Inhibition of gap junctional Intercellular communication in WB-F344 rat liver epithelial cells by triphenyltin chloride through MAPK and PI3-kinase pathways
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Organotin compounds (OTCs) have been widely used as stabilizers in the production of plastic, agricultural pesticides, antifoulant plaints and wood preservation. The toxicity of triphenyltin (TPT) compounds was known for their embryotoxic, neurotoxic, genotoxic and immunotoxic effects in mammals. The carcinogenicity of TPT was not well understood and few studies had discussed the effects of OTCs on gap junctional intercellular communication (GJIC) of cells.
In the present study, the effects of triphenyltin chloride (TPTC) on GJIC in WB-F344 rat liver epithelial cells were evaluated, using the scrape-loading dye transfer technique.
TPTC inhibited GJIC after a 30-min exposure in a concentration- and time-dependent manner. Pre-incubation of cells with the protein kinase C (PKC) inhibitor did not modify the response, but the specific MEK 1 inhibitor PD98059 and PI3K inhibitor LY294002 decreased substantially the inhibition of GJIC by TPTC. After WB-F344 cells were exposed to TPTC, phosphorylation of Cx43 increased as seen in Western blot analysis.
These results show that TPTC inhibits GJIC in WB-F344 rat liver epithelial cells by altering the Cx43 protein expression through both MAPK and PI3-kinase pathways.
KeywordsInhibitor LY294002 Organotin Compound Lucifer Yellow Newborn Calf Serum Immunotoxic Effect
Organotin compounds have been widely used as agricultural biocides, antifouling agents in boat paint, wood preservatives, and stabilizers for polyvinylchloride polymers (PVC) in industry [1, 2]. Triphenyltin (TPT) is an organotin compound which is widely used as fungicides on major food and food-stock crops. It is also used in anti-fouling paints to prevent growth of barnacles and other fouling organisms on boats and ships . Organotin compounds are known to be endocrine disruptors in marine species and may be mahuman beings [4, 5]. Tissue concentrations of TPT were correlated with the degree of imposex in rock shells [6, 7]. TPT compounds have embryotoxic, myotoxic, genotoxic and immunotoxic effects in mammals [8, 9, 10, 11]. The organotin compounds might be incorporated in the most abundant phospholipid of eukaryotic membrane and caused toxicity . Some toxic effects have been observed in aquatic and terrestrial organisms exposed to TPT, such as increased tumor incidence and immune suppression [13, 14]. Some studies have revealed that TPT might inhibit the cytotoxic function of human natural killer cells and triphenyltin hydroxide produced tumors in rats and mice [14, 15, 16].
Connexins (Cxs) are a group of at least 20 highly conserved proteins that provide the basis for communication through the direct exchange of ions, nutrients, second messengers, electrical coupling, and small metabolites from one cell to its neighboring cells [17, 18, 19, 20]. Cell proliferation, differentiation, apoptosis and adaptive responses of differentiated cells can occur as a consequence of the up- or down-regulation of GJIC [21, 22, 23]. Disruption in GJIC may cause loss of homeostatic and cell growth control [18, 24, 25, 26]. Growing evidence suggests that connexin 43 (Cx43), a major gap junction protein, functions as a tumor suppressor gene. Expression of Cx43 is often decreased in human tumor cells and tissues, including those involved in human mammary carcinoma, prostate cancer, human glioblastoma, skin squamous cell carcinoma, lung cancer, esophagus cancer, adrenocortical tumors, ovarian carcinoma, cervical cancer, endometrial carcinoma, and human mesothelioma [27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37]. It has been assumed that using pharmacological stimulation to efficiently restore GJIC in tumor cells might represent a strategy for anti-neoplastic therapies [38, 39, 40, 41, 42].
The carcinogenicity of TPT remained unclear. The present work was undertaken to define the effects of TPTC on GJIC in WB-F344 rat liver epithelial cells.
Materials and methods
Powder of TPTC was supplied by MERCK (Darmstadt, Germany).
Lucifer yellow, DMSO (dimethylsulfoxide), formaldehyde, MTT (3-[4,5-dimethyl-2-thiazolyl]-2,5-diphenyl-2H-tetrazolium bromide) were supplied by Sigma-Aldrich (St. Louis, MO, USA). D medium and newborn calf serum were from Gibco (Invitrogen cooperation, CA, USA), Trizole was from Invitrogen Life Technologies (Rockville, MD, USA) and 2 X SYBR green PCR master mix was from Applied Biosystems (Foster, CA, USA). The protein kinase C (PKC) inhibitor GF109203X, extracellular signal-regulated protein kinase (ERK) inhibitor PD98059 and PI3 kinase inhibitor LY294002 were from Sigma (St. Louis, MO, USA). Immobilon Western HRP Substrate Peroxide Solution and luminal reagent were supplied by Millipore Corporation (Billerica, MA). All chemicals used in the study were of the highest available purity.
Cell culture and treatment with chemicals
WB-F344 rat liver epithelial cells  were cultured in D medium supplemented with 5% fetal bovine serum and 1% [v/v] penicillin/streptomycin antibiotic. The cells were grown at 37°C in a 5% CO2 incubator before being used in the different experiments. Confluent cells, grown in plates, were exposed to various concentrations of TPTC. To prepare the TPTC stock solution, 0.01 g of TPTC powder was dissolved in 10 ml DMSO and then diluted to a final concentration of 1000 ppm.
Cell toxicity assay of TPTC
The effect of TPTC on the survival of WB F344 cells was assessed using MTT toxicity assay as described previously . In brief, the cells were plated in 100 μl media in 48-well plates (1 × 104/well). On the following day, the experimental medium containing different TPTC concentrations (0, 0.25, 0.5, 1, 2, 3, 4, and 5 ppm) was added, and then incubated for 30 and 60 minutes. Fifty μl of MTT solution (2 mg/ml in PBS) was added to each well and incubated for 6-8 hours. After careful removal of the medium, 150 μl of DMSO was added to each well, and then after careful shaking, the absorbance was read at 570 nm using an ELISA microplate reader (Zenyth 200rt with ADAP software, Anthos Labtec Instruments, Autria). Cell viability was expressed as a percentage of control cells not treated with TPTC and was designated as 100%.
Colony forming-efficiency assay
Colony forming-efficiency experiments were performed as previously described . In brief, exponentially growing cells were plated at 500 cells/100 mm tissue culture dish in 10 ml D medium, treated with different concentrations of TPTC. Following treatment, the plates were washed two times with the medium. The medium was not replaced, and colonies were fixed and stained after 14 days in culture by water: addition of methanol (1:1) containing crystal violet (1 g/l). Colonies with cell clusters containing more than 50 cells were counted under a dissecting microscope. Data indicate survival as a percentage relative to untreated cells.
GJIC inhibition assay
GJIC assay was carried out in 35 × 10 mm tissue culture dishes with 100% confluent monolayer cells grown in 2 ml D-medium supplemented with 5% newborn calf serum, 100 U/ml penicillin and streptomycin 100 μg/ml. GJIC was detected using the scrape-loading and dye transfer (SL/DT) technique developed by el-Flouly . Assays for different treatments and vehicle control were run in triplicate in cell culture dishes. Monolayer cells with 100% confluence were incubated with target compounds. For dose-dependent inhibition of GJIC, we treated cells with 0.5, 1.0, 1.5 and, 2.0 ppm TPTC for 30 min. For time-dependent inhibition of GJIC, analysis was performed with 1.5 ppm TPTC for 15, 30, 45, and 60 min. After exposure to the target compounds, the cells were rinsed three times with PBS and 1 ml of lucifer yellow solution was then added to the cell cultures and scrape-loaded with several scrapes using a steel surgical blade. The dye solution was left on the cell cultures for 3 min, and then discarded. The cell cultures were carefully rinsed three times with PBS to remove detached cells and background fluorescence. Several drops of 4% formalin in PBS were added to fix the cell cultures. An inverted fluorescence microscope equipped with a digital camera (Nikon Eclipse TE 2000-U system, Nikon ACT-1 version 2.62, Nikon Corporation, Japan) was employed to record the migration of the lucifer yellow dye from the edge cells of the scrape. The migration was measured on the micrograph. An average value of 30 measurements for each treatment (10 measurements per dish) was regarded as the migration of dye in the cell cultures. The percentage of migration of dye in cell cultures exposed to target compounds to the migration of dye traveling in the vehicle control was employed to evaluate the inhibition of GJIC. For inhibition studies, cultures were pre-incubated for 30 min with various pathway inhibitors prior to treatment with 1.5 ppm TPTC for 30 min.
Western blot analysis
WB F344 liver cells were treated with TPTC of 1.5 ppm for 15 and 30 min. After treatment, the medium was removed and cells were washed twice with PBS and lysed with 0.5% SDS. Lysates were stored at -80°C. Cell lysates were sonicated, and protein levels were determined using a protein detection assay (BioRad). Sample blue buffer (30% sucrose, 10% SDS, 0.1% bromophenol blue, and 0.2% dithiothreitol) was added and the samples were heated for 10 min at 100°C and loaded onto gels (10% SDS-PAGE). SDS-PAGE-separated proteins were blotted onto a PVDF membrane (Immobilon-PSQ, Millipore, Bedford, MA) using a semi-dry blotter (VWR), and the membrane was blocked with 5% milk in PBS-T buffer [1000 ml PBS with 1 ml Tween 20 (pH 7.4)] for more than 1 h at room temperature. The protein was probed with antibodies (Mouse IgG, Zymed) against connexin 43 at 4°C overnight and this was followed by incubation with horseradish peroxidase-conjugated secondary antibodies (Mouse anti-Goat IgG-HRP, Sigma). Protein visualization was carried out using an enhanced chemiluminescence kit (Pierce) according to the manufacturer's protocol.
Immunofluorescence staining experiment s were performed as previously described. In brief, WB F344 liver cells were plated in 100 μl media in 12 well-plates treated with 1.5 ppm TPTC for 30 min. After treatment, the medium was removed and sections were washed with PBS. 4% paraformaldehyde was added and washed sections with PBS 20 min later. 0.5% triton X-100 (Sigma) was added for 20 min and washed out with PBS. After treatment, diluted primary antibodies mouse IgG against connexin 43 (Santa Cruz Biotechnology, Inc.) with 4% triton X-100 was added and incubated sections for 1 h at room temperature. The sections were washed with PBS, and diluted mouse IgG secondary antibody (Alexa Fluor555 &488) with 4% triton X-100 was added and incubated sections for 1 h at room temperature. After treatment, 4,6'-diamidino-2-phenylindole (DAPI)(Sigma) was added and incubated sections for 10 min at room temperature. An inverted fluorescence microscope equipped with a digital camera (Nikon Eclipse TE 2000-U system, Nikon ACT-1 version 2.62, Nikon Corporation, Japan) was employed to record the fluorescent intensity of the cells.
Means ± SEM were calculated and the data are presented as a percentage of control. All data were analyzed by Sigma Plot 8.0 software using repeated measures. ANOVA (SPSS for window version 12.0.1; SPSS, Inc., Chicago, IL) was performed to examine the effect of independent variables (treatment, day, incubation time, time point). Tests for contrasts were carried out to compare the different levels of the independent variables. P values ≤ 0.05 were considered statistically significant.
TPTC dissolved easily in DMSO but not in water. To exclude the toxic effects of DMSO on cell viability and diffusion length of GJIC, tests involving exposure to DMSO were carried out. Results revealed that after exposure to 2% DMSO for 30 minutes, the diffusion length of GJIC did not obviously decrease as compared with that of the control group (p > 0.05).
Cytotoxicity of TPTC
Colony-forming efficiency in WB-F 344 cells was evaluated using TPTC of 0, 3, 9, 12, 15, 18 ppb. After 14 days of exposure, the colony-forming efficiency decreased significantly when TPTC concentration exceeded 12 ppb (Fig. 1B.)
Dose- and time- dependent inhibition of GJIC by TPTC
The effects of TPTC on GJIC were evaluated with cells exposed to TPTC for 15 min, 30 min, 45 min, and 60 min. After 15 min of exposure to 1.5 ppm of TPTC, the diffusion length was significantly decreased as compared with that of the control group (p < 0.05) (Fig. 2B). The diffusion length reduced gradually with time and became almost invisible after 60 min of exposure to 1.5 ppm of TPTC.
Effects of PKC, ERK and PI3 kinase on GJIC response
Neither GF109203X, LY294002 nor PD98059 alone at the indicated concentration had any notable effects on GJIC in these cells.
Effects of TPTC on connexin 43 protein level and phosphorylation
Effects of TPTC on connexin 43 in immunofluorescence staining
Carcinogenesis is a multistep process, including "initiation," "promotion," and "metastasis" ("progression") . Potter suggested that the initiation process prevents genetically altered stem cells from terminally differentiating , and, at the same time, GJIC restricts the growth of these cells. However, when exposed to tumor promoters, which inhibit GJIC, these transformed cells proliferate . The results of this study indicate that the TPTC inhibits GJIC in WB-F344 rat liver epithelial cells in a concentration- and time-dependent manner. In the present study, we demonstrate for the first time that exposure TPTC results in downregulation of Cx43 expression in liver cell cultures. Moreover, we show that TPTC modulates Cx expression predominantly through activation of MAPK and PI3K signaling pathways. Several in vivo and in vitro studies have revealed potential effects of organotins in broad spectrum including immunosuppressive, neurotoxic, endocrinopathic, reproductive, teratogenic, developmental, and possibly carcinogenic activity [3, 13, 72, 73, 74, 75]. Alterations in the phosphorylation status of connexins are a consequence of the activities of the protein kinase and/or protein phosphatases. GJIC recovered when pre-treated with PD 98059 (ERK inhibitor), and LY294002 (PI3-kinase inhibitor), but did not recover when GF109203X (Protein Kinase C inhibitor) was added. The reactions of fluorescence of Cx43 in WB-F344 cells after treatment with TPTC did decrease and the phosphorylation of Cx43 was found in Western Blot analysis. Some studies also showed that TPTC could inhibit the phosphorylation and ATP formation in chloroplasts and embryos of marine invertebrate [9, 76].
The inhibition of GJIC by TPTC was independent of PKC activity but clearly dependent upon the activation of both MAPK and PI3-kinase pathways. The loss of GJIC was also described in cancer cells [77, 78]. Alteration in expression of connexins may be involved in the expression of neoplastic phenotype  and changes in the phosphorylation pattern of connexins are also associated with GJIC inhibition by other tumor-promoting agents and oncogenes [80, 81, 82].
Hence, there is no evidence of a causal cross-talk between the two modulatory pathways, MAPK and PI3K. However, both PD58059 and LY294002 abolished completely the effect of TPTC downregulation of Cx43, implicating both MAPK and PI3K signaling cascades in a common mechanism of Cx regulation. It is possible that MAPK and PI3K act through a common downstream pathway, such as GSK-3 activation [83, 84, 85, 86], to control endothelial cellular function through Cxs.
In conclusion, the present study shows that TPTC inhibits GJIC in WB-F344 rat liver epithelial cells by altering the Cx43 protein expression through the MAPK and PI3-kinase pathways. However, to prove the carcinogenicity of TPTC still needs further study. This preliminary study could provide the possible mechanism for further evaluation of toxicity of TPTC.
This study was supported by a grant (NSC-93-2113-M-037-018) from the National Science Council, Taiwan.
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