Molecular characterization of retinal stem cells and their niches in adult zebrafish
© Raymond et al; licensee BioMed Central Ltd. 2006
Received: 11 May 2006
Accepted: 26 July 2006
Published: 26 July 2006
The persistence in adult teleost fish of retinal stem cells that exhibit all of the features of true 'adult stem cells' – self-renewal, multipotency, and the capacity to respond to injury by mitotic activation with the ability to regenerate differentiated tissues – has been known for several decades. However, the specialized cellular and molecular characteristics of these adult retinal stem cells and the microenvironmental niches that support their maintenance in the differentiated retina and regulate their activity during growth and regeneration have not yet been elucidated.
Our data show that the zebrafish retina has two kinds of specialized niches that sustain retinal stem cells: 1) a neuroepithelial germinal zone at the interface between neural retina and ciliary epithelium, called the ciliary marginal zone (CMZ), a continuous annulus around the retinal circumference, and 2) the microenvironment around some Müller glia in the differentiated retina. In the uninjured retina, scattered Müller glia (more frequently those in peripheral retina) are associated with clusters of proliferating retinal progenitors that are restricted to the rod photoreceptor lineage, but following injury, the Müller-associated retinal progenitors can function as multipotent retinal stem cells to regenerate other types of retinal neurons. The CMZ has several features in common with the neurogenic niches in the adult mammalian brain, including access to the apical epithelial surface and a close association with blood vessels. Müller glia in the teleost retina have a complex response to local injury that includes some features of reactive gliosis (up-regulation of glial fibrillary acidic protein, GFAP, and re-entry into the cell cycle) together with dedifferentiation and re-acquisition of phenotypic and molecular characteristics of multipotent retinal progenitors in the CMZ (diffuse distribution of N-cadherin, activation of Notch-Delta signaling, and expression of rx1, vsx2/Chx10, and pax6a) along with characteristics associated with radial glia (expression of brain lipid binding protein, BLBP). We also describe a novel specific marker for Müller glia, apoE.
The stem cell niches that support multi-lineage retinal progenitors in the intact, growing and regenerating teleost retina have properties characteristic of neuroepithelia and neurogenic radial glia. The regenerative capacity of the adult zebrafish retina with its ability to replace lost retinal neurons provides an opportunity to discover the molecular regulators that lead to functional repair of damaged neural tissue.
The identification and characterization of neural progenitors that produce neurons and glia in the central nervous system is a subject of intense investigation. It is now widely recognized that neural stem cells persist in specialized 'niches' in the adult mammalian forebrain where they generate large numbers of selected types of neurons [1–3]. One of the most intriguing recent discoveries is that these adult neural stem cells exhibit some properties of glial cells [4, 5] and that neurons in certain regions of the developing embryonic mammalian and avian brains also derive from radial glia . In the adult brain, the microenvironmental compartments called 'niches' provide an embryonic-like milieu to support the maintenance of neural stem cells with the essential properties of self-renewal and pluripotency, i.e. capacity for multi-lineage differentiation [5, 7]. Although still poorly understood, some defining characteristics of adult stem cell niches in the brain and elsewhere are beginning to emerge [8–13]. Some common features of neural stem cells and their niches include: prominent cadherin-mediated adhesive junctions, a rich extracellular matrix and contact with a specialized basal lamina via integrin-mediated junctions, close association with blood vessels, cell-surface carbohydrate markers (e.g., stage-specific embryonic antigen-1, SSEA-1, also called Lewis X, LeX or leukocyte cluster of differentiation 15, CD15), expression of BLBP (brain lipid binding protein, encoded by the gene brain-type fatty-acid binding protein 7, FABP7), expression of selected classes of intermediate filament proteins (e.g., nestin), responsiveness to extrinsic signals such as IGF (insulin-like growth factor), TGFβ/BMP (transforming growth factorβ/bone morphogenetic protein) family, Wnts, Shh (sonic hedgehog), Notch, and LIF (leukemia inhibitory factor). Probably not coincidentally, these extrinsic regulators represent all of the major families of signaling pathways that are essential for early embryonic development .
The neural retina is an embryonic derivative of the forebrain, but unlike the cerebral cortex, adult neural stem cells have not been described in mammalian retina in vivo. With the exception of fish and larval amphibians, retinal neurogenesis in vertebrates is completed during embryonic or early postembryonic development [15–17]. Neural progenitors with the capacity to generate retinal neurons can be recognized from the earliest stages of neural induction by regionalized expression of a series of transcriptional regulators that specify retinal identity [18, 19]. These early 'eye field transcription factors' include the paired-class homeobox genes Pax6 and Rx, a member of the sine oculis homeobox family, Six3, and a LIM-homeobox gene, Lhx. Additional members of the paired-class homeobox family, Chx10 (known as vsx2 in goldfish and zebrafish ) and Crx, appear at later stages in the developing optic cup . Continued co-expression of these homeobox transcription factors is a distinguishing feature of multipotent retinal progenitor cells [16, 21–24].
In larval amphibians and teleost fish, retinal neurogenesis continues postembryonically at the interface between neural retina and ciliary epithelium, a region called the ciliary marginal zone (CMZ) or circumferential germinal zone [25–29]. In these species the CMZ generates the majority of retinal tissue found in the adult eye [26, 30], but the specialized cellular and molecular characteristics of the CMZ niche that support the maintenance and regulate the activity of retinal stem cells in the adult fish eye have not yet been elucidated. A reduced and transient CMZ has been described recently in postnatal chicks and marsupial mammals  and a residual CMZ is seen in mice with a genetic lesion that increases activity of sonic hedgehog signaling . Although the ciliary epithelium of the adult mammalian retina may retain some neurogenic potential in vivo  and in vitro [33, 34], any endogenous capacity for neurogenesis in these species remains latent and without functional consequence.
In addition to the CMZ, another source of retinal progenitor cells persists in the adult teleost fish retina, although the identity and characteristics of these cells are not well understood. In the uninjured, differentiated retina, rod photoreceptors accumulate in central retina as the fish eye grows, and they are generated by rapidly dividing, lineage-restricted rod precursor cells located in the outer nuclear layer (ONL), among the nuclei of differentiated rods . The rod precursors are derived from more slowly proliferating progenitors in the inner nuclear layer (INL) that give rise to clusters of rapidly proliferating progenitors (transit amplifying cells), which migrate into the outer nuclear layer along the radial fibers of the Müller glial cells in larval  and adult [36, 37] fish. Not all of the Müller glia are associated with neurogenesis and the spatial distribution of rod precursors and clusters of INL progenitors varies in that they are present in greater density near the CMZ, i.e., in the most recently generated retina [36, 37]. The slowly dividing progenitors in the INL are immunoreactive for Pax6 , but it is not known whether they express other retinal progenitor transcription factors found in the CMZ. The rod precursors in the ONL do not express Pax6, but they do express the proneural bHLH transcription factor, NeuroD, suggesting that these ONL progenitors may be committed to the photoreceptor lineage .
Although their identity has not yet been established, it is clear that multipotent retinal stem cells (with the capacity to generate all types of retinal neurons, not just rod photoreceptors) persist not only in the germinal zone of the CMZ but also in central retina. Adult teleost fish have a robust capacity to regenerate retinal neurons and to restore the appropriate laminar retinal architecture following damage inflicted by surgical lesions, neurotoxins, laser or photic lesions [29, 39, 40]. All of these studies concluded that the source of regenerated neurons in central retina is an intrinsic progenitor population and not the CMZ. In the intact retina, the progeny of the INL progenitors differentiate only as rod photoreceptors, but several authors have speculated that these progenitors may retain the capacity to generate multiple lineages . Alternatively, it has been suggested that Müller glial cells, which proliferate rapidly in response to retinal damage, may retain a latent capacity to generate neurons in the fish retina [40–42].
In the present study we define the molecular profiles of retinal progenitor cells in the growing and regenerating adult zebrafish retina and we examine the properties of the cellular niches in which they reside. We introduce a simple heat lesion paradigm for analysis of retinal regeneration, we describe the time course of regeneration of cone photoreceptors, and we examine the molecular profile of the injury-induced proliferating progenitor cells that give rise to regenerated cones. Our data show that the adult fish retina has two types of specialized microenvironmental niches that sustain multipotent, self-renewing retinal stem cells: the peripheral CMZ and the microenvironment created by some Müller glia in differentiated retina. We further demonstrate that the retinal stem cell niches in the CMZ germinal zone and the injury-induced stem cell niche in the regenerating retina share a common molecular signature that includes activated Notch signaling, diffuse distribution of N-cadherin, expression of BLBP, and expression of the retinal homeobox genes rx1, pax6a and vsx2/Chx10. Müller glia form the retinal stem cell niche and may generate retinal stem cells in the regenerating retina. Like the neuroepithelial cells (retinal stem cells and progenitors) of the CMZ they are associated with the specialized basal lamina of blood vessels at the vitreal surface of the retina and their nuclei divide at the apical surface in contact with the subretinal space (an embryonic derivative of the ventricular lumen of the forebrain).
Molecular profile of retinal stem cells and progenitor cells in the zebrafish CMZ
Relative strength of in situ hybridization signals in the CMZ. The level of signal was estimated as strong (rank = 3), moderate (2), weak (1), or not detectable (0) in the four regions of CMZ (defined in Fig. 2; Peri. = Peripheral, Mid. = Middle, Cent. = Central). For each probe, 11 to 32 sections from 2 to 4 retinas were evaluated. The arithmetic means of the ranks are reported and the data for each probe are ordered by descending rank in the peripheral CMZ. Values greater than 1.0 are bolded for emphasis.
In the peripheral region of the germinal zone rx1, vsx2/Chx10, and pax6a show the highest signal levels of all the probes we examined (Table 1). Expression of pax6a is moderately high in the peripheral germinal zone and remains strong in middle and central-inner regions, consistent with the continued expression of this gene in differentiated amacrine cells. The level of rx1 signal is moderate in the peripheral germinal zone, and rx2 is slightly weaker. Both rx genes are sharply down-regulated in the middle germinal zone, but reappear in the central-outer region in differentiating cone photoreceptors. The profile of vsx2/Chx10 is similar to rx1/rx2 in that expression levels are highest in the peripheral CMZ and are sharply down-regulated in the middle CMZ. Expression of vsx2/Chx10 reappears in the differentiated INL, presumably in bipolar cells, but outside the CMZ . The expression domain of these transcription factors extends from the CMZ into the adjacent ciliary epithelium (Fig. 1C–F).
Other transcriptional regulators associated with retinal progenitors in several vertebrate species are members of the basic helix-loop-helix (bHLH) family of proneural genes . A zebrafish ortholog of mammalian/chick Mash1/Cash1, called ascl1a (formerly zash1a) has a moderate signal level in the peripheral CMZ, is reduced in the middle and is absent from central regions (Table 1). Proneural genes related to the atonal family, such as neuroD, are typically activated at later stages in the neuronal differentiation cascade and are associated with determination of specific neuronal cell types . In the retina, neuroD specifies photoreceptors in zebrafish . The neuroD probe produces only a very weak signal in the peripheral and middle CMZ, but increases sharply in the central regions, especially the outer part, where photoreceptors are differentiating (Table 1). All of these results are consistent with the idea that the most primitive (i.e., multipotent) retinal stem cells are located in the most peripheral region of the CMZ adjacent to the ciliary epithelium and more restricted retinal progenitors lie closer to the differentiated retina.
The Notch-Delta signaling pathway plays an important role in cell fate choice in the retina and in particular the decision of whether to differentiate as a neuron or a Müller glia or to remain undifferentiated [45, 46]. Several constituents of this bidirectional signaling pathway are expressed in the CMZ in larval and juvenile zebrafish, including the Notch ligands deltaA, deltaB, deltaC, deltaD, several Notch family members (notch1a, notch1b, notch 3) and downstream mediators of activated Notch, her6, the zebrafish ortholog of mammalian Hes1 and her2/Hes5 (Fig. 1G and data not shown). Analysis of relative expression levels shows that in the most peripheral region of the CMZ components of the Notch-Delta signaling cascade give moderate signals (Table 1). Expression levels are lower in the middle and central regions of the CMZ. The signals for notch3 are similar to the notch1 paralogs (data not shown). These data indicate that the Notch-Delta signaling pathway is activated in retinal progenitors including multipotent retinal stem cells that co-express a set of transcriptional regulators implicated in maintenance of multipotency and specification of retinal cell fate.
The microenvironment of the zebrafish CMZ has features typical of neural stem cell niches
The radial glia/astrocyte marker BLBP has been associated with adult neural stem cell niches in mammalian brain . We used a polyclonal antibody against a synthetic peptide of human BLBP that is 90% identical to the predicted amino acid sequence of the orthologous zebrafish gene, fabp7a . We show that retinal stem cells and progenitors in the CMZ and immature Müller glial cells are immunoreactive for BLBP (Fig. 1H). BLBP immunoreactivity extends throughout the CMZ and into the adjacent ciliary epithelium. In larval zebrafish retina (1-week-old), the CMZ and immature Müller glia distributed across the retina are BLBP+ (data not shown), but in 2-month-old juvenile fish only the recently generated, immature Müller glial cells closest to the CMZ are labeled (Fig. 1H). Thus, the BLBP protein is down-regulated with maturation of zebrafish Müller glia.
In mammals, the extracellular matrix-associated carbohydrate epitope SSEA-1/LeX/CD15 is a surface marker for embryonic stem cells and adult neural stem cells  as well as subpopulations of embryonic retinal progenitor cells . The antigen is the trisaccharide, 3-fucosyl-N-acetyl-lactosamine, which is a component of membrane glycolipids and glycoproteins from a variety of tissues. In zebrafish, the SSEA-1 epitope is present at high levels around the circumferential blood vessel [28, 50] that lies on the vitreal surface at the border between neural retina and ciliary epithelium overlying the CMZ (Fig. 1I) and around other blood vessels that line the vitreal surface (data not shown). A second site of high expression is a discrete laminar zone of undetermined identity in the inner plexiform layer (Fig. 1I), potentially on amacrine cell processes . The retinal pigmented epithelium (RPE) also expresses SSEA-1 (data not shown).
The calcium-dependent, homophilic cell adhesion protein N-cadherin (encoded by the gene Cadherin-2) is diffusely distributed on the basolateral plasma membranes of retinal stem cells and progenitors in the CMZ and adjacent ciliary epithelium (Fig. 1J), similar to the distribution of N-cadherin on undifferentiated neuroepithelial progenitors in the embryonic retinal primordium . Proliferating retinal progenitor cells in the CMZ are ensheathed in a network of cadherin-mediated adhesive interactions with neighboring cells. In contrast, in the differentiated retina, N-cadherin is targeted to the zonula adherens that form the outer limiting membrane (apical surface of the retina), to the synaptic (plexiform) layers and to axons of retinal ganglion cells (Fig. 1J and ).
Progenitors with the molecular profile of retinal stem cells are activated locally in differentiated retina by thermal lesions
Thermal lesions trigger a local increase in mitotic activity in the retina, which begins within 2 dpl (data not shown). In lesioned areas elongated clusters of cells associated with radial fibers of Müller glia appear by 3 dpl (Fig. 3D, E). Cells in these clusters incorporate BrdU (Fig. 3D). We confirmed that incorporation of BrdU reflects mitotic cell division and not DNA repair in response to damage  by immunostaining for proliferating cell nuclear antigen, PCNA (Fig. 3E). These mitotic cells are closely associated with radial fibers of Müller glia, all of which are strongly immunoreactive with antibodies against glial fibrillary acidic protein, GFAP (Fig. 3E). Nuclei of the activated Müller glia also reenter the cell cycle and migrate from the INL into the ONL (RLB and PAR, unpublished observations), as we showed previously in regenerating goldfish retina [42, 55].
At 4 and 5 dpl the injury-induced proliferating cells associated with GFAP+ radial Müller fibers co-express at high levels the retinal stem cell markers rx1, vsx2/Chx10 (Fig. 3F–L) and pax6a (data not shown). BrdU+ mitotic clusters show strong rx1 (Fig. 3F–I) and vsx2/Chx10 signals (Figs. 3J–L). The expression of these transcription factors within the lesion extends vertically beyond the laminar boundaries of their respective expression domains in the differentiated retina (Fig. 1C–F).
Injury induces a retinal stem cell niche that recreates the microenvironment of the CMZ
Müller glial cells activated by the lesion acquire several features characteristic of retinal stem/progenitor cells in the CMZ and in the embryonic retina. Activated Müller glial cells up-regulate expression of N-cadherin and the protein becomes distributed diffusely throughout the plasma membrane as it is in retinal stem cells and progenitors in the CMZ (Fig. 4E). The inset in Fig. 4E shows radial fibers of activated Müller glia co-labeled with a monoclonal antibody specific for zebrafish GFAP (zrf1) and polyclonal antibodies against zebrafish N-cadherin. In contrast, in the uninjured differentiated zebrafish retina, N-cadherin immunoreactivity primarily localizes to the adherens junctions formed by Müller glia at the apical surface of the retina (the outer limiting membrane), to the synaptic neuropil of the inner and outer plexiform layers, and to retinal ganglion cell axons . The injury-induced clusters of BrdU+ nuclei are tightly associated with radial Müller fibers that are immunoreactive for N-cadherin (Fig. 4F).
Activated Müller glia in the region of the lesion also up-regulate expression of BLBP (Fig. 4G, H), which is characteristic of retinal stem/progenitor cells in the CMZ and immature Müller glia (Fig. 1H). The boundary between BLBP+ and BLBP- Müller glia is very abrupt (Fig. 1G), which suggests that only the Müller glia directly impacted by the retinal injury dedifferentiate and reacquire an immature molecular profile.
Cone photoreceptors regenerate within a week
Some of the mitotically active cells induced by the thermal lesion are retinal stem/progenitor cells that differentiate into retinal neurons, thus repairing the retinal damage. To identify the retinal stem cells responsible for regenerating retinal neurons, we first needed to know when the regenerated neurons are born so we could focus on cells proliferating during and/or before that time. Not all of the mitotic cells at every interval following the lesion are retinal stem cells; for example, microglia proliferate rapidly in response to retinal injury [42, 57] and phagocytize the dead cells and debris. Differentiated Müller glia proliferate after injury, even in mammalian retinas that fail to regenerate neurons .
Identity of the injury-activated retinal stem cells/progenitors
The longitudinal birthdating analysis identified cells proliferating between 3 and 7 dpl as retinal progenitors whose progeny differentiate into cone photoreceptors. Since cone photoreceptors are not normally produced in the differentiated regions of the intact retina, these data demonstrate that multipotent retinal stem cells persist in central retina with the capacity to respond to injury by altering their lineage profile to compensate for loss of specific neuronal subtypes. As described above, most of the mitotic activity in the lesion area at this time is in elongated clusters of proliferating cells in the INL closely associated with the radial fibers of Müller glia (e.g., Fig. 3E–L, 4F, H). These proliferating cell clusters have been observed in all previous studies of retinal regeneration in teleost fish, and their similarity to the progenitors in the rod photoreceptor lineage of the uninjured retina has been noted . Another potential source of latent retinal stem cells are the Müller glia themselves [29, 41, 42, 65, 66]. This question has been difficult to resolve because of the tight association of retinal progenitors in the rod lineage with the radial fibers of Müller glia in both the uninjured retina  and the regenerating retina (Figs. 3E–L, 4F, H), and the complexity of Müller processes that enwrap neighboring cells . These intimate and complex anatomical relationships make it difficult to determine with fluorescent microscopy and the standard, cytoplasmic Müller-specific markers, e.g. GFAP, cellular retinaldehyde binding protein (CRALBP) and glutamine synthetase, whether a given BrdU+ nucleus belongs to the Müller cell or to an associated progenitor.
In an attempt to examine this question with better techniques, we sought a Müller-specific marker that is confined to the cell body. Apolipoprotein E (ApoE) is a small protein component of several different lipoproteins that is secreted by many cells including glia . To determine whether apoE is expressed by Müller cells, we used transgenic zebrafish  in which enhanced green fluorescent protein (GFP) is controlled by transcriptional regulatory elements of the zebrafish gfap gene. The GFP reporter in this transgenic line is cytoplasmic and fills the cell body and all the processes of Müller glia. We found that zebrafish apoE is expressed selectively and at high levels in gfap: GFP+ differentiated Müller glia, and the signal is largely confined to the cell bodies in the INL (Fig. 5E). The apoE probe also co-localizes with a probe that hybridizes to rlbp1-l (retinaldehyde binding protein 1-like) the zebrafish orthologue of the Müller glial marker CRALBP (cellular retinaldehyde binding protein)  (data not shown). It is therefore a useful marker to identify BrdU+ proliferating Müller glia.
If Müller glia function as retinal progenitors/stem cells in the injured retina, they should be proliferating before and/or during the interval when regenerated cone photoreceptors are being born (i.e., undergoing their terminal mitotic division), which we found is between 2 and 4 dpl. Very few cells incorporate BrdU at 1 dpl (data not shown), but at 2 dpl approximately 80% of the proliferating cells are apoE+/BrdU+ Müller glia (Fig. 6B). The fraction of apoE+/BrdU+ Müller glia in the population of proliferating cells dropped to ~50% by 3 and 4 dpl, while the total number of BrdU+ nuclei increased from a mean of 34 per section at 2 dpl, to 85 per section at 3 dpl, to 235 per section at 4 dpl (Fig. 6B). These data are consistent with several interpretations. Müller glia that express apoE constitute the vast majority (80%) of the proliferating cells at 2 dpl when the size of the BrdU+ population is smallest. The remaining 20% of the BrdU+ cells that are apoE- at this time could be progenitors in the rod lineage or dedifferentiated Müller glia or progeny of Müller glia that have down-regulated apoE expression. A closer examination of the rare BrdU+ cells at early intervals prior to 2 dpl with specific markers for retinal stem cells and progenitors (e.g., rx1, pax6a, vsx2, neuroD, crx) might answer this question. The decline in the Müller glia fraction of the expanding BrdU+ population at 3 and 4 dpl could be explained by dedifferentiation of proliferating Müller cells and/or a more rapid rate of proliferation of non-Müller retinal progenitors. Finally, these data are also consistent with the hypothesis that injury-induced retinal stem cells might derive from Müller glia that begin to proliferate at or before 2 dpl, dedifferentiate and give rise to retinal stem cells.
A separate type of retinal stem cell niche is created within the differentiated retina by some of the Müller glia. Retinal Müller glia are often compared with radial glia of the developing brain . Like radial glia, processes of Müller glia span the width of the retinal epithelium from the apical epithelial surface (outer limiting membrane) to the basal lamina at the vitreal surface and they express structural and functional markers of astrocytes (Fig. 7). In the intact retina of teleost fish, rapidly proliferating INL progenitors (the transit amplifying cells in the rod photoreceptor lineage) are clustered around radial Müller cell fibers and they use these radial processes as guides along which to migrate into the ONL [36, 64], as we showed previously by serial reconstruction electron microscopy . Not all Müller glia are associated with INL progenitors, and the frequency is highest near the retinal periphery (the youngest retina, most recently generated by the CMZ) [36, 64]. We do not yet know whether these neurogenic niches are associated with a specialized subpopulation of Müller glial cells. In the intact retina, the retinal progenitors in these putative Müller cell niches are directed exclusively into the rod lineage, but following injury, the frequency of neurogenic clusters increases , the fate of the retinal progenitors is altered , and the structural and molecular characteristics of the Müller glia change [41, 79] (present data). Müller glia in the injured fish retina exhibit many phenotypic changes associated with reactive gliosis, such as up-regulation of GFAP [42, 55], which is often considered an indicator of stress and pathological processes  and reentry into the cell cycle . Here we show that they also exhibit phenotypic changes suggestive of dedifferentiation, such as re-expression of BLBP and migration of their nuclei toward the apical surface, both of which are characteristic of immature Müller glia in the larval zebrafish retina (RLB, LKB and PAR, unpublished observations). The injury-induced retinal stem cells/multipotent progenitors are entwined in Müller processes, which in response to injury up-regulate components of the Notch-Delta signaling pathways and N-cadherin (cdh2) . The N-cadherin protein becomes distributed to the basolateral membranes of the activated Müller glia, similar to its distribution on neuroepithelial cells.
Radial glia in the embryonic mammalian brain are neurogenic progenitors [6, 82, 83] and specialized astrocytes in the adult mammalian brain function as neural stem cells [2, 4, 84], so it is not surprising that we and others have suggested that Müller glia might generate the injury-induced retinal stem cells in teleost fish [41, 42, 66, 79], although direct evidence that employs a selective and permanent lineage tracer for Müller glial fate mapping has not yet been accomplished. Fischer and Reh [57, 85] have proposed that a latent neurogenic capacity persists in Müller glia of early postnatal chick based on observations of BrdU incorporation and expression of neuronal markers in immature Müller cells following intraocular injection of neurotoxins (NMDA, kainate or colchicine) or growth factors (IGF and FGF2), and similar observations were made in rat retina . However, physiologically relevant, regenerative repair of retinal neuron loss has only been demonstrated in teleost fish  and some amphibians .
One of the most striking morphological changes in the injured fish retina is the migration of proliferating retinal progenitor cells and Müller nuclei to the apical surface and the subsequent reestablishment of a neuroepithelium; this anatomical organization is a necessary condition for regeneration of retinal neurons independent of the mechanism of injury [39, 55, 63]. For example, neurotoxins that selectively destroy retinal neurons in the inner layers of adult goldfish fail to elicit a retinal stem cell response and the missing neurons are not replaced. Only when photoreceptors are destroyed is the regenerative process triggered and the retina repaired including inner neurons as well as photoreceptors. One possible explanation for this differential response to injury is that damaged photoreceptors release factors that stimulate retinal stem cells and create a 'regeneration niche'. Another possibility, not mutually exclusive, is that in the absence of photoreceptors, the proliferating retinal progenitors reestablish contact with the apical surface thus recreating a neuroepithelial organization similar to that found in the CMZ. Migration of Müller nuclei to the apical surface following loss of photoreceptors is clearly not a sufficient trigger to elicit a regenerative stem cell response, since Müller glia in the mammalian retina undergo a similar behavior in the injured or dystrophic mammalian retina but do not generate neurons . The key unanswered question is what extrinsic signals are necessary and sufficient to provoke the formation of a regenerative retinal stem cell niche? Several extracellular factors associated with maintenance of the undifferentiated, multipotent state in neural progenitors in early development, promote glial differentiation at later stages, including activation of LIF and Notch signaling [88, 89]. In the developing retina, activation of Notch signaling either maintains undifferentiated progenitors or promotes Müller glia differentiation, depending on stage-dependent contextual cues [45, 46, 90]. The LIF pathway may also be implicated: Müller glia isolated from the neonatal mouse retina and induced to proliferate by exposure to growth factors express LIF , and LIF is necessary for injury-induced neurogenesis in mouse olfactory epithelium .
Our data indicate that Müller glia in the adult fish retina have a complex response to local injury that includes some features of reactive gliosis (up-regulation of GFAP and re-entry into the cell cycle) together with dedifferentiation and re-acquisition of phenotypic and molecular characteristics of multipotent retinal progenitors (diffuse distribution of N-cadherin, activation of Notch-Delta signaling, and expression of rx1, vsx2/Chx10, and pax6a and BLBP). The outcome of this injury-induced glial activation is not generation of more Müller glia and formation of a glial scar, as is typical in mammalian retina [80, 87], but instead a retinal stem cell niche is recreated with molecular and morphological features that mirror the neurogenic CMZ. Our data suggest that in the injured retina activated Müller glia cells define the retinal stem cell niche and our results are consistent with the proposal that retinal stem cells derive from proliferating Müller glia. This idea fits with the emerging view that adult neural stem cells in vivo are a subpopulation of radial glial-derived cells that retain a neurogenic potential.
Thermal retinal lesions
Zebrafish from our outbred wild-type colony were maintained according to standard procedures. Adult fish were anesthetized in 0.04% Tricaine (3-amino benzoic acidethylester; Sigma-Aldrich, St. Louis, MO) and positioned on their sides on the stage of a stereomicroscope. The dorsal scleral surface of the eyeball was exposed by exerting pressure on the ventral eye to torque it in its socket. A 0.2–0.3 mm diameter copper wire was attached with an alligator clip to a soldering pen (model #64-2055A, Radio Shack, Fort Worth TX), which was mounted on a micromanipulator and set at 15-watts. The heated copper wire was touched to the outer surface of the sclera for 5 seconds. Fish were revived and allowed to recover for 1 to 31 days post-lesion (dpl). The University Committee on Use and Care of Animals at the University of Michigan approved all experimental procedures.
Bromodeoxyuridine labeling of proliferating cells
Two methods were used to expose retinal cells to the thymidine analog, 5-bromo-2'-deoxyuridine (BrdU; Sigma-Aldrich). Zebrafish from 1 to 10 dpl were injected intraperitoneally with BrdU . Alternatively, fish were placed for 2 hours in aquarium system water containing 5 mM BrdU . From 4 hours to 31 days later, fish were killed and the eyes prepared for histology as described below.
Histology and immunocytochemistry
For histology, lesioned eyes were enucleated, fixed in 2.5% glutaraldehyde/1%paraformaldehyde in 0.08 M phosphate buffer, 3% sucrose, 1 mM MgSO4 (pH 7.4) and embedded in Eponate 12 Resin (Ted Pella, Redding, CA). Semithin (1 μm) sections were stained with 1% methylene blue, 1% azure II in 1% sodium borate.
For immunocytochemistry, larval zebrafish were treated with 0.2 mM PTU (1-phenyl-2-thiourea) starting at ~10 hpf to block formation of melanin in the RPE. Intact larval fish and juvenile (2-month-old) fish and enucleated eyes from and adult fish (≥ 1-year-old) were fixed in 4% paraformaldehyde in 0.1 M phosphate buffer and prepared for cryosectioning as described previously . Tissue used for PCNA (proliferating cell nuclear antigen) immunocytochemistry was fixed with 4% paraformaldehyde in 95% ethanol. Slides used for BrdU immunocytochemistry were pre-treated with 2N HCl for 30 min. Some slides were processed for antigen retrieval by incubation for 20 mins. at 98 C in 10 mM sodium citrate, pH 6.0, with 0.05% Tween20, then cooled and rinsed in 0.1 M phosphate buffered saline.
Primary antibodies and dilutions included: Monoclonal antibodies – anti-PCNA (Sigma-Aldrich), 1:1000; zrf1 (Zebrafish International Resource Center, ZIRC, Eugene, OR), 1:5; zpr1 (ZIRC), 1:200; rat anti-BrdU (Accurate Chemical, Westbury, NY), 1:50; 4C4 (from Jonathan Scholes, University College, London), 1:200; SSEA-1/LeX, carbohydrate epitope (MC-480, Developmental Studies Hybridoma Bank, Iowa City, IA), 1:5. Polyclonal antibodies – anti-human GFAP (DakoCytomation, Carpinteria, CA), 1:100; anti-human BLBP (Abcam, Cambridge, MA), 1:1000; affinity purified, anti-zebrafish N-cadherin (N-terminal peptide) , 1:500; anti-GFP (Invitrogen, Carlsbad, CA), 1:200.
Secondary antibodies used at 1:200 dilution included: anti-mouse IgG, Alexa 488 conjugate; anti-rat IgG, Alexa 647 conjugate; anti-rabbit IgG, Alexa 555 conjugate (Alexa conjugates from Invitrogen); anti-mouse IgM, FITC (fluorescein isothiocyanate)-conjugate; anti-mouse IgG, Cy-3, FITC and AMCA (7-amino-4-methylcoumarin-3-acetic acid) conjugates (Jackson ImmunoResearch Laboratories, Inc., West Grove, PA). Slides were mounted in ProlongGold antifade reagent (Invitrogen), premixed with the nuclear stain, DAPI (4', 6-diamidino-2-phenylindole).
In situ hybridization
Methods for synthesis and hybridization of digoxigenin (DIG)-labeled or fluorescein (FL)-labeled RNA probes  were modified as follows: Hauptmann hybridization buffer , hybridization temperature at 65 C, no RNase treatment, and increased posthybridization stringency . Probes transcribed from zebrafish cDNA templates (minimum length: 741 bp) were used at the concentrations indicated: notch1a, notch1b, notch2, notch3 (from Michael Lardelli, University of Adelaide) 0.8 μg/ml; her1, her6 (from Jose Campos-Ortega, deceased) 8 μg/ml; deltaA, deltaD (from Bruce Appel, Vanderbilt University) 8 μg/ml; deltaB, deltaC (from Julian Lewis, University College London) 8 μg/ml; rx1, rx2, rx3 (from Peter Mathers, University of West Virginia) 4 μg/ml; vsx2 (from Nisson Schechter, SUNY Stony Brook) 4 μg/ml; pax6a (from Nadean Brown, Cincinnati Children's Hospital) 1 μg/ml; gfap (from James Warren, Penn State) 8 μg/ml; ascl1a-DIG (from Nadean Brown) 4 μg/ml; neuroD (from Peter Hitchcock, University of Michigan) 4 μg/ml; apoE (from Susan Lyons, University of Michigan) 0.5 μg/ml; cone opsin genes sws1, sws2, rh2-1, lws-1 (from Thomas Vihtelic, University of Notre Dame), 250 ng/ml.
For two-color in situ hybridization  DIG-labeled and FL-labeled probes were mixed and hybridized to the tissue, then detected with anti-DIG or anti-FL antibodies conjugated to alkaline phosphatase (AP) or horseradish peroxidase (POD), respectively. Fast Red (FR) color substrate for AP (Roche Applied Science, Indianapolis, IN) was followed by the indirect Tyramide Signal Amplification (TSA) fluorescence system (TSA-biotin/avidin-FITC) to detect the POD-conjugated antibody (Perkin Elmer Life and Analytical Sciences, Boston, MA). Alternatively, to avoid any possibility that the dense FR precipitate would obscure the TSA-FITC signal, both anti-FL and anti-DIG antibodies were conjugated with POD. The FL-labeled probes were detected first by incubation with the anti-FL POD conjugated antibody followed by indirect TSA-biotin/avidin-FITC, as above. The POD was then inactivated by incubation with 3% H2O2 in 0.1 M PBS for 15 minutes, and sections were incubated with the anti-DIG POD-conjugated antibody and detected using direct TSA-Cy3 (Perkin Elmer).
Fish with lesioned retinas were injected intraperitoneally with BrdU at 3, 5, 7 or 10 dpl, retinas were fixed at 31 dpl and cryosectioned. DIG-labeled probes for zebrafish cone opsin genes (sws1, sws2, rh2-1, lws-1) were combined at a concentration of 250 ng/ml each, hybridized, and detected with anti-DIG (AP-conjugate visualized with FR), followed by BrdU immunofluorescent detection.
To determine the time course of photoreceptor regeneration, the area with regenerated photoreceptors was identified by BrdU+ nuclei in the INL. Labeling by in situ hybridization with the cone opsin cocktail identified cone photoreceptors, and those with BrdU+ nuclei were counted. BrdU+ rod nuclei within the segment of retina delimited by BrdU label in the INL were also counted. (Note that BrdU+ rod photoreceptors outside the lesioned zone are not regenerated neurons but instead are newly added in conjunction with normal retinal growth in teleost fish. These were not counted.) Between 4 and 17 sections per lesion were scored and the mean number of BrdU+ cones and rods per section was calculated.
To quantify the time course of proliferation in injury-activated Müller glial cells, retinas from fish labeled with a 2-hour pulse of BrdU at 2, 3 or 4 days post-lesion were processed for in situ hybridization with the Müller marker apoE. BrdU+ nuclei were counted in 2 to 9 sections from each retina and scored for double-labeling with ApoE. To maximize the number of BrdU+ nuclei in each sample we examined sections cut tangentially through the lesion.
For light microscopy we used epifluorescent compound microscopes (Zeiss Axioplan equipped with an Axiophot 2 camera or Zeiss AxioImager and ApoTome with an AxioCam MRM camera) supported by AxioVision software (Carl Zeiss, Jena, Germany), or an Olympus BX-51 epifluorescent compound microscope (Olympus, Tokyo, Japan). For laser scanning confocal microscopy we used an Olympus Fluoview 500, equipped with 405 nm blue diode, 458 nm, 488 nm, and 514 nm multiline argon, 543 nm helium neon green and 633 nm helium neon red lasers. Images were processed with Fluoview version 4.3 with Tiempo software. We used Adobe PhotoShop to adjust digital images for brightness, contrast and sharpness. Hues in RGB color space were adjusted with the Channel Mixer tool. Overlays of multiple fluorescent and differential interference contrast images from the same field of view were generated in PhotoShop with the Layer Style tool by selecting the Screen or Lighten option for the Blend Mode.
We would like to thank our colleagues who provided us with reagents (B. Appel, N. Brown, J. Campos-Ortega, P. Hitchcock, J. Lewis, M. Lardelli, S. Lyons, P. Mathers, N. Schechter, J. Scholes, T. Vihtelic, and J. Warren). We also thank Dilip Pawar for technical assistance. Supported by: NIH R01 EY004318 (PAR), NIH T32 EY013934 (RLB), NIH F31 NS047909 (RLB/PAR), and NIH T32 DC05341 (JJP).
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