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1From the Laboratories of Molecular Genetics and 2Neurohistology and Cell Biology, University Eye Hospital Tübingen, Tübingen, Germany; the 3Institute of Physiological Chemistry, University of Tübingen, Tübingen, Germany; and the 4Max Delbrück Center for Molecular Medicine, Berlin, Germany.
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METHODS. The rOpa1 cDNA was isolated by using reverse transcribed cDNA from total RNA obtained from a rat retinal ganglion cell line. The spatial and temporal expression patterns of OPA1 and its gene product were investigated by RNA in situ hybridization and immunohistochemistry in mouse and rat retinas. To characterize further the OPA1-positive neurons, retinal ganglion cells were retrogradely labeled by an immunogold fluorescent tracer or double labeled with OPA1 and choline acetyltransferase or calbindin antibodies.
RESULTS. Protein sequence alignment revealed a 96% identity between rat and human OPA1 mRNA. OPA1 expression was found as early as postnatal day 3 in the developing rodent retina. In the mature retina, the OPA1 gene and its protein were found not only in retinal ganglion cells, but also in starburst amacrine cells and horizontal cells, both of which are involved in lateral signal processing within the retina. However, OPA1 was absent from mitochondria rich nerve fibers and photoreceptor indicating a specific role for OPA1 in signal processing rather than in the requirement of mitochondrial energy supply in the retina.
CONCLUSIONS. The data suggest an important and specific function of the OPA1 protein, not only in the optic nerve forming ganglion cells but also in the intrinsic signal processing of the inner retina.
In 2000, we and others identified several mutant forms of the disease gene OPA1.17 18 This gene encodes a dynamin-related guanosine triphosphatase (GTPase) and is composed of 31 exons that are distributed across 
100 kb of genomic DNA on human chromosome 3 at q28-29. Several splice variants were recently reported19 caused by exclusion or inclusion of exons 4, 4b, or 5b. The full-length open reading frame (ORF) of 3045 bp translates into a predicted protein of 1015 amino acids, with a mitochondrial leader sequence at the N terminus of the protein and a characteristically conserved GTPase domain in the middle. The putative mitochondrial localization was experimentally confirmed by reporter gene analysis and colocalization with Hsp60 in HeLa cells.18 Most recent findings indicate that the OPA1 protein is anchored to the mitochondrial inner membrane facing the intermembrane space.20 Northern blot analysis of human RNA showed that OPA1 transcripts are present in all analyzed tissues but are most abundant in the retina.17
Recently, OPA1 immunoreactivity has been described in the mouse retina.21 However, until now, nothing has been known about the cellular expression and localization of the OPA1 gene and the identity of the cells containing this protein in the retina. In this study, we demonstrated spatial and temporal distribution of the OPA1 mRNA and its protein in the developing rat and mouse retina, as well as the expression pattern of the OPA1 protein in identified and distinct neurons of the adult rat retina. In addition, we report on identification of rOpa1, the rat orthologue of OPA1. Preliminary results have been published in abstract form (Pesch UEA, et al. IOVS 2001;42:ARVO Abstract 3521).
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To develop spliced transcripts, total RNA from the retina and RPE/choroid was isolated (RNeasy Total RNA-Kit; Qiagen, Hilden, Germany). First-strand cDNA was synthesized from 1 µg total RNA, using an oligo d(T)–primed reaction mixture (20 µL) with reverse transcriptase (Superscript RNase H; Invitrogen-Life Technologies Inc., Gaithersburg, MD) according to standard procedures. PCR amplification of rOpa1 isoforms was performed with the following primer pair: sense primer, 5'-CTC CCG CGT GGC CGT CT-3', and antisense primer, 5'-GAG TGT GCA GAA GTT CTT CC-3'. All PCR products were directly TA-cloned into pCR2 (Invitrogen, Carlsbad, CA) and sequenced.
In Vitro Transcription and Generation of Riboprobes
To generate the riboprobe, plasmid DNA containing the full-length human OPA1 cDNA (AB011139; GenBank; http://www.ncbi.nlm.nih.gov/Genbank; provided in the public domain by NCBI, Bethesda, MD) was linearized with either NotI (antisense probe) or SalI (sense probe). There is a 88% homology over the ORF on the nucleotide level between the human and rat and a 89% homology between the human and the mouse. For positive control experiments, plasmid DNA containing the rat rhodopsin cDNA (Z46957) was linearized by XhoI (sense probe) and NotI (antisense probe). The linearized DNA was purified by phenol-chloroform extraction and 1 µg purified linear DNA was used as the template to synthesize digoxygenin-labeled riboprobes (both sense and antisense) by in vitro run-off transcription with incorporation of digoxigenin-UTP (DIG-RNA labeling kit; Roche Diagnostics, Mannheim, Germany). These cRNA probes were finally hydrolyzed to obtain an appropriate probe length of 200 bp.
Antibody Production
To obtain a polyclonal antibody against OPA1, a peptide comprising the sequence ANTLRQQLTNTEVRRLEK (18-mer), which corresponds to amino acids 891-908 (100% conserved between human, rat, and mouse) of the C-terminal domain of the OPA1 protein was prepared by solid-phase peptide synthesis, using the Fmoc/But strategy. A Blast search was performed with the polypeptide sequence, and no other protein in the NCBI database showed any similarity. The peptide was purified by HPLC to a homogeneity of more than 95%, and the identity was confirmed by electrospray mass spectrometry. Each peptide was coupled to keyhole limpet hemocyanin (KLH) by the glutaraldehyde method. A polyclonal antiserum was raised in New Zealand White rabbits, according to standard immunization protocols (Charles River Service Laboratory System, Wilmington, MA). The antiserum was purified by protein Sepharose affinity chromatography and finally concentrated by ultrafiltration on a 20-kDa membrane to a concentration of 1.0 mg/mL.
Western Blot Analysis
Retina and brain tissue from adult rats was homogenized in ice-cold homogenization buffer (20 mM Tris-HCl [pH 7.4], 0.25 M sucrose, 1 mM EDTA, 0.5 g/L BSA, and 100 µM phenylmethylsulfonyl fluoride [PMSF]) supplemented with protease inhibitor (Set III; Calbiochem, Schwalbach, Germany) using standard protocols. HEK 293 cells were incubated at –80°C overnight and then suspended in the homogenization buffer–protease inhibitor cocktail.
All probes were mixed with Laemmli SDS-PAGE sample buffer, boiled for 5 minutes, separated on 10% SDS-polyacrylamide gels, and electrotransferred to nitrocellulose membranes. The membranes were blocked for 1 hour at room temperature with blocking solution (10 mM Tris-HCl [pH 8.0], 150 mM NaCl, 0.05% Tween 20, and 5% skim milk) and incubated overnight at 4°C, either with our own OPA1 antibody (1:500 in blocking solution) or an OPA1 antibody generated by Misaka et al.22 (1:1000 in blocking solution) against amino acids 938-960 of mouse OPA1. The reaction was visualized with horseradish peroxidase–conjugated secondary antibody and chemiluminescence reagent (ECL Plus; Amersham).
Animals and Tissue Preparation
All experiments performed in this study were in accordance with the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research. Retinas from Brown Norway rats and C57BL/6J mice from postnatal day (P)3 to adult (P76) were used (day of birth was P0). The animals were kept under a 12-hour light–dark cycle, with an illumination of 10 lux. Tissue samples were taken during the light phase between 9 AM and 5 PM.
Animals were killed with CO2. Eyes were enucleated and hemisected along the ora serrata. The anterior parts with cornea and lens were removed, and the posterior eye cups with the retina in place were fixed in 4% paraformaldehyde (PFA) in phosphate buffer (PB; pH 7.4) for 30 minutes at 4°C. Eye cups were cryoprotected by immersion in 30% sucrose in PB overnight at 4°C and embedded in freezing compound (Cryomatrix; Shandon, Pittsburgh, PA), and 10-µm cryosections were collected on tissue-adhesive–coated (Vectabond; Vector Laboratories, Burlingame, CA; for in situ hybridization) or gelatin-coated (for immunohistochemistry) glass slides.
In Situ Hybridization
Slide-mounted sections were preincubated with proteinase K buffer (PKB: 0.1 M Tris-HCl [pH 8.0] and 0.05 M EDTA [pH 8.0]) at 37°C for 5 minutes and then treated with proteinase K (0.3 µg/mL) in PKB at 37°C for 8 minutes. Slides were washed twice in diethyl pyrocarbonate (DEPC)-H2O (Sigma-Aldrich; Deisenhofen, Germany), fixed in 4% PFA in 0.2 M PB for 15 minutes, washed again three times, and dried at room temperature for 10 minutes.
The riboprobes were diluted in hybridization buffer (0.2 ng/µL) and heated to 68°C to 72°C for 10 minutes. Probes were applied to the retina sections and slides were incubated for hybridization in a humidified chamber at 62°C to 65°C overnight. Slides were then washed and treated for 30 minutes with blocking solution (10% blocking reagent in 0.1 M maleic acid and 0.15 M NaCl [pH 7.5]) before the incubation with anti-digoxigenin-AP, Fab-fragment antibodies (1:500). The detection reaction was performed out in AP-buffer with 400 µg/mL of both nitroblue tetrazolium chloride and 5-bromo-4-chlor-3-indolylphosphate in a humidified chamber in the dark for 5 to 48 hours at 4°C and then stopped in 0.1 M Tris-HCl and 0.01 M EDTA (pH 8.0; 15 minutes). Positive control experiments were performed with the generated rat rhodopsin riboprobes.
Immunohistochemistry
Sections were preincubated with 3% H2O2 and 40% methanol in phosphate-buffered saline (PBS) to block endogenous peroxidases. The OPA1 antibody was diluted 1:1000 in PBS containing 0.1% TritonX-100 and visualized with a biotinylated secondary antibody (goat anti rabbit; dilution 1:200) and an avidin-biotin peroxidase complex (Vector Laboratories) and diaminobenzidine, in combination with a nickel intensification as a chromogene. For control experiments, the primary antibody was preabsorbed with the antigenic peptide.
Retinal ganglion cells were retrogradely labeled with immunogold fluorescent tracer (Flurogold; Fluorochrome, Englewood, CO) injected into the lateral geniculate nucleus, and sections from these retinas were used for OPA1 immunohistology. For colocalizing OPA1 with choline acetyltransferase (CHAT) or calbindin (CALB), antibodies raised in mouse against CHAT or CALB (Chemicon, Hofheim, Germany) were diluted 1:100 and applied in combination with the OPA1 antibody in the same incubation steps. The appropriate secondary antibodies were conjugated with FITC or Cy3.
All histologic examination and documentation were performed with a multifunction microscope (AX70; Olympus, Tokyo, Japan). Photographs were digitized and adjusted for brightness and contrast (Photoshop; Adobe Systems, Mountain View, CA).
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(F/L/I)XX(G/S/T)XXXX that were found in mOpa122 24 and the consensus tripartite guanosine triphosphate (GTP)–binding motif needed for phosphate binding (GXXXGKS/T) and coordination of Mg2+ (DXXG) nucleotide binding (T/NKXD) and the dynamin sequence signature.25 Furthermore, two putative coiled-coil regions were also observed (Fig. 1A) . Thus, the greatest similarity was found in the region encoding the GTPase domain. Less sequence identity (85.5%) was observed in regions encoding the mitochondrial leader sequence at the N terminus of the protein. However, virtually all previously identified disease-causing missense mutations17 19 26 27 28 affect conserved amino acid residues.
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Western Blot Analysis of rOpa1
Western blot analysis using our own OPA1 antibody (Fig. 1B) showed a molecular mass of 90 kDa for Opa1 in the rat retina and the brain. In HEK 293 cells, which can be used as the negative for control Opa1,22 no cross-reactivity with other proteins was detectable with our antibody. To further confirm the antibody’s specificity, we analyzed rat brain samples in parallel with the antibody generated by us and an antibody generated by Misaka et al.,22 directed against a mouse (m)Opa1 sequence. Positive bands were detectable in the blots (Fig. 1B) with both antibodies at the same molecular mass.
Opa1 mRNA Expression in the Developing Rat and Mouse Retina
To determine cell-specific Opa1 expression in retinal neurons, we performed RNA in situ hybridization on rat (Fig. 2A) and mouse (Fig. 2B) retinal sections by using a human OPA1 antisense-riboprobe. The staining pattern in both species was the same. The most intense OPA1 expression occurred in the cell bodies of the GCL, labeling approximately 90% of the cells in the GCL of fully differentiated rat and mouse retinas (Figs. 2A 2B) . Because the GCL of rodents contains a roughly equal amount of ganglion and displaced amacrine cells, we concluded that both of these two cell types express Opa1. Labeled cells were also observed in the inner row of the inner nuclear layer (INL). These INL cells were faintly stained (Figs. 2A 2B) and represented approximately 3% to 4% of the cells in the inner row of the INL.
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In the developing rat (Fig. 2E) and mouse (Fig. 2F) retinas at P3, only the GCL and the adjacent inner plexiform layer (IPL) had already separated from the neuroblast layer (NBL). The GCL was still multilayered but was in the process of losing its supernumerous cells during the next days of development. At that stage, cells stained positive for OPA1 within all rows of the multilayered GCL in the rat. In addition, small stripes of labeled cytoplasm were present in the most apical part of some cells in the undifferentiated NBL located just along its inner border (Fig. 2E) . Thus, the in situ hybridization pattern was already generally the same in this early postnatal age as in the mature retina. The P5 retina showed the same cellular distribution as at P3 (Fig. 2E) . At P10, when the INL was separated from the outer parts of the retina, staining was clearly confined to the GCL and the inner row of the INL (Fig. 2E) . There was no alteration in the pattern and intensity of OPA1 staining after eye opening, which occurs in rats and mice at P15 (Fig. 2E ; P20).
Even though OPA1 staining was generally the same for rats (Fig. 2E) and mice (Fig. 2F) , its onset was delayed in mice, with no obvious positive staining before P5 (Fig. 2F) . Up to P10, there was a tendency for reaction deposits to be randomly scattered over the entire retina, including the outer layers (Fig. 2F) .
OPA1 Protein Distribution in the Mouse and Rat Retina
To examine cell-specific protein localization, we performed immunohistochemistry on postnatal rat (Fig. 3A) and mouse (Fig. 3B) retina sections, with polyclonal anti-OPA1 antiserum directed against the C-terminal part of OPA1, which is 100% conserved among human, rat, mouse, and salmon.
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P5 (Fig. 3B , white arrowheads) and OPA1-positive cells were subsequently found in the outermost row of the INL, adjacent to the outer plexiform layer (OPL) as soon as the OPL had formed and the INL was separated from the outer nuclear layer (ONL) at P10 (Fig. 3B , white arrowheads). Cell label resembling that in an adult retina was achieved at the end of the third postnatal week in both mice and rats (Fig. 3) . In the mature rat retina, strong staining of most of the neurons in the GCL was observed (Figs. 4A 4B) , with approximatively 10% to 15% of unlabeled cell bodies. In agreement with in situ hybridization experiments, cell bodies in the innermost row were stained (Fig. 4B) . These were classified as amacrine cells because of their position along the INL/IPL border. In contrast to the in situ hybridization results, we found immunoreactive cells in the outermost row of the INL (Fig. 4B) . These were easily identified as horizontal cells, because of their position and elongated horizontal shape. In addition, OPA1 immunoreaction was visible in horizontal processes in the OPL (Fig. 4B) and in two narrow stratified bands in the IPL (Fig. 4B) that were connected to cells in the INL (Figs. 4D 5B) , and GCL (Figs. 4E 5C) , respectively (see also OPA1 immunoreactivity in Fig. 5 ).
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Control experiments omitting the first antibody or preabsorbing the antiserum with the purified OPA1 protein used for antibody production (Fig. 4C) resulted in a complete absence of immunoreactivity over the entire retina.
To characterize further the OPA1-positive neurons, sections from retinas with ganglion cells retrogradely labeled with immunogold fluorescent tracer (Fluorogold; Fluorochrome) were used or retinal sections were double-labeled with the OPA1 antibody and antibodies directed either against CHAT, known to be specifically expressed in starburst amacrine cells, or calbindin (CALB), a marker for horizontal cells (Fig. 5) . OPA1 immunoreactivity was found in all ganglion cells stained by immunogold deposits (Fig. 5A , arrows); however, OPA1-positive cells that showed no colocalization of the gold deposits were also noted in the GCL, indicating the presence of OPA1 also in displaced amacrine cells (Fig. 5A , arrowheads). Double labeling of OPA1 and CHAT revealed that all CHAT-positive amacrine cells in the inner row of the INL as well as CHAT-positive displaced amacrine cells in the GCL coexpressed both proteins (Fig. 5B , arrows in the INL, arrowheads in the GCL). In contrast, some of the OPA1-positive amacrine cells in the INL did not necessarily coexpress CHAT (Fig. 5B3) . Processes of CHAT- and OPA1-positive neurons terminated in the same two sublayers of the IPL, and double labeling was observed in both bands (Fig. 5B , asterisks). There was a slightly broader band that occasionally seemed to consists of two layers of processes running in close proximity at sublayer 2 (Figs. 5B2 5B3 , single asterisk) and a finer and more distinct band at sublayer 4 (Figs. 5B2 5B3 , double asterisks). Horizontal cells were identified with an antibody directed against CALB. All CALB-positive processes in the OPL and all cell bodies stained in the outermost row of the INL colocalized with the OPA1 expression in this region of the retina (Fig. 5C , arrowheads).
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As a step toward characterizing the underlying pathophysiology of adOA, we investigated temporal and spatial Opa1 gene expression patterns during rat and mouse retina development. Our in situ hybridization data convincingly demonstrated that the Opa1 gene is specifically expressed in the GCL and occasionally in cells in the INL of both rat and mouse retinas. To us, this invariable presence of Opa1 in the retina indicates a fundamental need of retinal ganglion cells for Opa1 throughout the entire postnatal lifespan. These findings concur with the histologic investigations of eyes from donors who have had adOA that suggest that the fundamental pathologic characteristic of adOA is a primary degeneration of retinal ganglion cells.12 13 Besides ganglion cell degeneration, these first and early histopathologic examinations did not reveal any appreciable changes in the remaining retinal layers.
Our immunohistochemical data further confirmed the presence of the OPA1 protein in the GCL and the INL, leaving the photoreceptors and the optic nerve free of any staining. They are also in accordance with recent observations from the developing mouse retina21 which revealed first OPA1 immunoreactivity already in the undifferentiated neuroblast layer at embryonic day 16.
Furthermore, colocalization experiments showed that OPA1 is present in nearly all if not all RGCs and that CHAT-positive ganglion cells in the INL and GCL are additional sources of Opa1 expression. These CHAT-containing amacrine cells are starburst cells, which are very particular, in that they occur as two mirror-symmetric layers of cells with cell bodies located in the INL and GCL.28 CHAT cells located in the INL belong to the OFF amacrine cells, whereas those displaced to the GCL are ON amacrine cells.29 Whereas all the CHAT-positive cells in the INL and in the GCL express OPA1, the OPA1-positive amacrine cells in the INL do not necessarily do so. Starburst amacrine cells have been known for quite some time to be involved in the visual phenomenon of directional selectivity and connect with cone bipolar cells, other amacrine cells, and direction-selective (DS) ganglion cells.30 Experiments in transgenic mice with a specific ablation of starburst amacrine cells showed starburst cells to be the key players in the DS light response of ganglion cells.31 DS information is transmitted to the magnocellular layers in the lateral geniculate nucleus. We would expect such a transmission to be impaired in adOA patients, because of malfunctional OPA1 protein causing a loss of starburst amacrine cells. This would then contrast with findings that visual transmission to the parvocellular rather than to the magnocellular zone is affected in adOA patients. Future work will reveal the exact contribution of starburst cells to directional selectivity in vision and the underlying signaling circuits involving this particular cell population.
To our surprise, horizontal cells were strongly positive for OPA1 staining. This indicates for the very first time a possible role of this cell type in the pathologic course of adOA. A loss of horizontal cells would have remained unnoticed in sections of donor eyes of adOA patients, because of the numerous cell bodies in the INL. Also, electrophysiological examinations, such as ERG recordings, are unsuitable for the detection of horizontal cell loss of function. Horizontal cells can be divided into at least two types: Dendritic processes of type I horizontal cells contact M- and L-cones, whereas type II horizontal cells make extensive contacts with S-cones, but only sparse contact with M- and L-cones.32 Moreover, the latter type is not interconnected through gap junctions as is type I. It is striking that one very characteristic symptom, and often the very first one that is objectively measurable in adOA patients is a color vision disturbance.33 In many cases, a tritan color defect precedes a later total color disturbance. It has been speculated that the tritan color defect is attributable to a loss of RGCs. Now, however, our results point to a possible involvement of horizontal cells. Type II horizontal cells in particular seem to contribute directly to the integration of color visual information of blue components and are excellent candidates for being accountable for this clinical feature. From a clinical viewpoint, we hope that our results will trigger fresh ideas for psychophysical testing of visually impaired patients, such as those affected with adOA. Very first multifocal ERG recordings from the macular region of patients with optic atrophy showed alterations attributable to pathologic alterations in the inner retina (Leo-Kottler B, personal communication, 2003).
Concerning the presence of OPA1 in the horizontal cells, we have to consider that only the protein, not the mRNA, was detected in this cell type. A similar phenomenon was observed in early postnatal stages of the mouse retina. Opa1 mRNA levels in the horizontal cells below the detectable threshold of in situ hybridization and paralleled by accumulation of the protein may serve as an explanation for this discrepancy in expression profile obtained by the two methods. However, cross-reactivity of the antibody (which then has to be very specific for the horizontal cells) cannot be completely ruled out, even though the carefully examined specificity of the antiserum and the consistency of mRNA and protein expression in amacrine and ganglion cells argue against this.
OPA1 is imported into mitochondria,22 where it is possibly anchored to the mitochondrial inner membrane facing the intermembrane space.20 Mitochondrial biogenesis occurs in the somata of the retinal ganglion cells before they are transported to the synaptic terminals through the axons of the optic nerve.34 35 After myelination of the optic nerve axons posterior to the lamina cribrosa, the number of mitochondria drastically decreases.36 In addition, the inner segments of photoreceptor cells as well as the fiber layer have the greatest energy demand and contain the most mitochondria within the retina. Therefore, we expected to find OPA1 staining at least anterior to the lamina cribrosa and in the inner segments of the photoreceptors. However, both structures did not show any detectable signal for OPA1. This drastically differs from cyclo-oxygenase (COX) and serine dehydrase (SDH) activity measured in these and other layers in the human retina which have the requirement of mitochondrial energy supply. Thus, we can exclude OPA1 as an important regulator of the provision of adenosine triphosphate (ATP) generated through the respiratory chain. This may highlight a fundamental difference in the primary disease mechanism of adOA versus Leber’s hereditary optic neuropathy (LHON). The origin of disease in LHON is an impairment of complex I in the respiratory chain due to mutations in mitochondrially encoded reduced nicotinamide adenine dinucleotide dehydrogenase (NADH).37 Because OPA1 is clearly not present in mitochondria of the fiber layer and photoreceptors, it must be involved in other features of the mitochondrial cell biology. Especially the manifestation of disease symptoms in very early childhood and the early expression (at least at P3) of Opa1 mRNA in the developing rat retina convince us that a developmental defect in adOA should be proposed. Starburst amacrine cells, for instance, form the first identified network of internal neurons that directly participate in spontaneous rhythmic activities in the developing retina.38 These electrical waves depend on changes in intracellular neurotransmitter, ion, or second-messenger concentrations, which are partly known to be stored in mitochondria. OPA1 is a member of the protein family of large dynamin-related GTPases that are functionally specialized in fission and fusion events in membranes and vesicles.25 39 Recent studies have reported that mutant OPA1 protein affects mitochondrial morphology, altering it from the standard tubular to a vesicular shape.22 40 We hypothesize that OPA1 regulates or controls the release of mitochondrial cisternae, such as FeCa2+ stores. Neurons, which depend on proper buffering capabilities for Ca2+ during development, would be particularly at risk for the excitotoxic effects of mutant OPA1 protein.
The first evidence of possible OPA1 involvement in related diseases has been established by genetic testing of patients with normal-tension glaucoma (NTG) for genetic variations in the OPA1 gene.41 In contrast, no OPA1 mutations have been identified in any patients with LHON.27 The design of suitable animal models for adOA and related diseases has to be a next step in the process of conquering these disorders, because human donor tissue material is unavailable to the extent needed for appropriate research concerning the function of OPA1 as a disease gene. The cloning of the rat sequence in this study is a prerequisite for the generation of a rat model for adOA. In this context, the newly generated OPA1antibody will serve as a valuable tool for further investigation, especially in light of the fact that due to the 100% conservation of its target epitope, this antibody can be used in many different species.
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Submitted for publication November 19, 2003; revised June 23, 2004; accepted July 8, 2004.
Disclosure: U.E.A. Pesch, None; J.E. Fries, None; S. Bette, None; H. Kalbacher, None; B. Wissinger, None; C. Alexander, None; K. Kohler, None
The publication costs of this article were defrayed in part by page charge payment. This article must therefore be marked "advertisement" in accordance with 18 U.S.C. 
1734 solely to indicate this fact.
Corresponding author: Konrad Kohler, Laboratory of Neurohistology and Cell Biology, University Eye Hospital Tübingen, Röntgenweg 11, 72076 Tübingen, Germany; konrad.kohler{at}uni-tuebingen.de.
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) Proteins labeled in Western blots by our own polyclonal antibody raised against a peptide in the C terminus of OPA1. HEK cells were used as a negative control. No OPA1 protein was detectable with our antibody in these cells. Brain tissue was used as a positive control. In both rat brain and rat retina, a band is detectable with our OPA1 antibody at a molecular mass of approximately 90 kDa. *Band detected with an antibody directed against a mouse Opa1 sequence. Left: Positions of the molecular mass markers.
; ONL of the photoreceptors) leaving the inner retina unstained. (E, F) Radial sections of rodent retinas at various developmental stages between P3 and P20 hybridized with digoxigenin-labeled OPA1 riboprobes. In the developing rodent retina only the GCL and the adjacent IPL have already separated from the NBL at P3, with the GCL still being multilayered but in the process of losing its supernumerous cells during the next days of development. (E) In the rat retina, at P3 and P5, a clear OPA1 expression was present in cell bodies of the multilayered GCL (arrows) and in the proximal cytoplasm of cells located in the undifferentiated NBL along the IPL border (arrowheads). At P10, when the INL is completely separated from the photoreceptors, staining was confined to the GCL and the innermost row of the INL. This staining pattern then persisted in all later developmental stages. (F) In the developing mouse retina, the staining pattern was essentially the same as in rats. There was a slight temporal delay in OPA1 expression, which is consistent with the slower retinal development in the mouse compared with the rat—very faint, if any, positive reaction was visible before P5. Up to P10, there was a tendency for reaction deposits to be randomly scattered over the entire retina, including the outer layers (P5, 
). Scale bar, 50 µm.
