid-β neurotoxicity in vitro (6,7). In addition, cryptotanshinone (CTS), an active component of the medicinal herb Salvia miltiorrhiza, has been shown to improve learning and memory in several pharmacological models of Alzheimer's disease (8). Further research demonstrated that CTS improved the cognitive ability and promoted APP metabolism involving the non-amyloidogenic product pathway in rat cortical neuronal cells. Moreover, as the Indian diet is rich in herbs and spices, the incidence of Alzheimer's disease in India is considerably low (9,10). However, the precise molecular mechanisms of the therapeutic effects of medicinal herbs and spices are largely undefined, and limited data and a small body of convincing evidence exist at the molecular level (11). Therefore, basic research and development aimed at elucidating the mechanism of action underlying herbal effects should have high priority. We hypothesized that various herbs or spices may affect the γ-secretase proteolytic function. Therefore, we investigated the in vitro effect of several herbs on the expression of presenilin 1 in cultured human cells.

Materials and methods

Cell culture

The human cell lines, Jurkat, Daudi, U937 and K562, were maintained in RPMI-1640 supplemented with 10% fetal bovine serum (FBS), penicillin and streptomycin at 37°C in a humidified atmosphere containing 5% CO2.

Extract preparation

Herb and spice powders were purchased at a food market in Japan. The powders were dissolved in 80% ethanol and subsequently diluted in 40% ethanol at a stock concentration of 50 mg/ml. The mixtures were vortexed rigorously for 3 min followed by 3-min sonication. After centrifugation (1,500 × g, 5 min), the supernatants were collected and stored at −20°C until use. For the cell treatments, a range of 0.5–10 μl was added to 1 ml of the cell culture medium.

Reverse transcriptase-polymerase chain reaction (RT-PCR)

Presenilin 1 and GAPDH mRNAs were analyzed by semi-quantitative RT-PCR. Total RNA was extracted by an RNA isolation kit (Takara, Japan). Total RNA (2 μg) was reverse-transcribed using the Phusion RT-PCR kit (NEB) as described in the manufacturer's protocol. Cycle-based PCR was used to semi-quantitate the presenilin 1 gene level. GADPH was also used as an internal loading control. All the samples were evaluated within 3 months after collection. The primers used for the PCR were: presenilin 1 forward, GGTCCACTTCGTATGCTGGT and reverse, GCTGTTGCTGAGGCTTTACC (expected size 404 bp); GAPDH forward, TCCCATCACCATCTTCCA and reverse, CATCACGCCACAGTTTCC (expected size 376 bp). For real-time PCR, the reactions were performed in a real-time PCR system (Illumina, USA) using Kapa SYBR Fast reaction mix (Genetics, Japan). Thermocycling was performed according to the instructions at an annealing temperature of 60°C in a final volume of 10 μl, including Taq DNA polymerase. To correct for differences in both RNA quality and quantity between samples, data were normalized using the ratio of the target cDNA concentration to that of GAPDH.

Western blot analysis

Equal amounts of protein samples were used for Western blot analysis using anti-presenilin 1 (Genscript) and anti-Erk2 (Epitomics) antibodies, and quantified by densitometry. The Western blotting was repeated at least three times, and the representative data are shown.

Results and discussion

To investigate the possibility of using medicinal herbs to down-regulate presenilin 1 protein, extracts of many herbs and spices, including garlic, red pepper, cinnamon, phakchi, turmeric, basil and black pepper, were added to the cell culture medium of Jurkat, Daudi, U937 or K562 cells, and the levels of genes, including presenilin 1, were examined. RT-PCR analysis was employed to quantify the expression level of the genes. Total RNA was isolated 24 h after herbal extract treatment for the detection of presenilin 1, and the levels of presenilin 1 mRNA were determined by conventional semi-quantitative RT-PCR. As shown in Fig. 1, the expression level of the presenilin 1 gene was not altered by treatment of the herbal and spice extracts at a final concentration of 50 μg/ml, compared to the untreated ethanol vehicle. Expression of presenilin 2 (data not shown) and the housekeeping gene GAPDH were also unaltered (Fig. 1). In addition, similar results were also obtained from the quantitative real-time PCR analysis (Fig. 2). There was little difference in the results of the gene expressional profile among the Jurkat, Daudi, U937 and K562 cells (data not shown). To exclude the possibility of carry-over DNA contamination, reactions containing all RT-PCR reagents, including primers without sample RNA, were performed as negative controls. No such RNA contamination was detected (data not shown).

Figure 1. Semi-quantitative RT-PCR was performed using primers specific to presenilin 1 or GAPDH using 100 ng total RNA prepared from Jurkat cells treated without (lane 1) or with herbal extracts (lanes 2–8: garlic, red pepper, cinnamon, phakchi, turmeric, basil and black pepper, respectively) at a final concentration of 50 μg/ml for 24 h. Specific expression was determined in relation to the expression of the housekeeping gene GAPDH used as an internal loading control. At least four independent experiments were performed, and typical paired results are documented.

Figure 2. Fluorescence data for PCR amplification plots of presenilin 1 in Jurkat cells stimulated by the indicated herbs and spices. Data were generated by Thermal-Cycler software using the Illumina Real-Time PCR Detection system. No product was amplified in the no-template sample or when reverse transcriptions were omitted. Similar results were obtained when the PCR products of Daudi and K562 cells were analyzed.

To further examine the status of the level of protein expression, Western blotting was performed to analyze the presenilin 1 protein in the cells stimulated by the herbs and spices. As shown in Fig. 3, the turmeric and cinnamon extract dramatically reduced the protein expression of presenilin 1 in the Jurkat cells when the cell cultures were treated with the spices for 48 h. The down-regulation of presenilin 1 protein expression by the several herbal extracts was in approximate accord with the result of the long-term-treated cells (72 h after herbal stimulation) (Fig. 3, lower panels). After long-term stimulation, it was evident that red and black pepper, in addition to turmeric and cinnamon, down-regulated presenilin 1 protein expression. We then investigated whether curcumin, a major component of turmeric, reduces presenilin 1 expression. After treating the cells with different concentrations of curcumin, presenilin 1 protein, but not Erk2 protein expression was decreased with increasing concentrations of the curcumin extract. A final concentration of 100 μg/ml of the curcumin extract inhibited expression of presenilin 1 by >95% in the Jurkat cells (Fig. 4). The turmeric extract also down-regulated presenilin 1 in a dose-dependent manner in the K562 cells (data not shown).

Figure 3. Turmeric and cinnamon extract reduced the expression of presenilin 1 protein. (A) Jurkat cells were treated without (lane 1) or with extracts of herbs (lanes 2–8: garlic, red pepper, cinnamon, phakchi, turmeric, basil and black pepper, respectively) at a final concentration of 50 μg/ml for 48 or 72 h. After treatment, cell lysates were isolated and the levels of presenilin 1 protein were detected by Western blot analysis using an anti-presenilin 1 antibody. Western blots with an anti-Erk2 antibody were also shown as controls for equal levels of protein loading. At least three independent experiments were performed and typical paired results are shown.

Figure 4. Dose-dependent inhibition of presenilin 1 protein expression by curcumin. Jurkat cells were treated without (lane 1) or with curcumin extracts at a final concentration of 25 (lane 2), 50 (lane 3) and 100 μg/ml (lane 4) for 48 h. The levels of protein were detected by Western blot analysis using an anti-presenilin 1 antibody as explained in Fig. 3. Western blotting with an anti-Erk2 antibody was also shown as a control for equal levels of protein loading.

A recent in vivo study demonstrated that curcumin was able to reduce amyloid-β-related pathology in transgenic Alzheimer's disease mouse models via unknown molecular mechanisms (12). Curcumin is a small-molecule fluorescent compound found in the widely used culinary spice, turmeric, which possesses potent biological activities, including anti-inflammatory, anti-fibrilogenic and antioxidant, as well as chemopreventative effects and effects on protein trafficking. Curcumin has also been found to lower amyloid-β protein levels by attenuating the maturation of APP in the secretory pathway. Curcumin was demonstrated to promote a significant reversal of structural changes in dystrophic dendrites, including abnormal curvature and dystrophy size (13). The computed ionization potential and electron affinity show that curcumin has a low-molecular hardness, and the resulting charge undergoes delocalization throughout the structure, resulting in excitonic features. This feature appears to be important for its binding capability to human proteins, such as human serum albumin and amyloid-β (14). Together, these data suggest that curcumin reverses Alzheimer's disease pathology and propose a mechanism of action for the ability of curcumin to attenuate amyloid-β pathology. This approach may lead to more effective clinical therapies for the prevention of oxidative stress, inflammation and neurotoxicity associated with Alzheimer's disease.

In the present study, curcumin and the other spice components dose-dependently down-regulated presenilin 1 protein, which plays a pivotal role in γ-secretase activity. Recently, ubiquilin-1 was reported to regulate the proteasomal degradation of proteins, including presenilin (15). Since the proteasome is responsible for the removal of oxidatively damaged proteins in the cytosol and nucleus during oxidative stress (16), it is plausible that presenilin 1 protein may be degraded by the ubiquitin proteasome pathway (17). Various herbs and spices may accelerate this degradation. Further study including in vivo experiments must be undertaken to elucidate the precise molecular mechanisms of these herbs particularly in regard to the treatment of Alzheimer's disease.

Acknowledgements

This study was supported by grants-in-aid from the Ministry of Education, Culture, Sports, Science and Technology of Japan, and the Nara Women's University Intramural Grant for Project Research.

References