- Research article
- Open Access
Pax8 modulates the expression of Wnt4 that is necessary for the maintenance of the epithelial phenotype of thyroid cells
BMC Molecular Biology volume 15, Article number: 21 (2014)
The transcription factor Pax8 is expressed during thyroid development and is involved in the morphogenesis of the thyroid gland and maintenance of the differentiated phenotype. In particular, Pax8 has been shown to regulate genes that are considered markers of thyroid differentiation. Recently, the analysis of the gene expression profile of FRTL-5 differentiated thyroid cells after the silencing of Pax8 identified Wnt4 as a novel target. Like the other members of the Wnt family, Wnt4 has been implicated in several developmental processes including regulation of cell fate and patterning during embryogenesis. To date, the only evidence on Wnt4 in thyroid concerns its down-regulation necessary for the progression of thyroid epithelial tumors.
Here we demonstrate that Pax8 is involved in the transcriptional modulation of Wnt4 gene expression directly binding to its 5’-flanking region, and that Wnt4 expression in FRTL-5 cells is TSH-dependent. Interestingly, we also show that in thyroid cells a reduced expression of Wnt4 correlates with the alteration of the epithelial phenotype and that the overexpression of Wnt4 in thyroid cancer cells is able to inhibit cellular migration.
We have identified and characterized a functional Pax8 binding site in the 5’-flanking region of the Wnt4 gene and we show that Pax8 modulates the expression of Wnt4 in thyroid cells. Taken together, our results suggest that in thyroid cells Wnt4 expression correlates with the integrity of the epithelial phenotype and is reduced when this integrity is perturbed. In the end, we would like to suggest that the overexpression of Wnt4 in thyroid cancer cells is able to revert the mesenchymal phenotype.
Wnts are powerful regulators of cell proliferation and differentiation, and their signaling pathway involves proteins that directly participate in both gene transcription and cell adhesion . Over the past two decades, 19 members of the Wnt protein family have been found in mammals and have been subdivided into canonical signaling, with transforming activities in mammary epithelial cells, and non canonical signaling involved in the planar cell polarity (PCP) and in Calcium signaling . Member of the Wnt family, Wnt4 is classified as a non-canonical Wnt protein even though there is evidence that it is also able to activate the canonical signaling pathway . Wnt4 knockdown highlighted its crucial role in the development of several organs such as kidney, ovary and mammary gland [4, 5]. Moreover, Wnt4 null mice die within 24 h of birth, probably because of severe lack of kidney functions . In fact, during kidney development Wnt4 plays a key role in the mesenchymal to epithelial transition and in the morphogenesis required for tubule formation , and its expression is regulated by the transcription factor Pax2 . Interestingly, in humans defects in WNT4 are a cause of Rokitansky-Kuster-Hauser syndrome (RKH syndrome) characterized by utero-vaginal atresia in otherwise phenotypically normal female with a normal 46,XX karyotype . Homozygous null mutation in WNT4 is the cause of female sex reversal with dysgenesis of kidneys, adrenals, and lungs (SERKAL syndrome), demonstrating that this gene plays an essential role in human sex-determination and organogenesis . Furthermore, mutations in the WNT4 gene also cause WNT4 Müllerian aplasia and ovarian dysfunction .
Recently, Wnt4 was shown to be strongly down-regulated in human anaplastic carcinomas and to behave as a key factor in Ras-mediated transformation of rat epithelial cells . In addition, the analysis of the gene expression profile of FRTL-5 differentiated thyroid cells after the silencing of the transcription factor Pax8 identified Wnt4 among the down-regulated genes and by ChIP assay Wnt4 was defined as a novel direct target of Pax8 .
Pax8, a member of the Pax genes family, was shown to be required for both morphogenesis of the thyroid gland  and maintenance of the thyroid differentiated phenotype . Interestingly, mutations in the Pax8 gene have been associated with congenital hypothyroidism in humans [16–19]. During the embryogenesis Pax8 is expressed not only in the thyroid but also in other tissues such as the metanephros, the midhindbrain boundary region [20, 21], as well as in the Müllerian duct . In Pax8 knockout mice, the thyroid gland is barely visible and lacks the follicular cells; accordingly, the expression of the thyroid-specific markers thyroglobulin and thyroperoxidase cannot be detected in line with the crucial role that Pax8 plays in thyrocytes differentiation . Moreover, as a consequence of their athyroidism, Pax8 deficient mice are deaf, growth retarded, ataxic, and do not survive weaning. As in most cases of congenital hypothyroid patients, in Pax8-deficient mice the symptoms can be reversed by the TH replacement therapy if instituted within the first days of postnatal life [22, 23]. It is of interest to note that Pax8-/- mice that were properly substituted with TH and developed otherwise normally without any overt deficits did not become fertile . Indeed, the analysis of the male and female reproductive system demonstrated that the Pax8-/- mice fail to develop correctly .
Here, we investigated the involvement of Pax8 in the regulation of Wnt4 gene expression in thyroid cells. The in silico analysis of the 5’-flanking region of the Wnt4 gene identified several putative Pax8 binding sites and our data here reported show that indeed Pax8 is involved in the transcriptional regulation of the Wnt4 gene. All together, our results indicate that in thyroid cells Pax8 participates to Wnt4 gene expression directly binding to its 5′-flanking region and that a reduced expression of Wnt4 correlates with the alteration of the epithelial phenotype. Moreover, we also show that the overexpression of Wnt4 in thyroid cancer cells is able to inhibit cellular migration.
Wnt4 expression in thyroid cells is modulated by TSH
In the past, we observed that in FRTL-5 cells cultured in the absence of TSH, Pax8 mRNA and protein rapidly disappear, whereas upon TSH stimulation, both mRNA and protein are newly synthesized . To investigate the role of TSH in Wnt4 expression, FRTL-5 cells were starved for 4 days in 0.2% calf serum-medium and subsequently treated with TSH for 24 hours. The expression of both Pax8 and Wnt4 was analyzed at the protein level by immunofluorescence. As expected, Pax8 expression is strongly reduced upon starvation of the cells and reinduced upon TSH stimulation. Similarly, also the expression of Wnt4 turned out to be modulated by TSH in a way that well correlates with Pax8 expression profile suggesting that TSH regulation of Wnt4 expression could be mediated by Pax8 (Figure 1A).
Previous studies associated Wnt proteins with glycosaminoglycans in the extracellular matrix and bound tightly to the cell surface [27–29]. Beyond this information, the localization of Wnt proteins in vertebrates remains unclear. The immunofluorescence experiment in Figure 1A allowed us to obtain information also on the subcellular distribution of the Wnt4 protein in thyroid cells, showing the presence of Wnt4 exclusively in the cytoplasmic compartment of this cell type.To better clarify whether TSH stimulation of Wnt4 expression is entirely mediated by Pax8, we performed a Pax8 knock-down experiment. In details, FRTL-5 thyroid cells were transfected with siGENOME Pax8 siRNA (experimental) or siGENOME Non-Targeting siRNA (control), a scrambled sequence that does not show homology with any rat gene. Few hours after transfection, cells were starved in 0.2% calf serum medium for 24 hours and then stimulated for 3 hours with TSH. The expression of both Pax8 and Wnt4 was analyzed at the mRNA level by qRT-PCR. Interestingly, when Pax8 is inhibited by the silencing, the stimulation with TSH does not induce high levels of Wnt4 as it happens in the siCtrl- sample (Figure 1B). This result supports the hypothesis that a significant fraction of Wnt4 response to TSH stimulation is indeed mediated by Pax8.
The 5′-flanking region of the Wnt4 gene is responsive to Pax8
To determine whether Pax8 could regulate Wnt4 gene expression by directly binding to its regulatory genomic sequence, we performed a computational analysis using the MatInspector Software 8.0. We searched for Pax8 binding sites in a region of about 3 Kb in the Wnt4 5′-flanking region and the analysis showed the presence of several Pax8 binding sequences.To characterize more in detail the genomic region upstream the Wnt4 gene and to assess its transcriptional activity in thyroid cells, five different fragments corresponding to progressive deletions of the 5′-flanking region were subcloned in the pGL3-basic vector upstream the luciferase reporter gene. All the deletions were engineered taking into account the position of the Pax8 binding sites predicted by the MatInspector software (Figure 2A).To verify the transcriptional activity of each fragment, the deletion constructs were transiently transfected in FRTL-5 thyroid cells and in HeLa cells, the latter negative for the expression of Pax8. The results obtained demonstrate that all the constructs have a high transcriptional activity in thyroid cells. Interestingly, only the smallest construct carrying 190 bp of the Wnt4 5′-flanking region shows a strongly reduced activity in the FRTL-5 cells (Figure 2A). These data indicate that the 5′-flanking region of Wnt4 is transcriptionally active in thyroid cells and prompted us to further study the role of Pax8 in the modulation of Wnt4 expression. Initially, we tested the effect of Pax8 transient expression on the -300 and -190 promoter regions by luciferase assays (Figure 2B). Specifically, we performed transactivation assays in HeLa cells by transfecting the reporter constructs 300Wnt4LUC and 190Wnt4LUC together with increasing concentration of Pax8. As shown in Figure 2B, Pax8 is able to activate transcription from the 300Wnt4LUC reporter in a dose dependent manner but not from the smallest construct 190Wnt4LUC, suggesting that the region between -300 bp and -190 bp upstream the translational start site of the Wnt4 gene is required for Pax8 positive modulation. Subsequently, to further confirm the ability of Pax8 to physically interact with the Wnt4 promoter region in vivo, we performed chromatin immunoprecipitation (ChIP) assays on genomic DNA from FRTL-5 cells. The cross-linked chromatin was immunoprecipitated using a specific antibody against Pax8. The enrichment of the endogenous Wnt4 region was monitored by PCR amplification using specific primers designed to amplify the region of Wnt4 between -300 bp and -190 bp required for Pax8 transcriptional activation. The ChIP assay demonstrates that, in agreement with the transactivation data, Pax8 is able to bind in vivo the Wnt4 promoter (Figure 2C).
Identification of a Pax8 binding site on the Wnt4 proximal promoter region
The in silico analysis by the MatInspector software predicted two binding sites for Pax8 within the region spanning from -300 bp to -190 bp upstream the ATG of the Wnt4 gene that we named A and B, respectively. Specifically, site A was identified on the negative strand, while site B was identified on the positive strand of the DNA sequence, positioned on the rat promoter at -297 and -211 bp from the ATG, respectively. The alignment of the core sequence of the two putative Pax8 binding sites shows a high grade of conservation among the species, highlighting the potential relevance of these sites for Wnt4 expression (Figure 3A).To further characterize and verify the prediction obtained by the MatInspector analysis, we designed two oligo probes, containing the putative binding sites A and B, and we performed gel mobility shift experiments. Interestingly, the retarded band observed when the FRTL-5 protein extract was incubated with oligo A (Figure 3B, probe A, lane 2) is similar to that observed in the positive control (Figure 3B, probe A, lane 4). In contrast, the predicted binding site B could not be confirmed as a Pax8 binding site (Figure 3B, probe B). Afterwards, we demonstrated by competition and supershift assays that the shift observed when the FRTL-5 extract is incubated with oligo A is the result of a specific interaction (Figure 3B). All together, these results demonstrate that Pax8 is able to specifically bind to the sequence identified in this study.To demonstrate the functional relevance of Pax8 binding to the Wnt4 promoter, we generated a deletion mutant (260Wnt4LUC) that lacks the sequence predicted to be recognized by Pax8. Luciferase reporter constructs 300Wnt4LUC and 260Wnt4LUC were transiently transfected into FRTL-5 cells and the luciferase activity was measured 48 h later. As shown in Figure 3C, transfection of the 300Wnt4LUC construct produces high levels of luciferase activity, while the selective deletion of Pax8 binding site results in a reduced activity of the 260Wnt4LUC construct (about 50% reduction), indicating that the binding site A that we have identified is necessary for Wnt4 full promoter activity.
Wnt4 is responsible for the maintenance of the epithelial phenotype
Recently, Wnt4 was demonstrated to be essential for normal conversion of metanephric mesenchyme to the epithelia of the nephron . This evidence prompted us to investigate the involvement of Wnt4 in the EMT process also in epithelial thyroid cells. To this end, we inhibited Wnt4 expression in FRTL-5 by means of RNA interference and we analyzed by qRT-PCR the expression level of some EMT markers. Seventy-two hours after siRNA transfection, we analyzed the expression level of Wnt4, E-cadherin (E-cad) as an epithelial marker and α-Smooth muscle actin (α-SMA) and Vimentin (VIM) as mesenchymal markers. By qRT-PCR we show that upon Wnt4 knockdown, the mRNA level of E-cad is reduced while the expression level of the mesenchymal markers α-SMA and VIM is upregulated with respect to the FRTL-5 transfected with siCtrl- (Figure 4A).Our findings demonstrate that reduced levels of Wnt4 correlate with EMT, suggesting a relevant role of this gene in the maintenance of the epithelial phenotype of FRTL-5 thyroid cells. To better clarify the involvement of Wnt4 in this process, we generated FRTL-5 cells overexpressing Wnt4 and we analyzed, by qRT-PCR and Western blot, the expression level of the EMT markers above mentioned. The stable overexpression of Wnt4 is able to revert the mesenchymal phenotype; in fact, the upregulation of Wnt4 determines a stabilization of E-cad and a reduction of α-SMA and VIM (Figure 4B). The apparent difference between mRNA and protein level of VIM in our opinion could be due to the biological differences between transcript and protein abundance, underlining the importance of post-translational mechanisms controlling gene expression.
Wnt4 is down-regulated in human thyroid cancer cells and its overexpression inhibits cellular migration
We analyzed the expression level of Wnt4 in human thyroid cancer cell lines by qRT-PCR. In particular, we analyzed the WRO, Cal62, FB2 and BCPAP cells derived from follicular, anaplastic and papillary thyroid carcinoma, and a pool of six normal thyroid (N.T.) tissues as control. As expected, in all the thyroid cancer cell lines the expression level of Wnt4 is strongly reduced with respect to normal thyroid (Figure 5), indicating that a down-regulation of Wnt4 occurs in thyroid carcinoma. Interestingly, also the expression of PAX8 is significantly down-regulated in the same cell lines. The same result has been obtained by Western blot analysis (Figure 5, bottom panel). To further evaluate the involvement of Wnt4 in thyroid tumors we overexpressed Wnt4 in the BCPAP cell line and we selected a BCPAP-Wnt4 mass population. In parallel, we also generated a control mass population transfected with the backbone vector (BCPAP-pCEFL).To study whether elevated levels of Wnt4 might have a role in cell migration, we performed wound-healing assays using the two mass populations described above. The assay shows that after 12 hours the area of the wound is completely recovered by the BCPAP parental and the BCPAP-pCEFL cells. At difference, the motility of the BCPAP-Wnt4 cells appears strongly impaired, suggesting that Wnt4 overexpression significantly reduces the migration ability of human papillary thyroid cells (Figure 6).
In the last few years many data revealed that a set of transcriptional regulators, unique to the thyroid follicular cell type, has been identified as responsible for thyroid-specific gene expression. It comprises three transcription factors: TTF-1, Foxe-1 and Pax8, each of which is expressed also in cell types different from the thyroid follicular cells. Albeit, the specific combination of these factors is unique to the thyroid hormone producing cells, strongly suggesting that such combination plays an important role in the differentiation process of these cells [30, 31]. In particular, the transcription factor Pax8 is a master gene for thyroid differentiation, being necessary for the transcriptional activation of all the known differentiation markers . Moreover, Pax8 knockout mice show a severe thyroid phenotype  and are unfertile [24, 25]. In humans, patients carrying mutations in the Pax8 gene suffer from congenital hypothyroidism [16, 33].
Together with the transcription factor Pax2, Pax8 is also a central regulator of both nephron differentiation and branching morphogenesis in the developing kidney. Both transcription factors are necessary and sufficient for the formation of the pronephros and all subsequent kidney structures, regulating key target genes involved in pro/mesonephros formation [20, 34]. In parallel, a cooperative role for Pax2 and Pax8 in metanephric branching morphogenesis and nephron differentiation has been uncovered .
In thyroid, Wnt4 has been recently demonstrated to be a key player in Ras-mediated transformation of epithelial cells. Moreover, our recent data suggested that Wnt4 could be a direct target of Pax8 in FRTL-5 rat thyroid cells .
In this study, we show that Pax8 modulates the expression of Wnt4 at the transcriptional level. By EMSA, ChIP and transfection assays, we demonstrate that Pax8 directly binds to the Wnt4 promoter region and activates transcription from it.
It is well known that TSH is the main regulator of thyroid differentiation . Its role in this process has been studied in different model systems  and the expression of several thyroid-specific genes, such as Tg, TPO, TSHR and NIS has been shown to be modulated by TSH/cAMP. In the past, we demonstrated that in PCCl3 cells, TSH regulates the expression of Tg and Pax8 at the transcriptional level by a cAMP-mediated mechanism . Here, we show that in FRTL-5 rat thyroid cells also the expression of Wnt4 is under the control of TSH and that this control is likely mediated by Pax8. In fact, TSH deprivation causes a significant reduction of both Pax8 and Wnt4 and the kinetic of induction of Wnt4 expression upon TSH stimulation well correlates with that of Pax8. Interestingly, it has been demonstrated that TSH supports maintenance of thyroid follicular integrity in primary cultured pig thyrocytes, stabilizing E-cadherin at the cell surface and preventing its accelerated turnover to support the maintenance of thyroid follicular integrity . Therefore, we would like to propose that TSH promotes and ensures the maintenance of the architecture and integrity of the follicles also regulating the expression of Wnt4. Of course, this is currently a hypothesis that requires further investigations and experimental validations.
The epithelial-mesenchymal transition (EMT) is an orchestrated series of events in which cell-cell and cell-extracellular matrix (ECM) interactions are altered to release epithelial cells from the surrounding tissue. The cytoskeleton is reorganized to confer the ability to move through a three-dimensional ECM, and a new transcriptional program is induced to maintain the mesenchymal phenotype. Induction of EMT can compromise the mechanical and physiological integrity of the tissue, and inappropriate induction of this process can have disastrous consequences. EMT also acts in tumor progression by providing increased resistance to apoptotic agents [37, 38] and by producing supporting tissues that enhance the malignancy of the central tumor.
Recently, Wnt4 has been demonstrated to be critical for mesenchyme – epithelium transition of the epithelia of the nephron . In agreement with these data, we report in this manuscript that in FRTL-5 thyroid cells Wnt4 is involved in the maintenance of the epithelial phenotype. In fact, the EMT induced by Wnt4 down-regulation can be reverted in the cellular model system that stable overexpresses Wnt4. These results allow us to suggest that in thyroid cells, as in kidney cells, the expression of Wnt4 correlates with the integrity of the epithelial phenotype.
Many publications emphasize the role of the Wnt/β-catenin pathway in thyroid cancer. Recently, it has been shown that Wnt4 down-regulation is necessary for the progression of thyroid epithelial tumors toward a fully malignant phenotype . Moreover, it has been extensively demonstrated that a progressive decrease of Pax8 level occurs in thyroid tumors from follicular adenoma to differentiated carcinoma and then to anaplastic carcinoma, which parallels the progressive dedifferentiation and increasing malignancy of thyroid tumors . Here, we show that in human thyroid cancer cell lines, Wnt4 and PAX8 mRNA levels are strongly reduced. Moreover, the overexpression of Wnt4 in human papillary cancer cells is able to affect the stabilization of the epithelial state and to inhibit cellular migration.
In the future, it will be interesting to further clarify the role of Wnt4 in thyroid differentiation and tumorigenesis.
The results presented in this study demonstrate that the transcriptional factor Pax8 is involved in the transcriptional modulation of Wnt4 gene expression in differentiated thyroid cells. Furthermore, we show that a reduced expression of Wnt4 correlates with the alteration of the epithelial phenotype and that Wnt4 overexpression in thyroid cancer cells is able to inhibit cellular migration. Taken together, our data highlight a potential intriguing role of Wnt4 in the context of the thyroid cell.
Protein extracts and Western blot
Cells were washed twice with ice cold PBS and lysed in a buffer containing 50 mM HEPES (pH 7.5), 150 mM NaCl, 5 mM EGTA (pH 7.8), 10% glycerol, 1% triton X-100, 1 mM DTT and 1 mM PMSF. Protein concentration was determined using the Bio-Rad protein assay (Bio-Rad Laboratories, Inc., Hercules, CA). For Western Blot analysis, proteins were separated by SDS-PAGE. Gels were blotted onto Immobilon P (Millipore Corp., Bedford, MA) for 3 h, and the membranes were blocked in 5% nonfat dry milk for 1 h at room temperature. The antibodies used for immunoblotting were: Wnt4 (Mouse anti-WNT4, Invitrogen), Pax8 (kindly provided by Prof. R. Di Lauro), vimentin, E-cadherin, GAPDH (Santa Cruz Biotechnology, Inc.). Subsequently, the filters were developed using an enhanced chemi-luminescence detection method (Pierce Chemical Co., Madison, WI) according to the manufacturer’s directions.
FRTL-5 cells, grown on 12 mm diameter glass coverslips, were fixed with pre-chilled methanol at -20°C for 5 min, permeabilized for 10 min in 0.2% triton X-100 in PBS, and then rinsed with phosphate-buffered saline (PBS) to prepare them for immunostaining. Briefly, the cells were subsequently blocked with washing buffer containing 0.5% BSA for 1 h and treated with rabbit policlonal anti-WNT4 (Wnt4 antibody, Novus) O/N and then with Alexa Fluor® 594-conjugated secondary antibody (Invitrogen) for 30 min, followed by treatment with mouse monoclonal anti-PAX8 (BIOCARE MEDICAL) for 1 h and finally by an Alexa Fluor® 488-conjugated secondary antibody (Invitrogen). Several washes were interposed between the different antibodies incubations. Cell nuclei were identified by Hoechst staining. The coverslips were mounted on a microscope slide using a 70% (v/v) solution of glycerol in PBS and images were collected as previously described .
Promoter constructs and plasmids
Specific proximal promoter fragments of rat Wnt4 gene were amplified by PCR. The 3100Wnt4LUC was subcloned into MluI/BglII sites of the pGL3basic vector (Promega, Madison, WI), while all the other constructs were subcloned into XhoI/HindIII of the same vector.
Wnt4 cDNA (NCBI Reference Sequence NM_005923) was kindly provided by G. De Vita. The CMV-Pax8 construct was already described .
Cell culture and transfection assays
Rat thyroid follicular FRTL-5 cells were maintained in Coon’s modified F12 medium (EuroClone, MI, Italy) as previously described .
The starvation medium consisted of Coon’s modified Ham’s F12 medium supplemented only with 0.2% newborn calf serum (HyClone, Logan, UT). TSH treatment was performed by the addition of 1 mU/ml TSH (Sigma-Aldrich, St. Louis, MO) to the culture medium at 3 h or 24 h after starvation.
HeLa, WRO, FB2, Cal62 and BCPAP cells were grown in DMEM (EuroClone) supplemented with 10% (v/v) fetal bovine serum (HyClone, Logan, UT).
Transfections and luciferase assays were carried out as previously described .
ChIP was performed as previously described .
Precleared chromatin from FRTL-5 cells was incubated with 1 μg of affinity-purified rabbit polyclonal antibody anti-Pax8 (kindly provided by Prof. R. Di Lauro), unrelated antibody (α Tubulin, Santa Cruz) or no antibody and rotated at 4°C for 16 h. The immunoprecipitated DNA was analyzed by PCR using the following Wnt4 primers: 5′- GATCCAGAAGCGAGGTTTCGGAT -3′ and 5′-AACCTAGTCACTAGCGCTCGGG-3′.
Electrophoretic mobility shift assay (EMSA)
Double-strand oligonucleotides were labeled with γ-32P ATP and T4 polynucleotide kinase and used as probes. The binding reactions were carried out in a buffer containing 20 mM Tris–HCl (pH 7.6), 75 mM KCl, 1 mM dithiothreitol, 10% glycerol, 1 mg/ml BSA, and 3 mg/ml polydeoxyinosinic deoxycytidylic acid. After 30 min of incubation at room temperature, free DNA and DNA-protein complexes were resolved on a 6% non-denaturating polyacrylamide gel and visualized by autoradiography.
The oligonucleotides used in the competition assay and the antibodies used in the supershift experiments were incubated with the protein extract for 20 min before adding the probe.
Oligonucleotides were: probe A, 5′-GCGGGTCCAGCGGCGCGGGACACCCCCC-3′ and probe B, 5′-TCCGCCGCCACCGCCGCATCCCGGCTCTG-3′. The oligonucleotide mutated in the core sequence was: 5′-GCGGGTCCAGCGGATATGGACACCCCCCC-3′.
FRTL-5 cells were plated (8×104 cells) in a 24-well plate and were transfected in triplicate with 50 nM rat Wnt4 siRNA (Ambion, Life Technologies Ltd, UK), 50 nM siGENOME Non-Targeting #3 (Dharmacon, Lafayette, CO), or with 100 nM Pax8 siGENOME siRNA or siGENOME Non-Targeting #3 (DHARMACON) as scramble, using the DharmaFECT1 transfection reagent, following the manufacturer’s protocol.
RNA extraction, cDNA synthesis and quantitative RT-PCR
Total RNA was prepared using TRIzol Reagent (Invitrogen, San Diego, CA) according to the manufacturer’s directions. Total RNA (1 μg) was retrotranscribed using the iScript cDNA Synthesis kit (Bio-Rad Laboratories). Real-time PCR analysis was performed using an iCycler-iQ real-time detection system and SYBR green chemistry (Bio-Rad Laboratories).
Reactions were carried out in duplicate in three independent experiments. For each gene, values are means ± SD of three independent experiments, normalized by the expression of an housekeeping gene, and expressed as a percentage of the value measured in parental FRTL-5 or BCPAP cells. To calculate the relative expression levels, we used the 2-DDCT method .
Confluent BCPAP, BCPAP-pCEFL and BCPAP-Wnt4 cells plated on tissue culture dishes were wounded by manual scratching with 10-μl pipette tip, washed with PBS and incubated at 37°C in complete media. At the indicated time points, phase contrast images at specific wound size were captured.
Paired box transcription factor 8
Wingless-type MMTV integration site family, member 4
Electro mobility shift assay
Epithelial to mesenchymal transition
Thyroid stimulating hormone
Chromatin immuno precipitation
Planar cell polarity
α-smooth muscle actin
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We deeply thank G. De Vita, M. De Menna and S. Paladino for kindly providing reagents and helpful discussions.
This work was supported by grants from the Italian Ministry of Education, University and Research (MIUR-PRIN 2009), from the Italian Ministry of Economy and Finance to the CNR for the Project FaReBio di Qualità and by the grant Medical Research in Italy (MERIT) RBNE08YFN3_001.
The authors declare that they have no competing interests.
MGF carried the majority of the experiments and drafted the manuscript, TDP participated in the design of the study and carried out the ChIP assays, VL carried out the immunofluorescence analysis, MZ was responsible for the coordination and supervision of the entire study. All authors read and approved the final manuscript.
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Filippone, M.G., Di Palma, T., Lucci, V. et al. Pax8 modulates the expression of Wnt4 that is necessary for the maintenance of the epithelial phenotype of thyroid cells. BMC Molecular Biol 15, 21 (2014) doi:10.1186/1471-2199-15-21
- Transcriptional regulation
- Mesenchyme-to-epithelium transition
- Thyroid cancer