- Open Access
Nanog down-regulates the Wnt signaling pathway via β-catenin phosphorylation during epidermal stem cell proliferation and differentiation
© Cheng et al.; licensee BioMed Central. 2015
- Received: 15 July 2014
- Accepted: 16 January 2015
- Published: 27 January 2015
Skin tissue homeostasis is maintained by a balance between the proliferation and differentiation of epidermal stem cells (EpSCs). EpSC proliferation and differentiation are complex processes regulated by many factors and signaling pathways. This study aimed to explore the connection between the Nanog and the Wnt/β-catenin pathway in the proliferation and differentiation of EpSCs.
Our results demonstrated that during the study period, EpSC underwent differentiation when incubated in the presence neuropeptide substance P (SP), there was an opposing expression trend of Nanog and β-catenin after SP treatment, which could be antagonized by the Wnt antagonist, Dkk-1. The transduced EpSCs had a greater proliferative ability than the SP treatment group and they did not undergo differentiation upon SP treatment. More important, β-catenin expression was down-regulated but phosphorylated β-catenin expression and phosphorylated GSK-3β expression was up-regulated upon Nanog overexpression.
These results strongly suggest that Nanog plays an important role in maintaining the proliferation and differentiation homeostasis of EpSCs by promoting β-catenin phosphorylation via GSK-3β to inhibit the activity of the Wnt/β-catenin signaling pathway. This is important for precise regulation of proliferation and differentiation of EpSC in the application of tissue engineering.
- Epidermal stem cells
Skin is the largest organ of the human body; it plays a key role in protecting the body against pathogens. The homeostasis of skin tissue is maintained by rare but pluripotent epidermal stem cells (EpSCs) and their progeny, transient amplifying (TA) cells [1, 2]. As pluripotent cells, EpSCs not only have an unlimited self-renewal capability to maintain a certain population but they also differentiate to form structures such as hair follicles and sebaceous glands [2, 3].
Transcription factors and signals determine whether EpSCs undergo self-renewal or differentiation. Several studies have established the central role of Nanog in maintaining pluripotency and preventing differentiation [4–7]. Nanog simultaneously increases the expression of genes conferring pluripotency and decreases the expression of genes driving cell differentiation. Increasing evidence also supports the involvement of the Wnt/β-catenin signaling pathway in the self-renewal and differentiation of EpSCs [8–10]. β-catenin is of central importance in the Wnt/β-catenin signaling pathway. Numerous articles have also reported that the fate of EpSC is controlled by an intricate relationship between different signaling pathways and transcription factors, especially Nanog and the Wnt/β-catenin signaling pathway [11–14]. However, previous research has not been able to clearly reveal the underlying molecular mechanism of EpSC proliferation and differentiation. Thus, the relationship between Nanog and the Wnt/β-catenin signaling pathway in EpSC proliferation and differentiation is of great interest.
In this study, we evaluated the relationship between the Wnt/β-catenin signaling pathway and Nanog in the proliferation and differentiation of EpSCs. Rat EpSCs were infected with lentivirus overexpressing Nanog. SP,a neuropeptide present in primary sensory neurons,belongs to the tachykinin family and can activate Wnt/β-catenin signaling pathway . Transduced or untransduced cells were subsequently incubated in the presence or absence of SP. The effect of Nanog and SP on EpSC proliferation was tested in vitro. Subsequently, the expression of β-catenin and Nanog were evaluated in SP treated EpSCs using western blotting and PCR. In addition, the effect of Nanog on β-catenin expression was investigated in EpSCs using a lentivirus infection and/or SP treatment.
Characterization of EpSCs
Proliferative ability of EpSCs infected with lentivirus or treated with SP in vitro
The expression of Nanog and β-catenin in EpSCs treated with SP
The expression of Nanog and β-catenin in EpSCs infected with lentivirus
Negative feedback of Nanog on the Wnt /β-catenin signaling pathway
To explore how Nanog affects the Wnt/β-catenin signaling pathway, EpSCs infected with lentivirus encoding Nanog were incubated in the presence or absence of SP. Nanog, β-catenin and c-myc in Wnt/β-catenin signaling pathway were detected both at mRNA and protein level. At the mRNA level, Nanog expression in transduced cells in the absence or presence of SP was significantly higher than the control or SP-only treatment groups (Figure 6A) (P < 0.05). In contrast to Nanog expression, pt]?>β-catenin expression in transduced cells in the absence or presence of SP was significantly lower than the control or SP-only treatment groups (Figure 6B) (P < 0.05). C-myc, a downstream gene in the Wnt/β-catenin signaling pathway, trended with β-catenin expression (Figure 6C). The western blotting results were in accordance with q-PCR data. (Figures 5D, 5E, and 6 F).
As the primary barrier in the human body, skin protects humans from infection, radiation and wounds. However, skin, especially the epidermis, may be injured by external insults. The proliferation and differentiation of EpSCs and their progeny of TA cells greatly affect skin repair [2, 19, 20]. This process is controlled by an intricate relationship between different signaling pathways and transcription factors, especially the Wnt/β-catenin signaling pathway and Nanog [21–23].
Nanog is a pluripotent state-specific transcription factor that plays a critical role in regulating cell fate during embryonic development, maintaining pluripotent epiblasts and preventing differentiation [24, 25]. Nanog is also proposed as a transcription repressor that inhibits important genes for cell differentiation [7, 26]. Our results showed that the proliferation ability of transduced EpSCs is much greater than the control and SP treated groups (Figure 2). Additionally, transduced EpSCs treated with SP did not undergo differentiation (Figure 1I). These results using EpSCs agree with previous reports that Nanog can promote proliferation and inhibit differentiation of stem cells. On the other hand, accumulating evidence indicates that the Wnt/β-catenin signaling pathway plays a critical role in the lineage decision/commitment process [10, 23, 27, 28]. In contrast, there are also some reports that the Wnt/β-catenin signaling pathway plays a pivotal role in the maintenance of pluripotency as well as in the process of somatic cell reprogramming [9, 29–31]. These dramatically different observations upon activation of the Wnt signaling cascade have fueled enormous controversy concerning the role of Wnt signaling in the maintenance of differentiation potency and the induction of stem cells. Our results in EpSCs support the former conclusion. In this study, EpSCs were differentiated when they were treated with a Wnt agonist (Figure 1F) and the differentiation was antagonized by Dkk-1(Figure 1G). This result supports evidence that the Wnt/β-catenin signal pathway affects EpSCs differentiation.
It is noteworthy that treatment with 10-7 M SP caused a rapid proliferation of EpSCs into TA cells in the first twelve days, which subsequently had a limited proliferative ability (Figure 2). This result agrees with our previous study regarding the effect of SP on EpSCs . Previous reports also support our findings [33, 34]. From day 12, the EpSCs underwent differentiation, manifesting the typical morphology and expressing CK18, which is an EpSCs differential marker [35, 36] (Figures 1D, 1E). This is a new observation compared to our previous research. In this process, the expression of the pluripotency protein Nanog decreased significantly. However, β-catenin transcription and translation increased (Figure 3). Besides, the increase of β-catenin could be counteracted by Dkk-1 (Figure 4). The opposing expression trends of Nanog and β-catenin suggested that there should be an interaction between them (Figures 3 and 4).
To prove this hypothesis, we infected lentivirus-Nanog into EpSCs in vitro (Figure 1H). CCK-8 results revealed that the transduced EpSCs had a strong proliferative ability, while the control lentivirus vector infection showed no effect on the EpSCs proliferative ability (Figure 2). Besides, the control lentivirus vector infection also did not interfere with Nanog and β-catenin expression either (Figure 5). Nanog counteracted SP-induced cell differentiation (Figures 1I and 6A). The most important result is that β-catenin expression in the transduced EpSCs was notably decreased as measured by q-PCR and western blot (Figure 6). This result suggests that Nanog can inhibit EpSC differentiation by inhibiting β-catenin expression. C-myc, a downstream target of Wnt/β-catenin signaling pathway, binds to promoter sequences after activation by β-catenin-TCF complexes. Haegele et al. found that the activation of c-myc and its downstream targets Cyclin-dependent kinase 2 (CDK) and Cyclin A could up-regulate BMPs and cause embryonic stem cell differentiation . In the SP-treated groups, c-myc expression of the transduced EpSCs was also suppressed both at mRNA and protein level (Figures 6C, 6F). The change in c-myc expression agreed with β-catenin changes in the transduced EpSCs, which indirectly demonstrates that β-catenin is involved in EpSC differentiation. This result further proved that Nanog can maintain EpSC pluripotency and prevent differentiation by inhibiting the β-catenin expression.
To explore the potential mechanism of this process, we measured the levels of phosphorylated β-catenin protein, phosphorylated GSK-3β and total GSK-3β in each group. It is well known that the activity of the Wnt/β-catenin signaling pathway is affected by glycogen synthase kinase (GSK). GSK-3β is phosphorylated and results in β-catenin phosphorylation and its subsequent degradation by the ubiquitin-mediated pathway [29, 37]. In this experiment, we found that the ratio of phosphorylated β-catenin to total β-catenin paralleled Nanog expression in each group (Figure 7E), which is in common with the ratio of phosphorylated GSK-3β to total GSK-3β (Figure 7B). Therefore, we conclude that Nanog inhibits β-catenin activity through the phosphorylation of β-catenin via GSK-3β. Thus, we can infer the underlying process by which EpSCs execute their function. When skin is not injured, Nanog maintains the multi-potential and proliferative state of EpSCs through inhibiting β-catenin expression via β-catenin phosphorylation. However, when skin needs to repair an injury, negative feedback from β-catenin on Nanog suppresses its expression and induces EpSC differentiation. The whole process balances the differentiation and proliferation of EpSCs.
In summary, our study showed that Nanog and the Wnt/β-catenin signaling pathway are involved in the regulation of EpSC proliferation and differentiation, which is necessary to maintain EpSCs homeostasis in the skin. The underlying mechanism is that Nanog inhibits the activity of the Wnt/β-catenin signaling pathway via GSK-3β mediated β-catenin phosphorylation. This finding represents an important step towards understanding the precise regulation of EpSC proliferation and differentiation, which has important applications in tissue engineering.
Sprague–Dawley (SD) male rats were purchased from HUST Laboratory Animal Center (Wuhan, China). The Ethics Committee of Tongji Medical College, Huazhong University of Science and Technology, approved all animal care and experimental procedures. The EpSCs isolated procedure was regarded as a standard protocol which was first repoted by Liu Y . Skin tissue was obtained from the back of neonatal SD rats by plastic surgical procedures and was washed in phosphate-buffered solution (PBS). Connective tissue and subcutaneous fat were removed. The skin sample was sterilized with 70% ethanol for 5 min, rinsed in PBS, and minced into 5-mm wide strips using a sharp scalpel; the strips were treated with 0.25% Dispase (Roche, Switzerland) solution at 4°C overnight. The epidermis was mechanically separated from the dermis and incubated in 0.25% trypsin solution at 37°C for 15 min to dissociate the cells; enzyme activity was then blocked with Dulbecco’s modified Eagle’s medium (DMEM; Gibco, USA) containing 10% fetal bovine serum (FBS; Gibco, USA), and the cells were suspended with a pipette. To remove any remaining tissue pieces, the cell suspension was filtered through a stainless steel mesh attached to a 60-mm cell culture plate. The cells were transferred to a 15-ml centrifuge tube and collected by centrifugation for 5 min at 250 g. To select stem cells, 1x106 dissociated epidermal cells were plated onto collagen type IV (Sigma, USA) (100 μg/ml)-coated dishes at room temperature for 15 min. The unattached cells were removed, and the rapidly adherent epidermal cells were cultured with keratinocyte serum-free medium (K-SFM; Gibco, USA) supplemented with epidermal growth factor (EGF) (K-SFM; Gibco, USA), bovine pituitary extract (BPE; Gibco, USA), and 0.05 mM calcium chloride (CaCl2, Sigma, USA) at 37°C under 5% CO2 in a humidified incubator for two days before replacing the medium. The medium was changed every other day.
Lentivirus vector construction and EpSC infection
The coding sequence of rat Nanog was PCR amplified from GV208: rat-Nanog using primers with AgeI/AgeI overhangs and was cloned into pTZ58 (Fermentas, Vilnus, Lithuania). The AgeI/AgeI fragment was then sub-cloned into pUbi (AgeI/AgeI) and pEGFP-C1 (Clontech, Mountain View, CA) (AgeI/AgeI) to generate Ubi-Nanog-EGFP encoding plasmids, respectively. To produce lentivirus, the pBABE-puro plasmids were co-infected along with the helper plasmids into 293 T cells, and the medium was harvested 36 h and 72 h after infection. EpSC infection was performed by incubating the cells in virus-enriched medium for 12 h, which included 4 μg/ml polybrene. Transduced cells were identified for EGFP expression under a fluorescence microscope. The transduced EpSCs were divided into two groups: the first group of EpSCs was treated with SP for 12 days after infection; the second group of EpSCs was cultured for 12 days. EpSCs were also infected with control lentivirus vector and cultured for 12 days. EpSCs without any treatment were used as control.
The isolated cells were cultured in a 6-well plate (104 cells/well) for 24 h. The cells were rinsed five times with PBS, fixed with 4% paraformaldehyde solution for 15 min at room temperature, and permeated with 0.5% Triton X-100-PBS solution for 5 min. After blocking with 3% BSA in PBS for 30 min, the cells were respectively incubated with primary antibodies to anti-CD 34 antibody (rabbit polyclonal antibody, 1:50, Santa Cruz Biotechnology, Inc.) and anti-β1 integrin antibody (rabbit polyclonal antibody, 1:50, Boster Biological Technology, Ltd.) at 4°C overnight. The primary antibody binding was detected via the corresponding goat anti-rabbit IgG: Cy3 and goat anti-mouse IgG FITC (Boster Biological Technology, Ltd.). Staining was examined under a fluorescence microscope.
The isolated cells were cultured in a 6-well plate (104 cells/well) for 24 h. The cells were treated with 10-7 M SP or LiCl, a Wnt agonist, to induce differentiation for 12 days. The cells were rinsed five times with PBS, fixed with 4% paraformaldehyde solution for 15 min at room temperature, and permeated with 0.5% Triton X-100-PBS solution for 5 min. The cells were incubated with primary antibodies to anti-cytokeratin 18 antibody (CK18) (rabbit polyclonal antibody, 1:50, Santa Cruz Biotechnology, Inc.) at 4°C overnight. Subsequent procedures were performed according to the SP-9000 Histostain-Plus Kit instructions (ZSGB-BIO, Beijing, China). The cells were observed under a microscope (Bio-Rad, Hercules, CA, USA).
Cell Counting Kit-8 (CCK-8) assay
EpSCs were plated in 96-well plates (2 × 104 cells/well) and treated with collagen type IV. The cells were then divided into four groups: the first group was composed of cells without any treatment, the second group was composed of cells infected with control lentivirus vector, the third group was composed of transduced cells, and the forth group was composed of cells that were exposed to 10-7 M SP. Every other day after day 2 until day 12 post-treatment, 10 μL of CCK-8 (Boster, China) solutions were added to each well, and the samples were incubated for 2 h. The specific absorbance at 450 nm (A450) was determined using a Micro-plate Reader (Thermo Fisher, USA). All of the experiments were repeated independently at least three times, and each measurement was the average of 5 duplicate wells.
The total cell lysates of EpSCs that underwent the proliferation and differentiation were obtained by lysing the cells in RIPA buffer (Boster, China) containing 50 mM Tris–HCl, 150 mM NaCl, 1% NP-40, 0.1% SDS, 0.5% sodium deoxycholate, 2 mM sodium fluoride, 1 mM EDTA, 1 mM EGTA and a protease inhibitor cocktail. The protein concentration was determined using the bicinchoninic acid protein assay (Beyotime, China). The proteins were separated by SDS-PAGE, transferred to nitrocellulose, blocked with bovine serum albumin and incubated with the following primary antibodies: rat anti-β-catenin (CST, USA) diluted 1:1000, rat anti-p-β-catenin (CST, USA) diluted 1:1000, rat anti-c-myc (CST, USA) diluted 1:1000, rat anti-Nanog (CST, USA) diluted 1:2000, rat anti-GSK3β (CST, USA) diluted 1:1000, rat anti-p-GSK3β (CST, USA) diluted 1:1000 or rat anti-GAPDH (Beijing Biosynthesis Biotechnology, China) diluted 1:1000 that was used as a loading control. The membrane was washed and incubated with the respective secondary antibodies conjugated with peroxidase. Chemiluminescence (Bio-Rad, USA) was used to detect protein.
Real-time quantitative PCR
Total RNA was extracted using the TRIzol reagent (Invitrogen, USA), according to the manufacturer’s protocol. Using a spectrophotometer (Eppendorf, Germany), the RNA concentration and purity were determined by A260 and A260/A280 ratios, respectively. Total RNA was used to synthesize cDNA with a Super-Script II cDNA synthesis kit (Invitrogen Life Technologies, USA). The related genes of the Wnt/β-catenin signaling pathway and Nanog were assessed by quantitative real-time PCR using a SYBR-Green Master mix (Fermentas, Vilnius, Lithuania). Glyceraldehyde phosphate dehydrogenase (GAPDH) was selected as an internal control. The primer sequences are: Nanog (accession no. NM_001100781) forward, CCGTTGGGCTGACATGAGCGT and reverse, GGCAGGCATCGGCGAGGAAT; β-catenin (accession no. NM_053357) forward, AGCCCGTTGTACCGCTGGGA and reverse, CGCTGGGATGCCGCCAGATT; c-myc (accession no. NM_012603) forward, CATCATCCAGGACTGTATGTG and reverse, TGGAATCGGACGAGGTA; GAPDH (accession no. NM_017008) forward, TATGACTCTACCCACGGCAAGT and reverse, ATACTCAGCACCAGCATCACC.
All experiments were repeated independently at least three times. The data are presented as the mean ± standard deviation (SD). The results were analyzed using SPSS 18.0 statistical software. Statistically significant differences were identified using Student’s t-test and an analysis of variance (ANOVA). The significance level was set to P < 0.05.
This study was supported by the National Natural Science Foundation of China (No. 30872691 and No.81300828).
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