pH-mediated upregulation of AQP1 gene expression through the Spi-B transcription factor
© The Author(s) 2018
Received: 17 July 2017
Accepted: 6 March 2018
Published: 20 March 2018
Bicarbonate-based peritoneal dialysis (PD) fluids enhance the migratory capacity and damage-repair ability of human peritoneal mesothelial cells by upregulating AQP1. However, little is known about the underlying molecular mechanisms.
Here we used HEK-293T cells to investigate the effect of pH on AQP1 gene transcription levels. We found that AQP1 mRNA levels increases with pH. Transfection of HEK-293T cells with luciferase reporter vectors containing different regions of the AQP1 promoter identified an upstream region in the AQP1 gene between − 2200 and – 2300 bp as an enhancer required for pH-mediated regulation of AQP1 expression. Site-directed mutagenesis of this specific promoter region revealed a critical region between − 2257 and − 2251 bp, and gene knock-down experiments and ChIP assays suggested that the Spi-B transcription factor SPIB is involved in pH-mediated regulation of AQP1 expression.
We identified an upstream region in the AQP1 gene and the transcription factor SPIB that are critically involved in pH-mediated regulation of AQP1 expression. These findings provide the basis for further studies on the pH- and buffer-dependent effects of PD fluids on peritoneal membrane integrity and function.
End-stage renal disease (ESRD) has a poor prognosis and affects human populations around the world . Peritoneal dialysis (PD) is a well-established renal replacement therapy that takes advantage of the semi-permeability of the peritoneal membrane, to remove toxins and excess water from the circulatory system. Maintenance of the morphological and functional integrity of the peritoneum is essential for long-term PD patients. However, conventional acidic PD solutions cause peritoneal cell damage, cell shedding [2–4], peritoneal fibrosis and progressive vascularization [5–8], leading to ultrafiltration loss and eventually PD failure .
Novel PD solutions that separate glucose from the buffer at a very low pH contain fewer glucose degradation products (GDPs) and have a neutral to physiological pH after mixing. Several studies suggest that these solutions can reduce peritoneal cell damage and preserve the peritoneal membrane host defence and transport functions. The solutions contain lactate, bicarbonate or a mixture of both buffers. A prospective paediatric trial that compared a pure bicarbonate buffer to a purely lactate-based low GDP fluid demonstrated better preservation of ultrafiltration capacity over 10 months . However, the underlying mechanisms remained elusive, and the respective impacts of the solutions on cellular pH are unknown. The ultrafiltration capacity of the peritoneum is closely related to peritoneal aquaporin 1 (AQP1) expression. AQP1 is expressed in peritoneal capillaries, post-capillary venules and peritoneal mesothelial cells, which are critical for maintaining local peritoneal homeostasis [11–13]. AQP1 knockout mice have approximately 50% less peritoneal ultrafiltration capacity [14, 15]. Previously, via in vitro experiments, we demonstrated pH and buffer dependent upregulation of AQP1 in human peritoneal mesothelial cells and improved AQP1-dependent cell migration. Actinomycin D-based experiments further demonstrated that the pH-mediated effects on AQP1 occurred at the transcriptional level . Differences in the PD fluid buffer and pH may therefore play an important role through regulation of AQP1 gene expression.
Thus, here, we examined the underlying molecular mechanisms of pH- and buffer-dependent AQP1 expression in HEK-293T cells, which display reliable growth and have a propensity for transfection. We extensively explored the key transcription factors and their binding sites involved in pH-mediated regulation of AQP1 expression by cloning the AQP1 gene promoter region and various truncated forms of the promoter region.
Materials and methods
Plasmids and reagents
A Flag-tagged SPIB expression clone and the vector plasmid were purchased from GeneCopoeia (Guangzhou, China). Anti-IgG and anti-SPIB antibodies were purchased from Cell Signaling Technology, and anti-Flag and anti-β-actin antibodies were obtained from Sigma.
The HEK-293T cell line was purchased from ATCC (American Type Culture Collection). HEK-293T cells were cultured at 37 °C with 5% CO2 in DMEM supplemented with 10% foetal bovine serum and transfected using Lipofectamine 2000 reagent (Invitrogen) according to the manufacturer’s instructions. The total amount of plasmid DNA used for transfection was maintained at a constant level between experimental conditions through the addition of empty vector plasmid. To investigate the regulatory effects of pH on AQP1 gene expression, HEK-293T cells were seeded into 6-well plates. Once the cells attached to the culture surface, the regular culture medium was replaced with serum-free culture medium, and the cells were cultured in the serum-free medium for 24 h. Subsequently, the cells were treated with bicarbonate-buffered complete media in which the pH was adjusted to 6, 7 or 8 with HCl or NaOH. After treatment for 24 h, the cells were lysed.
RNA extraction and real-time PCR analysis
Total cellular RNA was extracted using Trizol reagent (Invitrogen Corporation). In total, 500 ng of RNA was reverse transcribed into cDNA using a PrimeScript Reverse Transcription Kit (Takara Biotechnology Co., Ltd); β-actin was used as an internal reference. The sequences of the specific primers for quantitative polymerase chain reaction (qPCR) were listed in Additional file 1: Table S1. The relative expression levels of target genes were calculated using the 2−ΔΔCT method.
Western blot analysis
Cells were harvested by scraping into an SDS sample buffer. Similar protein amounts were loaded onto a 7.5% SDS-PAGE gel, separated by electrophoresis, and transferred to a nitrocellulose membrane (Bio-Rad, Hercules, CA). The membrane was blocked with TBST (0.05% Tween 20 in TBS) containing 5% skim milk and then incubated overnight with the indicated antibodies at 4 °C. The membrane was washed three times in TBST and then incubated with an HRP-conjugated secondary antibody (Pierce, Rockford, IL) (1:2000) for 2 h at room temperature. The membranes were stripped of the primary antibodies and reprobed with antibodies as necessary. The immunocomplexes were detected using enhanced chemiluminescence (Pierce, Rockford, IL, USA).
Dual-luciferase reporter vector construction
Genomic DNA was extracted from HEK-293T cells using an AllPrep DNA/RNA Mini Kit (Qiagen). The isolated genomic DNA was used as a template for PCR amplification of the AQP1 promoter region. According to the genomic structure information for the AQP1 gene, the first base in the AQP1 coding sequence was numbered + 1. The AQP1 primer sequences were TTA CGC GTG CTA GCC CGG GCC TGC ACT TAG CAG AAG CTT CTG GCC AG (upstream primer) and GCT TAC TTA GAT CGC AGA TCA TGA AGA CAA AGA GGG TCG TGG CCA GG (downstream primer). The digested DNA fragments were ligated into a pGL3-Basic plasmid (Promega, Madison, USA). After verification via sequencing, the successfully constructed vector was named pGL3-AQP1-4K. Using pGL3-AQP1-4K, a series of luciferase reporter vectors containing various truncated forms of the AQP1 promoter were further constructed and named pGL3-AQP1-1K, pGL3-AQP1-2K, pGL3-AQP1-3K, pGL3-AQP1-2.2K, pGL3-AQP1-2.3K, pGL3-AQP1-2.4K, pGL3-AQP1-2.6K, pGL3-AQP1-2.8K, and pGL3-AQP1-2-3K. Using pGL3-AQP1-2.3K as the template and a QuikChange Lightning Site-Directed Mutagenesis Kit, a luciferase reporter vector containing a mutated AQP1 promoter fragment (pGL3-AQP1-2.3K mutant) was established. Additionally, the 0-1K and 2-3K regions in the AQP1 promoter were amplified via PCR. Subsequently, overlap PCR was performed to construct the pGL3-AQP1-3Δ2K vector.
Transfection of oligonucleotides
The EGR1, FOXL1, KLF5, NFIC, RFX5, SP1, THAP1, SPIB, and AQP1 siRNA duplexes and negative control (scrambled, has no significant sequence similarity to mouse, rat, or human gene sequences) were designed and synthesized by RiboBio (Guangzhou, China). For each cell of a six-well plate, cells were transfected with a pool of three siRNAs in a total volume of 5 μl (20 μM) and 5 μl Lipofectamine 2000.
HEK-293T cells were first seeded into 96-well plates at a density of 5 × 103 cells per well 24 h before transfection. The cells were transfected with a mixture of 50 ng firefly luciferase reporter and 5 ng pRL-CMV Renilla luciferase reporter using Lipofectamine 2000. The transfected HEK-293T cells were used in the subsequent assays.
Examination of luciferase activity
Twenty-four hours after transfection, the cells were covered with serum-free medium and cultured for an additional 24 h. Subsequently, the cells were incubated in culture medium with different pH values for 6 h. The firefly and Renilla luciferase activities of the cell lysates were measured using a Dual-Luciferase Reporter Assay System according to the manufacturer’s instructions (Promega). All activity values were normalized to those of the control vector pGL-basic 3.0 at pH 7. The results were assessed based on changes in the luciferase activity. All experiments were repeated three times.
Chromatin immunoprecipitation (ChIP)
HEK-293T cells were first seeded into 10-cm dishes and then transfected with plasmids the next day when the cells reached approximately 40% confluence using Lipofectamine 2000. For the ChIP assay, 4 × 106 cells were prepared using a SimpleChIP Enzymatic Chromatin IP kit (Cell Signaling Technology) according to the manufacturer’s instructions. Briefly, HEK-293T cells were fixed with 1% formaldehyde for 10 min at room temperature followed by glycine. Lysates were then digested with micrococcal nuclease into DNA/proteins fragments. Anti-flag or control IgG antibody was added, and the complex were co-precipitates and captured by protein G magnetic beads. After an overnight incubation at 4 °C, the complexes were purified, and the crosslinking was reversed at 65 °C. The resulting precipitated DNA samples were analyzed by PCR or real-time PCR using the primers listed in Additional file 1: Table S1.
Each group of experiments was repeated three times or more. Each time, three replicate wells were prepared. The measurement data were expressed as the mean ± standard error of the mean (SEM). Unless otherwise noted, Student t test (two-tailed) and one-way analysis of variance (ANOVA) followed by the Dunnett multiple comparisons test were used to compare differences between 2 groups and more than 2 groups, respectively. Two-way ANOVA was used to analyse the luciferase activity and AQP1 mRNA levels in HEK-293T cells with different pH treatment. A P value less than 0.05 indicated that the difference was statistically significant. The above statistical analyses were conducted using GraphPad software, and the results were plotted.
Effect of pH on AQP1 expression
Genomic structure of the AQP1 gene and construction of luciferase reporter vectors containing AQP1 promoter regions
The upstream region of the AQP1 gene was analysed using the UCSC Genome Browser database. According to existing knowledge, we hypothesized that a 4-kb region upstream of the AQP1 gene is the transcriptional regulatory region and contains binding sites for transcription factors. Therefore, we used HEK-293T genomic DNA as a template to clone the 4-kb upstream region of the AQP1 gene lying between − 4000 and 0 base pairs (bp; the first base in the AQP1 coding sequence was denoted as + 1). The resulting 4000-bp fragment was ligated into a pGL3-Basic vector to establish a luciferase reporter vector containing the potential AQP1 promoter region (pGL3-AQP1-4K). The luciferase activity of pGL3-AQP1-4K and the regulatory effects of pH on luciferase activity are shown in Fig. 1b. High pH upregulated the luciferase activity of pGL3-AQP1-4K in HEK-293T cells.
Identification of the AQP1 gene upstream promoter region
Prediction of transcription factors that interact with the enhancer region in the AQP1 gene (− 2300 to − 2200 bp)
SPIB is a potential transcription factor capable of influencing pH-regulated AQP1 expression
Our previous study demonstrated that a new bicarbonate-based PD solution enhances the migratory capacity and damage-repair ability of human peritoneal mesothelial cells by upregulating AQP1, thereby playing an important role in protecting the functional integrity of the peritoneum. AQP1 forms ultra-small pores in the peritoneum, is responsible for transporting water across cell membranes [17, 18] and mediates 50% of peritoneal ultrafiltration activities [14, 19]. Therefore, AQP1 is essential for maintaining PD [15, 20]. In recent years, other important biological effects of AQP1 have also been discovered, including its ability to promote cell migration, wound healing, tumour growth and metastasis and CO2 transport across the cell membrane [21–26]. Clearly, a variety of important biological therapeutic effects can be achieved by regulating AQP1. For example, downregulation of AQP1 inhibits tumour blood vessel proliferation and tumour metastasis and reduces cerebral oedema. Increased AQP1 gene expression improves the ultrafiltration function of the peritoneum  enhances the migratory and repair capabilities of peritoneal cells  and should therefore maintain the integrity of the peritoneum, thereby prolonging the time until PD failure. Thus, studying AQP1 gene expression regulation is of great significance.
AQP1 gene expression is regulated by a variety of factors, including glucocorticoids , hydrostatic pressure  and hypoxia . The promoter region in the AQP1 gene contains the glucocorticoid  and hypertonicity response element (GRE and HRE, respectively) [29–32], which upregulate AQP1 expression in response to glucocorticoid treatment and increasing hypertonicity and hyperoncoticity. Hypoxia-inducible factor 1-alpha (HIF-1α) binds to the AQP1 promoter and is involved in hypoxia-induced AQP1 gene expression [33, 34]. We now provide evidence that in addition to these regulatory mechanisms governing AQP1 gene expression, the AQP1 promoter contains a pH-sensitive region that upregulates AQP1 expression in response to increasing pH.
The present study first successfully replicated the findings of our previous study using the HEK-293T cell line as a research tool. AQP1 mRNA levels were gradually elevated in HEK-293T cells as the pH increased; this behaviour closely resembles the regulatory effects of pH on AQP1 gene expression in peritoneal mesothelial cells. This result indicates that AQP1 regulation at the gene transcriptional level is affected by pH. Then, the key transcription factors and their binding sites involved in the pH-mediated regulation of AQP1 gene expression were explored. The region between − 2300 and − 2200 bp was critical for the pH-induced regulation of AQP1 gene expression. By combining the above findings with JASPAR predictions and the experimental data obtained from the siRNA-mediated interference of gene expression and mutagenesis of the binding sites, we identified SPIB as a potential transcription factor that affects pH-mediated regulation of AQP1 gene expression. SPIB binds to the PU-box (5′-GAGGAA-3′) and activate transcription of a reporter plasmid containing PU boxes . SPIB has been reported to be involved in differentiation and maturation of plasmacytoid dendritic cells and to inhibit the differentiation of T, B and natural killer (NK) cells [36, 37]. PD solutions with a physiological pH may increase AQP1 gene expression and enhance peritoneal ultrafiltration by activating SPIB. Additionally, activated SPIB may participate in inhibition of inflammatory cell activation and reduction of inflammatory stimulation in the peritoneum, thereby achieving long-term protection of peritoneal function.
In the present study, we demonstrated that the pH-mediated upregulation of AQP1 gene expression was not observed after interference with SPIB gene expression, which indicates that SPIB is involved in pH-mediated regulation of AQP1 expression. Furthermore, we found that SP1 and THAP1 also affected the luciferase activity induced by pH. However, knockdown of SP1 and THAP1 inhibited the mRNA expression of AQP1, while knockdown of SPIB had no such effect. These results indicated that SPIB may play a major role in the pH-mediated upregulation of AQP1. The regulatory effect of SP1 and THAP1 on the mRNA expression of AQP1 need further investigation. Transcription factors activity are tightly regulated through many ways, such as transcriptional control, post-transcriptional modification, transcriptional co-activators and co-repressors, and interaction with enhancer. Using real-time qPCR and western blot analysis, we showed that different pH levels (pH 7 and pH 8) did not have significant effects on SPIB expression (Additional file 1: Fig S4), which indicates that pH-mediated activation of AQP1 transcription does not occur through the increase of SPIB protein level. Enhancers and their associated factors can regulate expression of genes located far upstream and downstream by looping to the promoters of these genes. The interaction of AQP1 promoter and SPIB protein may engender specific enhancer-gene interaction and are essential for AQP1 activation mediated by pH. However, additional experiments are needed to better define the role of pH-mediated SPIB activation.
In summary, the present study demonstrated that a region upstream of the AQP1 gene (− 2300 to − 2200 bp) contains an enhancer required for pH-mediated regulation of AQP1 gene expression. SPIB is a specific transcription factor that participates in pH-mediated regulation of AQP1 gene expression. The present study facilitates further elucidation of the mechanisms by which pH regulates AQP1 gene expression and the molecular mechanisms by which pH and buffer compounds in PD solutions affect peritoneal membrane integrity and function.
YZ and HX conceptualized the study. YZ performed the experiment and data analyses and wrote the manuscript. FS and CS helped prepared the manuscript. QS, JC and HL helped perform the analysis and provided constructive discussions. JL and JL helped perform the experiment and the data analysis. All authors read and approved the final manuscript.
We thank Prof. Xiliang Zha from the Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, Fudan University, for the helpful discussion.
The authors declare that they have no competing interests.
Availability of data and materials
Materials and datasets used for the preparation of the figures presented in the manuscript are available upon request.
Consent for publication
Ethics approval and consent to participate
Not applicable. The ethics committee of Children’s Hospital of Fudan University ruled that no formal ethics approval was required in this particular case.
This work is supported by grants from the National Natural Science Foundation of China (81300635), the Shanghai Natural Science Fund for Youth Scholars (12ZR1441300), and the Young Teachers Foundation Project supported by the Doctorate in Higher Education Institutions of Ministry of Education (20120071120096).
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