- Open Access
Microglia are not required for prion-induced retinal photoreceptor degeneration
Acta Neuropathologica Communications volume 7, Article number: 48 (2019)
Degeneration of photoreceptors in the retina is a major cause of blindness in humans. Often retinal degeneration is due to inheritance of mutations in genes important in photoreceptor (PR) function, but can also be induced by other events including retinal trauma, microvascular disease, virus infection or prion infection. The onset of apoptosis and degeneration of PR neurons correlates with invasion of the PR cellular areas by microglia or monocytes, suggesting a causal role for these cells in pathogenesis of PR degenerative disease. To study the role of microglia in prion-induced retinal disease, we fed prion-infected mice a CSF-1 receptor blocking drug, PLX5622, to eliminate microglia in vivo, and the effects on retinal degeneration were analyzed over time. In mice not receiving drug, the main inflammatory cells invading the degenerating PR areas were microglia, not monocytes. Administration of PLX5622 was highly effective at ablating microglia in retina. However, lack of microglia during prion infection did not prevent degeneration of PR cells. Therefore, microglia were not required for the PR damage process during prion infection. Indeed, mice lacking microglia had slightly faster onset of PR damage. Similar results were seen in C57BL/10 mice and transgenic mice expressing GFP or RFP on microglia and monocytes, respectively. These results were supported by experiments using prion-infected Cx3cr1 knockout mice without PLX5622 treatment, where microglial expansion in retina was delayed, but PR degeneration was not. Contrary to predictions, microglia were not a causative factor in retinal damage by prion infection. Instead, newly generated PrPSc accumulated around the inner segment region of the PR cells and appeared to correlate with initiation of the pathogenic process in the absence of microglia.
Prion diseases are transmissible neurodegenerative diseases of the CNS which occur in humans and animals. These diseases are caused by an infectious agent composed primarily of a misfolded host-derived protein known as prion protein (PrP or PrPC). Hallmarks of prion disease in the CNS are deposition of misfolded protease-resistant prion protein (PrPres or PrPSc), as well as microgliosis, astrogliosis, and vacuolation of gray matter followed by neurodegeneration [3, 20]. Typically, gliosis occurs prior to vacuolation or neuronal death, suggesting that activated glia might be involved both in causing the pathogenesis and in participating in the host response against the infection and damage. Although prion disease primarily involves brain and spinal cord, other tissues such as peripheral nerves, retina, intestines and lymphoid tissues are also infected.
In the current paper, we studied retinal degeneration caused by prion infection, which has been known for many years [1, 5]. Due to the devastating nature of the brain degeneration seen in typical human prion diseases, retinal damage is not considered a major clinical issue. However, the unique spatial organization of neurons and other cells in retina provides an opportunity to study prion-induced neuropathogenesis in a slightly less complex context than brain, perhaps allowing more accurate understanding of the detailed mechanisms of neuronal pathogenesis.
Destruction of photoreceptors and loss of photoreceptor (PR) cell bodies is a major feature of the retinal pathology induced by infection with both human and animal prions [5, 15, 17, 19]. High levels of prion infectivity can be detected in retinal tissue of animals by in vivo bioassay [6, 18, 22]. In humans with prion disease, infectivity could be detected in ocular tissue , and prion seeding activity has been detected by RT-QUIC in retinas from CJD patients . In multiple models, disease-associated PrPSc, astrogliosis, and microgliosis were observed in areas of degeneration in the PR areas [4, 17, 19, 22, 23, 39], thus mirroring the typical pathogenic findings in prion-infected brain.
The pathology of prion-induced retinopathy is similar to that seen in inherited PR degeneration diseases in humans. These diseases, known collectively as retinitis pigmentosa, are associated with over 44 different mutations in a variety of genes . Inherited PR degeneration is usually associated with an influx of activated microglia into the PR areas, including the outer segment (OS), inner segment (IS) and outer nuclear layer (ONL). Many observations suggest that these microglia contribute to damage of PR cells [40,41,42]. For example, microglia have been suspected of contributing to PR degeneration by secretion of chemotactic and inflammatory cytokines, generation of reactive oxygen and nitrogen species, and by aberrant phagocytosis of living PR cells [35, 40]. Because of the evidence suggesting that microglia contribute to inherited PR degeneration, coupled with the similarities in pathology between these inherited diseases and prion-induced PR degeneration, we suspected that microglia also have a causative role in prion-induced retinal disease. To determine more precisely the role of microglia in various pathologic conditions, ablation of microglia has been attempted by several methods including administration of toxins or drugs targeted to microglia or use of transgenic mice to express toxins in microglia . However, most of these methods have some technical drawbacks limiting their utility. Recently PLX5622, a new orally administered drug, which blocks the microglial CSF-1 receptor was found to rapidly eliminate most CNS microglia in vivo and has been beneficial in elucidating the role of microglia in a variety of systems [9,10,11, 37].
In our previous work using PLX5622 to study prion diseases, microglia could be suppressed for many months with continued drug administration . Furthermore, in this study, ablation of microglia by treatment with PLX5622 revealed that microglia were not required for induction of clinical prion brain disease and instead had an important beneficial effect in delaying progression of prion brain disease by 20 to 30 days.
In the present paper, we used PLX5622 to study the role of microglia in prion-induced retinal degeneration. Due to the above-mentioned similarities between inherited PR disease and prion-induced PR disease, we hypothesized that microglia might be required for prion-induced retinal disease and might not have a beneficial effect as was seen in our earlier brain experiments. However, the present experiments using microglia ablation by PLX5622 did not support this hypothesis. The results indicated that after prion infection of retina, microglia were not required for PR degeneration. Moreover, there was evidence suggesting that PR degeneration in the absence of microglia was more rapid than when microglia were present. Thus, the contribution of microglia in brain and retina appeared to be similar during prion infection.
All mice were housed at the Rocky Mountain Laboratories (RML) in an AAALAC-accredited facility in compliance with guidelines provided by the Guide for the Care and Use of Laboratory Animals (Institute for Laboratory Animal Research Council). Experimentation followed RML Animal Care and Use Committee approved protocol 2016–042.
C57BL/10SnJ mice were obtained from an in-house breeding colony, these mice are noted as C57BL/10 throughout the paper. TgGFP/RFP mice were generated by crossbreeding Cx3cr1 knockout mice homozygous for the Cx3cr1-GFP targeted mutation (B6.129P-Cx3cr1tm1Litt/J,The Jackson Laboratory, Stock No: 005582) with Ccr2 knockout mice homozygous for the Ccr2-RFP targeted mutation (B6.129(Cg)-Ccr2tm2.1Ifc/J,The Jackson Laboratory, Stock No:017586) [21, 34]. Resultant offspring had heterozygous expression of both Cx3cr1 and Ccr2. In addition, green fluorescent protein (GFP) was expressed under promoter for Cx3cr1, prominently expressed by microglia in the CNS and red fluorescent protein (RFP) was expressed under the promoter for Ccr2, prominently expressed by monocytes . All mice were group housed in transparent cages in a 12 h light (250-300 lx) /12 h dark cycle and food and water were available ad libitium.
Mice (4–6 weeks old) were injected intracerebrally (i.c.) in the left hemisphere with 30 μl of a 1% (wt/vol) dilution of brain homogenate pools from C57BL mice terminally ill from 79A scrapie. Titer was determined in previous i.c. endpoint titration experiments and was 9.6 × 107 LD50 (units = 50% infectious dose (ID50)/gm of brain) . Therefore, mice received 2.9 × 104 LD50 in a volume of 30 μl. Brain homogenates were diluted for inoculation in phosphate-buffered balanced saline (PBBS) pH 7.2, supplemented with 2% fetal bovine serum (Hyclone, Logan, UT). Observations were made daily to assess signs of scrapie disease, which included ataxia, altered gait, wasting, kyphosis, hind limb weakness, somnolence and immobility. Mice were judged clinical when they displayed severe, consistent neurologic signs. At selected time points, both pre-clinical and clinical, mice were euthanized by isoflurane anesthesia overdose followed by perfusion with 10 ml of saline. Eyes were collected for use in immunohistochemistry or whole retinal flat mount preparations.
To deplete retinal microglia, mice (C57BL/10 and tgGFP/RFP) were fed purified rodent diet AIN-76A (D10001, Research Diets, Inc.) with or without supplementation with compound PLX5622 (1200 mg/kg chow, kindly provided by Plexxikon Inc., Berkeley, CA). Specifically, C57BL/10 mice were fed control chow for 14 days after 79A scrapie-inoculation to allow mice to convalesce. Then “treated” mice were switched to PLX5622 supplemented chow and maintained on this diet until the experimental endpoint. TgGFP/RFP mice received a delayed treatment protocol; after inoculation with 79A scrapie, mice were fed control chow for 90 days, and then the “treated” group was switched to chow supplemented with PLX5622. Mice were then maintained on supplemented chow until the experimental endpoint.
Histology and Immunohistochemical detection of PrPSc, GFAP, Iba1, GFP and RFP
Eyes for immunohistochemistry were removed, placed in 10% neutral buffered formalin for 3 to 5 days and then processed by dehydration and embedding in paraffin. Each eye was embedded as a single block and 5 μm sections were cut using a standard Leica microtome, placed on positively charged glass slides, and air-dried overnight at room temperature. The following day slides were heated in an oven at 60 °C for 20 min. A Ventana automated Discovery XT stainer was used for deparaffinization, antigen retrieval and staining, unless noted otherwise below.
PrP antigens were exposed by incubation in CC1 buffer (Ventana) containing Tris-Borate-EDTA, pH 8.0 for 100 min at 95 °C. Staining for PrP was done using human anti-PrP monoclonal antibody D13  which was obtained from tissue culture supernatants made in our laboratory from CHO cells expressing the D13 antibody construct, which were kindly provided by Dr. R. Anthony Williamson, The Scripps Research Institute, La Jolla, CA. D13 culture fluid was used at a dilution of 1:100 for 2 h at 37 °C. The secondary antibody was biotinylated goat anti-human IgG at 1:500 dilution (Jackson ImmunoResearch, West Grove, PA.), and avidin-horseradish peroxidase was used with DAB as chromogen (DAB Map kit; Ventana Medical Systems, Tucson, AZ.).
Antigen retrieval for other targets was done using CC1 buffer at 100 °C for 44 min (Iba1), 60 min (RFP) or 20 min (GFAP). For GFP antigen retrieval, a Biocare Medical DC2002 Decloaking chamber with sodium citrate buffer at pH 6.0(0.01 M) was used for 20 min at 120 °C / 20 PSI and cooled to 80 °C. Microglia were stained with rabbit anti-Iba1 (1:2000) which was a gift from John Portis, Rocky Mountain Laboratories, Hamilton, MT. Retinal astrocytes and Müller cells were stained with rabbit anti-glial fibrillary acidic protein (GFAP) at (1:3500) (Dako). Green fluorescent protein (GFP) was stained using anti-GFP mouse monoclonal (Roche, ref.#11814460001, 1:200), and red fluorescent protein (RFP) was stained with anti-RFP rabbit polyclonal (ab124754, Abcam, 1:100). Primary antibodies were diluted in PBS with 1% normal goat serum and 0.1% Triton X-100. Diluent without antibody was used as a negative control. Ventana streptavidin-alkaline phosphatase protocol was used to detect Iba1 and GFAP as described previously  with the exception that Fast-Red chromogen was used. Detection of GFP and RFP also used the Ventana streptavidin-alkaline phosphatase protocol with secondary antibodies; biotinylated horse anti-mouse IgG (vector ba-2000) and biotinylated goat anti rabbit-IgG (Biogenex pre-dilute cat#HK3369R), respectively and DAB as chromogen. Slides were examined, and photomicrographs were taken and observed using an Olympus BX51 microscope and Microsuite FIVE software.
Flat mount preparation and confocal microscopy
After enucleation, tgGFP/RFP mouse eyes were placed in 10% neutral buffered formalin for 2 h. Formalin was removed, and eyes were washed with PBS. The eyes were transferred to a culture dish and under a dissection microscope, the anterior part of the eye was removed with a circular cut at the ora serrata. The lens, iris and optic nerve were removed and using micro-forceps, light pressure was applied to the posterior area of the sclera until the retina separated from the retinal pigment epithelium (RPE) and sclera. Once the retina was carefully removed, it was flattened, vitreal side up on a microscope slide. To avoid curling, radial cuts were made in a symmetrical four-leaf pattern. ProLong Gold (ThermoFisher) mounting media was applied and the retina was coverslipped for viewing. Analysis of retinal flat mounts was completed on a confocal laser-scanning microscope (Zeiss LSM 710, Carl Zeiss, Germany). A Z-stack of 40–70, 1 μm optical sections was taken for each retinal area photographed, and data were analyzed using IMARIS software (version 8.4.1).
The number of mice studied by retinal flat mounts was as follows: ND group, 3 uninfected, 12 infected; PLX group, 2 uninfected, 10 infected. At dpi = 82 (ND only), 104, 118, 129 (PLX only), 131, 134 (PLX only), 144 (ND only), and 153 (ND only), retinas from 1 to 3 mice of each group were examined.
Slide scanning,quantitative analysis of pathology and statistical analysis
Aperio Digital Pathology Systems (Aperio Technologies, Vista, CA) was used to scan, capture, and store whole slide images from histology samples. Immunohistochemical slides were scanned with the ScanScope® XT at 20X magnification. ImageScope™ software (Aperio ImageScope v220.127.116.110) and Aperio software (eSlide Manager Version 18.104.22.16829) was used to view, export and analyze e-slide images in JPEG format. Quantitative analysis of outer nuclear layer (ONL) thickness was performed on H&E-stained, 5 μm vertical sections showing complete retina at least 250 μm from the optic disc. To document disease-associated thinning of the ONL, three measurements, from the outer limiting membrane to the outer plexiform layer, were taken per mouse and averaged. The number of Iba1-positive, GFP or RFP cells in the photoreceptor layer was determined by counting the number of positive cells with nuclei in the IS and OS for two complete retinal sections. These numbers were averaged for each mouse. All statistical analysis was performed using GraphPad Prism software, version 7.04, details of statistical tests performed are described in the figure legends.
Deparaffinized sections (prepared as described above) were stained using a Click-iT TUNEL Alexa Fluor 488 Imaging assay kit (Life Technologies, #C10245) following the included protocol. Stained sections were analyzed using an Olympus BX51 fluorescent microscope and Microsuite FIVE software. In order to quantitate apoptosis, the number of TUNEL stained nuclei were counted in two complete retinal sections, per mouse eye and averaged.
Prion-induced retinal degeneration associated with gliosis and destruction of photoreceptor cells
In the present experiments, we studied the retinal degeneration process in mice after i.c. infection with scrapie strain 79A. In most experiments, we used double transgenic mice (tgGFP/RFP) in which microglia expressed GFP under control of the Cx3cr1 promoter and monocytes expressed RFP under control of the Ccr2 promoter, in order to be able to better distinguish microglia from monocytes [21, 34]. In some experiments C57BL/10 mice were also studied. After i.c. scrapie injection, prions infect the brain locally and rapidly spread via neuronal circuitry to retina as well as to various brain regions [17, 24]. In C57BL/10 mice and tgGFP/RFP mice, early clinical neurological signs such as abnormal gait and ataxia were noted starting as early as 125 dpi, and mice reached the clinical disease endpoint requiring euthanasia between 153 and 168 dpi.
To follow the onset and progression of eye disease mice were euthanized at various times, and brain and eye tissues were examined by histopathology. In both C57BL/10 and tgGFP/RFP mice, signs of retinal damage were initially noted at 118 to 128 dpi when thinning of the outer nuclear layer (ONL) was first observed, photoreceptors appeared to be disorganized, and mononuclear cells were seen in the PR areas. At 150 to 165 dpi, there was extensive retinal degeneration as indicated by loss of photoreceptor cells and their nuclei in the ONL, examples of retinas from prion-infected tgGFP/RFP mice at 124 and 153 dpi are shown in Fig. 1.
In our previous work on retinal degeneration induced by hamster scrapie prions, we found evidence for apoptosis as the mechanism of destruction of photoreceptor cells . Similarly, in the present studies, using scrapie strain 79A to infect tgGFP/RFP and C57BL/10 mice, apoptosis was noted by TUNEL assay in the photoreceptor cell nuclei located in the ONL (Fig. 2a-c). Furthermore, staining with anti-GFAP showed presence of activated astroglia (Müller cells) with bipolar processes often spanning the width of the retina (Fig. 2d-f), and staining with anti-Iba1 showed many positive cells with the morphology of activated microglial cells. This was seen in all retinal layers, but most strikingly in the PR (ONL,OS and IS) areas (Fig. 2h-i), where Iba1-positive cells were rarely seen in normal animals (Fig. 2g).
Depletion of microglia in retinas of uninfected mice after treatment with PLX5622
Although the preceding experiments detected microglia in retinas of scrapie-infected mice around the time of retinal degeneration, it was unclear whether these microglia were initiators of the damage or responders to the damage, or both. To investigate this matter, mice were given the CSF-1 receptor blocking drug, PLX5622, to ablate microglia to study their role in retinal degeneration. In uninfected tgGFP/RFP mice, oral administration of PLX5622 led to dramatic reduction of microglia in retina by 7 days post-treatment (Fig. 3a, b), and similar results were seen in retinas of C57BL/10 mice. This reduction was maintained as long as treatment was continued, in some cases over 180 days  .
PLX5622 treatment of scrapie-infected C57BL/10 mice
To investigate the effect of microglia depletion during scrapie infection, scrapie-infected C57BL/10 mice were started on PLX5622-containing chow at 14 dpi, similar to previous experiments studying scrapie brain disease . PLX5622-containing chow was maintained for the duration of the experiment (PLX group). Additional scrapie-infected mice received chow with no drug (ND group) to serve as a control group. In the ND group, early clinical signs were detectable around 125 dpi, and severe signs requiring euthanasia were seen between 155 and 165 dpi. In contrast, in the PLX group early clinical signs were noted around 105 dpi and severe signs were seen 129 and 139 dpi. Thus, as was reported previously , treatment with PLX5622 accelerated the clinical course of scrapie brain disease by about 20 days compared to untreated ND mice.
In the present experiments, retinas were removed at various times for histological examination. In C57BL/10 mice, in the ND group, Iba1-positive cells appeared in the IS and OS layers of the PR region starting at 125 dpi with a peak of around 30–40 cells per retinal section circumference between 140 and 160 dpi (Fig. 4a). However, in the PLX group, Iba1-positive cells were not present in any of the IHC sections analyzed. Therefore, PLX5622 appeared to abolish the host Iba1-positive cell response to scrapie infection in retina suggesting that the infiltrating cells might be mostly microglia.
As noted in our previous report  and above in Fig. 2a-c, apoptosis in the ONL region is an early feature of prion-induced retinal damage. Therefore, to investigate whether treatment of C57BL/10 mice with PLX5622 interfered with this damage, apoptosis was also studied in retinal tissue of scrapie-infected ND and PLX mice. In this experiment, similar levels of apoptosis were seen in the ONL of retinas in both ND and PLX groups starting at 118 dpi (Fig. 4b). Thus, scrapie-induced photoreceptor cell death appeared to proceed similarly in the presence or absence of Iba1-positive cells. Furthermore, progressive severe depletion of photoreceptor cells, as measured by thinning of the ONL occurred in both PLX and ND mice (Fig. 4c). There was a suggestion that ONL thinning appeared slightly earlier in the PLX group compared to the ND group; however, this difference was not statistically significant.
PLX5622 treatment of scrapie-infected tgGFP/RFP mice
To distinguish between microglia and monocytes, which are both Iba1-positive, we did similar scrapie infection experiments using tgGFP/RFP mice, which express GFP in microglia and RFP in monocytes as described in methods. In addition, we were concerned that early treatment with PLX5622 might influence the spread of scrapie from the brain injection site to the eye, so we waited until 90 dpi before starting PLX5622 treatment, as this schedule was also found previously to be highly effective in ablating microglia in brain .
In this experiment using TgGFP/RFP mice, we determined whether the Iba1-positive cells observed in retinal sections were microglia or monocytes by immunohistochemistry using anti-GFP or anti-RFP antibodies. Figure 5 shows examples of the IHC staining, where antibodies to Iba1, GFP and RFP were compared. In these studies, comparison of PLX versus ND groups in tgGFP/RFP mice gave very similar results to those seen previously using C57BL/10 mice. In the ND-group, Iba1-positive cells increased in the IS and OS layers of the PR region starting at 105 dpi with a peak between 118 and 145 dpi. In contrast, in the PLX group, rare Iba1-positive cells were detected in these same layers of the PR region at the latest time-points (Fig. 6a). Using IHC with anti-GFP and anti-RFP, large numbers of GFP-positive cells were detected in the retinal PR region of ND mice between 105 and 162 dpi, but numbers were much lower in the retinal PR region of PLX mice (Fig. 6b). In contrast, few RFP-positive cells were detected in either ND or PLX mice (Fig. 6c). Detailed data on all mice studied are shown in Table 1. Based on these data, we concluded that the detectable Iba1 cell response consisted mostly of microglia, and monocytes were only rarely detected. In addition, PLX5622 treatment abolished most of the microglial response in PLX retinas.
In spite of the difference in numbers of Iba1-positive microglial cells in the two treatment groups, apoptosis in the ONL was similar in both groups suggesting ongoing retinal degeneration (Fig. 6d). In addition, this retinal apoptosis was associated with direct evidence of thinning and degeneration of the ONL in both ND and PLX groups (Fig. 6e). Here thinning appeared to be faster in the PLX group, and this difference was statistically significant (P = 0.035). These data supported two conclusions: (1) Prion-induced retinal degeneration did not require presence of microglia or other Iba1-positive cells, and (2) lack of microglia appeared to accelerate the retinal degeneration observed.
Study of retinal flat mounts of ND and PLX mice by confocal microscopy
In order to obtain a 3-dimensional view of the ongoing degeneration process, intact retinas from infected ND and PLX tgGFP/RFP mice were gently fixed, and prepared as flat mounts for examination by confocal microscopy. In these preparations, expression of GFP and RFP was detected directly without the use of any antibodies. Data was gathered by obtaining 40 to 50 optical slices of approximately 1 μm thickness in selected areas.
Examination of the complete Z-stack of all 40–50 slices in the plane of the flat retina is shown for an uninfected mouse in Fig. 7a, where the GFP-expressing (green) microglia appeared to have small cell bodies and highly arborized processes typical of normal microglia. These cells were located mostly in the IPL and OPL regions as seen in the cross-section view of the stack. RFP-expressing (red) cells were very rare, and none were detected in this field.
In contrast, in the retina of a representative ND mouse at 159 dpi, microglia were much more abundant, and cell bodies were mostly large, and processes were short and stubby, consistent with activated microglia. Some cells had both green and red fluorescence, but the morphology of these cells was similar to the green-only microglia. In the cross-sectional view, many of these microglia were in the ONL/IS/OS region, similar to what was observed in the previously shown paraffin sections using IHC (Fig. 5b and d).
The retina of a representative PLX mouse from 134 dpi (Fig. 7c) showed a very low number of GFP-expressing microglia with an activated morphology, plus a few green/red cells also with microglial morphology. However, this retina also had several rounded red cells which appeared to be RFP-expressing monocytes. On the cross-sectional view, these cells were mostly located in the ONL/IS/OS regions.
For a more detailed view of the cell morphology, individual optical slices from each of these three mice were shown for three different levels. Figure 7d and e show normal microglia in the IPL and OPL regions with highly branched processes and small cell bodies. Rare microglia were seen in the ONL/IS/OS slice (Fig. 7f). In the ND mouse, a few microglia were detected in the IPL and OPL slices (Fig. 7g and h), but the majority of both the green and green/red microglia were in the ONL/IS/OS region (Fig. 7i). Here, the green/red cells appeared green over much of the cell body and the red appeared to be sequestered in cytoplasmic vacuolar structures resembling phagolysosomes. (see insert on Fig. 7i). Similar red fluorescent phagolysosomes were seen in prion-infected transgenic mice expressing GFP in microglia but lacking RFP expression, see Fig. 8c and d. This suggested that the red in these green/red cells was not RFP, but rather autofluorescence from phagocytosed outer segment material, as noted in other studies [25, 27].
In the PLX mouse, a few GFP expressing microglia were seen in the IPL and OPL regions (Fig. 7j and k), but in the ONL/IS/OS region fluorescent cells were either all red or mixed green/red (Fig. 7l). The round morphology of the all red cells was consistent with monocytes (Fig. 7l insert). However, the green/red cells were morphologically similar to activated microglia, which showed limited repopulation very late in disease .
In summary, microglial activation and invasion of the photoreceptors did not appear to be required for the process of prion-induced retinal degeneration. Monocytes were also likely not required, as they appeared late after the degeneration, consistent with a role in the clearance of the debris from dying cells.
Prion-induced photoreceptor degeneration in Cx3cr1 knockout mice
As a further test of the role of microglia in prion-induced photoreceptor degeneration, we also studied prion-induced retinal disease in mice homozygous for expression of a GFP transgene in place of the Cx3cr1 open reading frame, resulting in knockout of Cx3cr1 expression (tgGFP-Cx3cr1KO) . The Cx3cr1-Cx3cl1 axis, a neuron-to-microglia signaling chemokine axis, has been shown to influence microglial activation, migration and proliferation in several retinal disease models . In our experiment, these mice showed a delay in recruitment of microglia to the IS and OS following prion infection compared to TgGFP/RFP mice (Fig. 8a). However, this reduction in infiltrating microglia did not reduce the rate of prion-induced ONL thinning (Fig. 8b), suggesting that microglia were not required for prion-induced retinal PR degeneration. Thus, these results support the data obtained from the previous PLX5622-induced microglial ablation experiments.
Comparison of retinal flat mounts from these mouse strains by confocal microscopy revealed both green microglia and green/red microglia-like cells in both mouse strains (Fig. 8c and d). Since the GFP-Cx3cr1KO mice did not express RFP, the red in these mice cannot be RFP (Fig. 8d). Rather, as other studies have noted, this red fluorescence is likely to be autofluorescence of phagocytosed outer segment material by microglia, similar to what was suggested previously in tgGFP/RFP mice (Fig. 7b and i) [25, 27].
Detection of PrPSc in inner segment (IS) region of retinas at various times after scrapie infection
Microgliosis, astrogliosis and deposition of disease-associated PrPSc are important hallmarks of prion disease in brain and spinal cord, and gliosis and PrPSc often co-localize with neuronal damage. To detect areas of PrPSc deposition, scrapie-infected tgGFP/RFP retinas from the PLX and ND groups were examined by IHC using anti-PrP monoclonal antibody D13. This antibody is reactive with both the normal cellular PrPC and the disease-associated PrPSc isoform. In control uninfected mice, PrP staining was seen in multiple retinal layers, including ganglion cell layer (GC), IPL, INL, and OPL, as well as faint staining in the inner segment (IS) of the PR region (Fig. 9a). Because these mice were not scrapie-infected, this staining was assumed to be PrPC, which is the normal isoform of PrP and is seen in many cell types and tissues. In a representative scrapie-infected ND mouse at 104 dpi, in addition to the PrPC staining seen in uninfected mice, PrP staining was detected in the IS region of the PR cells (arrow, Fig. 9b). This staining was likely to be PrPSc, as it was not seen in uninfected mice. A time course of the development of PrPSc detection in the IS region is shown at higher magnification (Fig. 9c-k and in Table 2, where all the mice studied are indicated). In ND mice, the earliest PrPSc detection was scattered areas of granular punctate staining in the IS region at 82 dpi (Fig. 9d). Subsequently, at 104, 118 and 131 dpi, more numerous and sometimes confluent areas of staining were found in the IS region and also in scattered punctate spots in the ONL (Fig. 9e, f, and g). At 162 dpi near the clinical endpoint in ND mice, the OS and IS layers were mostly gone and the ONL layer was reduced to a thickness of 1–2 nuclei (Fig. 9h). PrP staining at this time was mostly in the IPL and OPL, and PrPSc could not be distinguished from PrPC.
In the PLX-treated group, PrPSc was detected at 104 and 118 dpi in the IS region and in the ONL and was similar to the findings in the ND group (Fig. 9i and j). There was no suggestion that PrPSc was deposited earlier or in higher amounts in PLX-treated mice versus ND mice (Table 2). Thus, absence of microglia did not appear to alter levels or pattern of PrPSc deposition in retina. At the clinical end point of 134 dpi in the PLX group, retinal degeneration was advanced, no distinct PR layer could be seen, and the ONL had a thickness of only 2–3 nuclei (Fig. 9k).
In conclusion, retinal PrPSc could be detected at increasing levels in the IS region of the photoreceptor cells. However, there was no definitive difference in the time course of appearance of this PrPSc in ND versus PLX mouse groups (Fig. 9d-k and Table 2).
In many types of photoreceptor degeneration, activated microglia have been detected near sites of retinal damage [32, 35]. Since microglial responses often involve secretion of proinflammatory cytokines and production of nitric oxide and reactive oxygen species, microglia have been thought to be an important causative factor in PR damage. In several experimental models, when microglia were genetically inhibited or blocked with drugs, pathology was decreased, indicating a pathological role for microglia [14, 41, 42]. In contrast, in our current experiments studying prion-induced PR degeneration, ablation of the microglia population using PLX5622 did not eliminate PR degeneration. Thus, microglia were not required for prion-induced retinal damage. In fact, the tempo of ONL thinning due to loss of PR cell nuclei was slightly faster in the absence of microglia (Fig. 4c and Fig. 5e). Therefore, microglia appeared to have an overall beneficial effect during prion retinal infection. Similar results were recently observed in an acute retinal detachment model where microglial elimination by PLX5622 did not block pathology, but instead, resulted in increased PR injury . This pattern was also seen in prion-infected brain, where microglia ablation by PLX5622 led to earlier onset of pathology and reduced survival times .
The fact that microglia were not required for prion-induced retinal degeneration suggested that PrPSc generated in the retina from PrPC precursor molecules might initiate pathogenesis directly. After prion infection, PrPSc aggregates were noted first in the IS region at 82 dpi (Fig. 9d) and later also in the ONL (Fig. 9e-g, j). One to two weeks later the PR in these areas became disorganized ultimately disappearing almost entirely. This prion-induced retinal degeneration appeared to be quite cell-specific, involving photoreceptor neurons, but not other types of neurons or glia in the retina. The primary association of PrPSc with the IS region may be an important clue as to the pathogenic mechanisms involved. PrPC is expressed at the IS, and PrPSc appeared to be generated at this same location. Early localization of retinal damage to the IS area was previously seen in scrapie-infected hamsters . The IS region is the site of most of the mitochondria of PR cells, and the IS is joined by the cilium to the outer segment of the PR cells containing the stacked discs of rhodopsin. Previous papers have suggested that normal PrPC might be colocalized to both mitochondria of brain cells [12, 13] and the ciliary basal body in neuroepithelial stem cells . Generation of PrPSc at such PrPC sites in PR cells might alter redox energy metabolism by mitochondria or protein transport by the connecting cilia. Furthermore, proteasome overload by accumulation of misfolded proteins such as PrPSc may favor ciliopathy and PR degeneration as seen in other models [26, 31].
In the present paper, using transgenic mice with GFP and RFP under control of microglial or monocytic promoters respectively, we were able to distinguish the types of Iba1-positive cells associated with retinal degeneration in prion-infected mice with and without microglia. When microglia were ablated by PLX5622, there were considerably fewer Iba1-positive cells detected. Some of these cells appeared to be regenerating microglia, and other cells with a rounded shape and strong diffuse red fluorescence in cytoplasm were suggestive of RFP-positive monocytes, which might have been recruited from the periphery to remove the damaged PR cells. In contrast, in ND mice with microglia present, the main cells in degenerating retina were GFP-positive, RFP-negative, suggesting that they were microglia. Late in disease some cells were both green and red and might be dual-positive microglia. However, the red fluorescence in these cells was localized to distinct cytoplasmic vacuoles similar to phagolysosomes, suggesting that this red fluorescence might be due to phagocytosed outer segment material from PR cells, rather than RFP. We found similar cells in scrapie-infected mice which did not have an RFP-expressing transgene (Fig. 8c and d) and, others have noted similar autofluorescence of phagocytosed outer segment material in microglia and macrophages [25, 27]. In summary, at the end stage of retinal degeneration, Iba1-positive cells in ND mice were mostly microglia, whereas in PLX mice Iba1-positive cells were very reduced in number and were a limited mixture of monocytes plus regenerating microglia. Both cell types appeared to phagocytose damaged PR cells, but this occurred so late in the degenerative process that it did not appear to be a major causal mechanism of damage.
In previous experiments by our group, PLX5622-induced ablation of microglia was able to reduce survival times from scrapie prion infection by 21–32 days . Thus, the presence of microglia in brain had an unexpected role in host defense against scrapie brain infection. In PLX5622-treated mice, PrPSc appeared in brain about 20 days earlier than in untreated mice suggesting that microglia might reduce PrPSc in brain by phagocytosis or other catabolic processes. In the present experiments studying retinal prion disease, microglial ablation by PLX5622 slightly accelerated prion-induced retinal degeneration. This effect might be due to the ability of microglia to catabolize PrPSc and reduce its damaging effects on retina as was suggested in previous brain experiments. However, the current retinal experiments were not able to detect differences between PLX-treated and ND mice in the amount of PrPSc in PR and ONL. More quantitative assays will be required to confirm this possibility. Moreover, it is possible that microglia can prolong retinal PR survival by other mechanisms, such as removing partially damaged PR cells to reduce bystander cell damage.
The ablation of microglia with the use of PLX5622 in the present experiments revealed that microglia were not required for prion-induced PR degeneration. This conclusion was unexpected as there are many similarities between the pathology of prion-induced PR degeneration and genetic models of PR degeneration, such as rd10, where microglia are thought to play an active role in retinal damage [40,41,42]. However, the mechanism of prion-induced retinal pathogenesis might be a more direct toxic effect of PrPSc on PR cells, whereas rhodopsin mutants, such as rd10, might act indirectly via stimulation of neurotoxic effects induced in microglia. To distinguish between these mechanisms, PLX5622 ablation of microglia would be interesting to test in models of retinitis pigmentosa, AMD and other retinal degenerative conditions to explore the possibility that microglia might have different or additional roles than are currently appreciated.
Ganglion cell layer
Inner nuclear layer
Inner plexiform layer
Inner segment of photoreceptor cells
Outer nuclear layer, containing PR cell nuclei
Outer plexiform layer
Outer segment of photoreceptor cells
Retinal pigment epithelium
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The authors thank Nancy Kurtz and Lori Lubke for technical histology assistance, Jeffrey Severson for animal husbandry, and Drs. Byron Caughey, Cathryn Haigh, Clayton Winkler and Karin Peterson for advice on manuscript preparation. The authors thank Dr. Karin Peterson for originally suggesting the use of the tgGFP/RFP transgenic mice. In addition, the authors kindly thank Plexxikon Inc., Berkeley, CA for providing the drug, PLX5622.
This research was supported by the Intramural Research Program of the NIH, National Institute of Allergy and Infectious Diseases.
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The data supporting the conclusions of this article are included within the article. Original slides, tissues and photographs are retained. All reagents and animals used in this study are available from scientific supply companies, except the anti-PrP antibody D13, which depending on supply, may be available upon request.
All mice were housed at the Rocky Mountain Laboratories (RML) in an AAALAC-accredited facility in compliance with guidelines provided by the Guide for the Care and Use of Laboratory Animals (Institute for Laboratory Animal Research Council). Experimentation followed RML Animal Care and Use Committee approved protocol 2016–04.
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Striebel, J.F., Race, B., Williams, K. et al. Microglia are not required for prion-induced retinal photoreceptor degeneration. acta neuropathol commun 7, 48 (2019). https://doi.org/10.1186/s40478-019-0702-x
- Müller cells
- Prion protein
- Cx3cr1 knockout