Molecular Vision 2013; 19:1747-1759
<http://www.molvis.org/molvis/v19/1747>
Received 11 January 2013 | Accepted 31 July 2013 | Published 04 August 2013
Molecular Vision 2013; 19:1747-1759
<http://www.molvis.org/molvis/v19/1747>
Received 11 January 2013 |
Accepted 31 July 2013 |
Published 04 August 2013
Kristopher G. Sheets,1 Bokkyoo Jun,1 Yongdong Zhou,1 Min Zhu,2 Nicos A. Petasis,2 William C. Gordon,1 Nicolas G. Bazan1
1Neuroscience Center of Excellence, Louisiana State University Health Sciences Center, School of Medicine, New Orleans, LA; 2Department of Chemistry and Loker Hydrocarbon Research Institute, University of Southern California, Los Angeles, CA
Correspondence to: Nicolas G. Bazan, Neuroscience Center of Excellence, School of Medicine, Louisiana State University Health Sciences Center, 2020 Gravier Street, Suite D, New Orleans, LA 70112; Phone: (504) 599-0831; FAX: (504) 568-5801; email: nbazan@lsuhsc.edu
Purpose: Neuroprotectin D1 (NPD1) attenuates laser-induced choroidal neovascularization (CNV) when administered intraperitoneally. Due to its lipophilicity and low molecular weight, NPD1 is well suited for topical delivery; thus, we investigated the efficacy of topically applied NPD1 in attenuating CNV. We also examined the effect of NPD1 on the recruitment and activation of microglia surrounding CNV lesions.
Methods: Mice were given laser-induced CNV and treated with NPD1 eye drops. CNV was evaluated by fluorescein leakage using a novel image analysis method and by isolectin B4 immunofluorescence of neovasculature. Microglia; recruitment was assessed by quantification. Using form factor, solidity, convexity, and fractal dimension, microglial activation was quantitatively assessed by two-dimensional, and for the first time, three-dimensional morphology. An ImageJ plugin, 3D Shape, was developed to enable this analysis.
Results: NPD1 attenuated leakage and neovascularization. The proximity of microglia to CNV lesions was significantly closer with NPD1. Consistent with the cellular ramification, microglia in NPD1-treated eyes were larger and exhibited a lower form factor and higher fractal dimension.
Conclusions: Our data show that NPD1 signaling induces a ramified, non-injury-inducing microglial phenotype coincident with attenuation of CNV. Since microglia are crucial participants in neurodegenerative diseases, the discovery that microglia are potential targets of NPD1 signaling warrants further investigation.
Choroidal neovascularization (CNV) rapidly deteriorates visual acuity and is responsible for most vision loss attributed to age-related macular degeneration. The current treatment options for CNV are limited to invasive laser photocoagulation, photodynamic therapy, and intravitreal injections of vascular endothelial growth factor (VEGF) scavengers [1]. Photoreceptor degeneration and CNV have been linked with the subretinal accumulation of microglia [2], but the role of microglia in these pathogenic events is not yet completely understood. Under physiological conditions, microglia are beneficial, releasing neuroprotective and anti-inflammatory factors [3]. In the diseased state, however, microglia are highly activated and appear to play a pathological role [4,5].
Recently, we demonstrated that a novel docosanoid, neuroprotectin D1 (NPD1), attenuates neovascularization and vascular leakage in a laser-induced model of CNV when injected intraperitoneally [6]. We also showed that NPD1 is a potent mediator of neuroprotection and inflammatory resolution [7-9]. Since microglia have the potential to resolve or exacerbate neuroinflammation, in this study, we examined the effect of NDP1 signaling on microglial cells in laser-induced CNV.
All animal experiments conformed to the Association for Research in Vision and Ophthalmology statement for the use of animals in ophthalmic and vision research and were approved by the Louisiana State University Institutional Animal Care and Use Committee. Male C57Bl/6 mice (8–12 weeks; 25–30 g) were obtained from Charles River Laboratories (Wilmington, MA) and maintained in the LSUHSC animal colony on a 12h:12h light-dark cycle (0600 h on; 1800 h off) with an average in-cage luminance of 20 lux at bedding level. Animals were fed normal mouse chow and supplied with water ad libitum. Twenty-four mice were used to assess retinal bioavailability and 20 mice were used for laser-induced CNV. Mice were anesthetized with ketamine (200 mg/kg) and xylazine (10 mg/kg) before deuterated NPD1 application, laser treatment, and fundus angiography. All mice were sacrificed by cervical dislocation.
Based on our previous results using intraperitoneal (ip) injection [6], NPD1 dosage was targeted at 1 mg per kg eye wet-weight (16 mg average wet-weight) and 16 ng NPD1 was delivered to the eye surface as a 1.6 μl drop (10 ng/μl NPD1 and 9.75% ethanol in saline) via micropipette. Ipsilateral eyes received NPD1, while contralateral eyes served as within-animal controls and received 1.6 μl of vehicle (9.75% ethanol in saline. The treatment solution was prepared and stored as 25 µl single-use aliquots at −20 °C. Treatments were administered rapidly, between 0900 and 1100, without anesthesia, using only gentle restraint. The treatment schedule was 1 h before laser treatment and once daily through 7 days post laser treatment. All information about each animal throughout the experimental procedures was hidden from the investigator performing the laser and NPD1 treatments.
The bioavailability of NPD1 in retinal tissue was determined using NPD1 labeled with two deuterium atoms [10]. Mice were anesthetized as above, and one eye per mouse received topical application of 1.5 μl of NPD1-d2 (100 ng/μl in 97.5% ethanol). This application represents a 10-fold higher concentration to ensure adequate detectability via mass spectrometry. To maintain this concentration of NPD1, the ethanol concentration was also 10-fold higher than the treatment levels. Contralateral eyes served as negative controls and received 2.5% methylcellulose to prevent corneal desiccation. Manual blinking of ipsilateral eyes was performed until mice were awake and moving normally. Mice were sacrificed, as above, at 0, 0.25, 0.5, 1, 2, and 4 h post-NPD1-d2 application. Immediately after this, eye surfaces were thoroughly washed and retinal tissue collected. Retinal tissue was extracted using a gentle pulling force applied with curved forceps behind the eye while the corneal surface was incised with a scalpel. NPD1-d2 was quantified in extracted retinal tissue by triple quadrupole tandem mass spectrometry. Selected parent and daughter ion pairs of NPD1-d2 were 361 and 208 m/z, respectively. Raw concentrations are reported as pictogram (pg) NPD1-d2 detected per mg of retinal protein analyzed. Variations in NPD1-d2 mass applied were corrected and normalized to the average retinal protein to determine the percent of applied NPD1-d2 present in each retina.
Mice given laser treatment were anesthetized as above, and pupils dilated with 1% tropicamide (Akorn, Inc., Buffalo Grove, IL). For optimal viewing of the retina and placement of laser lesions, corneal optics were negated by a coverslip adhered with a drop of 2.5% methylcellulose on the mouse cornea. To initiate retinal CNV, three laser spots (diameter 50 μm; duration 100 ms; energy 150 mW) were administered to each fundus using a Novus Spectra ophthalmic 532-nm diode laser (Lumenis, Inc., Santa Clara, CA) mounted on a slit lamp (Model SL-07; Topcon, Inc., Tokyo, Japan). The superior, nasal-inferior, and temporal-inferior fundus regions each received one lesion. Lesions were placed between two to three optic disc diameters from the optic nerve and between the retinal vessels. Inclusion criteria for successful laser-induced CNV were the formation of a bubble immediately after laser application, indicating penetration of Bruch’s membrane (Figure 1), and absence of subretinal hemorrhage. Lesions violating these criteria were excluded from the study. In total, only four lesions were rejected for lack of bubble, and no single mouse had more than one rejected lesion. After full recovery from anesthesia, mice were returned to the animal colony.
In vivo fundus fluorescein angiography of CNV lesions was performed 7 and 14 days post laser treatment using a Spectralis® HRA+OCT imaging system (Heidelberg Engineering, Inc., Vista, CA) equipped with high-resolution spectral domain optical coherence tomography and a confocal scanning laser ophthalmoscope. Mice were anesthetized and zero diopter contact lenses (Veterinary Specialty Products, Whitchurch, UK) were applied to improve image quality and protect corneas from desiccation. Following ip injection of 20 μl of 25% fluorescein (Hub Pharmaceuticals, Rancho Cucamonga, CA), angiograms were captured at approximately 0.5, 2, and 6 min post fluorescein injection.
Mice were sacrificed at 15 days post laser to allow fluorescein from the 14-day angiography to dissipate. Eyes were enucleated, corneas slit, and eyes fixed overnight (4 °C) with 4% paraformaldehyde (Electron Microscopy Sciences, Hatfield, PA) in PBS (potassium phosphate monobasic, 10.59 mM; sodium chloride, 1551.72 mM; sodium phosphate dibasic, 29.66 mM; without calcium chloride or magnesium chloride; pH 7.4; GIBCO, St. Louis, MO). After fixation, anterior segments and retinas were removed. The remaining eyecups were devoid of adhering retinal material (Figure 1C). These were washed in PBS (3×10 min), then permeabilized and blocked with 2% normal donkey serum (Sigma, St. Louis, MO) and 1% Triton-X (Invitrogen, Carlsbad, CA) in PBS (3×10 min). Eyecups were then incubated overnight (4 °C) with primary antibodies, 2% normal donkey serum (Sigma-Aldrich, St. Louis, MO), and 0.1% Triton-X in PBS. After primary labeling, eyecups were washed in 2% normal donkey serum and 0.1% Triton-X in PBS (3×10 min), then incubated overnight (4 °C) with fluorescent secondary antibodies and probes. Following a final wash with PBS (3×10 min), labeled eyecups were flattened with four peripheral radial cuts and coverslipped with ProLong Gold anti-fade medium (Invitrogen), forming a choroid flat mount. Antibodies and probes used were CD11b (20 μg/ml; AbD Serotec, Raleigh, NC), detected with AlexaFluor® 488 (5 μg/ml; Invitrogen); isolectin B4 (IB4) from Griffonia simplicifolia conjugated to AlexaFluor® 568 (25 μg/ml; Invitrogen); Hoechst 33,258 (10 μg/ml; Invitrogen); and phalloidin (to detect f-actin) conjugated to AlexaFluor® 488 (5 units/ml; Invitrogen).
Flat mounts were imaged on a Zeiss LSM-510 Meta laser confocal microscope using Zeiss objectives (Zeiss, Thornwood, NY). Tiled composites, or mosaics, were imaged using a Plan-Neofluar 10X/0.3 numerical aperture (NA) objective. Three-dimensional volumes were imaged using a Plan-Neofluar 40X/1.3 NA Oil DIC, Plan-Apochromat 63X/1.4 NA Oil DIC, or Plan-Apochromat 100X/1.4 NA Oil DIC objective. Optical slice thickness was equal across all channels and z-step intervals satisfied Nyquist sampling. Fluorophores were visualized as follows (excitation; emission): AlexaFluor® 568 (543 nm; 560–615 nm), AlexaFluor® 488 (488 nm; 505–550 nm), and Hoechst (405 nm; 420–490 nm).
To detail the effect of the laser on the retina, tissue was collected at 14 days post treatment and prepared for conventional histological analysis. Briefly, the corneas were slit and the eyes fixed in glutaraldehyde (2%) and paraformaldehyde (2%) in sodium cacodylate buffer (0.1 M) overnight. The cornea, iris, and lens were removed from each eye and fixation continued for one additional hour. Eyecups were rinsed in buffer and then postfixed in osmium tetroxide (1% in 0.1 M sodium cacodylate) for one hour, rinsed again, and dehydrated through an ethanol series to acetone. Infiltration and embedding occurred in an Embed-812/araldite epoxy mixture. Serial, 1 µm thick plastic sections were obtained through the laser lesions. These were contrasted with toluidine blue (1%) in 1% sodium borate and viewed by conventional light microscopy. Images were captured on a Nikon Optiphot-2 microscope (200X magnification) with a Nikon DS-Ri1 digital camera and displayed with NIS-Elements BR 3.00 software (Figure 1A,B).
Raw images of an angiography series were preprocessed (Figure 2) and lesion regions of interest (ROIs) were selected using an eight connected region growing method with manual subtraction of outlying regions. Leakage was measured as the area, mean intensity, and integrated density of each lesion at each phase and the exact fluorescein time of the phase recorded.
Based on the observed low variance of IB4 labeling along the Z-axis during our previous CNV analysis [6], we investigated CNV in the current study using area rather than volume. The CNV area was measured from the IB4 channel of choroid flat mount mosaics in Fiji by defining ROIs with eight connected region growing and the manual elimination of outlying pixels.
Microglia were identified by CD11b. Using a custom programmed macro in Fiji, sectors (origins at the optic nerve) were circumscribed ± 45 degrees about the centroid of each lesion in choroid flat mount mosaics. The radius of each lesion sector was 1080 μm, producing an area of 915,391 μm2. Microglia that did not overlap with the CNV lesion, hereafter referred to as peripheral microglia, were counted within each sector and the distance to the nearest lesion edge measured to assess their spatial distribution.
Microglia were segmented and their morphology assessed in two-dimensional (2D) and three-dimensional (3D) space. For 2D space, maximum intensity projections of the XY planes were used. ImageJ’s built-in analysis for circularity (shape descriptors form factor), solidity, convexity, area, and perimeter were measured in 2D, and 3D equivalents were measured using our custom 3D shape plugin. Fractal dimension was measured in 2D and 3D using the Fractal Count plugin [11].
Leakage, CNV, microglia count, and microglia spatial distribution were each analyzed separately using a mixed-model procedure [12] in SAS v9.1 (SAS Institute Inc., Cary, NC). Observations and denominator degrees of freedom (obs, den df) were as follows: leakage (168, 111); CNV area (50, 48); microglial count (33, 31); and microglial spatial distribution (965, 933). Treatment effects are represented by least squares and means±standard error reported p values are adjusted using the simulate option to increase robustness.
Analysis of microglial morphology was performed using the R statistical programming language. Treatment effects were assessed both nonparametrically using the Kruskal–Wallis and Wilcoxon tests and parametrically by a single-factor analysis of variance. Prior to analysis of variance testing, morphological measures rejected by the Shapiro-Wilk test of normality (α=0.1) were iteratively transformed using the method described by Goerg [13,14]. Data are presented as the transformed mean ± standard error of the mean; reported p values were White corrected [15].
The retinal bioavailability of topically applied NPD1 was assessed and found to have peak concentrations 2 h after application (Figure 3); no measurable quantity of nondeuterated NPD1, representing endogenous synthesis, was detected. It should be noted that NPD1 day 2 was applied in a 97.5% ethanol solution, which may have affected the aqueous humor dynamics of the mouse eye. From eye grooming behavior, it was inferred that mice experienced temporary irritation after both NPD1 and vehicle treatments, but otherwise tolerated them well; no corneal desiccation or cataract formation was observed in any eye during the treatment schedule.
Fluorescein angiography revealed striking differences between CNV lesions in control and NPD1-treated animals (Figure 4A). Leakage in NPD1-treated eyes was significantly lower (p<0.0001) than in controls at 7 days post laser (Figure 4B). By 14 days post laser, two of the three leakage measures remained significantly lower (p<0.05) in the treatment group (Figure 4C).
Immunohistochemical labeling of vascular endothelial cells with isolectin B4 also demonstrated striking differences between treatment groups. At 15 days post laser, the area of labeled neovasculature in the NPD1-treated group was significantly lower (p<0.05) at approximately half that of the control group (Figure 5). Despite measuring the area rather than the volume, this level of reduction was similar to our previous results [6]. It should be noted that there were some yellow/orange labeled cells, which may indicate colocalization of reactivity for isolectin B4 and immunoreactivity for CD11b. It has been reported that microglia can be labeled with isolectin B4.
Microglia peripheral to the CNV lesions were analyzed to assess density and recruitment effects induced by NPD1 (Figure 6). No difference in microglia counts was found between control and NPD1; control eyes had 24±2 microglia per lesion sector, while NPD1 eyes had 23±4 (Figure 6B). The spatial distributions within lesion sectors, however, were not homogenous, and revealed a significant difference between treatments. Microglia in control eyes were situated at an average of 344 μm from the CNV lesions, while NPD1 significantly reduced (p<0.0001) this distance by ~40% to 208 μm (Figure 6B).
Morphologically, microglial cells in the NPD1 treatment group had more than double the volume (p<0.0001), and a near twofold increase in surface area (p<0.0001; Figure 7A). Much of this cellular change occurred orthogonal to the Z-axis, as maximum intensity XY projections also revealed significant increases in analogous measures; the area increased 1.9-fold and the perimeter increased 1.8-fold (p=0.0002 and p=0.0014, respectively; Figure 7B).
We further investigated the continuum of alterations in reactive microglia using quantitative shape descriptors. The form factor expresses the spherical (circular for 2D) shape of an object. In both 3D and 2D, the form factor of the peripheral microglia was lower in the NPD1 group, indicating that microglia in the control group were more spherical and rounded (Figure 7C-F). Solidity, which conveys the spatial density of an object, was also lower in both 3D and 2D with NPD1 treatment, but not significantly different from controls (Figure 7E,F). Convexity was lower in the NPD1 group in 2D but not 3D (Figure 7E,F). Unlike the previous shape parameters, which are inherently linked to the image magnification, the fractal dimension evaluates the rate of change in the surface area (perimeter in 2D) with regard to scale and can be simply thought of as the roughness of the cell surface. NPD1 significantly increased the fractal dimension in both 3D and 2D (Figure 7E,F), implying that there were rougher cell surfaces than in control microglia. Visually, the differences in size and complexity between microglia were easily seen in the 3D rendering of representative microglia from control and NPD1 treatments (Figure 8).
NPD1 is well suited for topical delivery due to its lipophilicity and low molecular weight, both of which increase permeability in the cornea, conjunctiva, and retinal pigment epithelium (RPE) [16]. Thus, we investigated the efficacy of topically applied NPD1 to attenuate CNV. Because NPD1 is a potent mediator of neuroprotection and inflammatory resolution, it is tightly regulated, and in the absence of an initiating trigger, little to no NPD1 is synthesized. With topical eye drops being the least invasive ocular drug delivery method, NPD1 synthesis was not an expected outcome of our treatment process. The absence of endogenous NPD1 in our bioavailability assessment accords with this expectation. Despite the strict governance of NPD1 synthesis and release, exogenously applied NPD1-d2 was indeed present in retinal tissue at detectable levels. Considering our method of retina extraction, some degree of contamination by aqueous humor is assured, resulting in the high concentration at time zero. The decrease at plus 15 and 30 min suggests that the labeled NPD1 had moved out of the aqueous humor and into more distal tissues. A slower second NPD1-d2 peak at 2 h, however, supports the clear presence of NPD1 in retinal tissue. Our results demonstrate proof of principle that NPD1 can reach retinal tissue and that topical application is a viable delivery route for NPD1. Importantly, when diluted to therapeutic concentrations in saline, topical NPD1 treatment is well tolerated by the cornea.
One week after inducing CNV, NPD1 treatment significantly reduced leakage by approximately half compared to untreated controls. While NPD1-treated lesions in the second week did exhibit one-third less leakage than controls, the difference was not statistically significant, as the control lesions demonstrated a self-resolving leakage reduction of 27% from the first week. Considering that treatment was discontinued after the first week, these results demonstrate that NPD1 attenuates leakage before the normal resolution process observed in controls. As leakage reductions ceased when treatment did, it is possible that a continuous treatment paradigm may result in further leakage improvements. Topical NPD1 treatment also reduced the neovascular area by half. The leakage and CNV results observed with topical application correspond well to our previous study using ip delivery [6] and corroborate our previous findings that NPD1, whether applied topically or injected ip, attenuates CNV and associated leakage.
The ability of microglia to activate, proliferate, and migrate to sites of inflammation are requisite steps in the resolution of neuroinflammatory diseases. Here, we investigated the ability of NPD1 treatment to modulate microglial activation and recruitment. Our results showed similar quantities of microglia in both treatments. When we examined the spatial distribution of microglia, however, we found that microglia in NPD1 treated eyes were half the distance to lesions observed in control eyes. This suggests that NPD1 signaling facilitates microglial recruitment. In response to injury, microglia polarize toward the lesion and shield the injured area with an accumulation of microglial extensions [17]. The distribution pattern of microglia in NPD1-treated eyes is reminiscent of this shielding behavior. It has been observed in studies on hippocampal slices that activated microglia appear to wrap around capillaries to contain leakage sites [18]. Unfortunately, the limited immunolocalization of the present study did not permit visualization of this interaction. Here, it appears that microglia did not achieve this intimacy under either condition. However, since polarization, shielding, and migration are dependent on process motility [17-19], these results do suggest that NPD1 may enhance the dynamics of microglial processes responding to acute local injury signals.
Next, we evaluated differences in activation between treatments. As the functional phenotype of microglia is closely tied to their morphology, we used morphological shape as a proxy to assess differences in microglial activation. In normal healthy retinas, microglia are stratified into the outer and inner plexiform layers, as well as the ganglion cell layer [20,21]. In the surveillance state [22], originally termed “resting,” the resident microglia exhibit substantial ramification within their stratum [20]. Microglia present in choroid flat mounts are thus activated, but our results indicate that the degree of microglial activation differs between treatments. Indeed, it has been suggested that microglia may achieve various levels of activation under diverse conditions, in distinct regions, and in different tissues [23]. Morphologically, control microglia had smoother cell surfaces (lower fractal dimensions) and a more rounded form (higher form factor), and were half the size of microglia in the NPD1 group; all of these features are consistent with the morphology of amoeboid microglia [24,25]. Conversely, NPD1 treatment resulted in a more ramified morphology. This outcome may be simply a result of the CNV reduction induced by NPD1. Alternatively, NPD1 signaling may target microglia to affect the outcome of CNV. It is not yet clear whether microglial activation is caused by the initial damage from the laser treatment, or alternatively, because of some aspect of the development of the choroidal vessels. These neovessels could potentially leak, and instead provide signals secondary to the laser damage for activation of the microglia. Regardless, the lesion-associated microglia in the NPD1-treated eyes develop a highly ramified morphology that resembles microglia in their postactivated surveillance state, suggesting a condition more associated with resolution [23].
In our previous study, NPD1 was injected intraperitoneally 1 h before and 1, 3, 5, and 7 days following the initiation of the laser-induced CNV, and immunolabeling was performed on flat mount preparations 1 and 2 weeks following laser application. While NPD1 was administered only during the first week, we found continual reduction of leakage throughout the second week, indicating that NPD1 had an ongoing and direct effect on the underlying pathogenic process. Endothelial cell growth was affected in a similar manner; cell volume was significantly lower at the end of the first week and continued to decline during week 2 [6]. We noted similar results throughout the first week in this study, but observed a marked slowing of the decline during the following week, perhaps because of differing retinal NPD1 concentrations resulting from different modes of delivery.
We have suggested that the NPD1-induced reduction of laser-CNV leakage may occur through inhibition of cyclooxygenase 2 (COX-2) expression and nuclear factor kappa B (NF-κB) activation [9], and have shown that COX-2 and vascular endothelial growth factor (VEGF) expression increase when retinal choroidal cells are stimulated with interleukin (IL)-1β [26]. Moreover, NPD1 downregulates IL-1β and tumor necrosis factor (TNF)-α gene expression [27], both of which are known to increase permeability of the pericyte/endothelial cell complex [28]. Accordingly, NPD1-induced inhibition of CNV-associated leakage may result from the reduction of IL-1β and TNF-α expression, as well as the inhibition of NF-κB, a common downstream transcription factor in both pathways. Decreased permeability (i.e., vascular leakage) at the pericyte/endothelial cell complex and a reduction in VEGF expression would result from this, reducing the growth and permeability of endothelial cells.
NPD1 potently promotes cell survival. We have demonstrated that RPE cells are protected from oxidative stress– and inflammation-induced apoptosis by NPD1 [7,8]. Promoting RPE cell survival may encourage the resynthesis of Bruch’s membrane and help to maintain RPE tight junctions, resulting in the reestablishment of an intact subretinal space that is protected from neovascular signaling with the choroid. Moreover, neuronal and glial cell inflammatory Aβ-42-triggered apoptosis and optic nerve damage–induced retinal ganglion cell death are inhibited by NPD1 [27,29], indicating that photoreceptors and Müller glial cells may be protected from CNV inflammatory signaling by NPD1.
In the present study, laser-induced CNV created large neovascularized wound sites with associated microglia, but did little to affect the distribution of microglia that had migrated into the subretinal space. In contrast, treatment with NPD1 exerted neuroprotective action at the laser damage sites, decreasing the volume of the wound site and its neovascular tissue and stimulating microglial migration from the subretinal space to accumulate at the lesions.
It was recently demonstrated that activated microglia can respond to tissue damage by expressing TNF-α [30]. However, we have shown that NPD1 downregulates proinflammatory substances such as IL-1β and TNF-α [27], and the present study suggests that NPD1 treatment blocked the proinflammatory effects of microglia but promoted both tissue aggregation of microglia at the damage site and an anti-inflammatory response. In addition, as in the previous study, NPD1 administration occurred only during the first week, but analysis after 2 weeks demonstrated marked differences in microglial distribution and morphology when compared to untreated retinas undergoing CNV, again suggesting that the effect of NPD1 on the pathoangiogenesis of laser-induced CNV may be long lasting.
These observations suggest that NPD1 may trigger multiple effects on activated microglia, resulting in the promotion of anti-inflammatory responses. Taken together, these results strongly suggest that NPD1 signaling exerts multiple effects on the cross-talk between microglia and the retina/RPE/choroidal complex.
In the present study, we have demonstrated that topical application of NPD1 to the eye surface is well tolerated, reaches retinal tissue, and ameliorates experimental CNV. Importantly, this study corroborates our previous findings of NPD1 attenuating CNV and affirms that NPD1 signaling imparts significant neuroprotection and is capable of resolving neuroinflammatory conditions. The discovery of the redistribution and ramification of microglia concomitant with NPD1-attenuated CNV suggests that NPD1 signaling may function to initiate phenotypic changes within microglia. Since microglia are crucial participants in neurodegenerative diseases, the discovery of microglia as potential targets of NPD1 signaling warrants further investigation.
The authors would like to thank Brittney Chiappinelli for her histology work during her time in the LSUHSC Summer Undergraduate Neuroscience program. Support: NIH/NEI NRSA F31-EY020115 “The Role of Neuroprotectin D1 in Choroidal Neovascularization” PI: Kristopher G. Sheets NIH/NEI Grant R01-EY005121 “RPE Messengers, Transcription and Photoreceptor Renewal” PI: Nicolas G. Bazan NIH/NIGMS Grant P30-GM103340 “Mentoring Neuroscience in Louisiana: A Biomedical Program to Enhance Neuroscience” PI: Nicolas G. Bazan Beckman Initiative for Macular Research Grant 1101 “Neuroprotective bioactivity of neuroprotectin-D1 with nanoparticle-enhanced delivery in experimental retinal degeneration” PI: Nicolas G. Bazan, NIH/NIGMS Grant P01GM095467 "Total Synthesis of Novel Specialized Pro-resolving Lipid Mediators" PI: Nicos A. Petasis.