Platelet-derived growth factor (PDGF)-C inhibits neuroretinal apoptosis in a murine model of focal retinal degeneration.

Platelet-derived growth factor (PDGF)-C is a member of the PDGF family and is critical for neuronal survival in the central nervous system. We studied the possible survival and antiapoptotic effects of PDGF-C on focal retinal lesions in Ccl2(-/-)/Cx3cr1(-/-) on C57BL/6N [Crb1(rd8)] (DKO rd8) background mice, a model for progressive and focal retinal degeneration. We found no difference in transcript and protein expression of PDGF-C in the retina between DKO rd8 mice and wild type (WT, C57BL/6N). Recombinant PDGF-CC protein (500 ng/eye) was injected intravitreally into the right eye of DKO rd8 mice with phosphate-buffered saline as controls into the left eye. The retinal effects of PDGF-C were assessed by fundoscopy, ocular histopathology, A2E levels, apoptotic molecule analysis, and direct flat mount retinal vascular labeling. We found that the PDGF-CC-treated eyes showed slower progression or attenuation of the focal retinal lesions, lesser photoreceptor and retinal pigment epithelial degeneration resulting in better-preserved photoreceptor structure. Lower expression of apoptotic molecules was detected in the PDGF-CC-treated eyes than in controls. In addition, no retinal neovascularization was observed after PDGF-CC treatment. Our results demonstrate that PDGF-C potently ameliorates photoreceptor degeneration via the suppression of apoptotic pathways without inducing retinal angiogenesis. The protective effects of PDGF-C suggest a novel alternative approach for potential age-related retinal degeneration treatment.

Introduction

Platelet-derived growth factor (PDGF)-C is a PDGF family member.[1, 2] It is a polypeptide of 345 amino acids with potent pleiotropic effects and functions as a homodimer, PDGF-CC.[3] PDGF-C possesses a CUB (complement C1r/C1s, Uegf, Bmp1) domain preceding the PDGF homology core domain. It is necessary for the CUB domain to be proteolytically removed to allow the PDGF core domain to bind to the PDGF receptor (PDGFR).[1, 4, 5] PDGFR-C has two receptors: PDGFR-α and PDGFR-β. PDGF-CC preferentially binds to the PDGFR-αα homodimer but can also bind to the PDGFR-αβ heterodimer when PDGFR-α and PDGFR-β are coexpressed in the same cell.[5-7]

Although PDGF-C is a novel molecule discovered a decade ago, it has been found to be essential in many biological processes. It has been reported that Pdgfc knockout mice on a 129 background cannot survive the perinatal period due to feeding and respiratory difficulties.[8] PDGF-C is abundantly expressed in multiple cell types, including endothelial cells,[7, 9] vascular smooth muscle cells,[7, 9, 10] pericytes, and vascular fibroblasts.[7, 11] Additionally, PDGF-C is highly expressed in the central nervous system, including the retina,[12, 13] brain,[1, 12] and spinal cord.[14] As a broad-acting neuroprotective factor, PDGF-C has been shown to have pro-survival effects on neurons via both direct and indirect pathways.[5] In the retina, specifically, PDGF-C exhibits protective effects on retinal ganglion cells and neurons in the inner/outer nuclear layers (INL/ONL) and regulates the expression of apoptotic and survival genes.[12] It has been shown that PDGF-C also induces human retinal pigment epithelium (RPE) proliferation and migration in vitro.[15] Moreover, PDGF-C is a potent angiogenic factor during development and under pathological conditions. Related studies have demonstrated that PDGF-C plays a role in promoting proliferation, survival, and migration of vascular smooth muscle cells, pericytes, and vascular endothelial cells and their progenitors.[11, 16–18] PDGF-C inhibition could effectively suppress both choroidal and retinal neovascularization under pathological conditions.[18]

Age-related macular degeneration (AMD) is a multifactorial neurodegenerative disease characterized by progressive degeneration of photoreceptor/RPE complex primarily in the retinal macula. It has become the major cause of irreversible central vision loss in the elderly worldwide.[19-21] Because the photoreceptors and RPE are closely associated, a change in any single component of this complex could ultimately result in photoreceptor death.[22] Prior evidence reveals a link between photoreceptor degeneration and AMD.[23-25] Many clinical and experimental studies have linked AMD neurodegeneration to a variety of factors, including aging, oxidative stress, parainflammation, genetic predisposition, and environmental elements.[26-32] In certain conditions, the photoreceptor/RPE complex is exposed to numerous stimuli, such as oxidants, cytokines, and/or neurotoxins, which ultimately contribute to AMD pathogenesis.[33] In addition, studies have shown that apoptosis of RPE and photoreceptors plays a vital role in geographic atrophy AMD.[34, 35]

Given the reported survival effects of PDGF-C in the neurons, the aim of this study was to evaluate the neuroprotective and anti-apoptotic effects of PDGF-C on the retinal lesions in a Ccl2 on C57BL/6N [Crb1] (DKO rd8) background mouse model of progressive and focal retinal degeneration, mimicking certain features of human AMD in additional to typical retinal dystrophy secondary to rd8 background.[36, 37]

Materials and Methods

Animals and treatment

We generated the DKO rd8 mouse as a model of progressive, focal retinal degeneration,[38, 39] mimicking certain features resembling human AMD lesions.[36] In addition to the Ccl2/Cx3cr1 double knockout, the C57BL/6N mouse line has the crumbs-like 1 (Crb1) mutation in homozygous form.[40] The DKO rd8 mouse has earlier onset and higher penetrance than Ccl2 and Cx3cr1 single knockout strains.[36, 41] The DKO rd8 mice and age-matched wild type (WT, C57BL/6N [Crb1]) mice were bred in-house. The mouse number in our study was determined by power analysis, considering the following factors as P value, power, effects, and alternative hypothesis (two-tailed). All animal experiments were performed under protocols approved by the National Eye Institute’s Institutional Animal Care and Use Committee and were in compliance with the Association for Research in Vision and Ophthalmology Statement for the Use of Animals in Ophthalmic and Vision Research. The right eyes of 6-week-old DKO rd8 mice were intravitreally injected with core domain of recombinant His-tagged PDGF-CC protein (500 ng/eye) diluted in phosphate buffered saline (PBS). Left eyes were injected with the vehicle control PBS and served as controls.

Retina isolation

Mouse retina was isolated from eyes of WT and DKO rd8 mice at 6–8 weeks of age. Briefly, experimental animals were euthanized and their eyes were enucleated. The globes were dissected free of periocular connective tissue, the anterior segment was removed, and the retina was dissected free from the underlying RPE-choroidal eyecups. The isolated retina was collected to measure mRNA and protein expression of PDGF-C by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and Western blot, respectively.

RNA isolation and qRT-PCR

Total RNA was isolated from the primary retina using an RNeasy Mini Kit (Qiagen, Hilden, Germany). One µg RNA was reverse transcribed with Superscript II RNase H Reverse Transcriptase (Invitrogen, Grand Island, NY, USA) to 20µl cDNA. qRT-PCR was performed on the resulting cDNA using Brilliant SYBR Green QPCR Master Mix (Stratagene, La Jolla, CA, USA). The comparative cycle threshold value method, representing log transformation, was used to establish relative quantification of the fold changes in gene expression using ABI 7500 System (Applied Biosystems, Foster City, CA, USA). Each 25 µl reaction volume contained 2× PCR master mix (SYBR Green/Rox; SABiosciences, Frederick, MD, USA), 0.4 µM of each primer, and 1 µl cDNA. The cDNA was amplified with specific primers for 40 cycles. β-actin was used as an internal control. Primers of β-actin, pdgfc, Fas ligand (Fasl), Fas, B-cell CLL/lymphoma-2 (Bcl2) and Bcl2-associated X protein (Bax) were purchased from SABiosciences (Frederick, MD, USA).

Western blot

Preparation of whole cell lysates and Western blot analysis were performed as described previously.[42] Cell extracts from mouse retina (30 µg/lane) were fractionated on 4–12% gradient SDS-PAGE (Invitrogen). Antibodies used included PDGF-C (R&D Systems, Minneapolis, MN, USA) and β-Actin (Santa Cruz Biotechnology, Santa Cruz, CA, USA). Preimmune serum was used in parallel as controls and signals were detected with a HRP-conjugated secondary antibody (Zymed Laboratories) using the ECL-PLUS system (Amersham, Arlington Heights, IL, USA). Assays were repeated in 4 WT and 5 DKO mice. Image-J software is used to measure the band intensity in pixels.

Fundus photography and clinical grading

Fundoscopy was performed before injection and 2 months following the PDGF-CC protein injection. A Karl Storz veterinary otoendoscope (Karl Storz, Tuttlingen, Germany) coupled with a Nikon D90 digital camera was used for taking mouse fundus photographs. Mice were given intraperitoneal injection of ketamine (1.4 mg/mouse) and xylazine (0.12 mg/mouse) for systemic anesthesia and topical 1% tropicamide ophthalmic solution (Alcon Inc, Fort Worth, TX, USA) for pupil dilation. We assigned lesion grades by comparing the same quadrant of fundus area in all 65 mice over the 2-month course.[43, 44] Progression was defined as a >10% increase in the number of the retinal lesions (+1), a >50% increase in the lesion size in at least 1/3 of the lesions (+2), >5 fused lesions or the appearance of >2 chorioretinal scars (+3), and diffuse chorioretinal scars (+4). Regression was defined as a >10% decrease in the number of retinal lesions (−1), a >50% decrease in lesion size in at least 1/3 of the lesions (−2), a >50% disappearance of retinal lesions (−3), and total disappearance of retinal lesions (−4).[43] A masked observer conducted the grading.

Direct labeling and visualization of retinal vessels in flat-mounted retina

Blood vessels in the retina were directly labeled by cardiac perfusion of an aqueous solution containing 1,1’-dioctadecyl-3,3,3’,3’-tetramethylindocarbocyanineperchlorate (DiI, D-282, Invitrogen/Molecular Probes, Carlsbad, CA, USA), a lipophilic dye that labels endothelial cell membranes as previously described.[45] Briefly, DKO rd8 mice were euthanized by carbon dioxide inhalation and the thoracic cavity opened to expose the heart. A volume of 100 µl of DiI stock solution (6 mg/ml in 100% ethanol) was dissolved in 5 ml of diluent comprising of PBS and 5% glucose in a ratio of 1:4. The resulting solution was applied via cardiac perfusion at a rate of 1–2 ml/min. This was immediately followed by the perfusion of 5–10 ml of PBS and 5–10 ml of 4% paraformaldehyde at a rate of 1–2 ml/min. The eyes were harvested, and the neuroretina was dissected free from the underlying RPE-choroidal eyecups. These flat-mount preparations were mounted on glass slides in mounting medium (Fluoromount; Sigma, St. Louis, MO, USA) with the ganglion cell layer uppermost. The slides were covered and examined under an Olympus FV1000 Confocal Scanning Microscope. Retinal z-stack scan was used to examine all the retinal vascular layers. The total scanned thickness was 50 µm and slices within the stack were separated by a distance of 5 µm. Image-J software is used to measure the fluorescence intensity in pixels per whole retina in each image.

A2E extraction and quantification

[2,6-dimethyl-8-(2,6,6-trimethyl-1-cyclohexen-1-yl)-1E,3E,5E,7E-octatetra-enyl]-1-(2-hydroxyethyl)-4-[4-methyl-6(2,6,6-trimethyl-1-cyclohexen-1-yl) 1E,3E,5E,7E-hexatrienyl]-pyridinium (A2E) is a lipofuscin generated from the visual cycle flux of all-trans-retinol and is relevant to aging and AMD pathogenesis.[46] Whole eyes were removed in a dark room under dim red light and homogenized. A2E was extracted with chloroform/methanol as previously described.[47] The extracts dissolved in methanol were separated by high-performance liquid chromatography (HPLC, Agilent 1100 LC, Wilmington, DE, USA) and detected by ultraviolet light at a wavelength of 435 nm. A gradient of 40–95% acetonitrile/H2O in 0.1% trifluoracetic acid was used to elute A2E on a reverse-phase C18 column (Agilent, eclipse XD8-C18, 5 µm, 4.6×150 mm) at a flow-rate of 1.0 ml/min. A2E was quantified using external A2E standards.[48]

Histopathology

Eyes were fixed for 30 min in 4% gluteraldehyde followed by 10% formalin for at least 24 h. Fixed eyes were embedded in methacrylate and serially sectioned in the vertical pupillary-optic nerve plane. Each eye was cut through the vertical pupillary-optic nerve axis (P-O sections) into 4–6 sections and stained with hematoxylin and eosin. All lesions on the whole retina of each P-O section were analyzed and examined under a light microscope.

Transmission electron microscopy (TEM)

The mouse eyes were fixed in 2.5% gluteraldehyde, dehydrated, and embedded with Spurr's epoxy resin. Ultrathin sections (90 nm) were prepared and double-stained with uranyl acetate and lead citrate and viewed using a JEOL JEM 1010 transmission electron microscope.

Frozen sections, TUNEL assay and immunohistochemistry

Eyes were harvested following euthanasia of mice, snap frozen and embedded in Tissue-Tek OCT Compound (Sakura Finetek USA Inc., Torrance, CA, USA). Serial sections were cut along the vertical pupillary-optic nerve plane and stored on slides at −70°C. Frozen mouse eye slides were fixed in 4% paraformaldehyde for 15 min, washed in PBS. The fixed slides were labeled using a terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit according to the manufacturer's instructions (Roche, Nutley, NJ, USA). In additional, the fixed slides were blocked in ICC buffer with 5% normal goat or rabbit serum for 30 min at 4°C. Samples were incubated overnight with primary antibodies to the following antigens: FasL, 1:50 (Abcam, Inc., Cambridge, MA, USA); Fas, 1:200 (Santa Cruz); Bax, 1:200 (Santa Cruz); and Bcl2, 1:200 (Santa Cruz). After washing with ICC buffer, 4',6-diamidino-2-phenylindole dihydrochloride (DAPI, 1:1000, Invitrogen) and secondary antibodies conjugated to either Alexa-488 or Alexa-555 (1:400, Invitrogen) were added and incubated at room temperature for 1 h. All the slides with immunohistochemical staining were examined under an Olympus FV1000 Confocal Scanning Microscope. Image-J software was used to measure the fluorescence intensity in pixels per area in each image and expressed as fluorescence intensity ratio.

Statistical analysis

Statistical analyses were performed using GraphPad Prism 5 (GraphPad Software, San Diego, CA, USA). The data of qRT-PCR, A2E, TUNEL assay and fluorescence intensity were compared using paired t-test. The data of clinical fundus scores were compared using Mann-Whitney U test. A P value less than 0.05 was considered statistically significant.

Results

PDGF-C expression in neuroretina is comparable between WT and DKO rd8 mice

We compared protein and mRNA transcript levels of PDGF-C in freshly isolated neuroretina from WT and DKO rd8 mice. Both Pdgfc transcripts (Figure 1A) and PDGF-C protein (Figure 1B and 1C) were expressed in the retina of both WT and DKO rd8 mice. No significant differences were measured between the two mouse strains.

Figure 1

PDGF-C level in the retina of DKO rd8 and WT

A) Pdgfc transcript levels in freshly isolated retina from WT (n=4) than DKO rd8 (n=5) mice using quantitative reverse transcription-polymerase chain reaction. Pdgfc transcript is comparably expressed between WT and DKO rd8 mice. B) The PDGF-C protein ratio of Western blot is calculated relative to β-actin (loading control). Image-J software is used to measure the band intensity in pixels. C) Western blot detected PDGF-C expression in the retina in both WT and DKO rd8 mice. The size of molecular weight is given in kDa.

PDGF-C attenuated focal retinal lesions of DKO rd8 mice

To test whether PDGF-C would positively affect the retinal lesions in the DKO mice, we administered purified recombinant PDGF-CC protein into the eyes of 65 mice in 3 independent experiments. The experimental replicates yielded similar data. Fundoscopy revealed that PDGF-CC-treated eyes at 2 months had significant improvement over PBS controls, with fewer and smaller deep retinal lesions (arrows, Figure 2A and 2B). Histopathologically, the PBS-injected retina showed focal photoreceptor degeneration, focal loss of inner/outer segment (IS/OS, Figure 2C, asterisks), and RPE vacuolation/pigmentary alteration in addition to the rd8 associated photoreceptor dystrophic lesions in the outer plexiform layer (OPL, Figure 2C, arrows). In contrast, PDGF-CC-treated retina presented fewer/smaller photoreceptor lesions, relatively healthy photoreceptor IS/OS, and normal RPE. However, most rd8 associated focal photoreceptor dystrophic lesions remained (Figure 2C, arrows). A total of 25 pairs of eyes were histologically examined, 17/25 mice had AMD-like lesions and 23/25 mice had rd8-associated lesions (Figure 2D). For AMD-like lesion comparison, 14 of 17 (82.4%) mice showed fewer lesions in the PDGF-CC-treated eyes compared with PBS-injected controls. For rd8 lesion comparison, no statistical differences were found between the eyes injected with PDGF-CC and PBS. Moreover, PDGF-C treatment tended to reduce the levels of lipofuscin A2E, 11 of the 15 mice (below the dashed line) tested appeared to have decreased A2E while the remaining 4 mice (above the dashed line) had increased expression (Figure 2E). To further investigate the protective effects of PDGF-C in mouse retinal vasculature, ultrastructural changes were compared. The pericytes of retinal vessels (asterisk) in PBS-injected eyes showed disintegration but were healthier in the PDGF-CC-injected retina (Figure 2F).

Figure 2

Retina-protective effect of PDGF-C in DKO rd8 mouse retina

A) The fundus of PBS-injected and PDGF-CC-treated DKO rd8 mouse eyes was taken by a Nikon D90 digital camera illuminated with a Karl Storz veterinary otoendoscope. Representative fundus findings showed changes in yellowish deep retinal lesions (arrows) in both eyes of the same mouse before and 2 months after PDGF-CC treatment. B) Fundus scores of 65 pairs of eyes based on the fundus photographs showing altered progression scores between the two eyes at the end of 2 months after PDGF-CC treatment. C) DKO rd8 mouse eyes were enucleated and embedded in methacrylate. Representative histopathological findings showed retinal lesions of both DKO (asterisks) and rd8 (arrows) associated lesions. Scale bar = 50 µm. D) Histological comparison of AMD-like lesions and rd8-associated lesions between each mouse. The lesions in the PDGF-CC-treated eye are compared with that in PBS-injected eye of the same mouse. E) PBS-injected and PDGF-CC-treated DKO rd8 mouse eyes were enucleated and homogenized for A2E extraction with chloroform/methanol (n=15). The 11 eyes below the dashed line showed decreased A2E. F) DKO rd8 mouse eyes were enucleated and embedded with Spurr's epoxy resin. PDGF-C maintained pericytes (asterisks, scale bar = 2 µm) in retinal tissues when compared with PBS-injected eyes. *P<0.05.

PDGF-C has anti-apoptotic effects on neuroretina of DKO rd8 mice

As a useful tool to detect DNA fragmentation of apoptotic cells, TUNEL assay showed less apoptotic cells in PDGF-CC-treated than PBS-injected retina in the ganglion cell layer, INL and ONL (Figure 3A and 3B). Several apoptosis-related molecules were measured to investigate whether PDGF-C could attenuate retinal lesions via apoptotic pathways. Between the PDGF-CC-treated and control eyes, Fasl (Figure 3C), Fas (Figure 3D), Bax (Figure 3E) and Bcl2 (Figure 3F) transcripts were compared between PDGF-CC-treated and PBS-injected eyes. The levels of Fas (Figure 3D) and Bax (Figure 3E) transcripts were significantly decreased in PDGF-CC-treated retina compared to the controls. While there was an overall decrease in Fasl (Figure 3C) and Bcl2 (Figure 3F) in PDGF-CC treated retina compared to controls, the difference was not statistically significant. Immunohistochemistry showed less immunoreactivity against FasL in the ganglion cell layer, IPL, INL and OPL (Figure 3G), Fas in the ganglion cell layer, IPL, INL, OPL and IS/OS (Figure 3H) and Bax in the INL, OPL and IS/OS (Figure 3I) but more expression of Bcl2 in the IPL, OPL and IS/OS (Figure 3J) in PDGF-CC-treated retina than PBS-injected retina.

Figure 3

Anti-apoptotic effects of PDGF-C on the neuroretina in DKO rd8 mice

A) The frozen sections of PBS-injected and PDGF-CC-treated DKO rd8 eyes were stained with TUNEL assay (green color, n=4). B) The percentage of TUNEL positive cells per total cells in the neuroretina is calculated by Image-J software (n=4). C–F) Whole retina of PBS-injected and PDGF-CC-treated DKO rd8 eyes was harvested, and total RNA was isolated and converted to cDNA. Quantitative reverse transcription-polymerase chain reaction analysis was then performed to determine the levels of targeted gene transcripts as follows: (C) Fasl, (D) Fas, (E) Bax and (F) Bcl2 (n=4). The frozen sections of the PBS-injected eye with thinner and irregular ONL and the PDGF-CC-treated DKO rd8 eyes with relatively intact ONL were stained with apoptosis related antibodies and immunoreactivity (red color) were evaluated under an Olympus FV1000 Confocal Scanning Microscope. Image-J software is used to measure the fluorescence intensity in pixels per area in each image and expressed as fluorescence intensity ratio. The same molecules were analyzed as follows: (G) anti-FasL, (H) anti-Fas, (I) anti-Bax and (J) anti-Bcl2 (n=5). The nuclei were stained with DAPI (blue). Scale bar = 50 µm. *P<0.05; **P<0.01; ***P<0.001.

PDGF-C does not induce leakage and neovascularization in neuroretina of DKO rd8 mice

To further investigate whether PDGF-C would cause vascular leakage and vascularization in the retina of DKO rd8 mice, retinal vasculature was examined using DiI staining. Differences in vascular neovascularization were noted between PDGF-CC-treated and PBS-injected mice, the sizes and amount of vascular leakages were moderately smaller and less in the eyes received PDGF-CC (Figure 4).

Figure 4

Effects of PDGF-C on retinal vessels in the neuroretina of DKO rd8 mice

Z stacks of retinal vasculature stained with DiI showed less vessel leakage or vascularization in PDGF-CC-treated than PBS-injected retina (n=4). Image-J software is used to measure the fluorescence intensity in pixels per whole retina in each image. *P<0.05.

Discussion

This study demonstrates that PDGF-C level is equally expressed in the retina of DKO rd8 and WT mice. Local administration of recombinant PDGF-CC protein ameliorates focal photoreceptor degeneration in this mouse model with focal retinal degeneration. PDGF-CC-treated eyes showed fewer clinical and histopathological lesions in the retina. More importantly, the neuroprotective effect of PDGF-C is associated with anti-apoptotic activities on retinal neuronal cells. Molecular studies demonstrated decreased apoptosis with exogenous PDGF-CC compared with PBS controls. In addition, the used dosage of PDGF-CC that is effective for neuroprotection also can protect retinal vessel pericytes but not induce retinal angiogenesis.

PDGF-C is widely expressed in multiple cell types and displays broad neuroprotective activities.[7, 9–11] Inside the eye, it has protective effects on retinal ganglion cells and INL/ONL neurons in mouse models with optic nerve crush and N-methyl-D-aspartic acid (NMDA) injury.[12] Given the neuroprotective and anti-apoptotic effects of PDGF-C, we propose that intravitreal administration of PDGF-CC protein may serve to protect the neuroretina in DKO rd8 mice with AMD-like lesions and could be a potential therapeutic agent for treatment.

Maintenance of normal photoreceptor function is closely related with RPE based on its nutrient transportation for photoreceptors and phagocytosis of shed photoreceptor outer segments. Lipofuscin accumulates as a byproduct of phagocytosis of photoreceptor outer segments. Excessive levels of lipofuscin during aging can greatly compromise essential RPE functions and contribute to the AMD pathogenesis.[46, 49] Thus, A2E, the major component of lipofuscin, is regarded as a biomarker in AMD.[46, 50] Our study showed decreased A2E levels in 11 of 15 mice with PDGF-CC treatment compared with PBS controls. This suggests that PDGF-C has the effect to reduce A2E level in the RPE of DKO rd8 mice, which can preserve RPE, thus potentially help uphold the photoreceptor integrity.

One of the major causes of human AMD is photoreceptor apoptosis mediated by both extrinsic and intrinsic pathways. Upregulation of FasL/Fas extrinsic pathway has been reported in human AMD specimens.[34] Meanwhile, both the extrinsic FasL/Fas pathway and intrinsic Bcl2/Bax system are involved in photoreceptor/RPE apoptosis in DKO rd8 mice.[51, 52] Our previous study demonstrated an elevation of FasL-associated photoreceptor apoptosis of DKO rd8 mice than that of WT in physiological conditions.[52] We also reported an upregulation of Bax transcript and a lower ratio of Bcl2/Bax in DKO rd8 mouse eyes compared with WT.[53] Interestingly, in DKO rd8 eyes, PDGF-C decreased apoptotic retinal cells with less FasL and Fas protein expressions. We did not detect a significant decrease of Fasl transcript in the DKO rd8 retina with PDGF-CC treatment, which could be due to the discordant expression of transcript and protein of FasL in DKO rd8 eyes or limited number of experimental animals.[30, 53] In the current study, PDGF-C significantly down-regulated pro-apoptotic Bax protein and transcript levels. This finding is in agreement with the antiapoptotic effects of PDGF-C in the retina of optic nerve crush mouse model.[12] Additionally, we found an up-regulation of anti-apoptotic Bcl2 protein in PDGF-CC-treated DKO rd8 eyes. Bcl2 confers negative control in the apoptosis pathway and the actions of Bax in vivo are partially dependent on the formation of homo-oligomers.[54, 55] The cytoprotective mechanism of Bcl2 has been shown to involve the formation of Bcl2/Bax heterodimer that prevents Bax oligomerization, which subsequently evokes a survival signal for the cells.[54-56] Thus, the total effect of PDGF-C on Bcl2 family members is anti-apoptotic. This effectively results in a survival trend in the DKO rd8 retina.

We have previously reported that PDGF-CC protein can activate both PDGFR-α and PDGFR-β in the mouse retina.[12] Furthermore, their neutralizing antibodies can largely block the neuroprotective effect of PDGF-CC on retinal ganglion cells in vivo. The neuroprotective effect of PDGF-C was mediated by both PDGFR-α and PDGFR-β. We further identified that the neuroprotective effect of PDGF-C was achieved by regulating GSK3β phosphorylation and expression. GSK3β is a pro-apoptotic gene that plays an important role in neuronal apoptosis.[57] This is in accordance with our current study, showing the effect of PDGF-C on neuroretina is via anti-apoptosis pathway.

Another important issue of PDGF-C treatment is the angiogenic effect in target tissues. Prior studies have shown that PDGF-C and PDGFRs are abundantly expressed by a variety of vascular cells, including pericytes.[7, 9–11] The highest density of pericytes in the body is found in vessels of the neural tissues, including the brain and retina.[58] Pericytes play an important role in the integrity of structural vessels and the blood-retinal barriers.[58, 59] Thus, pericyte abnormality and degeneration would result in vascular defects. PDGF-C has a critical role in promoting blood vessel growth and maturation, and one of the target routes is through pericytes.[16, 17] It also induces new blood vessel formation by increasing the number and integrity of pericytes.[60] PDGF-C drives the recruitment and differentiation of pericytes, resulting in better basement membrane integrity and a more mature, stable vascular wall with a lower permeability.[61] Thus, with the supportive effect of PDGF-C on pericytes, the treated mice revealed better-preserved pericytes in the retinal vessels with PDGF-CC treatment than PBS controls. It also guarantees the relatively normal vessel function to provide blood supply for the retinal neurons, which contributes to PDGF-C’s neuroprotective effects. More importantly, under the effective dosage for neuroprotection in this study, less vascular leakage and no neovascularization were noted in any of the PDGF-CC-treated eyes.

In summary, our data show that local application of PDGF-CC protein stabilizes focal photoreceptor degeneration in DKO rd8 mice. The mechanism of the protective role is through the anti-apoptotic pathway. PDGF-CC treatment under the effective neuroprotective dosage does not damage vascular pericytes, thus avoid retinal neovascularization in this mouse model. The neuroprotective and survival effects of PDGF-CC may provide a novel treatment for retinal degeneration diseases, such as AMD.