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Article

Effect of Perfluorooctanoic Acid on the Epigenetic and Tight Junction Genes of the Mouse Intestine

by
Faizan Rashid
1,2,†,
Saeed Ahmad
1,3,† and
Joseph Maria Kumar Irudayaraj
1,2,3,4,5,*
1
Biomedical Research Center in Mills Breast Cancer Institute, Carle Foundation Hospital, Urbana, IL 61801, USA
2
Department of Comparative Biosciences, College of Veterinary Medicine, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA
3
Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA
4
Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA
5
Cancer Center at Illinois, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA
*
Author to whom correspondence should be addressed.
†
Equal credit co-first authors.
Toxics 2020, 8(3), 64; https://doi.org/10.3390/toxics8030064
Submission received: 7 August 2020 / Revised: 24 August 2020 / Accepted: 25 August 2020 / Published: 28 August 2020
(This article belongs to the Special Issue Biological Fate and Potential Hazards of Per- and Polyfluorinated Alkyl Substances (PFAS))
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Abstract

:
Perfluorooctanoic acid (PFOA) has been implicated in various toxicities including neurotoxicity, genotoxicity, nephrotoxicity, epigenetic toxicity, immunotoxicity, reproductive toxicity, and hepatotoxicity. However, information on the accumulation of PFOA in the intestine and its toxic effects on intestinal epigenetics and tight junction (TJ) genes is sparse. CD1 mice were dosed with PFOA (1, 5, 10, or 20 mg/kg/day) for 10 days, and its accumulation and induced alterations in the expression of epigenetic and tight junction genes in the small intestine and colon were evaluated using LC–MS and qPCR techniques. PFOA reduced the expression levels of DNA methyltransferases (Dnmt1, Dnmt3a, Dnmt3b) primarily in the small intestine whereas, in the colon, a decrease was observed only at high concentrations. Moreover, ten-eleven translocation genes (Tet2 and Tet3) expression was dysregulated in the small intestine, whereas in the colon Tets remained unaffected. The tight junction genes Claudins (Cldn), Occludin (Ocln), and Tight Junction Protein (Tjp) were also heavily altered in the small intestine. TJs responded differently across the gut, in proportion to PFOA dosing. Our study reveals that PFOA triggers DNA methylation changes and alters the expression of genes essential for maintaining the physical barrier of intestine, with more profound effects in the small intestine compared to the colon.

1. Introduction

Perfluorooctanoic acid (PFOA) is an eight-carbon chain (C8) compound which belongs to a group of synthetic chemicals known as perfluoroalkyl and polyfluoroalkyl substances (PFASs). Since the 1950s, PFAS compounds have been widely used in the synthesis of various household and industrial products such as greaseproof papers, stain repellants, non-stick cookware, cleaners, carpets, aqueous film-forming foam and in wetting agents [1,2]. Among PFASs, PFOA has been used excessively because of its polymerization properties in the synthesis of various fluoropolymers used in the production of commercial products, such as Gore-Tex and Teflon [3].
PFOA has been detected in house dust, [4] surface and drinking water, [5,6], indoor and outdoor air [7], and animal tissues [8,9]. Humans are exposed to PFOA through diet, primarily eggs, fish products, poultry products, cereals, vegetables and drinking water, inhalation of dust particles, and in commercial products [5,10,11,12]. PFOA has strong carbon–fluorine bonds which makes it a highly persistent compound, and its bioaccumulation may eventually lead to adverse health effects [13]. Public concern of PFOA has increased since its detection in blood serum and breast milk of humans [14,15]. PFOA levels may remain high for an extended period of time owing to their long half-life of 2 to 3 years in human serum [16,17].
The bioaccumulation of PFOA in human serum and tissues has led to adverse effects on human health, such as an increase in levels of uric acid, cholesterol, and liver enzymes, reduced fetal growth, and ulcerative colitis [3,18,19,20]. This may also suggest the possibility of a PFOA role in several human pathologies such as liver diseases, cardiovascular diseases, chronic renal disease, and abnormal fetal development. Animal studies have revealed accumulation and distribution of PFOA in tissues leading to several toxicities including neurotoxicity, genotoxicity, nephrotoxicity, epigenetic toxicity, immunotoxicity, reproductive and developmental toxicity, and hepatotoxicity [21,22,23,24,25,26]. Studies have shown that PFOA can alter the activities of liver enzymes [27], cause anti-inflammatory effects by modulating the levels of proinflammatory cytokines [28], and exert cytotoxic effects on liver and thyroid cells [29,30]. PFOA has been found to cause testicular, liver, and other cancers in rats [31]. An increase in kidney and testicular cancers was also observed among people living close to chemical plants [32]. Several studies have demonstrated the alterations in metabolic pathways as a result of PFOA exposure, such as increased oxidative stress and fibrotic markers [26,33], peroxisome proliferator-activated receptor (PPARs) activation [34], initiation of P450 [35], altered expression of lipid metabolism and cell cycle genes [24], and disruption of efflux transporters—for example, Bcrp, which has an important role in the elimination of drugs and environmental chemicals from kidney and liver [36].
Through the consumption of drinking water and food contaminated with PFOA, the intestinal wall is the initial line of contact with the contaminant. PFOA was found to be stored in the intestines of various organisms such as bivalves, fishes, and crabs [37]. In vivo studies in rats revealed poor excretion of PFOA in feces which may suggest increased bioaccumulation of PFOA after repeated exposures, which may lead to significant toxicity [38]. The bioaccumulation of PFOA was found to be increased in a dose-dependent manner within the tissues of several animal models. The higher PFOA bioaccumulation was found in the intestine and liver of fishes compared to other organs such as ovary, brain, and gall bladder [37,39]. The increased bioaccumulation potential of PFASs in the intestine compared to gonads was also found in other organisms such as Holothuria tubulosa. Accumulation in intestinal tissue was dependent on the perfluoroalkyl chain lengths, thus PFOA and perfluorooctane sulfonate (PFOS) were found to have higher bioaccumulation potential than shorter-chain compounds [40]. It has been reported that PFOA levels in serum were positively correlated to ulcerative colitis in humans [20]. Furthermore, other commonly used PFASs, such as PFOS, were also found to alter the intestinal microbiome [41]. However, the mechanisms underlying the toxicity of PFOA in the human intestine are still unclear.
Research examining the toxic effects of PFOA in human intestinal cells is limited. It has been observed that PFOA alters the calcium homeostasis and decreased the viability of colon carcinoma (HCT116) cells over time [42,43]. Another study described the increased invasive ability of colorectal cancer cells (DLD-1 cells) via NF-κB facilitated matrix metalloproteinase-2/-9 expression after PFOA exposure [44]. This may suggest the role of PFOA in cancer metastasis. Nevertheless, although in vitro studies are common, they also raise the question as to whether in vivo models would respond in the same way to PFOA.
Despite these studies, there is still limited evidence on the toxicity of PFOA on intestinal epigenetics and tight junction (TJ) genes. From our previous studies, we observed significant alterations in mRNA expression of epigenetic genes in liver (HepG2) cells and mice kidney tissues due to acute PFOA exposure which promoted early indicators of fibroblast activation in mice kidney tissues [23,24,25,26]. The changes in the DNA methylation patterns were also found to be linked with alteration of disease-related genes in inflammatory bowel disease (IBD) and inhibition of various tumor suppressor genes in cancers [45]. Various studies published recently indicate the number of mechanisms by which epigenetic changes regulate intestinal development [46] and cause various intestinal disorders such as intestinal adenomas [47], colorectal cancer [40], intestinal inflammation [48], and inflammatory bowel disease including Crohn’s disease [49,50]. The role of epigenetics in the regulation of tight junction genes is also evident from the literature. It has been reported that metastatic and tumorigenic properties of various cancer cells were promoted by epigenetic inhibition of Occludin [51]. Similarly, DNA hypomethylation was found to cause overexpression of membranous Claudin-4 which inhibited the invasion and migration of tumor cells in gastric carcinoma [52]. These studies suggest that PFOA exposure can possibly disrupt the intestinal barrier through epigenetic alterations.
Intestinal TJs in epithelia are essential for the maintenance of the physical barrier in the intestine and regulate the flow of substances, such as solutes, ions, and water across the epithelial cells in the intestine [53]. They are also involved in various other physiological functions, from appropriate hydration to nutrient uptake, to protection against infectious agents. Several cancers and key signaling pathways involved in cell metastasis, invasion, proliferation, and transformation were found to be associated with TJ dysregulation [54]. Studies have also revealed the association of TJ dysfunction with various inflammatory and metabolic disorders, such as celiac disease, IBD, obesity, and type 1 diabetes [55,56,57,58,59]. This was further supported by the positive correlation of PFOA serum levels with the incidence of ulcerative colitis in the human population [20]. This indicates the possibility of the dissemination of PFOA and associated metabolites through a compromised intestinal barrier into different locations of the body. However, there is no study to date examining the toxic effect of PFOA on intestinal epigenetics and tight junctions.
In the current study, we examined the bioaccumulation of PFOA in the small intestine and colon tissues and the relative expression of (1) epigenetic effector genes, which are DNA methyltransferase (Dnmts) and ten–eleven translocation (Tets), and (2) intestinal TJ genes (i.e., occludin (Ocln), claudins (Cldns) and zonula occludens (ZOs)), which have a key role in the maintenance of physical barriers in the intestine. Previous studies have mostly been conducted on colon cell lines which may not appropriately represent in vivo conditions and undermine the major anatomical differences in the intestine. Further, dose-dependent effects of PFOA have been noted in colon cancer cell lines [43]. Therefore, the focus of our work is to assess the effect of PFOA on intestinal epigenetics and tight junction genes in the small intestine and colon. We expect our findings to further assess the effect of PFOA in methylation and modulation of the intestinal barrier due to its toxicity.

2. Materials and Methods

2.1. Test Chemical and Dosing Concentrations

PFOA (C8HF15O2, CAS# 335-67-1, 96% purity) and Tween-20 were purchased from Sigma-Aldrich (St. Louis, MO, USA). Four different dosing concentrations 1, 5, 10, and 20 mg/kg/day of PFOA along with vehicle control (no PFOA) were prepared in 0.5% Tween-20 in deionized water. The concentrations were selected based on the reported amount of PFAS levels in the serum of people both from the environmental/community and occupational exposure. The highest concentration of PFOA reported in the blood serum of 506 fluorochemical production employees was 92.03 μg/mL with an average of 2.21 μg/mL [60]. A community exposure study showed PFOA serum concentration in the range of 7–4525 ng/mL with a primary source of PFOA in drinking water [61]. In mice studies, blood serum has been reported in a concentration range of 100–200 μg/mL dosed with 20 mg/kg/day of PFOA for different duration [62,63]. We decided our dosing concentrations (from low–high) and duration (10 days) taking into consideration the community and fluorochemical production workers’ exposure limits to PFOA.

2.2. Animals Housing, Dosing, and Tissues Collection

CD1 mice, an outbred strain, commonly used in toxicology were dosed to assess the adverse effect of PFOA. Animal experiments were conducted with an approved protocol (Toxicology of Endocrine Disrupting Chemicals, Protocol# 19037; Approved 4/11/2019) by the University of Illinois at Urbana-Champaign, Institutional Animal Care and Use Committee (IACUC) per National Institute of Health (NIH) guidelines. Female mice were obtained from Charles River, USA, and randomly divided into 5 groups (n = 3 mice per group). They were housed in polysulfone, ventilated cages at 25 °C on a 12:12 h light: dark cycle and given free access to the Teklad Rodent Diet 8604 and purified water. Mice were dosed by oral gavage after acclimatization to the new environment and reaching the age of 30 days. Different doses (1, 5, 10, and 20 mg/kg/day) of PFOA along with vehicle control were administered daily for the next 10 days.
After the completion of dosing, mice were euthanized using CO2 asphyxiation. Intestinal tissues were collected immediately after euthanasia, and intestinal contents were flushed with sterile phosphate-buffered solution (PBS). The washed tissues were stored in liquid nitrogen at the site of surgery and later transferred to a −80 °C freezer.

2.3. Isolation of RNA and cDNA Synthesis

Small intestine and colon tissue were processed to extract total RNA by the Trizol method (Ambion, Thermofisher, Waltham, MA, USA) and dissolved in diethyl pyrocarbonate (DEPC) treated water. The concentration and purity of RNA were analyzed by NanoDrop 1000 spectrophotometer (Thermo Fisher Scientific Inc., Waltham, MA, USA). Then, 1 μg of extracted RNA from each sample was used to transcribe cDNA using the high capacity cDNA synthesis kit (Applied Biosystems, Thermofisher, Waltham, MA, USA). The synthesized cDNA was diluted (1:20) in molecular grade water (Corning Mediatech, Inc., Manassas, VA, USA).

2.4. Assessing Gene Expression Variation Using Real-Time PCR

Variation in the expression pattern of specific tight junction and epigenetic genes was studied with quantitative real-time PCR (StepOnePlus Real-Time PCR Systems; v 2.0 Applied Biosystems, Waltham, MA, USA). Primers for these genes were designed and ordered using PrimerQuest Tool (Integrative DNA Technologies, Inc., Commercial Park Coralville, IA, USA). Then, 5 μL of diluted cDNA and 20 μL of Powerup SYBR Green PCR master mix (primers added) (Thermo Fisher Scientific Inc., Waltham, MA, USA) were placed in each well of the plate and qPCR was run according to their optimized annealing temperature. Glyceraldehyde 3- phosphate dehydrogenase (GAPDH) a housekeeping gene was used as an exogenous reference to normalize the transcription and the subsequent data were analyzed by the ΔΔCt method.

2.5. Quantification of PFOA Accumulated in the Intestine

PFOA extraction from the tissue was performed following the method of Mamsen et al., 2017, with some modifications [64]. Tissues were homogenized at a ratio of 10 parts 70% HPLC grade acetonitrile (in DI water) to one-part tissue using Omni THQ—Digital Tissue Homogenizer for 2 min. Samples were shaken for half an hour at room temperature, then centrifuged at 10,000× g and the clear supernatant containing the extracted PFOA was separated. The supernatant was diluted in 70% acetonitrile in 1:1 and then injected into Ultra Performance Liquid Chromatography–Mass Spectrometry (UPLC–MS) using SYNAPT G2-Si system (Waters Corp., Milford, MA, USA). The mobile phase used was solvent A: 5 mM Ammonium acetate (NH4OAc·H2O) and solvent B: Acetonitrile. The mobile phase was kept at 100% for 2 min, and 98% B for the next 3 min. The column was then conditioned at 100% solvent A for the last 2 min. Calibration curve was built using known concentrations of PFOA (0.78125, 0.390625, 0.195313, 0.097656, 0.048828, 0.024414, 0.012207, and 0.006104 μM) in 70% acetonitrile. Electrospray ionization (ESI) in the mass spectrometry was set in negative ion mode for PFOA detection.

2.6. Data Processing and Statistical Analysis

Data analysis was performed with the IBM SPSS Statistics for Windows (Version 25.0, IBM Corp., Armonk, NY, USA). Due to the relative smaller sample size, we assumed that the data were not normally distributed and therefore a non-parametric analysis, Mann–Whitney U two independent test was used. Statistical values were considered significant at p-value ≤ 0.05 (denoted by “*”) and less significant at p-value > 0.05 but < 0.1 (denoted by “^”) reported from two-tailed tests.

3. Results

3.1. Accumulation of PFOA in the Intestinal Tissues

PFOA, the persistent perfluoroalkyl substance, has a high potential to accumulate in human and animal bodies and shows a large variation in concentration across the different tissues [65]. Extended half-life and high bio-accumulative characteristics increased its toxicity in living organisms [17]. After 10 days of PFOA exposure, small intestine and colon tissues of the female CD1 mice were noted to have a significant amount of PFOA accumulation compared to the control group in which no PFOA was detected. Accumulation of PFOA gradually increased in the tissue with an increase in dosing concentrations (Figure 1). The mean concentration of PFOA detected was 1002.62, 2298.06, 4427.71, and 6533.69 ng/g in the small intestine and 211.12, 412.73, 513.45, and 1834.27 ng in colon tissue for the treatment groups 1, 5, 10, and 20 mg/kg/day, respectively.
Overall, there was a very high dose-dependent bioaccumulation rate in intestinal tissues with much higher bioaccumulation in the small intestine compared to the colon, which may suggest dose-dependent effects of PFOA on gut epigenetics and permeability explored in the current work.

3.2. PFOA Induced Alteration of the Epigenetic Regulators

The DNA methylation is predominantly regulated by DNMT and TET enzymes. DNMTs have various isoforms and in the current study, we primarily focused on DNMT3a, DNMT3b, and DNMT1. These isoforms were principally selected because in the early development, the de novo DNMTs (i.e., DNMT3a and DNMT3b) play an important role in forming the 5 mC patterns in the genome and these genomic patterns were then maintained by DNMT1. In the small intestine, there is a significant decrease in the expression pattern of the genes Dnmt1 and Dnmt3b in all of the treatment groups (Figure 2A). Dnmt3a was expressed more in low dosing groups: 1 and 5 mg/kg/day and under-expressed at higher concentrations of 10 and 20 mg/kg/day. In colon tissues, we observed that after PFOA exposure the Dnmt3b expression level in higher concentrations was significantly reduced and the Dnmt3a expression level for the 10 mg/kg PFOA exposure was also found to be significantly reduced; hence, affecting the DNA methylation levels in the colon. Unlike Dnmt3b and 3a, Dnmt1 had no significant change in its expression level when exposed to increasing concentrations of PFOA (Figure 2B).
Next, we evaluated the mRNA expression levels of TETs enzymes. TETs are a family of three protein enzymes, which include TET1, TET2, and TET3. These three enzymes catalyze a set of reactions which include oxidation of 5 mC to 5 hmC, 5-formylcytosine, and then finally to 5-carboxylcytosine [66,67], therefore resulting in DNA demethylation. In the small intestine, Tet1 expression increased significantly at low and high concentrations, while Tet2 shows a significant increase at all dose levels. In contrast, Tet3 expression reduced significantly in all treatment groups (Figure 2C). In colon tissues, the mRNA expression for Tet3 significantly decreased after exposure to 10 mg/kg of PFOA, and Tet1 expression decreased after exposure to 20 mg/kg only. No significant change in mRNA expression of Tet2 after exposure to PFOA (Figure 2D) was noted. Therefore, our data suggest that at higher concentrations a concentration-dependent effect on the mRNA expression of key enzymes that regulate DNA methylation is possible, suggesting strong evidence of PFOA-induced epigenetic effects in colon tissue.

3.3. PFOA Induced Alteration of Tight Junction Genes

3.3.1. mRNA Expression Analysis of Cldns Genes

The structural integrity, barrier and transport functions of the gut epithelial lining are primarily regulated by tight junction proteins [54]. In the current study, we examined seven members of Cldn (transmembrane protein family), which were Cldn2, Cldn3, Cldn4, Cldn7, Cldn8, Cldn12, and Cldn15. In the small intestine, Cldn2 mRNA expression significantly decreased at all PFOA dosings, while Cldn8 and Cldn12 showed low expression at 5, 10, and 20 mg/kg/day doses. Cldn4 expression significantly increased at exposure levels of 5 mg/kg and gradually decreased with an increase in PFOA concentration but still higher than the untreated/control mice. Likewise, the Cldn3 gene has a higher expression at 5 and 10 mg/kg, but the mRNA level decreased at 20 mg/kg compared to control. Cldn15 expression pattern was significantly elevated at 1, 5 and 10 mg/kg/day treatment groups whereas Cldn7 expressed more at lower doses and then significantly decreased in expression at 20 mg/kg/day (Figure 3A).
In colon tissues, Cldn 2 expression was found to be significantly increased when exposed to the highest concentration (20 mg/kg) of PFOA. Similarly, Cldn 3 and Cldn 8 mRNA expression levels also increased at higher concentrations. However, Cldn 7 expression level was reduced at higher PFOA dose levels. Unlike Cldn 2, Cldn 3, Cldn 7, and Cldn 8, other Cldns (Cldn 4, Cldn 12, and Cldn 15) were not affected by the exposure (Figure 3B).

3.3.2. mRNA Expression Analysis of Tjps and Ocln Genes

To further explore the effect of other TJ components on intestinal permeability, we observed the mRNA expression levels of zonula occludens, i.e., TJ proteins (Tjp-1 and Tjp-2) and occludin (Ocln) genes. In the small intestine, Tjp1 was significantly upregulated at 5 mg/kg/day of PFOA dosing but gradually decreased in expression at higher levels of exposure. Conversely, Tjp2 expression was very low at 1 and 5 mg/kg/day and high at an exposure level of 10 mg/kg/day, whereas Ocln expression remained unaffected (Figure 4A). In the colon, the mRNA expression levels for Tjp1 and Ocln were found to decrease at 20 mg/kg concentration. Whereas, Tjp2 expression remained unaffected due to PFOA exposure (Figure 4B). These expression profiles showed a significant effect of PFOA on these protective barriers to indicate a possible dysregulation in the linked pathways.

4. Discussion

PFOA is a commonly used synthetic chemical that has a high persistence and bioaccumulation in environmental media and the human body [13]. Recently, another commonly used PFAS compound, perfluorooctane sulfonate (PFOS) was found to disrupt the intestinal microbiome in mice, causing intestinal tissue damage [41]. In the current study, we expect that PFOA exposure could compromise the expression of epigenetic genes and intestinal barrier function in mice.

4.1. Orally Administered PFOA Accumulates in the Intestine

The intestinal wall is an initial contact barrier to environmental chemicals after being ingested through food or drinking water. PFOA has a reduced elimination rate in feces which may lead to its bioaccumulation in various organs including the intestine [38]. In our experiments, a significant dose-dependent increase in PFOA concentration was observed in the small intestine and colon tissues (Figure 1). Higher levels of accumulation were noted in the small intestine compared to colon tissues. In vivo exposure studies conducted in the past have also demonstrated a significant amount of PFOA, as well as the accumulation of other PFAS compounds in intestinal tissues compared to other organs [37,39,40]. The current study is in line with the studies conducted in the past.

4.2. PFOA Alters Expression of DNA Methylation Genes in the Intestine

To explore the epigenetic mechanisms that can cause gene expression changes in the small intestine and colon tissues exposed to PFOA, we specifically studied the mRNA expression changes of genes involved in DNA methylation mechanisms. Various studies published recently indicate a number of mechanisms by which epigenetic changes regulate intestinal development [46] and cause various intestinal disorders [40,48], thus providing the opportunities to identify new epigenetic biomarkers as treatment targets.
There are a limited number of studies available that explore the epigenetic alterations in the intestine due to PFOA exposure. The studies available are mostly performed on blood samples collected from the PFOA-exposed population [68,69]. One of these studies has revealed the hypomethylation of glutathione-S-transferase Pi in liver cells [70]. The previous studies from our group have also reported significant alterations in DNA methylation in vitro in HepG2 cells [24] and in vivo in mice kidney and liver tissues [23,26]. However, the effect of PFOA on the epigenetic alterations of intestinal tissues has not been studied to date.
For examination of the mRNA expression levels of Dnmts and Tets, key regulators of DNA methylation and demethylation, respectively, we observed a significant decrease in the mRNA expression levels of Dnmt1 and Dnmt3b in small intestine tissue. Dnmt3a level was found to be significantly reduced when exposed to higher concentrations of PFOA (i.e., 10 and 20 mg/kg), thus affecting the de novo methylation of DNA and maintenance of these genomic patterns (Figure 2A). Similarly, in colon tissues, Dnmt3b expression levels were found to be reduced when exposed to 1, 10, and 20 mg/kg of PFOA for 10 days, whereas the Dnmt3a level was found to be reduced only when exposed to 10 mg/kg of PFOA. No significant changes were observed for the Dnmt1 levels (Figure 2B). This may suggest the effect of PFOA on de novo methylation in the colon, but the maintenance of these DNA methylation patterns in the colon may remain unaffected due to insignificant changes in Dnmt1 levels. However, these could be explored in the future with further experiments. More severe effects of the expression levels of Dnmts in the small intestine could be due to a higher accumulation of PFOA in the small intestine compared to the colon especially at higher dose levels. Nevertheless, the reduction in the expression of Dnmts can possibly have a beneficial effect in preventing diseases such as colorectal carcinoma by reactivation of the tumor suppressor genes in the intestinal tissue [71].
The demethylation of CpG is a result of hydroxymethylation, which is mediated by ten–eleven translocation enzymes (TET1, TET2, and TET3). Past studies have demonstrated the reduced mRNA expression of Tet1 in intestinal tumors and gastric cancers [72,73]. Further, Tet3 expression was found to be reduced in the disease model of experimental fibrosis, whereas Tet2 expression was not found to be significantly reduced in disease conditions [74]. Our study also reveals reduced expression of Tet3 in the small intestine in all the treatment groups and colon tissues from the 10 mg/kg treatment group. The Tet1 expression in the colon was also found to be reduced in the 20 mg/kg treatment group (Figure 2D). This reduction in expression levels of Tet3 and Tet1 could be due to the result of a decrease in the levels of Dnmts to balance the net amount of DNA methylation within the tissue. However, we observed an increase in Tet1 and Tet2 expression levels in small intestinal tissues after PFOA exposure (Figure 2C) that may potentially lead to change in expression levels of other functional genes in the small intestine and colon. Alterations in the expression of epigenetic regulators seem to be more profound in the small intestine, possibly due to the higher accumulation of PFOA compared to the colon. These evaluations suggest that direct environmental and occupational exposure to PFOA can possibly lead to epigenetic alterations in the intestinal tissues. These methylation anomalies can be of potential significance in the development of human pathologies as is evident from previous studies in animal models, which showed their association with inflammatory bowel disease (IBD) [45], compromised intestinal development [46], intestinal adenomas [47], colorectal cancer [40], intestinal inflammation [48], and inflammatory bowel disease including Crohn’s disease [49,50]. The epigenetic changes can also lead to overexpression and inhibition of various TJ genes which can promote tumorigenic and metastatic properties of gastric cancer cells [51,52]. Future work can focus on evaluation of methylation levels of TJ genes and other key signaling pathways involved in intestinal tumors in PFOA-exposed mice to explore the direct effect of methylation changes in the development of intestinal pathologies.

4.3. PFOA Alters Expression of TJ Genes in the Intestine

As the gastrointestinal tract (GIT) is the primary route of exposure to the PFOA present in the drinking water and food chain, it can affect the structural integrity and function of the gut epithelial lining. The integrity and barrier function of the gut lining are maintained by tight junction proteins that seal the adjacent cells to regulate transport and avoid leakage [75]. Tight junction proteins either localize as transmembrane proteins such as Cldn and Ocln or cytoplasmic proteins, Tjp [76,77]. Dysfunctionality in these proteins has been implicated in several disorders, as in impaired blood–brain barrier and blood–retinal barrier, inflammatory bowel disease, breast cancer, celiac disease and even in heredity diseases such as deafness [78,79,80].
Several studies have shown an increase in permeability of the gut due to environmental inducers such as synthetic food additives (emulsifiers and surfactants), nanoparticles, and alcohol which disrupt tight junction proteins that lead to leaky gut [81,82]. Further, many viral and bacterial infections are known to destroy these junction proteins and cause leakage in epithelial linings [83,84]. The adverse effects of environmental toxicants on the tight junction proteins are an unexplored area. There is a need to evaluate the GIT integrity and function in PFAS-exposed tissue to mimic the exposure route of these toxicants through water and food. Therefore, we examined the variation in the mRNA expression pattern of key tight junction genes (Cldn, Ocln, and Tjp) in the small intestine and colon tissue in orally administered mice with PFOA.
The results from the present study show that PFOA had an effect on these tight junction genes and there is a substantial change in mRNA expression between the control and treatment group mice. Further, a variation in the expression pattern between the small intestine and colon suggests that these tissues are affected differently by PFOA treatment. We examined seven members of the Cldn protein family, which either functions as a paracellular barrier or channel depending upon the extracellular regions of these proteins [85,86]. In the small intestine, expression of Cldns was significantly affected, in proportion to the PFOA concentration and type of Cldn member. The change in the expression pattern can be linked to the elevated level of PFOA accumulation in the small intestine. Further, Dnmts are previously reported to be linked with the change in the expression profile of Cldn in different carcinomas [52,87]. This is an indication that the heavily altered expression pattern of Dnmts in the current study would have affected Cldn transcription in the small intestine. In the colon, Cldn 2, Cldn 3, and Cldn 8 expression was greater at higher levels of exposure to PFOA. Since PFOA was detected in the colon in high amounts, especially in the higher concentration treatment groups, its effect was proportional to the expression pattern of some of the Cldns.
Occludin (Ocln), a transmembrane tight junction that is indirectly involved in the barrier function through regulation of other tight junction proteins [57], remained unchanged in the small intestine whereas in the colon it was downregulated at the highest PFOA dose level. The knockout of the Ocln gene in mice model has shown chronic inflammation and poor tight junction integrity [88]. Tjps genes, which encode the cytoplasmic proteins to bridge transmembrane and cytoskeletal proteins [57], showed dysregulation in mRNA expression across the intestine. Mutation in Tjp2 inhibits its linkage to Cldn and leads to biliary disease [89]; while knockdown of the Tjp1 gene induces the condition of leaky gut [90].
The change in the expression profile of tight junction genes was more conspicuous in the small intestine compared to the colon. Our results show that PFOA accumulation was greater in the small intestine compared to the colon which is a distal part of the GIT. Further, it is evident from our previous study that PFOA accumulation was almost six-fold more in the liver compared to the small intestine [23]. Our results suggest that orally administered PFOA accumulates in the small intestine and is absorbed in higher levels from here to the liver and in trace amounts as it passes to the distal colon. Hence, more significant changes in gene expression were observed in the small intestine than in the colon.

5. Conclusions

In the current study, the expression of epigenetic and tight junction genes was found to be altered in intestinal tissues with more profound effects in the small intestine due to increased accumulation of PFOA. The alterations in the expression levels of tight junction genes evaluated may be due to the epigenetic toxicity at high concentrations of PFOA found in the intestinal tissues. Nevertheless, further research is needed to examine the methylation profiles of the tight junction genes to confirm the direct epigenetic effect of PFOA on the regulation of genes expressed in intestinal tissues. It would also be prudent to assess how sub-acute and chronic PFOA exposure could affect epigenetic factors and the pathways triggered. Transgenerational studies could provide valuable insights on how these effects are propagated.

Author Contributions

F.R. and S.A. contributed equally. They were responsible for investigation, experiments, data collection, analysis, and writing. J.M.K.I. was responsible for conceptualization, writing, funding, overall project supervision, and administration. All authors have read and agreed to the published version of the manuscript.

Funding

J.M.K.I. is supported by University of Illinois at Urbana-Champaign startup grants and the Planning Grant Award from the Cancer Center at Illinois.

Acknowledgments

Support from the staff at Beckman Institute is greatly appreciated in animal studies.

Conflicts of Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

References

  1. Kissa, E. Fluorinated Surfactants and Repellents; CRC Press: Boca Raton, FL, USA, 2001; Volume 97. [Google Scholar]
  2. Kannan, K. Perfluoroalkyl and polyfluoroalkyl substances: Current and future perspectives. J. Environ. Chem. 2011, 8, 333–338. [Google Scholar] [CrossRef] [Green Version]
  3. Steenland, K.; Fletcher, T.; Savitz, D.A. Epidemiologic evidence on the health effects of perfluorooctanoic acid (PFOA). Environ. Health Perspect. 2010, 118, 1100–1108. [Google Scholar] [CrossRef] [PubMed]
  4. Scher, D.P.; Kelly, J.E.; Huset, C.A.; Barry, K.M.; Yingling, V.L. Does soil track-in contribute to house dust concentrations of perfluoroalkyl acids (PFAAs) in areas affected by soil or water contamination? J. Expo. Sci. Environ. Epidemiol. 2019, 29, 218–226. [Google Scholar] [CrossRef] [PubMed]
  5. Guelfo, J.L.; Adamson, D.T. Evaluation of a national data set for insights into sources, composition, and concentrations of per- and polyfluoroalkyl substances (PFASs) in U.S. drinking water. Environ. Pollut. 2018, 236, 505–513. [Google Scholar] [CrossRef] [PubMed]
  6. Liu, Y.; Li, X.; Wang, X.; Qiao, X.; Hao, S.; Lu, J.; Duan, X.; Dionysiou, D.D.; Zheng, B. Contamination Profiles of Perfluoroalkyl Substances (PFAS) in Groundwater in the Alluvial–Pluvial Plain of Hutuo River, China. Water 2019, 11, 2316. [Google Scholar] [CrossRef] [Green Version]
  7. Goosey, E.; Harrad, S. Perfluoroalkyl substances in UK indoor and outdoor air: Spatial and seasonal variation, and implications for human exposure. Environ. Int. 2012, 45, 86–90. [Google Scholar] [CrossRef]
  8. Xie, S.; Cui, Y.; Yang, Y.; Meng, K.; Pan, Y.; Liu, Z.; Chen, D. Tissue distribution and bioaccumulation of 8:2 fluorotelomer alcohol and its metabolites in pigs after oral exposure. Chemosphere 2020, 249, 126016. [Google Scholar] [CrossRef]
  9. Bogdanska, J.; Borg, D.; Bergström, U.; Mellring, M.; Bergman, Å.; DePierre, J.; Nobel, S. Tissue distribution of 14C-labelled perfluorooctanoic acid in adult mice after 1–5 days of dietary exposure to an experimental dose or a lower dose that resulted in blood levels similar to those detected in exposed humans. Chemosphere 2020, 239, 124755. [Google Scholar] [CrossRef]
  10. Kedikoglou, K.; Costopoulou, D.; Vassiliadou, I.; Leondiadis, L. Preliminary assessment of general population exposure to perfluoroalkyl substances through diet in Greece. Environ. Res. 2019, 177, 108617. [Google Scholar] [CrossRef]
  11. Bao, J.; Yu, W.-J.; Liu, Y.; Wang, X.; Jin, Y.-H.; Dong, G.-H. Perfluoroalkyl substances in groundwater and home-produced vegetables and eggs around a fluorochemical industrial park in China. Ecotoxicol. Environ. Saf. 2019, 171, 199–205. [Google Scholar] [CrossRef]
  12. Gomis, M.I.; Vestergren, R.; MacLeod, M.; Mueller, J.F.; Cousins, I.T. Historical human exposure to perfluoroalkyl acids in the United States and Australia reconstructed from biomonitoring data using population-based pharmacokinetic modelling. Environ. Int. 2017, 108, 92–102. [Google Scholar] [CrossRef] [PubMed]
  13. Buck, R.C.; Franklin, J.; Berger, U.; Conder, J.M.; Cousins, I.T.; de Voogt, P.; Jensen, A.A.; Kannan, K.; Mabury, S.A.; van Leeuwen, S.P. Perfluoroalkyl and polyfluoroalkyl substances in the environment: Terminology, classification, and origins. Integr. Environ. Assess. Manag. 2011, 7, 513–541. [Google Scholar] [CrossRef] [PubMed]
  14. Sochorová, L.; Hanzlíková, L.; Černá, M.; Drgáčová, A.; Fialová, A.; Švarcová, A.; Gramblička, T.; Pulkrabová, J. Perfluorinated alkylated substances and brominated flame retardants in serum of the Czech adult population. Int. J. Hyg. Environ. Health 2017, 220, 235–243. [Google Scholar] [CrossRef] [PubMed]
  15. Jin, H.; Mao, L.; Xie, J.; Zhao, M.; Bai, X.; Wen, J.; Shen, T.; Wu, P. Poly- and perfluoroalkyl substance concentrations in human breast milk and their associations with postnatal infant growth. Sci. Total Environ. 2020, 713, 136417. [Google Scholar] [CrossRef]
  16. Bartell, S.M.; Calafat, A.M.; Lyu, C.; Kato, K.; Ryan, P.B.; Steenland, K. Rate of decline in serum PFOA concentrations after granular activated carbon filtration at two public water systems in Ohio and West Virginia. Environ. Health Perspect. 2010, 118, 222–228. [Google Scholar] [CrossRef] [PubMed]
  17. Li, Y.; Fletcher, T.; Mucs, D.; Scott, K.; Lindh, C.H.; Tallving, P.; Jakobsson, K. Half-lives of PFOS, PFHxS and PFOA after end of exposure to contaminated drinking water. Occup. Environ. Med. 2018, 75, 46–51. [Google Scholar] [CrossRef] [Green Version]
  18. Fletcher, T.; Galloway, T.S.; Melzer, D.; Holcroft, P.; Cipelli, R.; Pilling, L.C.; Mondal, D.; Luster, M.; Harries, L.W. Associations between PFOA, PFOS and changes in the expression of genes involved in cholesterol metabolism in humans. Environ. Int. 2013, 57–58, 2–10. [Google Scholar] [CrossRef]
  19. Lam, J.; Koustas, E.; Sutton, P.; Johnson, P.I.; Atchley, D.S.; Sen, S.; Robinson, K.A.; Axelrad, D.A.; Woodruff, T. The Navigation Guide—Evidence-based medicine meets environmental health: Integration of animal and human evidence for PFOA effects on fetal growth. J. Environ. Health Perspect. 2014, 122, 1040–1051. [Google Scholar] [CrossRef] [Green Version]
  20. Steenland, K.; Zhao, L.; Winquist, A.; Parks, C. Ulcerative colitis and perfluorooctanoic acid (PFOA) in a highly exposed population of community residents and workers in the mid-Ohio valley. Environ. Health Perspect. 2013, 121, 900–905. [Google Scholar] [CrossRef]
  21. Shane, H.L.; Baur, R.; Lukomska, E.; Weatherly, L.; Anderson, S.E. Immunotoxicity and allergenic potential induced by topical application of perfluorooctanoic acid (PFOA) in a murine model. Food Chem. Toxicol. 2020, 136, 111114. [Google Scholar] [CrossRef]
  22. Kmecick, M.; Vieira da Costa, M.C.; Oliveira Ribeiro, C.A.d.; Ortolani-Machado, C.F. Morphological evidence of neurotoxic effects in chicken embryos after exposure to perfluorooctanoic acid (PFOA) and inorganic cadmium. Toxicology 2019, 427, 152286. [Google Scholar] [CrossRef]
  23. Wen, Y.; Chen, J.; Li, J.; Arif, W.; Kalsotra, A.; Irudayaraj, J. Effect of PFOA on DNA Methylation and Alternative Splicing in Mouse Liver. Toxicol. Lett. 2020, 329, 38–46. [Google Scholar] [CrossRef] [PubMed]
  24. Wen, Y.; Mirji, N.; Irudayaraj, J. Epigenetic toxicity of PFOA and GenX in HepG2 cells and their role in lipid metabolism. Toxicol. Vitro 2020, 65, 104797. [Google Scholar] [CrossRef] [PubMed]
  25. Liu, W.; Irudayaraj, J. Perfluorooctanoic acid (PFOA) exposure inhibits DNA methyltransferase activities and alters constitutive heterochromatin organization. Food Chem. Toxicol. 2020, 141, 111358. [Google Scholar] [CrossRef] [PubMed]
  26. Rashid, F.; Ramakrishnan, A.; Fields, C.; Irudayaraj, J. Acute PFOA exposure promotes epigenomic alterations in mouse kidney tissues. Toxicol. Rep. 2020, 7, 125–132. [Google Scholar] [CrossRef]
  27. Franco, M.E.; Sutherland, G.E.; Fernandez-Luna, M.T.; Lavado, R. Altered expression and activity of phase I and II biotransformation enzymes in human liver cells by perfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS). Toxicology 2020, 430, 152339. [Google Scholar] [CrossRef]
  28. Brieger, A.; Bienefeld, N.; Hasan, R.; Goerlich, R.; Haase, H. Impact of perfluorooctanesulfonate and perfluorooctanoic acid on human peripheral leukocytes. Toxicol. Vitro 2011, 25, 960–968. [Google Scholar] [CrossRef]
  29. Huang, Q.; Zhang, J.; Martin, F.L.; Peng, S.; Tian, M.; Mu, X.; Shen, H. Perfluorooctanoic acid induces apoptosis through the p53-dependent mitochondrial pathway in human hepatic cells: A proteomic study. Toxicol. Lett. 2013, 223, 211–220. [Google Scholar] [CrossRef]
  30. Coperchini, F.; Awwad, O.; Rotondi, M.; Santini, F.; Imbriani, M.; Chiovato, L. Thyroid disruption by perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA). J. Endocrinol. Investig. 2017, 40, 105–121. [Google Scholar] [CrossRef]
  31. Biegel, L.B.; Hurtt, M.E.; Frame, S.R.; O’Connor, J.C.; Cook, J.C. Mechanisms of extrahepatic tumor induction by peroxisome proliferators in male CD rats. Toxicol. Sci. 2001, 60, 44–55. [Google Scholar] [CrossRef]
  32. Barry, V.; Winquist, A.; Steenland, K. Perfluorooctanoic acid (PFOA) exposures and incident cancers among adults living near a chemical plant. Environ. Health Perspect. 2013, 121, 1313–1318. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Arukwe, A.; Mortensen, A.S. Lipid peroxidation and oxidative stress responses of salmon fed a diet containing perfluorooctane sulfonic-or perfluorooctane carboxylic acids. Comp. Biochem. 2011, 154, 288–295. [Google Scholar] [CrossRef] [PubMed]
  34. Abbott, B.D.; Wood, C.R.; Watkins, A.M.; Tatum-Gibbs, K.; Das, K.P.; Lau, C. Effects of perfluorooctanoic acid (PFOA) on expression of peroxisome proliferator-activated receptors (PPAR) and nuclear receptor-regulated genes in fetal and postnatal CD-1 mouse tissues. Reprod. Toxicol. 2012, 33, 491–505. [Google Scholar] [CrossRef] [PubMed]
  35. Kurtz, A.E.; Reiner, J.L.; West, K.L.; Jensen, B.A. Perfluorinated alkyl acids in Hawaiian cetaceans and potential biomarkers of effect: Peroxisome proliferator-activated receptor alpha and cytochrome P450 4A. Environ. Sci. Technol. 2019, 53, 2830–2839. [Google Scholar] [CrossRef]
  36. Eldasher, L.M.; Wen, X.; Little, M.S.; Bircsak, K.M.; Yacovino, L.L.; Aleksunes, L.M. Hepatic and renal Bcrp transporter expression in mice treated with perfluorooctanoic acid. Toxicology 2013, 306, 108–113. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Hong, S.; Khim, J.S.; Wang, T.; Naile, J.E.; Park, J.; Kwon, B.-O.; Song, S.J.; Ryu, J.; Codling, G.; Jones, P.D. Bioaccumulation characteristics of perfluoroalkyl acids (PFAAs) in coastal organisms from the west coast of South Korea. Chemosphere 2015, 129, 157–163. [Google Scholar] [CrossRef]
  38. Cui, L.; Liao, C.-Y.; Zhou, Q.-F.; Xia, T.-M.; Yun, Z.-J.; Jiang, G.-B. Excretion of PFOA and PFOS in Male Rats during a Subchronic Exposure. Arch. Environ. Contam. Toxicol. 2010, 58, 205–213. [Google Scholar] [CrossRef]
  39. Ulhaq, M.; Sundström, M.; Larsson, P.; Gabrielsson, J.; Bergman, Å.; Norrgren, L.; Örn, S. Tissue uptake, distribution and elimination of 14C-PFOA in zebrafish (Danio rerio). Aquat. Toxicol. 2015, 163, 148–157. [Google Scholar] [CrossRef]
  40. Martín, J.; Hidalgo, F.; García-Corcoles, M.T.; Ibáñez-Yuste, A.J.; Alonso, E.; Vilchez, J.L.; Zafra-Gómez, A. Bioaccumulation of perfluoroalkyl substances in marine echinoderms: Results of laboratory-scale experiments with Holothuria tubulosa Gmelin, 1791. Chemosphere 2019, 215, 261–271. [Google Scholar] [CrossRef]
  41. Zhang, L.; Rimal, B.; Nichols, R.G.; Tian, Y.; Smith, P.B.; Hatzakis, E.; Chang, S.-C.; Butenhoff, J.L.; Peters, J.M.; Patterson, A.D. Perfluorooctane sulfonate alters gut microbiota-host metabolic homeostasis in mice. Toxicology 2020, 431, 152365. [Google Scholar] [CrossRef]
  42. Kleszczyński, K.; Gardzielewski, P.; Mulkiewicz, E.; Stepnowski, P.; Składanowski, A.C. Analysis of structure–cytotoxicity in vitro relationship (SAR) for perfluorinated carboxylic acids. Toxicol. Vitro 2007, 21, 1206–1211. [Google Scholar] [CrossRef]
  43. Kleszczyński, K.; Składanowski, A.C. Mechanism of cytotoxic action of perfluorinated acids. III. Disturbance in Ca2+ homeostasis. Toxicol. Appl. Pharmacol. 2011, 251, 163–168. [Google Scholar] [CrossRef] [PubMed]
  44. Miao, C.; Ma, J.; Zhang, Y.; Chu, Y.; Li, J.; Kuai, R.; Wang, S.; Peng, H. Perfluorooctanoic acid enhances colorectal cancer DLD-1 cells invasiveness through activating NF-kappaB mediated matrix metalloproteinase-2/-9 expression. Int. J. Clin. Exp. Pathol. 2015, 8, 10512–10522. [Google Scholar] [PubMed]
  45. Yi, J.M.; Kim, T.O. Epigenetic alterations in inflammatory bowel disease and cancer. Intest. Res. 2015, 13, 112–121. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Yu, D.-H.; Gadkari, M.; Zhou, Q.; Yu, S.; Gao, N.; Guan, Y.; Schady, D.; Roshan, T.N.; Chen, M.-H.; Laritsky, E.; et al. Postnatal epigenetic regulation of intestinal stem cells requires DNA methylation and is guided by the microbiome. Genome Biol. 2015, 16, 211. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Abu-Remaileh, M.; Bender, S.; Raddatz, G.; Ansari, I.; Cohen, D.; Gutekunst, J.; Musch, T.; Linhart, H.; Breiling, A.; Pikarsky, E.; et al. Chronic Inflammation Induces a Novel Epigenetic Program That Is Conserved in Intestinal Adenomas and in Colorectal Cancer. Cancer Res. 2015, 75, 2120. [Google Scholar] [CrossRef] [Green Version]
  48. Yara, S.; Lavoie, J.-C.; Beaulieu, J.-F.; Delvin, E.; Amre, D.; Marcil, V.; Seidman, E.; Levy, E. Iron-Ascorbate-Mediated Lipid Peroxidation Causes Epigenetic Changes in the Antioxidant Defense in Intestinal Epithelial Cells: Impact on Inflammation. PLoS ONE 2013, 8, e63456. [Google Scholar] [CrossRef]
  49. Fogel, O.; Richard-Miceli, C.; Tost, J. Epigenetic changes in chronic inflammatory diseases. In Advances in Protein Chemistry and Structural Biology; Elsevier: Amsterdam, The Netherlands, 2017; Volume 106, pp. 139–189. [Google Scholar]
  50. Kelly, D.; Kotliar, M.; Woo, V.; Jagannathan, S.; Whitt, J.; Moncivaiz, J.; Aronow, B.J.; Dubinsky, M.C.; Hyams, J.S.; Markowitz, J.F.; et al. Microbiota-sensitive epigenetic signature predicts inflammation in Crohn’s disease. JCI Insight 2018, 3, e122104. [Google Scholar] [CrossRef]
  51. Osanai, M.; Murata, M.; Nishikiori, N.; Chiba, H.; Kojima, T.; Sawada, N. Epigenetic Silencing of Occludin Promotes Tumorigenic and Metastatic Properties of Cancer Cells via Modulations of Unique Sets of Apoptosis-Associated Genes. Cancer Res. 2006, 66, 9125. [Google Scholar] [CrossRef] [Green Version]
  52. Kwon, M.J.; Kim, S.-H.; Jeong, H.M.; Jung, H.S.; Kim, S.-S.; Lee, J.E.; Gye, M.C.; Erkin, Ö.C.; Koh, S.S.; Choi, Y.-L.; et al. Claudin-4 overexpression is associated with epigenetic derepression in gastric carcinoma. Lab. Investig. 2011, 91, 1652–1667. [Google Scholar] [CrossRef] [Green Version]
  53. Lee, B.; Moon, K.M.; Kim, C.Y. Tight Junction in the Intestinal Epithelium: Its Association with Diseases and Regulation by Phytochemicals. J. Immunol. Res. 2018, 2018, 2645465. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Buckley, A.; Turner, J.R. Cell Biology of Tight Junction Barrier Regulation and Mucosal Disease. Cold Spring Harb. Perspect. Biol. 2018, 10, a029314. [Google Scholar] [CrossRef] [PubMed]
  55. Meddings, J. The significance of the gut barrier in disease. Gut 2008, 57, 438–440. [Google Scholar] [CrossRef] [PubMed]
  56. McCole, D.F. IBD candidate genes and intestinal barrier regulation. Inflamm. Bowel. Dis. 2014, 20, 1829–1849. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Chelakkot, C.; Ghim, J.; Ryu, S.H. Mechanisms regulating intestinal barrier integrity and its pathological implications. Exp. Mol. Med. 2018, 50, 103. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  58. Lerner, A.; Matthias, T. Changes in intestinal tight junction permeability associated with industrial food additives explain the rising incidence of autoimmune disease. Autoimmun. Rev. 2015, 14, 479–489. [Google Scholar] [CrossRef] [Green Version]
  59. Norén, E.; Almer, S.; Söderman, J. Genetic variation and expression levels of tight junction genes identifies association between MAGI3 and inflammatory bowel disease. BMC Gastroenterol. 2017, 17, 68. [Google Scholar] [CrossRef]
  60. Olsen, G.W.; Burris, J.M.; Ehresman, D.J.; Froehlich, J.W.; Seacat, A.M.; Butenhoff, J.L.; Zobel, L.R. Half-life of serum elimination of perfluorooctanesulfonate, perfluorohexanesulfonate, and perfluorooctanoate in retired fluorochemical production workers. Environ. Health Perspect. 2007, 115, 1298–1305. [Google Scholar] [CrossRef]
  61. Emmett, E.A.; Shofer, F.S.; Zhang, H.; Freeman, D.; Desai, C.; Shaw, L.M. Community exposure to perfluorooctanoate: Relationships between serum concentrations and exposure sources. J. Occup. Environ. Med. 2006, 48, 759–770. [Google Scholar] [CrossRef]
  62. Yan, S.; Wang, J.; Zhang, W.; Dai, J. Circulating microRNA profiles altered in mice after 28d exposure to perfluorooctanoic acid. Toxicol. Lett. 2014, 224, 24–31. [Google Scholar] [CrossRef]
  63. Lau, C.; Thibodeaux, J.R.; Hanson, R.G.; Narotsky, M.G.; Rogers, J.M.; Lindstrom, A.B.; Strynar, M.J. Effects of perfluorooctanoic acid exposure during pregnancy in the mouse. Toxicol. Sci. 2006, 90, 510–518. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Mamsen, L.S.; Jönsson, B.A.G.; Lindh, C.H.; Olesen, R.H.; Larsen, A.; Ernst, E.; Kelsey, T.W.; Andersen, C.Y. Concentration of perfluorinated compounds and cotinine in human foetal organs, placenta, and maternal plasma. Sci. Total Environ. 2017, 596–597, 97–105. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Mamsen, L.S.; Björvang, R.D.; Mucs, D.; Vinnars, M.T.; Papadogiannakis, N.; Lindh, C.H.; Andersen, C.Y.; Damdimopoulou, P. Concentrations of perfluoroalkyl substances (PFASs) in human embryonic and fetal organs from first, second, and third trimester pregnancies. Environ. Int. 2019, 124, 482–492. [Google Scholar] [CrossRef] [PubMed]
  66. Tahiliani, M.; Koh, K.P.; Shen, Y.; Pastor, W.A.; Bandukwala, H.; Brudno, Y.; Agarwal, S.; Iyer, L.M.; Liu, D.R.; Aravind, L.; et al. Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1. Science 2009, 324, 930–935. [Google Scholar] [CrossRef] [Green Version]
  67. Ito, S.; Shen, L.; Dai, Q.; Wu, S.C.; Collins, L.B.; Swenberg, J.A.; He, C.; Zhang, Y. Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine. Science 2011, 333, 1300–1303. [Google Scholar] [CrossRef] [Green Version]
  68. Watkins, D.J.; Wellenius, G.A.; Butler, R.A.; Bartell, S.M.; Fletcher, T.; Kelsey, K.T. Associations between serum perfluoroalkyl acids and LINE-1 DNA methylation. Environ. Int. 2014, 63, 71–76. [Google Scholar] [CrossRef] [Green Version]
  69. Kobayashi, S.; Azumi, K.; Goudarzi, H.; Araki, A.; Miyashita, C.; Kobayashi, S.; Itoh, S.; Sasaki, S.; Ishizuka, M.; Nakazawa, H.; et al. Effects of prenatal perfluoroalkyl acid exposure on cord blood IGF2/H19 methylation and ponderal index: The Hokkaido Study. J. Expo. Sci. Environ. Epidemiol. 2017, 27, 251–259. [Google Scholar] [CrossRef] [Green Version]
  70. Tian, M.; Peng, S.; Martin, F.L.; Zhang, J.; Liu, L.; Wang, Z.; Dong, S.; Shen, H. Perfluorooctanoic acid induces gene promoter hypermethylation of glutathione-S-transferase Pi in human liver L02 cells. Toxicology 2012, 296, 48–55. [Google Scholar] [CrossRef]
  71. Cai, Y.; Geutjes, E.J.; de Lint, K.; Roepman, P.; Bruurs, L.; Yu, L.R.; Wang, W.; van Blijswijk, J.; Mohammad, H.; de Rink, I.; et al. The NuRD complex cooperates with DNMTs to maintain silencing of key colorectal tumor suppressor genes. Oncogene 2014, 33, 2157–2168. [Google Scholar] [CrossRef] [Green Version]
  72. Wu, B.-K.; Brenner, C. Suppression of TET1-Dependent DNA Demethylation Is Essential for KRAS-Mediated Transformation. Cell Rep. 2014, 9, 1827–1840. [Google Scholar] [CrossRef] [Green Version]
  73. Tricarico, R.; Madzo, J.; Scher, G.; Maegawa, S.; Jelinek, J.; Scher, C.; Chang, W.-C.; Nicolas, E.; Zhou, Y.; Slifker, M.; et al. TET1&TDG suppress intestinal tumorigenesis by down-regulating the inflammatory and immune response pathways. bioRxiv 2019, 676445. [Google Scholar] [CrossRef] [Green Version]
  74. Tampe, B.; Tampe, D.; Müller, C.A.; Sugimoto, H.; LeBleu, V.; Xu, X.; Müller, G.A.; Zeisberg, E.M.; Kalluri, R.; Zeisberg, M. Tet3-mediated hydroxymethylation of epigenetically silenced genes contributes to bone morphogenic protein 7-induced reversal of kidney fibrosis. J. Am. Soc. Nephrol. 2014, 25, 905–912. [Google Scholar] [CrossRef] [PubMed]
  75. Groschwitz, K.R.; Hogan, S.P. Intestinal barrier function: Molecular regulation and disease pathogenesis. J. Allergy Clin. Immunol. 2009, 124, 3–20. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  76. Günzel, D.; Yu, A.S. Claudins and the modulation of tight junction permeability. Physiol. Rev. 2013, 93, 525–569. [Google Scholar] [CrossRef] [Green Version]
  77. Cereijido, M.; Contreras, R.G.; Flores-Benítez, D.; Flores-Maldonado, C.; Larre, I.; Ruiz, A.; Shoshani, L. New diseases derived or associated with the tight junction. Arch. Med Res. 2007, 38, 465–478. [Google Scholar] [CrossRef]
  78. Yamazaki, Y.; Shinohara, M.; Shinohara, M.; Yamazaki, A.; Murray, M.E.; Liesinger, A.M.; Heckman, M.G.; Lesser, E.R.; Parisi, J.E.; Petersen, R.C.; et al. Selective loss of cortical endothelial tight junction proteins during Alzheimer’s disease progression. Brain J. Neurol. 2019, 142, 1077–1092. [Google Scholar] [CrossRef]
  79. Jauregi-Miguel, A.; Fernandez-Jimenez, N.; Irastorza, I.; Plaza-Izurieta, L.; Vitoria, J.C.; Bilbao, J.R. Alteration of tight junction gene expression in celiac disease. J. Pediatr. Gastroenterol. Nutr. 2014, 58, 762–767. [Google Scholar] [CrossRef]
  80. Ivanova, E.; Alam, N.M.; Prusky, G.T.; Sagdullaev, B.T. Blood-retina barrier failure and vision loss in neuron-specific degeneration. JCI Insight 2019, 5, e126747. [Google Scholar] [CrossRef] [Green Version]
  81. Wang, Y.; Tong, J.; Chang, B.; Wang, B.; Zhang, D.; Wang, B. Effects of alcohol on intestinal epithelial barrier permeability and expression of tight junction-associated proteins. Mol. Med. Rep. 2014, 9, 2352–2356. [Google Scholar] [CrossRef] [Green Version]
  82. Orr, S.E.; Gokulan, K.; Boudreau, M.; Cerniglia, C.E.; Khare, S. Alteration in the mRNA expression of genes associated with gastrointestinal permeability and ileal TNF-α secretion due to the exposure of silver nanoparticles in Sprague-Dawley rats. J. Nanobiotechnol. 2019, 17, 63. [Google Scholar] [CrossRef]
  83. Troeger, H.; Loddenkemper, C.; Schneider, T.; Schreier, E.; Epple, H.J.; Zeitz, M.; Fromm, M.; Schulzke, J.D. Structural and functional changes of the duodenum in human norovirus infection. Gut 2009, 58, 1070–1077. [Google Scholar] [CrossRef] [PubMed]
  84. Guttman, J.A.; Samji, F.N.; Li, Y.; Vogl, A.W.; Finlay, B.B. Evidence that tight junctions are disrupted due to intimate bacterial contact and not inflammation during attaching and effacing pathogen infection in vivo. Infect. Immun. 2006, 74, 6075–6084. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  85. Zihni, C.; Mills, C.; Matter, K.; Balda, M.S. Tight junctions: From simple barriers to multifunctional molecular gates. Nat. Rev. Mol. Cell Biol. 2016, 17, 564–580. [Google Scholar] [CrossRef] [PubMed]
  86. Tsukita, S.; Tanaka, H.; Tamura, A. The Claudins: From Tight Junctions to Biological Systems. Trends Biochem. Sci. 2019, 44, 141–152. [Google Scholar] [CrossRef]
  87. Xu, X.; Jin, H.; Liu, Y.; Liu, L.; Wu, Q.; Guo, Y.; Yu, L.; Liu, Z.; Zhang, T.; Zhang, X.; et al. The expression patterns and correlations of claudin-6, methy-CpG binding protein 2, DNA methyltransferase 1, histone deacetylase 1, acetyl-histone H3 and acetyl-histone H4 and their clinicopathological significance in breast invasive ductal carcinomas. Diagn. Pathol. 2012, 7, 33. [Google Scholar] [CrossRef] [Green Version]
  88. Schulzke, J.D.; Gitter, A.H.; Mankertz, J.; Spiegel, S.; Seidler, U.; Amasheh, S.; Saitou, M.; Tsukita, S.; Fromm, M. Epithelial transport and barrier function in occludin-deficient mice. Biochim. Biophys. Acta 2005, 1669, 34–42. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  89. Carlton, V.E.; Harris, B.Z.; Puffenberger, E.G.; Batta, A.; Knisely, A.; Robinson, D.L.; Strauss, K.A.; Shneider, B.L.; Lim, W.A.; Salen, G.; et al. Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. Nat. Genet. 2003, 34, 91–96. [Google Scholar] [CrossRef]
  90. Anderson, J.M.; Van Itallie, C. Physiology and function of the tight junction. Cold Spring Harb. Perspect. Biol. 2009, 1, a002584. [Google Scholar] [CrossRef]
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Figure 1. Bioaccumulation of PFOA in the intestinal tissues of CD1 mice. Mice were treated with control (0.5% Tween-20 in water) or 1–20 mg/kg/day PFOA for 10 days. (A) Quantification of PFOA in ng/gram in small intestine tissue; (B) quantification of PFOA in ng/gram of colon tissue using UPLC chromatography.
Figure 1. Bioaccumulation of PFOA in the intestinal tissues of CD1 mice. Mice were treated with control (0.5% Tween-20 in water) or 1–20 mg/kg/day PFOA for 10 days. (A) Quantification of PFOA in ng/gram in small intestine tissue; (B) quantification of PFOA in ng/gram of colon tissue using UPLC chromatography.
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Figure 2. Effect of PFOA on the expression levels of DNA methylation (Dnmts) and DNA demethylating genes (Tets) in intestinal tissues of CD1 mice. Mice were treated with control (0.5% Tween-20 in water) or 1–20 mg/kg/day PFOA for 10 days. (A) Change in the mRNA expression level of Dnmt1, Dnmt3a and Dnmt3b genes in the small intestine; (B) change in the mRNA expression level of Dnmt1, Dnmt3a and Dnmt3b genes in the colon; (C) change in the mRNA expression level of Tet1, Tet2 and Tet3 genes in the small intestine; (D) change in the mRNA expression level of Tet1, Tet2 and Tet3 genes in the colon. Statistical values were considered significant at p-value ≤ 0.05 (denoted by “*”) and less significant at p-value > 0.05.
Figure 2. Effect of PFOA on the expression levels of DNA methylation (Dnmts) and DNA demethylating genes (Tets) in intestinal tissues of CD1 mice. Mice were treated with control (0.5% Tween-20 in water) or 1–20 mg/kg/day PFOA for 10 days. (A) Change in the mRNA expression level of Dnmt1, Dnmt3a and Dnmt3b genes in the small intestine; (B) change in the mRNA expression level of Dnmt1, Dnmt3a and Dnmt3b genes in the colon; (C) change in the mRNA expression level of Tet1, Tet2 and Tet3 genes in the small intestine; (D) change in the mRNA expression level of Tet1, Tet2 and Tet3 genes in the colon. Statistical values were considered significant at p-value ≤ 0.05 (denoted by “*”) and less significant at p-value > 0.05.
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Figure 3. Effect of PFOA on the expression levels of tight junction gene Cldn in intestinal tissues of CD1 mice. Mice were treated with control (0.5% Tween-20 in water) or 1–20 mg/kg/day PFOA for 10 days. (A) Change in the mRNA expression level of Cldn2, Cldn3, Cldn4, Cldn7, Cldn8, Cldn12, and Cldn15 genes in the small intestine; (B) change in the mRNA expression level of Cldn2, Cldn3, Cldn4, Cldn7, Cldn8, Cldn12, and Cldn15 genes in the colon. Statistical values were considered significant at p-value ≤ 0.05 (denoted by “*”) and less significant at p-value > 0.05 but < 0.1 (denoted by “^”) reported from two-tailed tests.
Figure 3. Effect of PFOA on the expression levels of tight junction gene Cldn in intestinal tissues of CD1 mice. Mice were treated with control (0.5% Tween-20 in water) or 1–20 mg/kg/day PFOA for 10 days. (A) Change in the mRNA expression level of Cldn2, Cldn3, Cldn4, Cldn7, Cldn8, Cldn12, and Cldn15 genes in the small intestine; (B) change in the mRNA expression level of Cldn2, Cldn3, Cldn4, Cldn7, Cldn8, Cldn12, and Cldn15 genes in the colon. Statistical values were considered significant at p-value ≤ 0.05 (denoted by “*”) and less significant at p-value > 0.05 but < 0.1 (denoted by “^”) reported from two-tailed tests.
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Figure 4. Effect of PFOA on the expression levels of tight junction genes Tjps and Ocln in intestinal tissues of CD1 mice. Mice were treated with control (0.5% Tween-20 in water) or 1–20 mg/kg/day PFOA for 10 days. (A) Change in the mRNA expression of Tjp1, Tjp2, and Ocln genes in the small intestine; (B) change in mRNA expression of Tjp1, Tjp2, and Ocln genes in the colon. Statistical values were considered significant at p-value ≤ 0.05 (denoted by “*”) and less significant at p-value > 0.05.
Figure 4. Effect of PFOA on the expression levels of tight junction genes Tjps and Ocln in intestinal tissues of CD1 mice. Mice were treated with control (0.5% Tween-20 in water) or 1–20 mg/kg/day PFOA for 10 days. (A) Change in the mRNA expression of Tjp1, Tjp2, and Ocln genes in the small intestine; (B) change in mRNA expression of Tjp1, Tjp2, and Ocln genes in the colon. Statistical values were considered significant at p-value ≤ 0.05 (denoted by “*”) and less significant at p-value > 0.05.
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MDPI and ACS Style

Rashid, F.; Ahmad, S.; Irudayaraj, J.M.K. Effect of Perfluorooctanoic Acid on the Epigenetic and Tight Junction Genes of the Mouse Intestine. Toxics 2020, 8, 64. https://doi.org/10.3390/toxics8030064

AMA Style

Rashid F, Ahmad S, Irudayaraj JMK. Effect of Perfluorooctanoic Acid on the Epigenetic and Tight Junction Genes of the Mouse Intestine. Toxics. 2020; 8(3):64. https://doi.org/10.3390/toxics8030064

Chicago/Turabian Style

Rashid, Faizan, Saeed Ahmad, and Joseph Maria Kumar Irudayaraj. 2020. "Effect of Perfluorooctanoic Acid on the Epigenetic and Tight Junction Genes of the Mouse Intestine" Toxics 8, no. 3: 64. https://doi.org/10.3390/toxics8030064

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