MCP-1–Activated Monocytes Induce Apoptosis in Human Retinal Pigment Epithelium

This study provides the first evidence that monocyte chemoattractant protein-1 (MCP-1)–activated monocytes induce intracellular Ca²⁺ signaling and subsequent reactive oxygen species (ROS) accumulation that promotes RPE apoptosis and that cluster of differentiation 14 (CD14) and cyclic adenosine diphosphate ribose (cADPR) may contribute to these changes. Understanding the complex interactions among CD14, cADPR, Ca²⁺, and ROS may provide new insights and treatments of retinal diseases, including age-related macular degeneration (AMD).

Abstract

Purpose.

The inflammatory response in age-related macular degeneration (AMD) is characterized by mononuclear leukocyte infiltration of the outer blood–retina barrier formed by the retinal pigment epithelium (RPE). A key mechanistic element in AMD progression is RPE dysfunction and apoptotic cell loss. The purpose of this study was to evaluate whether monocyte chemoattractant protein (MCP)-1–activated monocytes induce human RPE apoptosis and whether Ca²⁺ and reactive oxygen species (ROS) are involved in this process.

Methods.

A cell-based fluorometric assay was used to measure intracellular Ca²⁺ concentrations ([Ca²⁺]_i) in RPE cells loaded with fluorescent Ca²⁺ indicator. Intracellular RPE ROS levels were measured by using the 5- and 6-chloromethyl-2′,7′-dichlorodihydrofluorescence diacetate acetyl ester (CM-H₂DCFDA) assay. RPE apoptosis was evaluated by activated caspase-3, Hoechst staining, and apoptosis ELISA.

Results.

MCP-1–activated human monocytes increased [Ca²⁺]_i, ROS levels, and apoptosis in RPE cells, all of which were inhibited by 8-bromo-cyclic adenosine diphosphoribosyl ribose (8-Br-cADPR), an antagonist of cADPR. Although the ROS scavengers pyrrolidinedithiocarbamate (PDTC) and N-acetylcysteine (NAC) significantly inhibited ROS production and apoptosis induced by activated monocytes, they did not affect induced Ca²⁺ levels. The induced Ca²⁺ levels and apoptosis in RPE cells were inhibited by an antibody against cluster of differentiation antigen 14 (CD14), an adhesion molecule expressed by these cells.

Conclusions.

These results indicate that CD14, Ca²⁺, and ROS are involved in activated monocyte-induced RPE apoptosis and that cADPR contributes to these changes. Understanding the complex interactions among CD14, cADPR, Ca²⁺, and ROS may provide new insights and treatments of retinal diseases, including AMD.

The retinal pigment epithelium (RPE), the key supportive retinal epithelium, is interposed between the outer retina and its choroidal blood supply as part of the blood–retina barrier. The RPE is believed to be a key participant in the development of age-related macular degeneration (AMD).^1–5 RPE atrophy characterizes atrophic or dry AMD that may evolve to exudative or wet AMD. Mononuclear phagocyte infiltration of the outer blood–retina barrier has been linked to retinal diseases that are leading causes of blindness in the United States. These diseases include AMD, uveitis, endophthalmitis, proliferative vitreoretinopathy (PVR), and proliferative diabetic retinopathy (PDR).^4,6–11 Previous studies have described RPE-to-mononuclear phagocyte contact and RPE apoptosis within AMD lesions^4,12–16 and suggest an association between reactive oxygen species (ROS) and AMD.^17–19 However, the mechanisms that underlie the development of AMD are poorly understood. As Ca²⁺ and ROS have been implicated in apoptosis in other systems,^20–24 monocyte chemoattractant protein-1 (MCP-1)—the most potent monocyte chemoattractant and stimulator—is produced by RPE as well as retinal and choroidal microvascular endothelial cells, and activated mononuclear phagocytes induce RPE apoptosis,^25,26 we hypothesized that MCP-1–activated monocytes induce RPE apoptosis and that Ca²⁺ and ROS are involved in apoptosis. In the present study, we provide evidence that MCP-1–activated monocytes induce intracellular Ca²⁺ signaling and subsequent ROS accumulation that promotes RPE apoptosis. We also show that this pathway may be mediated by activation of cyclic adenosine diphosphate ribose (cADPR), which is known to induce intracellular Ca²⁺ signaling, ROS accumulation, and apoptosis.^27–33

Methods

Materials

Flasks (Falcon and Primaria) were purchased from Becton-Dickinson Inc. (Lincoln Park, NJ) and 35-mm glass-bottom culture dishes were purchased from MatTek Corporation (Ashland, MA). Separation media (Ficoll-Paque Plus and Fico/Lite-Monocytes) were purchased from Amersham Biotechnologies (Arlington Heights, IL) and Atlanta Biologics (Atlanta, GA), respectively. MCP-1 was purchased from R&D Systems (Minneapolis, MN). Dulbecco's modified Eagle's medium (DMEM)/F12, phenol red-free DMEM/F12, papain, Hoechst 33342, 8-bromo-cyclic adenosine diphosphoribosyl ribose (8-Br-cADPR), 1,2-bis(2-aminophenoxy) ethane-N,N,N′,N′-tetraacetic acid tetrakis(acetoxymethyl ester) (BAPTA-AM), pyrrolidinedithiocarbamate (PDTC), N-acetylcysteine (NAC), and poly-d-lysine–coated 96-well plates were purchased from Sigma-Aldrich (St. Louis, MO). PBS, Hanks' balanced salt solutions (HBSS), Trizol reagent, and Taq DNA polymerase were obtained from Invitrogen (Carlsbad, CA). An assay kit (NucView 488 caspase-3 assay kit) was purchased from Biotium, Inc., Hayward, CA. A fluorescent Ca²⁺ indicator dye (Fura red-AM; acetoxymethyl ester) and 5- and 6-chloromethyl-2′,7′-dichlorodihydrofluorescence diacetate, acetyl ester (CM-H₂DCFDA) were purchased from Molecular Probes (Eugene, OR). A DNA removal kit (DNAfree) and a first-strand cDNA synthesis kit (RETROscript) were purchased from Ambion (Austin, TX). Oligonucleotides were synthesized by Integrated DNA Technologies, Inc. (Coralville, IA).

Human RPE Cell Culture

Human eyes from 17 donors 50–86 years of age were obtained from enucleation at the University of Michigan. Human RPE cells were isolated from donor eyes within 4 hours after enucleation by enzymatic digestion as previously described.^34,35 The protocol adhered to the provisions of the Declaration of Helsinki for the use of human tissue in research. In all experiments, simultaneous, parallel assays were performed on cultured human RPE cells between passages 2 and 6. At least three RPE cell lines from different donors were used for each set of experiments. For imaging experiments, RPE cells were seeded on 22 × 22 mm coverslips in 35-mm culture dishes or on 35-mm glass-bottom culture dishes and grown in phenol red-free complete medium for at least 4 days.

Monocytes and Treatment

Human peripheral monocytes were isolated as previously described.³⁶ Human monocytic U937 cells were purchased from American Type Culture Collection (Rockville, MD) and cultured at 37°C with 5% CO₂ in RPMI-1640 medium supplemented with 10% heat-inactivated FBS, l-glutamine (2 mM), streptomycin (100 μg mL⁻¹), and penicillin G (100 U mL⁻¹). Freshly isolated human peripheral monocytes or cultured human monocytic U937 cells were preincubated with RPMI culture medium containing MCP-1 (40 ng/mL) for 24 hours before co-culturing with RPE monolayers. Functional blocking antibody against cluster of differentiation antigen 14 (CD14), which was characterized by our previous studies,^25,37,38 was included in selected assays to antagonize the effects of MCP-1–activated monocytes.

Cell-Based Fluorometric Assay

Intracellular Ca²⁺ levels were quantitatively determined by a cell-based fluorometric assay using a fluorescent Ca²⁺ indicator (Fura red-AM). RPE cells grown on 96-well culture plates were incubated with the Ca²⁺ indicator (Fura red-AM; 10 μM) for 1.5 hours at 37°C in the dark, after which RPE cells were washed, and control medium, MCP-1, monocytes, or MCP-1–activated monocytes were added to RPE cells. The dye was excited at 420 nm and 480 nm, and the fluorescence emission was measured at 660 nm using a fluorometer (FlexStation Scanning Fluorometer; Molecular Devices, Sunnyvale, CA). The fluorescence ratio (F420/F480) was used as a direct index of intracellular Ca²⁺ concentrations ([Ca ²⁺]_i).

Measurement of Intracellular ROS Production

Intracellular ROS production by human RPE cells in response to monocytes was measured based on deacetylation and oxidation of nonfluorescent reduced CM-H₂DCFDA into fluorescent CM-DCF as described previously.^26,35

Detection of Activated Caspase-3

Activated caspase-3 was measured by a commercially available caspase-3 substrate assay kit (NucView 488; Biotium, Inc.) as previously described.²⁶ In brief, after treatment, RPE-monocytes co-cultures were incubated with 5 μM caspase-3 substrate (NucView 488) in the dark for 30 minutes and washed once with HBSS/HEPES. The coverslips were mounted onto slides and the cell staining was observed under a fluorescence microscope using a FITC filter. The numbers of stained RPE (green) were scored as activated caspase-3–positive cells.

Hoechst 33342 Staining of Nuclei

After challenge, RPE cells were washed with HBSS/HEPES and then stained with the membrane-permeable and nuclear-specific fluorescent dye Hoechst 33342 (5 μg/mL in HBSS/HEPES) for 10 minutes in the dark at room temperature as described previously.²⁶ After two HBSS/HEPES washes, the coverslips were mounted on microscope slides with HBSS/HEPES and immediately viewed in a microscope using a UV filter. The numbers of stained RPE that exhibited apoptotic nuclear condensation and fragmentation were scored as apoptotic.

Cell Death Detection ELISA

RPE apoptosis was also evaluated by DNA fragmentation as measured using a kit (Cell Death Detection ELISA^PLUS kit; Roche Applied Science, Indianapolis, IN) following procedures outlined by the manufacturer.

Total RNA Isolation

Total RNA was isolated from cultured human RPE cells using reagent (Trizol; Invitrogen) following the manufacturer's instructions. The concentration of total RNA was measured by ultraviolet spectrophotometry.

RT-PCR Analysis

Total RNA was treated with DNase I (DNAfree) and reverse transcribed with random decamers using reverse transcriptase (RETROscript) as previously described.³⁹ PCR was performed with cluster of differentiation 38 (CD38)-specific primers, with the forward primer sequence: 5′-TTG GGA ACT CAG ACC GTA CCT TG-3′ and the reverse primer sequence: 5′-CCA CAC CAT GTG AGG TCA TC-3′. The housekeeping gene hypoxanthine guanine phosphoribosyl transferase 1 (HPRT1) served as a control. The forward primer for HPRT1 was 5′ACCGTGTGTTAGAAAAGTAAGAAG-3′ and the reverse primer was: 5′-AGGGAACTGCTGACAAAGATTC-3′.⁴⁰ The PCR products were generated by adding Taq DNA polymerase and cycled 40 times for CD38 or HPRT1 (1 minute at 94°C, 0.5 minute at 64°C, 0.5 minute at 72°C), followed by a 7-minute extension at 72°C. The RT-PCR products were separated by 1.5% agarose gel electrophoresis.

Statistical Analysis

Data are expressed as mean ± SE (SEM) and evaluated by unpaired Student's t-test or ANOVA followed by Newman-Keul's post test. P < 0.05 is considered statistically significant.

Results

MCP-1–Activated Monocytes Increase Ca²⁺ Levels in RPE Cells

To examine the effects of MCP-1–activated monocytes on [Ca²⁺]_i in RPE cells, confluent monolayers of RPE cells loaded with fluorescent Ca²⁺ indicator dye (Fura red-AM) were exposed to MCP-1–activated human monocytic U937 cells, and fluorescence ratio (F420/F480) of emissions was measured after excitation at 420 nm and 480 nm, as a direct index of [Ca²⁺]_i of RPE cells. As shown at the right-hand side of Figure 1A, the MCP-1–activated U937 cells (40 ng/mL for 24 hours) mediated an increase in F420/F480 ratio compared to control (RPE alone) or RPE stimulated with unactivated U937 cells (RPE/U937) (n = 9; P < 0.05). To determine whether this increase in F420/F480 ratios was Ca²⁺ specific, RPE cells were pretreated with an intracellular Ca²⁺ chelator, BAPTA-AM, then exposed to MCP-1–activated U937 cells in the presence or absence of BAPTA-AM. As shown in Figure 1B, the heightened F420/F480 ratios were blocked by BAPTA-AM treatment. To determine whether this response was also observed using human monocytes, human peripheral blood monocytes were freshly isolated and activated with MCP-1 (40 ng/mL for 24 hours). Figure 1C shows that MCP-1–activated freshly isolated human monocytes also induced an increase in F420/F480 ratios in RPE cells. Unstimulated monocytes had no significant effect on the F420/F480 ratio in RPE cells (Fig. 1C).

Figure 1.

Activated monocytes stimulate Ca²⁺ signals in RPE cells. (A) RPE cells were preloaded with 10 μM fluorescent Ca²⁺ indicator dye (Fura red-AM; Molecular Probes), and fluorescence intensities were measured from RPE cells exposed to control medium (RPE alone), U937 cells (RPE/U937), or MCP-1–activated U937 cells (RPE/U937/MCP-1). (B) Fluorescent Ca²⁺ indicator dye–preloaded RPE cells were preincubated with or without 10 μM BAPTA-AM for 30 minutes, and then exposed to control medium (RPE alone) or MCP-1–activated U937 cells in the presence (RPE/U937/MCP-1+BAPTA-AM) or absence (RPE/U937/MCP-1) of BAPTA-AM. Fluorescence intensities were measured. (C) Fluorescent Ca²⁺ indicator dye–preloaded RPE cells were exposed to control medium (RPE alone), monocytes freshly isolated from human peripheral blood (RPE/Mo), or MCP-1–activated monocytes (RPE/Mo/MCP-1). Data represent the mean ± SEM (n = 3–20). *P < 0.05, **P < 0.01, ***P < 0.001, compared to control or RPE/Mo; ^###P < 0.001, compared to RPE/U937/MCP-1.

Activated Monocytes Induce ROS Accumulation in RPE Cells

Previous studies have shown that Ca²⁺ signaling is required for ROS production.^41–43 As ROS are involved in apoptosis^21–24 and retinal degeneration,^17–19 ROS production due to RPE exposure to activated monocytes was studied using the ROS-sensitive fluorescent dye CM-H₂DCFDA. RPE cells were loaded with nonfluorescent CM-H₂DCFDA that becomes fluorescent in the presence of ROS. As shown in Figure 2A, MCP-1–activated U937 cells promoted intracellular ROS accumulation in RPE cells. This result was confirmed using MCP-1–activated freshly isolated human monocytes in a second assay in which intracellular ROS levels were determined by monitoring DCF fluorescence with a fluorometer (FlexStation Scanning Fluorometer; Molecular Devices) (Fig. 2B). ROS-induced fluorescence levels in RPE cells exposed to monocytes (P < 0.05) or MCP-1–activated monocytes (P < 0.01) were significantly higher than those of control RPE cells (Fig. 2B).

Figure 2.

Activated monocytes induce ROS production in RPE cells. (A) RPE cells were preloaded with 5 μM CM-H₂DCFDA, and then exposed to control medium (RPE alone), or MCP-1–activated U937 cells (RPE/U937/MCP-1) for 1 hour. Differential interference contrast (DIC) and fluorescence images of intracellular ROS deposition were displayed. Scale bar, 20 μm. (B) RPE cells were preloaded with 5 μM CM-H₂DCFDA, and then exposed to control medium (RPE alone), monocytes (RPE/Mo), or MCP-1–activated monocytes (RPE/Mo/MCP-1) for 1 hour. Intracellular ROS production was measured with a fluorometer (FlexStation Scanning Fluorometer; Molecular Devices). Data are presented as mean ± SEM (n = 3). *P < 0.05, **P < 0.01, compared with RPE alone (control).

Activated Monocytes Provoke Apoptosis in RPE Cells

One potential important consequence of Ca²⁺ and ROS signaling is the induction of apoptosis, a key mechanism of RPE loss during AMD. Thus, we examined whether MCP-1–activated monocytes could induce RPE apoptosis. Figure 3A shows fluorescence images of cells stained with Hoechst 33342 and caspase-3 substrate (NucView 488; Biotium, Inc.). The Hoechst 33342 dye is a fluorescent indicator that binds specifically to the nuclear chromatin, which is traditionally used to monitor the apoptotic status of cells. As shown in the middle panel of Figure 3A, the RPE cells co-cultured with MCP-1–activated U937 cells had condensed nuclei, which is the hallmark of cells undergoing apoptosis. We stained RPE cells with propidium iodide and did not find propidium iodide–positive RPE cells under the same condition (data not shown), indicating that MCP-1–activated U937 cells induced RPE apoptosis rather than necrosis. In contrast, RPE cells exposed to control medium remained healthy with normal nuclear structure with no apparent chromatin condensation. We also confirmed our observations using a more specific activated caspase-3 assay (Fig. 3A, right panel). In this assay, caspase-3 substrate is cleaved by activated caspase-3 to release a high-affinity DNA dye that accumulates as a green nuclear stain. Thus, this assay is used to detect apoptotic cells containing activated caspase-3. Figure 3B quantifies the detection of apoptotic cells with activated caspase-3 and summarizes the results from four independent experiments. A significant increase in RPE apoptosis was observed when RPE monolayers were co-cultured with MCP-1–activated U937 cells. Treatment of RPE cells with activated U937 cells led to a sixfold increase in the number of activated caspase-3–positive RPE cells (Fig. 3B; P < 0.05). The RPE apoptosis, as measured by a third assay, cell death detection ELISA, was also significantly increased by U937 cells and MCP-1–activated U937 cells (Fig. 3C), or by MCP-1–activated freshly isolated human monocytes (Fig. 3D).

Figure 3.

Activated monocytes induce apoptosis in RPE cells. (A) Differential interference contrast (DIC) and fluorescence images of cells stained with Hoechst 33342 and caspase-3 substrate (NucView 488; Biotium, Inc.) in RPE cells exposed control medium (RPE alone), unstimulated U937 cells (RPE/U937), or MCP-1–activated U937 cells (RPE/U937/MCP-1). Scale bar, 10 μm. (B) A quantitative analysis of activated caspase-3–positive RPE cells. Activated caspase-3–positive RPE cells were determined after staining with caspase-3 substrate. (C) RPE cells were treated as described in (A) for 6, 12, and 24 hours. DNA fragmentation or released mono- and oligonucleosomes were measured by a cell death detection ELISA. (D) RPE cells were treated with MCP-1–activated freshly isolated human monocytes (RPE/Mo/MCP-1) for 24 hours. DNA fragmentation or released mono- and oligonucleosomes were measured by a cell death detection ELISA. Data are presented as mean ± SEM (n = 3–6). *P < 0.05, ***P < 0.001, compared with RPE alone (control).

Effects of cADPR Antagonist on Activated Monocyte-Induced Ca²⁺ Levels, ROS Accumulation, and Apoptosis in RPE Cells

The results show that activated monocytes trigger RPE Ca²⁺ signaling, ROS generation and apoptosis (Figs. 1–3). There is increasing evidence that cADPR participates in Ca²⁺ signaling, ROS production, and apoptosis.^27–33 To assess the potential role of cADPR in the activated monocyte-induced increase in RPE Ca²⁺, ROS, and apoptosis, first the effect of the cAPDR antagonist 8-Br-cAPDR on the activated monocyte-induced Ca²⁺ levels was tested. As shown in Figure 4A, exposure of RPE to activated monocytes increased F420/F480 ratios, indicating an increase in intracellular Ca²⁺ in RPE cells. Pretreatment of RPE with 8-Br-cAPDR inhibited this increase. Next the effect of 8-Br-cAPDR on activated monocyte-induced ROS production was examined. RPE pretreatment with 8-Br-cAPDR, which was effective in reducing activated monocyte-induced F420/F480 ratios (Fig. 4A), also inhibited ROS accumulation (Fig. 4B). The effect of 8-Br-cAPDR on the activated monocyte-induced RPE apoptosis was also examined. RPE pretreatment with 8-Br-cAPDR also inhibited activated monocyte-induced RPE apoptosis (Fig. 4C). CD38 cyclizes nicotinamide adenine dinucleotide (NAD⁺) to produce cADPR, and human monocytes express CD38.⁴⁴ To examine whether human RPE could express CD38, RT-PCR analysis and immunofluorescence microscopy were performed. Both CD38 transcript (Fig. 4D) and protein (Fig. 4E) were expressed by human RPE cells. These parallel sets of observations in Figure 4 suggest that cADPR signaling may contribute to RPE apoptosis.

Figure 4.

Effects of cADPR antagonist on activated monocyte-induced RPE Ca²⁺ levels, ROS production, and apoptosis. (A) Fluorescent Ca²⁺ indicator–preloaded RPE cells were preincubated with or without cADPR antagonist 8-Br-cADPR for 30 minutes, and then exposed to control medium (Control) or MCP-1–activated monocytes (RPE/Mo/MCP-1) in the presence or absence of 8-Br-cADPR. (B) CM-H₂DCFDA–prelabeled RPE cells were preincubated with or without 8-Br-cADPR for 30 minutes, and then exposed to control medium or MCP-1–activated monocytes in the presence or absence of 8-Br-cADPR. Fluorescence intensities were measured. (C) RPE cells were preincubated with or without cADPR inhibitor, 8-Br-cADPR, for 30 minutes, and then exposed to MCP-1–activated monocytes. After 6 hours, the number of cells with activated caspase-3 was determined after staining with caspase-3 substrate. (D) RT-PCR analysis of CD38 expression in human RPE cells. Total RNA isolated from human RPE cells was treated with DNase I and reverse transcribed (RT). PCR was performed using a primer set specific for CD38 or hypoxanthine phosphoribosyltransferase 1 (HPRT1), which serves as an endogenous control or reference. Lanes 1 to 3 indicate RPE cells derived from three different donors. (E) Immunofluorescence labeling of CD38 in human RPE cells. Isotype-matched IgG2a serves as a control. Data are presented as mean ± SEM (n = 3–12). *P < 0.01, **P < 0.001, compared to control; ^#P < 0.05, compared to RPE/Mo/MCP-1 without 8-Br-cADPR.

Effects of ROS Inhibitors on Activated Monocyte-Induced Ca²⁺ Levels, ROS Accumulation, and Apoptosis in RPE Cells

The effects of the ROS inhibitors PDTC and NAC on induced Ca²⁺ levels, ROS generation, and apoptosis in RPE cells were tested. PDTC and NAC did not significantly affect activated monocyte-induced Ca²⁺ levels (Fig. 5A), although RPE pretreatment with NAC and PDTC abolished and inhibited ROS generation, respectively (Fig. 5B). Pretreatment with PDTC and NAC, which were effective in the suppression of activated monocyte-increased ROS levels (Fig. 5B), inhibited activated monocyte-induced RPE apoptosis (Fig. 5C).

Figure 5.

Effects of ROS scavengers on activated monocyte-induced RPE Ca²⁺ levels, ROS production, and apoptosis. (A) Fluorescent Ca²⁺ indicator–preloaded RPE cells were preincubated with or without ROS scavenger, NAC, or PDTC for 30 minutes, and then exposed to MCP-1–activated monocytes in the presence or absence of NAC or PDTC. (B) CM-H₂DCFDA-prelabeled RPE cells were preincubated with or without NAC or PDTC for 30 minutes, and then exposed to unstimulated monocytes (Control), MCP-1–activated monocytes in the presence or absence of NAC or PDTC. Fluorescence intensities were measured. (C) RPE cells were preincubated with or without ROS scavenger (PDTC or NAC) for 30 minutes, and then exposed to MCP-1–activated monocytes. The number of cells with activated caspase-3 was determined after staining with caspase-3 substrate (NucView 488; Biotium, Inc.). Data are presented as mean ± SEM (n = 3–12). **P < 0.01, ***P < 0.001, compared with control. ^#P < 0.05, ^###P < 0.0001, compared with RPE/Mo/MCP-1.

Taken together, the findings suggest that Ca²⁺ signaling may be required for activated monocyte-induced ROS generation in RPE cells and that activated monocytes induce RPE apoptosis via both intracellular Ca²⁺ signaling and ROS production.

Effects of Anti-CD14 Antibody on Activated Monocyte-Induced Ca²⁺ Levels, ROS Accumulation, and Apoptosis in RPE Cells

To identify functionally whether adhesion molecule CD14 was involved in activated monocyte-induced intracellular Ca²⁺ in RPE cells, the activated monocyte-induced Ca²⁺ rise in the presence or absence of anti-CD14 antibody was tested. As shown in Figure 6A, the activated monocyte-induced F420/F480 ratio was significantly inhibited by anti-CD14 antibody, indicating that CD14 may be involved in activated monocyte-induced increase in intracellular Ca²⁺ in RPE cells.

Figure 6.

Effects of anti-CD14 on activated monocyte-induced RPE Ca²⁺ levels, ROS production, and apoptosis. (A) Activated monocytes-induced RPE Ca²⁺ levels were measured using a fluorometer (FlexStation Scanning Fluorometer; Molecular Devices) in the presence or absence of antibody directed against CD14. RPE cells were loaded with a Ca²⁺ indicator dye (Fura red-AM; 10 μM), for 1.5 hours at 37°C. After incubation with anti-CD14 antibody for 1 hour, RPE cells were challenged with MCP-1–activated monocytes (RPE/Mo/MCP-1). (B) CM-H₂DCFDA–prelabeled RPE cells were preincubated with or without anti-CD14 antibody for 1 hour, and then exposed to MCP-1–activated monocytes in the presence or absence of anti-CD14 antibody. Fluorescence intensities were measured. (C) Differential interference contrast (DIC) and fluorescence images of cells stained with Hoechst 33342 and caspase-3 substrate (NucView 488; Biotium, Inc.) in RPE cells exposed control medium (RPE alone), or MCP-1–activated U937 cells (RPE/U937/MCP-1) in the presence or absence of anti-CD14 antibody for 6 hours. Scale bar, 20 μm. (D) RPE cells were preincubated with or without anti-CD14 antibody for 1 hour, and then exposed to control medium (RPE alone), monocytes (RPE/Mo), or MCP-1–activated monocytes in the presence or absence of anti-CD14 antibody. After 6 hours, the number of cells with activated caspase-3 was determined after staining with caspase-3 substrate. (E) RPE cells were treated as described in (C) for 24 hours. DNA fragmentation or released mono- and oligonucleosomes were measured by a cell death detection ELISA. Data are presented as mean ± SEM (n = 3–12). *P < 0.05, ***P < 0.001, compared with control or RPE/Mo/MCP-1 (without antibody); ^##P < 0.01, ^###P < 0.001, compared with RPE/Mo/MCP-1 or RPE/U937/MCP-1 (without antibody).

As the activated monocyte-induced Ca²⁺ levels were significantly inhibited by anti-CD14 antibody (Fig. 6A), it was tested whether activated monocytes induced RPE ROS production and apoptosis via CD14. Functional blocking antibody against CD14 significantly reduced activated monocyte–induced apoptosis by different assays: Hoechst 33342 staining for condensed nuclei (Fig. 6C) and caspase-3 substrate staining (Fig. 6C) and quantitative measurement (Fig. 6D) for activated caspase-3, and apoptosis ELISA for DNA fragmentation (Fig. 6E). However, anti-CD14 antibody had no effect on the activated monocyte-induced ROS generation (Fig. 6B). Thus, CD14 appears to be responsible for activated monocyte–induced Ca²⁺ increase and apoptosis in RPE cells.

Discussion

As monocytic infiltration is a key component of retinal diseases such as PVR, AMD, and uveitis, as evidenced by their presence in histopathologic lesions,^{4,6,7,10,11,45–50} and MCP-1 plays an important role in regulation of the monocytic infiltration, and is associated with AMD and retinal detachment,^51–53 it is important to examine how monocytes induce RPE apoptosis. Both RPE cells and monocytes have critical regulatory functions in the development of these diseases, and monocytes and monocyte-derived cytokines influence RPE functions and integrity.^34,54–60 It is well established that activated monocytes and macrophages are capable of directing apoptosis in various types of cells, including RPE cells.^{25,26,51,61–68} The present authors previously reported that, using a human RPE culture model, RPE apoptosis was induced by activated monocytes.²⁵ The association of superoxide anions with mononuclear phagocyte-induced apoptosis in mouse RPE cells from wild-type and heterozygous superoxide dismutase 2-knockout (Sod2^±) mice was also examined.²⁶ Mononuclear phagocyte–induced mouse RPE apoptosis involved enhanced intracellular O₂^·− generation, loss of mitochondrial membrane potential, and caspase activation, especially when mononuclear phagocytes were immunologically activated and RPE Sod2 gene was partially knocked out.²⁶ This suggested that elevated O₂^·− levels due to genetic abnormalities of Sod2 or immunologic activation of mononuclear phagocytes lead to greater levels of RPE apoptosis.²⁶ Our present study adds new facets to the mechanisms of activated monocyte-induced RPE apoptosis in that CD14, Ca²⁺, and ROS are involved in the induced RPE apoptosis and that the induced Ca²⁺ and ROS may be mediated by cADPR.

This study demonstrates increases in intracellular Ca²⁺, ROS, and apoptosis when RPE cells are exposed to activated monocytes (Figs. 1–3). Our data are consistent with previous studies in other cell systems showing that several apoptotic stimuli cause Ca²⁺ increase, ROS induction, and apoptosis.^{21,22,69–71}

We also evaluated the potential pathways involved in activated monocyte-induced Ca²⁺ signaling, ROS accumulation, and apoptosis in RPE cells. Previous evidence implicates CD38 and cADPR in Ca²⁺ signaling, ROS production, and apoptosis induced by various stimuli in other cell types.^27–33 Although a possible link among cADPR, Ca²⁺, and ROS production has not been studied in RPE cells, CD38 is expressed in rat RPE cells.⁷² The present study shows that human RPE cells also express CD38 (Figs. 4D, 4E). CD38 binds to its substrate, NAD⁺, and catalyzes the cleavage of NAD⁺ into cADPR with its ADP-ribosyl cyclase activity.⁷³ We show that pretreatment of RPE with 8-Br-cAPDR, a selective and potent antagonist of cADPR-mediated Ca²⁺ signaling,⁷⁴ inhibited the induced Ca²⁺ increase, ROS production, and subsequent apoptosis in RPE cells (Fig. 4). Therefore, we speculate that cAPDR may mediate activated monocyte-induced Ca²⁺ signaling, ROS production, and apoptosis.

It has been reported that antioxidants inhibited apoptosis induced by various apoptotic stimuli.^69,75–80 In the present study, two antioxidants, NAC and PDTC, were used to test their effects on activated monocyte-induced Ca²⁺, ROS, and apoptosis in RPE cells. Pretreatment RPE with NAC completely blocked ROS production and partially inhibited apoptosis induced by activated monocytes, but this pretreatment did not inhibit activated monocyte-induced Ca²⁺ increase, indicating Ca²⁺ signaling may precede ROS production in RPE cells. Similarly, pretreatment of RPE with PDTC inhibited the induced ROS production and apoptosis, but did not significantly inhibit the induced Ca²⁺ increase. Although NAC completely blocked the induced ROS production, it did not completely inhibit the induced apoptosis of RPE, suggesting that other signaling molecule(s) may play a role in RPE apoptosis.

Previous studies demonstrated that CD14 is involved in the regulation of apoptosis and apoptotic cell clearance.^81–84 In addition, lipopolysaccharide (LPS)-mediated activation of microglial and peripheral blood mononuclear (PBM) cells increases cADPR, intracellular calcium levels, and ROS accumulation.^85,86 Anti-CD14 antibody was shown to block the increase in cADPR in LPS-activated PBM cells, but its effects on intracellular calcium levels and ROS accumulation were not studied.⁸⁶ Removal of monocytes from the activated-PBM cells also inhibited the cADPR increase.⁸⁶ This indicates that activated monocytes and CD14 may both be involved in the activation of cADPR. The present study shows that anti-CD14 antibody significantly inhibited MCP-1–activated monocyte-induced Ca²⁺ and apoptosis in RPE cells. As the activated monocyte-induced RPE Ca²⁺ rise (Fig. 1) precedes the induced RPE apoptosis (Figs. 3 and 6), these findings support the role of CD14 in activated monocyte-induced RPE apoptosis through Ca²⁺ signaling.

Monocyte and macrophage infiltration are observed in murine AMD models.^87,88 Both RPE and microvascular endothelial cells produce MCP-1. The finding in the current study that MCP-1–activated monocytes induce RPE apoptosis implicates that in addition to RPE, microvascular endothelial cells might also be involved in atrophic or dry AMD via MCP-1 secretion. Thus it is possible that both MCP-1 and CD14 could be used as therapeutic targets for AMD.

In summary, activated monocytes increased intracellular Ca²⁺ levels, ROS generation, and apoptosis in RPE cells. In addition, inhibition of cADPR with 8-Br-cADPR reduced the induced increase in Ca²⁺, ROS production, and apoptosis. The generation of ROS and apoptosis, but not the Ca²⁺ increase, was inhibited by NAC or PDTC. The induction of Ca²⁺ and apoptosis, but not ROS generation, was incompletely blocked by anti-CD14 antibody. Activated monocytes may induce cADPR formation through CD38 activation, and the generated cADPR could increase RPE Ca²⁺ levels, ROS production, and apoptosis. Understanding how CD38 is activated, how cADPR is regulated, and further elucidating the role of CD14 in RPE cells might therefore provide new insights into retinal diseases, including AMD, and potential therapeutic targets.