Effect of 7-methylxanthine on human retinal pigment epithelium cells cultured in vitro

Tissue source

This study was approved by the Ethics Committee of Sun Yat-sen University (China) and complied with the Declaration of China for Research Involving Human Tissue and with the Declaration of Helsinki. This study was approved by the Ethics Committee of Sun Yat-sen University (China) and complied with the Declaration of China for Research Involving Human Tissue, the Declaration of Helsinki, as well as the ARVO statement on human subjects. Three myopic adult human eyes (from 27-year-old men) were obtained from the eye bank of Zhongshan Ophthalmic Center (Sun Yat-sen University).

RPE cells isolation and primary culture

The eyes were dissected, and the anterior segment and the retina were removed. The eyecups were rinsed with calcium- and magnesium-free balanced salt solution and incubated with 0.25% trypsin-0.02% EDTA (Gibco, Invitrogen Inc., Carlsbad, CA) for 1 h at 37 °C. The incubation buffer with the released cells was removed, and ten times the volume of Dulbecco’s modified Eagle medium (DMEM/F12; Gibco, Invitrogen Inc.) with 20% fetal bovine serum (FBS; Gibco, Invitrogen Inc.), 1.2 g/l sodium bicarbonate (Fisher Scientific, Hampton, NH), and 10 ml/l L-glutamine-penicillin G-streptomycin (2 mM to 100 U/ml to 0.1 mg/ml; Sigma, St. Louis, MO) were added.

Primary RPE cells were cultured in a humidified incubator and kept at 37 °C in 5% CO₂. The medium was changed every 2 to 3 days. At passage 3, cells were photographed, and immunochemistry was performed to detect cytokeratin 18 expression. Then when a monolayer (80% confluence) was achieved, cells were trypsinized in 0.25% trypsin-0.02% EDTA solution in PBS (1X; 155.2 mM NaCl, 1.1 mM KH₂PO₄, 3.0 mM Na₂HPO₄-7H₂O, pH 7.4).at room temperature for 2 min and subcultured (i.e., passage 4) for the 7-MX treatment and subsequent examination.

Immunochemistry assay

The RPE cells were cultured on cover glasses in six-well plates until 70–80% confluence. The cells were washed with PBS three times and fixed with 4% paraformaldehyde for 10 min. After washing with PBS, the glasses were immersed in 3% H₂O₂ solution to block endogenous peroxidase and then incubated with 5% normal goat serum (containing 0.5% Triton X-100) at room temperature for 20 min. The slices were incubated at 4 °C overnight with the primary antibody (rabbit anti-human keratin 18 monoclonal antibody; Sigma) diluted at 1:100 in PBS. A negative control was run in which the cells were incubated in PBS without primary antibody. Then the slices were washed with PBS and incubated with goat anti-rabbit immunoglobulin G (IgG) secondary antibody (Chemicon, Temecula, CA) diluted at 1:100 in PBS at room temperature for 30 min. Finally, the slices were colored with 3,3′-diaminobenzidine (DAB) using the DAB developing kit (Maixin Biotech Development, Fuzhou, China) and restained with hematoxylin.

MTT proliferation assay

The RPE cells were seeded in a 96-well plate at a density of 1 × 10⁴/200 µl per well. Incubation took place in the previously described medium until a confluence of 80% was achieved. After a 24-h phase of deficiency in 0.1% FBS-containing DMEM/F12, the primary cultured RPE cells were cultured with different concentrations of 7-MX (from 1 nmol/l to 1 mmol/l; 0 nmol/l was used as control; Sigma) in a FBS-free medium. The control cells were cultured in FBS-free medium without 7-MX treatment.

The proliferation rate was measured dynamically at 24, 48, 72, and 96 h of 7-MX treatment. At the end of the incubation interval, 20 μl of MTT solution (5 mg/ml; Sigma) were added to each well and incubated for 4 h at 37 °C. Thereafter, 150 μl of dimethyl sulfoxide (DMSO; Sigma) were added and incubated at room temperature for 15 min. Optical density (OD) was measured using a microplate reader. Each experiment was repeated three times.

Flow cytometry

Apoptosis and cell cycle distribution were determined with flow cytometry. The RPE cells were cultured in DMEM/F12 with or without 10 µmol/l 7-MX for 24, 48, and 72 h and digested with 0.25% trypsin. Cells without 7-MX treatment were used as control. The medium and the cells were centrifuged at 1,000 ×g and 4 °C for 10 min. Precipitates were washed three times with PBS, fixed with 70% alcohol for at least 24 h, and kept at 4 °C until assayed. Then, 1 × 10⁶ cells in 100 µl were washed twice with PBS. Precipitates were dyed with 300 µl of DNA dying solution (PI 100 µg/ml and RNase A 20 U/ml; Sigma) for 30 min. The cells were then read with a FACScalibur system (BD Biosciences, Franklin Lake, NJ). The experiments were performed three times. Cell cycle and apoptosis were analyzed with Multicycle AV analysis software.

RNA isolation and qPCR analysis

The RPE cells with 10 µmol/l 7-MX for 0, 24, 48, and 72 h were harvested and washed with PBS. Total RNA was isolated with TRIzol (Invitrogen Inc.), according to the manufacturer’s instructions. The quality and quantity of total RNA were estimated spectrophotometrically. Subsequently, RNA was reverse-transcribed into cDNA using a RevertAid First Strand cDNA synthesis kit (Fermentas, Burlington, Canada). Quantitative PCR (qPCR) was performed as described in a previous study [21]. Reactions were incubated at 50 °C for 2 min and 95 °C for 10 min, followed by 40 cycles of 15 s at 95 °C and 1 min at 60 °C. The primers and probes for A1R (Rn00567668_m1), A2aR (Rn00583935_m1), A2bR (Rn00567697_m1), and GAPDH (Rn01775763_g1) were obtained from Applied Biosystems (Grand Island, NY). The amplification was performed in an ABI 7500 Fast Real-Time PCR system (Applied Biosystems). The 2^{-ΔΔ Ct} method was used for relative quantification of the gene expression.

Immunofluorescence assay

The RPE cells with 10 µmol/l 7-MX for 24 and 48 h were subcultured on cover glasses in six-well plates until 70–80% confluence; cells without 7-MX treatment were used as control. The cells were washed with PBS three times, fixed with cool acetone for 15 min, air-dried, and kept at −20 °C until use. The slices were washed three times with PBS, covered with 10% normal goat serum diluted in PBS, and incubated for 20 min at 37 °C. The slices were incubated at 4 °C overnight with the primary antibody (anti-ADORA1, anti-ADORA2A, and anti-ADORA2B; Chemicon) diluted at 1:500 in PBS. A negative control was run in which the cells were incubated in PBS without primary antibody. The slices of the antibody-treated and the negative control samples were washed with PBS and exposed to fluorescein isothiocyanate (FITC)–conjugated goat anti-rabbit IgG antibody (Zhongshan Golden Bridge Biotechnology, Beijing, China) diluted at 1:50 in PBS at 37 °C for 30 min. The slices were washed with PBS three times, and propidium iodide (PI) was added for 5 min to dye the nuclei in red. Immunofluorescence images were taken using a laser scanning confocal microscope (LSM 510 META, Carl Zeiss GmbH, Oberkochen, Germany). Four cells with clear boundaries in each image were randomly chosen for analysis. The mean fluorescence intensity of cells was measured using the Axio Vision 4.8 software. The experiments were repeated three times.

Statistical analysis

Data analysis was performed using SPSS 16.0 (SPSS Inc., Chicago, IL). The data were expressed as mean ± standard deviation. The ANOVA (ANOVA) was applied to compare variables among multiple groups. P values of less than 0.05 were considered statistically significant.

In vitro culture and identification of human RPE cells

Primary human RPE cells were flat or angular, and rich in brown pigment granules in the cytoplasm. After two to four passages, the pigment granules were gradually reduced, and the cells were spindle-shaped or irregularly shaped (Appendix 1). The cultured cells had cytokeratin expression in the cytoplasm, indicating that they were RPE cells (Appendix 1).

Effects of 7-MX on RPE cell proliferation

To observe the growth of cells treated with 7-MX, primary human RPE cells were incubated with different concentrations (from 1 nmol/l to 1 mmol/l) of 7-MX. No statistically significantly growth alteration was noted at 24, 72, and 96 h (Figure 1A). A slightly decreased cell proliferation rate was seen with 100 µmol/l 7-MX at 48 h, but without statistically significant differences compared to the other concentrations (all p>0.05; Figure 1A). We considered 10 μM a safe dose that would not suppress the growth of the cells. Based on previous studies [4,9], the dosages used in animal experiments and clinical trials were around 10 μM. Thus, we chose 10 μmol/l for further experiments.

Effects of 7-MX on cell cycle distribution and apoptosis level of RPE cells

Human RPE cells were cultured in vitro with 10 µmol/l 7-MX for 24, 48, and 72 h. Flow cytometry was used to analyze changes in the cell cycle distribution and apoptosis level. The proportion of RPE cells in the G1 stage was slightly increased at 24 h (p=0.035) but decreased at 48 h (p=0.0045) upon 7-MX treatment; and the proportion was restored to normal at 72 h (Table 1). The apoptosis level in RPE cells without 7-MX treatment increased with time (Figure 1B). We suppose that it may be the basal characteristics of in vitro cultured RPE cells even without any treatment, as observed previously [22]. Compared with the non-treated group, no statistically significant change in cell apoptosis was found when RPE cells were cultured with 7-MX for 24, 48, or 72 h (Figure 1B).

Dynamic changes in ADOR mRNA levels with 7-MX treatment

To observe the effects of 7-MX on the mRNA levels of ADORs, RPE cells were cultured with 10 μmol/l 7-MX for 24, 48, and 72 h. The ADOR mRNA levels were analyzed with qPCR (Figure 2). After 24 h treatment with 7-MX, there were no statistically significant changes in the mRNA levels of ADORA1, ADORA2A, or ADORA2B, compared to 0 h. However, the mRNA levels of all three ADORs were statistically significantly decreased at 48 h, compared to 0 h or 24 h (p<0.01 or p<0.001; Figure 2A–C). The mRNA levels of ADORA2A and ADORA2B appeared to rebound at 72 h, compared to 48 h (p<0.05 or p<0.01; Figure 2B,C).

Dynamic changes in ADOR protein levels with 7-MX treatment

To further verify the effects of 7-MX on ADOR expression, RPE cells were cultured with 10 μmol/l 7-MX for 24 and 48 h. The ADOR protein levels were evaluated with immunofluorescence (Figure 3A, Figure 4A, and Figure 5A). The ADORA1 protein level was decreased after 24 h of 7-MX treatment (p<0.01) and was more obviously decreased at 48 h, compared to 0 h (p<0.001; Figure 3B). The ADORA2A protein was statistically significantly inhibited at 24 and 48 h compared to 0 h (p<0.001; Figure 4B). The ADORA2B protein level declined statistically significantly at 48 h compared to 0 h (p<0.05; Figure 5B).