Effects of ganoderic acid A on lipopolysaccharide-induced proinflammatory cytokine release from primary mouse microglia cultures.

For several thousand years, Ganoderma lucidum (Ling-Zhi in Chinese and Reishi in Japanese) has been widely used as a traditional medication for the prevention and treatment of various diseases in Asia. Its major biologically active components, ganoderic acids (GAs), exhibit significant medicinal value due to their anti-inflammatory effects. Dysregulation of microglial function may cause seizures or promote epileptogenesis through release of proinflammatory cytokines, including interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α. At present, only little information is available on the effects of GAs on microglia-mediated inflammation in vitro and/or in vivo. The present study aimed to investigate the role of GA-A on microglia-mediated inflammation in vitro. In addition, the effect of GA-A on lipopolysaccharide (LPS)-evoked alterations in mitochondrial metabolic activity of microglia was evaluated. The results of the present study demonstrated that GA-A significantly decreased LPS-induced IL-1β, IL-6 and TNF-α release from mouse-derived primary cortical microglial cells in a concentration-dependent manner. GA-A treatment reduced LPS-induced expression of nuclear factor (NF)-κB (p65) and its inhibitor, demonstrating that non-toxic suppression of IL-1β, IL-6 and TNF-α production by GA-A is, at least in part, due to suppression of the NF-κB signaling pathway. In addition, the LPS-induced stimulation of mitochondrial activity of microglial cells was abolished by co-treatment with GA-A. Thus, GA-A treatment may be a potential therapeutic strategy for epilepsy prevention by suppressing microglia-derived proinflammatory mediators.

Introduction

For several thousand years, Ganoderma (G.) lucidum (Ling-Zhi in Chinese and Reishi in Japanese) has been widely used as a traditional medication for the prevention and treatment of various human diseases in Asia (1). The major biologically active components of G. lucidum are polysaccharides and the secondary metabolites ganoderic acids (GAs), including GA-A, -B, -C, -D, -E and -F. Most GAs have a significant pharmacological potential; they were demonstrated to exhibit significant medicinal value with activities including inhibition of histamine release and cholesterol synthesis as well as antitumor and anti-inflammatory effects (2).

It was demonstrated that inflammation participates in the mediation of acute and chronic neurological disorders, including epilepsy and seizure (3). In human epilepsy patients and in experimental models of epilepsy, inflammatory processes, including activation of microglia and release of proinflammatory cytokines, have been described (4–6). Emerging evidence thus supports the hypothesis that inflammation may contribute to epileptogenesis. Microglia are intimately associated with diverse neuronal functions, such as modulation of synaptic function and plasticity, regulation of the delivery of energy substrates and enforcement of cellular immunity in the brain to restore function and promote healing, which helps to maintain tissue homeostasis (7). However, dysregulation of microglial functions may cause seizures or promote epileptogenesis. Activation of microglia through increases of excitability and inflammation is a prominent feature of epileptic foci in the human brain and in experimental epilepsy models (8–10). Uncontrolled microglia-mediated immunity may cause sustained release of inflammatory cytokines, including interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α, to facilitate epileptogenesis (11).

GAs, the triterpenoid components of G. lucidum mushroom extracts, are attractive sources of anti-inflammation products. Although numerous studies have reported that GAs exhibit anti-inflammatory and antitumor properties in animal models mainly through the induction of cytokines such as IL-1, IL-6, interferon-γ and TNF-α in monocytes/macrophages and T lymphocytes (12–14), encouraging the potential use of GAs in combination therapy against inflammation and cancer, little information is available on their in vitro and in vivo effect on microglia-mediated inflammation. The present study aimed to investigate the role of GA-A on microglia-mediated inflammation in vitro. In addition, the effect of GA-A on lipopolysaccharide (LPS)-evoked alterations in mitochondrial metabolic activity of microglia was evaluated.

Materials and methods

Reagents and chemicals

GA-A, poly-L-ornithine hydrobromide, dimethyl sulphoxide (DMSO), deoxyribonuclease I from bovine pancreas (DNaseI), penicillin-streptomycin, MTT and LPS were purchased from Sigma-Aldrich (Merck KGaA, Darmstadt, Germany). Mouse monoclonal anti-CD68 antibody conjugated to phycoerythrin (PE) was purchased from eBioscience (San Diego, CA, USA; cat. no. 12-0681-82). Mouse monoclonal anti-CD11b antibody conjugated to fluorescein isothiocyanate was purchased from ProSpec-Tany Technogene Ltd. (East Brunswick, NJ, USA; cat. no. ANT-136). High-glucose Dulbecco's modified Eagle's medium (DMEM), PBS, 0.05% (w/v) trypsin-EDTA and fetal bovine serum (FBS) were obtained from Thermo Fisher Scientific, Inc. (Waltham, MA, USA).

Isolation and culture of primary microglia

The primary microglia cultures were established as follows: Mixed glial cultures from male C57BL/6 mice, purchased from the Animal Centre of the Xiangya Third Hospital (Changsha, China) were established from neonatal cortices (postnatal day 0–1; n=5; mean weight, 1.4 g) (15). Cells were cultured in high-glucose DMEM supplemented with 10% FBS, penicillin and streptomycin in a humidified atmosphere of 95% air and 5% CO2 at 37°C. The culture medium was replaced with fresh medium 24 h after the initial preparation and every 3 days thereafter. Following 1 week of culture, microglia were obtained by mechanical shaking of the mixed glial cell cultures for 1 h. Cells were routinely monitored for purity by fluorescence-activated cell sorting and the population of CD11b+ CD68+ cells was >80% (Fig. 1). All experimental procedures were approved by the Xiangya Third Hospital Ethics Committee for Experimentation on Animals (Changsha, China), where the cultures were established.

Figure 1.

Primary microglial cells were isolated from mice cerebral cortex and identified by fluorescence-activated cell sorting following staining with anti-CD11b-FITC and CD68-PE antibodies. CD11b- and CD68-positive cells were indicated as microglial cells (~80%). FITC, fluorescein isothiocyanate; PE, phycoerythrin.

Cell treatment

To induce the release of proinflammatory cytokines, microglia were treated with DMEM containing 0.1 µg/ml LPS or vehicle for 24 h. To investigate the role of GA-A in LPS-induced release of cytokines, microglial cells were treated with a range of concentrations of GA-A (10, 20, 50 or 100 µg/ml), or co-treated with LPS. Cells treated with vehicle were used as a control.

RNA extraction and SYBR green quantitative polymerase chain reaction (qPCR) analysis

Total RNA was extracted from cells using TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc.). RevertAid™ First Strand cDNA Synthesis kit (Thermo Fisher Scientific, Inc.) was used to reverse transcribe the mRNA to cDNA according to the manufacturer's protocol. Briefly, 0.5 ng of the template RNA, 1 µl Oligo(dT)18 Primer and 12 µl RNase free water were mixed, and incubated at 65°C for 5 min, then cooled down on ice. The mixture was added to Reaction Buffer (4 µl), RiboLock RNase inhibitor (1 µl), 10 mM dNTP mix (2 µl) and RevertAid Reverse Transcriptase (1 µl), and incubated at 42°C for 1 h. Finally, the mixture was heated to 70°C for 5 min to obtain the cDNA. The expression of IL-1β, IL-6 and TNF-α in cells was detected using a SYBR Fast qPCR mix (cat. no. RR430A; Takara, Dalian, China) at following condition: 95°C for 30 sec, followed by 40 cycles of 95°C for 5 sec and 60°C for 10 sec. Expression of β-actin was assessed as an endogenous control. The mRNA levels were quantified using the 2−ΔΔCq method (16).

Measurement of the release of IL-1β, IL-6 and TNF-α

Levels of IL-1β, IL-6 and TNF-α were measured in supernatants of the primary mouse microglia cell culture with commercially available ELISA kits (Sigma-Aldrich; Merck KGaA) according to the manufacturer's instructions. Measurements were performed in three independent experiments.

Western blot analysis

Immunoblotting was performed to detect the expression of IL-1β, IL-6 and TNF-α in the cell lysate, as well as the levels of nuclear factor (NF)-κB and phosphorylated inhibitor of NF-κB (p-IκBα) in microglial cells. Cultured or transfected cells were lysed in radioimmunoprecipitation assay buffer with 1% phenylmethane sulfonyl fluoride. The concentration of protein was determined using the BCA Protein Assay kit (cat. no. P0011; Beyotime Institute of Biotechnology, Haimen, China) according to the manufacturer's protocol. A total of 60 µg/lane of protein was loaded into a 12% SDS-PAGE minigel, electrophoresed and transferred onto a polyvinylidene difluoride membrane (Wuhan Boster Biological Technology, Ltd., Wuhan, China). The membranes were probed with antibodies directed against IL-1β (cat. no. I3767; 1:1,000), IL-6 (cat. no. SAB4301665; 1:1,000) and TNF-α (cat. no. SAB4502982; 1:2,000) from Sigma-Aldrich (Merck KGaA); p-IκBα (cat. no. 9246S; 1:1,000) and NF-κB (cat. no. 8242; 1:3,000) from Cell Signaling Technology, Inc. (Danvers, MA, USA); GAPDH (cat. no. ab9485; 1:3,000) from Abcam (Cambridge, UK) at 4°C overnight. The blots were subsequently incubated with horseradish peroxidase-conjugated secondary antibodies (cat. no. ab7090 and ab97040; 1:5,000; Abcam) for 1 h at 37°C. Signals were visualized using enhanced chemiluminescence substrate (EMD Millipore, Billerica, MA, USA). GAPDH was used as an endogenous protein for normalization.

Measurement of the mitochondrial metabolic activity

The mitochondrial activity of microglial cells was determined by measurement of MTT reduction to MTT formazan by cellular mitochondrial dehydrogenases. After incubation with GA-A for 24 h, MTT (0.5 mg/ml) was added to the medium, followed by incubation for 4 h at 37°C. Subsequently, dimethyl sulfoxide (150 µl) was added to dissolve the formazan crystals and the absorbance was measured at 570 nm using a microplate reader (Paradigm Detection Platform; Beckman Coulter, Brea, CA, USA); this value was proportional to the number of viable cells with intact mitochondria. Measurements were performed in three independent experiments.

Statistical analysis

Values are expressed as the mean ± standard error. Statistical analysis was performed using SPSS software (version 20; IBM Corp., Armonk, NY, USA). Student's t-test was performed for two-group comparisons, while one-way analysis of variance with Tukey's post-hoc test was performed for multiple-group comparisons. P<0.05 was considered to indicate a statistically significant difference.

Results

Effects of GA-A on LPS-induced release of IL-1β, IL-6 and TNF-α from cortical microglial cells in culture

To investigate the role of GA-A on LPS-induced release of IL-1β, IL-6 and TNF-α from mouse cortical microglial cells, the cells were treated with 0.1 µg/ml LPS for 24 h. Treatment with LPS resulted in a potent, 80-, 42- and 110-fold increase in IL-1β, IL-6 and TNF-α release, respectively (Fig. 2A). In addition, the microglial cells were treated with a range of concentrations of GA-A (10, 20, 50 and 100 µg/ml) for 24 h. The results indicated that GA-A treatment slightly but not significantly altered the release of IL-1β, IL-6 and TNF-α (Fig. 2B-D). GA-A increased IL-1β at 20 µg/ml, and IL-6 at 10 and 20 µg/ml; GA-A at 100 µg/ml decreased the release of IL-1β, IL-6 and TNF-α to ~75% of that in the control group, but this effect was not statistically significant (Fig. 2B-D).

Figure 2.

Effects of LPS on the release of IL-1β, IL-6 and TNF-α from mouse cortical microglial cells in culture. (A) The cells were treated with LPS (0.1 µg/ml) for 24 h, and ELISA were used to determine the release of IL-1β, IL-6 and TNF-α. (B-D) The cells were treated with GA (10, 20, 50 or 100 µg/ml) for 24 h and ELISA was used to determine the release of (B) IL-1β, (C) IL-6 and (D) TNF-α. Values are expressed as the mean ± standard error of the mean and relative to the control. Three independent experiments were performed. ***P<0.001 vs. control. IL, interleukin; TNF, tumor necrosis factor; LPS, lipopolysaccharide; GA, ganoderic acid A.

Furthermore, it was determined whether GA-A treatment was able to abolish the LPS-induced release of IL-1β, IL-6 and TNF-α from mouse cortical microglial cells. First, RT-qPCR was performed to detect whether the levels of IL-1β, IL-6 and TNF-α were affected at the transcriptional level, revealing that GA-A treatment (50 µg/ml) did not significantly alter the cellular mRNA expression of IL-1β, IL-6 and TNF-α (Fig. 3A). However, ELISAs indicated that GA-A treatment (10, 20, 50 or 100 µg/ml) for 24 h caused a statistically significant reduction of LPS-stimulated release of IL-1β from primary mouse microglial cells in a concentration-dependent manner (Fig. 3B). At lower concentrations (10 µg/ml), the drug did not cause any significant decrease of IL-6 and TNF-α release (Fig. 3C and D). However, IL-6 and TNF-α release were markedly reduced at higher concentrations of the drug (50 and 100 µg/ml; Fig. 3C and D). The most prominent effect was observed at a dose of 100 µg/ml (a decrease by 30, 32 and 22% for IL-1β, IL-6 and TNF-α, respectively). These results were confirmed by western blot analysis for IL-1β, IL-6 and TNF-α expression in cell lysate (Fig. 3E).

Figure 3.

Effects of GA on LPS-induced release of IL-1β, IL-6 and TNF-α from mouse cortical microglial cells in culture. (A) The cells were treated with GA (50 µg/ml) for 24 h, and total RNA was then extracted. Quantitative polymerase chain reaction was used for analysis of the mRNA levels of IL-1β, IL-6 and TNF-α. (B-D) The cells were treated with LPS alone or co-treated with LPS and GA (10, 20, 50 and 100 µg/ml) for 24 h, and ELISA was used to determine the release of (B) IL-1β, (C) IL-6 and (D) TNF-α. (E) Western blot was performed to analyze the expression of IL-1β, IL-6 and TNF-α in cell lysate after the indicated treatments (left) and quantification (right). Values are expressed as the mean ± standard error of the mean and relative to the control that was treated with LPS alone. Three independent experiments were performed. *P<0.05, **P<0.01 vs. control. IL, interleukin; TNF, tumor necrosis factor; LPS, lipopolysaccharide; GA, ganoderic acid A.

GA-A inhibits LPS-induced NF-κB pathway activation

Microglial cells were then treated with GA-A (0, 10 or 50 µg/ml) and stimulated with LPS (0.1 µg/ml). Western blot analysis of the total protein extract indicated that treatment with GA-A at 10 and 50 µg/ml reduced LPS-induced p-IκBα and NF-κB (p65) expression, with 50 µg/ml being more effective (Fig. 4A). These results revealed that GA-A inhibited LPS-induced NF-κB pathway activation, which may suggest that that non-toxic suppression of IL-1β, IL-6 and TNF-α production by GA-A is, at least in part, due to suppression of the NF-κB signaling pathway.

Figure 4.

Effect of GA on LPS (0.1 µg/ml)-induced changes in the NF-κB signaling pathway and mitochondrial activity of mouse cortical microglial cells in culture. (A) Western blot was performed to analyze the expression of p-IκB and p-p65 in microglial cells after the indicated treatments (left), and quantification (right). (B) The cells were treated with GA (10, 20, 50, 100 µg/ml), or vehicle (control) for 24 h, and MTT were used to determine the mitochondrial activity of microglia cells. (C) The cells were treated with LPS alone, or co-treated with LPS and GA (10, 20, 50 or 100 µg/ml), or vehicle (control) for 24 h, and the MTT assay was used to determine the mitochondrial activity of microglial cells. Values are expressed as the mean ± standard error of the mean and relative to the control treated with vehicle. Three independent experiments were performed. #P<0.05 vs. control, *P<0.05, **P<0.01 vs. LPS alone. GA, ganoderic acid A; LPS, lipopolysaccharide; NF-κB, nuclear factor κB; p-IκBα, phosphorylated inhibitor of NF-κB.

GA-A reduces LPS-induced increases in mitochondrial activity of mouse cortical microglia cells

GA-A treatment (10, 20, 50 or 100 µg/ml for 24 h) did not significantly alter the mitochondrial activity of microglial cells (Fig. 4B), while cells stimulated with LPS (0.1 µg/ml) for 24 h exhibited a significant increase in their mitochondrial activity by 50% (Fig. 4C). The increase of mitochondrial activity induced by LPS was markedly attenuated by treatment of the cells with GA-A used at 10 and 20 µg/ml, and was abolished by higher concentrations of the drug (50 and 100 µg/ml; Fig. 4C).

Discussion

The present study demonstrated, for the first time, to the best of our knowledge, the effects of GA-A on LPS-stimulated release of proinflammatory cytokines from primary mouse microglia cultures. To date, only a few studies have examined the effects of GA-A on microglia-mediated inflammation (17). Microglial cells are brain-resident macrophage-like cells that contribute to innate immune mechanisms (18). Microglia-mediated inflammation was reported to have an important role in the pathogenesis of epilepsy (19). In response to stressors, microglia are activated, leading to the release of proinflammatory mediators that may promote seizures and epileptogenesis, particularly when uncontrolled inflammation occurs (5). Of note, the extent of microglia activation correlates with the frequency and duration of seizures (20).

Activated microglial cells release cytokines that induce transcriptional and post-transcriptional signaling. For instance, microglia release a variety of pro-inflammatory and cytotoxic soluble factors, including IL-1β and IL-6, and subsequent activation of the proinflammatory IL-1 receptor/Toll-like receptor (IL1R/TLR) system (21). In epilepsy models, this IL1R/TLR signaling is activated, which promotes the onset and recurrence of seizures (22). Of note, pharmacological blockade or genetic inactivation of the IL1R/TLR system drastically reduces seizure activity (23). IL-1β increases glutamate release via TNF-α production, resulting in elevated extracellular glutamate levels and hyperexcitability (24). Furthermore, IL-1β also stimulates IL-6 release (25). After a febrile seizure, children had significantly higher serum IL-6 levels than a healthy control group (26), and IL-6 levels had a descending trend during the time of recovery from the seizure in the intractable epilepsy group and the non-intractable epilepsy group (27), indicating that high IL-6 levels may be a pathogenetic factor in epilepsy.

LPS is a component of the wall of Gram-negative bacteria, which may induce immediate focal epileptic-type discharges in the mouse neocortex mediated by IL-1β release (28). LPS activates microglia via TLR4. Endogenous ligands of TLR4, including IL-1β, may be generated by microglia following brain injury, mimicking the effect of LPS (29). An animal study indicated that activated microglia release proinflammatory molecules to decrease the seizure threshold (30). Consequently, microglia may help generate seizures by releasing, and responding to, endogenous inflammatory mediators, including IL-1β and TNF-α (31). For instance, chemokine-activated microglia cooperated with astrocytes to release TNF-α and other cytokines, thereby contributing to cell loss and seizures (32).

Anti-inflammatory molecules then help to resolve the inflammatory tissue response. Clinical anti-inflammatory or immunosuppressive treatments may control seizures in certain epileptic syndromes. For instance, intravenous immunoglobulin (IVIG) increases circulating levels of IL-1 receptor antagonist and blocks IL-1β signaling (33,34). IVIG suppresses seizures, which may be partially mediated by the reduction of proinflammatory cytokines and suppression of microglia activation (35).

Numerous studies have indicated that GAs enhance the immune system. Akihisa et al (36) identified four GAs isolated from the fruiting bodies of the fungus G. lucidum and identified that these GAs inhibit 12-O-tetradecanoylphorbol-13-acetate-induced inflammation in mice. The triterpene extract from G. lucidum markedly suppressed the secretion of the inflammatory cytokines TNF-α and IL-6, as well as the inflammatory mediator nitric oxide from LPS-stimulated murine RAW264.7 cells (37). In addition, natural killer cell activity was significantly enhanced by intraperitoneal administration of GA-Me (38). The anti-inflammatory properties of purified GAs encourage the potential use of GAs in combination therapy against inflammation.

The present study demonstrated that GA-A significantly decreased LPS-induced IL-1β, IL-6 and TNF-α release from primary mouse cortical microglial cells in a concentration-dependent manner. Furthermore, GA treatment did not alter the mRNA expression of IL-1β, IL-6 and TNF-α, but decreased the release of IL-1β, IL-6 and TNF-α in the cell culture medium, indicating that GA may target the release of cytokines. LPS induces proinflammatory cytokines, including IL-1β, IL-6 and TNF-α, through the activation of several intracellular signaling pathways such as NF-κB (39). A previous study demonstrated that G. lucidum extracts significantly and non-toxically suppressed TNF-α production by murine macrophages induced by peripheral blood mononuclear cells from asthma patients (12). Furthermore, the inhibitory effect of G. lucidum extracts on LPS-induced TNF-α production by macrophages was associated with the suppression of NF-κB signaling. In line with these previous studies, the results of the present study indicated that GA treatment reduced LPS-induced p-IκBα and NF-κB (p65) expression, suggesting that non-toxic suppression of IL-1β, IL-6 and TNF-α production by GA is, at least in part, due to suppression of NF-κB signaling. Although the results of the present study indicate GA regulates the IL-1β, IL-6 and TNF-α production through NF-κB at transcriptional level, other mechanism by which GA control the cytokines protein production cannot be excluded, such as the ubiquitin pathway (40).

Since the alterations of microglial function have an impact on neuronal excitability and epileptic activity, the present study also examined the effect of GA-A on the metabolic activity in mitochondria. In line with other studies (41,42), the results of the present study indicated that LPS stimulation resulted in significant increase in mitochondrial activity of microglial cells, and this effect was abolished by co-treatment with GA-A. A previous study identified that GA-T treatment resulted in a reduction of mitochondrial membrane potential and release of cytochrome C, as well as subsequent apoptosis in lung cancer cells, suggesting that the apoptosis induction of GA-T may be mediated by mitochondrial dysfunction (43). However, incubation in GAC2-conditioned media attenuated mitochondrial defects in a 3-nitropropionic acid (3-NP) cell model, and G. lucidum treatment therapeutically restored neuronal loss in mice with 3-NP-induced behavioral impairment and striatal degeneration (44). Whether the effects of GA-A on LPS-induced changes in mitochondrial activity of microglial cells are involved in the drug's action on the release of proinflammatory cytokines remains to be elucidated.

In conclusion, the results of the present study demonstrated that GA-A reduced the LPS-induced release of proinflammatory cytokines, IL-1β, IL-6 and TNF-α from mouse cortical microglial cells in culture at least in part via suppression of the NF-κB signaling pathway, and suppressed the LPS-stimulated increase in mitochondrial metabolic activity of the cells. Thus, treatment with GA-A may be potential therapeutic strategy for epilepsy via suppression of microglia-derived proinflammatory mediators.