We generated self-induced retinal ganglion cells (RGCs) with functional axons from human induced pluripotent stem cells. After development of the optic vesicle from the induced stem cell embryoid body in three-dimensional culture, conversion to two-dimensional culture, achieved by supplementation with BDNF, resulted in differentiation of RGCs at a rate of nearly 90% as indicated by a marginal subregion of an extruded clump of cells, suggesting the formation of an optic vesicle. Axons extended radially from the margin of the clump. Induced RGCs expressed specific markers, such as Brn3b and Math5, as assessed using by quantitative PCR and immunohistochemistry. The long, prominent axons contained neurofilaments and tau and exhibited anterograde axonal transport and sodium-dependent action potentials. The ability to generate RGCs with functional axons uniformly and at a high rate may contribute to both basic and clinical science, including embryology, neurology, pathognomy and treatment of various optic nerve diseases that threaten vision.
Retinal disorders are an important cause of blindness throughout the world1,2. Of the various types of retinal cells, photoreceptors and ganglion cells are primarily affected by retinal disorders; photoreceptors are generally affected by retinitis pigmentosa and retinal dystrophy3,4, while ganglion cells are generally affected by optic neuropathy and glaucoma5. Research aimed at achieving regeneration of the diseased retina has identified several candidate structures that contain precursors of key retinal cells, including the iris6,7, ciliary epithelium8 and Muller glial cells9,10. Two dimensional (2D) cell culture methods have been employed in this work; however, efficient regeneration of photoreceptors and the other retinal cells has not been achieved without application of exogenous factors that relate to retinal morphogenesis11,12,13, whereas self-induction by endogenous factors would have been ideal. The establishment of embryonic stem cell (ESC) and induced pluripotent stem cell (iPSC) technologies has recently allowed further advances in the generation of retinal cells.
The development of three-dimensional (3D) culture systems has led to more advanced work on differentiation of neural tissues from ESs and iPSCs, facilitating self-organisation of brain cortical tissue14, the pituitary gland15 and the retina starting from mouse and human ESCs16,17. First, the optic vesicle and continuous optic cup, which are two early developmental stages of the eyeball, were generated from ESC embryoid bodies. These tissues were then cut with scissors and continuously incubated in a floating culture system under a high-oxygen atmosphere, resulting in self-induction of almost all retinal layers15,16, including the ganglion cell and photoreceptor cell layers. In further advancements to this method, all layers of the murine retina were generated from ESCs and iPSCs and retinal sheets were successfully transplanted into the subretinal space of mice with advanced retinal degeneration (rd1), which lacked the outer nuclear layer of the retina18.
Another series of 3D culture systems has been developed, enabling generation of the 3D retinal structure, including retinal ganglion cell and photoreceptor cell layers. In the primary experiment, adherent human embryonic stem cells and iPS cells were picked up mechanically and transferred to floating culture to be induced into an optic vesicle (OV)-like structure with retinal precursor characteristics. This structure was then reattached to a 2D culture dish, where it differentiated into the retinal cell lineage19,20. In subsequent experiments in 3D culture systems, the entire retinal layer, including the retinal ganglion cell layer and functional photoreceptors, was established from human iPSCs mainly using intrinsic cues21 and addition of small amounts of exogenous factors, as reported in previous studies22,23,24,25,26. In this experiment, an OV-like structure was directly differentiated into a retina without the process of optic cup formation. There is a critical difference between these two major methods; in the former, the OV-like structures were extruded from the embryoid body, while in the latter, aggregates of human iPSCs or ESCs were directly induced into OV-like structures. In both methods17,21, the entire retinal layer is regenerated, containing thick outer layers with well-differentiated photoreceptors and thin, immature inner layers comprised of RGCs. Moreover, the formation of RGC axons has not been realised using either 3D retinogenesis method.
The RGCs located in the ganglion cell layer of the retina typically have long axons, enabling them to connect the retina to various visual centres in the central nervous system, represented by the lateral geniculate body27. RGCs play roles in transmitting image-forming and non-image-forming visual information28, processed by photoreceptors, horizontal cells, amacrine cells and bipolar cells, to higher visual centres via converging non-myelinated nerve fibres in the retina that continue into the myelinated optic nerve. Thus, the long axons of RGCs are crucial to transmitting visual images from the retina to the brain.
However, although culture of isolated RGCs with tiny axons from animal and human retinas has been achieved by immunopanning methods29,30,31, no study has reported the generation of RGCs exhibiting characteristic long, prominent axons in an in vitro culture system, with the exception of one report in which RGCs were developed from mouse iPSCs that carried an Atoh/Math5 lineage reporter32 and another report in which almost 30% of attached aggregates of RGCs derived from human iPSCs exhibited elongated axons with action potentials33.
Here, we describe a novel in vitro method that generated RGCs with long, functioning axons exhibiting action potentials and axonal transport, by combining cultivation of 3D floating aggregates with a subsequent 2D adhesion culture. This advance may facilitate both basic research on RGCs and translational research aimed at finding treatments for retinal diseases.
Protocol for self-induction of RGCs from human iPSCs
For purposes of generating RGCs, we modified a previously established17 3D retinal regeneration protocol (Fig. 1). This method called for addition of both foetal bovine serum (FBS) and Matrigel to the culture medium; these components were not required by other protocols20,21, which also produced retinal cells efficiently. Therefore, we investigated the effects of FBS concentrations (1%–10%) on D12–18 and Matrigel concentrations (0.5%–2.0%) on D1–18. At all concentrations, embryoid bodies (EBs) were well organised and OVs, which were maintained over the duration of the study, extruded from nearly 90% of the EBs (Table S1 and Fig. S1). In order to establish RGCs with long axons in a relatively short period, we changed the OV culture conditions from floating (3D) to dish (2D) to obtain cell attachment because the incipient ganglion cell layer was located on the surface of the OV. Initially, we severed the OVs from the EBs, which is predicted to lead to differentiation into neural retinal cells, as demonstrated previously17. However, maintenance of the cut OVs did not succeed, as documented in another report34. Therefore, we directly attached the OVs to the dish while still connected to the EBs and the attached OVs were further differentiated into an extruded clump of cells on the dishes. Around 2 days after attachment, massive axonal growth from the margin of the clump was realised. The optimal timing of attachment was also evaluated. Attachment on D26–29 was ideal for elongation of axons from the marginal portion of the clump, which was thought to represent the RGC region (RGCR), while attachment prior to D24 or after D30 seemed suboptimal for efficient development of axons (Fig. S2). When retinoic acid was added 3 days prior to the attachment, axonal growth was promoted (Fig. S3); in contrast, if retinoic acid was continuously supplemented after adhesion, axons grew by around D32, but died back by around D40 (Fig. S4). Finally, following addition of BDNF (100 ng/mL) to promote neuronal survival beyond 3 days of retinoic acid administration, RGCs and their axons were stabilised until around D50 (Fig. S5).
The time course of expression of transcription factors and protein markers associated with retinal development
The OV is derived from the eye field in the forebrain, a process in which several transcription factors, called eye-field transcription factors, play principal roles35. The retinal homeobox gene, Rx and the paired box gene 6, Pax6, which belong to this group of eye-field transcription factors, are crucial in early retinogenesis36. During the period of attachment of the cultured EB with its extruded OV to a dish, temporal gene expression analysis clearly revealed that upregulation of Rx began on D6, when the EB had maturely formed and peaked on D18, when the OVs began to develop. This was followed by upregulation of its downstream target Pax6. Math5, the bHLH transcription factor, is expressed in post-mitotic retinal precursor cells under direct control by Pax637. Math5 crucially regulates RGC formation and Math5 mutant mice lack RGCs38,39. In humans, Math5 mutation results in optic nerve aplasia40. Brn3b, known as the most reliable RGC marker, is a member of the POU-domain family of transcription factors and its expression is controlled by Math541. Brn3b is believed to determine RGC fate by acting as a repressor of differentiation to non-RGC cell types42, a process in which Islet1, an LIM-homeodomain factor, acts as a coregulator43. In our experiments, expression of Brn3b was relatively low until D18 and then dramatically increased until D24, when the OVs were well developed from the floating EBs following an increase in Math5 expression. Chx10 is associated with the proliferation of retinal progenitor cells. It is initially expressed in all retinal progenitors, but later is restricted to bipolar cells44. In our experiments, expression of Chx10 became apparent at D18 and was maintained until at least D34, when RGCs and axons developed after attachment of the EB. Crx, a cone-rod-containing gene, shows restricted expression in premature and mature cells of photoreceptor lineage45,46. Crx expression was also first observed at D18, following Chx10 expression. Amacrine cells start to differentiate immediately after RGC differentiation47. In our experiments, syntaxin, an amacrine cell marker48,49, showed delayed expression following Brn3b expression. The markers associated with horizontal and bipolar cells, both of which develop at later stages of retinogenesis, showed little expression until D34. The time course of gene expression was quite consistent with that in human retinogenesis. Mitf, a microphthalmia-associated transcription factor and the master regulator of melanocyte and retinal pigment epithelium (RPE) development50, was not highly expressed in the present study, suggesting that our induction protocol induced human iPSCs into the neural retinal lineage but not into the RPE lineage (Fig. 2a).
Immunohistochemistry also showed expression of Rx and Pax6 in both OVs and the clump, while expression of Brn3b and Math5 was observed only in the clump, localised within the margins of the clump. In contrast, low expression of Crx was observed within the clump (Fig. 2b). Calbindin and PKCα were not detected in either the OV or the clump (Fig. S6).
Structure of human iPSC-derived RGCs by light and electron microscopy
We investigated the structure of the RGCs by light and electron microscopy. After the OV became attached around D26–29, it became complanate, filled with cells and showed radiation of numerous axons from the outer margin at the dish surface. The cells in the clump were apparently different from those in the main body of the EB, which was filled with small round cells. The cells in the clump showed relatively large cell bodies (range: 16.1–23.6 μm; average: 21.6 μm, n = 10) with clear cytoplasms and nuclei and spindle-shaped or round cell bodies, sometimes accompanied by a prominent axon. These findings were identical to those of RGCs in vivo, whose cell body sizes ranged from 12 to 25 μm51. Notably, several cells located peripheral to the structure had Nissl bodies (Fig. S7), which is considered characteristic of RGCs52. However, Nissl bodies were not detected in other types of cells, including those in rosettes. The axons were eosinophilic, had few branches and grew radially from the clump (Fig. 3a, b).
Electron microscopy of D35 specimens demonstrated that the RGCs, which had axons, seemed to be relatively large (range: 16.0–24.1 μm; average: 20.6 μm, n = 10) and were stratified at the margin of the clump. These RGCs contained prominent rough endoplasmic reticulum, which represented the Nissl bodies that were observed by light microscopy. The axons developed from the axon hillock, which exhibited a characteristic conical cell body with neurotubules but no rough endoplasmic reticulum (Fig. 3c), which have also been detected in RGCs in vivo53,54 and define the end of the soma of neurons. The axons contained numerous neurotubules. The diameters of the axons varied (range: 1.7–2.2 μm; average: 1.8 μm, n = 10) and the axons were not myelinated (Fig. 3d). These findings were identical to those of axons in the retinal nerve fibre layer and in the optic nerve anterior to the lamina cribrosa, whose diameters range from 0.6 to 2.0 μm51.
Determination of RGC lineages
To confirm that the cells with axons in the margin of the clump differentiated from the OV were RGCs, we examined the expression and distribution of typical markers associated with RGCs. Real-time PCR revealed a more than 30-fold increase in the expression of Brn3b, Math5, Islet1, γ-synuclein (Sncg) and Tuj1. Brn3b, the most specific marker in this group, showed a nearly 3,000-fold increase in expression at D34 compared with D0 (Fig. 4a). Immunohistochemistry showed positive staining for all markers except Tuj1 in the marginal portion of the clump, which was therefore thought to be the incipient RGC layer. Math5, an upstream transcription factor for Brn3b and Sncg, another RGC marker and contributor to neurofilament integration55, showed similar distributions in the marginal portion of the clump. Islet1, a marker of RGCs and amacrine cells, was positive both in the margin and further toward the interior of the clump, suggesting that amacrine cells also developed there. Notably, Brn3b-positive cells apparently localised to the outermost margin of the clump at the surface of the dish, which strongly indicated that the margin was the RGCR and that the long radial axons originated from the RGCR. The costaining of Brn3b and Tuj1 demonstrated that the axons originated from the Brn3b-positive cells (Fig. 4b).
Sectional gene expression associated with RGCs and other retinal cells
For further confirmation of the presence of localised RGCs in the supposed RGCR, we mechanically divided the adherent structural complex into three parts: the RGCR, OVR and MBEB (Fig. 5a). Notably, Brn3b showed nearly four-fold higher expression in the RGCR than that in the MBEB. In addition, Crx expression was strongly suppressed in the RGCR. These results obviously demonstrated that the RGCR was highly specified into the ganglion cell lineage. Islet1 (a marker for ganglion and amacrine cells) was also up regulated in both the RGCR and OVR, which was consistent with the distribution of Islet1 expression confirmed by immunostaining (Fig. 5b). We also noticed that the isolated RGCR survived for approximately 10 days after separation from the OVR, which suggests that mechanical purification of RGCs is possible after growth of abundant axons.
RGC axon-related protein expression and determination of types of neurofilament proteins in early retinal gangliogenesis
To confirm that the apparent axons emanating from the RGCR resembled typical axons, we used tau and neurofilament (NF) immunostaining (Fig. 6b). The time-series expression of all NF components—neurofilament-light (NFL), neurofilament-medium (NFM) and neurofilament-heavy (NFH)—was studied in parallel (Fig. 6a). Microtubules, NFs, microtubule-associated proteins (MAPs) and actin play crucial roles in axonal development56. Tau, which is a MAP, contributes to polymerisation, stabilisation and organisation of microtubules and promotes axonal growth and effective axonal transport57. Once tau is hyperphosphorylated, the axonal transport process and cell survival of RGCs are compromised58. The axons detected in our study were clearly stained for tau and associated with evidence of axonal transport. NFs are the intermediate filaments of neurons and are especially abundant in CNS axons, where they occur as heteropolymers made up of four subunits, namely NFL, NFM, NFH and α-internexin59. NFs have essential roles in radial axonal growth and maintenance of axon calibre, therefore mediating the ability to transmit action potentials60. Both NFL and NFM appear early in retinogenesis, while synthesis of NFH is delayed61. In our experiments, NFL and NFM were already highly expressed at D34 and expression continued until D50, while expression of NFH was quite low at D34 and gradually increased until D50. Specimens from D34 showed positive staining for NFL/M but weak staining for NFH, in agreement with the expression time series study. We observed temporally varying gene expression not only of transcription factors but also of genes associated with structural components of RGCs.
Axonal transport in human iPSC-derived RGCs
To establish axonal function, we tested for axonal transport in the apparent axons that radiated from the RGCR. Axonal transport showed two characteristic flows, slow and fast, both of which had anterograde and retrograde components. RGCs and their axons are known to be rich in mitochondria and to maintain homeostasis by axonal transport, as in other neurons. Neurotrophic tyrosine kinase receptor 1 (NTRK1), a member of the neurotrophic tyrosine kinase receptor family, is the receptor for nerve growth factor and is expressed in RGCs, especially when the cells are damaged62,63,64. Using NTRK1 and mitochondria as tracers, we directly introduced plasmid vectors composed of GFP-NTRK1 with a CMV promoter and mCherry-mitochondria with a CMV promoter into the cell body of RGCs around D34 by electroporation to analyse anterograde rapid axonal transport. Several axons demonstrated anterograde axonal transport after approximately 7–10 h post-introduction. The cell bodies corresponding to these axons expressed these factors as well (Fig. 7a).
To detect a time series of axonal transport, Alexa-Fluo-555 conjugated cholera toxin B, which is also known as a tracer of axonal transport58, was administrated. Slow and fast anterograde axonal flow were clearly observed by injection of the toxin into RGCR (Fig. 7b, Fig. S8, Supplemental Video 1). The transport was blocked by an addition of 1 mM colchicine (Fig. S9, Supplemental Video S2 and S3).
Human iPS cell-derived RGCs showed neuronal excitability
To determine whether iPSC-derived RGCs could generate action potentials, we examined the RGCs in the RGCR (Fig. 8a). The RGCs each had a long axon process extending to the filter paper side and possessed some dendritic processes (Fig. 8b). Electrophysiological analysis of cells with an axon process revealed repetitive action potentials in response to current injection through the recording pipette in current clamp mode (4 of 5 cells; Fig. 8c). The resting membrane potential and the amplitude of the first action potential were −81.8 ± 26.8 mV and 56.8 ± 24.6 mV, respectively (n = 4). The cells that generated action potentials exhibited tetrodotoxin (TTX)-sensitive sodium-dependent currents with a maximum amplitude of 1,248 ± 573 pA (n = 4), followed by outward currents (Fig. 8d).
In this study, we generated RGCs with functioning axons from human iPSCs. The present quantitative PCR and immunohistochemistry results showed a gene expression profile and protein markers characteristic of RGCs, including Brn3b, Math5, Islet1, Sncg and Tuj1. RGCs induced from ESCs and iPSCs in previous studies carried markers characteristic of RGCs17,21,65, but were not accompanied by long axons. RGCs have also been generated in 3D culture systems, but without observation of the axons that would be expected with formation of the nerve fibre layers of the retina and the nerve fibre bundle of the optic nerve. In contrast, RGCs observed in the present study had long, prominent axons expressing NFs, Tuj1 and tau and growing in straight lines on the culture plate. The functionality of the axons was demonstrated by observation of axonal flow and action potentials. Anterograde axonal transport was identified by induction of both NTRK1- and mitochondria-specific vital stains and cholera toxin B into cell bodies. Sodium-dependent action potentials were demonstrated by patch clamp techniques.
RGCs were generated mostly in an OV-like clump of cells extruded from an EB where the layers of neural retina were supposed to differentiate. Most RGCs were localised to the marginal portion of the clump that adhered to the bottom of the culture dish. Because RGCs in vertebrates are located in the most anterior layer of the retina, which coincides with the marginal portion of the OV and optic cup in both embryogenesis and in previously established 3D culture systems, it is not surprising that our RGCs differentiated specifically at the surface of the clump, the inner portion of which may be an agglomerate of other retinal cell types. Relatively large cells with prominent nuclei, consistent with RGC morphology, were stratified at the marginal portion of the clump and were positive for Brn3b, the most specific marker for RGCs. Sectional analysis of RNA expression also confirmed that Brn3b expression was highest at the marginal portion of the clump without accompanying Crx expression, implying that the marginal portion of the clump had been specified purely into RGCs. This marginal portion, the RGCR, was able to survive for several weeks separated from the parent clump of cells (Fig. S3), suggesting the possibility of mechanically purifying RGCs for use in further investigations. Retinal cell determination progresses via a well-organised spatio-temporal pattern, in which RGCs appear initially and are followed by amacrine cells, photoreceptors, horizontal cells, bipolar cells and Muller cells, a process that is highly conserved among species47,66In monkeys, RGC development begins around D2567 and Brn3b, a characteristic transcriptional factor, is expressed in the retina of the human foetus at least by 8 weeks of gestation68. Thus, the timing of the marker expression and development of RGCs in our experiment resembles the process of the genesis of RGCs in vivo.
The axonal growth pattern differs significantly between 2D (on-dish) and 3D cultures. Two-dimensional culture methods for CNS neurons, including hippocampal69, cortical70,71 and hypothalamic cells72,73, have been well established. These primary cultures can be augmented by coating the bottom of the culture dish with extracellular matrix components, including laminin, fibronectin, cadherin and collagen, through which axons can extend74. In addition, neuroprotective agents, including BDNF75,76, nerve growth factor77 and CTNF78,79, can easily be provided to the cells uniformly by adding them to the culture medium to further support neuron and axonal growth.
In contrast, the 3D culture approach has recently achieved in vitro organogenesis of CNS structures80,81, including the retina16,17,34, the pituitary gland15 and heterogeneous neural tissue82, in which axons generally extend into an extracellular matrix gel that contains collagen, fibronectin, or cadherin. Although 3D-cultured neurons seem more suitable for investigating stratified structures, branching and synaptogenesis, the formation of long axons has not been obtained by previous 3D culture methods for retinogenesis. Achieving differentiation to normal RGCs by these methods may be too challenging because the surface of the self-induced retina directly contacts homogeneous culture fluid, which contains no extracellular matrix geometries capable of providing a foothold for horizontal extension of axons from RGCs. Expecting to achieve targeted horizontal extension of axons along the surface of the retina towards the optic nerve head, probably guided by extracellular signals such as Shh, BMP and BDNF83, would be even more difficult because self-induced retinas lack both the optic stalk and the nerve head.
Even in the environment of 2D culture where concentrations of multiple growth factors can be reliably controlled, neither self-induction of retinal layers nor prominent outgrowth of axons from RGCs have been achieved thus far. In the present study, axons extended from RGC bodies in response to a switch of the culture method from 3D to 2D at an optimal time, when the polarity and location of the new RGCs had just been determined. Supplementation with BDNF, a protective agent for RGCs, further supported axon growth. These spatio-temporal steps may be requirements for axon growth from RGCs. However, development of axons by a purely 3D culture method merits further research. RGC axons grown by the 3D to 2D culture method we established were formed uniformly, at a high rate and in a short time and may contribute to various endeavours in basic and clinical science on human RGCs. For example, embryogenesis, nerve path finding, synaptogenesis and interactions between nerve and glial cells in coculture may be easily investigated in vitro.
Our RGCs, which possessed long axons, also provided an excellent tool for investigating the pathogenesis and pathophysiology of optic nerve diseases. The optic nerve is composed of some 800,000–1,000,000 RGC axons51 and can be anterogradely or retrogradely damaged by various crises, including ischemia, infection, trauma, inflammation, tumours and genetic disorders. These can result in cell death and clinically severe visual impairment or blindness, such as glaucoma. Glaucoma, a disease caused by high intraocular pressure, is an important cause of blindness globally. The pathogenesis and pathophysiology of many diseases associated with RGCs remain to be elucidated because of the difficulty of clinical examination of the deepest portions of the eyeball. RGCs induced by iPSCs derived from patients with RGC-associated diseases, especially genetic diseases, may further our understanding of the underlying molecular mechanisms of pathogenesis and pathophysiology. Precedents for this are already documented for other neurodegenerative diseases, including Parkinson' disease and Alzheimer's disease84,85. Moreover, the efficacy and toxicity of drugs for neuroprotection and support of axonal outgrowth and regeneration relevant to human RGC-associated diseases could be examined in vitro with our system with far more ease, accuracy and safety than in the era of animal models. Indeed, an in vitro clinical study relevant to cardiac disease has already started86,87. In addition, future therapies involving isolation of human RGCs for transplantation to repair damaged optic nerves may benefit from our method, though several issues remain to be elucidated, including how to induce complex axonal projection patterns and synaptogenesis in the CNS target areas.
The Ethics Committee of the National Institute for Child and Health Development (NCCHD) approved all experimental protocols (approval number #686, July 3, 2013). All experiments handling human cells and tissues were carried out in accordance with the Tenets of the Declaration of Helsinki.
Human iPSC culture
Human iPSCs (HPS0007_409B2 cell passage 29) were obtained from RIKEN BRC (Japan) and were maintained on a feeder layer of mouse embryonic fibroblasts (MEFs) inactivated by irradiation in Primate ES medium (ReproCELL) supplemented with 10 ng/mL recombinant human basic fibroblast growth factor (bFGF; Invitrogen). For passaging, hiPSC colonies were detached and recovered from the feeder layer by treatment with dissociation solution (ReproCELL) at 37°C for 8 min. The detached hiPSC clumps were broken into smaller pieces consisting of several tens of cells by gentle pipetting. Cell passaging was performed at a 1:3 to 1:4 split ratio.
Induction of differentiation to RGCs
The induction of hiPSC differentiation employed a procedure based on SFEB methods17. hiPSCs were dissociated to single cells in TrypLE Express (Invitrogen) containing DNase I (0.05 mg/mL; Roche) and Y-27632 (10 μM; Wako) and were resuspended in retinal differentiation medium (RDM; G-MEM supplemented with 20% KSR, 0.1 mM nonessential amino acids, 1 mM pyruvate, 0.1 mM 2-mercaptoethanol, 100 U/mL penicillin and 100 μg/mL streptomycin) containing Y-27636 and IWR-1e (20 and 3 μM, respectively; Merck Millipore). After separation from the feeder cells by decantation (the feeder cells adhered to the gelatine-coated bottom of the dish), the floating hiPSCs collected from the medium were seeded into V-bottomed low-cell-adhesion 96-well plates (Sumitomo Bakelite) at 9,000 cells per well. Matrigel (growth factor-reduced; BD Bioscience) was added to a final concentration of 0.5%–2% in the medium on day 2 (the day the suspension culture was initiated was defined as D0). On D12, the aggregates were transferred to low-cell-adhesion 24-well plates and the medium was replaced with RDM containing Matrigel (0.5%–2%) and FBS (1%–10%). On D15, CHIR99021 (3 μM; Wako) and SAG (100 nM; Enzo Life Science) were added to the medium and the suspension culture was continued for another 3 days. On D18, the aggregates were transferred to retinal maturation medium (RMM; DMEM/F12-Glutamax medium containing the N2 supplement, 100 U/mL penicillin and 100 μg/mL streptomycin) and were then cultured in the absence of FBS. The adhesion culture started when the aggregates were transferred to poly-d-lysine/laminin-coated 24-well plates (BD Bioscience) in RMN medium containing FBS and 100 ng/mL BDNF (R&D Systems). The start day varied from D26 to D29 and the addition of retinoic acid (0.5 μM; Sigma) 3 days prior to the start of adhesion culture was preferred. The concentration of FBS was increased stepwise from 1% up to 10% over the course of the adhesion culture.
Real-time reverse transcription polymerase chain reaction (RT-PCR)
Total RNA was extracted from cells using an RNeasy Mini Kit (QIAGEN). The expression levels of the mRNAs in each RNA sample were determined using the StepONE Sequence Detection System (Applied Biosystems). RT-PCR was performed using a One Step SYBR PrimeScript PLUS RT-PCR Kit (TaKaRa Bio). The primers used in this study are listed in Supplementary Table 1. The thermocycler conditions were as follows: an initial hold at 42°C for 5 min; incubation at 95°C for 10 s; and then 40 cycles at 95°C for 5 s and 60°C for 31 s. The expression of mRNA was assessed by evaluating threshold cycle (CT) values. The CT values were normalised to the expression level of hypoxanthine phosphoribosyltransferase 1 (HPRT1) and the relative amount of mRNA specific to each of the target genes was calculated using the 2−ΔΔCT method.
To perform sectional gene expression analysis, adherent tissues of EBs and extruding OVs were defined as three parts: the RGCR, which was located at the outermost 2–3 layers of cells in the clump of cells; the OVR, which was an adherent structure of OVs excluding the RGCR; and the MBEB, which was an adherent structure of the EB. The regions were obviously identified under a SZ61 stereomicroscope (Olympus) and mechanical separation using a 25-G needle was performed under the same microscope.
Frozen section preparation
Specimens were fixed in 4% paraformaldehyde in 100 mM phosphate buffer for 3 h at 4°C, then rinsed in phosphate buffer, osmotic pressure-conditioned in a graded series of sucrose solutions in phosphate buffer up to 30% and embedded in OCT compound (Tissue-Tek; Sakura Finetek). Each block was serially sectioned at 5-μm thickness using a CryoStar NX70 (Thermo Fisher Scientific).
Immunostaining was performed using frozen sections or whole cells fixed on the dish. Whole cells specimens were fixed with 4% paraformaldehyde (pH 7.0) for 20 min at room temperature. After two rinses with PBS, specimens were incubated with 0.1% Triton X-100 for 15 min at room temperature and then washed three times with PBS for 5 min each. Specimens of frozen sections or whole cells were then incubated with 3% bovine serum albumin (BSA) for 30 min at room temperature followed by primary antibody incubation for 16 h at 4°C. The primary antibodies used in this study and their dilutions are listed in Supplementary Table 2. Secondary antibody reactions were carried out by incubation with the corresponding species-specific Alexa Fluor-488-conjugated antibodies (1:500, Invitrogen) for 1 h at room temperature in the dark. After four washes with PBS for 5 min each, specimens were mounted with ProLong Gold Antifade Reagent with DAPI (Invitrogen) and viewed with an IX71 inverted research microscope (Olympus) or BZ-9000E (KEYENCE).
Haematoxylin and eosin staining
Specimens were fixed in 4% paraformaldehyde in 100 mM phosphate buffer for 3 h at 4°C, rinsed in water, dehydrated in a graded series of alcohols/xylene and embedded in paraffin. Each block was serially sectioned at a 3-μm thickness. Deparaffinized sections were then stained with haematoxylin and eosin.
Transmission electron microscopy
Specimens were fixed in 2% glutaraldehyde in 100 mM cacodylate buffer for 2 h, followed by 1% osmium tetroxide in 100 mM cacodylate buffer for 1 h. Specimens were then dehydrated in a graded series of alcohols/xylene, permeated with propylene oxide and embedded in epoxy resin. Ultrathin sections of representative areas were stained with uranyl acetate and lead citrate and viewed with a JEM-1200EX electron microscope (Japan Electron Optics Laboratory).
Axonal flow observation
The NTRK1 expression vector (RG213091; ORIGENE), the pPAmCherry-Mito Vector (TaKaRa Bio) and the pcDNA™6.2/C-EmGFP Vector (Invitrogen) were electroporated into cultured cells. For electroporation, NEPA21 (NEPAGENE) with platinum electrodes was used. The cultured colony was injected with fast green-dyed DNA solution using a sharp glass pipette, placed between the electrodes and electroporated with voltage pulses (poring pulse: voltage 100 V, width 2.5 ms, interval 50 ms, two times; transfer pulse: voltage 20 V, width 50 ms, interval 50 ms, five times). The cultured cells were then allowed to develop in humidified incubators. Observations were made with an IX71 inverted research microscope (Olympus).
The time series of anterograde axonal flow was conducted by injection of Alexa Fluo-555 conjugated cholera toxin subunit B (Life Technologies) into the RGCR. Time-lapse analysis was performed immediately after the injection of cholera toxin B with a DeltaVision ELITE (CORNES Technologies).
Colonies were cultured on mixed cellulose ester filter papers (0.2-μm pore size; ADVANTEC) for 1 week. After removal of filter paper bearing colonies from the medium, suction was applied to the bottom of the filter to cause the colonies to attach firmly. Slices 200 μm thick were then cut vertically with a custom-made tissue chopper and fixed to the glass bottom of a recording chamber having a volume of 1.5 mL with a small amount of silicone grease (Dow Corning). All experiments were performed at physiological temperatures (35–37°C) using a ThermoClamp-1 (Automate Scientific). The chamber was continuously perfused at 1.5 mL/min with extracellular solution containing 120 mM NaCl, 3 mM KCl, 2.5 mM CaCl2, 1 mM MgCl2, 10 mM glucose and 25 mM NaHCO3 equilibrated with 95%/5% O2/CO2 (pH 7.4). Chemicals were purchased from Sigma unless otherwise noted. Whole-cell patch-clamp recordings were made from the retinal ganglion cells located on the outer perimeter of the cultured colony. Recordings were performed with an Axopatch 200B amplifier (Molecular Devices) using pCLAMP 9.2 software (Molecular Devices). The slice preparations were visualised using an upright microscope (BX50WI; Olympus) equipped with DIC optics and a 60× water-immersion objective. The voltage or current trace was low-pass filtered (Bessel filter, corner frequency 10 kHz) and sampled at 20–50 kHz with a Digidata 1322A interface (Molecular Devices). Voltage-dependent Na+ currents were measured with leakage and capacitive current subtraction (P/-5 protocol) and were averaged over three trials. In some experiments, we added 1 μM tetrodotoxin (TTX) to the extracellular solution to block voltage-dependent Na+ channels. The recording pipettes (6–8 MΩ) were filled with an intracellular solution containing 120 mM K gluconate, 6 mM KCl, 2 mM NaCl, 1 mM CaCl2, 1 mM MgCl2, 5 mM EGTA, 10 mM HEPES, 4 mM Na2ATP and 0.5 mM GTP (pH 7.2). In all experiments, Lucifer Yellow CH dilithium salt (LY; 0.05%) was added to the intracellular solutions to visualise the morphology of the recorded cells. Liquid junction potentials (−11 mV) were corrected. The average series resistance (Rs) was 29.4 ± 4.77 MΩ (n = 5). Rs was compensated by 40%. Data with Rs values of more than 35 MΩ were excluded from the analyses. The average membrane capacitance during the recordings was 7.20 ± 2.84 pF (n = 5). Current and voltage data were acquired using pCLAMP 9.2 software and saved on a custom-built personal computer (Physio-Tech). Analyses were performed with Clampfit 9.2 (Molecular Devices) and OriginPro 8J (OriginLab). Images of LY-filled cells were captured using a high-gain colour camera (HCC-600; Flovel) and saved using INFO.TV Plus software (Infocity). The images were adjusted for brightness and contrast and complemented by pasting in a part of another image obtained from a different depth of the slice preparation using Photoshop CS6 software (Adobe Systems). All data are presented as means ± SDs.
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We thank Dr H. Akutsu for technical instruction on primary culture of iPSCs. This work was supported by a Grant from the Ministry of Health, Labour and Welfare (H24-Nanchi-Ippan-031), JSPS KAKENHI (grant numbers 22390327 and 24659770) and a grant from the National Centre for Child Health and Development 25-7.
The authors declare no competing financial interests.
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Tanaka, T., Yokoi, T., Tamalu, F. et al. Generation of retinal ganglion cells with functional axons from human induced pluripotent stem cells. Sci Rep 5, 8344 (2015). https://doi.org/10.1038/srep08344
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