Apigenin and luteolin modulate microglial activation via inhibition of STAT1-induced CD40 expression
- Kavon Rezai-Zadeh†1,
- Jared Ehrhart†1,
- Yun Bai1,
- Paul R Sanberg2,
- Paula Bickford2, 3,
- Jun Tan1, 2 and
- R Douglas Shytle1, 2Email author
© Rezai-Zadeh et al; licensee BioMed Central Ltd. 2008
Received: 16 January 2008
Accepted: 25 September 2008
Published: 25 September 2008
It is well known that most neurodegenerative diseases are associated with microglia-mediated inflammation. Our previous research demonstrates that the CD40 signaling is critically involved in microglia-related immune responses in the brain. For example, it is well known that the activation of the signal transducer and activator of transcription (STAT) signaling pathway plays a central role in interferon-gamma (IFN-γ)-induced microglial CD40 expression. We and others have previously reported that microglial CD40 expression is significantly induced by IFN-γ and amyloid-β (Aβ) peptide. Recent studies have shown that certain flavonoids possess anti-inflammatory and neuroprotective properties distinct from their well-known anti-oxidant effects. In particular, flavonoids, apigenin and luteolin have been found to be effective CD40 immunomodulators.
Cultured microglia, both N9 and primary derived lines, were treated with flavonoids in the presence of IFN-γ and/or CD40 ligation to assess any anti-inflammatory effects and/or mechanisms. CD40 expression on microglia was analyzed by fluorescence activated cell sorting (FACS). Anti-inflammatory effects and mechanisms were confirmed by ELISA for interlekin-6 (IL-6) and TNF-α, lactate dehydrogenase (LDH) assay, and STAT1 Western blotting.
Apigenin and luteolin concentration-dependently suppressed IFN-γ-induced CD40 expression. Apigenin and luteolin also suppressed microglial TNF-α and IL-6 production stimulated by IFN-gamma challenge in the presence of CD40 ligation. In addition, apigenin and luteolin markedly inhibited IFN-γ-induced phosphorylation of STAT1 with little impact on cell survival.
Our findings provide further support for apigenin and luteolin's anti-inflammatory effects and suggest that these flavonoids may have neuroprotective/disease-modifying properties in various neurodegenerative disorders, including Alzheimer's disease (AD).
Multiple lines of evidence suggest microglia, the resident immune cells of the central nervous system (CNS), play a critical role in the etiology of various neurodegenerative diseases. Chronic activation of microglia is believed to trigger and maintain an inflammatory response, which may ultimately lead to neuronal cell death such as that observed in Alzheimer's disease (AD), HIV-dementia, Parkinson's disease, prion disease, amyotrophic lateral sclerosis, and multiple sclerosis [1–11]. In fact, this chronic activation exposes the CNS to elevated levels of a wide array of potentially neurotoxic molecules including pro-inflammatory cytokines, complement proteins, proteinases, and reactive oxygen species (ROS) [12–17]. Conversely, an alternative view suggests that dysregulation of microglial activation may prevent appropriate immune responses necessary to respond to neuroinsults . Essential to microglial activation is the stimulatory signal from CD40 ligation. CD40 and its ligand (CD40L) are key immunoregulatory molecules that provide co-stimulatory input to cells from both the innate and adaptive arms of the immune system [19–22]. The classical stimulatory signal for microglial activation is propagated by T-cell release of interferon-gamma (IFN-γ), which consequently sensitizes the microglia by upregulating the expression of various immunoregulatory molecules, including CD40, on their cell surfaces [23, 24]. Furthermore, it is well known that the activation of the Janus kinase/signal transducer and activator of transcription (JAK/STAT) signaling pathway plays a central role in this IFN-γ-induced microglial CD40 expression [25, 26]. We have previously reported that microglial CD40 expression is significantly increased by IFN-γ in the presence of β-amyloid (Aβ) peptide via STAT1 activation [27, 28]. Accordingly, modulation of the JAK/STAT signaling pathway may not only prove to be an effective means for suppressing microglial-mediated inflammation but also an important target for neurodegenerative disease therapy.
While several anti-inflammatory drugs have been found to prevent microglial-mediated inflammation, their underlying mechanisms remain unclear and the search for more effective practical compounds continues. Recent research has focused on the analysis of flavonoids, which epidemiological study suggest are beneficial against the neurodegeneration and aging processes [29–33]. Flavonoids, a group of phenolic phytochemicals, are common in vascular plants and are abundant in particular spices, vegetables, and fruits. They are considered important constituents in the human diet, although their daily intake varies with dietary habits [34, 35]. Several medicinal properties have been ascribed to flavonoids, notably anti-oxidant [36, 37], anti-carcinogenic [38, 39], and anti-inflammatory activity [40–42]. One such flavonoid, apigenin, and its phase I metabolite, luteolin, have been found to reduce CD40 and CD40L expression on dendritic cells and basophils, respectively [43, 44]. Previous research has also shown apigenin's ability to inhibit pro-inflammatory cytokines production by monocytes, macrophages, and microglia and further substantiates this compound as versatile immunomodulator [45–49].
In the present study, we investigate the potential anti-inflammatory effects and mechanisms of these flavonoids, apigenin and luteolin, in cultured microglia. Our findings demonstrate that treatment of both N9 and murine-derived primary microglia cell lines with apigenin and luteolin significantly reduces CD40 expression induced by IFN-γ. This reduction is paralleled by significant decreases in the release of the pro-inflammatory cytokines interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) by the microglia. Furthermore, data show that apigenin and luteolin treatments achieve these reductions through inactivation of STAT1 and suggest a mechanism whereby these compounds may prove to be an effective therapy for neurodegeneration.
Animals and microglial cell cultures
Breeding pairs of BALB/c mice were purchased from Jackson Laboratory (Bar Harbor, ME) and housed in the animal facility at the University of South Florida, College of Medicine. Murine primary culture microglia were isolated from mouse cerebral cortices and grown in RPMI 1640 medium supplemented with 5% FCS, 2 mM glutamine, 100 U/ml penicillin, 0.1 μg/ml streptomycin, and 0.05 mM 2-mercaptoethanol according to previously described methods . Briefly, cerebral cortices from newborn mice (1–2 day-old) were isolated under sterile conditions and were kept at 4°C before mechanical dissociation. Cells were plated in 75 cm2 flasks and complete medium was added. Primary cultures were kept for 14 days so that only glial cells remained and microglial cells were isolated by shaking flasks at 200 rpm in a Lab-Line incubator-shaker. More than 98% of these glial cells stained positive for microglial marker Mac-1 (CD11b/CD18; Boehringer Mannheim, Indianapolis, IN; data not shown). All animal protocols were approved by the Committee of Animal Research at the University of South Florida, in accordance with the National Institutes of Health guidelines. N9 microglial originally generated from myc-immortalized mice were cultured as previously described [50, 51]. Briefly, N9 microglial cells were maintained and plated in 75 cm2 flasks with MEM medium supplemented with 5% FCS and 2 mM glutamine.
Flow cytometric analysis of microglial CD40 expression
Primary cultured microglial cells were plated in 6-well tissue culture plates at 5 × 105 cells/well and incubated with apigenin and luteolin at different doses in the presence or absence of IFN-γ (100 U/ml). Eight hours after incubation, these microglial cells were washed with flow buffer [PBS containing 0.1% (w/v) sodium azide and 2% (v/v) FCS] and re-suspended in 250 μl of ice-cold flow buffer for fluorescence activated cell sorting (FACS) analysis, according to methods described previously . Briefly, cells were pre-incubated with anti-mouse CD16/CD32 monoclonal antibody (clone 2.4G2, PharMingen, Los Angeles, CA) for 10 min at 4°C to block non-specific binding to Fc receptors. Cells were then spun down at 5,000 g washed 3 times with flow buffer and then incubated with hamster anti-mouse CD40-FITC or isotype control antibody-FITC (1:100 dilution; PharMingen) in flow buffer. After 30 min incubation at room temperature, cells were washed twice with flow buffer, re-suspended in 250 μL of flow buffer and analyzed by a FACScan™ instrument (Becton Dickinson, Franklin Lanes, NJ). A minimum of 10,000 cells were accepted for FACS analysis. Cells were gated based on morphological characteristics such that apoptotic and necrotic cells were not accepted for FACS analysis using CellQuest™ software (Beckton Dickinson). Percentages of positive cells (i.e. CD40-expressing) were calculated as follows: for each treatment, the mean fluorescence value for the isotype-matched control antibody was subtracted from the mean fluorescence value for the CD40-specific antibody.
TNF-α, IL-6, and LDH analyses
Murine primary cultured microglial cells were plated in 24-well tissue-culture plates (Costar, Cambridge, MA) at 1 × 105 cells per well and stimulated for 12 hr with either IFN-γ (100 U/ml)/CD40 agonistic antibody (2 μg/ml) (R&D Systems, Minneapolis, MN) in the presence or absence of apigenin and luteolin at a range of concentrations. Cell-free supernatants were collected and stored at -70°C until analysis. TNF-α and IL-6 levels in the supernatants were examined using ELISA kits (R&D Systems) in strict accordance with the manufacturers' protocols. Cell lysates were also prepared and the BCA protein assay (Pierce Biotechnology, Rockford, IL) was performed to measure total cellular protein. Results are shown as mean pg of TNF-α or IL-6 per mg of total cellular protein (+/- SD). Cell death was measured from lactate dehydrogenase (LDH) release in the cell-free supernatants using a CytoTox 96® Non-Radioactive Cytotoxicity Assay kit (Promega, Madison, WI).
STAT1 signaling pathway analysis
Primary culture microglial cells were plated in 6-well tissue culture plates at a density of 5 × 105 cells per well and co-incubated with IFN-γ (100 U/mL) in the presence or absence of a dose range of apigenin or luteolin for 30 min. At the end of the treatment period, microglial cells were washed in ice-cold PBS three times and lysed in ice-cold lysis buffer. After incubation for 30 min on ice, samples were centrifuged at high speed for 15 min, and supernatants were collected. Total protein content was estimated using the BCA protein assay (Pierce Biotechnology). Aliquots corresponding to 100 μg of total protein was electrophoretically separated using 10% Tris gels. Electrophoresed proteins were then transferred to PVDF membranes (Bio-Rad, Richmond, CA), washed in dH2O, and blocked for 1 hour at ambient temperature in TBS containing 5% (w/v) non-fat dry milk. After blocking, membranes were hybridized for 1 h at ambient temperature with various primary antibodies. Membranes were then washed 3 × for 5 min each in dH2O and incubated for 1 hour at ambient temperature with the appropriate HRP-conjugated secondary antibody (1:1,000, Pierce Biotechnology). All antibodies were diluted in TBS containing 5% (w/v) of non-fat dry milk. Blots were developed using the luminol reagent (Pierce Biotechnology). Densitometric analysis was conducted using a FluorS Multiimager with Quantity One™ software (BioRad, Hercules, CA). For STAT1 phosphorylation, membranes were probed with a phospho-Ser727 STAT1 antibody or a phospho-Tyr701 STAT1 antibody (Cell Signaling Technology, Danvers, MA) and stripped with stripping solution and then re-probed with antibody that recognize total STAT1 (Cell Signaling Technology).
All data were normally distributed; therefore, in instances of single mean comparisons, Levene's test for equality of variances followed by t-test for independent samples was used to assess significance. In instances of multiple mean comparisons, analysis of variance (ANOVA) was used, followed by post-hoc comparison using Bonferonni's method. Alpha levels were set at 0.05 for all analyses. The statistical package for the social sciences release 10.0.5 (SPSS Inc., Chicago, IL, USA) was used for all data analysis.
Apigenin and luteolin suppress IFN-γ-induced CD40 expression in N9 and murine-derived primary microglial cells
Apigenin and luteolin oppose the effects of IFN-γ/CD40 ligation on TNF-α and IL-6 production in N9 and murine-derived primary microglial cells
Apigenin and luteolin inhibit IFN-γ-induced STAT1 phosphorylation in N9 and murine-derived primary microglial cells
Compounds that modulate microglial activity would be indispensable tools in neurodegenerative disease therapy. Here, we identify two flavonoids, apigenin and luteolin, that reduce CD40 expression on microglia and elucidate a mechanism whereby these compounds may prevent harmful neuroinflammation. The transcription factor STAT1 has been a potential therapeutic target in our previous neurodegeneration research. It is becoming evident that STAT1 and related signaling proteins may be regulated by flavonoids. Apigenin and luteolin appear to affect the phosphorylation status of tyrosine 701 and serine 727, which is required for STAT dimerization and maximal activation of transcription, respectively [53, 54]. Even though we do observe slight increases in serine 727 STAT1 phosphorylation with flavonoid treatment alone (Fig. 4 and 5), it is likely that this phenomenon is related to these compounds' pro-apoptotic effects evidenced in tumor cell lines [55, 56]. In a study by Elsisi and colleagues, apigenin was found to induce apoptosis in the BV-2 microglial cell line after 24 hours of incubation . However, in our present study it is apparent that a 25 μM concentration of apigenin may be at worst cytostatic towards both the primary derived and the "transformed/immortalized" N9 microglia with treatment times under 24 hours (Fig. 2C and 2D). It has been reported that regulation of apoptosis via STAT1 is dependent upon serine 727 phosphorylation [58–60]. In contrast, we observe significant reductions in serine 727 phosphorylation with apigenin in N9 microglia and luteolin in both N9 and primary microglia in the presence of IFN-γ (Fig. 4 and 5). Therefore, it may be likely that the pro-apoptotic/anti-carcinogenic and immunomodulatory mechanisms of these flavonoids interface at the level of STAT1, a molecule qualified to function in this capacity. Still, distinct differences between these mechanisms may be dependent on the microenvironment and remain to be established.
While phosphorylation of tyrosine residue 701 on STAT1 is an event essential for STAT dimerizaton and translocation, it neither is a required precursor to serine 727 phosphorylation nor a mediator of apoptosis [58–60]. However, it appears to be as necessary as serine 727 phosphorylation for STAT1 signaling as apigenin effectively reduces CD40 expression in the presence of IFN-γ in primary microglia (Fig. 2B). Interestingly, we find that apigenin appears to regulate tyrosine 701 phosphorylation, but not serine 727 phosphorylation, of STAT1 in primary microglia, which suggests that it has a distinct target/mechanism separate from that of luteolin. Furthermore, these mechanistic differences underscore the differences inherent between primary derived and N9 microglia.
The ability of these flavonoids to regulate CD40-CD40L interaction and consequently pro-inflammatory mediators may be useful in the treatment of many inflammatory diseases. Nonetheless, inflammation in neurodegenerative disease represents a specific immunoprofile, involving discrete units made up of glial cells and neurons. Complete abolishment of CD40-CD40L interactions between microglia, astrocytes, and neurons may prove to be hazardous, as we have previously shown that ligation of CD40 protected neuronal cells from nerve growth factor-β (NGF-β) or serum withdrawal-induced injury and promoted differentiation . Rather, modulation of immune reactions in CNS would appear to be the most appropriate course of action for treating neurodegenerative disease. While it would be quite difficult to achieve this modulation with conventional drugs, flavonoids appear to be uniquely fitted to this task as we observe their ability to affect multiple converging signaling pathways. For instance, apigenin and luteolin appear to regulate serine 727 phosphorylation of STAT1 at levels that are potentially conducive to apoptosis, all the while keeping a damper on levels in the presence of IFN-γ (Fig. 4 and 5). It is in this way that these compounds are essentially promoters of homeostasis.
It is quite clear from both the present study and previous research that apigenin and luteolin are potentially safe and effective immunomodulators, although their direct molecular targets have not been identified. What seems to be apparent is that these compounds prevent STAT1 signaling, which consequently may prevent the transcription of its target genes. Even as these compounds affect STAT1, it is more likely that upstream kinases or phosphatases are directly involved. Phosphatidylinositol 3-kinase (PI3K), its effector kinase Akt, JAK1, and JAK2 are all required for phosphorylation of both serine 727 and tyrosine 701 of STAT1 . Accordingly, these kinases are all potential molecular targets of apigenin and luteolin. Previous reports also suggest that similar flavonoids mediate their effects through protein tyrosine phosphatases. Furthermore, CD45, a protein tyrosine phosphatase important for immune regulation and function, has been identified as an upstream regulator of STAT1 signaling via dephosphorylation of JAKs . In light of these findings, it may be important to evaluate the effects of these flavonoids on other potential immunoregulatory signaling molecules to better ascertain both safety and efficacy.
While a major limitation in the use of these flavonoids as immunomodulators or anti-inflammatory agents is their low bioavailability, apigenin, in particular, may hold some promise as a suitable therapeutic agent. Recent pK studies suggest that apigenin exhibits a slow metabolism, absorption, and elimination phase (92 hours in rats) [64–66]. Moreover, in one human pK study, apigenin was also found to significantly reduce measures of oxidative stress in blood . Like many aglycone forms of flavonoids, apigenin and luteolin potentially reach their molecular targets by passive diffusion through cell membranes. This means of cellular uptake may explain the onset (<30 mins) of STAT1 inactivation as we observed following apigenin and luteolin treatment (Fig. 3). Despite the possibility of sustainable therapeutic concentrations, future work with these compounds will certainly need to address blood-brain-barrier permeability.
In summary, flavonoids apigenin and luteolin may prevent microglial-mediated inflammation by modulating the induction of CD40 in response IFN-γ. This decrease in expression modulates CD40-40L interactions, which are critical to microglial activation. Apigenin and luteolin's mechanism of action appears to be targeted at regulating STAT1 activation. These studies may lay the foundation for the development of neurodegenerative disease modifying therapies focused on preventing harmful inflammation while maintaining proper glia-neuron interactions.
analysis of variance
central nervous system
fluorescence activated cell sorting
janus kinase/signal transducer and activator of transcription
nerve growth factor beta
reactive oxygen species
tumor necrosis factor alpha.
This work was supported in part by grants from the Johnnie B. Byrd, Sr. Alzheimer's Center & Research Institute (RDS and JT) and, in part, from grants R21AG031037 (RDS) and PO104418P2 (JT) from the National Institute on Aging.
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