Introduction
Human skin is composed of the epidermis, dermis, hair, hair follicles and sebaceous glands. These multicellular structures consisting of a hair follicle and sebaceous glands are known as a pilosebaceous unit. In the pilosebaceous unit, the sebaceous glands store sebum, a lipid produced by sebocytes found in the skin of mammals (1,2). Human sebocytes are specialized epithelial cells that secrete sebum through an accumulation of neutral lipid droplets within the cytoplasm and thus undergo terminal differentiation into adipocytes (3). Sebaceous lipogenesis results in the secretion of sebum that contains triglycerides, wax esters, squalene, cholesterol esters, cholesterol and free fatty acids. Thus, these characteristics of sebocytes are related to the functional persistence of skin by controlling the moisture balance and protecting the skin from harmful factors, such as pathogens or ultraviolet (UV) light (4–6). On the contrary, the production of excessive sebum is associated with a common inflammatory disorder of the pilosebaceous units which, along with microbial infection, is known as acne vulgaris. The pathogenesis of acne vulgaris involves a variety of factors, including increased sebum production, follicular hyperkeratinization and the induction of inflammation by Propionibacterium acnes (P. acnes) (7). Current treatments for acne vulgaris utilize topical retinoids, benzoyl peroxide, antibiotics and systemic isotretinoin (13-cis retinoic acid). It is the potent inhibition of sebum production that results in a marked reduction in the size of and the secretion of sebum by the sebaceous glands (8–10).
The growth and differentiation of sebocytes and sebum secretion are regulated by diverse factors, as well as by peroxisome proliferator-activated receptor (PPAR), liver X receptor (LXR) and insulin-like growth factor (IGF)-1. PPAR isoforms (α, β/σ, γ) are ligand-activated transcription factors found in the skin and other organs that regulate adipogenesis and lipid metabolism through cell proliferation and differentiation. In addition, PPAR isoforms are all expressed in the human sebaceous glands where lipid synthesis occurs. Furthermore, PPAR activators, such as BRL-49653, WY-14643 and linoleic acid (LA) are potent lipid inducers that result in the production of lipids through sebocyte differentiation (11–13). Studies have indicated that IGF-1 increases sebocyte proliferation and promotes sebaceous gland lipogenesis by enhancing the expression of the sterol response element binding protein-1 (SREBP-1), a transcription factor regulating lipid formation (14,15). Furthermore, it has been demonstrated that IGF-1 is associated with the activation of the mitogen-activated protein-kinase/extracellular signal-regulated protein kinase (MAPK/ERK) pathway and the stimulation of the phosphatidylinositol 3-kinase (PI3-K)/Akt pathway in several cell types (16,17). ERK and Akt are serine/threonine protein kinases that play a critical role in cell growth and cell survival in various cell types (18,19). Taken together, both signaling pathways are known to be important for cell growth. Moreover, these pathways have been implicated in the activation of sebocytes (16,20). Thus, in this study, we investigated the potential involvement of ERK and Akt in the effects exerted by treatment with resveratrol.
Resveratrol (trans-3,4′,5-trihydroxystilbene) is a naturally occurring polyphenolic compound and a phytoalexin present in food products, red wine, grape skin and various plants and is produced as a reaction to environmental stresses, such as infection by plant pathogens (21). Previous studies have suggested that resveratrol exerts a variety of pharmacological effects, including antiproliferative, antioxidant, anti-inflammatory, anti-angiogenic and antimetastatic effects in many different cell lines (21–23). It has been reported that resveratrol has chemotherapeutic properties in several cell culture models and in an in vivo cancer model (22,24). Previous studies have reported the inhibitory effects of resveratrol on cell cycle progression in tumor cells, which results in a reduction in the number of cells in the G0/G1 phase of the cell cycle and the downregulation of cyclin D1 and cyclin-dependent kinase (CDK)4 (24–27). In addition, it has been shown that resveratrol downregulates the phosphorylation of Akt and ERK in cancer cells (28). Moreover, previous studies have reported that resveratrol inhibits the proliferation of normal cells, such as smooth muscle cells and normal human keratinocytes (29,30). It has also been shown to reduce the synthesis of lipids by repressing PPAR-γ in differentiated adipocytes (31–33). Despite our understanding of the antiproliferative and pro-apoptotic properties of resveratrol in other cells, the antiproliferative signaling mechanisms of resveratrol in human sebocytes remain uncertain. Thus, in this study, in order to investigate the association between the antiproliferative effects of resveratrol and cell cycle progression, we evaluated the epxression of p21WAF1/CIP1 (p21), p27KIP1 (p27) and cyclin D1 in human sebocytes.
The aim of the present study was to investigate the underlying molecular signaling pathways through which resveratrol inhibits the proliferation of human immortalized sebocytes and thus attenuates cell cycle progression. Due to the importance of cell cycle regulators in proliferation, we determined whether the levels of these regulators are affected by resveratrol. Therefore, we assessed the effects of resveratrol on cell cycle regulators in human sebocytes, and investigated the effects of this potent inhibitor of sebum production in a model of lipid droplet formation.
Materials and methods
Materials
Antibodies against phosphorylated ERK (p-ERKl; Thr202/Tyr204, #9101S), ERK (#9102), phosphorylated Akt (p-Akt; Ser473, #9271S), Akt (#9272), cyclin D1 (#2922), p21 (#2946) and p27 (#3688) were purchased from Cell Signaling Technology, Inc. (Beverly, MA, USA). The antibodies to PPAR-γ (B-5, #sc-271392) and β-actin (I-19, #sc-1616) were obtained from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA). Reagents including, LA, formaldehyde, Thiazolyl Blue tetrazolium bromide (MTT), Tris-HCl, sodium dodecyl sulfate (SDS), β-mercaptoethanol, phenylmethylsulfonyl fluoride (PMSF), sodium orthovanadate (Na3VO4), sodium fluoride (NaF), ethylenediaminetetraacetic acid (EDTA), Oil Red O and Gill’s hematoxylin were purchased from Sigma-Aldrich Co. (St. Louis, MO, USA). LY294002 (19–142, a PI3-K inhibitor) and PD98059 (19–143, a MEK inhibitor) were obtained from Calbiochem (San Diego, CA, USA). LA was dissolved in ethanol and stored at −20°C. Further dilutions were made in a vehicle solution (ethanol) prior to use.
Cell culture
Immortalized human sebocytes, SZ95 (34), were maintained in Sebomed® basal medium (Biochrom GmbH, Berlin, Germany) containing 10% fetal bovine serum (HyClone Inc., Logan, UT, USA), 1% penicillin (10,000 U/ml) and 1% streptomycin (10,000 g/ml) (Gibco-BRL, Grand Island, NY, USA), 1mM CaCl2 and 5 ng/ml human epidermal growth factor (EGF; Sigma-Aldrich Co.). The cultures were maintained at 37°C in a humidified 5% CO2 incubator and the medium was replaced every 2–3 days. The SZ95 human sebocytes used for the experiments were between passages 31 and 35.
Determination of cell proliferation by MTT assay and microscopy
The cells were examined under a phase contrast microscope (Olympus Optical Co., Tokyo, Japan) and photographed using a DCM300 digital camera (ScopeTek, Inc., Hangzhou, China), which was supported by Scope Photo software (Scopetek, Inc.). Cell proliferation was determined using the MTT reduction assay. To determine proliferation, SZ95 human sebocytes were seeded (1×104 cells/well) on 24-well culture plates for 24 h and incubated with resveratrol-containing medium at 37°C in 5% CO2. Treatment with increasing concentrations of resveratrol was carried out for 24, 48 and 72 h. At the end of the resveratrol incubation period, the cells were incubated with the test substances for the indicated periods of time at 37°C in 5% CO2. Subsequently, 100 μl of MTT at 5 mg/ml were added to each well, and incubation was continued for 4 h. Supernatants were removed and formazan crystals resulting from mitochondrial enzymatic activity on the MTT substrate were solubilized with dimethylsulfoxide (DMSO; Sigma-Aldrich Co.). The absorbance was measured at 540 nm using an enzyme-linked immunosorbent assay (ELISA) reader (VersaMax; Molecular Devices, Sunnyvale, CA, USA).
Oil Red O staining
The human SZ95 sebocytes were seeded (1×105 cells/well) in 6-well culture plates and incubated for 24 h. To induce the differentiation of the sebocytes, 100 μM LA were added to the culture medium and the cells were then treated with 10 μg/ml resveratrol for 48 h. The cells treated with the vehicle (ethanol) served as the controls. At the end of the treatment period, the cells were washed with phosphate-buffered saline (PBS; WelGene Inc., Daegu, Korea) and fixed in 4% paraformaldehyde for 5 min at room temperature. After 5 min, the cells were washed with PBS, and the fixed cells were then stained with Oil Red O solution, a mixture of Oil Red O (1% in isopropanol) and dH2O at a ratio of 6:4 (vol/vol), for 15 min, and washed with PBS. The cell nuclei were stained with Gill’s haematoxylin for 5 min, as previously described in the study by Zouboulis et al (34). The stained cells were visualized under a microscope. Cell morphology was observed under a DP70 microscope using DP Controller software (Olympus Optical Co.). The Oil Red O staining of the lipid droplets in the cells was quantified by elution into isopropanol, and 200 μl aliquots of the elution were then placed in 96-well plates, and the optical density of each well was determined using an ELISA reader (VersaMax; Molecular Devices) at 500 nm. In some wells, the concentration of cellular protein from these cells was measured using a protein assay kit from Bio-Rad Laboratories, Inc. (Hercules, CA, USA). The lipid content was expressed as the percentage of living cells relative to the controls.
Determination of cell cycle changes
Following treatment of the SZ95 cells with resveratrol (0–50 μg/ml) for 24 h, culture supernatants were collected to remove floating dying and apoptotic cells. The adherent cells were then harvested by trypsinization and then adjusted to 1×106 cells/tube, washed with ice-cold PBS and resuspended in 2 ml ethanol. Following incubation at 4°C for 1 h, the ethanol was removed and 100 μl of ribonuclease solution (10 mg/ml, Sigma-Aldrich, Co.) were added to each tube. The tubes were then incubated at room temperature for 30 min and 500 μl of analysis solution (37 mM EDTA and 0.1% Triton X-100 in PBS) and 100 μl of propidium iodide (PI) solution (1 mg/ml, Sigma-Aldrich Co.) were added. The samples were stored in the dark at 4°C and analyzed using a flow cytometer (FACSCalibur; Becton-Dickson, San Jose, CA, USA). The population of the cells in the sub-G0/G1 phase with a low DNA content was considered to be apoptotic cells.
Western blot analysis
Sebocytes were prepared in cell lysis buffer contains 62.5 mM Tris-HCl (pH 6.8), 2% SDS, 5% β-mercaptoethanol, 2 mM PMSF, 1 mM Na3VO4, 50 mM NaF and 10 mM EDTA, and protease inhibitors (Roche Diagnostics, Indianapolis, IN, USA). SDS-polyacrylamide gel electrophoresis was performed using 10 μg of protein per lane. The gels were blotted onto polyvinylidene fluoride (PVDF; Millipore Corp., Billerica, MA, USA) membranes that were then saturated with 5% dried milk in Tris-buffered saline (TBS) with 0.5% Tween-20 (Sigma-Aldrich, Co.). The blots were incubated with the specific primary antibodies against p-ERK, ERK, p-AKT, AKT, PPAR-γ, cyclin D1, p21, p27 and β-actin overnight at 4°C. After washing, secondary antibodies (Cell Signaling Technology, Inc.) conjugated with horseradish peroxidase were used. Bound antibodies were detected using an ECL™ Prime Western Blotting Detection substrate (Amersham Pierce Biotechnology Inc., Rockford, IL, USA).
Statistical analysis
One-way ANOVA followed by Dunnett’s T3 test were used to assess statistical significance with thresholds of P<0.05, P<0.01 and P<0.001 indicating significant and highly significant differences, respectively.
Results
Resveratrol inhibits the proliferation of human SZ95 sebocytes
To investigate the effects of resveratrol on the proliferation of human sebocytes, we used a human SZ95 sebocyte cell line which was established by the simian virus-40 transformation of primary sebocytes derived from a human sebaceous gland (34). In the present study, in order to determine whether resveratrol exerts an antiproliferative effect on sebocytes, we treated the cells with various concentrations of resveratrol by adding it to the culture medium. Cell proliferation was assessed by MTT assay, and we found that resveratrol significantly decreased the proliferation of the SZ95 sebocytes in a dose- and time-dependent manner. Whereas cell proliferation was unaffected in the SZ95 sebocytes treated with resveratrol for 24 h, a significant inhibitory effect of resveratrol was observed at the indicated concentration after 72 h of incubation (Fig. 1A). After 72 h, treatment with resveratrol at concentrations of 1, 5, 10, 25 and 50 μg/ml decreased the cell numbers by 2.4±3.54, 22.3±7.47, 33.24±3.47, 72.53±8 and 66.46±3.49%, respectively, compared to the control levels. As shown in Fig. 1B, the cell numbers were distinctly reduced following treatment with resveratrol in a dose-dependent manner. This observation indicates that resveratrol exerts antiproliferative effects on SZ95 sebocytes.
Resveratrol induces the inactivation of ERK and Akt in human SZ95 sebocytes
We demonstrated that resveratrol inhibited the proliferation of SZ95 sebocytes. In order to determine the signaling pathways through which resveratrol inhibits sebocyte proliferation, we measured the changes in ERK and/or Akt protein levels following treatment with various concentrations of resveratrol. Our results revealed that the activation of ERK was decreased by treatment of the SZ95 sebocytes with resveratrol, and that the activation of Akt was markedly inhibited in the resveratrol-treated SZ95 sebocytes (Fig. 2A). Additionally, we analyzed cell cycle distribution using DNA flow cytometry following treatment with resveratrol for 72 h. Under the control conditions, the proportion of cells in the G0/G1 phase remained constant during the 72-h incubation period. On the contrary, the proportion of cells in the G0/G1 phase in the cells incubated with resveratrol was altered, and this decline was observed following treatment with 1–25 μg/ml of resveratrol. At high concentrations, this effect was reversible. The cell cycle distribution of the cells treated with 50 μg/ml of resveratrol only differed slightly from the values obtained for the control cells (Fig. 2B). Our results revealed that treatment with resveratrol resulted in a significant increase in the number of cells in the sub-G0/G1 phase of the cell cycle. Furthermore, we evaluated the effects of resveratrol on cell cycle progression by measuring the protein expression levels of cyclin D1, p21WAF1/CIP1 (p21) and p27KIP1 (p27). As shown in Fig. 2A, the protein level of cyclin D1 decreased in a dose-dependent manner following treatment with resveratrol, whereas the levels of p21 and p27 increased following treatment with resveratrol. These results suggest that the resveratrol-mediated cell cycle arrest is associated with the inactivation of the ERK and Akt signaling pathways.
Resveratrol enhances the antiproliferative effects exerted by PD098059 or LY294002 in human SZ95 sebocytes
The resveratrol-treated sebocytes were cultured for 72 h in the presence of PD098059 (a MEK inhibitor) or LY294002 (a PI3-K inhibitor), and cell proliferation was measured by MTT assay. As shown in Fig. 3A, at a concentration 10 μg/ml, resveratrol induced a 33±3.4% decrease in cell growth compared with the untreated controls. In order to determine the association of the ERK and Akt signaling pathways in the resveratrol-induced growth inhibitory effects, we treated the cells with the specific inhibitors, PD098059 and LY294002, and examined the antiproliferative effects of resveratrol and the inhibitors either alone or in combination. The SZ95 sebocytes were pre-treated with 50 μM PD098059, a specific inhibitor of MEK, for 1 h and or with 50 μM LY294002, a specific inhibitor of PI3-K, for 10min, and subsequently treated the cells with resveratrol. As shown in Fig. 3A, PD098059 alone inhibited sebocyte growth, and this PD098059-mediated inhibition was enhanced by resveratrol. In parallel, LY294002 alone inhibited sebocyte proliferation, and the combination treatment of LY294002 and resveratrol had a stronger inhibitory effect than the combination with PD098059. As a result, the inhibitory effects of resveratrol in combination with PD098059 (51.27±6.25%) and with LY294002 (77.94±4.09%) were demonstrated (Fig. 3A). In addition, the decrease in Akt protein levels was significantly enhanced by combination treatment with LY294002 and resveratrol (Fig. 3B). These results indicate that the Akt signaling pathway is important for sebocyte proliferation.
The induction of lipogenesis by LA in human SZ95 sebocytes is blocked by resveratrol
SZ95 immortalized human sebocyte differentiation is characterized by the intracellular accumulation of cytoplasmic lipid droplets, including neutral lipids (3). Lipid synthesis in SZ95 sebocytes is increased by diverse stimuli, such as androgens and fatty acids (35,36). LA and arachidonic acid are a known as free fatty acids and induce the accumulation of lipids in SZ95 sebocytes, which activates PPAR (37,38). In addition, the treatment of human sebocytes with LA (100 μM) has been shown to lead to the activation of all PPAR subtypes (12). In this study, to determine the role of resveratrol during sebocyte differentiation, we examined the inhibition of lipid formation in SZ95 sebocytes by treatment with resveratrol in the presence of LA. The sebocyte lipid content was detected by Oil Red O staining and then by ELISA, and cell morphology was determined by microscopic examination, as described in the Materials and Methods. When the SZ95 sebocytes were treated with 100 μM LA, Oil Red O staining revealed intracellular lipids and an enlarged number of lipid droplets in the cytoplasm surrounding the nucleus. Of note, although the intracellular lipid accumulation was further decreased in the SZ95 sebocytes following treatment with resveratrol and LA in comparison to treatment with LA alone (Fig. 4B), it was not influenced by treatment with the vehicle or by treatment with resveratrol alone. Additionally, the enhancement of lipogenesis by LA was significantly decreased in a dose-dependent manner by treatment with both resveratrol and LA (Fig. 4A), as evidenced by the results of microscopic visualization after Oil Red O staining.
To evaluate the inhibitory effect of resveratrol on PPAR-γ activation in LA-treated cells, we examined inactivation of PPAR-γ by resveratrol in the cells treated with LA. We found that the expression of PPAR-γ decreased in a dose-dependent manner in the SZ95 sebocytes treated with resveratrol (Fig. 2A). As shown in Fig. 4B, LA enhanced PPAR-γ expression in the SZ95 sebocytes, while treatment with resveratrol and LA inhibited the activation of PPAR-γ. Moreover, the activation of PPAR-γ was inhibited by treatment with resveratrol alone in comparison to the untreated SZ95 sebocytes (Fig. 4B). These results provide evidence of the effectiveness of resveratrol against sebocyte differentiation. Thus, our results suggest that lipid production is reduced by resveratrol and that this reducing effect by resveratrol is mediated through the inactivation of PPAR-γ in human sebocytes.
Discussion
The effectiveness of resveratrol (trans-3,4′,5-trihydroxystilbene) in the inhibition of cell growth, cell cycle arrest and apoptosis has been investigated in several human cancer cells, and has been shown to induce anticancer effects when used as a cancer therapy (22,24). In addition, a few studies have reported the antiproliferative effects of resveratrol on cell growth in normal cell types, although to date, the molecular mechanisms through which these effects occur are unknown (29,30). By contrast, the antioxidant effects of resveratrol on human skin cells have been shown to be mediated by protection against hydrogen peroxide through the prevention of lipid peroxidation and programmed cell death (14,15). Despite this fact, the antiproliferative effects of resveratrol in human sebocytes are not yet well understood and the mechanisms leading to the resveratrol-dependent cell growth inhibition have not been fully elucidated.
Studies utilizing a variety of cells have demonstrated the involvement of cell cycle arrest as a contributor to cell growth inhibition (24,39,40). Cell cycle progression is a complex biological process that includes cell growth and mitosis. This process is controlled by CDKs, CDK inhibitors and phosphorylation events (41). Therefore, the upregulation of the p21 and p27 inhibitors of CDKs has been associated with the disruption of the cell cycle and, conversely, the decreased expression of p21 has been shown to lead to increased proliferative activity (42). A number of cell types have been shown to respond to resveratrol treatment by cell cycle arrest (24–26), the accumulation of p21 (43,44) and the downregulation of cyclin D1 and CDK4 (27). In this study, to examine the association between cell growth inhibition by resveratrol and cell cycle arrest, we evaluated the involvement of the cell cycle progression machinery during the inhibition of proliferation by resveratrol in sebocytes. Our results demonstrated that the inhibition of cell growth by resveratrol involved a decrease in the expression of cyclin D1 and an enhanced expression of p21 and p27, which confirms that resveratrol exerts antiproliferative effects on SZ95 sebocytes by inducing cell cycle arrest. In addition, we demonstrated that the resveratrol-mediated cell cycle arrest resulted in an increase in the proportion of cells in the sub-G0/G1 phase, suggesting that resveratrol leads to the abrogation of DNA synthesis.
This study provides evidence that resveratrol significantly inhibits cell proliferation in a dose-dependent manner. Cell proliferation is regulated by a complex series of events that trigger intracellular signals, which included the activation of the ERK and Akt pathways (16–19). Therefore, as further elucidation is required, we investigated the mechanisms leading to cell growth inhibition by resveratrol in SZ95 sebocytes. The ERK pathway, one of the MAPK family proteins, is known to play key roles in cellular events, such as proliferation, differentiation and apoptosis and is activated by growth factors, such as EGF and platelet-derived growth factor (PDGF) (45,46). Resveratrol has previously been shown to promote growth inhibition by inhibiting the ERK pathway in K562 leukemia cells and normal human keratinocyte (47). In SZ95 sebocytes, we found that treatment with resveratrol resulted in a decrease in ERK phosphorylation in a concentration-dependent manner. In addition, our results revealed that the inhibition of the ERK pathway by PD98050 treatment, which is known to be a typical MEK inhibitor, caused cell growth inhibition, suggesting that the resveratrol-induced inactivation of ERK may be associated with an antiproliferative effect. Among the signaling pathways controlling cell growth, the Akt pathway plays a critical role in mediating both cell growth and apoptosis. Akt phosphorylation, a target signaling molecule of PI3-K, is activated when cells are exposed to IGF-1 or other growth factors (17). Our result revealed that resveratrol inactivated Akt in a dose-dependent manner, indicating that the antiproliferative effects of resveratrol are linked to the inactivation of the Akt pathway. Furthermore, in order to investigate the cell growth inhibition resulting from the inactivation of Akt by LY294002, a specific PI3-K inhibitor, we evaluated cell proliferation by MTT assay. Our data revealed that the inhibition of Akt by LY294002 induced cell growth inhibition, indicating that the inhibition of Akt phosphorylation by resveratrol may be involved in the growth-inhibiting mechanisms in SZ95 sebocytes.
Subsequently, we examined the effects of resveratrol on the proliferation of human sebocytes using specific inhibitors. SZ95 sebocytes were treated with resveratrol alone, or with resveratrol in combination with LY294002 or PD98050. We demonstrated that pre-treatment with PD98050 enhanced the resveratrol-mediated cell growth inhibition. In parallel, the resveratrol-induced inhibition of cell growth was increased by pre-treatment with LY294002 (Fig. 3A). Of note, the level of cell growth inhibition resulting from treatment with resveratrol in the presence LY294002 was greater than the antiproliferative effects of resveratrol in the presence PD098059. As shown in Fig. 3A, >67.02±4.09% of the cells were inhibited by treatment with resveratrol in the presence LY294002, compared with those treated with resveratrol only. Moreover, the phosphorylation of Akt in the resveratrol- and LY-treated cells decreased considerably to 57.23±0.26% in comparison to the cells treated with resveratrol alone (Fig. 3B). These findings suggest that resveratrol regulates cell proliferation through Akt activation, thereby suggesting a possible mechanism of action for resveratrol.
Currently, the majority of experimental and clinical studies using sebocytes are mainly focused on lipogenesis. Sebocytes are similar to adipocytes in that both cells accumulate lipids within their cytoplasms and comparable transcription factors are involved in lipid production. However, it has been reported that the secreted lipids in sebocytes differ from adipocytes-derived lipids (5). In addition, the excessive production of sebum in the sebaceous glands is pivotal in the pathogenesis of acne (7). During the process of sebum production, several transcription factors, including SREBP-1 and PPARs, are involved in lipogenic gene expression in sebocytes and are consequently involved in the pathogenesis of acne (13,16,48). PPAR-γ, one of 3 PPARs subsets, has been implicated in modulating the differentiation of adipocytes and sebocytes, and its activation also enhances lipid metabolism (11,49,50). In addition, it is known that the transcriptional activation of PPAR-γ requires the activation of both the PKA and PI3-K/Akt pathways. During lipid synthesis, PI3-K/Akt signaling is an important regulatory pathway for lipogenesis in sebocytes and adipocytes, and the lack of this pathway results in a complete defect in the differentiation process (16,51). Therefore, previous studies have demonstrated that resveratrol inhibits adipogenesis in 3T3-L1 adipocytes through the downregulation of PPAR-γ and Akt signaling (31,52). In addition, resveratrol has been found to inhibit lipid synthesis in rat liver and 3T3-L1 preadipocytes (32,33). On the other hand, the results of a previous study investigating the effects of inhibiting lipogenesis and the mechanisms of resveratrol in sebocytes were less conclusive (53). In the present study, in order to further examine the potential anti-lipogenic effects of resveratrol, we extended our experiments to sebocyte cells. We determined the effects of resveratrol on LA-induced lipogenesis. LA is a well-established lipid inducer in sebocytes and is known to stimulate sebocyte differentiation through the upregulation of PPAR-γ (11,54,55). In the current study, resveratrol was found to decrease the lipid content and PPAR-γ expression in LA-stimulated lipogenesis. The treatment of the cells with resveratrol at concentrations >5 μg/ml resulted in a significant reduction in their lipid content (Fig. 4A). A similar effect on cell morphology visualized by Oil Red O staining was observed using resveratrol at 10 μg/ml, whereas resveratrol alone did not result in these changes in morphology (Fig. 4B). In addition, the effects on the expression of PPAR-γ resulting from resveratrol treatment were investigated in human SZ95 sebocytes. Our results revealed that resveratrol resulted in a marked decrease in the expression of PPAR-γ in a concentration-dependent manner (Fig. 2A). Moreover, as shown in Fig. 4B, resveratrol abolished the activation of LA-stimulated PPAR-γ expression, indicating a possible mechanism of action for resveratrol. These data indicate that the potent anti-sebum effect of resveratrol is mediated through the inactivation of PPAR-γ transcription.
In conclusion, our results demonstrated that treatment with resveratrol resulted in a dose-dependent inhibition of proliferation and induced cell cycle arrest in human SZ95 sebocytes, which was associated with the stimulation of the p21 and p27 proteins and a decrease in cyclin D1 levels. Our results demonstrated that resveratrol reduced the phosphorylation levels of ERK and Akt. LY294002 as a chemical inhibitor of the Akt pathway further enhanced the antiproliferative effects of resveratrol in contrast to the effects observed in the PD098050-treated cells, indicating that the inactivation of Akt may play a critical role in the growth inhibitory effects of resveratrol. Furthermore, resveratrol also blocked the LA-induced transcription of PPAR-γ and sebocyte lipogenesis. These data suggest that treatment with resveratrol may be used as a therapeutic approach for the treatment of acne vulgaris.