Immune response in the eye following epileptic seizures
© The Author(s). 2016
Received: 9 December 2015
Accepted: 8 June 2016
Published: 27 June 2016
Epileptic seizures are associated with an immune response in the brain. However, it is not known whether it can extend to remote areas of the brain, such as the eyes. Hence, we investigated whether epileptic seizures induce inflammation in the retina.
Adult rats underwent electrically induced temporal status epilepticus, and the eyes were studied 6 h, 1, and 7 weeks later with biochemical and immunohistochemical analyses. An additional group of animals received CX3CR1 antibody intracerebroventricularly for 6 weeks after status epilepticus.
Biochemical analyses and immunohistochemistry revealed no increased cell death and unaltered expression of several immune-related cytokines and chemokines as well as no microglial activation, 6 h post-status epilepticus compared to non-stimulated controls. At 1 week, again, retinal cytoarchitecture appeared normal and there was no cell death or micro- or macroglial reaction, apart from a small decrease in interleukin-10. However, at 7 weeks, even if the cytoarchitecture remained normal and no ongoing cell death was detected, the numbers of microglia were increased ipsi- and contralateral to the epileptic focus. The microglia remained within the synaptic layers but often in clusters and with more processes extending into the outer nuclear layer. Morphological analyses revealed a decrease in surveying and an increase in activated microglia. In addition, increased levels of the chemokine KC/GRO and cytokine interleukin-1β were found. Furthermore, macroglial activation was noted in the inner retina. No alterations in numbers of phagocytic cells, infiltrating macrophages, or vascular pericytes were observed. Post-synaptic density-95 cluster intensity was reduced in the outer nuclear layer, reflecting seizure-induced synaptic changes without disrupted cytoarchitecture in areas with increased microglial activation. The retinal gliosis was decreased by a CX3CR1 immune modulation known to reduce gliosis within epileptic foci, suggesting a common immunological reaction.
Our results are the first evidence that epileptic seizures induce an immune response in the retina. It has a potential to become a novel non-invasive tool for detecting brain inflammation through the eyes.
Epilepsy is a neurological disorder characterized by spontaneous seizures, affecting almost 1 % of the population worldwide . An epileptic seizure is an abrupt abnormal synchronized activity affecting the entire—or parts, of the brain. When a seizure engages the entire brain, called a generalized seizure, the patients experience disturbed consciousness and often tonic-clonic muscle movements. Seizures initiated in parts of the brain are named focal seizures and may induce a plethora of symptoms often correlated to the function or lack of function of that particular brain region. The etiology of epilepsy varies. It may arise due to a brain infection, trauma, ischemia, tumor, neurodegenerative disease, or genetic predisposition. A large proportion is cryptogenic. Almost 40 % of epilepsy patients are resistant to current anti-epileptic therapy, which makes investigation of new therapeutic targets and biomarkers for patient stratification warranted.
Pathological hallmarks in the brain associated with epilepsy include imbalance in synaptic transmission, neuronal damage, and an exaggerated immune response [2–6]. During the acute innate immune response in the brain following seizures, microglia release pro- and anti-inflammatory mediators , undergo phenotypic changes, and migrate towards the epileptic foci where they phagocytize cell debris [8, 9]. Moreover, astrocytes change their activity state and exhibit disturbed buffering capacity of ions and glutamate uptake . In addition to the innate immune reaction, seizures may cause blood-brain barrier dysfunction and activation of vascular-associated and blood-derived immune cells . Hitherto, a seizure-induced immune response has primarily been described within the epileptic foci of the brain, such as in hippocampal sclerosis in medial temporal lobe epilepsy, the most common form of epilepsy . However, recent findings support the idea that seizures may be viewed as a disturbance of entire brain networks, including subcortical nodes for seizure propagation . More remote areas of the brain, such as the retina, have not yet been investigated at all. Recently, we reported microglial activation in both cortical and subcortical brain areas even before behavioral seizures had developed in a genetic mouse model of epilepsy . Therefore, the relationship between brain inflammation and epileptogenesis may also be further understood by studying the immune response in remote areas to the epileptic foci that are not known to either generate or propagate seizures.
In the present study, we therefore decided to explore whether a post-seizure immune response can extend beyond an epileptic focus within the temporal lobes and, hence, be detected as far as the retina of adult rats. The retina lines the back of the eyeball and constitutes a remote extension of the brain, so far not considered to exhibit seizure-induced pathology. It is a light-sensitive neural structure with several layers of strictly interconnected neurons . The innate and adaptive immune response of the retina involves, similar to other brain regions, the activation of microglia and macroglial cells (i.e., astrocytes and Müller cells), vascular pericytes, and leucocytes that cross the blood-retina barrier (BRB) [14–16]. Since the retinal immune response is more accessible than the cerebral immune response for non-invasive investigations, it may become an attractive biomarker of brain inflammation if it reflects the immune response in the rest of the brain. Here, we evaluated micro- and macroglial activation, leukocyte infiltration, and number of vascular pericytes in the retina, acutely and late after electrically induced temporal status epilepticus. We also investigated whether a seizure-induced retinal immune response may be modulated by intracerebroventricular infusion of an antibody (Ab) against the chemokine receptor CX3CR1.
Adult male Sprague Dawley rats (n = 78) weighing between 200 and 250 g were procured from Charles River (Germany). The animals were housed in a 12-h light/dark cycle with ad libitum food and water. All experimental procedures followed the guidelines set by the Malmö-Lund Ethical Committee in Sweden for the use and care of laboratory animals, and the ARVO statement for the use of animals in ophthalmic and vision research.
Animals were divided into three survival groups following electrically induced temporal status epilepticus (SE) and corresponding non-stimulated controls (NSC): 6 h (SE n = 4 and NSC n = 5 were perfused, SE n = 4 and NSC n = 4 were homogenized), 1 week (SE n = 9 and NSC n = 8 were perfused, SE n = 6 and NSC n = 6 were homogenized), and 7 weeks (SE n = 6, SE + CX3CR1 antibody n = 7 and NSC + saline infusion n = 9 were perfused SE n = 5 and NSC n = 5 were homogenized).
Surgeries, drug infusions, and electrically induced temporal status epilepticus
For biochemical analyses, rats were decapitated and the eyes, excluding the lenses, were immediately collected, frozen on dry ice, and stored in −80 °C. For immunohistochemistry, rats were perfused with ice-cold 0.9 % saline and paraformaldehyde (PFA) (4 % in 0.1 M phosphate-buffered saline (PBS), pH 7.4). The eyes were enucleated and post-fixed in PFA for 4 h, rinsed in PBS, incubated in 10 % sucrose (16 h) and 25 % sucrose (16 h), consecutively embedded in a Yazulla medium (30 % egg albumin, 3 % gelatin), and finally cut in 20 μm-thick sagittal cryosections (Microm HM 560, US) and stored at −20 °C.
Multiplex enzyme-linked immunosorbent assay (ELISA)
Samples were homogenized on ice in buffer (pH 7.6) containing (in millimolars) 50.0 Tris-HCl, 150 NaCl, 5.0 CaCl2, 0.02 % NaN3, and 1 % Triton X-100, and then centrifuged at 17,000g for 30 min at 4 °C. The supernatant was collected into a microcentrifuge tube, where the total protein concentration was determined by BCA protein assay (BCA, Pierce, Rockford, IL) as per manufacturer’s instructions. Levels of interleukin (IL)-1β, tumor necrosis factor (TNF)-α, interferon (IFN)-γ, IL-4, IL-5, IL-6, IL-10, IL-13, and keratinocyte chemoattractant/growth-related oncogene (KC/GRO) were measured by sandwich immunoassay methods using commercially available electrochemiluminescent detection system, plates, and reagents (V-PLEX Proinflammatory Panel 2 (rat) kit, Meso Scale Discovery (MSD), Gaithersburg, MD, USA) as per manufacturer’s instructions with minor modifications. Briefly, 100 μg (50 μl) of the protein sample was loaded per well in the MSD plate. The samples were incubated overnight at 4 °C with shaking. For each assay, samples were analyzed in duplicates and compared with known concentrations of protein standards. Plates were analyzed using the SECTOR Imager 2400.
Western blot analysis
Western blot analyses were performed as previously described . The following primary Abs were used: mouse monoclonal anti-β actin (1:10,000; Sigma-Aldrich, MO, US), rabbit monoclonal anti-glyceraldehyde 3-phosphate dehydrogenase (GAPDH) (1:2000; Cell Signaling Technologies, CA, USA), rabbit polyclonal anti-CX3CR1 (1:500; Abcam, Cambridge, UK), and mouse monoclonal anti-postsynaptic density-95 (PSD-95) (1:200, Abcam). Secondary Abs used were either horseradish peroxidase-conjugated anti-mouse or anti-rabbit (both 1:5000; Sigma-Aldrich). Band intensities were quantified using ImageJ software (NIH, USA), and β-actin or GAPDH was used as a loading control.
Sections were washed with potassium PBS, hydrated, and pretreated with 0.06 % potassium permanganate for 15 min, rinsed with distilled water, and treated with 0.001 % Fluoro-Jade (Histo-Chem, Jefferson, AR, USA) for 30 min. They were then washed with distilled water, dehydrated by treatment with ethanol and xylene, and coverslipped with PERTEX mounting medium.
Immunohistochemistry and hematoxylin-eosin staining
Immunohistochemistry was performed as previously described . The following primary Abs were used: rabbit polyclonal anti-Iba1 (1:1000; Wako, Japan), mouse anti-rat CD68/ED1 (1:200; AbD Serotec, NC, USA), rabbit anti-CD-45 (1:100; Santa Cruz Biotechnology, TX, USA), mouse anti-neuron glial antigen 2 (NG2) (1:200; Millipore, MA, USA), mouse anti-glial fibrillary acidic protein (GFAP) (1:400; Sigma-Aldrich), goat anti-Iba1 (1:250; AbD Serotec), mouse anti-PSD-95 (1:500; Abcam), rabbit anti- IL-6 (1:400; Abcam), rabbit anti-IL-4 (1:100, Abcam), and goat anti-IL-1β (1:100; Santa Cruz Biotechnology). Sections were incubated with appropriate primary Abs overnight at 4 °C and secondary antibody for 1 h at room temperature. For each immunohistochemical assessment, some eye sections went through the entire protocol without primary Abs incubation to serve as the negative controls. The following secondary Abs were used: Cy3-conjugated donkey anti-mouse/rabbit/goat (1:200; Jackson ImmunoResearch, UK), Alexa-488 conjugated donkey anti-mouse/rabbit (1:200; Invitrogen, NY, USA), and Cy2-conjugated donkey anti-rabbit (1:200; Jackson ImmunoResearch). For counterstaining of nuclei, the sections were coverslipped using 496-diamidino-2-phenylindole (DAPI)-containing VECTASHIELD mounting medium (Vector Laboratories, Burlingame, CA, USA) and stored in −20 °C until cell quantification. For gross morphological analyses, sections were stained with hematoxylin-eosin (Htx-eosin) for 1 min, dehydrated, and coverslipped using PERTEX mounting medium (HistoLab, Sweden).
Morphological analyses, cell countings, and intensity measurements
First, an overall gross morphological analysis of retinal lamination was performed throughout the entire retina using light microscopy, in four sections from ipsi- and contralateral eyes, respectively. Second, detailed analyses were performed with regard to nuclear layer morphology using the ranking system 0–2 (0 = normal nuclear layer morphology and the presence of 0–10 pyknotic (shrunken) nuclei; 1 = islands of disseminated nuclear layers without nuclei (typically the size of 1–2 cells) and 11–20 pyknotic nuclei; 2 = completely disseminated nuclear layers and >20 pyknotic nuclei) as described previously .
Semi-quantitative analysis of GFAP expression was performed in 12 representative images from four sections/eye, using Olympus BX61 epifluorescence microscope. The density of GFAP+ radial Müller cell processes was graded according to a 0–5 scale in IPL (0 = none, 1 = 1–5, 2 = 6–10, 3 = 11–20, 4 = 21–50, 5 = >50 processes) and a 0–3 scale in INL + OPL and ONL, respectively (0 = none, 1 = 1–5, 2 = 6–10, 3 = >10 processes). In addition, number of GFAP+ retinal astrocytes was manually quantified in 12 representative images of the inner retina from four sections/eye.
Intensity measurements of GFAP expression in the GCL, NFL, and ILM were performed in fluorescence images from 12 sections/eye (each image corresponding to 13 × 103 μm2), using an Olympus BX61 epifluorescence microscope (Leica, Germany). Intensity measurements of PSD-95 expression in IPL, INL, OPL, and ONL, respectively, were performed with confocal laser scanning microscope (Zeiss, Germany) with a 561-nm excitation filter, ×63 oil-immersion objective, and ×5 zoom. Intensity measurements of IL-6, IL-4, and IL-1β expression in IPL, INL, OPL, and ONL, respectively, were carried out with a 488-nm and 561-nm excitation filter, ×40 oil-immersion objective, and ×5 digital zoom. Images were taken from three representative areas from each animal. Each image was acquired in a z-stack at an interval of 0.2 μm, on average 50 slices per z-stack. The images were analyzed in ImageJ software and the brightness and contrast corrected and noise reduced using the built-in ImageJ functions. Background intensity was measured in every image and subsequently subtracted from the mean gray value from each image in order to obtain a background-corrected mean gray value per animal.
To ensure the lack of bias, all analyses were conducted by an observer blind to the treatment conditions.
Statistical analyses were performed with the unpaired Student’s t test when comparing two groups, using GraphPad Prism software, except for analyses of gross morphology and grading of GFAP+ processes where Mann-Whitney’s rank sum test for non-parametric variables was applied. Microglial morphology was analyzed with two-way analysis of variance (ANOVA) followed by a Bonferroni post hoc test. Data are presented as means ± SEM, apart from gross morphology and GFAP+ process evaluations, which are presented as median ± range with upper quartile range. Differences were considered statistically significant at p ≤ 0.05.
Lack of acute changes in the expression of immune mediators, glial activation, and cell death in the eyes after temporal status epilepticus
Next, biochemical analyses of pro- and anti-inflammatory mediators in the protein homogenates from the eye tissue excluding the lens at 6 h following SE were evaluated. At this time point, several immune factors are upregulated in the epileptic focus of the hippocampus (Avdic U, Ahl M, Ekdahl CT, unpublished observation). However, even though the chemokine KC/GRO, chemokine receptor CX3CR1, and the cytokines IL-6, IL-5, and IL-1β were detectable in the eyes, the levels were unaltered compared to the NSC group, both ipsi- and contralateral to the epileptic focus (Fig. 3d, e).
Lack of subacute changes in the expression of immune mediators, glial activation, and cell death in the eyes after temporal status epilepticus
We next performed cytoarchitectural analyses of the eye tissue 1 week post-SE. At this time point, neuronal necrosis and apoptotic cell death are readily observed in varying degree within temporal structures, including the hippocampus [17, 22]. However, in the retina, again, no obvious pathological signs were found at the gross cytoarchitectural level. Detailed morphological analysis of the retina showed no differences between SE and NSC group in the ipsi- and contralateral eyes, with both retinas displaying well-preserved nuclear layer morphology and only occasional pyknotic cells and disseminated GCL (ipsilateral SE 0.25 u = 0.875 vs NSC 0.5 u = 0.5 and contralateral SE 0 u = 0.75 vs NSC 0.25 u = 0.458 score) (Fig. 2c). Less than three Fluoro-Jade+ cells per animal were observed in both groups.
Delayed glial activation in the retina after temporal status epilepticus
We hypothesized that a seizure-induced tissue injury may be delayed in the retina compared to other brain structures and, therefore, we extended our analyses to a later time point, i.e., 7 weeks after SE. Again, no changes in retinal laminar organization or significant changes in the cytoarchitecture (ipsilateral SE 1.0 u = 1 vs NSC 0.5 u = 0.75 and contralateral SE 0.25 u = 0.375 vs NSC 0.333 u = 0.50 score) could be detected (Fig. 2d). The quantification of Fluoro-Jade+ cells in the retina never exceeded three cells per eye.
Less than 1–2 single-labeled ED1+ cells and Iba1+/ED1+ cells per retina were detected at 7 weeks post-SE (data not shown). The cells were uniformly distributed among the retinal layers (Fig. 5k). In order to evaluate a possible systemic contribution of leukocytes to the immune response in the retina after SE, numbers of CD45+ cells were evaluated at 7 weeks, but again, very low cell numbers were found with no differences between the two groups (ipsilateral SE 0.38 ± 0.13 vs NSC 0.97 ± 0.22, contralateral SE 0.88 ± 0.38 vs NSC 1.53 ± 0.34). At both 1 and 7 weeks, CD45+ cells were primarily located in the subretinal layers, not overlapping with the Iba1 staining (Fig. 5l).
In an attempt to define whether the immune response in the retina was associated with a subtle microvascular disturbance, we also analyzed the numbers of vascular NG2-expressing pericytes . NG2+ cells were found in the same retinal layers as the Iba1+ cells, but their expressions did not overlap (Fig. 5m). Often, the NG2+ cells were aligned in a cluster of 2–3 cells, as if embracing a microvessel (Fig. 5m inset). However, the cell numbers did not differ between SE and NSC group neither 1 nor 7 weeks post-SE (1 week ipsilateral SE 9.64 ± 0.40 vs NSC 8.76 ± 0.62 and contralateral SE 8.67 ± 0.29 vs NSC 9.60 ± 0.51; 7 weeks ipsilateral SE 7.97 ± 0.64 vs NSC 8.38 ± 0.31, contralateral SE 7.47 ± 0.51 vs NSC 8.16 ± 0.76).
Altered synaptic protein expression in the retina after temporal status epilepticus
Intracerebroventricular CX3CR1 antibody infusion decreases micro- and macroglial activation in the retina after temporal status epilepticus
Here, we provide the first evidence that epileptic seizures arising within the temporal lobes of the adult rat brain lead to glial activation in the retina. The activation includes both micro- and macroglia and is delayed in the retina compared to the epileptic focus. The seizures originated from one hemisphere, but the retinal glial activation occurred both ipsi- and contralaterally. Furthermore, we show that the seizure-induced retinal glial activation can be significantly reduced with intracerebroventricular infusion of the same CX3CR1Ab as we have previously demonstrated to reduce microglial activation within the epileptic focus. This suggests common immunological features in the retina and the epileptic focus.
Although the retina exhibited a pronounced glial reaction, retinal neurodegeneration was subtle compared to the pathology within the epileptic focus [5, 17, 19, 23]. We found no evidence for prominent retinal neuronal death in terms of disseminated retinal lamination, increased numbers of pyknotic cells, or Fluoro-Jade-positive cells at the time points studied. Still, the increased number of activated microglia, often in clusters, disarranged the normally very strict territorial distribution of the retinal microglia , and is most likely reflecting alterations in their normal function as regulators of synaptogenesis and synaptic transmission [30, 31]. Similarly, the decreased levels of the excitatory synaptic scaffolding protein PSD-95 in the ONL, where we observed seizure-induced aberrant microglia processes, may indicate a homeostatic imbalance in excitatory transmission. The technique for intensity measurements was not sensitive enough for detecting minor differences in high intensity regions, which may explain why we did not detect changes in synaptic plexiform layers with strong PSD-95 expression . Future electrophysiological recordings of retinal neuronal networks will be important for validating synaptic transmission and functional deficiencies.
Interestingly, other neurological diseases have also recently been described to induce retinal inflammation but with more pronounced neurodegeneration. In experimental and clinical studies on stroke, Parkinson’s, Huntingtons’, and Alzheimer’s diseases, reduced retinal ganglion cell numbers, and nerve fiber layer thinning are evident, causing visual disturbances . Activation of micro- and macroglia, mononuclear infiltrations, and microvascular abnormalities have also been reported [33–39]. In addition, demyelinating diseases like multiple sclerosis show optic disc and nerve dysfunction . Notably, experimental AD studies linked increased retinal glial activation to astrocyte changes in the brain . However, since the presented delayed upregulation of GFAP in macroglia after SE is an early indicator of reactive gliosis , we cannot rule out that the pathology may progress beyond 7 weeks post-SE and with additional seizures. Conversely, since there was a high variation in retinal GFAP expression within both the SE and NSC group 6 h and 1 week after SE, we cannot rule out that there may be changes occurring acutely that were not detected with our analyses. The significance of the small decrease in GFAP at 6 h after SE also remains to be clarified.
Another important distinction between the current and previous studies on stroke and neurodegenerative diseases is the fact that the temporal seizures were initiated from implanted electrodes within a very localized area of an initially healthy brain, without genetic susceptibility or systemic immunological/vascular deficiencies. Hence, the retinal changes could only have occurred as a result of the SE insult, the SE-induced spontaneous seizures, and/or SE-induced epileptogenesis and not due to an underlying disease, which is otherwise often the case in epilepsy. Future correlation studies of seizure numbers and degree of retinal inflammation as well as studies on retinal inflammation in other models of epilepsy may give more answers to what extent retinal inflammation is a biomarker of epileptogenesis or merely a reaction to seizures per se.
There are at least four possible scenarios that may explain the underlying mechanisms of the seizure-induced retinal immune response. First, temporal seizures initiate an acute systemic immune response which may spread through the BRB. Common inflammatory mediators are upregulated in both the hippocampus and enthorinal cortex 24 h after SE . However, when evaluating the same immune factors at an earlier time point in eye homogenates, no such increase was found. Instead, subtle changes in cytokine/chemokine levels were observed with a delay. A systemic immune response may also trigger a delayed infiltration of leukocytes from the retinal vessels in the subretinal or retinal layers. Though, we did not observe such an adaptive response, it may still occur at other time points. We also did not find changes in numbers of vascular pericytes, as in, i.e., diabetic retinopathy [42, 43]. Vascular pericytes are situated along endothelial cells in the wall of small blood vessels [44, 45] and sense microvascular dysfunction [46, 47]. Here, we cannot rule out that seizures lead to altered BRB function and a more subtle microvascular reorganization. Moreover, there are studies describing retinal microglial activation without prominent infiltrating leukocytes during a systemic inflammation and viral infections .
Secondly, the seizures may change the intracranial pressure (ICP) and influence the intraocular pressure (IOP) within the eyes. An imbalance between the anterior IOP and posterior ICP fluid pressures on the optic nerve may lead to abnormal function and nerve damage in GCL and ONL due to changes in axonal transport or altered blood flow, as seen in glaucoma [48, 49]. Initial signs of increased IOP may include altered PSD-95 expression and gliosis [50, 51].
Thirdly, the immune response in the epileptic focus may spread to other brain areas involved in the temporal seizure networks, including subcortical structures, and via the visual pathways initiate changes as far as the retina. It is likely that such a scenario would induce a stronger immune response close to the entrance of the optic nerve and inner part of the retina. Accordingly, we found macroglia activation primarily in the inner retina. However, the microglial cells did not gather within the inner layers but were evenly distributed within synaptic layers and aberrantly in the ONL. Detailed investigations of the nerve fiber tract and optic disc may reveal more subtle local changes in favor of a direct rostral cerebrum-to-retina signaling. In support, studies in AD patients suggest that inflammation may, through soluble pathogenic factors such as small nucleic acids, spread from the limbic structures both into the visual cortex, optic nerve, and the retina [39, 52].
Fourthly, an epileptic seizure may induce a retrograde current through the optic nerve, initiating an imbalance in excitatory/inhibitory transmission in the retinal network and thereby a glial activation. Whether the retinal neurons may have the properties to exhibit abnormal synchronized firing similar to a seizure among cortical neurons is to our knowledge not known. Activated Müller cell processes in the inner retina may perhaps contribute to epileptic discharges, as suggested for astrocytes in the rest of the brain .
The seizure-induced glial activation was evident in the retina both ipsi- and contralateral to the temporal epileptic focus. A previous case report on Rasmussen’s encephalitis, a severe inflammatory epileptic encephalopathy engaging only one brain hemisphere, described an ipsilateral ocular inflammation in the patient . The authors speculated to what extent an immune reaction in the eye after focal seizures may also be associated with clinical manifestations. However, apart from small alterations in cytokine/chemokine levels in the ipsilateral retina only, we could not find significant differences between the two retinas after focal temporal seizures helping in determining whether the rat exhibited left or right temporal lobe seizures. In the current study, we did not differentiate between lateral and medial parts of the retina; and therefore, we cannot define whether the retinal inflammation may be correlated to the left or right hemisphere-innervated visual field. This will be important to analyze in future studies.
A reduced glial activation both in the retina and within epileptic foci following intracerebroventricular CX3CR1 Ab treatment suggests that the two immune responses, despite being remotely located, share similar activated signaling pathways. The fractalkine-CX3CR1 pathway is involved in the activation and migration of immune cells [27, 54, 55], and an increased expression of CX3CR1 in the epileptic focus suggests a dysfunctional neuron-glial cross talk [19, 56, 57]. Thus, a reduced immune response in the eye after CX3CR1 Ab treatment may be due to a reduced propagation of the immune response from the epileptic focus/network, which could be a result of both a reduced microglia activation and neurodegeneration within the epileptic focus and a direct inhibition of the migratory capacity of the immune cells. However, CX3CR1 deficiency has been associated with eye-related disorders [58–60]; thus, we do not know the functional consequences of inhibiting seizure-induced retinal immune response with CX3CR1 Ab. During healthy conditions, the glial cells are important for keeping the homeostasis. The seizure-induced retinal immune response or the remaining immune response after CX3CR1 Ab treatment may be dysfunctional. As for the immune response in the rest of the brain, the retinal immune response is likely to both contribute to and restore pathology . However, we believe that the mere existence of a retinal glial activation may turn out to be a potential novel biomarker of seizure-induced or epileptogenesis-associated brain inflammation. The fact that the retina is more accessible than many other parts of the brain makes it more attractive for diagnostic purposes. Studying the immune reaction in the eyes of epilepsy patients and correlating it to the seizure semiology, development, and prognosis may turn out to be clinically relevant.
To what extent a visual dysfunction in patients with temporal epilepsy exists and correlates to a glial activation in the retina and brain remains to be shown. Patients with epilepsy do not commonly describe visual disturbances, except for those with visual cortical involvements or drug-induced side effects. Therefore, we do not currently know if patients have retinal inflammation and visual disturbances subclinically. In the present study, we have also not addressed the question as to what extent rodents with temporal epileptic seizures suffer from functional retinal deficiencies. Future studies with pattern evoked electroretinography and multi-electrode array analysis of retinal physiology will be highly relevant [62, 63].
These are the first evidence that epileptic seizures lead to an immune response in the retina. The finding has a potential to become a novel non-invasive tool for detecting brain inflammation through the eyes.
Ab, antibody; AD, Alzheimer’s disease; BRB, blood-retina barriers; DAPI, 496-diamidino-2-phenylindole; EEG, electroencephalographic; ELISA, enzyme-linked immunosorbent assay; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; GCL, ganglion cell layer; GFAP, glial fibrially acidic protein; Htx-eosin, hematoxylin-eosin; ICP, intracranial pressure; IFN-γ, interferon gamma; IL-1β, 4–6, 10, 13, interleukin 1beta, 4-6, 10, 13; IML, inner limiting membrane; INL, inner nuclear layer; IOP, intraocular pressure; IPL, inner plexiform layer; KC/GRO, keratinocyte chemoattractant/growth-related oncogene; MSD, Meso-Scale Discovery; NFL, nerve fiber layer; NG2, neuron glial antigen 2; NSC, non-stimulated control; ONL, outer nuclear layer; OPL, outer plexiform layer; PBS, phosphate-buffered saline; PFA, paraformaldehyde; PSD-95, postsynaptic density-95; SE, status epilepticus; TNF-α, tumor necrosis factor alpha
This work was supported by the Swedish Research Council, ALF Grant for funding medical training and research, Zoega’s Foundation, Tore Nilson’s Foundation, and Åhlens’ Foundation. The research leading to these results has received funding from the European Union’s Seventh Framework Programme (FP7/2007-2013) under grant agreement no. 602102 (EPITARGET). We thank biomedical analysts Susanne Jonsson, Hodan Abdshill, and Birgitta Stenström for technical support.
This work (including data collection, analysis, interpretation, and writing of paper) was supported by the Swedish Research Council, ALF Grant for funding medical training and research, Zoega’s Foundation, Tore Nilson’s Foundation, and Åhlens Foundation. The research leading to these results has also received funding from the European Union’s Seventh Framework Programme (FP7/2007-2013) under grant agreement no. 602102 (EPITARGET).
Availability of data and materials
Datasets for all experiments are available through corresponding author.
MA partly acquired data shown in Figs. 2, 3, 4, 5, and 8. UA contributed with data shown in Figs. 6 and 7 and partly Figs. 3, 4, 5, and 8. UA, IA, and DC provided the animal material in the study. CS contributed with the data shown in Fig. 2. UEJ and CE provided the experimental design and most of the writing. All authors reviewed the results, took part in the writing, and approved the final version of the manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
All experimental procedures followed the guidelines set by the Malmö-Lund Ethical Committee in Sweden for the use and care of laboratory animals.
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