Porphyromonas gingivalis-induced miR-132 regulates TNFα expression in THP-1 derived macrophages
© The Author(s) 2016
Received: 22 February 2016
Accepted: 18 May 2016
Published: 17 June 2016
Periodontitis is a chronic inflammatory disease induced by periodontopathogens such as Porphyromonas gingivalis (P. gingivalis). MicroRNAs (miRNAs) are small single-stranded noncoding RNAs that regulate gene expression at the level of translation. MiRNAs have been reported to be involved in inflammatory processes. In this study, we examined the effects of P. gingivalis-induced inflammatory miRNAs expression on TNFα production in THP-1 derived macrophages.
Porphyromonas gingivalis induced the expression of miR-132. P. gingivalis-induced miR-132 expression was significantly inhibited by TLR2/4 knock-down and NF-κB inhibitor. Additionally, miR-132 antagomir strongly repressed production of TNFα. The expression of NFE2L2 and NFAT5, the putative target genes of miR-132 involved in regulation of TNFα, decreased in response to P. gingivalis. Furthermore, miR-132 antagomir rescued P. gingivalis-induced suppression of NFE2L2 and NFAT5.
These results suggest that the induction of miR-132 by P. gingivalis can modulate the pathogenesis of periodontitis induced via regulatory expression of TNFα.
Inflammation is central to effective host defense against invading pathogens. Periodontitis, which is one of the most common human diseases, is an infection-driven chronic inflammatory disease of periodontium and the major cause of tooth loss. Periodontitis is initiated by pathogenic bacteria, such as Porphyromonas gingivalis (P. gingivalis), Tannerella forsythia, and Treponema denticola (Byrne et al. 2009; Socransky and Haffajee 1992). P. gingivalis is a gram negative anaerobic short rod that expresses various virulence factors, including outer membrane vesicles, lipopolysaccharides (LPS), fimbriae, lipoproteins, and gingipains (Pathirana et al. 2000; Zhou and Amar 2006). P. gingivalis modulates the expression of pro-inflammatory cytokines, such as interleukin (IL)-1β, IL-6, IL-8, and TNF-α in human and murine monocytes and macrophages (Agarwal et al. 1995; Park et al. 2014a). The differential regulation of inflammatory cytokines in response to infection is important for recruitment of immune cells in periodontitis tissue and required for orchestration or activation of innate and adaptive immune response.
MicroRNAs (miRNAs) are small single-stranded noncoding RNAs (18–25 nt) that post-transcriptionally regulate gene expression by binding to the 3′ untranslated region (UTR) of target mRNA, leading to mRNA degradation and translational repression (Stoecklin-Wasmer et al. 2012). More than 1000 human miRNAs have been identified in mammals to date (miRBasev.18) (Dai and Ahmed 2011), and they have been found to be associated with diverse biological processes including cell differentiation/proliferation, metabolism, tumorigenesis, and immunity (Ambros 2004; Gregory and Shiekhattar 2005; Taganov et al. 2007).
Recently, several miRNAs related to periodontal inflammation have been reported. In a previous study, we reported differential miRNA expression in healthy and periodontitis tissues (Lee et al. 2011). MiR-132 and miR-146 are inflammatory miRNAs related to bacterial infection. MiR-146 induces a negative feedback mechanism in response to bacterial products-induced TLR signaling to prevent excessive inflammation via suppression of IL-1β, IL-6, IL-8, and TNF-α (Marques-Rocha et al. 2015; Staedel and Darfeuille 2013). Overexpression of miR-132 is sufficient to promote activation of NF-κB and production of IL-8 and MCP-1 (Strum et al. 2009). Although these studies shed some light on the relationship between inflammation and miRNA, bacterial infection-induced miR132 function on inflammatory response is poorly understood. Furthermore, limited data describing the role of miRNAs related to periodontitis or periodontopathogens and the effects of P. gingivalis on the expression of various types of miRNA are available.
In the present study, we investigated whether P. gingivalis can affect the expression of inflammatory miRNAs involved in networks that control innate immunity and extend beyond TLR regulation in THP-1 derived macrophages. We found that P. gingivalis induced miR-132 via TLR2/4 and NF-κB signaling. Moreover, the inhibition of miR-132 expression strongly suppressed the production of TNF-α. The expression of NFE2L2 and NFAT5, potential target molecules of miR-132, decreased in response to P. gingivalis and was recovered by miR-132 antagomir treatment. These results suggest the role of miR-132 in the pathogenesis of periodontitis induced by P. gingivalis.
Porphyromonas gingivalis (strain 381) wild type and various mutants (MT10, MT10W, DPG) were grown in GAM broth (Nissui Pharmaceutical, Japan) with 5 mg/ml hemin and 0.5 mg/ml vitamin K under anaerobic conditions at 37 °C. An OD of 1.0 (650 nm) was determined to correlate to 109 CFU/ml. The bacteria were washed and suspended in serum free-RPMI media to infect THP-1 derived macrophages at various multiplicity of infections (MOIs).
THP-1 cells were cultured in RPMI 1640 medium with 10 % heat-inactivated fetal bovine serum (FBS; Gibco), 100 U of penicillin/ml, and 100 μg of streptomycin/ml at 37 °C in a 5 % CO2/95 % air incubator. THP-1 cells were differentiated into macrophage-like cells with 50 ng/ml of Phorbol 12-mystristate 13-acetate (PMA; Sigma).
Real-time quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR)
Total RNA was extracted with TRIzol (Invitrogen, USA) according to the manufacturer’s instructions. For miRNA analysis, 10 ng of RNA from each sample was used for quantitative stem-loop reverse transcription and real-time PCR (qRT-PCR). Quantification of expression of mature miRNAs was performed using a TaqMan micro-RNA RT kit, TaqMan Universal PCR Master Mix, and gene-specific primers and fluorogenic Taqman probes (Applied Biosystems, USA). MiRNA expression values were calculated using human RNU44 as an endogenous reference. For miRNA target gene analysis, the reverse transcription of total RNA to cDNA was performed using AccuPower RT PreMix (Bioneer Co, South Korea). The mRNA expression levels were quantified by real-time PCR using a Light Cycler instrument (Roche Applied Science, Mannheim, Germany) with SYBR Green PCR Master Mix (Qiagen, USA) according to the manufacturer’s instructions.
For RNA interference assay, human siRNAs for TLR2, TLR4, and non-targeting control oligonucleotides were obtained from Qiagen. The siRNA oligonucleotides in this pool were as follows: TLR2, TLR4, and non-targeting control siRNA oligonucleotides. For siRNA experiments in THP-1 cells, cells were seeded in 6-well plates at a density of 1 × 106 cells per well in the presence of 50 nM PMA. The differentiated cells were then transfected with siRNA oligonucleotides (1200 ng) for 48 h using Attractene Transfection Reagent (Qiagen, USA) in 1 ml of RPMI. MiR-132 functional analyses were performed by transfecting synthetic antagomir (20 pmol) in THP-1 cells using Attractene Transfection Reagent.
NF-κB DNA binding assay
Binding of p65 to the double-stranded NF-κB oligonucleotide was measured using a NF-κB Combo Transcription Factor Assay kit (Cayman Chemical Company, USA).
Measurement of TNF-α and IL-1β
To determine the amount of TNF-α and IL-1β released into the culture media after P. gingivalis stimulation, we analyzed the amount in accordance with the manufacturer’s instructions using an ELISA kit (eBioscience, San Diego, CA, USA).
Cells were washed in ice-cold PBS and lysed, after which a total of 50 μg proteins were separated by 15 % SDS-PAGE, transferred to a PDVF membrane and probed with the indicated antibodies. Reactivity was determined using HRP-conjugated anti-mouse, anti-rabbit or anti-mouse IgG secondary antibody (Jackson Immuno Research Laboratories, USA) (diluted 1:5000) and the signals were visualized using Super Signal West Femto maximum sensitivity substrate (Pierce, USA) with a LAS-4000 FUJIFILM Luminescent Image Analyzer (Fujifilm, Japan).
ASC pyroptosome quantitation in live cells
THP-1/ASC-GFP cells were seeded in 8 well chambers and then primed with PMA (50 nM). THP-1/ASC-GFP cells were transfected with miR-132 antagomir and further challenged with P. gingivalis. ASC pyroptosome formation was observed by confocal Laser-Scanning Microscopy (Carl Zeiss, USA) at various time points. At least 400 cells were counted to enumerate the number of cells containing the ASC-GFP pyroptosome at the end of each period. The percentage of cells with ASC pyroptosome was calculated by dividing the number of cells with ASC pyroptosome by the total cells counted.
Statistically significant differences between samples were analyzed with an unpaired, one-tailed Student’s t test. The data are shown as the mean ± standard deviation (SD).
Porphyromonas gingivalis infection up-regulates miR-132 expression in THP-1 derived macrophages
Porphyromonas gingivalis induces miR-132 expression through TLR2/4 signaling and NF-κB signaling in THP-1 derived macrophages
The inhibition of miR-132 expression down-regulates the expression of TNFα, but not IL-1β, induced by P. gingivalis infection in THP-1 derived macrophages
Inhibition of miR-132 expression restored the expression of NFE2L2 and NFAT5 decreased by P. gingivalis infection in THP-1 derived macrophages
In this study, we investigated the effects of P. gingivalis on the expression of inflammatory miRNAs, miR-132 and miR-146, and the role of miR-132 in live P. gingivalis-challenged THP-1-derived macrophages. P. gingivalis induced miR-132 expression via TLR2/4 and NF-κB signaling, and the enhanced miR-132 expression was closely associated with the increased production of TNFα (Fig. 4c).
MiRNAs are abundant in the human genome and control various important cellular processes, including proliferation, differentiation, metabolism, apoptosis and inflammation (Ambros 2004; Zhang and Su 2009). A single miRNA is loaded into the RNA-induced silencing complex (RISC) and guides this complex to the 3′ UTRs of target mRNA, leading to suppressed target protein expression. Several lines of evidence suggest that miRNAs play critical roles in a number of chronic inflammatory diseases (Plank et al. 2013; Zhang et al. 2014). In innate immune response, specific miRNAs can be up- or down-regulated by inflammatory stimuli. The miRNAs significantly linked to inflammatory response were miR-146, miR-155, miR-21, miR-9 and miR-132 (Dai and Ahmed 2011; Schetter et al. 2010), among which miR-132, miR-146, and miR-155 are inflammatory miRNAs. miR-146 and miR-155, but not miR132, are known to be associated with periodontal disease (Xie et al. 2011). MiR-146 expression increased in periodontal-disease gingival tissue (Lee et al. 2011; Xie et al. 2011) and P. gingivalis-LPS induced miR-146 expression in THP-1 cells/THP-1-derived macrophages (Honda et al. 2012) and human gingival fibroblasts (Xie et al. 2013). Honda et al. (2012) suggested that P. gingivalis-LPS-induced miR-146 expression did not modulate proinflammatory cytokines production. Consistent with the above reports, we found that P. gingivalis induced miR-146 in THP-1-derived macrophages. Although these studies demonstrated the involvement of miRNA in periodontitis, the association of miR-132 with periodontitis has not yet been reported.
MiR-132 is well characterized in brain neurons and plays an important role in inflammation, angiogenesis, and neural development (Magill et al. 2010; Mulik et al. 2012; Shaked et al. 2009). MiR-132 modulates neuronal survival in AD neurodegeneration (Wong et al. 2013) and attenuates inflammation in the mouse brain by targeting acetylcholinesterase (Shaked et al. 2009). In innate immune response, miR-132 plays important roles in TLR2 ligand–induced tolerance and cross-tolerance by targeting IRAK4 (Nahid et al. 2013). Nevertheless, the function of miR-132 has been described in only a few studies and is still poorly understood in innate immune response. Our data are the first to reveal the relationship between miR-132 and P. gingivalis-mediated inflammatory response in THP-1-derived macrophages. The bacterial cell surface components facilitate growth, nutrient acquisition, colonization, biofilm formation and evasion of host defense (Yoshimura et al. 2009). Several reports suggest that gingipains is critical for proinflammatory response in periodontal disease progression (Kataoka et al. 2014; Tancharoen et al. 2015). Fimbriae are potent stimulators of inflammation (Takahashi et al. 2006), and P. gingivalis fimbriae significantly induced TNFα production via TLR2 in macrophages (Aoki et al. 2010). Interestingly, our data showed that gingipain mutants (MT10 and MT10 W) and fimbriae mutant (DPG) of P. gingivalis resulted in less increase of miR-132 compared to wild-type. Even though involvement of gingipain and fimbriae in miR132 expression has not yet been investigated, these reports coupled with our results support the possibility that gingipain and fimbriae contribute to production of TNFα via miR-132 induction.
In our study, live P. gingivalis induced miR-132, and its regulation was dependent on TLRs. TLRs recognize pathogens and activate signaling pathways including immune and inflammatory response to regulate cytokines, chemokines, and adhesion molecules and eliminate pathogens. Several reports recently revealed that TLR signaling modulates various miRNAs (Nahid et al. 2011; O’Neill et al. 2011). miR-146, miR-155 and miR-21 have been central in many miRNA studies due to their expression levels following TLR activation (Quinn and O’Neill 2011). Furthermore, miR-9, miR-147, miR-27b, miR-223, and let-7e are induced by TLR stimulus or pathogen infection (He et al. 2014). However, only a few studies have investigated TLR-mediated miR-146 expression in periodontal disease (Honda et al. 2012; Xie et al. 2013). Indeed, this study is the first study to suggest P. gingivalis induces miR-132 via TLR signaling.
The expression of most TLR-responsive miRNAs described to date depends on NF-κB activity. MiR-155 positively regulates inflammation through the TLR-NF-κB pathway in response to Francisella (Cremer et al. 2009). MiR-9, miR-146, miR-181b and miR-21 are also directly regulated through the NF-κB-dependent pathway (Ma et al. 2011). Conversely, miR-29b, let-7i, miR-98, miR-107, miR-27a, and miR-532-5p are negatively regulated by the TLR-NF-κB pathway (He et al. 2014). We found that inhibition of TLR signaling or NF-κB abolished P. gingivalis-induced miR-132 expression. Although this suggests that miR-132 may be directly regulated by the TLR2/4-NF-κB signaling pathway, further studies are needed to better understand the exact mechanism.
Cytokines are key modulators of inflammatory response classified as proinflammatory (IL-1, IL-6, IL15 and TNFα) or anti-inflammatory (IL-4, IL-10, TFGβ and IFNα) (Schetter et al. 2010). Among various cytokines, TNFα affects many functions such as inflammation, tumor promotion, and anti-microbial immunity (Sedger and McDermott 2014). The expression of TNFα was higher in periodontitis patients than healthy controls, and periodontal bacteria stimulate expression of TNFα (Preshaw and Taylor 2011). Consistent with the above data, we previously reported that TNFα was higher in the GCF of periodontitis patients and P. gingivalis-LPS induced gene expression and protein synthesis of TNFα (Han et al. 2005; Park et al. 2014a). Similar to TNFα, IL-1β is a pro-inflammatory cytokine critical to inflammatory response against pathogens that is well known for involvement in periodontal disease. We recently found that the levels of IL-1β and inflammasome components increased in periodontitis patients and P. gingivalis induced IL-1β release via TLR2/TLR4-NLRP3/AIM2 inflammasome-caspase-1 pathway activation (Park et al. 2014b). In the current study, we found that miR-132 positively regulates TNFα, but not IL-1β. Furthermore, miR-132 did not affect inflammasome activation. However, some studies suggest that IL-1β is a target of miR-132, in contrast to our results (Fen et al. 2014; Hanieh and Alzahrani 2013). The precise reasons for this difference are not clear, but these results may be dependent on cell type and stimuli; accordingly, these mechanisms should be further investigated.
Nuclear factor E2-related factor 2 (NFE2L2 or Nrf2) is a master transcription factor essential for protection from oxidative stress via modulation of ARE-dependent genes, including hemo oxygenase-1 (HO-1), a well-known anti-inflammatory enzyme (Hu et al. 2010; Kim et al. 2010). Park et al. recently reported that the anti-inflammatory effect of Schisandrin on P. gingivalis-LPS-stimulated macrophages was due to induction of HO-1 and activation of Nrf-2. Inhibition of miR-132 restored the ochartoxin-driven decrease of Nrf2 and HO-1 expression as well as the increase in ROS production (Stachurska et al. 2013). Our study also found that inhibition of miR-132 rescued P. gingivalis-mediated deduction of Nrf-2 expression. Moreover, our results indicated that P. gingivalis-induced production of TNFα may be enhanced by miR-132 via miR-132-mediated suppression of Nrf2 expression and anti-inflammatory effect of Nrf2. Nuclear factor of activated T cells 5 (NFAT5) is a transcription factor involved in immune response by regulating TNFα expression via direct binding to TNF promoter and enhancing TNF transcription (Esensten et al. 2005). Although NFAT5 positively regulates TNFα, our results showed that P. gingivalis and P. gingivalis-induced miR-132 negatively regulated NFAT5 expression. We assume that these results occurred due to a negative-feedback loop in which P. gingivalis-induced miR-132 attenuated pro-inflammatory effects of P. gingivalis by targeting NFAT5 expression. Since we do not yet fully understand how miR-132-targeted NFAT5 affects the expression of TNFα by P. gingivalis, the exact involvement of miR-132 and NFAT5 in P. gingivalis-induced inflammation will be confirmed later.
In this study, live P. gingivalis infection induced miR-132 via TLR signaling and activation of NF-κB. Furthermore, inhibition of miR-132 expression strongly repressed the production of TNFα and increased NFE2L2 and NFAT5. This is the first study to describe the novel role of miR-132 in the pathogenesis of P. gingivalis. These results support the concept that miR-132 modulates TNFα via inhibition of its target genes, which may provide a new window of opportunity to investigate therapeutic intervention for P. gingivalis-induced TNFα associated diseases such as periodontitis.
The work presented here was carried out in collaboration among all authors. PMH, PEJ, NSH and CJ designed the research. PMH and PEJ analyzed the data, interpreted the results. PMH drafted the manuscript, which was proofread by KHJ, NHS and CJ. All authors read and approved the final manuscript.
This work was supported by the National Research Foundation of Korea (NRF) Grant funded by the Korea Government (NRF-2011-0012897).
The authors declare that they have no competing interests.
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