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(Investigative Ophthalmology and Visual Science. 2007;48:1401-1409.)
© 2007 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.06-0865
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Identification of Intracellular Phospholipases A2 in the Human Eye: Involvement in Phagocytosis of Photoreceptor Outer Segments

Miriam Kolko,1,2,3 Jinmei Wang,1,3,4 Chen Zhan,1,3 Kristian A. Poulsen,5 Jan Ulrik Prause,1 Mogens Holst Nissen,3 Steffen Heegaard,1 and Nicolas G. Bazan6

1From the Eye Pathology Institute, the 3Department of Medical Anatomy, The Panum Institute, and the 5Institute of Molecular Biology and Physiology, University of Copenhagen, Copenhagen, Denmark; the 2Department of Ophthalmology, Glostrup University Hospital, Copenhagen, Denmark; the 4Department of Ophthalmology, Second Clinical Hospital, Jilin University, Changchun, Peoples Republic of China; and the 6Neuroscience Center of Excellence and Department of Ophthalmology, Louisiana State University Health Sciences Center School of Medicine, New Orleans, Louisiana.


   Abstract
Top
 Abstract
Methods
 Results
 Discussion
 References
 
PURPOSE. To identify intracellular phospholipases A2 (PLA2) in the human retina and to explore the role of these enzymes in human retinal pigment epithelium (RPE) phagocytosis of photoreceptor outer segments (POS).

METHODS. PCR amplification and Western blot analysis were used to identify mRNA and protein expression of intracellular PLA2 subtypes in the retinal pigment epithelial cell line ARPE-19. Immunohistochemical staining of normal human eye sections was performed to reveal the cellular location of the enzymes. A model of RPE phagocytosis of POS was used to explore the role of intracellular PLA2 in phagocytosis. An activity assay was used to evaluate PLA2 activity, and inhibitors of specific PLA2 were applied to evaluate the role of PLA2 in RPE phagocytosis.

RESULTS. Genes encoding calcium-independent (i)PLA2, group VIA; calcium-dependent cytosolic (c)PLA2, groups IVA, IVB, and IVC; and iPLA2, group VIB, were identified in the human RPE cell line ARPE-19. Furthermore, protein of iPLA2-VIA, cPLA2-IVA, and iPLA2-VIB were identified in ARPE-19 cells and in various parts of the normal human eye. iPLA2-VIA protein levels were upregulated during phagocytosis, and iPLA2-VIA activity was found to be specifically increased 12 hours after ARPE-19 cells were fed with POS. Finally, RPE phagocytosis was inhibited by the iPLA2-VIA inhibitor bromoenol lactone.

CONCLUSIONS. Various intracellular PLA2 subtypes are present in the human retina. iPLA2-VIA may play an important role in the regulation of RPE phagocytosis of POS and may also be involved in the regulation of photoreceptor cell renewal.

The retinal pigment epithelium (RPE) is essential to maintaining a functional neuroretina. One of the most important functions of RPE is to phagocytize the shed tip of photoreceptor cells. During this process, photoreceptor outer segments (POS) are constantly formed at the base of the POS and are phagocytized by the adjacent RPE in a tightly regulated intracellular signaling pathway coupling phagocytosis with expression of POS-degradative enzymes.1 The essential role of RPE phagocytosis is highlighted by the rapid degeneration of photoreceptors in Royal College of Surgeon’s rats, which carry an autosomal recessive mutation that impairs RPE phagocytosis, resulting in subretinal accumulation of POS.

Phospholipids (PLs) represent major constituents of POS. Published values for the percentage of PL in bovine POS varies between 30% and 60%, depending on the procedure for POS preparation.2 3 Phosphatidylcholine (PC) and phosphatidylethanolamine (PE) account for 80% of the PL in POS; followed by phosphatidylserine with 13%; and finally by phosphatidylinositol, sphingomyelin, and lipids in the solvent (phosphatidic acid, phosphatidylglycerol, diphosphosphatidylglycerol, and dipalmitoylphosphatidylethanolamine), which makes up the rest.4 5

Even though recent studies emphasize the differences between macrophage and RPE phagocytosis, the two processes show many similarities, and much can be learned from macrophage studies to further our understanding of RPE phagocytosis.6 Among other mediators of phagocytosis. phospholipases A2 (PLA2) have been found to be involved in macrophage engulfment.7 8 9 PLA2 is a group of enzymes catalyzing the hydrolysis of sn-2 fatty acyl chains, thereby releasing free fatty acids and lysophospholipids. PLA2 can be divided into various groups according to their cellular location, calcium dependency, and substrate specificity. The most recent classifications divide PLA2 into high-molecular-weight cytosolic calcium-dependent (c)PLA2, groups IVA, IVB, IVC, and IVD; high-molecular-weight calcium-independent (i)PLA2, groups VIA and VIB; low-molecular-weight secretory (s)PLA2, groups IB, IIA, IIC, IID, IIE, IIF, III, V, X, and XIIA; and the substrate-specific platelet-activating factor-acetylhydrolases (PAF-AH), groups VIIA, VIIB, VIIIA, and VIIIB.10 11 12 Macrophage studies have revealed involvement of cyclooxygenases (COX) and prostaglandins as a result of PLA2 activity in the regulation of phagocytosis.8 13 14 Most evident is the role of cPLA2 and sPLA2, group V in regulation of phagocytosis.7 15 Recent studies furthermore indicate a role of iPLA2 in phagocytosis since PLA2-induced cleavage of PC in dying cells leads to phagocytosis of these by adjacent macrophages.9 There is only limited evidence of the involvement of PLA2 in RPE phagocytosis. However, RPE has been shown to elicit PLA2 activity,16 17 and RPE phagocytosis of POS has been shown to induce prostaglandins by COX activation.18 Preliminary findings have revealed the highest abundance of the high-molecular-weight PLA2 in the human RPE cell line ARPE-19 compared with the low-molecular-weight sPLA2. The present study therefore evaluated the known high-molecular-weight PLA2 in human RPE cells and explored their possible role in ARPE-19 phagocytosis of POS.


   Methods
Top
 Abstract
 Methods
Results
 Discussion
 References
 
ARPE-19 Cultures
Human ARPE-19 cells (purchased from ATTC-LGC Promochem AB, Boras, Sweden) were maintained at 37°C in a humidified chamber of 5% CO2 in Dulbecco’s modified Eagle’s medium- F12 (DMEM) containing 5 mM glucose and supplemented with 15% fetal bovine serum (FBS), 100 U/mL penicillin, and 100 µg/mL streptomycin (Invitrogen-Gibco, Carlsbad, CA). The cells were grown in six-well plates, and the culture medium was replaced with fresh medium twice a week. The cells were harvested at different time points and kept at –80°C until use.

PCR Amplification
Total RNA was extracted from 2-week-old ARPE-19 cultures. cDNA was then generated (ThermoScript cDNA kit; Invitrogen-Gibco). One microgram of total RNA was used for each reaction with polyT primers and amplified (AmpliTaqGold; (Applied Biosystems, Foster City, CA). To exclude genomic contamination, controls were made by excluding the polyT primers during reverse transcription. Furthermore, primer sets were all designed to span an intron. Volumes of cDNA used were 5 µL (from 100 ng RNA) for each of the PLA2s. Amplification was performed in an automated thermal cycler (model 2400; Perkin Elmer, Boston, MA). Primers were as outlined in Table 1 . PCR products were ligated into PCR-II vectors (Invitrogen-Gibco) and sequenced, thereby confirming the specificity of the PCR reactions.


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  		TABLE 1. RT-PCR Primers Used for PCR Cloning of Intracellular PLA2 Subtypes

 
Western Blot Analysis
ARPE-19 cells were kept in growth medium and incubated with POS or PBS. The cells were collected after 12 and 24 hours and homogenized in 500 µL lysis buffer. Samples were centrifuged at 4000g for 25 minutes at 4°C, and samples containing 25 µg protein were loaded. Blots were preincubated overnight in TBS (0.2 mM Tris-HCl [pH 7.5], 150 mM NaCl, 0.1% Tween 20) containing 5% nonfat dry milk and incubated with one of the following primary antibodies in TBS-1% bovine serum albumin for 3 hours at room temperature: iPLA2-VIA (CAY-160507, 1:500; Cayman Chemical, Ann Arbor, MI); cPLA2-IVA (SC-454, 1:500; Santa Cruz Biotechnology, Santa Cruz, CA); or iPLA2-VIB (1:100), prepared as described by Poulsen et al. (manuscript submitted). Extracellular signal-regulated kinase (ERK) expression did not change during phagocytosis and blots incubated with an antibody recognizing ERK were used as loading controls (see Fig. 4B ). Blots were washed in TBS and incubated with goat anti-rabbit IgG alkaline phosphatase secondary antibody (TriChem ApS; Interkemi, Frederikssund, Denmark) followed by visualization using BCIP/NBT (5-bromo-4-chloro-3-indoyl phosphate-nitroblue tetrazolium) substrate (VWR International ApS, Albetslund, Denmark).


Figure 1
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  		FIGURE 1. (A) PCR amplification and semiquantitative analysis of genes encoding iPLA2-VIA, cPLA2-IVA, and iPLA2-VIB. (B) PCR amplification of genes encoding iPLA2-VIA splice variants and cPLA2-IV subtypes.

 

Figure 2
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  		FIGURE 2. (A) Western blot analysis using iPLA2-VIA-, cPLA2-IVA-, and iPLA2-VIB-specific antibodies on protein isolated from ARPE-19 cells and bovine POS. (B) Immunohistochemical staining of normal human retinas with antibodies specifically recognizing iPLA2-VIA, cPLA2-IVA, and iPLA2-VIB. Note strong reactivity in the RPE with iPLA2-VIA and only weak reactivity with the other two antibodies. RPE, retinal pigment epithelium; OS, photoreceptor outer segments; POS, photoreceptor outer segments; IS, photoreceptor inner segments; ONL, outer nuclear layer. (C) Immunohistochemical staining of ARPE-19 cells. Red: iPLA2-VIA reactivity; green: cytoskeleton, stained by Alexa 488-phalloidin. Note the iPLA2-VIA reactivity in the cytosol of the ARPE-19 cells. Bar, 5 µm.

 

Figure 3
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  		FIGURE 3. Immunohistochemical staining of normal human eyes with antibodies specifically recognizing iPLA2-VIA, cPLA2-IVA, and iPLA2-VIB. (A–D) Staining with iPLA2-VIA; (E–H) staining with cPLA2-IVA; (I–L) staining with iPLA2-VIB; (M) staining with rabbit serum. (N) Staining with preimmune serum from rabbits used to produce iPLA2-VIB antibody. e, Corneal epithelium; k, corneal keratocytes; en, corneal endothelium; pe, pigmented epithelium; npe, nonpigmented epithelium; nfl, nerve fiber layer; g, ganglion cell layer; ipl, inner plexiform layer; inl, inner nuclear layer; opl, outer plexiform layer; onl, outer nuclear layer; is, photoreceptor inner segments; os, photoreceptor outer segments; POS, photoreceptor outer segments; rpe, retinal pigment epithelium; le, lens epithelium; lf, lens fibers. Magnification: (A–C, E–G, I–K, M, N) x200; (D, H, L) x600.

 

Figure 4
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  		FIGURE 4. (A) Fluorescence absorbance at various time points after addition of POS to 3-week-old ARPE-19 cells. (B) Western blot analysis, using antibodies against iPLA2-VIA, cPLA2-IVA, and iPLA2-VIB, on protein isolated from ARPE-19 cell before and after POS phagocytosis. ERK staining was used as the loading control. *Significance level P < 0.05.

 
Immunoprecipitation
Protein was isolated from 3-week-old ARPE-19 cells as just described. Precleared supernatant was incubated with a goat anti-iPLA2-VIA antibody (SC-14463; 1:400; Santa Cruz Biotechnology, Inc.) overnight at 4°C. To monitor nonspecific binding, we omitted the antibody from a similar sample. After incubation, 50 µL of protein G-Sepharose beads (GE Healthcare, Hillerød, Denmark) was added, and samples were incubated at 4°C for a further 4 hours. The resin was collected by centrifugation and washed five times in buffer. Bound protein was eluted by boiling the resin in 40 µL of 2x loading buffer and resolved by SDS gel electrophoresis. Blots were stained with a rabbit anti-iPLA2-VIA (CAY-160507, 1:200; Cayman Chemical).

Immunohistochemistry
Human eyes were obtained from the Eye Pathology Institute, University of Copenhagen, in accordance with the guidelines of the Declaration of Helsinki for research involving human tissue. Sections were deparaffinized, boiled for 20 minutes in a microwave in TE buffer (pH = 9.5) for antigen retrieval and incubated with 3% H2O2 for 8 minutes at room temperature, to inhibit endogenous peroxidase activity. Sections were exposed to antibodies that specifically recognize iPLA2-VIA (1:200), iPLA2-VIB (1:200), or cPLA2-IVA (1:200); washed twice with PBS; and exposed to biotinylated anti-rabbit IgG followed by incubation with a dilution of streptavidin peroxidase complex reagent and finally visualized by the use of AEC (3-amino-9-ethylcarbazole) chromogen (Dako Inc., Copenhagen, Denmark). Relevant positive and negative controls were used. Immunostained sections were examined by light microscopy.

Confocal Microscopy
ARPE-19 cells were detached with trypsin, transferred to glass coverslips in 24-well plates, and incubated in normal glucose medium. The cells were grown to confluence and stained with an iPLA2-VIA-specific antibody (SC-160507; 1:200) overnight at 4°C. They were washed three times with PBS and fixed in formaldehyde 3.7% for 15 minutes at room temperature, followed by membrane permeabilization by 0.2% Triton X-100 in TBS for 10 minutes. They were washed three times in blocking buffer (TBS+5% BSA), and Alexa 488-phalloidin (1:20; Invitrogen-Gibco) was added to for 2 hours at room temperature in the dark. Finally, the cells were washed three times in blocking buffer. Coverslips were moved to slides and sealed with fluorescence-preserving mounting medium (Vector Laboratories, Burlingame, CA). A confocal laser scanning image system (LSM 510; Carl Zeiss Meditec GmbH, Düsseldorf, Germany) was used to detect immunofluorescence.

Isolation of POS
Normal bovine eyes were obtained from an abattoir, and preparation was initiated within 6 hours after enucleation. POS isolation was performed as described by Hall.1 The retina was removed and transferred into PBS. The retinal tissue was trypsinized on ice and fragmented by a magnetic stirrer for 30 minutes. Large tissue fragments were eliminated by precipitation for 20 minutes at 4°C, and supernatants were centrifuged at 800g for 10 minutes. The samples were rinsed twice with PBS, and aliquots containing 40 x 106 POS were stored at –70°C until use.

Labeling of POS and Quantification of POS Phagocytosis by ARPE-19 Cells
POS were labeled with the biotin-streptavidin method described by Schraermeyer and Stieve.19 POS suspended in PBS were centrifuged at 1000g for 10 minutes. The pellet, containing the outer segments, was then biotinylated with 1:5 (wt/vol) 0.8 mg/mL NHS-LC biotin (Sigma-Aldrich, St. Louis, MO) dissolved in PBS for 1 hour in the dark and on ice. POS was washed twice in PBS and in a second step, the biotin residues on the outer segments were labeled 1:5 (wt/vol) with 0.05 mg/mL streptavidin-AlexaFluor568 red (Jackson ImmunoResearch, West Grove, PA) for 1 hour in the dark and on ice and washed twice in PBS to remove unbound conjugates. Finally, POS was resuspended 1:2 (wt/vol) in PBS. RPE cells were grown in 96-well plates. Media were removed, and 200 µL of Locke’s solution (154 mM NaCl, 5.6 mM KCl, 10 mM glucose, 2.2 mM CaCl2, and 5 mM HEPES buffer adjusted to pH 7.4) was added to all wells. Five microliters POS was gently added on top of confluent monolayer cultures of ARPE-19 cells grown in 96-well plates. Five microliters of Locke’s was added to the control wells. Incubations were continued in darkness for various time intervals at 37°C in an atmosphere of 5% CO2 and 95% air. Phagocytized fluorescent POS were detected with a gel and blot imager (Typhoon 9410; GE Healthcare) equipped with a 532-nm excitation filter. Background fluorescence of the system, as assayed without cells, was very low and was automatically subtracted. Bromoenol lactone (BEL; 0.1. 1, 5, 10, or 20 µM), arachidonyl trifluoromethyl ketone (AACOCF3; 10 µM) or propranolol (150 µM) was added to cells simultaneously with the POS. To evaluate the phagocytosis of POS, we added Alexa-red-labeled POS to ARPE-19 cells grown on glass coverslips, as described earlier. After 12 hours, the cells were washed three times with PBS and fixed. Alexa 488-phalloidin (1:20; Invitrogen) was added to the cells for 2 hours at room temperature without light. Finally, the cells were washed and visualized with a confocal laser scanning image system.

Cytotoxicity Assay
After an overnight incubation with different concentrations of BEL (n = 6 for each condition) cell viability was determined by a colorimetric method, which is based on the conversion of yellow MTT salt (3-(4.5-dimethylthiazol-2-yl)-2.5-diphenyl tetrazolium bromide; Sigma-Aldrich) to an insoluble purple formazan dye by mitochondrial dehydrogenase of living cells. Briefly, the assay was performed by removing the cell culture medium and replacing it with 100 µL fresh culture medium containing 5.0 mg/mL MTT. After 4 hours of incubation at 37°C, the cells were solubilized overnight with 100 µL of a solution containing 50% dimethylformamide and 20% SDS (pH 4.7), and absorbance was measured at 560 nm. The background readings (blank wells with medium, MTT, and solubilization buffer) were subtracted from the average absorbance readings of the BEL-treated wells, to obtain an adjusted absorbance reading that represented cell viability. This reading was divided by the adjusted absorbance reading of untreated cells in control wells, to obtain the percentage of cell survival.

Measurement of PLA2 Activity
ARPE-19 cells, with or without preincubation with POS, were collected and homogenized in 150 µL lysis buffer (50 mM HEPES, 1 mM EDTA, 1 mM Na-orthovanadate, and protease inhibitor cocktail [1:100; Sigma-Aldrich]). Samples were centrifuged at 2000g for 30 minutes at 4°C. The supernatants were collected and subsequently spun though 30-kDa cutoff filters (12 minutes, 14,000g; Microcon YM-30; Millipore, Hundested, Denmark). Arachidonoyl thio-PC was used as a synthetic substrate to detect PLA2 activity. Hydrolysis of the arachidonoyl thioester bond at the sn-2 position by PLA2 releases free thiol, which is detected by Ellman’s reagent. PLA2 activity was determined in the supernatant with a cPLA2 assay kit (Cayman Chemical), in the presence and absence of a specific inhibitor of iPLA2, BEL, which was incubated for 15 minutes at 25°C at a concentration of 10 µM before the assay. Activity was calculated by measuring the absorbance at 405 nm, using the 5.5'-dithiobis(2-dinitrobenzoic acid; DTNB) extinction coefficient of 10.66/mM, and reported as nanomoles per minute per gram cytosolic protein.

Statistics
Quantitative results are expressed as the mean ± SD. Statistical significance between experimental groups was assessed by Student’s t-test.


   Results
Top
 Abstract
 Methods
 Results
Discussion
 References
 
Expression of mRNAs and Proteins of Intracellular PLA2s in ARPE-19 Cells
Primers recognizing genes encoding iPLA2-VIA, cPLA2-IVA, and iPLA2-VIB revealed significantly higher expression of iPLA2-VIA than of cPLA2-IVA and iPLA2-VIB. cPLA2-IVA (P < 0.001, n = 4) and iPLA2-VIB (P < 0.001, n = 4) mRNA expression was 12% and 67% of iPLA2-VIA mRNA expression (n = 4), respectively (Fig. 1A) . RT-PCR primers designed to detect splice variants of iPLA2-VIA documented the expression of the known alternative genes encoding the iPLA2-VIA region, with and without exon 9, ankyrin 1, and ankyrin 2.20 We furthermore identified a new splice variant containing intron 4 (Fig. 1B) . Finally, primers specifically recognizing cPLA2-IVA, cPLA2-IVB, or cPLA2-IVC revealed mRNA expression of these genes in ARPE-19 cells (Figs. 1A 1B) . A primer set recognizing cPLA2-IVD did not amplify a product (not shown).

Western blot analysis, using antibodies against human iPLA2-VIA, human cPLA2-IVA, and human iPLA2-VIB, revealed protein expression of all the intracellular PLA2s in ARPE-19 cells. POS did not express any of the known PLA2s (Fig. 2A) . iPLA2-VIA identified a ~85-kDa band and a ~70-kDa band, previously described in the literature.21 The cPLA2-IVA antibody recognized a ~100-kDa band and finally iPLA2-VIB recognized a ~88, ~77, ~63, and ~48-kDa band. Immunohistochemical staining of ARPE-19 cells confirmed the protein expression of all the intracellular PLA2s (Fig. 2B) . The authenticity of the ~70-kDa protein to which the CAY-160507 (Cayman Chemical) antibody reacts, was evaluated by immunoprecipitation. An iPLA2-VIA-directed antibody (SC-14463; Santa Cruz Biotechnology, Inc.) was used to immunoprecipitate iPLA2-VIA from ARPE-19 cells. In this precipitate, both the ~85- and the ~70-kDa proteins were recognized by Western blot analysis using the CAY-160507 antibody, strongly indicating that this protein is an iPLA2-VIA protein product (data not shown).

Cellular Location of Intracellular PLA2 in the Normal Human Eye
Six normal eyes were used for evaluation of the expression pattern of intracellular PLA2. Antibodies recognizing iPLA2-VIA, cPLA2-IVA, and iPLA2-VIB were used as described in the Methods section. Table 2 presents the reactivity of the various ocular structures.


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  		TABLE 2. Staining Intensity of iPLA2-VIA, cPLA2-IVA, and iPLA2-VIB Protein Expression in the Human Eye

 
In the cornea, moderate detectable expression of iPLA2-VIA was found in the epithelial cells, whereas strong iPLA2-VIA expression was observed in the endothelium (Fig. 3A) . Weak to moderate iPLA2-VIA expression was found in the dilator and sphincter muscles. Pigmented and nonpigmented ciliary epithelial cells (Fig. 3B) as well as the ciliary muscle revealed moderate iPLA2-VIA expression. Strong expression of iPLA2-VIA was observed in various layers of the retina (Fig. 3C) . The most abundant expression was detected in the RPE cells, the ganglion cells, and the nerve fiber layer. Moderate iPLA2-VIA expression was found in the photoreceptor inner segment and the inner and outer plexiform layers, whereas no expression appeared in the nuclear layers and the POS (Figs. 2B 3C) . Moderate iPLA2-VIA expression appeared in both the anterior (Fig. 3D) and equatorial lens epithelium.

cPLA2-IVA expression also showed widespread expression in the human eye. In the cornea moderate detectable expression was found in the epithelial cells and in the endothelium (Fig. 3E) . Pigmented epithelial cells of the ciliary body (Fig. 3F) as well as the ciliary muscle revealed moderate cPLA2-IVA expression, whereas strong staining appeared in the nonpigmented epithelial cells (Fig. 3F) . Moderate expression was detected in the photoreceptor inner segment of the retina (Fig. 3G) . Weak expression of cPLA2-IVA was found in the anterior (Fig. 3H) and equatorial lens epithelium.

In contrast to the expression of iPLA2-VIA and cPLA2-IVA, iPLA2-VIB appeared both in the cytosol and the nuclei of various cells in the human eye. Strong iPLA2-VIB was found in the corneal epithelium and moderate expression was detected in the corneal endothelium (Fig. 3I) . Pigmented and nonpigmented epithelial cells of the ciliary body (Fig. 3J) and ciliary muscle revealed moderate iPLA2-VIB expression. In the retina, moderate iPLA2-VIB expression was found in the photoreceptor inner segment, the inner nuclei layer, in the ganglion cells, in the nerve fiber layer and in the RPE (Fig. 3K) . Strong iPLA2-VIB expression appeared in both the anterior (Fig. 3L) and equatorial lens epithelium. In control eyes stained with rabbit serum, no reactivity appeared (Fig. 3M) . In control eyes stained with preimmune serum from the rabbits used to produce the iPLA2-VIB antibody, weak reactivity appeared in the photoreceptor inner segment, in the inner and outer plexiform layers, and in the nerve fiber layer (Fig. 3N) .

Cellular Location of iPLA2-VIA in ARPE-19 Cells
ARPE-19 cells stained with an iPLA2-VIA-specific antibody confirmed the location of iPLA2-VIA in the cytosol of the RPE cells (Fig. 2C) .

Validation of POS and Latex Bead Uptake by ARPE-19 Cells
ARPE-19 cells were incubated with Alexa-red–labeled POS or beads for 12 and 24 hours. The identity of the fluorescence-labeled cells was confirmed by confocal microscopy revealing perinuclear localization of POS or beads in RPE cells. No staining was evident when nonlabeled POS were added to the cells or when no POS or beads were added to the media (data not shown).

ARPE-19 Phagocytosis of POS
Alexa red–labeled POS (n = 3) or latex beads (n= 3) were added to ARPE-19 cultures as described in the Methods section. The cells were washed after 1, 2, 4, 6, 8 10, 12, 16, and 24 hours. Maximum absorbance was found 12 hours after addition of both POS (Fig. 4A) and beads (data not shown).

Expression of PLA2 after POS Phagocytosis
ARPE-19 cells were fed with POS, as described in the Methods section. After 12 and 24 hours of incubation, the cells were harvested and the protein isolated for Western blot analysis. The 70-kDa iPLA2-VIA was upregulated by 1.6-fold after 12 hours (P < 0.001, n = 4) and 1.7-fold after 24 hours (P < 0.001, n = 4; Fig. 4B ), whereas the 85 kDa iPLA2-VIA was downregulated by 0.2-fold after 12 and 24 hours (P < 0.05, n = 4). cPLA2-IVA and iPLA2-VIB revealed no significant change in expression after POS phagocytosis (n = 4; Fig. 4B ).

No change in iPLA2-VIA, cPLA2-IVA or iPLA2-VIB expression was found after phagocytosis of the beads (data not shown).

Induction of iPLA2-VIA Activity by ARPE-19 Phagocytosis of POS
ARPE-19 cultures were fed with POS, and protein was isolated 4, 8, and 12 hours after POS addition. PLA2 activity was measured in conditions with and without POS and was found to be 0.24 micromoles/per milligram protein in untreated ARPE-19 cells (n = 14). In ARPE-19 cells fed with POS PLA2, activity was measured to be 0.24 micromoles/per milligram protein (P < 0.05, n = 4) after 4 hours, 0.34 micromoles/per milligram protein (P < 0.05, n = 4) after 8 hours, and 0.35 micromoles/per milligram protein (P < 0.001, n = 18) after 12 hours (Fig. 5A) . The iPLA2-VIA-specific inhibitor BEL (10 µM) was added to the proteins to estimate PLA2 activity and was found to inhibit all activity induced by phagocytosis of POS (Fig. 5A) . Addition of beads to the ARPE-19 cells did not induce iPLA2-VIA activity, which was measured at 0.23 micromoles/per milligram protein after 12 hours (n = 8; Fig. 5A ). Inhibition with the specific cPLA2-IVA inhibitor AACOCF3 did not reveal a significant role of cPLA2-IVA in the increased PLA2 activity induced by phagocytosis (not shown).


Figure 5
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  		FIGURE 5. (A) PLA2 activity in ARPE-19 cells fed with POS or beads. Bars represent total PLA2 activity (±SD). Black portions indicate iPLA2-VIA-specific activity. (B) Inhibition of ARPE-19 phagocytosis of POS by the specific iPLA2-VIA inhibitor BEL (10 µM) or the cPLA2-IVA inhibitor AACOCF3 (10 µM). Bars representthe mean percentage of inhibition (±SD). (C) Irreversible inhibition of ARPE-19 phagocytosis of POS 24, 48, and 72 hours after addition of BEL. POS was repeatedly added every 12 hours. Bars represent the mean BEL inhibition (±SD). (D) Cytotoxicity of various concentrations of BEL using an MTT assay. Bars represent the mean percentage of cytotoxicity after addition of the different BEL concentrations (±SD). (E) Inhibition of ARPE-19 phagocytosis of POS by different BEL concentrations. Bars represent mean percentage of inhibition (±SD). Significance levels: *P < 0.05, **P < 0.001.

 
Inhibition of ARPE-19 Phagocytosis by BEL
The specific iPLA2-VIA inhibitor BEL (10 µM) significantly reduced ARPE-19 phagocytosis of POS (24%; P < 0.01, n = 16; Fig. 5B ). The inhibition was sustained after readdition of POS after 24, 48, and 72 hours (21%; P < 0.05, n = 4), 26% (P < 0.05, n = 4), and 32% (P < 0.05, n = 4), respectively (Fig. 5C) . BEL toxicity was evaluated by MTT as described in the Methods section. Significant toxicity was observed when cells were exposed to BEL concentrations above 20 µM (Fig. 5D) . BEL concentrations between 5 and 20 µM had an equal inhibitory effect on ARPE-19 phagocytosis of POS (Fig. 5E) . The cPLA2-IVA inhibitor AACOCF3 (n = 15; Fig. 5B ) and propranolol (n = 15; data not shown) did not significantly reduce phagocytosis.


   Discussion
Top
 Abstract
 Methods
 Results
 Discussion
References
 
RPE phagocytosis of POS is essential for retinal function, and it has been suggested that alterations in POS degradation may lead to age-related macular degeneration (AMD), the most common cause of irreversible blindness in the Western world.21 22 Besides phagocytizing POS, RPE cells have various additional physiological functions such as supporting the neuroretina, creating part of the blood–brain barrier, and transporting metabolites and water.23 Studies of other phagocytizing cells may be helpful in understanding RPE phagocytosis of POS. PLA2 activity has been demonstrated in macrophages, and it has been shown that PLA2 activity increases during phagocytosis. Among other specific PLA2 subtypes, iPLA2-VIA has been shown to be essential in macrophage phagocytosis.7 9 24 25 Lyso-phosphatidylcholine, a metabolite of iPLA2-VIA activity, seems to generate a signal for phagocytosis, and macrophage phagocytosis can be inhibited by the iPLA2-specific inhibitor BEL.9 Evidence on cPLA2-IVA involvement in macrophage phagocytosis has also been suggested,13 26 whereas no studies have explored a role of iPLA2-VIB in phagocytosis.

In the retina, the literature has described PLA2 activity in the RPE cells as well as in the neuroretina. However, no specific PLA2 has been identified in these tissues, and the current knowledge is based on indirect evidence of substrate-specific PLA2 activity.16 17 27 Based on the previous findings, the purpose of this study was to identify intracellular PLA2 in the human eye, with emphasis on the outer retinal layers, and to evaluate the role of intracellular PLA2 in RPE phagocytosis of POS. Intracellular PLA2 expression was found in various parts of the eye, as outlined in Table 2 . Abundant expression of genes encoding iPLA2-VIA were present in the human ARPE-19 cell line, whereas RPE expression of cPLA2-IVA and iPLA2-VIB was less abundant (Fig. 1A) . The various known splice variants of iPLA2-VIA were identified, including a new splice variant without exon 4, which creates a frameshift and thereby a new possible regulator of iPLA2-VIA activity (Fig. 1B) . Because all splice variants of iPLA2-VIA seem to be present in the ARPE-19 cells, there may be tightly regulated functions of iPLA2-VIA, not only in the phagocytosis of POS but also in other functions of these multifunctional cells. However, the physiological relevance of the splice variants remains to be shown.

On the protein level, expression of iPLA2-VIA, cPLA2-IVA, and iPLA2-VIB were identified, both in the normal human eye sections and the ARPE-19 cells (Fig. 2) . Western blot analysis of iPLA2-VIA revealed ~85- and ~70-kDa bands. The ~85-kDa band has been shown to be a catalytically active iPLA2-VIA, and evidence from pancreatic islets and insulinoma cells shows the significance of the ~70 kDa iPLA2-VIA.28 In the present study the specificity of the ~70 kDa band was furthermore strengthened by immunoprecipitation.

The ~70 kDa band of iPLA2-VIA was upregulated 12 and 24 hours after the addition of POS to ARPE-19 cells indicating a role in RPE phagocytosis. It has been suggested that the high-molecular-weight iPLA2 is proteolytically cleaved to create the low-molecular-weight iPLA2.29 Because the present Western blot analysis reveals decreased expression of the high-molecular-weight iPLA2-VIA in phagocytizing ARPE-19 cells, the induction of the ~70-kDa band may be due to cleavage of the ~85-kDa band. Furthermore, the ~85-kDa band has been shown to include a membrane-binding site,28 and it is therefore tempting to suggest that cleavage possibly leads to the smaller ~70-kDa band, which may relocalize and thereby obtain ability to act in the phagocytosis process. Future studies are necessary, however, to clarify these issues.

Previous studies have shown a role of COX-2 in rat RPE phagocytosis and it is possible that cPLA2-IVA may play a role in this induction.18 However, no significant upregulation of cPLA2-IVA was found (Fig. 4B) and the present study could not confirm an involvement of this subtype in RPE phagocytosis of POS. Finally, no significant regulation of iPLA2-VIB was observed (Fig. 4B) . Involvement of sPLA2 in macrophage phagocytosis has previously been shown7 15 26 and this subgroup of PLA2 may also be involved in RPE phagocytosis of POS. However, the present study did not evaluate possible roles of sPLA2, and future studies should investigate this question. In comparison with published data on PLA2 activity in different cell types, basal PLA2 activity in ARPE-19 cells appears to be relatively high.30 31 In the present study, we showed increased PLA2 activity in phagocytosing RPE cells 8 (not shown) and 12 hours (Fig. 5A) after ARPE-19 cells were fed with POS, whereas no upregulation was seen 4 hours after addition of POS. The delay on increased PLA2 activity suggests that PLA2 activity may be a response to POS engulfment and thereby a mechanism to degrade the membranes and thereby regulate phagocytosis. Of interest, the increased activity could be blocked by BEL, which strongly supports the role of iPLA2-VIA in RPE phagocytosis of POS (Figs. 5B 5C) . When inhibiting phagocytosis with the iPLA2-VIA specific inhibitor BEL, we significantly reduced phagocytosis, whereas no effect was found with the cPLA2-IVA-specific inhibitor AACOCF3. Because PLA2-VIA activity has been implicated in the involvement of normal phospholipid remodeling and several reports have suggested that iPLA2-VIA is one of the main modulators of PC catabolism, our present data support this hypothesis.32 33

In conclusion, in the present study, we explored intracellular PLA2 in the human retina. We confirmed that RPE elicits PLA2 activity and identified iPLA2-VIA, cPLA2-IVA, and iPLA2-VIB on both the mRNA and the protein levels. We report a significant role of iPLA2-VIA in RPE phagocytosis of POS, whereas cPLA2-IVA and iPLA2-VIB do not seem to be essential in this process. Because RPE phagocytosis is critical for vision and is damaged during pathologic processes such as AMD, it is tempting to suggest that iPLA2-VIA could be a target for future pharmacological intervention.


   Acknowledgements
 
The authors thank Sven Erik Nilsson and Staffan Sundelin for valuable help with the isolation and labeling of POS.


   Footnotes
 
Supported by the Hørslev Fonden, The Danish Eye Research Foundation, The Danish Eye Health Society, the Augustinus Fonden, the Fam. Hede Nielsens Fond, the Dir. Ib Henriksens Fond, Civilingeniør Lars Andersens Legat, the Alice and Jørgen A. Rasmussens Mindelegat, Chr. Andersen and hustru Ingeborg Andersen, f. Schmidts legat, and National Eye Institute Grant EY05121.

Submitted for publication July 26, 2006; revised November 2, 2006; accepted January 22, 2007.

Disclosure: M. Kolko, None; J. Wang, None; C. Zhan, None; K.A. Poulsen, None; J.U. Prause, None; M.H. Nissen, None; S. Heegaard, None; N.G. Bazan, None

The publication costs of this article were defrayed in part by page charge payment. This article must therefore be marked "advertisement" in accordance with 18 U.S.C. §1734 solely to indicate this fact.

Corresponding author: Miriam Kolko, Eye Pathology Institute, Frederik d. V’s vej 11, 1st floor, 2100 Copenhagen, Denmark; mkolko{at}dadlnet.dk.


   References
Top
 Abstract
 Methods
 Results
 Discussion
 References
 

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