- Research article
- Open Access
Progressive ganglion cell loss and optic nerve degeneration in DBA/2J mice is variable and asymmetric
© Schlamp et al; licensee BioMed Central Ltd. 2006
- Received: 22 May 2006
- Accepted: 03 October 2006
- Published: 03 October 2006
Glaucoma is a chronic neurodegenerative disease of the retina, characterized by the degeneration of axons in the optic nerve and retinal ganglion cell apoptosis. DBA/2J inbred mice develop chronic hereditary glaucoma and are an important model system to study the molecular mechanisms underlying this disease and novel therapeutic interventions designed to attenuate the loss of retinal ganglion cells. Although the genetics of this disease in these mice are well characterized, the etiology of its progression, particularly with respect to retinal degeneration, is not. We have used two separate labeling techniques, post-mortem DiI labeling of axons and ganglion cell-specific expression of the βGeo reporter gene, to evaluate the time course of optic nerve degeneration and ganglion cell loss, respectively, in aging mice.
Optic nerve degeneration, characterized by axon loss and gliosis is first apparent in mice between 8 and 9 months of age. Degeneration appears to follow a retrograde course with axons dying from their proximal ends toward the globe. Although nerve damage is typically bilateral, the progression of disease is asymmetric between the eyes of individual mice. Some nerves also exhibit focal preservation of tracts of axons generally in the nasal peripheral region. Ganglion cell loss, as a function of the loss of βGeo expression, is evident in some mice between 8 and 10 months of age and is prevalent in the majority of mice older than 10.5 months. Most eyes display a uniform loss of ganglion cells throughout the retina, but many younger mice exhibit focal loss of cells in sectors extending from the optic nerve head to the retinal periphery. Similar to what we observe in the optic nerves, ganglion cell loss is often asymmetric between the eyes of the same animal.
A comparison of the data collected from the two cohorts of mice used for this study suggests that the initial site of damage in this disease is to the axons in the optic nerve, followed by the subsequent death of the ganglion cell soma.
In a systematic examination of intraocular pressure (IOP) in inbred mice, John and colleagues described elevated levels of IOP and the subsequent development of an optic neuropathy in the DBA/2J (D2) line . The development of elevated IOP in these mice is linked to mutations in two genes, Gpnmb and Tyrp1, which encode a protein found in melanosomal membranes and an enzyme involved in melanin synthesis, respectively [2, 3]. Recessive inheritance of both of these mutant genes causes the breakdown of the iris stroma and the release of pigment clumps into the anterior chamber of the eye. The association of these proteins with melanosomes has lead to the theory that toxic byproducts generated by the biosynthesis of melanin are released from the melanosome leading to the atrophy of the iris. In some respects, this disease resembles human pigment dispersion syndrome in that displaced pigment accumulates in the trabecular meshwork (TM) leading to elevated IOP and glaucoma. It is also clear that disease in the D2 mouse has an immune component that may contribute to both iris atrophy and the pathology of the TM. D2 mice exhibit a decrease in ocular immune privilege as they age. Leakage of the blood brain barrier leads to infiltration of monocytes and neutrophils into the anterior chamber and the iris , possibly in response to increasing amounts of toxic melanin byproducts accumulating in the anterior chamber. Bone marrow transplants into D2 mice, from genetically different donors, can effectively prevent the age-related decrease in immune privilege leading to a substantial reduction in both the anterior chamber disease and the subsequent increase in IOP.
The temporal course of the pathology of the anterior chamber disease is relatively predictable, but by no means synchronous in D2 mice. In general, defects in the iris, as determined by transillumination, begin to occur in mice at ~6 months of age. Elevation in IOP is detected in animals anytime from 9–12 months, and is variable within the population . Early studies of the time course of retinal ganglion cell death indicated that a majority of animals exhibited significant cell loss and optic nerve degeneration by 12 months  and TUNEL studies showed that peak cell death in the ganglion cell layer of these mice occurred between 10 and 13 months . Similarly, DBA/2NNia mice, a substrain of the DBA/2J line, also exhibited ganglion cell loss between 12 and 15 months of age [7–9]. Several studies have characterized the neuronal populations affected in this disease. Jakobs and colleagues described that the dying cells at this age were almost entirely made up of different sub-types of retinal ganglion cells, while other retinal cell-types, such as amacrine cells, were unaffected . A study by Moon et al showed a similar depletion of ganglion cells, but also noted changes in a subset of amacrines . An ultrastructural electron microscope study, conducted by Scheuttauf and colleagues, described two patterns of neurodegeneration as D2 mice age . Although this study relied on qualitative observations, it concluded that ganglion cell apoptosis was more prevalent in mice under 6 months of age, while necrotic cell death was more prevalent in older mice. In addition to necrosis, mice at ages of 8 and 11 months exhibited ischemic retinal changes, and showed evidence of activated Müller's cells and an increase in neoangiogenesis. Aged retinas showed no signs of inflammatory cells or damage to other retinal cell layers, such as the photoreceptors. These observations may be quite significant, because they indicated that necrosis was the principal mechanism of cell death during the period of elevated IOP. This assessment was made using relatively general morphological criteria on very few animals, however, and more recent studies using Bax knock out animals have demonstrated that intrinsic apoptosis is the primary pathway of cell death associated with elevated IOP in D2 mice .
In this study, we report on the timing and pattern of both optic nerve and retinal degeneration in two separate cohorts of D2 mice. In both cases, the disease exhibits variable and asymmetric progression in mice as they age and has features that are consistent with glaucoma in humans. Additionally, a comparison of the onset of damage between the two, suggests that optic nerve degeneration precedes measurable damage in the retina, implicating the optic nerve as the initial site of damage in this disease.
Evaluation of optic nerve degeneration in aging D2 mice
Evaluation of retinal ganglion cell loss in aging D2 mice
The asymmetry and timing of degeneration in D2 mice
The difference in retinal score between eyes of the same mouse was also calculated and graphed (Fig. 9B). Eyes that differed by less than 0.5 on our grading scale were considered the same based on the level of variability observed in scorer agreement analysis. Forty percent of the mice (58/145 mice) had scores that differed between the eyes by more than 0.5 on our grading scale, again with no significant preference between left and right eyes (P > 0.50, χ2 analysis). A total of 13 mice (9% of the entire cohort) had scores that differed by more than 2.0 on the grading scale, which was similar to the percentage of mice exhibiting complete asymmetry of optic nerve degeneration.
The results from two separate cohorts of aging D2 mice are reported here. In the first cohort, anterograde DiI-labeling and confirmatory histology showed a marked increase in degeneration of the optic nerve in a majority of mice when they reach 9 months of age. In the second cohort, ganglion cell loss was followed as a function of histochemical staining activity of the ROSA3 (Fem1cR3/+) βGeo reporter gene product. Using this method, a majority of mice exhibit moderate to severe damage by 10.5 months of age.
Degeneration of the optic nerve
The timing of optic nerve degeneration we observed in our mice followed a similar pattern recently reported by Libby et al. , with the exception that we detected signs of degeneration at 9 months of age, or 1 month earlier than the Libby study. A variety of factors may account for this difference, including different sensitivities in the methods used to evaluate the nerves, the numbers of mice analyzed at critical ages, and different housing and feeding conditions that could affect the timing of the disease in different colonies.
By combining the data collected using silver staining of optic nerve sections and the DiI-labeling technique, we speculate that axons damaged in glaucoma start to degenerate in regions throughout the nerve, proximal to the laminar region. The overall pattern of degeneration, however, occurs in a retrograde direction. A similar pattern of retrograde degeneration has been reported in tibial nerves of mice after nerve crush . Interestingly, the pattern of degeneration of axons is different if a more acute lesion (transection) is performed on the tibial nerve. In this latter paradigm, Wallerian degeneration occurs in an anterograde direction and is initiated more rapidly than in nerves after crush. The direction of degeneration we observe in D2 mice suggests that the nerve lesion in glaucoma is more akin to crush in severity.
In addition to the retrograde direction of loss, we also observed the "preservation" of peripheral tracts of axons in a significant number of nerves examined. The lack of uniform degeneration across the whole diameter of the nerve suggests that damage to the axons is probably more focal than diffuse. A similar condition has been reported in the nerves of humans with glaucoma [14–17] and non-human primates with experimental glaucoma . In these cases, glaucomatous degeneration followed a classic "hourglass" pattern of axon loss in the inferior and superior regions of the optic nerves, which has been associated with structural differences in the collagen beams of the lamina cribrosa . Similarly, mice with experimental ocular hypertension (as apposed to the chronic disease exhibited by D2 mice) exhibit initial axon loss in the superior optic nerve . Although we have not detailed any predictable pattern of loss in DBA/2J mice, when present, the preserved axon tracts are found predominantly in the nasal optic nerve. Structural studies of the optic nerve head in some strains of mice have not found any evidence of an extracellular lamina cribrosa , but this does not preclude the possibility that mice also have some kind of increased structural support in different regions of the optic nerve.
The method of DiI-labeling also allowed us to rapidly evaluate the symmetry of optic nerve damage in each mouse. A majority of animals exhibited more damage in one nerve over the other, with no preference between left and right eyes. Like the non-uniform degeneration of axons we observed in some optic nerves, asymmetric degeneration between eyes is also similar to the natural history of this disease in humans. Several independent studies in which visual field defects and changes to the optic disc were analyzed, have reported marked asymmetry of disease progression in glaucoma patients [21–25].
Degeneration of the retina
Using βGEO activity to mark ganglion cells, the earliest detectable changes in the retina we observed were at 8–10 months of age, with a peak in the number of animals showing degeneration occurring by 10.5–11 months of age. Our data showing peak disease at this age are consistent with the TUNEL data reported by Libby et al  and the loss of fluorogold-labeled ganglion cells in DBA/2NNia mice, a substrain of DBA/2J , indicating that the progression of disease is not unduly influenced by the presence of a single R3 allele. Our results contradict the observations made by Scheuttauf and colleagues , however, in that we found no obvious increase in cell loss in 6 month old mice. Since the Scheuttauf group did not quantify the amount of cell loss they observed, it is not known if the reported increase in cell death they observed was large enough to detect using the βGeo staining method. It is also clear that the timing of retinal degeneration is highly variable in a population of aging D2 mice and because this other study used relatively small numbers of mice for their studies, their data may not be representative of the general population.
The βGeo staining method also provided us with some insight on the pattern of cell loss exhibited in the D2 retina. The majority of mice showed a diffuse pattern of loss throughout the retina. Many mice in the early stages of retinal degeneration, however, clearly showed regional cell loss, often in the form of large pie-shaped sectors of retina extending from the optic nerve to the periphery. An identical pattern of ganglion cell loss was independently observed in aged D2 mice by Jakobs and colleagues  and may be consistent with the "patchy" cell loss reported in DBA/2NNia mice by others [8, 9], although these mice appear to lose cells preferentially from the central retina rather than in sectors . In each of these studies, ganglion cell depleted regions of the retina were typically bordered by normal regions of retina, suggesting that damage had occurred initially to discrete bundles of axons in the optic nerves of these animals. Since the only region of the nerve where discrete bundles exist is in the laminar region (see Fig. 3), this is the likely site of initial insult in glaucoma. Histological evaluation of the laminar regions of nerves from eyes with regional cell loss also showed similar patterns of discrete areas of axon loss supporting this hypothesis.
Like the optic nerve studies, we also observed asymmetry in the loss of βGeo positive cells in the two eyes of single mice, indicating that the disease progresses independently in each eye. This finding is also consistent with ERG response changes reported in the DBA/2NNia mice , where the decrease in amplitude of the b-wave form was much more variable between the two eyes of aged (15 month) mice compared to younger animals. Although the exact cause of the ERG changes was not elucidated, the authors attributed it primarily to retinal damage.
Comparison of the timing of optic nerve and retinal degeneration
In summary, this study of the pattern of optic nerve and retinal degeneration in D2 mice provides some interesting insights into the sequence of events in the pathology of the disease. Analysis of the timing of both optic nerve and retinal degeneration suggests that the nerve is affected first. Axons begin to degenerate posterior to the lamina in intermittent regions throughout the nerve, but are more prevalent in the proximal regions, making the overall pattern of degeneration appear retrograde by DiI staining. The loss of ganglion cells in the retina is delayed by about 1 month, and often first occurs in discrete wedges of cells. Since damage likely occurs first in the optic nerve, it is reasonable to assume that the discrete pattern of damage observed in the retina is due to damage to adjacent bundles of axons, which are only found in the laminar region. Thus, the lamina is probably the initial site of damage in glaucoma in these mice, analogous to previous studies suggesting a similar etiology in humans [14, 15, 17].
Handling of animals and generation of DBA/2J ROSA3 mice
Experiments using mice were conducted in accordance with the Association for Research in Vision and Ophthalmology statement on the use of animals for ophthalmic research and the University of Wisconsin Animal Care Committee. A colony of D2 mice was established from breeders purchased from the Jackson Laboratory (JAX – Bar Harbor, ME) and routinely backcrossed onto new founders from JAX in order to reduce genetic drift in the colony. The ROSA3 line of mice was initially generated in the laboratory of Philip Soriano  using the promoter trap gene βGeo (a fusion protein of β-galactosidase and neomycin phosphotransferase). In this line, the βGeo trap gene was inserted into the first intron of Fem1c. Adult animals express this gene in distinct populations of neurons in the CNS. In the retina, βGeo is expressed predominantly in the majority of retinal ganglion cells . The ROSA3 allele (Fem1cR3 - R3) was crossed into the D2 background by successive breeding through 10 generations. D2 mice, heterozygous for the R3 allele, were generated by crossing homozygous animals (Fem1cR3/R3) with wild-type D2 mates obtained from JAX. Mice were maintained on a 4% fat diet (8604 M/R Diet, Harland Teklad, Madison, WI) in a 12 hr light/dark cycle.
Post-mortem DiI labeling of optic nerves
Optic nerve histology
After DiI staining and imaging, optic nerves were removed from the mouse heads and processed for histology. Nerves were dissected with a small region of the globe still attached to help define regions proximal and distal to the retina. Nerves were fixed for 4 hr at 22°C in 10% Formalin in PBS, embedded in JB-4 Plus plastic (glycol methacrylate, Polyscience, Warrington, PA), and sectioned at 2 μm thickness. Cross sections were taken within 1.0 mm of the globe (distal segment) and within 1.0 mm of the chiasm (proximal segment). Some nerves were also sectioned longitudinally. Sectioned nerves were stained using a silver impregnation technique, which selectively stains the axons . Optic nerves were digitally photographed using an Olympus BH-2 photomicroscope (Mellville, NY).
Histochemical staining for βGeo enzyme activity and scoring of retinal wholemounts
Mice were euthanized at the appropriate ages and the superior region of each eye was marked using an ophthalmic cautery to place a small burn in the cornea. Eyes were then enucleated, and the anterior chamber and lens of each was removed after a relaxing cut was made in the superior retina in line with the cautery mark. Retinas were stained with X-Gal (1 mg/mL) as described previously , with the exception that enucleated eye cups were stained for a standard period of 21–22 hrs at 37°C in an effort to ensure all eyes were stained an equal period of time. After staining, retinas were removed from the eye cups and flat mounted on charged glass Plus microscope slides (Fisher Scientific, Chicago, IL) using care to maintain retinal orientation based on the superior retina. Three additional relaxing cuts were then made to flatten the tissue onto the slide. This procedure resulted in retinas with 4 relatively equal sized lobes corresponding to the superonasal, superotemporal, inferonasal, and inferotemporal quadrants. To estimate the staining intensity of each retina, each individual lobe was scored separately by 3 observers using a 1 to 5 point scale. Briefly, each lobe was divided into 4 regions (2 central and 2 peripheral) and each region was scored independently from 1 to 5. A score of 1 was given to retinas with a dense staining pattern. A score of 2 was given to retinas that exhibited reduced, but still widespread distribution of positive cells. Correlative cell counts from sample retinas indicated that these retinas had at least 50% of the positive cells in the ganglion cell layer remaining. A score of 3 was given to retinas with markedly reduced staining, to a maximum of approximately 75% cell loss. A score of 4 indicated sparse distribution of positive cells in the ganglion cell layer, while a score of 5 was given to retinas with no evidence of positive cells in the ganglion cell layer. The mean of the 4 scores for each lobe was considered the score for that lobe, and the mean score of each of the 4 lobes was considered the mean score for that retina. This scoring method created data sets that enabled statistical analysis of cell loss between the peripheral and central retina, between different lobes of each retina, and between different retinas. An example of a scored retina is shown in Figure 11. A weighted Kappa statistic revealed a high level of agreement among the scorers using this method (κ = 0.667, 95% CI = 0.32 to 1.0).
This work was supported by a grant from The Glaucoma Foundation (RWN), grants from The National Eye Institute (R03 EY13790 and R01 EY12223 to RWN, and CORE grant P30 EY016665 to the Department of Ophthalmology and Visual Sciences), and an unrestricted grant from Research to Prevent Blindness. The authors would like to thank Ms. Inna Larsen for assistance in breeding the Rosa3 allele onto the DBA/2J genetic background.
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