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vß3
From the Departments of Ophthalmology* and Medical Biophysics and Radiation Biology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; the Department of Ophthalmology, Kagoshima University School of Medicine, Kagoshima, Japan; Apoptosis and Immune System, Centre National de la Recherche Scientifique, Institut Pasteur, Paris, France; and the Centre National de la Recherche Scientifique,¶ Institut Gustave Roussy, Villejuif, France
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Abstract |
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vß3 revealed that phagocytotic clearance involves the PSR as well as integrin vß3 in vivo. Importantly, the level of blockade obtained with these reagents was different. Although anti-PSR increased the frequency of apoptotic cells that fail to bind to macrophages, GRGDSP prevented the engulfment (but not the recognition) of apoptotic photoreceptor cells by macrophages. To our knowledge, this is the first report describing the mechanisms through which apoptotic photoreceptors are selectively eliminated via a directional process in the subretinal space.
Cells dying from apoptosis attract phagocytes, presenting as so-called "eat me" signals, probably by exposing or releasing ligands for receptors on phagocytes. Apoptotic cells develop numerous changes including the exposure of phosphatidylserine (PS) and the alteration of membrane carbohydrates on the cell membrane surface. Several receptors are implicated in the phagocytotic uptake of apoptotic cells by phagocytes, such as phosphatidylserine receptor (PSR),4,5
the vitronectin receptor (vß3 and vß5 integrins),6-8
CD14,9
CD36,10,11
or the scavenger receptor class A.12
The ligand and receptor systems have been well investigated in vitro. However, both their functions and relative importance remain to be established in vivo.13-17
The retina is a highly differentiated neural tissue for vision and exhibits characteristic features of neural apoptosis in various pathologies. As a result, retinal detachment (RD) causes the selective apoptotic demise of retinal photoreceptors. The induction phase of photoreceptor apoptosis in RD has been characterized to some extent,1,18,19 establishing that it involves a caspase-independent apoptotic process3 that can be inhibited by the intraocular injection of brain-derived neurotrophic factor (BDNF).3,20 Importantly, the inhibition of apoptosis allows for the maintenance of the retinal function and the prevention of RD-induced blindness.21 Although the induction phase of photoreceptor apoptosis in RD has been previously reported,1,3,18,21 their clearance phases are still unknown. Identifying the phagocytotic process, including the infiltrating phagocytes, their distribution and recognition systems for apoptotic photoreceptors thus remain an obviously important issue to prevent tissue destruction by their released contents. The destruction of these tissues causes retinal gliosis, and an excessive amount of gliosis is sometimes harmful for the maintenance of retinal regular structure and function.22 Previous studies have identified candidate phagocytes of retinal apoptotic cells in the developmental or pathological processes,23-26 without, however, providing any insight into the mechanism of these processes. Apoptotic photoreceptors have thus been thought to be phagocytosed in the original location of the outer nuclear layer by a diverse range of cells including retinal pigment epithelium (RPE), retinal microglia, infiltrated macrophages, tissue macrophages, glial cells, or neighboring cells.27-29
To elucidate the mechanisms accounting for the elimination of apoptotic photoreceptors, we used a rodent model of RD-induced retinal degeneration.3,21
Unexpectedly, we found that apoptotic photoreceptors are eliminated from their original location, the outer nuclear layer, and thereafter move into the subretinal space, where they are phagocytosed by infiltrating macrophages derived from freshly recruited circulating monocytes. In addition, we also report that the PSR and the integrin vß3 play an instrumental role in the phagocytotic recognition and internalization of apoptotic photoreceptors in vivo.
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Materials and Methods |
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All procedures conformed to the Association for Research in Vision and Ophthalmology’s statement for the Use of Animals in Ophthalmic and Vision Research. Brown Norway rats (Kyudo, Fukuoka, Japan), postnatal 8 weeks, were studied as follows. Rat experimental RD was produced by a previously described method.3,28 Briefly, the rats were anesthetized with an intraperitoneal injection of pentobarbital and their pupils were dilated with topical 1% tropicamide and 2.5% phenylephrine hydrochloride. The retinas were detached using a subretinal injection of 1% sodium hyaluronate (Healon; Pharmacia, Uppsala, Sweden). Sodium hyaluronate (0.05 ml) was gently injected through the sclera into the subretinal space to enlarge the RD. Because the volume of the vitreous space is relatively small, the injection of 0.05 ml sodium hyaluronate reproducibly produced similar RDs (half of the retina). Biomicroscopy (Kowa, Tokyo, Japan) demonstrated that the same portion of the retina remained detached for more than 28 days after treatment. The detached retinas that reattached spontaneously were thus excluded from the further studies. Eyes with an anterior chamber puncture, scleral incision, and no injection of sodium hyaluronate were used as controls. The rats were sacrificed at 6 and 12 hours and on days 1, 3, 5, 7, 14, and 28 after treatment and then their eyes were harvested for the following studies.
Chimera Mouse by Transplantation with Green Fluorescent Protein (GFP)-Transgenic Bone Marrow Cells
Previously, the phagocytes that infiltrated after RD were reported to be RPE, retinal microglia, or monocyte-derived macrophages, however, this identification remains unclear.27,29 To characterize the infiltrating phagocytes, we produced chimera GFP mice, by a previously described method. Briefly, we used transgenic mouse lines with an enhanced GFP (EGFP) cDNA under the control of a chicken ß-actin promoter and cytomegalovirus enhancer (a generous gift from Dr. Masaru Okabe, Osaka University, Osaka, Japan).30,31 All of the tissues from these transgenic lines, with the exception of erythrocytes and hair were green under excitation light. The established transgenic mouse was used as a cell source for GFP-positive bone marrow cells. The GFP-positive cells were transplanted intravenously in C57/B6 mice after irradiation with 9 Gy of X-rays. The eyes were protected with lead shields for prevention of radiation retinopathy. A successful bone marrow transplantation was confirmed by the identification of GFP-positive cells in the blood 2 weeks after irradiation. RD was produced in these chimera mice as described above. These eyes were harvested 3 days after RD, cryosectioned, acetone-fixed, and then were observed by fluorescent microscopy (Olympus, Tokyo, Japan). The eyes from wild-type (wt) mice were used as control eyes.
Terminal dUTP Nick-End Labeling (TUNEL)
Apoptotic photoreceptor degeneration was detected by TUNEL. Four-µm-thick sections were made from samples fixed in 4% paraformaldehyde and embedded in paraffin. TUNEL staining was performed with the ApopTag Fluorescein Direct in Situ Apoptosis Detection Kit (Intergen Company, New York, NY) according to the manufacturer’s protocol. The sections were co-stained with propidium iodide (Molecular Probes, Eugene, OR), thus allowing the observation of the cell nuclei by a fluorescence microscope (Olympus). Ten sections for each eye specimen were randomly selected and observed by masked observers (six eyes for each time point). The results are presented as the means ± SD.
AIF, ED1, and ED2 Immunohistochemistry
Apoptosis-inducing factor (AIF) is a novel, caspase-independent apoptogenic mediator in apoptosis, which is normally confined to the mitochondrial intermembrane space, yet translocates to the cytosol and the nucleus in the apoptotic process.32 In a previous report, we confirmed that the mitochondrio-nuclear relocalization of AIF occurred in this model.3 To clarify whether AIF participated in the late phase of apoptosis in the subretinal apoptotic nucleus, we examined this issue immunohistochemically. Samples were fixed in 4% paraformaldehyde, embedded in paraffin, deparaffinized in xylene, rehydrated in ethanol, and washed in phosphate-buffered saline (PBS), as described above. A 1:100 dilution of anti-AIF rabbit serum was produced by a previously described method32 and incubated at 4°C overnight. A nonimmune serum and a preabsorbed antiserum (with 1 µg/µl of recombinant AIF) were used as negative controls. To characterize the infiltrating phagocytes, anti-ED1, ED2 antibodies (Serotec, Oxford, UK), F4/80 antibody (Caltag Laboratories, Burlingame, CA), anti-pan cytokeratin (DAKO, Glostrup, Denmark), and control IgG were used at a 1:100 dilution. Anti-ED1 antibody recognized monocytes/macrophages, anti-ED2 recognizes tissue macrophages in rat,33 F4/80 antibody recognizes mouse macrophages,34 anti-pan cytokeratin recognizes RPE. Cy5-labeled secondary antibody (Zymed Laboratories, San Francisco, CA) was used at a dilution of 1:200 for 20 minutes. The sections were co-stained by TUNEL and observed by fluorescence microscopy.
Transmission Electron Microscopy and Immunoelectron Microscopy
The eyes were enucleated and the posterior segments were fixed in 1% glutaraldehyde and 1% paraformaldehyde in PBS. The detached retinas were removed and postfixed in veronal acetate buffer osmium tetroxide (2%), dehydrated in ethanol and water, and embedded in Epon. Ultrathin sections were cut from blocks and mounted on copper grids. For immunoelectron microscopy, the eyes were fixed in 1% paraformaldehyde in PBS, and the detached retinas were rinsed with PBS, incubated in NH4Cl, and embedded in London Resin white blocks (London Resin, London, UK). Primary antibody for AIF was used at a 1:150 dilution, and the sections were incubated at 4°C overnight. A nonimmune serum was used as a negative control. Anti-rabbit antibody conjugated with 10-nm gold particles (British BioCell, Cardiff, UK) was used as a secondary antibody at a dilution of 1:30 for 90 minutes. The specimens were observed with a JEM 100CX electron microscope (JEOL, Tokyo, Japan).
Scanning Electron Microscopy
The removed retinas were postfixed in veronal acetate buffer osmium tetroxide (2%), and dehydrated in ethanol and water. The retinas were saturated in t-butyl alcohol, and critical point drying was performed (Eiko, Tokyo, Japan). The tissue was then placed on stubs by means of self-adhering carbon tabs and sputtered with Au of 20-nm thickness by argon plasma coater (Eiko). Next, the subretinal surface of the detached retina was studied by a JEM 840 scanning electron microscope (JEOL).
Inhibition of Phagocyte Infiltration by Preventing Apoptosis Development
It was reported that BDNF inhibited photoreceptor apoptosis after RD.3,20,21 To investigate the relationship between photoreceptor apoptosis and phagocyte infiltration, we administered BDNF (2.5 ng per eye; R&D Systems, Minneapolis, MN) into the subretinal space. To clarify whether apoptotic photoreceptors attract phagocytes, the phagocyte infiltration into the subretinal space was determined on day 3. The number of cells per 1-mm retina in 10 histological sections for each eye was measured and six eyes were analyzed using analysis software (MacScope; Mitani, Fukui, Japan). The results were expressed as the means ± SD.
Blockade of Phagocytotic Process by Inhibiting Receptor Systems
To investigate the participation of candidate receptors for phagocytosis of apoptotic photoreceptors, we used RGD peptide (Bachem, Bubendorf, Switzerland), anti-integrin ß3 antibody (clone F11; BD Pharmingen, San Diego, CA) for integrin vß3, and anti-PSR antibody (Cascade BioScience, Winchester, MA). The integrin vß3 and PSR are shown to be present on monocyte-derived macrophages.10,35
The function-blocking hexapeptide GRGDSP including the integrin vß3-binding motif RGD, and nonfunctioning control hexapeptide GRGESP were administered into the subretinal space mixed in 1% sodium hyaluronate at a concentration of 2.0 mg/ml. Anti-integrin ß3 antibody, which blocks integrin vß3 binding, and control IgG were injected with 1% sodium hyaluronate at a concentration of 1.0 mg/ml. Anti-PSR antibody, which blocks phosphatidylserine binding, and control IgM were injected at a concentration of 1.0 mg/ml. The eyes were then harvested on day 3 and analyzed by immunohistochemistry, transmission electron microscopy, and scanning electron microscopy. The number of cells per 1-mm retina in 10 histological sections for each eye was measured and six eyes were analyzed using analysis software (MacScope). The results were expressed as the means ± SD. Student’s t-test was used to calculate the probability by comparing data between the groups and P < 0.05 was considered to be significant.
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Results |
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After the injection of sodium hyaluronate into the subretinal space of rats, RD was followed macroscopically and histologically for 28 days. Macroscopically, the detached area remained unchanged during this period. TUNEL-positive apoptotic cells appeared mainly in the photoreceptors starting 12 hours after RD, reached a maximum on day 3 (Figure 1, A and B
, arrowheads), and then gradually decreased.3
Although most TUNEL-positive signals were observed in the outer nuclear layer, some signals were observed in the outer segment layer and subretinal space (Figure 1
, arrows). In control eyes without RD, no TUNEL-positive signals were observed in any of the layers (Figure 1C)
.
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RD-induced apoptotic morphological alterations, including chromatin condensation, cell shrinkage, and apoptotic body formation were observed in the photoreceptors (Figure 2
; A to D). In the apoptotic body formation process, nucleolar components are tightly aggregated (Figure 2B)
, separated into semi-dense granular masses (Figure 2C)
and forms electron-dense linear strands (Figure 2D)
. As electron-dense apoptotic body formation developed, the electron-dense materials became detectable in the inner and outer segment layers and the subretinal space (Figure 2
; E to G). Figure 2E
shows the electron-dense materials just passing through the outer limiting membrane, which consisted of portions of Müller cells with adherent junctions. These electron-dense materials are apparently mixed with other cytosolic structures such as mitochondria (Figure 2E)
. The electron-dense materials were found among the normal outer segments in outer segment layer (Figure 2, F and G)
.
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Apoptotic photoreceptor nuclei stain positively with an antibody specific for the AIF protein, thus indicating the translocation of this protein from the mitochondria to the nucleus (Figure 3, A and B)
.3
As photoreceptor apoptosis developed, TUNEL-positive signals were also detected in the outer segment layer, and these are still positive for AIF (Figure 3A)
. Immunoelectron microscopy showed the electron-dense materials in the outer segment layer to be AIF-positive by gold particles (Figure 3C)
. The nonimmune serum and preabsorbed serum showed no positive staining for AIF (data not shown).
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Phagocyte infiltration into the subretinal space occurred 2 days after RD. Most infiltrating phagocytes contained in the subretinal space (88%) bore the characteristic phenotype of monocyte-derived macrophages (ED1+, ED2-; Figure 4
; A to C) while a minority was consisted of cells bearing the specific phenotype of RPE (pan cytokeratin+; Figure 4D
). Most if not all ED1+ cells were located in the outer segment layer of photoreceptors or the subretinal space of the detached retina (Figure 4A)
. A low frequency of ED2+ cells, namely tissue macrophages, were detected in the inner layers of the detached retina (Figure 4B)
, yet were never found to phagocytose apoptotic debris. Double-staining experiments confirmed that ED1+ macrophages phagocytosed TUNEL+ apoptotic bodies (Figure 4C)
. The free RPE that migrated into the peripheral area of the detached retina were positive for a specific marker, pan cytokeratin (Figure 4D)
.
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To further elucidate the origin of phagocytes, we used chimera mice, reconstituted with bone marrow-expressing transgenic GFP. Although such mice normally lack bone marrow-derived (GFP+) macrophages in their retina (Figure 5A)
, they exhibit infiltrating GFP+ phagocytes several days after RD (Figure 5B)
. The infiltrated GFP+ phagocytes are positive for mouse macrophage marker F4/80 (Figure 5C)
. The 84% of the total infiltrated phagocytes are GFP+, F4/80+ cells in the chimera mouse. The GFP+ cells were never seen in the wild-type control mice after RD (Figure 5D)
.
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Ultrastructural observations could differentiate two types of infiltrating cells. One is a middle-sized (10 µm) macrophage-like cell abundant with lysosomes and finger-like processes (Figure 6
; A to C), whereas the other is a large (15 µm), round cell abundant with melanin granules (Figure 6
; D to F). The infiltrating macrophage-like cells phagocytosed apoptotic condensed nuclei rather than degenerated outer segment debris (Figure 6A)
. These macrophage-like cells apparently infiltrated from choroidal vessels, and migrated through the Bruch’s membrane and RPEs toward the subretinal space (Figure 6C)
. The other melanin-rich round cells also migrated and infiltrated into the subretinal space from the peripheral area of the detached retina (Figure 6
; D to F). Early after RD, the macrophage-like cells mostly phagocytosed the apoptotic nuclei (Figure 6A)
, while later on the pattern of digestion changed. As the apoptotic photoreceptor decreased on days 14 and 28, these cells instead phagocytosed the degenerated outer segment of the photoreceptors (data not shown).
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In control retina without RD, both apoptotic photoreceptors and apoptotic debris were rarely seen (Table 1
and Figure 1C
). No phagocyte infiltration was noted in subretinal space of control retina (Table 1)
. RD induced photoreceptor apoptosis as well as phagocyte infiltration in the subretinal space. The subretinal injection of a neurotrophic factor, BDNF, dramatically reduced photoreceptor apoptosis and phagocyte infiltration into subretinal space (Table 1)
. In contrast, the injection of anti-PSR antibody, RGD peptide, and anti-integrin ß3 antibody increased apoptotic debris and phagocyte infiltration (Table 1)
.
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An antibody specific for the PSR, capable of blocking the interaction between PSR and PS,35
was administered into the subretinal space when RD was induced. Eyes were harvested 3 days later, and then were fixed and embedded in paraffin. The sections were double-stained by TUNEL and propidium iodide and 10 sections for each eye specimen were randomly selected and observed in a masked manner (n = 6). The subretinal apoptotic bodies were classified as free, as bound to macrophages, or as phagocytosed (Figures 7 and 8)
. Anti-PSR significantly blocked the uptake of apoptotic photoreceptor debris by macrophages (Figures 7 and 8)
. As a result, the free apoptotic debris increased from 10 per 1-mm retina in controls injected with a control IgM to 17 per 1-mm retina in animals treated with anti-PSR (Figure 8
, anti-PSR IgM, P < 0.05). These data indicate that the PS-PSR interaction has a rate limiting effect on the macrophage-mediated recognition of apoptotic photoreceptor cells from the subretinal space.
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The hexapeptide GRGDSP includes the integrin vß3-binding motif RGD and thus blocks the interaction between vß3 and vß3 ligands such as vitronectin.10
The local injection of this peptide blocked macrophage phagocytosis of apoptotic photoreceptors (Figures 7 and 8)
. Although the infiltrated macrophages recognized and collected apoptotic debris, which apparently bound to their surface, subsequent internalization was blocked by GRGDSP (Figures 7 and 8)
. Scanning electron microscopy revealed that macrophages selectively recognized and collected apoptotic debris yet failed to engulf apoptotic bodies (Figure 7F)
. As an internal control, the peptide GRGESP (which lacks the RGD sequence) did not block the phagocytotic uptake of apoptotic debris, and never caused an increase of bound apoptotic debris on the infiltrated phagocytes (Figure 8)
. The results were confirmed by the antibody clone F11 (anti-integrin ß3 antibody), which blocks the integrin vß3. This antibody also blocked the internalization of apoptotic bodies by phagocytes, thus resulting in an increased amount of bound apoptotic debris and infiltrating phagocytes (Figure 8
and Table 1
). These data underscore the importance of an interaction between integrin vß3 and an RGD motif-containing vß3 ligand for the engulfment of apoptotic cells in our model.
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Discussion |
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vß3 participates in internalization of the apoptotic photoreceptors in vivo. Apoptotic Photoreceptors Eliminated from the Retina in the Late Phase of Apoptosis
Photoreceptor apoptosis after RD has attracted the interest of neural researchers and has been studied extensively.1,3,18-21,36
In this process, photoreceptors develop the characteristic morphological features of apoptosis (initial phase), followed by a clearance process that, schematically, can be subdivided into the subsequent steps of recognition, binding, engulfment, and digestion of apoptotic bodies by phagocytes (late phase). The initial phase has been studied in detail, however, the late phase has not yet been reported. In this study, we clearly showed this late phase of photoreceptor apoptosis after RD for the first time. Previously, Erickson and colleagues37
reported that a loss of photoreceptors occurred both by necrosis and by the migration of photoreceptor into the subretinal space after RD. However, both the origin and mechanism of the late phase still remain unclear. In this study, we demonstrated apoptotic photoreceptors to show chromatin condensation (Figure 2B)
, electron-dense apoptotic body formation (Figure 2C)
, and electron-dense linear strands (Figure 2D)
. As apoptotic body formation developed, the electron-dense materials became detectable in the inner and outer segment layer and the subretinal space (Figure 2
; E to G). To detect the apoptotic DNA degradation, we examined TUNEL. Although most TUNEL-positive signals were observed in the outer nuclear layer, some signals were observed in the outer segment layer and subretinal space. In this process, we found that AIF, an apoptogenic protein that translocates from the mitochondria to the nucleus after apoptosis, was observed in these electron-dense materials in the outer segment layer, suggesting that these are derived from apoptotic nuclei (Figure 3)
.
Considering the ultrastructural findings as well as TUNEL and AIF immunohistochemistry, because photoreceptor nuclei are normally located in the outer nuclear layer and are usually not found in the inner and outer segment layers or the subretinal space, these electron-dense materials are likely to be displaced apoptotic photoreceptor nuclei from their original location.
During this process, the nuclei translocated from the original nuclear layer into the subretinal space, thus crossing the outer limiting membrane and the outer segment layer. The mechanism through which this active transport of nuclei occurs remains unclear. On theoretical grounds it could be a cell-autonomous process involving an active contraction of the outer part of the cell or it could involve passive processes depending on the specific architecture of the retina. Excreted nuclei from dead photoreceptor cells were effectively phagocytosed by monocyte-derived macrophages that remained confined to the subretinal space. As a result, the neural retina was not invaded by destructive inflammatory cells.
Characterization of Infiltrating Phagocytes after RD
Although detailed ultrastructural studies have been made on infiltrating phagocytes after RD, their characterization and origin have remained elusive.27,28,38,39
In this study, we used three antibodies that positively identify monocyte-derived macrophages (ED1), differentiated tissue macrophages (ED2), or RPE (pan cytokeratin), respectively. Those phagocytes that infiltrated into the subretinal space were either ED1+ macrophages (88% of total infiltrated phagocytes) or pan cytokeratin+ RPEs (12%) (Figure 4)
. The ED1+ macrophages infiltrated into the subretinal space after RD (Figure 4A)
, and selectively phagocytosed TUNEL-positive apoptotic debris (Figure 4C)
. To confirm the origin of these infiltrating phagocytes, we produced chimera mice, namely wild-type C57/B6 mice transplanted with bone marrow cells from GFP-transgenic mice. In such chimera mice, no GFP-positive cells were found in the normal retina (Figure 5A)
, and GFP-positive cells only infiltrated into the subretinal space after RD (Figure 5, B and C)
. These results provide compelling evidence that the phagocytes that remove dead photoreceptor nuclei are derived from the transplanted GFP+ bone marrow cells, and not from retinal cells such as glial cells. Scanning electron microscopy showed two different types of infiltrating phagocytes in the subretinal space (Figure 6)
. Considering the results in immunophenotypic studies, these phagocytes were macrophages and RPEs. These macrophages infiltrated from choroidal vessels into the subretinal space beyond the RPE layer (Figure 6C)
. Surprisingly, the subretinal injection of a neurotrophic factor, BDNF dramatically reduced both photoreceptor apoptosis and macrophage infiltration into the subretinal space (Table 1)
. The results indicate that monocyte-derived macrophages are selectively called for phagocytotic clearance by apoptotic photoreceptors, not by surgical injury itself.
In addition to macrophages, a small amount of RPE was found to migrate and infiltrate into the subretinal space in the peripheral area of the detached retina (Figure 4D
and Figure 6
; D to F), as previously described.27,28,38,39
RPEs (ED1-ED2-GFP-pancytokeratin+) can be readily distinguished from the macrophages by electron microscopy, based on their pigment content, round surface, and the large size (Figure 6
; D to F). Scanning electron microscopy also showed that the RPEs migrated from the RPE layer beneath the detached retina (Figure 6F)
, as described previously.27
As a result, the infiltrating phagocytes were macrophages and RPEs, and most infiltrating phagocytes were confirmed to be ED1+, monocyte-derived macrophages, participating in the clearance of photoreceptors.
Phagocytotic Clearance of Apoptotic Photoreceptors Depends on the PSR for the Recognition and the Integrin vß3 for Internalization
The phagocytotic processes of apoptosis may include the recognition, binding, internalization, and digestion of apoptotic cells. In our model of RD, the infiltrating macrophages reached apoptotic bodies by elongating filopodia (Figure 7D)
. The anti-PSR antibody inhibited the selective elongation of filopodia to the apoptotic body, presumably by blocking the interaction between PS on the apoptotic photoreceptors and the PSR on macrophages (Figure 7, B and E)
. Although macrophages did phagocytose apoptotic bodies, the internalization process is seldom observed under normal conditions. This may be because of the rapid execution of the internalization process. Surprisingly the function-blocking hexapeptide GRGDSP including integrin vß3-binding motif RGD, and anti-integrin ß3 antibody, effectively inhibited this internalization process but did not affect either the recognition or binding processes (Figure 7, C and F
, and Figure 8
). Scanning electron micrographs clearly demonstrated that many apoptotic bodies were trapped and accumulated on the macrophage surface, yet were not engulfed (Figure 7F)
. These data demonstrate that effective phagocytotic clearance depends on the PSR for apoptotic photoreceptor recognition, and on the integrin vß3 for the internalization of apoptotic photoreceptors in vivo.
In conclusion, the present study revealed the mechanisms through which the selective elimination of apoptotic photoreceptors can be performed in a unique way, which guarantees the conservation of overall retinal tissue architecture after RD. One unresolved issue remains concerning the question as to how apoptotic photoreceptor nuclei translocate from the neural retina to the subretinal space. Further studies are thus called for to clarify this conundrum.
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Acknowledgements |
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Footnotes |
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Supported in part by grants-in-aid for Scientific Research from the Ministry of Education, Science, Sports, and Culture of the Japanese Government (nos. 09671804 and 09470382) and the Japan National Society for the Prevention of Blindness (Tokyo).
Accepted for publication February 26, 2003.
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