INTRODUCTION
Inflammatory bowel disease (IBD) is a chronic disease of the gut thought to involve an altered immune response to unknown microbial related threats of genetically susceptible individuals. The composition of the gut microbiota in IBD patients differs from that of healthy individuals, with reports of lower abundance of butyrate-producing bacteria of the Firmicutes phylum such as Roseburia hominis and Faecalibacterium prausnitzii [
1,
2]. Further, reduced colonic levels of butyrate, possibly related to disease activity, have been demonstrated in IBD patients [
3,
4].
Butyrate, a short-chain fatty acid and the main end-product of intestinal microbial fermentation of dietary fiber in the colon, is a histone deacetylase inhibitor [
5] and has been suggested to have anti-inflammatory effects, as shown by the ability to ameliorate disease in animal models of colitis [
6‐
8]. Hence, results primarily obtained from mouse models and
in vitro systems suggest that butyrate improve intestinal barrier integrity[
9], increase secretion of antimicrobial peptides[
10,
11], down-regulate Toll-like receptor (TLR) expression and secretion of pro-inflammatory cytokines[
12], and inhibit the activity of granulocytes[
8] and lymphocytes[
13]. Moreover, butyrate may promote T regulatory cell generation [
14,
15] and inhibit inflammatory signaling including the AKT [
16] and NF-κB pathways[
17].
Given its potential anti-inflammatory properties, butyrate has been proposed as a therapeutic option for IBD patients, although results so far have been indecisive. Several clinical trials investigating efficacy of butyrate supplementation suggested the compound to be beneficial for IBD patients[
18‐
21], whereas other studies were not able to show any effect on intestinal inflammation [
22,
23]. More recently, attempts to restore the gut microbiota balance by fecal microbiota transplantation (FMT), which may result in increased abundance of butyrate-producing bacterial taxa, have been implemented. A meta-analysis based on randomized controlled trials for patients with UC, including 4 studies with 277 participants, demonstrated that significantly more patients receiving donor FMT achieved clinical remission (42.1%) compared with those receiving control interventions (22.6%), and therefore concluded that FMT appears promising as treatment to induce remission, although long-term durability still remains unclear[
24]. Recently, a randomized controlled trial using anaerobically prepared pooled donor FMT or autologous FMT in UC patients reached the primary outcome with a higher likelihood of remission at week 8 in donor compared with autologous FMT [
25].
The somewhat diverging results of butyrate induction or supplementation may result from design of studies, and could also be due to that butyrate has different effects on the immune system of the host during inflamed and non-inflamed conditions. Hence, we aimed to determine and compare effects of butyrate on the intestinal immune profile of UC patients with active disease and non-inflamed controls, to potentially identify factors explaining the lack of convincing therapeutic effects on intestinal inflammation of butyrate.
MATERIALS AND METHODS
Study Subjects and Sample Collection
Study subjects were recruited among patients at the outpatient clinic at the Sahlgrenska University Hospital, Gothenburg, Sweden. Inflamed (sigmoid colon) and non-inflamed (ascending colon) biopsies were obtained from the same UC patients. Non-inflamed biopsies (sigmoid and ascending colon) were obtained from the same control subjects undergoing colonoscopy for other indications (polyps, weight loss). All biopsies were taken according to a clinical routine using the same diameter endoscopic forceps. Disease activity was determined by Mayo score [
26]. The study was performed after receiving informed written consent from all subjects, and the protocol was approved by the Regional Ethical Review Board at the University of Gothenburg.
Cell Cultivation Assay
Six biopsies were obtained from each site and the four most even-sized were used for cultivation. The same laboratory technician performed the handling of all samples to ensure conformity and all samples were cultivated in duplicates. Biopsies were cultivated in 0.2 mL Iscove’s medium supplemented with 10% human FBS, 100 μg/ml gentamicin (Sigma-Aldrich, St Louis, USA), and 3 μg/ml L-glutamine (Sigma-Aldrich) without or with 1.6 mM butyrate (B5887, Sigma Aldrich), at 37 °C and 5% CO2. After 6 h, the duplicate biopsies were collected and pooled for RNA purification and supernatants were pooled and frozen for cytokine analysis. Butyrate concentration was chosen by titration from 0.1 to 6.4 mM on biopsies from healthy controls with reduction of IL-6 expression in the supernatant as readout, lowest concentration exhibiting IL-6 suppression was selected.
Cytokine Analysis
Quantities of cytokines IL-1β, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12p70, IL-13, IL-17A, GM-CSF, TNF, and IFN-γ secreted in culture supernatants were measured by MSD® Multi-Spot Assay system (Meso scale diagnostics, MD, USA), according to the manufacturer’s instructions. Sigmoidal samples were analyzed for all 13 cytokines while samples from ascending colon were analyzed for 8 out of 13 cytokines (IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, TNF, and IFN-γ).
Total mRNA from biopsies was extracted using Nucleospin® DNA, RNA, and protein purification kit (Macherey-Nagel, Düren, Germany) according to the manufacturer’s protocol. Concentration and purity of the RNA was measured using a NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, Delaware, USA) with 260/280 and 260/230 ratios of ̴ 2 and 2.1–2.2, respectively.
Mucosal Gene Expression Array Analysis
Gene expression array analysis was performed as previously described [
27]. Briefly, cDNA was prepared using the RT
2 First Strand Kit (Qiagen, Hilden, Germany) according to the manufacturer’s protocol. The RT
2 Profiler PCR arrays for “antibacterial response” (PHAS-148Z, Qiagen) and “innate and adaptive immune responses” (PAHS-052Z, Qiagen) were analyzed in a Quantstudio 12K Flex Real-Time PCR System (Applied Biosystems, Foster City, CA, USA) by the use of RT
2 qPCR SYBR Green ROX MasterMix (Qiagen). Data was analyzed in the RT
2 Profiler PCR Array Data Analysis version 3.5 (Qiagen). All samples passed the quality checks for PCR array reproducibility, RT efficiency, and genomic DNA contamination. ACTB, B2M, and RPLP0 were used as housekeeping genes and normalized values are expressed as 2
−(Target-Housekeeping). For genes present in both arrays (
n = 34), mean values from the two arrays were used. A complete list of the genes from the arrays, including annotation of duplicates and undetected genes (
n = 14), is shown in Supplementary table
1.
Data Analyses
Principle component analysis (PCA) was conducted on logarithm-transformed gene expression data using the prcomp-algorithm and visualized using the pca3d-package in R (version 3.3.2) [
28].
To examine the relationship between gene expression without and with butyrate (Y-variable) and mRNA levels (X-variables), multivariate factor analysis (SIMCA-P+ software; Umetrics, Umeå, Sweden) was used. Orthogonal Projections to Latent Structures Discriminant Analyses (OPLS-DA) were implemented to correlate selected
Y-variables and
X-variables with each other in linear multivariate models. The quality of the OPLS-DA was based on the parameters R2, that is, the goodness of the fit of the model (values of ≥ 0.5 defines good discrimination, best possible fit, R2 = 1) and Q2, that is, the goodness of prediction of the model (values of ≥ 0.4 defines high predictive ability, best possible predictive ability Q2 = 1).[
29] A variable influence on projection (VIP) cut-off of > 1.2 was used as a variable selection based on discriminatory power, since VIP > 1 is most influential for the model and most relevant for explaining the Y observations[
29]. Significance of the separation between the groups in the OPLS-DA was calculated using CV-ANOVA.
Parameters identified by OPLS-DA as VIP > 1.2 were logarithm transformed and subject to univariate analysis using Student’s T test. Mean values were back transformed and fold changes (FC) were calculated between butyrate 1.6 mM and none for each gene and evaluated using Ingenuity Pathway Analysis (IPA, version 2.3) (Qiagen). Cut-off used for IPA was p < 0.05. Gene expression data are presented as FC on a log2 scale where log2FC = 1 and − 1 define a 2-fold increase and decrease, respectively. Activation z-scores are calculated by the IPA software and predict whether a specific pathway, disease or function is increased (z-score > 2.0) or decreased (z-score < − 2.0) based on the experimental dataset.
For cytokine expression, the Mann-Whitney U test was used to determine differences between two independent groups and Wilcoxon signed-rank test was used for comparison of related samples. Data are shown as median (range) unless otherwise stated.
All statistical analyses were performed using IBM SPSS Statistics 23; p values < 0.05 were considered as statistically significant. Boxplots and the heatmap were generated using the ggplot2-package in R.
DISCUSSION
In this study, we have demonstrated that butyrate alters the intestinal gene expression profile of both UC patients and non-inflamed controls. Nevertheless, butyrate had a different effect on intestinal gene expression during inflamed and non-inflamed conditions. Hence, butyrate more potently down-regulated expression of inflammatory pathways in intestinal biopsies from non-inflamed controls than in inflamed biopsies from UC patients.
In the absence of butyrate, the cytokine secretion and gene expression of cultured sigmoidal biopsies differed substantially between the two study groups. The higher cytokine secretion as well as expression of genes encoding pro-inflammatory cytokines, chemokines, and receptors for recognition of microbial products in inflamed UC patients than non-inflamed controls reflected the inflammatory status of UC patients with active disease. Few changes were detected in cytokine expression due to butyrate, which was not surprising given the short incubation time. However, paired samples from inflamed and non-inflamed tissue of the UC patients as well as paired samples from sigmoid and ascending colon from controls revealed that the few butyrate-induced differences in cytokine secretion were inherent to the inflammation, not to the disease. Undeniably, butyrate had similar effects on the regulation of the expression of a smaller share of genes in UC patients and non-inflammatory controls. Similarities of gene regulation in the presence of butyrate in the two groups included down-regulated expression of
NFKB1, along with reduced secretion of the NF-κB-induced pro-inflammatory cytokines TNFα and IL6. Indeed, in CD patients, butyrate has been demonstrated to inhibit NF-κB activation and IκBα degradation [
30] and control ROS-mediated NF-kB activation [
31]. Also, genes expressed by T regulatory cells, i.e., RORC and FOXP3, were down-regulated by butyrate in UC patients and non-inflammatory controls, respectively. While butyrate has been reported to support induction of FOXP3
+ T regulatory cells in animal models [
14,
15], data from the human setting are so far lacking, and our results do not support butyrate-induced expression of genes related to this admittedly anti-inflammatory cell population. Furthermore, the gene expression of a few cytokines and growth factors was regulated similarly in both groups. Hence, the effect of butyrate on the expression of a limited numbers of genes is shared during inflamed and non-inflamed conditions.
The most prominent finding of our study was that butyrate had different effects on regulation of gene expression with only minor overlaps between the non-inflamed controls and UC patients. Based on the intestinal gene expression, IPA identified Neuroinflammation Signaling pathway to be inhibited in non-inflamed controls, but not in UC patients with active disease. IPA also predicted different regulation of the biological diseases and functions Inflammatory response and Binding of leucocytes for the two groups with a stronger decrease for controls. Hence, our data suggest that butyrate more prominently down-regulate genes alluring to inflammatory pathways during the healthy state, but not during chronic inflammatory conditions.
There are few previous studies of the individual genes that were differently regulated by the presence of butyrate in health and disease. Nevertheless, XIAP expression, found to be down-regulated by butyrate in UC patients but not in non-inflamed controls, has been reported to be reduced by butyrate addition to Caco-2 cells [
32]. Additionally, similar to our finding, butyrate has been reported to substantially down-regulate the expression of CD80 on human dendritic cells [
33]. Opposite to reports of butyrate having effects on epithelial function expression of antimicrobial peptides such as cathelecidin [
11], RegIIIγ, and β-defensins [
10,
34], we found no evidence for regulation of genes encoding for antimicrobial peptides. Potentially, the conflicting results may reflect that previous studies have made use of epithelial cell lines, whereas our data were based on cultured biopsies, where the epithelial barrier only constitutes a smaller part of the whole tissue. Still, the effect of butyrate on the human intestinal immune profile, irrespective of presence of inflammation, is under-investigated and needs further attention.
The altered regulation of genes of several inflammatory pathways in UC patients with active inflammation as described in our study may be due to impaired butyrate metabolism. Possibly, inflammatory conditions can result in down-regulated expression of genes encoding enzymes involved in butyrate metabolism and oxidation, as demonstrated in inflamed mucosa of UC patients [
35]. This is supported by the fact that in UC patients responding to anti-TNF therapy the mucosal expression of butyrate metabolism/oxidation genes are increased [
35]. Another study, promoting that butyrate has different effects on intestinal cells during health and disease, demonstrated that addition of butyrate alone to intestinal primary epithelial cultures increased the epithelial resistance, whereas butyrate in the presence of pro-inflammatory cytokines led to a drop in resistance [
36]. In line with this, a recent study showed that TNFα reduces the ability of the intestinal epithelium to take up and metabolize butyrate [
37]. Hence, others and our data imply that butyrate effects on the host are altered by inflammation and butyrate supplementation alone may be insufficient to resolve inflammation and regain gut homeostasis.
Recently, manipulation of the gut microbiota by fecal transplantation, potentially increasing the abundance of butyrate-producing taxa, has been proposed as a target for IBD therapy [
38]. So far, the treatment efficacy seems highly variable and may be related to microbiota composition of the donor and/or recipient. Interestingly, sustained remission in UC patients undergoing fecal transplantation has been associated with increased abundance of butyrate-producing bacteria and overall increased butyrate production capacity, while relapse was associated with persisting high relative abundance of Proteobacteria and Bacteroidetes [
39]. Our data, along with the reports of impaired butyrate metabolism during inflammatory conditions described above, imply that improved long-term effects of butyrate induction, or local supplementation, may be best achieved while distributing butyrate during non-inflamed conditions. Hence, butyrate may be more potent to maintain rather than induce remission.
The fact that we only determined the effects of butyrate on intestinal gene expression, not including analyses of certain cell populations or protein expression, is a potential weakness of this study. Further, the number of study subjects included is limited and addition of consecutive time-points or several concentrations of butyrate for our analyses might have revealed another pattern of gene regulation and cytokine secretion by the addition of butyrate. Indeed, underdosing may be a reason for the differences detected in our study and in clinical studies of butyrate supplementation. However, our approach, analyzing pathway-focused gene expression using verified PCR assays, allows for a broad and still relatively detailed analysis including a wide range of targets in specific pathways. Also, coherent analysis methods, including multivariate tools and Ingenuity Pathway Analysis, admit for better understanding of the overall picture, rather than isolated findings. To the best of our knowledge, this study is the first of its kind, comparing effects of butyrate on human gene expression ex vivo, making use of intestinal biopsy cultures during inflammatory conditions in ulcerative colitis patients and non-inflammatory controls.
To conclude, although butyrate altered the intestinal gene expression profile of both UC patients and non-inflamed controls, butyrate regulated a different set of genes during inflamed and non-inflamed conditions. Inflammatory pathways were more potently down-regulated by butyrate in non-inflamed controls than UC patients at active inflammation. These discrepancies may at least partly explain why anticipated anti-inflammatory effects of local butyrate induction or supplementation in UC patients are not always obtained.
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