Vision 2012; 18:1402-1410
Received 27 February 2012 | Accepted 29 May 2012 | Published 01 June 2012
1Singapore Eye Research Institute, Singapore; 2Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; 3Department of Orthopedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; 4Singapore National Eye Center, Singapore
Correspondence to: Adjunct Associate Professor Jodhbir S. Mehta, Singapore National Eye Centre, 11 Third Hospital Avenue, Singapore, 168751; Phone: (65) 63224512; FAX: (65) 63224599; email: email@example.com
Purpose: To investigate the role of WW Domain Containing Transcription Regulator (WWTR1/TAZ) protein in regulating the proliferation of normal human conjunctiva epithelial cells and epithelial cells from pterygium tissue.
Methods: Conjunctiva epithelial cells were cultured in keratinocytes growth medium and treated with transformation growth factor β (TGFβ) to analyze the expression and translocation of TAZ protein by immunostaining and BrdU analysis. Immortalized conjunctiva epithelial cells (NHC) were treated with TGFβ, targeting siRNA, TGFβ receptor antibody or TGFβ receptor inhibitor, to study the involvement of TAZ and TGFβ signaling pathway in conjunctiva cell proliferation by cell adhesion assay. Conjunctiva tissues from a normal human eye and an eye with pterygium disease were collected for histological analyses and western blot to evaluate the TAZ protein expression in vivo.
Results: TAZ expression was upregulated in mitotic conjunctiva epithelial cells, proliferating conjunctiva epithelial cells, TGFβ treated conjunctiva epithelial cells and human pterygium epithelium. TAZ siRNA induced less conjunctiva epithelial cell growth. Moreover, TGFβ receptor antibody and TGFβ receptor inhibitor rescued this anti-proliferative effect of TAZ siRNA.
Conclusions: TAZ is involved in human conjunctiva epithelial cells proliferation via regulating TGFβ signaling pathway.
Pterygium is a common ocular disease characterized by a fibrovascular membrane advancing on the corneal surface. Pterygium is caused by the abnormal growth and differentiation of the conjunctival epithelial cells of the corneal limbus [1,2]. Previous studies have shown an overexpression of transforming growth factor β (TGFβ) signaling in pterygia tissue when compared with normal conjunctiva. Therefore, the proliferation of conjunctiva epithelium in pterygium may be attributed to the activities of TGFβ.
TGFβ regulates important biologic functions, including cell growth, differentiation, migration and apoptosis, which have been extensively investigated and reviewed [3-5]. In the mature mammalian epithelium, TGFβ signal induces cell cycle arrest, apoptosis, cell adhesion and cytokine secretion [6-8]. Biologic signals for TGFβ are transduced through transmembrane serine/threonine kinase receptors to a family of intracellular mediators known as mothers against decapentaplegic homolog (Smad) proteins . Smad proteins are activated to either propagate or inhibit the TGFβ signal by interacting with other modulators. The TGFβ superfamily receptors have been found to have a distinct and specific distribution in the conjunctiva epithelium, indicating that conjunctiva epithelial cells respond to TGFβ cytokine and that TGFβ may have important autocrine and/or paracrine roles in the growth and metabolism of ocular tissues in vivo [10,11].
WW Domain Containing Transcription Regulator (WWTR1/TAZ) protein is a transcriptional co-activator, which contains a 14–3-3 binding fragment, a single WW domain and a PDZ-binding motif . Mutations of TAZ protein have been reported to be related to a dysfunction of caspase activities in mammalian cells [13,14]. Recently, TAZ was reported to be essential in regulating hippo pathway and β-catenin/wnt pathway during organ size control, tissue regeneration and stem cell self-renewal [15-17]. Additionally, the WW domain of the TAZ protein was found to be able to bind with the PPXY motif of the transcription factor runt-related transcription factor 2 (RUNX2 [18-20]. This opens up the possibilities that other PPXY sequences containing transcription factors, such as myocyte enhancer factor 2B (MEF2B), Smad, and sex determining region Y-box (SOX) family molecules, are also possible binding candidates of TAZ . Subsequently it was found that TAZ binds with Smad 2/3 to shuttle the TGFβ stimulated nucleus translocation of Smad proteins to regulate human embryonic stem cell proliferation . Currently, there are no reports in the literature regarding the study of TAZ in ocular tissues.
In the present study, we sought to investigate the involvement of TAZ protein and TGFβ signaling in regulating conjunctival epithelial cell proliferation. Moreover, we aimed to investigate the expression and location of TAZ protein in human conjunctiva epithelium and epithelium from pterygium samples.
All human tissue related studies were performed in accordance with the tenets of the Declaration of Helsinki and the study protocol was approved by the Institutional Review Board of the Singapore Eye Research Institute and Singapore National Eye Centre. Informed written consent was obtained from each participant.
Pterygium biopsies were collected from patients undergoing routine surgery for pterygium removal. A small piece of normal conjunctiva (1×3 mm) was removed from the super bulbar region, 10–15 mm from the limbus. For cell isolation and culture, tissue biopsies were briefly rinsed with phosphate buffer saline, followed by stirring in buffer containing 30 mM HEPES, 4 mM glucose, 3 mM KCL, 1 mM Na2HPO4 and 1.2% dispase. Epithelial cells were collected by centrifugation and cultured in serum-free keratinocyte growth medium (KGM) with supplements of bovine pituitary and epithelial growth factor (EGF). For TGFβ stimulation experiments, conjunctiva epithelial cells were cultured in KGM medium without supplements for 2 days before treatment.
Immortalized normal human conjunctiva cells (NHC cells) were cultured in Dulbecco’s modified eagle medium (DMEM) supplemented with 10% fetal calf serum and grown on round shape glass coverslips, which were inserted on the bottom of the 24 well plate dishes. BrdU (10 µm) was added into the culture medium for 24 h before fixation with 4% paraformaldehyde. After treatment with 2 N hydrochloric acid (HCL) for 15 min, cells were stained with monoclonal anti-BrdU (Sigma, St. Louis, MO) and polyclonal anti-TAZ (Santa Cruz Biotechnology, Santa Cruz, CA). 4',6-diamidino-2-phenylindole (DAPI) was applied in the mounting medium as a nucleus counter stain. Images of the cells after staining were taken by LSM510 confocal microscope (Carl Zeiss, Jena, Germany) and the fluorescent intensity of the defined area was measured by Image J (NIH) software. Briefly, the staining pictures were converted into monochrome images and measured with the intensity tools. The intensities of the cells at cell cycle resting stage or TGFβ non-treated cells were defined as “1.” The fluorescence intensities of testing cells were normalized to the readings of cells at control group and defined as “relative fluorescence intensity.”
TAZ siRNA (Santa Cruz) is a combination of three siRNA sequences targeting the human TAZ gene (NM_013595): A; GUA CUU CCU CAA UCA CAU Att, UAU GUG AUU GAG GAA GUA Ctt: B; CUA GGA AGG CGA UGA AUC Att, UGA UUC AUC GCC UUC CUA Gtt: C; GGA UGU AGC CAU GAC CUU Att, UAA GGU CAU GGC UAC AUC Ctt. Both TAZ siRNA and mock siRNA (Santa Cruz Biotechnology) were transiently transfected into NHC cells with lipofectamine 2000 (Invitrogen, Carlsbad, CA) as a carrier, according to the protocol provided by the manufacturer. NHC cells were collected at 24 h after transfection for further processing. For cell density analysis, NHC cells were stained with 0.5% commassie brilliant blue before scanning. The scanning pictures were converted into monochrome images and measured with the intensity measurement tools of Image J (NIH) software. The averaged intensities of the scanning images for non-treated specimens were defined as “1.” The intensities of the scanning images for treated specimens were normalized to the readings of control group and defined as “relative cell density.”
For the luciferase reporter assay, NHC were grown on Costar® white 96-well dish and transfected with 10–4-cyclin E-lux cDNA (addgene plasmid 8458) with lipofectamineTM 2000 (Invitrogen). 10–4-cyclin E–lux (50 ng) was transfected into NHC cells with a combination of mock siRNA or siTAZ. Luciferase activity in cell lysate was measured using the Bright-GloTM luciferase assay system (Promega, Madison, WI) in a TecanTM Xfluor 4 Geniospro V4.5 luminometer (Tecan, Seestrasse, Männedorf). Data were collected from 3 repeats.
NHC cell line or primary human conjunctiva epithelial cells after treatment were fixed with 4% paraformaldehyde and washed by phosphate buffer saline with 0.2% triton-x 100. Normal conjunctiva or pterygium tissue after dissection was fixed with 4% paraformaldehyde before cryopreserving with 20% sucrose. Eight µm thickness sections were collected with a cryostat (Leica, Wetzlar, Germany). The primary antibodies for immunostaining include polyclonal anti-TAZ and anti-Smad4 (Cell signaling Technology, Danvers, MA). Secondary antibodies include Alexflour 488 or Alexflour 555 conjugated goat anti-mouse or goat anti-rabbit secondary antibody (Invitrogen). Images of the specimens after staining were taken by LSM510 confocal microscope (Carl Zeiss, Jena, Germany).
Conjunctiva epithelial cells were plated on a 9 cm × 9 cm culture dish till 80% to 90% confluence. After treatment, the cells were collected and lysed in RIPA buffer (50 mM Tris-HCL, 1 mM EDTA, 0.25% sodium deoxycholate, 150 mM sodium chloride, and 1% NP-40) containing 1 mM DTT, protease inhibitor cocktail, 1 mM Na3VO4, and 1 mM PMSF. A total of 30 µg of each protein was loaded for SDS–PAGE gel analysis. Primary antibodies for western blot were anti-TAZ (Santa Cruz Biotechnology) and anti-β-actin (Sigma, St. Louis, MO).
Secondary antibodies for western blot included horseradish peroxidase conjugated sheep anti-mouse/rabbit IgG (GE Healthcare, Buckinghamshire, England).
We performed TAZ immunostaining on primary normal human conjunctiva epithelial cells to investigate the role of TAZ protein in cell proliferation. Nucleus DAPI counterstaining was applied to indicate the cell dividing stage. We observed that the fluorescence intensity of TAZ protein was strongly upregulated in dividing cells compared with that of neighbor cells at the resting stage (Figure 1A). A total of 120 cells from three independent repeats were collected for analysis. The averaged fluorescence intensity of TAZ protein in mitotic cells was around 5.2±0.4 fold higher than that of the resting cells (Figure 1B). Upregulation of TAZ protein expression was also observed in proliferating cells during other cell cycle phases, which were reflected by the DAPI staining pattern (Figure 2). We treated conjunctiva epithelial cells with 2N HCL for 15 min (Figure 2A) or 40 min (Figure 2B) to allow for permeabilization of TAZ antibody. We found that in dividing conjunctiva keratinocyte, TAZ protein concisely co-localizes with DAPI, an indicator for DNA. We did transcriptional response assay to determine the involvement of TAZ in cell cycling/proliferation, which was accessed by transcriptional activities of 10–4-cyclin E promoter. 10–4-cyclin E promoter is required for the mammalian cell transition from G1 to S phase. TAZ siRNA induced significant less transcriptional activities of 10–4-cyclin E promoter in NHC cells and this effect is dosage dependent (Figure 2C).
BrdU analysis was performed to further examine whether TAZ protein is upregulated in proliferating conjunctiva epithelial cells. We observed that in BrdU positive cells, TAZ protein was found clustering in the nucleus of the cells, while in cells that were BrdU negative, TAZ protein was predominantly expressed in the cytoplasm (Figure 3). Moreover, the fluorescence intensity of TAZ signal in BrdU positive cells was also observed to be much higher than that of BrdU negative cells. This result is consistent with our previous observation that TAZ protein was highly upregulated during epithelial cell division and proliferation; therefore, the activation and translocation of TAZ protein are closely associated with epithelial cell proliferation.
It was recently reported that TAZ is responsive to TGFβ cytokine, forming a complex with Smad protein at the cytoplasm, which facilitated the nucleus translocation of Smad proteins in human embryonic stem cells . In our study, we aimed to investigate whether the TAZ signal in human conjunctiva epithelial cells is also responsive to TGFβ. Our data showed that the fluorescence intensity of endogenous TAZ signal in epithelial cells that were treated with TGFβ is higher than that of cells without TGFβ treatment (Figure 4A). Smad4 staining was simultaneously performed as an indicator of the cells that were responsive to TGFβ. The relative quantitative fluorescence intensity in the nucleus of the epithelial cells was measured (Figure 4B). A total of 100 cells from three repeated experiments were analyzed. We found that after TGFβ treatment, fluorescent intensity of TAZ protein in the cell nucleus is about 2.5±0.3 times higher than that of untreated cells (Figure 4B). Western blot analysis further confirmed that the TAZ protein expression was upregulated in TGFβ treated cells (Figure 4C). Altogether, these results indicate that TAZ protein is responsive to TGFβ stimuli in human conjunctiva epithelial cells.
We initially did western blot and commassie brilliant blue staining to confirm the effect of TAZ siRNA. Western blot images (Figure 5A) indicated that there was down-regulation of TAZ gene expression by TAZ siRNA. Commassie brilliant blue staining images (Figure 5B) indicated that TAZ silencing induced lower conjunctiva cell attachment and cell growth. We then sought to investigate whether TAZ regulates the growth rate of NHC cells by interacting with a TGFβ signal. NHC is an immortalized cell line, which was derived from the normal human conjunctiva epithelium and shared a lot of characteristics with primary conjunctiva epithelial cells . TGFβ receptor I antibody was added to block the signal transduction of TGFβ. We found that silencing of the TAZ gene significantly suppressed the proliferation rate of NHC cells (Figure 6A, “a”). However, this suppression was rescued by the treatment of anti-TGFβ Receptor I antibody (10 µg/ml, Figure 6A, “b”). Our data indicated that TAZ regulated the epithelial cell proliferation by interacting with the TGFβ signal. NHC cells were also treated with the specific TGFβ receptor inhibitor, SB431542. Silencing of the TAZ gene suppressed the cell growth rate of NHC cells and this effect was significantly rescued by SB431542 (10 nm, Figure 6B).
We then examined the expression of TAZ protein in human normal conjunctiva epithelium and pterygium conjunctiva epithelium. TAZ protein was blotted from the total lysate of the epithelial layers of conjunctiva tissues. We found that TAZ expression in pterygium tissue was much higher than that of normal tissue (Figure 7A). Intensity of the blotting bands showed that the expression level of TAZ protein in pterygium epithelium is around 10 times higher than that of the normal conjunctiva tissue (Figure 7B). Immunostaining of the pterygium conjunctiva tissue revealed that TAZ protein is highly clustering in the epithelial layer of conjunctiva tissue (Figure 7C).
The TGFβ signaling pathway controls a diverse set of cellular activities and is regulated by various receptors and transcription factors. Here, we addressed the role of TAZ in the regulation of conjunctiva epithelial cell proliferation by interacting with the TGFβ signaling pathway. TAZ protein expression was found to be upregulated in the mitotic conjunctiva epithelial cells and pterygium epithelium, which is a novel observation and has never been reported before. Moreover, TGFβ receptor antibody and TGFβ receptor inhibitor partially rescued cell growth inhibition, which was induced by TAZ siRNA. Hence, TAZ is involved in regulating conjunctiva cell proliferation via the TGFβ pathway.
Previous studies revealed that Smad family protein functions by directly binding with DNA promoters and consensus fragments resulting in the activation of target genes [23-25]. A growing number of DNA binding factors, such as Fas-activated serine/threonine kinase (FAST), activator protein 1 (AP1)-containing elements and transcription factor E (TFE), as well as TAZ, have been identified to facilitate the Smad-induced gene activation . In our study, we found the co-localization of TAZ protein with DAPI signal in mitotic cells, which indicated that TAZ is related to cell cycle regulation and TAZ protein is a transcriptional factor that may act by binding with Smad and DNA promoters or consensus after stimulation.
Several WW domain containing ubiquitin ligases have been identified to negatively regulate the TGFβ signal by targeting and degradation of Smad family proteins [26,27]. The HECT-type WW domain containing ubiquitin ligase, Smurf2, was reported to down-regulate the TGFβ signal by binding with the proline-rich domain of Smad7 and form a complex with TGFβ receptors [28-30]. Smurf2 was also reported to degrade the receptor binding Smad protein, Smad 1 . Another receptor binding Smad protein, Smad2, was also found to be able to form assembly with Smurf2 and be degraded by Smurf2 [32,33], while the co-Smad, Smad4, can be targeted indirectly by Smurf2 and be degraded simultaneously with R-Smad and I-Smad . The WW domain containing protein, TAZ, shares a similar structure with smurf2 . TAZ functions by binding with Smad family proteins and TAZ antagonised the TGFβ induced cell growth inhibition. Altogether, these findings indicate that TAZ and smurf family proteins probably serve separate but perhaps overlapping functions. Hence, TAZ may be an ubiquitin co-activator that negatively regulates the TGFβ/Smad signaling pathway to regulate mammalian cell proliferation.
Many tumor cells are resistant to TGFβ induced apoptotic effect. The mechanisms are reported to be associated with the mutation of the receptors or components of the Smad pathways [35,36]. TGFβ has a biphasic role in tumor genesis. In the initial phases it acts as a tumor suppressor, whereas during the late phases it has been shown to function as a tumor promoter . TGFβ stimulates the de-differentiation of epithelial cells into malignant invasive and metastatic fibroblastic cells. This procedure was regulated by various co-factors. Recently, Yes-associated protein 1 (YAP1), a protein that shares its homological structure with TAZ, was reported to play a critical role in regulating the expression of cancer gene tumor protein 73 (p73) and in regulating tumor cell migration . These reports indicate that other transcriptional co-factors, such as TAZ, may also interact with the TGFβ signal and regulate cancer cell migration and invasion. In our studies, we found that TAZ expression was upregulated in the epithelial tissue with pterygium disease compared with that of the normal conjunctiva tissue (Figure 6). The pterygium is studied as a benign tumor whose genotype is highly associated with the mutation of tumor suppressor gene p53 [38,39]. Our findings at least indicated that TAZ is possibly involved in the pathology of pterygium by regulating the TGFβ signal. Further mechanism and in vivo studies are necessary to clarify this.
In conclusion, we found that TAZ regulates human conjunctiva epithelial cell proliferation via inhibiting TGFβ signaling. We also found that TAZ is upregulated in pterygium tissue. This finding provides an important clue to the mechanisms of TGFβ signaling in the regulation of conjunctiva cell proliferation and pterygium progression. Furthermore, TAZ may also play an important role in the pathogenesis of other ocular diseases, such as TGFβ related fibrogenesis diseases, corneal wound healing and protein aggregation.
We could like to acknowledge the technical support from Dr Wu Hong, Singapore Eye Research Institute, Singapore.
In this article by Xiao Wei Tan and
the following corrections were made:
In the title, abstract, and introduction,
the gene symbol
TAZ was corrected to be WW Domain Containing Transcription