Immunometabolism: Molecular Mechanisms, Diseases, and Therapies 2018View this Special Issue
Research Article | Open Access
Mirian Samblas, J. Alfredo Martínez, Fermín Milagro, "Folic Acid Improves the Inflammatory Response in LPS-Activated THP-1 Macrophages", Mediators of Inflammation, vol. 2018, Article ID 1312626, 8 pages, 2018. https://doi.org/10.1155/2018/1312626
Folic Acid Improves the Inflammatory Response in LPS-Activated THP-1 Macrophages
DNA methylation has been suggested as a regulatory mechanism behind some inflammatory processes. The physiological actions of methyl donors, such as folic acid, choline, and vitamin B12 on inflammation-related disease have been associated with the synthesis of the universal methyl donor S-adenosyl methionine (SAM). The aim of this study was to evaluate the effects of folic acid, choline, vitamin B12, and a combination of all on preventing the lipopolysaccharide- (LPS-) induced inflammatory response in human THP-1 monocyte/macrophage cells. Folic acid and the mixture of methyl donors reduced interleukin 1 beta (IL1B) and tumour necrosis factor (TNF) expression as well as protein secretion by these cells. Folic acid and choline decreased C-C motif chemokine ligand 2 (CCL2) mRNA levels. In addition to this, the methyl donor mixture reduced Cluster of differentiation 40 (CD40) expression, but increased serpin family E member 1 (SERPINE1) expression. All methyl donors increased methylation levels in CpGs located in IL1B, SERPINE1, and interleukin 18 (IL18) genes. However, TNF methylation was not modified. After treatment with folic acid and the methyl donor mixture, ChIP analysis showed no change in the binding affinity of nuclear factor-κB (NF-κB) to IL1B and TNF promoter regions after the treatment with folic acid and the methyl donor mixture. The findings of this study suggest that folic acid might contribute to the control of chronic inflammation in inflammatory-related disease.
Inflammation is traditionally defined as the short-term adaptive response to fight against injury, caused by pathogens or biological and chemical stimuli . Although acute inflammation is a crucial component for maintaining homeostasis in the body, persistent and chronic inflammation is involved in the development of several clinical manifestations and diseases. During inflammatory disease, monocytes and macrophages produce cytokines in response to different stimuli, such as lipopolysaccharide (LPS) . The proinflammatory molecules released by macrophages in the inflamed regions orchestrate the enhancement of monocyte recruitment from blood to tissue. Recruited monocytes differentiate into macrophages to continue the inflammatory response . Alongside this, studies have described that epigenetic mechanisms contribute to the pathogenesis of several chronic inflammatory-related diseases by regulating important steps such as macrophage infiltration or cytokine secretion [4, 5]. For instance, inflammatory genes like interleukins (IL) IL6, IL4, IL8, IL1B, or interferon INF-γ have been described to be methylated differently in several chronic inflammatory diseases [4, 6].
Methionine, folate, betaine, choline, and vitamins B2, B6, and B12 are considered methyl donor precursors naturally occurring in the diet . These substances participate in the methionine pathway for the synthesis of S-adenosyl methionine (SAM), which is the universal methyl donor for DNA methylation reactions . The anti-inflammatory effects exerted by some of these compounds in a variety of inflammatory diseases have been described in previous research. For example, folic acid supplementation improved disease outcomes in subjects with hypertension, diabetes, and stroke by reducing levels of inflammatory markers (CRP, VCAM-1, IL-1β, and TNF-α) . In addition to this, the combined supplementation of folate and vitamin B12 ameliorated inflammation during pregnancy by modifying the concentration of inflammatory cytokines . Lastly, vitamin B12 has been negatively associated with proinflammatory cytokines and low-grade systemic inflammation . On the other hand, deficiencies in the abovementioned methyl donors have also been shown to lead to adverse effects [10, 12]. For example, vitamin B12 deficiency has been related to metabolic disturbances such as hyperhomocysteinemia, obesity, hypertension, and insulin resistance . Choline deficiency has been associated with the development of fatty liver disease and demonstrated to worsen the outcome of liver fibrosis in patients with nonalcoholic steatohepatitis (NASH) . Interestingly, NASH patients that were choline-deficient exhibited amelioration of steatohepatitis after choline supplementation . Similarly, methyl donor supplementation prevented HFS diet-induced liver fat accumulation in rats fed an obesogenic diet .
The anti-inflammatory effect of methyl donors in monocytes before differentiation and LPS-induced inflammatory response in macrophages, along with the role of DNA methylation in this process, have been scarcely studied. For this reason, the aim of this study was to investigate the effects of methyl donors, both individually and together, on the attenuation of LPS-induced inflammatory response and the possible underlying epigenetic mechanisms in human THP-1 monocyte/macrophage cells. Monocytes were incubated with folic acid, choline, and vitamin B12 or a methyl donor mixture of folic acid, choline, and vitamin B12. Monocytes were then differentiated into macrophages and an inflammatory response was induced with LPS.
2. Material and Methods
Folic acid, vitamin B12, and choline chloride were supplied from Sigma-Aldrich (MO, USA). Phorbol 12-myristate 13-acetate (TPA) (Sigma-Aldrich) was used for differentiating THP-1 monocytes into macrophage-like cells. LPS from E. coli K12 strain (Invitrogen, CA, USA) was applied to activate macrophages. Thiazolyl Blue Tetrazolium Bromide (MTT) (Sigma-Aldrich) was used to investigate the toxic effects of methyl donors on THP-1 cells.
2.2. Cell Culture and Treatments
Human monocyte THP-1 cells were purchased from American Type Cell Culture (ATCC® TIB-202™, VA, USA). Cells were maintained at 37°C and 5% CO2 in RPMI-1640 medium (Gibco) modified to contain 2 mM L-glutamine, 1 mM sodium pyruvate, 4.5 g/l glucose, and 1.5 g/l sodium bicarbonate and supplemented with 10% fetal bovine serum (GIBCO), 100 U/ml penicillin, and 100 μg/ml streptomycin.
THP-1 cells were treated with 11.3 μM folic acid, dissolved in 1 M NaOH, 105 μM choline chloride, 18.5 nM vitamin B12, and a mixture of methyl donors consisting of folic acid, choline chloride, and vitamin B12 at the concentrations previously indicated. Concentrations were determined by multiplying ten times the basal concentration present in the RPMI-1640 medium for each compound. After 24 h, cells were differentiated into macrophages by incubation with 25 ng/ml TPA for 48 h and then were activated with 100 ng/ml LPS for 24 hours. Finally, RNA and DNA were extracted and supernatants were collected for ELISA analysis.
2.3. Cell Viability Analysis
For the viability assay, THP-1 cells were pretreated with methyl donors at the selected concentrations during 24 h, as described above, in a 96-well plate. After the treatments, 20 μl MTT (5 mg/ml) was added to each well and plates were incubated for 2 h at 37°C. Formazan crystal formation was solubilised in 100 μl/well DMF-glacial acetic acid-SDS solution consisting of 40% DMF, 2% glacial acetic acid, and 16% w/v sodium SDS. Formazan production was quantified by absorbance at 570 nm using a microplate reader (Multiskan Spectrum, Thermo Electron Corporation, Finland). The results were expressed as relative cell viability (%).
2.4. Analysis of mRNA Expression by Quantitative Real-Time PCR
Total RNA was extracted from cells with TRizol® Reagent (Invitrogen). RNA quality and concentration were measured using the Nanodrop Spectrophotometer ND1000 (Thermo Fisher Scientific, MA, USA). Approximately 1 μg of total RNA was reverse-transcribed into cDNA by the MultiScribe™ Reverse Transcriptase Kit, following the manufacturer’s instructions (Thermo Fisher Scientific, MA, USA). Real-time PCR was performed using ABI Prism 7900HT Sequence Detection System and Taqman Universal Master Mix (Applied Biosystems, CA, USA). Predesigned TaqMan primers and probes for IL1B (Hs01555410_m1), TNF (Hs00174128_m1), IL18 (Hs01038788_m1), SERPINE1 (Hs01126606_m1), CD40 (Hs01002913_g1), CCL2 (Hs00234140_m1), and TLR4 (Hs00152939_m1) genes were used (Applied Biosystems). The levels of these mRNAs were normalized to the level of GAPDH (Hs02758991_g1) mRNA expression. Relative expression was determined by using the comparative method.
2.5. Cytokine Secretion Analysis by Enzyme-Linked Immunosorbent Assay (ELISA)
Culture supernatants were collected after the treatments and stored at −80°C for further cytokine analysis. Protein concentrations of IL-1β, TNF-α, PAI1, and CD40 were measured with standard ELISA kits (R&D Systems Europe, UK), according to the manufacturer’s protocols. Absorbance was measured at 450 nm using a microplate reader (Multiskan Spectrum, Thermo Electron Corporation, Finland).
2.6. DNA Methylation Analysis by MALDI-TOF Mass Spectrometry
DNA was isolated using MasterPure™ DNA Purification Kit (Illumina, WI, USA), according to the manufacturer’s guidelines. Genomic DNA was sodium bisulfite-converted using the EpiTect Bisulfite Kit (Qiagen, CA, USA). DNA methylation quantification was performed by MassARRAY EpiTYPER technology (Sequenom Inc., CA, USA). This method uses matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry in combination with RNA base-specific cleavage (MassCLEAVE). Four amplicons covering 32 CpG sites were selected. EpiDesigner software (Sequenom Inc.; http://www.epidesigner.com/start3.html) was used to design PCR primers for the amplicons of interest: IL1B (chr2: 112,837,566–112,837,895), TNF (chr6: 31,575,209–31,575,481), SERPINE1 (chr7: 101,127,068–101,127,411), and IL18 (chr11: 112,163,853–112,164,105). The designed primers are shown in Supplementary Table 1 and the complete amplicon sequences are reported in Supplementary Figure 1. The complete methodology was previously explained .
2.7. Chromatin Immunoprecipitation (ChIP) Assay
ChiP assay was performed with the ChIP-IT™ Express Enzymatic Kit (Active Motif, CA, USA), following the manufacturer’s guidelines. THP-1 cells were cultured for 24 hours with methyl donors and were then differentiated with TPA (25 ng/μl) for 48 hours and activated with LPS (100 ng/μl) over 24 hours. The cell medium was discarded and 36.5% formaldehyde was added directly to the cell surface for 10 min. Cross-linking between proteins and DNA was stopped by the addition of glycine for 5 min at room temperature and cells were collected by scraping. Then, cells were incubated with lysis buffer for 30 min at 4°C and DNA was fragmented via enzyme-based digestion for 10 min at 37°C. Chromatin was immunoprecipitated using rabbit polyclonal antibody to nuclear factor-κB (NF-κB; ab7970, Abcam, MA, USA). After immunoprecipitation, cross-linking of protein-DNA complexes was reversed. Real-time quantitative PCR was performed using primers for IL1B: sense 5-agcaacaaagctgccactta-3 and antisense 5-tgacgtgctgtgtgaatttg-3, and TNF: sense 5-ggagaatgtccagggctatg-3 and antisense 5-tcctggaggctctttcactc-3.
2.8. Transcription Factor-Binding Site Analysis
In order to identify the putative transcription factor binding site in the CpG sites of the IL1B gene, a bioinformatic analysis was performed through LASAGNA-Search 2.0 using TRANSFAC matrices and aligned models, as described elsewhere .
2.9. Statistical Analysis
Normality was assessed by Kolmogorov-Smirnov and Shapiro-Wilk tests. For the statistical analysis of the results, a one-way ANOVA followed by Dunnett’s test for multiple comparisons between groups and an unpaired Student t-test, for the direct comparisons between two groups, were used. Differences were considered significant at value < 0.05. Statistics were performed using Prism 5.0 (GraphPad Software, CA, USA).
3.1. Methyl Donors Did Not Affect Cell Viability
Cell viability was measured by MTT assay after incubation with folic acid at 11.3 μM, choline at 105 μM, vitamin B12 at 18.5 nM, and the methyl donor mixture. The selected concentrations were within the range proposed by previous studies [9, 17, 18]. Cell viability was not significantly affected by methyl donors at these concentrations (Supplementary Figure 2).
3.2. Effects of Methyl Donors on the Expression of Genes Associated with the Inflammatory Response in THP-1 Macrophages Activated with LPS
Treatment of THP-1 cells with the different compounds before the differentiation with TPA and activation with LPS altered the expression of most of the inflammation-related genes compared to the control treatment (Figure 1). Folic acid and the methyl donor mixture reduced IL1B ( for folic acid; for the methyl donor mixture) and TNF ( for folic acid; for methyl donor mixture) mRNA expression. Folic acid also reduced TLR4 () and CCL2 (), but increased SERPINE1 () gene expression. Moreover, methyl donor mixture incubation reduced the levels of CD40 () but increased SERPINE1 (). Choline decreased the expression of CCL2 (). However, no statistically significant changes were observed after vitamin B12 incubation.
3.3. The Pretreatment with Folic Acid and Methyl Donor Mixture Reduced IL-1β and TNF-α Secretion of LPS-Activated Macrophages
Concerning cytokine secretion, the incubation with folic acid and the methyl donor mixture reduced the levels of IL-1β () and TNF-α ( and , resp.), but not CD40 and PAI-1. However, no changes were observed with the other methyl donors (Figure 2).
3.4. Incubation with Methyl Donors Increased DNA Methylation in the Inflammatory Genes
The regions studied in the genes IL1B, SERPINE1, and IL18 displayed an overall gain of methylation when LPS-activated macrophages were treated with the different methyl donors. This hypermethylation was especially significant after the incubation with folic acid. As shown in Table 1, folic acid significantly increased () the methylation levels of CpG_1 (190%), CpG_5 (680%), and CpG_6 (200%) of IL1B, CpG_1 (750%), CpG_2 (88%), CpG_3.4 (136%), CpG_7 (1003%), and CpG_9 (88%) of SERPINE1, and CpG_4 (53%) and CpG_5 (27%) of IL18 when compared with the methylation percentage of the nontreated LPS-activated macrophages. No changes in methylation were noted in the analyzed region of TNF after the treatment. Regarding choline chloride, vitamin B12, and the methyl donor mixture, incubation with these compounds also significantly increased () the methylation levels of some CpG sites concerning the studied genes (Table 1).
3.5. NF-κB Binding to IL-1β and TNF-α Was Not Affected after the Incubation with Folic Acid and the Methyl Donor Mixture
IL1B and TNF gene expression and secretion decreased after the incubation with folic acid and the methyl donor mixture (Figures 1 and 2). IL1B DNA methylation levels increased; TNF methylation levels did not. To determine the effect of DNA methylation in the sequence of proinflammatory genes on NF-κB binding to IL1B and TNF promoters, a ChIP assay was performed. The analysis showed no significant changes in NF-κB binding to IL1B and TNF promoter regions in THP-1 cells treated with folic acid and the methyl donor mixture (Figure 3).
Previous studies in humans have analyzed the association between folic acid and inflammation. For example, a case-control study showed a reduction of cytokine levels after a 12-week treatment with folic acid . In addition, folic acid supplementation in patients with a high risk of coronary artery disease was associated with a reduction in proinflammatory cytokines (e.g., monocyte chemoattractant protein 1 or MCP-1) in human monocytes . In the present study, we demonstrated that folic acid and a mixture of methyl donors reduced the expression of proinflammatory genes (e.g., TNF, IL1B, CD40, CCL2, and TLR4) in THP-1 monocytes, when the monocytes were differentiated into macrophages and activated with LPS. In agreement with our results, the incubation of murine monocyte RAW 264.7 cells with folic acid reduced the expression of proinflammatory genes during LPS activation  . In contrast, folic acid deficiency in the same cell line enhanced the expression of proinflammatory genes .
Current data revealed that folic acid and the methyl donor mixture not only reduce proinflammatory gene expression in THP-1 monocytes, but also decrease the secretion of TNF-α and IL-1β cytokines when cells were differentiated to macrophages and activated by LPS.
During the inflammatory response, the proinflammatory mediators, specially MCP-1 (encoded by the CCL2 gene), contribute to the migration of circulatory monocytes into the surrounding tissue , by specifically attracting monocytes towards the inflamed area, promoting tissue damage and disease. In this context, our results suggest that folic acid and a mixture of methyl donors could reduce the inflammatory response of the monocytes and the macrophages derived from these monocytes would decrease cytokine and chemokine secretion.
The specific mechanisms for the beneficial effects of folic acid or methyl donors on inflammation have not been clearly elucidated. One of the possible explanations is epigenetics, via DNA and histone methylation . Folate, choline, and vitamin B12 directly participate in the formation of S-adenosyl methionine (SAM), which is the major donor of methyl groups for DNA methylation . In the current trial, folic acid and the methyl donor mixture increased methylation levels of IL1B, SERPINE1, and IL18. However, only IL1B presented lower gene expression and protein secretion, which was associated with hypermethylation after folic acid supplementation. This result suggests that IL1B gene expression may be modulated by changes in DNA methylation induced by folic acid. However, the methylation changes of SERPINE1 and IL18 did not correlate with changes in gene expression. Incubation with methyl donors was for 24 hours and then the monocytes were differentiated for 48 hours and activated by LPS for a further 24 hours. A recent study of IL18 expression in LPS-stimulated murine macrophages showed that the maximum level of expression of this interleukin was 3–6 hours after induction. No changes were found after 24 hours suggesting an earlier enzymatic activation of poly(ADP-ribose) polymerase 1 (PARP-1) that induces IL18 expression . In this context, the time or the concentration of supplements might have been insufficient to evidence subtle changes in IL18 and SERPINE1 expression.
Unexpectedly, no changes in DNA methylation levels in the TNF gene were found after the treatment with methyl donors. In line with these results, Kolb and Petrie  found that although folate deficiency in murine macrophages reduced DNA methyltransferase expression, TNF DNA methylation did not change. In addition, in murine macrophages incubation with exogenous SAM attenuated the LPS-stimulated expression of TNF . The reduction in TNF expression without a change in methylation could be due to folic acid causing upstream methylation. Recent studies have uncovered a new epigenetic mechanism for gene expression regulation: mRNA methylation. In vitro data has shown that methyladenine of mRNA influences mRNA transcription, splicing, nuclear export, translation, and mRNA stability [26, 27]. Therefore, RNA methylation may also be a regulatory mechanism altering TNF expression after the supplementation with the methyl donors.
Transcriptional activation of TNF and IL1B by LPS requires the stimulation of a set of pathways and transcription factors, including NF-κB, early growth response protein 1 (EGR-1), and activator protein 1 (AP-1) . Available data in such research reveals that the binding levels of the NF-κB transcription factor to the IL1B promoter were similar to the TNF promoter and to macrophages without the methyl donors’ supplementation. These results suggest that DNA methylation does not directly affect the binding affinity of NF-κB to IL1B. Similarly, Feng et al.  reported that folic acid decreased TNF-α and IL-1β production by inhibiting the NF-κB pathway without modifying NF-κB binding affinity. Taking into account these results, other molecular mechanisms could be affected by the tested molecules. For example, the bioinformatic analysis of the selected sequence of IL1B identified a putative PU.1 (Spi-1) transcription factor binding site, which could be involved in the regulation of the expression of this gene. PU.1 binds to GC-rich regions of genes to activate transcription, hence DNA methylation might impair the binding of PU.1 to the analyzed sequence and downregulate gene transcription. Interestingly, the PU.1 transcription factor is involved in macrophage differentiation and also in the transcriptional control of genes in mature macrophages [29, 30].
THP-1 is a human monocytic cell line derived from peripheral blood, which has been widely used to investigate the inflammatory response due to its ability to differentiate into macrophage-like cells. A known limitation of the use of cell lines in research is the difference to the natural environment, however previous studies have found that LPS mimics the inflammatory environment when added to THP-1 . Despite this, direct extrapolation to human disease is not possible because more proinflammatory molecules and more than one cell type are involved in the response. Nevertheless, results of this investigation suggest a direct effect of methyl donors in the methylation of proinflammatory genes in LPS-activated THP-1 cells and the reduction of expression and production of proinflammatory cytokines. In addition, although methyl donor supplementation did not modify TNF promoter methylation, it reduced LPS-induced TNF-α production. However, the binding affinity of NF-κB to proinflammatory genes was unaffected, suggesting a minor role of this protein complex in the transcriptional regulation of these genes in response to folic acid and other methyl donors.
The findings of this study evidenced that monocyte pretreatment with specific methyl donors, particularly folic acid, reduced the inflammatory response in LPS-activated THP-1 macrophages, which could in part be mediated by increased DNA methylation in some CpG sites of important proinflammatory genes. In addition, folic acid decreased the expression of cytokines and chemokines (i.e., CCL2), suggesting a protective role through the recruitment of monocytes to the inflamed tissue.
Access to data will be considered by the author upon request.
Conflicts of Interest
The authors have nothing to declare concerning this issue.
The authors thank the technical assistance of Enrique Buso (UCIM, University of Valencia) for the MassARRAY® measurements. The authors are also grateful to Catherine Graham (St Mary’s University, UK) for English proofreading. The authors acknowledge the financial support of MINECO (Nutrigenio Project reference AGL2013-45554-R) and Spanish Centro de Investigación Biomédica en Red de la Fisiopatología de la Obesidad y Nutrición (CIBERobn). Mirian Samblas holds a FPI grant from the MECD (BES-2014-068409).
Supplementary Table 1: primer sequences used for MassARRAY EpiTYPER assay. Supplementary Figure 1: genomic localization and nucleotide sequences of CpG sites covered by the MassARRAY EpiTYPER probes for the study of DNA methylation levels of IL1B, TNF, SERPINE1, and IL18 genes. The number on the left of each sequence represents the positions with respect to the start of the transcription or TSS. Nucleotides in the box are the sequences selected for each gene. CpGs underlined and highlighted in bold are those that were quantified by MassARRAY EpiTYPER. Transcription start site (TSS). Coding DNA sequence (CDS). Supplementary Figure 2: relative cell viability (measured by MTT assay) after THP-1 monocyte incubation with folic acid (11.3 μM), choline (105 μM), vitamin B12 (18.5 nM), and methyl donor mixture. Data are shown as the means ± SD (). Differences between groups were analyzed by one-way ANOVA. (Supplementary Materials)
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