Cell determination in the retina has been under intense investigation since the discovery that retinal progenitors generate clones of apparently random composition (Price, J., D. Turner, and C. Cepko. 1987. Proc. Natl. Acad. Sci. USA. 84:156–160; Holt, C.E., T.W. Bertsch, H.M. Ellis, and W.A. Harris. 1988. Neuron. 1:15–26; Wetts, R., and S.E. Fraser. 1988. Science. 239:1142–1145). Examination of fixed tissue, however, sheds little light on lineage patterns or on the relationship between the orientation of division and cell fate. In this study, three-dimensional time-lapse analyses were used to trace lineages of retinal progenitors expressing green fluorescent protein under the control of the ath5 promoter. Surprisingly, these cells divide just once along the circumferential axis to produce two postmitotic daughters, one of which becomes a retinal ganglion cell (RGC). Interestingly, when these same progenitors are transplanted into a mutant environment lacking RGCs, they often divide along the central-peripheral axis and produce two RGCs. This study provides the first insight into reproducible lineage patterns of retinal progenitors in vivo and the first evidence that environmental signals influence the orientation of cell division and the lineage of neural progenitors.
Isolated retinal progenitors give rise to clones of cells in vitro that are similar in size and cellular composition to clones that such progenitors generate in vivo (Cayouette et al., 2003). This suggests the existence of preestablished lineage programs in retinal progenitors. But what are these programs and what factors control them?
The ath5, a bHLH transcription factor, is necessary and sufficient for the development of retinal ganglion cells (RGCs), which are the earliest born cell type in the vertebrate retina (Kanekar et al., 1997; Brown et al., 2001; Kay et al., 2001; Wang et al., 2001). In ath5 mutants, there is a delay in the first cells to exit the cell cycle, which is consistent with the failure of any population of cells to exit the cell cycle at the time when RGCs are normally born. Similarly, when ath5 is transfected into retinal progenitors, those cells tend to leave the cell cycle early in histogenesis at the time when RGCs are normally born, and then about half of these cells become RGCs (Ohnuma et al., 2002). In a recent study, an ath5:GFP transgenic line faithfully recapitulating ath5 expression in the zebrafish retina was used to show that ath5 and RGC determination is switched on in a spatio-temporal pattern that depends on intrinsic properties of the neuroblasts themselves (Kay et al., 2005). Together, these data are consistent with the idea that the lineage of neuroblasts is determined by the expression of ath5.
Although recent findings suggest that cell-intrinsic properties of neuroblasts play a major role in affecting the cell lineage during retinal development (Cayouette et al., 2003; Kay et al., 2005; Mu et al., 2005), environmental factors have also been proposed to affect the lineage of retinal progenitors. In particular, negative feedback from developing RGCs has been shown to limit the production of new RGCs (Waid and McLoon, 1998; Gonzalez-Hoyuela et al., 2001). This is known because ganglion cell production can be restored in these progenitors when ganglion cells are depleted from the older cell population. Interestingly, selective depletion of RGCs in the differentiating mouse retina in vivo leads to an increase in the number of progenitors expressing ath5 (Mu et al., 2005), providing a possible link between extrinsic and intrinsic coordination of cell division and cell fate.
For these reasons, we wanted to see whether ath5-expressing progenitors showed any reproducible lineage patterns and whether these patterns could be influenced by negative feedback. We reasoned that the best way to see these things was by using an in vivo time-lapse approach.
Time-lapse imaging studies on explanted pieces of developing ferret cortex suggested that the orientation of cell division is associated with different daughter cell fates (Chenn and McConnell, 1995). Similarly, the examination of rat retinal explants revealed that daughters with similar fates derived mostly from divisions in the plane of the retinal surface, whereas orthogonal (apical-basal) divisions generated different daughter cells (Cayouette and Raff, 2003). To reconstruct cell divisions in the fully intact developing retina, researchers turned to the transparent embryonic zebrafish embryo (Das et al., 2003). Three dimensional (3D) time-lapse observations of fluorescently labeled progenitors in this preparation showed that the orientation of cell division shifts from central-peripheral to circumferential over development. Interestingly, that study also showed that the normal shift in the orientation of cell division was affected in the ath5 mutant lakritz, raising the issue of how the orientation of cell division correlates with specific cell fates.
In this study, we used the ath5:GFP transgenic line of zebrafish (Masai et al., 2003) combined with 3D time-lapse video microscopy. This allowed us, for the first time, to determine reproducible features in lineages of ath5-expressing progenitors in a normal embryo and to demonstrate that environmental signals affect lineage pattern and orientation of cell division.
ath5-expressing cells go through mitosis before they differentiate
Recent BrdU experiments describe ath5 expression as a post–S-phase marker of retinal progenitors (Masai et al., 2005). However, GFP driven by the ath5 promoter and enhancer is detectable before RGCs complete their differentiation and possibly before their final mitosis (Masai et al., 2005). Therefore, we used these transgenic ath5:GFP fish embryos to perform long-term time-lapse imaging of ath5:GFP-expressing retinal progenitors to see when in the cell cycle these cells began to express GFP. Embryonic retinas that were imaged in 15-min intervals with optical sections 0.5 μm apart were taken through a volume up to 50 μm in depth for a minimum of 10 h starting from ∼32 h after fertilization (Fig. 1 A). A schematic describing the main features of the developing retinal neuroepithelium is shown in Fig. 1 B. These image sets were reconstructed into 3D time-lapse videos. ath5:GFP cells could be clearly seen undergoing M phase of the cell cycle at the apical surface (Fig. 1 C and Video 1). In a few instances, we transplanted ath5:GFP blastomeres that had been injected with a membrane-targeted RFP construct (growth-associated protein [GAP]–mRFP) and used double labeling to highlight cells as they first turned on GFP. Although the RFP label was weak and faded rather quickly in these experiments, we were able to focus on dividing cells that became GFP positive during the recording sessions. In these cases, GFP first became visible in RFP-labeled cells as the nuclei of these cells were migrating toward the apical surface before metaphase (Fig. 1 D and Video 2). This apically oriented phase of interkinetic nuclear migration is generally associated with the G2 phase of the cell cycle (Seymour and Berry, 1975). Finally, ath5:GFP cells could be seen acquiring the anatomical characteristics of RGCs. Differentiation into RGCs is characterized by the retraction of the apical process, the migration of the cell body to the RGC layer of the retina near the vitreal surface, and the extension of a growth cone–tipped axon that grows along the vitreal surface toward the future optic nerve head (Fig. 1 E and Video 3).
To test the fidelity of GFP expression in these transgenic embryos, we examined ath5 RNA expression in the retina at stages when these signals first become visible. The level of ath5 mRNA is unaffected by the expression of GFP from the transgenic promoter, as quantitative RT-PCR analysis reveals that transgenic and wild-type embryos express indistinguishable amounts of ath5 mRNA (not depicted). Moreover, GFP and ath5 mRNA can often be seen in the same cells, including dividing precursors (Fig. 1, F–H). These colocalization results agree with and extend those of previous studies (Kay et al., 2005; Masai et al., 2005).
ath5-expressing progenitors divide once and produce one RGC daughter
ath5 is necessary for RGC development, yet not all ath5-positive cells differentiate as RGCs. ath5 mutants of zebrafish (called lakritz; Kay et al., 2001) and Math5 knockouts in mice (Brown et al., 2001; Wang et al., 2001) have a strong reduction in RGCs, whereas lipofection experiments in Xenopus laevis show that Xath5 promotes RGC fate in approximately half of the misexpressing cells (Kanekar et al., 1997). Moreover, the effects of Xath5 on cell fate appear to be stage dependent; misexpression at early stages primarily promotes RGC fates, whereas the same experiment at later stages promotes other retinal neuronal fates (Moore et al., 2002). Math5 expression was also found to be associated with the differentiation of multiple retinal neuron types in the developing mouse (Yang et al., 2003) and in developing transgenic Xenopus retinas (Hutcheson et al., 2005). These results raise the issue of how ath5 expression affects the lineage and fate of precursors in vivo during normal development.
ath5 mRNA is rapidly lost from differentiating progenitors and is not visible even in mature RGCs. However, the persistence of stable GFP protein in transgenic zebrafish allowed us to track the fate of ath5:GFP-positive cells to later stages. Therefore, we analyzed the distribution of positive cells in 5-d postfertilization retinas, when all retinal cell layers are differentiated and distinguishable. Histological sections through the central retina showed GFP-positive cells in the ganglion cell layer (GCL) as expected. These cells colabeled with the RGC-specific antibody zn-5. There were also many GFP-positive cells in the inner nuclear layer (INL) and outer nuclear layer (ONL; Fig. 2, A–C). GFP-positive INL cells could often be identified by their morphologies and positions as either horizontal or amacrine cells (Fig. 2 C). Interestingly, we found that the INL GFP-positive cells do not colabel with the bipolar marker PKCβ1; on the other hand, some colabel with the amacrine-specific marker calretinin (Fig. 2, E and F), further suggesting that at least a number of these INL cells are amacrines. The GFP-positive cells in the ONL had the morphology of photoreceptors and expressed the photoreceptor-specific marker zpr-1 (Fig. 2 D). These results show that RGCs are not the exclusive fate choice of ath5-expressing retinal progenitors in the zebrafish retina.
To map out the lineage relationships between the ath5:GFP-positive RGCs and the other ath5:GFP-positive cells in the retina, we examined the dividing ath5:GFP progenitors and followed their descendents by 3D time lapse. This was difficult to do in the “normal” transgenic fish embryos because the high density of ath5:GFP-positive cells made it difficult to pick out lineages in our time-lapse videos. Therefore, to see these progenitors more clearly, we transplanted blastula-stage cells from ath5:GFP transgenic fish into the blastulas of nontransgenic host embryos. This early stage transplantation ensured that the transgenic cells had fully integrated normally into their wild-type hosts while allowing the density of transgenic cells in the retinas to be low enough for good observation. We then imaged several individual ath5:GFP-expressing progenitors in host retinas starting from 32–35 h after fertilization. We saw no cell deaths in the population of ath5:GFP-positive cells or their progeny within the time period studied (unpublished data). Anaphase and cytokinesis of ath5:GFP progenitors always occurred at the apical surface of the retina and parallel to it, as previously observed for all cell divisions in the zebrafish retina (Das et al., 2003). We were able to trace the GFP label in the daughters of 14 ath5:GFP dividing progenitors for many hours. All ath5:GFP-positive progenitors gave rise to two daughter cells. After separation, the two daughter cells reextended toward the basal surface but then usually migrated in opposite directions and acquired different morphologies. One daughter invariably migrated basally, withdrew its apical process, and began acquiring, through laminar position and axon extension, the characteristics of an RGC. The other daughter withdrew its basal process and migrated back to the apical surface. Fig. 3 shows an example of this lineage pattern (Video 4). This apical cell often changed in shape and began to look like an immature photoreceptor. When we tried to track the fate of this cell by extending our video recording, we observed the GFP signal becoming fainter, eventually disappearing from the focal plane. Although we were not able to show a clear fate for the apical daughter cell, our observations indicated that these apical cells did not divide again even within the extended time frame of these recordings, which is consistent with the observations that ath5-positive cells were always BrdU negative (Masai et al., 2005). Thus, the lineage pattern of these ath5:GFP progenitors seems to be reproducibly programmed to give rise to two postmitotic daughters, one of which becomes an RGC.
Removal of RGCs affects the fate and lineage of ath5:GFP progenitors
Previous in vitro studies suggested that inhibitory feedback signals secreted from differentiated RGCs prevent undifferentiated retinal cells from choosing the RGC fate (Waid and McLoon, 1998; Gonzalez-Hoyuela et al., 2001). If ath5:GFP-positive retinal progenitors respond to such cues, we might expect that the absence of RGCs should change the developmental potential and lineage of these progenitors. We used the lakritz mutant to investigate this question. In lakritz, RGCs fail to differentiate because of a loss of function mutation in the ath5 locus. As a result, the first wave of cells exiting the cell cycle and differentiating as RGCs is missing in lakritz. Instead, the cells that would have differentiated as RGCs appear to stay in the cell cycle for an extra round of division and differentiate into other retinal cell types (Kay et al., 2001). Wondering whether the absence of the inhibitory feedback signals from previously generated RGCs would influence the lineage of wild-type ath5-expressing progenitors, we transplanted blastula-stage cells from ath5:GFP transgenic fish into the blastulas of lakritz mutant host embryos. Fig. 4 shows that there were proportionally more RGCs generated by ath5:GFP cells transplanted to lakritz hosts (∼70%) than there were RGCs generated by the same progenitors transplanted to wild-type embryos (∼40%). The proportion of other ath5:GFP-positive cell types was concomitantly lower (Fig. 4 and see Fig. 6). These data suggest that the lack of RGCs in lakritz hosts indeed biases the developmental behavior of the ath5-expressing progenitors toward an RGC fate.
A likely explanation for the increase in the proportion of ath:GFP-positive RGCs in lakritz versus wild-type hosts is that the lineage of the ath5:GFP progenitors is changed in these circumstances. Therefore, we traced the lineages of a number of dividing ath5:GFP cells in lakritz hosts. Again, no cell deaths were observed in the transplanted population of ath5:GFP-positive cells, and progenitors displayed normal interkinetic nuclear movements. Strikingly, these dividing progenitors showed different lineage patterns in lakritz than in wild-type hosts. In many instances, both daughter cells began to differentiate as RGCs (Fig. 5 A and Video 5), and, in two cases, a progenitor divided twice, giving rise to one RGC with each division (Fig. 5 B and Video 6). A diagram comparison of the 14 lineages that we were able to follow in each of the two environments are shown in Fig. 6 A. Clearly, there is a striking difference between these two populations. Moreover, if it is the case that all RGCs normally arise from ath5-expressing progenitors, the changes in lineage programs represented in this study are enough to account for the increase in RGCs when ath5:GFP progenitors are transplanted into an environment lacking RGCs (Fig. 6 B).
Orientation of cell division
Apical-basal cell divisions, occurring with the cleavage plane parallel to the retinal surface, have been suggested to be a source of asymmetric cell fates in the vertebrate nervous system (Chenn and McConnell, 1995; Zhong et al., 1996, 1997; Wakamatsu et al., 1999; Cayouette et al., 2001; Cayouette and Raff, 2003). It was previously reported that progenitors in the zebrafish retina do not divide along the apical-basal axis even when they are giving rise to postmitotic daughters (Das et al., 2003). In agreement with this study, we found that all divisions of ath5:GFP cells occurred parallel to the retinal surface (i.e., with the cleavage plane perpendicular to the retinal surface). Interestingly, the same study showed that the proportion of cells dividing in the circumferential axis (>45°) increased over time at the expense of divisions orientated in the central-peripheral or radial axis (<45°; Fig. 7 A and Videos 7 and 8). Das et al. (2003) also suggested that the more circumferentially orientated divisions could be asymmetric in nature, whereas the radial divisions could be more symmetric, and showed that the normal shift in orientation was compromised in lakritz mutants. In this study, we show that only 10% of ath5:GFP progenitors transplanted into a wild-type environment divided radially (Fig. 7 B), whereas 45% of these same progenitors transplanted to the lakritz environment divided radially (Fig. 7 B). What is more telling is that we are able, for the first time, to classify asymmetric fate divisions and symmetric fate divisions among normal ath5:GFP-positive progenitors and, thus, to correlate the orientation of division directly with lineage outcome. In asymmetric divisions, one daughter cell became a RGC, whereas the other did not. In symmetric divisions, both daughter cells became RGCs. We found that circumferential divisions tended to give rise to asymmetric or different fates, whereas the radial divisions tended to give rise to symmetric or similar fates (Fig. 7 C).
Recent studies provide evidence for the sufficiency of intrinsic programs for retinal cell diversification (Cayouette et al., 2003; Kay et al., 2005; Mu et al., 2005). This is consistent with the findings that wild-type retinal progenitors can turn on ath5 and differentiate into RGCs when transplanted into a lakritz environment, suggesting that they do not need positive signals deriving from differentiated RGCs (Kay et al., 2005). It is particularly striking that all 14 ath5:GFP progenitors we followed in the wild-type environment displayed very similar lineages, strongly suggesting the presence of stereotyped and intrinsically determined lineage programs in the retina. However, such a conclusion must be treated with caution, as we were examining these lineages only during a narrow time window, and the results of transplanting the same cells into a lakritz mutant suggest that even in a wild-type environment, earlier ath5-positive progenitors developing in an environment devoid of previously generated RGCs might show a different lineage program.
The reproducible lineage patterns that we found among ath5-expressing progenitors helps explain why ath5 is necessary for RGC fate but does not necessarily correlate with RGC fate (Kanekar et al., 1997; Brown et al., 2001; Kay et al., 2001; Wang et al., 2001; Yang et al., 2003; Masai et al., 2005). All ath5 progenitors produce RGCs, but not all ath5-expressing progenitors become RGCs. In wild-type animals, we found that an ath5:GFP-positive progenitor divides once and only one of the two daughters (the one that expresses ath5:GFP more strongly) becomes a RGC. The other daughter usually becomes a different cell type and down-regulates ath5:GFP expression. Interestingly, we observed that this cell usually ended up in the ONL and assumed an immature photoreceptor-like morphology, suggesting that, at least during the period of our video recordings, ath5:GFP progenitors tend to be restricted to a lineage that produce one RGC and one other cell type, usually a photoreceptor.
ath5 is first expressed in post–S-phase retinal precursors (Yang et al., 2003; Ma et al., 2004; Masai et al., 2005). In our study, we recorded many ath5:GFP retinal progenitors undergoing cytokinesis at the apical surface and found that ath5 mRNA colocalizes with ath5:GFP expression in M-phase progenitors. Interestingly, we found that the onset of ath5:GFP expression in dividing progenitors was almost always shortly before they entered M phase and while their nuclei were undergoing interkinetic migration toward the apical surface, suggesting that ath5 usually turns on in retinal progenitors at G2 of the final cell cycle (Miale and Sidman, 1961). Other cases have been described in which intrinsic factors begin to be expressed in G2; for example, Prox1, a homeobox protein that is required for the determination of horizontal cells in the vertebrate retina, is initiated at G2 (Dyer et al., 2003), but in these cases, the fates of the daughter cells have not been followed.
It has been previously argued that the distinct clones seen in the retina could have been sculpted out of a highly conserved lineage program by random cell death (Voyvodic et al., 1995). The differences we see among ath5:GFP progenitor clones in which one of the daughter cells becomes an RGC and the other becomes a different cell type or, in the lakritz environment, becomes another RGC are clearly not results of cell death but are caused by different lineage patterns.
Our results clearly also show that the lineage programs of ath5:GFP-expressing cells respond to negative feedback signals in the normal environment, at least during the developmental time window of this study when the first RGCs are already present. Previous studies have shown that the environment plays an important role in regulating the proportion of RGCs generated (Waid and McLoon, 1998; Gonzalez-Hoyuela et al., 2001). Indeed, we found that after transplantation of wild-type cells into a wild-type host, about half of ath5:GFP-positive cells are RGCs, but this percentage is increased by ∼30% when the same cells are transplanted to a lakritz mutant environment. By following individual ath5:GFP progenitors over time, we found that the environment can dramatically influence their lineage patterns, leading to a predicted increase in RGC production of ∼30%. A greater number of dividing ath5:GFP progenitors give rise to two RGCs compared with one in the wild-type environment.
Recent data has shown that GDF11 is a potential negative feedback factor for RGC production (Kim et al., 2005). In mice mutant for GDF11, the histogenetic window for ath5 expression and RGC production is extended. In these mutants, extra RGCs are generated at the expense of later born cell types. Follistatin antagonizes GDF11, and follistatin mutants show a shortened period of ath5 expression and RGC production in the retina. These results fit well with our findings of extra rounds of division and a switch from asymmetrical fate to symmetrical RGC-generating divisions in ath5 progenitors transplanted to the lakritz environment.
Apical-basal cell divisions have been found in the vertebrate nervous system, including the retina, and some of them have been shown to be asymmetric in nature (Chenn and McConnell, 1995; Zhong et al., 1996, 1997; Wakamatsu et al., 1999; Cayouette et al., 2001; Cayouette and Raff, 2003). Planar divisions, however, can also be asymmetric (Adams, 1996; Gho and Schweisguth, 1998; Wodarz and Huttner, 2003; Kosodo et al., 2004; Malicki, 2004; Sun et al., 2005). In the chick retina, cells dividing apico-basally are a small percentage of dividing cells, and this percentage does not seem to account for all of the asymmetric behavior of daughter cells (Silva et al., 2002). Both in the zebrafish retina and neural tube, apical-basal divisions are entirely absent (Das et al., 2003; Geldmacher-Voss et al., 2003; Lyons et al., 2003). Within the plane of the ventricular surface in the zebrafish retina, however, cells may divide along a more circumferential or radial axis (Das et al., 2003). Interestingly, we found that circumferential divisions in ath5:GFP-positive progenitors tend to give rise to different or asymmetric fates. One possible explanation for this relates to the neurogenic wave, which spreads primarily in the circumferential axis (Neumann and Nuesslein-Volhard, 2000). Consequently, circumferential divisions could produce two daughter cells that are differentially exposed to any potential signals that are associated with this wave. Differences in the intrinsic ability to respond to extrinsic signals may also account for asymmetric behavior of daughter cells. Indeed, a recent study found that unequal segregation of the EGF receptor during mitosis in dividing cortical progenitor cells plays a part in generating asymmetric behavior of the daughter cells (Sun et al., 2005). Alternatively, these circumferential divisions may favor the unequal partitioning of an intrinsic determinant. It will be interesting to investigate which of these possibilities is at play in this system.
In this study, we found that radial divisions tend to give rise to similar or symmetric fates (in this case, two RGCs). In the Das et al. (2003) study (Lyons et al., 2003), all dividing cells were examined, including those early dividing cells in which presumably both daughters remained in the cell cycle. The conclusion from that study was that early progenitors might also divide primarily in a radial orientation. If that is so, the results here suggest that radial cell divisions can give rise to two progenitors at early stages or two similar postmitotic daughters at later stages.
It has always been an aspiration of scientists in this field to directly observe clone formation and to watch how different cell types arise in vivo. This time-lapse analysis is the beginning of such work, and we have used this beginning to show, for the first time, a major role for the environment in influencing the orientation of division and lineage pattern of a distinct class of retinal precursors in their final mitosis.
Materials And Methods
Fish were maintained at 26.5°C. Embryos were raised at 28.5°C and staged in hours after fertilization. Embryos used for imaging were of wild-type strains (wik), were homozygous for the lakritz (lakth241) mutation (a gift from H. Baier, University of California, San Francisco, San Francisco, CA), or were ath5:GFP transgenic (Masai et al., 2003). All embryos were treated with 0.003% phenylthiourea (Sigma-Aldrich) from 11 to 24 h after fertilization to delay pigment formation in the eye.
A pCS2 + GAP-mRFP plasmid, which consists of mRFP preceded by a palmitoylation signal from GAP43, was used to label the membrane of retinal progenitors in ath5:GFP transgenic donor embryos before they started to express ath5:GFP. The DNA was injected at a concentration of 10 ng/μl in the cell of one-cell stage embryos.
In vivo imaging
Both transgenic and transplanted embryos were screened 24 h after fertilization under a fluorescent dissecting stereo microscope (MZ FLIII; Leica) for those with strong eGFP expression in the retina. Chosen embryos were mounted in 0.7% agarose, pH 7.4, containing 0.04% MS-222 and 0.01 M Hepes onto a No. 0 coverslip that served as the bottom of a 30-mm petri dish. Embryos were also orientated such that the lateral side of the eye was closest to the coverslip. The petri dish was then filled with embryo medium containing 0.04% MS-222 and placed in a heated stage at 30°C on an inverted microscope (DMIRBE; Leica). Both mRFP and eGFP fluorescence in the specimens was imaged with a confocal laser scanning microscope (model TCS-NT; Leica) using a 63× NA 1.2 water immersion objective (Leica) with a long working distance (0.225 mm). A 488-nm line from an argon laser was used for GFP excitation, and a krypton laser providing a 568-nm laser line was used for RFP excitation. Emission was detected using individual descanned photomultiplier tube detectors. For time lapses, optical sections 0.5 μm apart were taken through a volume of the retina up to 50 μm in depth and Kallmann averaged once. Time points were between 10 and 15 min apart. Image data was acquired and stored as TIFF files using TCS-NT or confocal software (Leica).
Visualization and cell tracking
Acquisition was performed using macros provided by R. Adams (University of Cambridge, Cambridge, UK). To visualize the acquired data as time-resolved volumes, images were processed on a Macintosh computer using Volocity (Improvision). All projections in each dataset were assembled into Quicktime videos. Cell tracking was performed using the Volocity classification module (Improvision) as well as a tracking program provided by R. Adams. At the end of each video recording, a whole mount antibody staining with the ganglion cell marker zn-5 was performed on the imaged retina in order to further verify the identity of the final fate of the tracked cells.
Imaging of wild-type and lakritz transplanted embryos
The lakritz phenotype does not become apparent until 4 d after fertilization, but it can be easily identified by tissue genotyping (Kay et al., 2001). To identify the genotype of embryos obtained from lakritz heterozygous matings 24 h after fertilization, a small portion of the tip of the tail was cut and used for tissue genotyping. The protocol used was described previously (Kay et al., 2001), with few modifications. This method allowed us to efficiently genotype the embryo in a short time and start the time-lapse imaging ∼32 h after fertilization.
Transplantations were performed as previously described (Ho and Kane, 1990). Approximately 10–50 cells were transplanted from blastula-stage ath5:GFP transgenic embryos into the animal pole of blastula-stage embryos that were obtained from lakritz heterozygous matings. For imaging on retinal sections, host embryos were left to grow in embryo medium until 4 d after fertilization, when they were fixed, cryosectioned, labeled with antibody, and analyzed by confocal microscopy. For whole-mount immunostaining and live imaging, embryos where grown in embryo medium containing 0.003% phenylthiourea (Sigma-Aldrich) from 11 to 24 h after fertilization and either fixed at 4 d or genotyped as described above for time-lapse imaging.
Whole-mount in situ hybridization was performed on ath5:GFP transgenic embryos using ath5 as a probe. A fluorescent signal was obtained by using Fast Red as a substrate for alkaline phosphatase (Sigma-Aldrich) followed by antibody labeling for GFP and confocal analysis. Antibody labeling was performed on 10-μm–thick cryosections or on whole embryos and was analyzed with a confocal microscope (model TCS-SP-MP; Leica). The following antibodies were used: anti–rabbit GFP (Invitrogen), anti–rabbit polyclonal calretinin (1:500; Chemicon), anti–rabbit PKCβ1 (1:50; Santa Cruz Biotechnology, Inc.), anti–mouse zn-5 (1:200; University of Oregon), and anti–mouse Zpr-1 (1:500; University of Oregon). Bound antibodies were detected using anti–rabbit AlexaFluor488, anti–rabbit AlexaFluor594 (both at 1:1,000; Invitrogen), and anti–mouse Cy3 (Chemicon). Nuclei were stained at 1:50 DAPI in PBS for 10 min.
Analysis of the orientation of cell division
Analysis of the orientation of cell division was performed as previously described (Das et al., 2003).
Online supplemental material
Video 1 shows ath5:GFP progenitors dividing at the apical surface. Video 2 shows ath5:GFP expression occurring during apically oriented interkinetic nuclear migration. Video 3 shows ath5:GFP retinal progenitors extending axons toward the basal surface while differentiating in RGCs. Video 4 depicts the common lineage program of ath5:GFP progenitors in a wild-type environment. Video 5 shows the lineage program of an ath5:GFP progenitor generating two RGCs in a lakritz environment. Video 6 shows the lineage program of an ath5:GFP progenitor generating one RGC and another progenitor in the lakritz environment. Video 7 depicts a circumferential division. Video 8 shows a radial or central-peripheral division.
We thank Jeremy Skepper for help in using the confocal microscope and Ingrid Pradel for helping with embryo genotyping. Many thanks go to Richard Adams for providing macros for acquisition and cell tracking. We thank the Zebrafish International Resource Center for providing antibodies
This work was supported by a grant (#RR12546) from the National Institutes of Health National Center for Research Resources. We also thank the European Commission and the Wellcome Trust for funding this work.
The authors have no conflicting financial interests.
Abbreviations used in this paper: 3D, three dimensional; GAP, growth-associated protein; GCL, ganglion cell layer; INL, inner nuclear layer; ONL, outer nuclear layer; RGC, retinal ganglion cell.