Establishment of an immortalized human endometrial stromal cell line with functional responses to ovarian stimuli
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Studies on the mechanisms of decidualization and endometriosis are often hampered by lack of primary endometrial cells. To facilitate in vitro studies, we established a human endometrial stromal cell line, KC02-44D, immortalized with human telomerase reverse transcriptase. Upon exposure to ovarian stimuli, KC02-44D cells showed similar cytoskeletal marker or gene expression and biochemical phenotype to primary endometrial stromal cells. KC02-44D would be useful for studies of human endometrial function and its associated pathologies.
KeywordsEndometriosis Reverse Transcription Polymerase Chain Reaction Decidualization Capacity Ovarian Steroid Progesterone Receptor Expression
List of abbreviations used
3',5'-cyclic adenosine monophosphate
dextran-coated charcoal-treated fetal bovine serum
Dulbecco's modified Eagle's medium
enzyme-linked immunosorbent assay
endometrial stromal cell
human estrogen receptor-alpha
human telomerase reverse transcriptase
insulin-like growth factor-binding protein-1
a lentivirus encoding hTERT
protein kinase A
reverse transcription polymerase chain reaction
Tris-buffered saline containing 0.1% Tween-20
tumor necrosis factor-alpha
p38 mitogen-activated protein kinase
Decidualization is the process of differentiation of the endometrium, the mucosa lining the uterine lumen. In endometrial decidualization, estrogen receptor (ER) and progesterone receptor (PR) expressions strictly regulate the tissue responsiveness to cognate ligands. Estrogen can autoregulate ER expression, and PR is a classical estrogen target [1, 2, 3]. In humans, decidualization occurs independently of a blastocyst signal during the second half of the menstrual cycle and is controlled as a progesterone- and 3',5'-cyclic adenosine monophosphate (cAMP)-dependent event. Its initiation requires elevated intracellular cAMP levels and sustained activation of the protein kinase A (PKA) pathway; progestin and cAMP synergistically induce decidualization in primary cultured human endometrial stromal cells (ESCs) . Decidual cells exhibit morphological changes and abundant secretion of decidualization enhancers such as prolactin and insulin-like growth factor-binding protein-1 (IGFBP-1) .
Endometriosis is the growth of endometrial epithelial and stromal cells at ectopic sites outside the uterine cavity. Interleukin (IL)-1β, a proinflammatory cytokine, is considered to play an important role in the pathogenesis of endometriosis [5, 6]. However, the relationship between IL-1β and abnormal growth of endometrial cells is not clearly understood.
For investigations on the mechanisms of decidualization and endometriosis, cultured human ESCs are desirable tools; however, the applicability of these cells is largely restricted by the long cell-culture time and difficulty in maintaining the primary ESC phenotype. Several attempts have been made to immortalize human ESCs by oncogenic transformation  or prolongation of cell division by introducing human telomerase reverse transcriptase (hTERT) [8, 9, 10, 11]. However, the synergistic effect of progestin and cAMP on the decidualization capacity and the induction of the PR by estradiol (E2) have not been fully reproduced in these cell lines. In this study, we established an hTERT-immortalized ESC line, KC02-44D, to facilitate in vitro studies. KC02-44D cells responded in a similar manner to primary human ESCs, showing the synergistic induction of decidualization by progestin and cAMP, and PR upregulation by E2.
Human tissue samples
Endometrial tissue was obtained from the uterus of a 45-year-old woman who had undergone total hysterectomy because of leiomyoma, after her written informed consent and Keio University Hospital approval. Primary human ESCs were purified as described previously . In brief, the tissue specimens were washed in Dulbecco's modified Eagle's medium (DMEM; Sigma-Aldrich, St. Louis, MO) and minced with scissors into pieces less than 1 mm3 in size. The tissues were then gently agitated in tubes for 2 h at 37°C in DMEM with 0.2% (wt/vol) collagenase (Wako Pure Chemical Industries, Osaka, Japan), 0.05% DNase I (Life Technologies, Inc., Gaithersburg, MD), 10% fetal bovine serum (FBS), and 1% antibiotic-antimycotic mixture (Life Technologies, Grand Island, NY). After enzymatic digestion, cell clumps were dispersed by pipetting. Most of the digested human ESCs, presenting as single cells or small aggregates, were filtered sequentially through a 70 μm cell-strainer nylon filter (Falcon 2350; BD Biosciences, Franklin Lakes, NJ) to remove gland cells, layered onto Ficoll-Paque (GE Healthcare Life Sciences, Uppsala, Sweden), and centrifuged at 500 × g for 15 min at 4°C to remove erythrocytes. The isolated human ESCs were collected from the Ficoll interface and resuspended in DMEM with 10% FBS and 1% antibiotic-antimycotic mixture.
Recombinant lentivirus preparations
Recombinant lentiviruses were prepared using the ViraPower Lentiviral Expression System (Life Technologies), according to the manufacturer's instructions. Full-length cDNA of human telomerase reverse transcriptase isoform 1 (hTERT; GenBank accession number NM_003219) was amplified by PCR from the total RNA of a colon cancer cell line. The first-strand DNA was synthesized using hTERT 3'-noncoding primer 5'-TGACAGGGCTGCTGGTGTCTG and ReverTra Ace reverse transcriptase system (Toyobo, Tokyo, Japan). The cDNA of the N-terminus half of hTERT (1-2304) was amplified using forward primer 5'-CACCATGCCGCGCGCTCCCCGCTGCCGA and reverse primer 5'-GCCTTCTGGACCACGGCATACCGA, and that of the C-terminus half (1977-3399) was amplified using forward primer 5'-CACCGGCACTGTTCAGCGTGCTCAACTACGAG and reverse primer 5'-TCAGTCCAGGATGGTCTTGAAGTC. Each cDNA was ligated to the pLenti6/V5-D TOPO vector. Kozak sequences were introduced according to the instruction manual. The fragment between SpeI (in the vector) and EcoRV sites from the N-terminus half was then recloned in the same sites of the C-terminus half to obtain the full-length hTERT plasmid (pLenti6-hTERT). The DNA sequence of pLenti6-hTERT was completely confirmed by DNA sequence analysis. pLenti6-hTERT was then transfected to near-confluent 293FT cells (Life Technologies) with helper plasmids (pLP1, pLP2, and pLP/VSVG) to produce a lentivirus encoding hTERT (LtV-hTERT). After 2 days of incubation at 37°C, the conditioned mediums of the lentivirus-producing 293FT cells were harvested and centrifuged at 3000 rpm for 15 min at 4°C. The supernatants were separated into aliquots and stored at -80°C until use.
Immortalization of human ESCs
For immortalization, human ESCs were infected with LtV-hTERT in the presence of polybrene (6 mg/ml, Sigma). The cells were grown in phenol red-free DMEM supplemented with 10% dextran-coated charcoal-treated FBS (DCC-FBS; Life Technologies) in the presence of 10 nM 17-b-estradiol (E2; E8875, Sigma) for 7-8 days until uninfected cells died in the presence of 2 mg/ml blasticidine (Life Technologies). Then, the cells were trypsinized and limiting-diluted in 96-well plates. Immortalized clones were obtained in the presence of E2 under selection with blasticidine. The obtained clones were maintained in DMEM supplemented with 10% FBS, 100 U/ml penicillin, 100 mg/ml streptomycin, and 2 mg/ml blasticidine at 37°C under 5% CO2 in a humidified incubator. The clones were tested for marker expression and response to ovarian steroids and cAMP, as described below. Finally, KC02-44D was selected as the most responsive clone to the ovarian stimuli. We did not obtain any clones responsive to these stimuli when primary human ESCs were cultured in the absence of E2.
In vitro decidualization and cytokine assay
KC02-44D cells were precultured in phenol red-free DMEM supplemented with 10% DCC-FBS, 100 U/ml penicillin, and 100 mg/ml streptomycin at 37°C over 4 days. They were then stimulated with or without 10 nM E2, 1 μM 6α-methyl-17α-hydroxy-progesterone acetate (MPA; M-1629, Sigma), and/or 0.125 mM dibutyryl cAMP (D0627, Sigma) in combination with the indicated concentrations of cytokines for different time periods according to the experimental procedures. Cell images were acquired using a phase-contrast microscope (Nikon). In the IL-1β experiment, KC02-44D cells were treated with 1.0 ng/ml IL-1β (201-LB-005, R&D Systems, Minneapolis, MN) for 3-7 days, as described in the figure legends.
KC02-44D cells were cultured in 96-well tissue culture plates and characterized by immunofluorescence staining. The cells were fixed with 4% paraformaldehyde (PFA; Wako Pure Chemical Industries) solution for 30 min at room temperature. After washing and permeabilization with phosphate-buffered saline (PBS) containing 0.1% Triton X-100, the cells were blocked with PBS-5% FBS at 4°C. The fixed cells were incubated in PBS-10% FBS containing Cy3-labeled mouse anti-vimentin (C9080, 1:200; Sigma), mouse anti-CD10 (clone SS2/36, 1:25; Dako, Glostrup, Denmark), mouse anti-CD13 (clone WM-47, 1:50; Dako), or mouse anti-cytokeratin (clone MNF116, 1:50; Dako) antibody. After washing in PBS, the cells were incubated with Alexa Fluor 488-labeled anti-mouse secondary antibody (1:500; Molecular Probes, Eugene, OR), washed again, and examined for each marker expression under a fluorescence microscope (BZ-8000; Keyence, Osaka, Japan).
Western blot analysis
Total proteins from KC02-44D cells were extracted with Cell Lysis Buffer (Cell Signaling Technology, Beverly, MA) containing 1 mM phenylmethanesulfonyl fluoride (Sigma) on ice. The lysate was scraped and sonicated for 5 s by using an ultrasonic disruptor at output 1 (Tomy Digital Biology, Tokyo, Japan). The sonicate was centrifuged at 15,000 rpm for 10 min at 4°C, and the protein contents of the supernatant were measured using the Bradford protein assay (Bio-Rad, Hercules, CA). After the addition of lithium dodecyl sulfate sample buffer (Life Technologies, Grand Island, NY) containing 2-mercaptoethanol (Sigma), the samples were reduced at 70°C for 10 min. Equal amounts of total proteins were then electrophoresed on 4-12% NuPAGE Bis-Tris gels (Life Technologies, Grand Island, NY) and transferred onto polyvinylidene difluoride membranes (Immobilon-P; Millipore, Bedford, MA), followed by blocking with 5% nonfat dry milk in Tris-buffered saline containing 0.1% Tween-20 (TBS-T). The membranes were then immunoblotted with the primary antibody against the PR (clone PgR636, 1:800, mouse monoclonal; Dako), IGFBP-1 (06-106, 1:1000, rabbit polyclonal; Upstate, Millipore), or β-actin (1:3000, goat polyclonal; Santa Cruz Biotechnology, Santa Cruz, CA) in TBS-T for 1 h at room temperature. After washing thrice with TBS-T, the membranes were further incubated with horseradish peroxidase-conjugated anti-mouse, anti-rabbit (1:10,000; GE Healthcare, Buckinghamshire, UK) or anti-goat (1:5000; Jackson ImmunoResearch Laboratories, West Grove, PA) secondary antibody in TBS-T for 1 h at room temperature. After washing thrice with TBS-T again, proteins were detected with ECL Plus reagent (GE Healthcare) and visualized with LumiImager (Roche Diagnostics, Penzberg, Germany).
Enzyme-linked immunosorbent assay (ELISA)
KC02-44D cells were plated at a density of 2 × 105 cells per well in 6-well plates. Two days later, the medium was changed and the cells were stimulated with E2, MPA, and dibutyryl cAMP alone or in combination at the indicated concentrations. The supernatants were collected 6 or 7 days later, and the amounts of IGFBP-1, PGE2, and IL-8 proteins were measured using ELISA kits for IGFBP-1 (DY871, R&D Systems), prostaglandin E2 (PGE2; KGE004, R&D Systems), and IL-8 (GE Healthcare), respectively. Each treatment was performed in triplicate wells.
Reverse transcription polymerase chain reaction (RT-PCR)
Total RNA was extracted from cultured KC02-44D cells by using an RNeasy mini kit (Qiagen, Valencia, CA). RT-PCR was carried out with 200 ng total cellular RNA by using a One-Step RT-PCR kit (Qiagen). The primers used for amplification were as follows: human estrogen receptor-alpha (ERα), forward primer 5'-CAGGGGTGAAGTGGGGTCTGCTG-3' and reverse primer 5'-ATGCGGAACCGAGATGATGTAGC-3'; cyclooxygenase-2 (COX-2), forward primer 5'-TGTCTTGACATCCAGATCAC-3' and reverse primer 5'-ACATCATGTTTGAGCCCTGG-3'; β-actin, forward primer 5'-CCCAGGCACCAGGGCGTGATC-3' and reverse primer 5'-TCAAACATGATCTGGGTCAT-3'. Preliminary experiments determined the optimum PCR cycle number within the linear range of amplification for each gene being measured. After PCR amplification, the samples (15 μl aliquots) were electrophoresed in 2% agarose gels, followed by photographic recording of ethidium bromide-stained gels with FAS-III MINI (Toyobo). All data from the RT-PCR analysis represent the results of three independent experiments.
Cell proliferation was determined using a Click-iT EdU Alexa Fluor Imaging kit (Life Technologies, Grand Island, NY), a modified 5-bromo-2'-deoxyuridine (BrdU) system to detect DNA replication. In brief, KC02-44D cells (1.0-1.5 × 103) were seeded onto 96-well culture plates with phenol red-free DMEM containing 10% DCC-FBS and stimulated with cytokines 48 h later. EdU (5-ethynyl-2'-deoxyuridine) was added to a final concentration of 10 μM in the cell-culture medium and the cells were incubated for 24 h at 37°C. After fixation with 4% PFA and permeabilization with 0.1% Triton X-100 in PBS, the cells were treated with the reaction cocktail containing Alexa Fluor 488 azide. The EdU intensity was measured using an ArrayScan VTi HCS reader (Thermo Scientific Cellomics, Pittsburg, PA). The colocalization bioapplication protocol was used to acquire images with the appropriate filter sets in two separate fluorescence channels: channel 1, Hoechst 33342 (nuclear reference and object identification); channel 2, EdU labeled with Alexa Fluor 488 azide (identification of DNA-replicating S-phase cells in the cell cycle). The cells were imaged with a 20 × objective and 0.63 numerical aperture with exposure times of 0.2 s (Hoechst 33342) and 0.1 s (Alexa Fluor 488 azide). The images were collected as nine fields per well, and the values were expressed as the mean average fluorescence intensity.
All quantitative experiments were conducted at least three times each in triplicate wells. The results were then analyzed using ANOVA and Tukey's test. The data shown in figures was the Mean ± SEM for triplicate wells from one representative experiment.
Characterization of KC02-44D cells
Responses to ovarian steroids and cAMP
KC02-44D cells were also tested for their response to ovarian steroids and dibutyryl cAMP to induce IGFBP-1, a decidualization marker . MPA or dibutyryl cAMP significantly but very weakly induced IGFBP-1 expression in the presence of E2. However, the protein expression was greatly induced by the combination of MPA, dibutyryl cAMP, and E2 (Figure 2b), consistent with the findings of a previous study on primary human ESCs . Prolactin, another decidualization marker, showed similar responses to IGFBP-1 (See Additional file 1 Figure S1). KC02-44D cells maintain their response to estradiol, progestin, and cAMP even at high passage numbers (See Additional file 2 Figure S2).
We then assessed PR expression under stimulation by ovarian steroids. Exposure of KC02-44D cells to E2 strongly upregulated the expression of both isoforms (A and B) of PR, a target gene of ERα in the endometrium [14, 15, 16, 17, 18]. The E2-induced PR expression was significantly downregulated after stimulation with MPA (Figure 2c), consistent with reports on the endometrial decidualization phase [7, 13, 19]. Therefore, KC02-44D cells were considered to possess ESC characteristics, displaying similar biochemical properties as well as cytoskeletal marker and gene expression patterns to primary ESCs, without any structural abnormalities.
Responses of KC02-44D cells to IL-1β
Regulation of inflammatory responses by IL-1β
Downregulation of decidualization capacity by IL-1β
Counteraction of ovarian steroid- and cAMP-induced growth arrest by IL-1β
We established the KC02-44D cell line and found similar characteristics to primary human ESCs, showing the synergistic induction of decidualization by progestin and cAMP. Moreover, our cell line showed upregulation of PR expression upon E2 stimulation, which is critical for the progestin-dependent decidualization capacity of ESCs. According to reports of immortalized cell lines, a simian virus 40 large T antigen (SV40T)-immortalized ESC line did not respond to E2 stimulation for PR expression and prostaglandin production, possibly by nonfunctional ERα , and another temperature-sensitive SV40T-immortalized ESC line showed an adequate decidualization phenotype only with cAMP stimulation, even in the absence of progestin . A recent hTERT-immortalized cell line showed a robust response to progestin stimulation, but the synergistic effect of cAMP in this cell line was not examined . Another hTERT-immortalized line showed progestin and cAMP synergy, but in contrast to our clone, PR induction by E2 was not noted in this cell line . The reasons for these discrepancies are not clear, but the differences in human ESC sources or E2-supplemented culture conditions for clone selection might affect the ability of each cell line.
Human ESCs respond to IL-1β through induction of COX-2 expression and PGE2 production. In primary human ESCs, COX-2 mRNA is induced by IL-1β in a p38 mitogen-activated protein kinase (p38MAPK)-dependent manner and this induction is diminished by progesterone or 8-bromo-cAMP through p38MAPK inhibition , which is consistent with the results regarding the inflammatory responses of KC02-44D cells. Further, we observed induction of IL-8 production upon IL-1β stimulation. However, progestin and/or cAMP seemed to have no inhibitory effect on IL-8 expression. A previous study using endometriotic tissues showed a similar observation, indicating the menstrual cycle phase-independent expression of IL-8 and progestin resistance of IL-1β-induced IL-8 production . However, the mechanism of progestin resistance of IL-8 induction is currently unclear; a PR-dependent mechanism might be responsible. At least distinct responses were observed for COX-2 and IL-8 induction by IL-1β in our cell line.
In the menstrual cycle, estrogen induces PR expression in the proliferative phase, and a high level of PR expression is observed in the late proliferative phase; this expression is downregulated according to the elevation in the serum progesterone level, followed by the initiation of decidualization in the secretory phase [29, 30]. We have shown the regulation of PR expression in this study. E2 strongly upregulated the expression of the PR, and the E2-induced PR expression was significantly downregulated after the stimulation with MPA (Figure 2c). Compared with paired ectopic endometrial specimens, a drastic loss of PR-B expression has been observed in endometriotic tissues, resulting in progesterone resistance in endometriosis . IL-1β-induced inhibition of the decidualization capacity [24, 25, 26], activation of cell proliferation, and downregulation of PR-B expression have been observed in primary ESCs . We confirmed the effects of IL-1β on these responses in KC02-44D cells.
We established an immortalized human ESC line, KC02-44D, by introducing the hTERT gene into primary ESCs. This clone showed characteristics such as decidualization capacity and responses to IL-1β similar to primary human ESCs. The KC02-44D cell line would be useful to investigate the mechanisms of normal and pathological human reproductive processes.
We thank Dr. H. Masuda for collecting the endometrial sample. We also thank Dr K. Taniguchi for the helpful discussion and Ms. N. Aoyama for her expert technical assistance. Editorial and publication support was provided by Editage.
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