Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Highlights
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CRISPR/Cas9 engineering of OPTN(E50K) glaucomatous hPSCs and isogenic controls
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RNA sequencing displays important pathways linked to glaucomatous neurodegeneration
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OPTN(E50K) RGCs encompass numerous neurodegenerative mechanisms
Summary
Retinal ganglion cells (RGCs) serve as the connection between the eye and the brain, with this connection disrupted in glaucoma. Numerous cellular mechanisms have been associated with glaucomatous neurodegeneration, and useful cellular models of glaucoma allow for the precise analysis of degenerative phenotypes. Human pluripotent stem cells (hPSCs) serve as powerful tools for studying human disease, particularly cellular mechanisms underlying neurodegeneration. Thus, efforts focused upon hPSCs with an E50K mutation in the Optineurin (OPTN) gene, a leading cause of inherited forms of glaucoma. CRISPR/Cas9 gene editing introduced the OPTN(E50K) mutation into existing lines of hPSCs, as well as generating isogenic controls from patient-derived lines. RGCs differentiated from OPTN(E50K) hPSCs exhibited numerous neurodegenerative deficits, including neurite retraction, autophagy dysfunction, apoptosis, and increased excitability. These results demonstrate the utility of OPTN(E50K) RGCs as an in vitro model of neurodegeneration, with the opportunity to develop novel therapeutic approaches for glaucoma.
Graphical Abstract
Keywords
Introduction
Glaucoma is a devastating optic neuropathy which causes the progressive degeneration of retinal ganglion cells (RGCs), leading to irreversible loss of vision and eventual blindness ( , , ). Various animal models have been developed that have led to a greater understanding of glaucomatous neurodegeneration ( , , , ), although these models often exhibit physiological features that do not precisely reflect those present within human patients. Furthermore, recent studies demonstrating significant variability between rodent and primate RGCs ( ) suggest that there may be important differences in how these cells respond to glaucomatous injuries between species. As such, there is a strong need to develop new approaches to complement these glaucoma models to determine RGC pathogenesis and mechanisms leading to their degeneration and death.Human pluripotent stem cells (hPSCs) provide an attractive option as a model for studies of cellular development and disease progression as they can be cultured indefinitely and induced to differentiate into all cell types of the body ( ), including RGCs ( , , , , , , ). When harboring genetic mutations associated with disease states, the derivation of these cells from patient-specific sources allows for the ability to study mechanisms underlying diseases, such as glaucoma ( , , , ). In addition, gene-editing approaches, including CRISPR/Cas9 technology allow for the ability to create isogenic controls from these patient-derived cells and also introduce disease-causing mutations in unaffected cells, leading to the generation of new disease models ( , , ). Among the gene mutations associated with glaucoma, those mutations in the Optineurin (OPTN) gene are known to result in glaucomatous neurodegeneration in the absence of increased intraocular pressure ( , , ). These mutations directly affect RGCs, with the OPTN(E50K) mutation previously shown to result in a particularly severe degenerative phenotype ( , , , , , ). As such, the generation of hPSCs harboring the OPTN(E50K) mutation, along with corresponding isogenic controls, allows for the in vitro analysis of mechanisms underlying the degeneration of RGCs in glaucoma.Thus, the efforts of the current study were initially focused upon the generation of hPSCs with the OPTN(E50K) mutation as well as their corresponding isogenic controls through the use of CRISPR/Cas9 gene editing. Upon initial differentiation of these cells into three-dimensional retinal organoids and subsequent RGC purification, OPTN(E50K) and isogenic control cells both developed in a similar manner, yielding a comparable number of RGCs. Conversely, at later stages of RGC maturation, OPTN(E50K) RGCs demonstrated numerous characteristics associated with glaucomatous neurodegeneration, including neurite retraction, autophagy dysfunction, and increased excitability. The results of this study provide the most comprehensive analysis of glaucomatous neurodegeneration to date using hPSC-based models, including the demonstration of CRISPR/Cas9 gene editing to provide essential disease models and corresponding isogenic controls for glaucoma.
Results
CRISPR/Cas9-Edited OPTN(E50K) Disease Models and Isogenic Controls
The ability to precisely edit genes in hPSCs through CRISPR/Cas9 gene-editing technology allows for new insights into disease modeling, including the generation of isogenic controls ( , , ). When properly applied, CRISPR/Cas9 gene editing allows for the enhanced ability to analyze disease phenotypes due to relevant mutations by minimizing genetic variability between cell lines. As such, CRISPR/Cas9 gene editing was utilized in the current study to examine the E50K mutation in the OPTN protein, a known genetic determinant for glaucoma.To introduce the OPTN(E50K) mutation in hPSCs (Figure 1), the homology-directed repair (HDR) template was designed to include the mutant nucleotide c.458G > A that altered the 50th amino acid from glutamic acid (E) to lysine (K), with an additional two silent mutations (c.454G > C and c.460G > A). The first silent mutation altered an Hpy188III restriction site, which was used for PCR screening of prospective gene-edited clones. The second silent mutation was introduced to prevent Cas9 from cutting the donor template by modifying the PAM site. A plasmid containing the OPTN(E50K) HDR template as well as the guide RNA was co-transfected with pCas9-GFP, with the GFP signal used to sort for presumptively edited cells (Figures 1A–1C). Clonal populations were screened by PCR amplification of the edited region and enzymatic digestion with Hpy188III, with prospectively edited clones further sequenced to ensure proper editing of the target gene (Figure 1D). Likewise, patient-specific hiPSCs harboring the OPTN(E50K) mutation utilized a similar strategy to correct the OPTN(E50K) mutation (Figure 1E). Following CRISPR/Cas9 gene editing, the karyotypes of each cell line were analyzed to reveal normal karyotypes (Figure S1). The results of these experiments demonstrated the successful establishment of hPSC lines harboring the OPTN(E50K) mutation along with their corresponding isogenic controls.
Figure 1CRISPR/Cas9 Gene Editing for the Generation of OPTN(E50K) hPSCs and Corresponding Isogenic Controls
OPTN(E50K) Glaucomatous RGCs Demonstrate Morphological Deficits and Gene Downregulation after Prolonged Culture
The degeneration of RGCs in glaucoma severely affects the visual pathway, leading to blindness ( , , , ). This degeneration is commonly associated with advanced age, as the initial development of the retina is unaffected by the disease state. As such, the early differentiation of OPTN(E50K) and isogenic control hPSCs yielded similar formation of optic vesicle-like and optic cup retinal organoids and a comparable number of RGCs (Figure 2).
Figure 2The OPTN(E50K) Mutation Does Not Affect Early Stages of Retinal Differentiation
Figure 3OPTN(E50K) RGCs Demonstrate Neurite Deficits at Later Stages of Maturation
Figure 4OPTN(E50K) RGCs Downregulate RGC-Associated Transcription Factors
Functional Consequences of the OPTN(E50K) Glaucomatous Mutation
Previous studies have demonstrated changes in RGC excitability associated with the glaucomatous disease state ( ) and, as such, patch-clamp analyses determined if functional changes were present in OPTN(E50K) RGCs (Figure 5). Within 4 weeks of RGC maturation, both OPTN(E50K) and isogenic control RGCs demonstrated functional properties, including ionic currents as well as spontaneous firing of action potentials (Figures 5A and 5B). No significant changes were detected in the resting membrane potential (Figure 5C), although OPTN(E50K) RGCs displayed a significantly lower cell capacitance, higher input resistance, as well as lower action potential current threshold (Figures 5D–5F), suggesting possible changes to excitable properties. To test this, current-clamp recordings demonstrated that OPTN(E50K) RGCs fired significantly more action potentials (Figures 5G and 5H). These results demonstrated an increased excitability of OPTN(E50K) RGCs, suggesting that excitotoxicity may play a key role in the early stages of RGC degeneration in glaucoma.
Figure 5OPTN(E50K) RGCs Display Increased Excitability
RNA Sequencing Demonstrated Differential Gene Expression in OPTN(E50K) RGCs
To elucidate gene expression differences and the specific cellular pathways affected by the OPTN(E50K) mutation, RNA sequencing was conducted on RGCs purified from OPTN(E50K) and isogenic control retinal organoids (Figure 6). Initial analysis demonstrated 75 downregulated genes and 117 upregulated genes associated with OPTN(E50K) RGCs when compared with isogenic control RGCs (Figure 6B). Of the downregulated genes, a number of genes were associated with the clearance of aggregated proteins, protein trafficking, and neurite outgrowth. Pathway analyses revealed changes in gene expression associated with a variety of neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS) and Alzheimer disease, as well as the downregulation of pathways related to autophagy and neurite outgrowth (Figure 6C). Thus, as RNA sequencing results demonstrated differential gene expression and pathways suggesting autophagy dysfunction, opportunities to examine deficits in autophagy associated with this mutation were further pursued.
Figure 6RNA Sequencing Revealed Differential Gene Expression and Pathway Analysis in OPTN(E50K) RGCs
OPTN(E50K) RGCs Exhibit Autophagy Disruption and Increased Susceptibility to Apoptosis
The OPTN protein plays an important role as an autophagy receptor ( , , , ), with mutations to the OPTN protein, such as the E50K mutation disrupting the autophagy pathway leading to the damage and degeneration of RGCs ( , , , , ). As such, to elucidate possible disruptions to the autophagy pathway, retinal organoids were examined for the expression of LC3, particularly the accumulation of this protein as a hallmark of autophagy dysfunction (Figure 7). Compared with isogenic controls, OPTN(E50K) organoids exhibited profound LC3 accumulation exclusively within inner layers where RGCs reside, indicating a differential effect upon these cells (Figures 7A–7F). To test the possibility of rescuing this phenotype, the autophagy pathway was enhanced through treatment with rapamycin, leading to a significant reduction of LC3 accumulation within OPTN(E50K) organoids (Figures 7G–7I). As such, disruptions to the autophagy pathway likely contribute to the degeneration of OPTN(E50K) RGCs, with rescue of this phenotype by rapamycin suggesting modulation of autophagy may rescue degenerative phenotypes.
Figure 7OPTN(E50K) Retinal Organoids Demonstrate Autophagy Dysfunction through LC3 Accumulation
To determine if autophagy disruption was correlated with a decrease in RGC viability, retinal organoids were similarly examined for apoptosis, with OPTN(E50K) organoids exhibiting significantly increased levels of activated caspase-3 found largely within inner layers of these organoids (Figures 7M–7P). In addition, OPTN(E50K) organoids contained significantly fewer BRN3-expressing RGCs, while the number of photoreceptors quantified by expression of OTX2 revealed no significant differences (Figure S3). Retinal organoids were then treated with rapamycin to determine if an association existed between apoptosis and autophagy. When treated with rapamycin, OPTN(E50K) organoids displayed decreased levels of active caspase-3 (Figures 7Q–7S), suggesting an important link between autophagy dysfunction and apoptosis.
Discussion
hPSCs have been used as a reliable model system for studying both the development of many retinal cell types ( , , , , ) as well as diseases which result in the degeneration of these cells ( , , ). The current understanding of glaucomatous neurodegeneration has been established in part by the use of animal models mimicking RGC degeneration and injury ( , , , ). Although these studies have been instrumental in discovering various disease phenotypes, important differences exist between rodent and primate retinas ( ). As such, the use of hPSCs provides a powerful and complimentary model to study RGC development and disease that helps to bridge the gap between rodent studies and human glaucoma patients. Results of the current study demonstrate the most in depth phenotypic and functional characterization of RGCs grown from OPTN(E50K) hPSCs, revealing numerous neurodegenerative phenotypes including autophagy deficits and neurite retraction, allowing for a greater understanding of mechanisms leading to the degeneration and death of RGCs in glaucoma.CRISPR/Cas9 gene editing provides exciting opportunities for the precise engineering of cells to generate new experimental models ( , , ). Of particular interest for this study, CRISPR/Cas9 gene editing allowed for the insertion of disease-causing mutations in hPSCs as well as the correction of these mutations in patient-specific hPSCs, minimizing effects due to variability between cell lines. As previous studies have demonstrated variability in the capacity of numerous hPSC lines to differentiate into retinal cells ( , ), this variability complicates the definitive identification of disease-related phenotypes apart from inherent differences between cell lines. The use of CRISPR/Cas9 gene editing in the current study allowed for the definitive identification of disease-related phenotypes directly linked to the OPTN(E50K) mutation. As such, the results of this study provide the foundation for utilizing CRISPR/Cas9 gene editing of hPSCs for the study of other genetically inherited forms of glaucoma as well as other neurodegenerative diseases of the retina to discover mechanisms of degeneration.The age-related loss of RGCs in glaucoma is characteristic of the loss of neurons found in many neurodegenerative diseases ( , , , , , , , , , ). In this context, RGCs differentiate normally during early retinogenesis, with degeneration associated with age and disease progression. As such, it is crucial for model systems of glaucoma to demonstrate this type of disease progression in vitro. Results of the current study suggested that OPTN(E50K) and isogenic control hPSCs both differentiated into early optic cup-like retinal organoids that displayed a lamination of retinal layers. When organoids were dissociated and resultant cells grown in two-dimensional cultures, no significant differences were observed in the initial expression of RGC-associated markers as well as the morphological features of neuronal maturation. Disease phenotypes including neurite retraction, autophagy dysfunction, and apoptosis were only identified in OPTN(E50K) cells after prolonged culture, with this progression somewhat recapitulating the age-related phenotypes observed in glaucomatous neurodegeneration.The downregulation of RGC-associated transcription factors has been previously established in experimental glaucoma as well as RGC injury models, which provides an early indicator of degeneration in the retina ( , ). Results of the current study demonstrated the downregulation of the RGC-associated transcription factors BRN3 and ISL1 in OPTN(E50K) RGCs compared with isogenic controls. Importantly, this downregulation of BRN3 and ISL1 was only identified after prolonged culture, with quantification at earlier time points indicating no significant differences between OPTN(E50K) RGCs and isogenic controls. In future experiments using fluorescent reporters to identify RGCs in hPSC disease models, it will be necessary to account for the downregulation of these reporters to identify those RGCs at advanced stages of the disease state.The OPTN protein performs a variety of functions within the cell, including its role as an autophagy receptor ( , , , , ). As such, OPTN interacts with a variety of essential autophagy proteins, with the E50K mutation in this protein leading to a disruption in this pathway. Autophagy pathway disruption has also been linked to neurodegeneration in a number of other diseases, including ALS, Alzheimer, and Parkinson diseases, with the possibility of deficits in this pathway conserved as a mechanism leading to the degeneration of neurons ( , , , , , , , ). In this study, results demonstrated profound accumulation of LC3 and significantly higher levels of apoptosis within inner layers compared with both the outer layers of these same organoids as well as the presumptive RGC layers of isogenic controls. When treated with rapamycin, an activator of the autophagy pathway, these phenotypes were reduced back to levels comparable with isogenic controls, reflecting an important balance between the autophagy and apoptotic pathways linked to the OPTN(E50K) mutation.The overstimulation of cells through excitotoxic mechanisms has been implicated in a variety of neurodegenerative diseases including glaucoma ( , , ). Results of this study demonstrated that OPTN(E50K) RGCs exhibited a significantly lower action potential current threshold than isogenic controls, leading to the firing of significantly more action potentials, with these results suggesting that the increased excitability of OPTN(E50K) RGCs may serve as a key contributor to their degeneration. Importantly, both OPTN(E50K) and isogenic control RGCs were identified for patch-clamp recordings based upon their expression of BRN3B:tdTomato fluorescence. Given that the results of this study also documented the downregulation of BRN3B:tdTomato in more advanced stages of OPTN(E50K) RGC maturation, the possibility exists that the phenotypes observed may represent an earlier stage of the degenerative process, with these phenotypes more severe in those RGCs which are more advanced in their degeneration and have downregulated the tdTomato reporter.Although glaucoma is often overlooked as a neurodegenerative disease, it bears many similarities to other CNS diseases, such as Parkinson, ALS, and Alzheimer, which ultimately result in the degeneration of neurons in either the brain or spinal cord ( , , , , , , , , ). Similar to previous studies of RGC damage as well as cortical neurons in Alzheimer disease ( , , , ), results of this study identified numerous deficits including the downregulation of important RGC transcription factors, neurite retraction, autophagy disruption, and apoptosis, as well as heightened excitability of RGCs, all of which have previously been associated with other neurodegenerative diseases. As such, the results and assays conducted in this study are not only relevant to the study of glaucoma, but also to many other diseases of the CNS, with the possibility to work collectively on targeted therapeutics at these distinctive pathways.Overall, the results of this study demonstrate a detailed characterization of the OPTN(E50K) mutation and how it affects the degeneration of RGCs. More so, this study extensively utilized CRISPR/Cas9 gene-editing technology for the generation of disease models as well as isogenic controls for studies of glaucoma, with an important emphasis on the discrimination between mutation-causing phenotypes and cell line variability. In future studies using hPSC-based models of glaucomatous neurodegeneration, the identification of other unique neurodegenerative phenotypes and specific pathways leading to those phenotypes should be considered to better target therapeutic strategies.
Experimental Procedures
CRISPR/Cas9 Gene Editing
The OPTN(E50K) mutation was inserted into H7BRN3B:tdTomatoThy1.2-hESCs ( , ) and an hiPSC line harboring the OPTN(E50K) mutation ( ) was corrected (see Supplemental Experimental Procedures for details). Electroporation was performed using the Neon transfection system and, subsequently, cells were plated onto Matrigel-coated plates in mTeSR1 medium with CloneR supplement (STEMCELL Technologies). Forty-eight hours after electroporation, GFP-positive cells were isolated by FACS to enrich for edited cells. After initial growth, clonal populations were isolated and expanded. To screen for the insertion/correction, genomic DNA from individual clones was extracted, and the portion of the OPTN gene containing the 50th codon was amplified by PCR. This PCR product was then enzymatically digested by Hpy188III and run on a 1% gel. Properly edited clones were further confirmed by Sanger sequencing, and chromosomal abnormalities were analyzed by G-banded karyotyping.Maintenance of hPSCs
hPSCs were cultured from OPTN(E50K) disease lines and corresponding isogenic controls based on previously described protocols ( , , ). In brief, hPSC colonies were maintained on a Matrigel-coated six-well plate in mTeSR1 medium, with daily medium changes. hPSCs were passaged every 4–5 days based upon their confluency. Before passaging, hPSCs were marked for areas of spontaneous differentiation and those areas were mechanically removed. At 70% confluency, hPSCs were enzymatically passaged with dispase (2 mg/mL) for approximately 15 min and split at a ratio of 1:6 onto a new six-well plate freshly coated with Matrigel.Differentiation of RGCs
hPSCs were differentiated into retinal organoids and RGCs using an established protocol with minor modifications ( , ). In brief, enzymatically passaged hPSC colonies were grown in suspension to produce embryoid bodies (EBs). Within the first 3 days of differentiation, EBs were slowly transitioned from mTesR1 medium into neural induction medium. On day 6 of differentiation, BMP4 (50 ng/mL) was added to the flask ( ). The same medium was used at day 8 to induce adherence of EBs to a plate supplemented with 10% fetal bovine serum. Half of the medium was changed at day 9 and 12 to slowly reduce the concentration of BMP4. At day 15, early optic vesicle colonies were mechanically lifted and transferred into retinal differentiation medium, with a medium change every 2 to 3 days. At 30 days of differentiation, early retinal organoid cultures were supplemented with GlutaMAX and 2% fetal bovine serum to aid in retinal organization. By day 45, retinal organoids were either enzymatically dissociated in Accutase for RGC purification, or preserved as floating organoids for cryosectioning. For some experiments, retinal organoids were treated with rapamycin (2 μM) for 24 h and then fixed for immunocytochemistry.To purify RGCs, retinal organoids were enzymatically dissociated into single cells using Accutase for 20 min at 37°C. Single-cell suspensions were then enriched for RGCs with the Thy1.2 surface receptor using the MACS cell separation kit ( ). A total of 10,000 RGCs were plated on poly-D-ornithine and laminin-coated 12-mm coverslips and maintained for up to 4 weeks in BrainPhys medium ( , ). To analyze neurite complexity, RGCs were transfected with GFP using lipofectamine 2 days before fixation to aid in identification of individual RGC neurites along with BRN3:tdTomato expression.Immunocytochemistry
Samples were fixed with 4% paraformaldehyde in phosphate-buffered solution (PBS) for 30 min followed by 3 PBS washes. Retinal organoids were then prepared for cryosectioning through an incubation in 20% sucrose solution for 1 h at room temperature, followed by an incubation in 30% sucrose solution overnight at 4°C. The following day, retinal organoids were transferred into OCT cryostat molds and snap-frozen on dry ice. Sections (12 μm) were cut and used for immunocytochemical analyses.
Following fixation or sectioning, samples were permeabilized in 0.2% Triton X-100 for 10 min at room temperature. Samples were then washed with PBS and blocked with 10% donkey serum for 1 h at room temperature. Primary antibodies (Table S1) were diluted in 0.1% Triton X-100 and 5% donkey serum and applied overnight at 4°C. The next day, the primary antibody was removed and samples were washed three times with PBS and blocked with 10% donkey serum for 10 min at room temperature. Secondary antibodies were diluted at 1:1,000 ratio in 0.1% Triton X-100 and 5% donkey serum and applied to samples for 1 h at room temperature. The secondary antibodies were then removed and samples were washed three times with PBS before mounting onto slides for imaging. Immunofluorescent images were obtained using a Leica DM5500 fluorescence microscope.
Data Quantification
Isogenic control and OPTN(E50K) RGCs were collected at 1, 2, 3, and 4 weeks after purification and analyzed based on neurite complexity, neurite length, and soma size. Several immunofluorescent images were taken of RGCs co-expressing tdTomato and GFP, and soma area and neurite complexity were quantified using ImageJ and Photoshop, with the NeuronJ plugin used to quantify the length of RGC neurites.
Organoids from isogenic control, OPTN(E50K), and OPTN(E50K) plus rapamycin sources were collected at 2.5 months of differentiation and quantified for expression of BRN3, OTX2, and caspase-3 using the cell counter plugin in ImageJ. LC3 puncta number, size, and area were quantified using the ImageJ particle analyzer. Organoid areas were also quantified using ImageJ plugins. For caspase-3 quantification, organoid sections were imaged and the inner and outer layers were traced based on the expression of BRN3:tdTomato in Photoshop. The areas of inner and outer layers were determined using ImageJ and the cell counter plugin was used to quantify caspase-3 fragments in each layer.
Statistical Analyses
Statistical significance for neurite complexity, soma size, neurite length, and electrophysiological recordings was performed using two-tailed Student's t test and significance based on a p value of < 0.05. Significance for BRN3 and ISL1 quantifications were achieved by a Student's t test based on a p value of < 0.05. For BRN3, OTX2, caspase-3, and LC3 accumulations, a one-way ANOVA followed by a Tukey's post hoc analysis was used to determine significance based on a p value < 0.05.
Electrophysiology
Whole-cell patch-clamp recordings were performed at room temperature (~22°C) using a HEKA EPC-10 amplifier as described previously ( ), with detail provided in Supplemental Experimental Procedures. RGCs were identified by tdTomato fluorescence. To enhance comparisons between cells during action potential activity recording, current was injected to bias the cell membrane potential to −70 mV. Current threshold for action potential generation was obtained by a series of 1-ms stimuli of increasing intensity, with the maximum number of action potentials elicited measured during a series of 500-ms stimuli of increasing intensity. Voltage-clamp recordings were obtained from each cell at the end of the series of current-clamp protocols. The peak amplitudes of sodium and potassium currents were measured using a standard I-V protocol with a holding potential at −80 mV. The current density was calculated by normalizing current amplitude to the capacitance of each cell.RNA Sequencing Preparation and Analysis
RGCs were immunopurified from organoids after 45 days of differentiation and grown in adherent cultures for 10 days in BrainPhys medium. RNA was collected using the PicoPure RNA isolation kit. Total RNA was evaluated for its quantity and quality using an Agilent Bioanalyzer 2100. Approximately 30 million reads per library were generated. The sequencing data were next assessed using FastQC (Babraham Bioinfomatics, Cambridge, UK) and then mapped to the human genome (GRCH38) using STAR RNA sequencing aligner ( ). Differentially expressed genes were tested by using DESeq2 with a false discovery rate < 0.05 as the significant cutoff ( ). Pathway enrichment analysis were conducted by hypergeometric test against human gene ontology and MsigDB v.6 canonical pathways, with p < 0.01 as the significant cutoff ( ). The RNA sequencing experiments reported in this paper have been deposited in the Gene Expression Omnibus database, www.ncbi.nih.gov/geo (accession no. GSE145069).Author Contributions
K.B.V. and K.-C.H. designed the experiments, collected and analyzed the data, and wrote the manuscript. Y.P., S.S.L., P.T., and C.Z. collected and analyzed the data. C.M.F., A.R.A., and K.A.L. collected the data. H.C.T. designed the experiments. T.R.C. designed the experiments and analyzed the data. J.S.M. designed the experiments, analyzed the data, and wrote and approved the manuscript.
Acknowledgments
We thank Dr. Amelia Linnemann for helpful discussions about autophagy analyses and the sharing of antibodies. We also thank Dr. Don Zack and Dr. Valentin Sluch for sharing the BRN3B:tdTomato:Thy1.2 vectors used in the generation of RGC reporter cell lines. Grant support was provided by the National Eye Institute ( R01 EY024984 and R21 EY031120 to J.S.M.), the Indiana Department of Health Spinal Cord and Brain Injury Research Fund (grant no. 26343 to J.S.M.), and an Indiana CTSI Core Pilot grant (to J.S.M.). This publication was also made possible with partial support from a University Fellowship (to K.C.-H.) and from an Indiana CTSI pre-doctoral research fellowship (UL1TR002529, A. Shekhar, PI) from the NIH , National Center for Advancing Translational Sciences , Clinical and Translational Sciences Award (to K.B.V.).
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