- Research article
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Functional consequences of enhanced expression of STIM1 and Orai1 in Huh-7 hepatocellular carcinoma tumor-initiating cells
BMC Cancervolume 19, Article number: 751 (2019)
The endoplasmic reticulum (ER) Ca2+ sensor, stromal interaction molecule1 (STIM1) activates the plasma membrane (PM) channel Orai1 in order to mediate store-operated Ca2+ entry (SOCE) in response to ER store depletion. Enhanced expression of STIM1 in cancer tissue has been associated with poor patient prognosis. Therefore, this study investigated the functional consequences of enhanced expression of STIM1 and Orai1 in a tumor-initiating subpopulation of Huh-7 hepatocellular carcinoma (HCC) cells that express epithelial cell adhesion molecule (EpCAM) and Prominin 1 (CD133).
We performed qRT-PCR, intracellular Ca2+ monitoring, protein analyses, and real-time cell proliferation assays on EpCAM(+)CD133(+) subpopulation of tumor-initiating Huh-7 HCC cells expressing high levels of STIM1 and/or Orai1. Statistical significance between the means of two groups was evaluated using unpaired Student’s t-test.
Enhanced STIM1 expression significantly increased ER Ca2+ release and proliferation rate of EpCAM(+)CD133(+) cells.
STIM1 overexpression may facilitate cancer cell survival by increasing ER Ca2+-buffering capacity, which makes more Ca2+ available for the cytosolic events, on the other hand, possibly preventing Ca2+-dependent enzymatic activity in mitochondria whose Ca2+ uniporter requires much higher cytosolic Ca2+ levels.
Hepatocellular carcinoma (HCC) appears to be the third leading cause of cancer-related deaths worldwide [1,2,3,4,5,6,7,8,9,10,11]. The primary issue in HCC cases is the high recurrence rates  possibly due to the existence of chemotherapy-resistant tumor-initiating cell (TIC) subpopulations . Tumor-initiating cells constitute 0.01–1% of tumor mass [14, 15]. These cells express certain cell surface antigens used for separating them from other cell types within the heterogeneous tumor cell lines . Epithelial cell adhesion molecule (EpCAM) and Prominin 1 (CD133) are frequently used to identify Huh-7 human HCC TICs [17, 18] as NOD/SCID mice developed tumor after receiving Huh-7 cells expressing these two antigens .
SOCE, a major Ca2+ influx through Ca2+-release activated Ca2+ (CRAC) channels in non-excitable cells [20,21,22,23,24,25], has been shown to be operational both in normal hepatocytes and HCC . SOCE components are the ER-resident Ca2+ sensor stromal interaction molecule 1 (STIM1)  and the PM Ca2+ channel Orai1 [28,29,30]. The roles of STIM1 and Orai1 in carcinogenesis, tumor initiation, proliferation and metastasis have recently attracted significant attention [27, 31]. Indeed, altered expression of STIM1 and Orai1 is a hallmark of many cancer types, suggesting their potential value as prognostic biomarkers in cancer [27, 32,33,34,35].
TICs appear to be responsible for high recurrence rates as well as for chemoresistance . HCC cells are a non-excitable cell type, where SOCE plays a crucial role in Ca2+ homeostasis and signaling . In many cancer types including HCC, enhanced expression of STIM1 and Orai1 have been shown to enhance carcinogenesis including proliferation, migration and invasion processes [26, 38, 39]. Previous studies have reported that STIM1 and Orai1 molecules mix at a specific ratio to encode functional CRAC channel assembly [40, 41]. Based on crystallographic and electrophysiological studies, STIM1 exists as a dimer under resting conditions, and binds to Orai1 in a nonlinear fashion such that all six Orai1 binding sites must be occupied for the activation of SOCE . However, the structural basis of STIM1 interaction with Orai1 within the channel assembly is not known. Therefore, the purpose of this study is to investigate the functional impact of altered stoichiometry of STIM1 and/or Orai1 by employing overexpression plasmid vectors on intracellular Ca2+ dynamics as well as carcinogenic properties of Huh-7 EpCAM(+)CD133(+) cells.
Human HCC cell lines (Huh-7) were provided by Dr. Ozturk (IBG İzmir), originally from Dr. Jack Wands Laboratory (Massachusetts General Hospital, Boston, MA) as a gift, and tested for authenticity via DNA profiling (Applied Biosystem’s Identifier kit, PN 4322288) at DNA Sequencing & Analysis Shared Resource, University of Colorado Cancer Center. The authenticity was reconfirmed by Idexx Bioresearch Company (Germany) just before initiating our studies. In addition to these, the cells have been also checked regularly in our laboratory for mycoplasma contamination by using MycoAlert Mycoplasma Detection kit (Lonza). Parental Huh-7 HCC cells and the sorted cells after Fluorescence Activated Cell Sorting (FACS, FACSAria III, BD) were maintained in complete growth medium (Dulbecco’s modified Eagle medium, DMEM, Sigma) containing 10% heat-inactivated fetal bovine serum (FBS, Biowest), 2 mM L-glutamine (Sigma) and 0.1 mM non-essential amino acids (Sigma).
Selection of EpCAM(+)CD133(+) and EpCAM(−)CD133(−) Huh-7 cells with FACS
Huh-7 HCC cells were trypsinized, washed, and resuspended in FACS buffer (1XPBS, 1 mM EDTA, 25 mM HEPES, 1% FBS) and filtered through 0.2 μm filter. Cells were passed through cell strainers with pore diameters of 100 and 30 μm (Miltenyi) to eliminate cell aggregates. Cells (15 × 106) were centrifuged to obtain pellets, then, resuspended in 105 μl FACS buffer followed by reincubation with 30 μl FcR blocking reagent (Miltenyi), 15 μl EpCAM-FITC (Miltenyi) and 15 μl CD133-PE (Miltenyi) for 10 min on ice. After incubation, cells were washed with FACS buffer and sorted via a fluorescence-activated cell sorter (FACS Aria III, BD Biosciences). Cells with and without EpCAM and/or CD133 were separately collected inside FBS containing tubes. After sorting, purity percentages for EpCAM(+)CD133(+) were determined with FACSCalibur (BD Biosciences) on the fifth day.
Transfection of EpCAM(+)CD133(+) Huh-7 cells with STIM1 and Orai1 overexpression plasmids
Cells were seeded on 6 well-plate (105 cells/well) and transfection was performed after 24 h with X-tremeGENE HP DNA Transfection Reagent (Roche). Following removal of the cell media, serum-reduced media (Opti-MEM) were added and incubated for additional 1 h. 100 μl Opti-MEM, 1.5 μg plasmid DNA (MO70-STIM1-eYFP, pDEST501-Orai1-CFP and pCMV6 empty vector as a control) and 1 μl X-tremeGENE HP DNA Reagent-containing transfection mix was added to each well and incubated for 30 min at room temperature. Transfection mix was added on the cells dropwise and shaked gently. Plasmids were gently provided by Dr. M Trebak (Penn State University).
RNA isolation and cDNA synthesis
Cells were seeded on 6-well plate (15 × 104/well). Total RNA was isolated by using High Pure RNA Isolation (Roche) according to the manufacturer’s instructions. cDNA synthesis from the total RNA samples were performed by using Transcriptor First Strand cDNA Synthesis Kit (Roche) according to the manufacturer’s instructions.
Real-time quantitative RT-PCR (qRT-PCR)
FastStart DNA Master SYBR Green I kit was used in real-time qRT-PCR experiments performed (LightCycler 1.5, Roche Applied Science). Primer sequences are shown in Table 1. All expression levels were normalized to that of internal 18S rRNA ([Target gene]/[18S rRNA] × 100).
Protein isolation and Western blot
Protein isolation was performed on 15 × 104 cells seeded on 6-well plate by cOmplete Lysis-M, EDTA-free (Roche) according to the manufacturer’s instructions. Protein extracts, separated by SDS-PAGE were transferred onto PVDF membranes, then, incubated with antibodies targeted against STIM1 (3 μg/μl, Abcam), Orai1 (1:750, Abcam) and β-actin (1:5000, Sigma) overnight at 4 °C. Membranes were incubated with secondary antibodies (1:5000, anti-rabbit or anti-mouse, LI-COR) for 1 h via shaking at room temperature. Protein bands were visualized in an infrared imager (Odyssey, LI-COR) based on the appropriate channel properties (680RD or 800CW) of secondary antibodies.
Cells seeded on circular coverslips were loaded with 5 μM Fura-2/AM (Molecular Probes) in HEPES-buffered saline. Changes in intracellular Ca2+ levels were monitored via a front-surface spectrofluorometer (PTI QM8/2005) as described earlier .
Real-time monitoring of proliferation by real-time cell analyzer (RTCA)
Real-time label-free impedance-based monitoring of cellular proliferation assay was performed by using xCELLigence MP (Roche Applied Science). Transfected cells were incubated in 6-well plates for 48 h. After the incubation period, 5000 cells/well were seeded in E-plate 96. Cell proliferation was monitored at every 15 min for 72 h. Changes in proliferation rate were expressed as “cell index” (RTCA software 1.2.1, Roche Applied Science).
Data expressed as mean ± standard error of the mean (S.E.M.). “n” denotes the number of samples. Statistical significance between the means of two groups was evaluated using Student’s t-test (unpaired data). Significance was accepted at 0.05 level of probability.
Selection of EpCAM(+)CD133(+) and EpCAM(−)CD133(−) Huh7 cells
EpCAM(+)CD133(+) and EpCAM(−)CD133(−) Huh-7 cells were selected from a parental Huh-7 cell line via a FACS. Figure 1a and b show the percentages of EpCAM(+)CD133(+) and EpCAM(−)CD133(−) cells after sorting (Day 0) and on the 5th day (Day 5) Fig. 1c. On Day 5, as cells reach about 70% confluency in order to be ready for the transfection procedure, the EpCAM(+)CD133(+) cell population decreased from 96.6 to 64.3%.
In addition to microscopic examinations, overexpression (OE) efficiency of STIM1 and Orai1 in all experimental conditions (STIM1-OE, Orai1-OE, STIM1 + Orai1-OE) on EpCAM(+)CD133(+) cells was confirmed via real time qRT-PCR. STIM1 and Orai1 expression levels were not significantly different between EpCAM(+)CD133(+) and EpCAM(−)CD133(−) cells (data not shown). In STIM1-OE and STIM1 + Orai1-OE EpCAM(+)CD133(+) cells (Fig. 2) STIM1 increased both in STIM1-OE (p < 0.05, Fig. 2a) and STIM1 + Orai1-OE cells (**p < 0.01, Fig. 2b) as expected.
Orai1 mRNA level increased in Orai1-OE (**p < 0.01, Student t-test, unpaired data n = 4, Fig. 3a) and STIM1 + Orai1-OE (**p < 0.01, Student t-test, unpaired data, n = 4, Fig. 3b) EpCAM(+)CD133(+) cells (Fig. 3) comparable to the control, which is similar to that of STIM1 mRNA expression levels revealed in previous data.
In STIM1-OE EpCAM(+)CD133(+) Huh-7 cells, STIM1 protein level was significantly higher (3 fold) than that of the control (**p < 0.01, Student t-test, unpaired data, Fig. 4a and b).
Although not statistically significant, the Orai1 protein level was lower in STIM1-OE samples comparable to that of the control (Fig. 5).
STIM1 protein levels decreased in STIM1 + Orai1-OE EpCAM(+)CD133(+) cells (p < 0.01, Fig. 6) possibly due to administration of STIM1 and Orai1 plasmids together.
Intracellular basal Ca2+ levels were significantly higher in EpCAM(+)CD133(+) comparable to those of EpCAM(−)CD133(−) cells. Although Ca2+ elevation due to ER release was significantly higher in EpCAM(+)CD133(+) cells (*p < 0.05, Student t-test, unpaired data, n = 4–6), SOCE was not altered (Fig. 7).
Although there was an apparent increase both in ER Ca2+ release and SOCE, the data did not reach statistical significance in STIM1-OE EpCAM(+)CD133(+) cells (Fig. 8). No significant change was observed in basal, ER Ca2+ release (expected) and SOCE, possibly due to increased coupling efficiency between depleted ER and Orai1. Although ER Ca2+ release and SOCE decreased in Orai1-OE EpCAM(+)CD133(+) cells, the data were not statistically significant (Fig. 9). SOCE increased significantly (p < 0.05, Fig. 10) in STIM1+ Orai1-OE cells without any change in ER Ca2+ release.
Cell proliferation patterns in EpCAM(+)CD133(+) and EpCAM(−)CD133(−), STIM1-OE and STIM1 + Orai1-OE EpCAM(+)CD133(+) cells
Elevations in impedance (cell index) in RTCA show an increased cellular proliferation rate in real-time. In this study, differences in the cell proliferation pattern were monitored in two groups [EpCAM(+)CD133(+) vs. EpCAM(−)CD133(−) cells and STIM1-OE and STIM1 + Orai1-OE EpCAM(+)CD133(+) cells]. The proliferation rate at 48th h was significantly higher in EpCAM(−)CD133(−) cells comparable to that of EpCAM(+)CD133(+) (**p < 0.01, Fig. 11).
We also monitored the effects of STIM1 and STIM1 + Orai1 overexpression on cell proliferation in EpCAM(+)CD133(+) Huh-7 cells. Comparable to the control, STIM1-OE cells at 72nd h showed the highest proliferation rate (p < 0.01, Fig. 12); higher than that of STIM1 + Orai1-OE.
The difference in multidrug resistance gene (MDR1) expression between tumor-initiating cells and tumor cell lines as well as the effects of STIM1 and Orai1 overexpression on MDR1 transcription in a number of experimental settings were investigated as increases in SOCE appeared to be associated with chemoresistance . MDR1 mRNA levels were significantly higher in EpCAM(+)CD133(+) cells that in EpCAM(−)CD133(−) cells (**p < 0.01, Student t-test, unpaired data, n = 4, Fig. 13). Elevation of MDR1 in EpCAM(+)CD133(+) was potentiated by inducing STIM1 or an Orai1 expression and drastically increased (6-fold) by STIM1 + Orai1 overexpression (*p < 0.05, Student t-test, unpaired data, n = 4, data not shown).
In addition to being involved in intracellular Ca2+ homeostasis mechanism of non-excitable cells, SOCE appears to be operational in hepatocellular carcinogenesis . In this study, the role of SOCE components, STIM1 and Orai1, reportedly involved in intracellular Ca2+ regulation was investigated on Huh-7 TICs expressing cell surface antigens EpCAM and CD133 through monitoring intracellular Ca2+ dynamics (ER Ca2+ release and SOCE), proliferation and MDR1 expression responsible partly for drug resistance. High intracellular Ca2+ concentration comprises toxic and proapoptotic conditions for cells. Excessive Ca2+ is buffered by certain proteins (e.g., calsequestrin and calreticulin) inside ER and by mitochondria. ER Ca2+ release and SOCE are significantly higher in EpCAM(+)CD133(+) cells comparable to that of EpCAM(−) CD133(−).
Overexpression of STIM1 and Orai1 is shown in many cancer types like prostate cancer, breast cancer, glioblastoma and hepatocellular carcinoma . More specifically, STIM1 overexpression is commonly seen in HCC [26, 39]. Among the three overexpression groups of EpCAM(+)CD133(+) Huh-7 cell subpopulation in our study, STIM1-OE showed the highest ER Ca2+ release. As STIM1 has Ca2+ binding EF hand domains located on the intracellular part of ER , its overexpression may buffer more Ca2+, leading to more Ca2+ available to be released from ER following SERCA blockade by CPA. STIM1 is the key initiating molecule in SOCE. After ER depletion, as a sensor of ER Ca2+ content, STIM1 accumulated in ER membrane closely located to PM with Orai1. At this ER and PM junctions, STIM1 interacts with Orai1 as a result SOCE is activated . Lower ER release and SOCE in Orai1 OE EpCAM(+)CD133(+) Huh-7 cells comparable to the control cells could be due to changes in coupling stoichiometry between STIM1-Orai1 for SOCE . Higher levels of the PM channel subunit (Orai1) might decrease effective coupling of two molecules (STIM1 and Orai1) yielding SOCE inhibition. Increases of ER release and SOCE in STIM1 + Orai1-OE EpCAM(+)CD133(+) cells, show presence of appropriate coupling stoichiometry between STIM1 and Orai1 for SOCE as both molecules are freely available for random interaction . Similar SOCE elevations were also seen in STIM1 + Orai1-OE and only STIM1-OE DU145 (prostate cancer cell line) and HEK (human embryonic kidney) cells, respectively [40, 48, 49]. Overexpression of Orai1 in DU145 and HEK cells also inhibited SOCE, as observed in EpCAM(+)CD133(+) cells in our study [40, 47, 48].
TICs tended to remain in a quiescence state . These EpCAM(+)CD133(+) cells have slow proliferation rates comparable to that of EpCAM(−)CD133(−) [49, 51] as was also observed in the present study. This may support their survival strategy in a cytotoxic environment [34, 52, 53]. The higher proliferation rate of STIM1-OE cells, comparable to that of STIM1 + Orai1-OE cells, showed that upregulation of these two genes (STIM1 and Orai1) suppresses the cell division/proliferation possibly through attenuated Ca2+ buffer capacity of ER. Again, the significantly higher proliferation rate observed with STIM1-OE cells over that of EpCAM(+)CD133(+) cells overexpressing both STIM1 and Orai1 (present data) confirms the poor prognosis of several cancer types with overexpressed STIM1 [54,55,56].
Cancer cells show resistance to chemotherapeutic treatments. This may result from drug inactivation, changing drug targets, DNA damage repair, and efflux of drug from cells by ABC transporters . Because of the upregulated ABC transporters, cancer cells can pump chemotherapeutics out of the cell . The “slow and steady” feature might also be maintained by higher MDR1 (an ABC transporter family member) expression. Upregulated MDR1 in EpCAM(+)CD133(+) Huh-7 cells in the present study is also in accordance with the increased MDR1 gene expression in lung cancer , ovary cancer , osteosarcoma  and glioblastoma’s  cancer stem cells. The signaling pathways (JAK/STAT, PI3K/AKT, MAPK/ERK), which take place in drug resistance, are regulated by Ca2+/calmodulin dependent protein kinase II (CaMKII), suggesting an interaction between Ca2+ and MDR mechanisms in liver cancer .
Based on the higher proliferation rates observed in STIM1-overexpressing EpCAM(+)CD133(+) Huh7 cells compared to that of STIM1 + Orai1-OE constructs, one may conclude that HCC stem cells might undergo a phenotypical switch process from a quiescent to proliferative stage by increasing ER Ca2+ buffering capacity due to higher levels of Ca2+-binding protein, STIM1. Furthermore, one may also speculate that increased ER Ca2+ buffering prevents Ca2+- dependent processes in mitochondria localized within the ER microenvironment by inhibiting Ca2+ uptake via low affinity/high capacity Ca2+ uniporter of mitochondria.
Availability of data and materials
The datasets used and/or analyzed in the present study are available from the corresponding author.
Bovine Serum Albumin
Clustering Domain 133 (Prominin 1)
Calcium release-activated calcium
Dulbecco’s modified eagle medium
Epithelial cell adhesion molecule
Fluorescence-activated cell sorting
Real-time cell analyzer
Sodium dodecyl sulfate polyacrylamide gel electrophoresis
Store-operated calcium entry
Stromal interaction molecule
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Authors acknowledge Dr. Xiaozhou Hu (Izmir Biomedicine and Genome Center, Dokuz Eylul University, Izmir, Turkey) for an excellent technical support in flow cytometry, Dr. Mehmet Ozturk (Izmir Biomedicine and Genome Center, Dokuz Eylul University, Izmir, Turkey) and Dr. Mohamed Trebak (Dept. of Cellular and Molecular Physiology, Penn State Cancer Institute, Hershey, PA, USA) for providing Huh-7 cells and plasmid vectors, respectively. Authors also thank Dr. Trebak and Dr. Donald Staub (School of Foreign Languages at Izmir University of Economics, Izmir, Turkey) for their critical comments on the manuscript.
This work was supported by the Scientific and Technological Research Council of Turkey (TUBITAK 113S399 to MT).
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