- Research article
- Open Access
The neuroepithelial basement membrane serves as a boundary and a substrate for neuron migration in the zebrafish hindbrain
Neural Development volume 5, Article number: 9 (2010)
The facial branchiomotor neurons of cranial nerve VII undergo a stereotyped tangential migration in the zebrafish hindbrain that provides an ideal system for examining the complex interactions between neurons and their environment that result in directed migration. Several studies have shown the importance of the planar cell polarity pathway in facial branchiomotor neuron migration but the role of apical-basal polarity has not been determined. Here we examine the role of the PAR-aPKC complex in forming the basal structures that guide facial branchiomotor neurons on an appropriate migratory path.
High resolution timelapse imaging reveals that facial branchiomotor neurons begin their migration by moving slowly ventrally and posteriorly with their centrosomes oriented medially and then, upon contact with the Laminin-containing basement membrane at the rhombomere 4-rhombomere 5 boundary, speed up and reorient their centrosomes on the anterior-posterior axis. Disruption of the PAR-aPKC complex members aPKCλ, aPKCζ, and Pard6gb results in an ectopic ventral migration in which facial branchiomotor neurons escape from the hindbrain through holes in the Laminin-containing basement membrane. Mosaic analysis reveals that the requirement for aPKC is cell-nonautonomous, indicating that it is likely required in the surrounding polarized neuroepithelium rather than in facial motor neurons themselves. Ventral facial motor neuron ectopia can be phenocopied by mutation of lamininα1, suggesting that it is defects in maintenance of the laminin-containing basement membrane that are the likely cause of ventral mismigration in aPKCλ+ζ double morphants.
Our results suggest that the laminin-containing ventral basement membrane, dependent on the activity of the PAR-aPKC complex in the hindbrain neuroepithelium, is both a substrate for migration and a boundary that constrains facial branchiomotor neurons to the appropriate migratory path.
Spatial information along the anterior-posterior and dorsal-ventral axes is used to specify neuronal identity during vertebrate brain development. The position at which a neuron's fate is specified, however, frequently does not correspond to the position at which it must perform its function. Instead, neurons frequently migrate from their place of birth to their final functional position. This process of neuronal migration involves a tightly choreographed interaction between a migrating cell and the complex environment through which it is migrating, requiring the organism to lay down the appropriate cues, substrates, and boundaries that guide migration at the appropriate time during development .
The tangential migration of the facial branchiomotor neurons (FBMNs) of cranial nerve VII in the zebrafish hindbrain provides an ideal system for examining the complex interactions between migrating neurons and their environment. FBMNs are continuously differentiating in rhombomere 4 (r4) starting at 16 hours post-fertilization (hpf). They migrate posteriorly to r6 and r7, the migration lasting 4 to 6 hours for each FBMN, and the entire migration of about 100 to 150 μm is concluded by 48 hpf . During this period the zebrafish hindbrain constitutes a richly patterned and dynamic environment. Early in migration, the hindbrain is a pseudostratified neuroepithelium composed of neural progenitor cells that, over the course of the time that migration progresses, undergo neurogenesis and gliogenesis .
The early hindbrain neuroepithelium is polarized both apico-basally and within the plane of the epithelium. This latter form of polarity, known as planar cell polarity (PCP), has been shown to be required for FBMN migration. Mutations in the PCP genes vangl2[4, 5], prickle1b, frizzled3a, and celsr2 all result in a failure of FBMNs to migrate out of r4. It has been proposed that PCP proteins function by excluding FBMNs from the more dorsal neuroepithelium and keeping them on their appropriate migratory pathway [7, 8]. The role of apical-basal polarity in FBMN migration, however, has not been assessed. FBMNs undergo the majority of their migration apposed to the ventral pial surface, which corresponds to the basal domain of the neuroepithelial progenitor cells. The apical domain of these progenitors is located at the midline where the lumen is forming during this stage of development .
A key regulator of apical-basal polarity in many systems is the PAR-aPKC complex, composed of two scaffold proteins, PAR-3 and PAR-6, and a serine/threonine kinase, aPKC . In zebrafish there is one PAR-3 gene, pard3, two aPKC genes,aPKCλ and aPKCζ, and four PAR-6 genes, pard6a, pard6b, pard6ga, and pard6gb[10, 11]. The PAR-aPKC complex functions to polarize epithelial cells by establishing apical membrane domains and promoting the formation of apical structures such as tight junctions . Members of the PAR-aPKC complex have also been shown to have a role in polarizing migrating cells by reorienting the centrosome in migrating wound-edge astrocytes , and controlling the saltatory migration of cortical neurons along their glial guides .
The PAR-aPKC complex also functions indirectly to maintain basal structures of epithelia by maintaining the basolateral localization of proteins such as PAR-1 and the Lgl-Dlg-Scrib complex. The basement membrane is a sheetlike extracellular matrix composed of a network of Laminin and type IV Collagen crosslinked and decorated with various other protein components. It anchors the basal domain of epithelia and functions in their polarization . Basement membrane components are secreted by epithelial cells and organized into basal sheets by basally located Dystroglycan complex that anchors and allows for the polymerization of Laminin . The basal localization of the Dystroglycan complex requires basally-localized Par1, which in turn requires apical localization of PAR-3-PAR-6-aPKC .
Here we show that FBMN migration requires the basal structures produced by a properly polarized neuroepithelium. We observe that FBMNs undergo a change in their migratory behavior upon contact with the ventral Laminin-containing basement membrane. Depletion of PAR-aPKC complex members or of Laminin itself results in defects in the basement membrane that allow FBMNs to mismigrate ventrally, escaping the hindbrain entirely. This suggests that the ventral Laminin-containing basement membrane is both a substrate for FBMN migration and a barrier that constrains that migration to its appropriate trajectory.
FBMNs undergo a change in velocity and centrosome orientation upon contact with the ventral basement membrane
Facial branchiomotor neurons are born in hindbrain r4, first becoming detectable by Isl1:GFP expression at 16 hpf, and migrate posteriorly to r6 and r7 by 48 hpf. This is apparent in tg(hoxb1aBAC:RFP); tg(isl1:GFP) double transgenic fish, where cells born in r4 express red fluorescent protein (RFP) and branchiomotor neurons (including FBMNs) express GFP. In these double transgenics, most FBMNs in r6 and r7 are GFP- and RFP-positive, indicating their r4 origins (Figure 1A).
In order to better visualize the migration of FBMNs in live embryos, we created a transgenic line in which a membrane-targeted monomeric RFP  is expressed in branchiomotor neurons under the control of the minimal islet1 enhancer, zCREST1 . This transgenic line, tg(zCREST1:memb-mRFP1), allows for timelapse movies that show the cellular behaviors of migrating FBMNs in greater detail than has previously been possible. New FBMNs immediately begin their posterior migration, moving in an amoeboid manner without a prominent leading process. FBMNs appear to rappel down the hindbrain, playing out their axons behind them. This axon tract seems to serve as a scaffold, allowing later born neurons to migrate in close apposition with the axons of earlier born neurons and for FBMNs to crawl over each other as they migrate (Additional files 1, 2 and 3).
Crossing the tg(zCREST1:memb-mRFP1) transgenic line with a tg(krox20BAC:GFP) transgenic line that expresses GFP in r3 and r5 allowed us to measure the posterior migratory velocity with respect to the r4-r5 boundary (Figure 1B; Additional file 1).
We measured the extent of individual FBMN posterior migration over time for 14 FBMNs from 12 different embryos, with the onset of imaging occurring between 18 and 28 hpf. When we pooled these data and compared the average velocity for all observed FBMNs in r4 (0.11 ± 0.01 μm/minute) versus their average velocity in r5 (0.17 ± 0.01 μm/minute), we observed a statistically significant increase in velocity in r5 (t-test; P < 0.01). In order to determine the nature of this increase in velocity, we plotted the extent of posterior migration versus time and compared the fit of various models to the data. We found that for 7 of the 14 cells, the data was best fit by a bilinear model , indicating a single change in velocity (Figure 1C, left graph), while for the other 7 cells, the data was equally well fit by a bilinear model or by a single line, indicating a constant velocity (Figure 1C, right graph). In no cases was an exponential model superior to the bilinear model (data not shown). When we re-centered these plots so that the origin of the graph corresponded to the point of contact with the r4-r5 boundary, it became apparent that the change in velocity occurred within 7 μm (about one cell diameter) from the r4-r5 boundary (Figure 1D, FBMN#1 to FBMN#7).
We wondered what was occurring near the r4-r5 boundary that might explain this change in velocity. We performed a three-dimensional analysis of Isl1:GFP transgenic embryos  stained with anti-Laminin antibody. This analysis revealed that FBMNs begin their migration by moving ventrally as well as posteriorly until they reach the ventral Laminin-containing basement membrane. After this, migration is purely posterior (Figure 1E). To determine where on the anterior-posterior axis FBMNs reach the basement membrane, we immunostained tg(isl1:GFP) embryos for Laminin and EfnB2a, which is expressed in rhombomere 4 (r4). This staining revealed that the point of contact with the ventral basement membrane occurs at approximately the r4-r5 boundary (Figure 1F). The slow phase of migration, then, correlates with the ventro-posterior movement that occurs before neurons reach the basement membrane while the fast phase correlates with purely posterior movement that occurs in close apposition to the basement membrane.
The velocity measurement we made is the posterior component of a velocity vector that points ventro-posteriorly during the slow phase of migration and then points posteriorly after cells have reached the ventral basement membrane. As such, the change in posterior velocity might be explained simply by this change in direction. To correct for the ventral component of migration, we calculated the average angle (θ) between the line of ventrally migrating neurons and the ventral basement membrane (Figure 1G) and multiplied the initial velocity measurement by the correction factor of 1/cosθ to arrive at the magnitude of the ventro-posterior velocity vector. Even after this correction factor is applied, FBMNs migrate with an average velocity of 0.11 ± 0.01 μm/minute during the ventral-directed phase while they migrate at a significantly different velocity of 0.21 ± 0.01 μm/minute during the posterior phase (t-test; P < 0.0005). This indicates that apposition with the basement membrane correlates with an increased rate of migration. FBMNs that migrated at a constant velocity (for example, Figure 1D, FBMN#8) did so with an average velocity of 0.18 μm/minute, so we speculate that most of these FBMNs are migrating in the fast, posterior phase of migration, suggesting that they may have contacted the basement membrane before we began recording.
In many migratory cell types, such as wound-edge astrocytes and fibroblasts [12, 21] or migrating cortical neurons , the centrosome localizes between the nucleus and the leading edge, where it organizes the microtubule cytoskeleton in a polarized fashion. We asked whether the change we observed in migratory velocity might be associated with changes in polarity as assayed by centrosome position. We found that before contact with the ventral basement membrane, most centrosomes in FBMNs are found in the ventral half (75%; n = 36 FBMNs from 4 embryos) and in the medial quadrant (75%; n = 36 FBMNs from 4 embryos) of the cell (Figure 2A, D, E). Medial centrosome orientation is similar to that observed in the surrounding neuroepithelial progenitor cells whose centrosomes are found at the (apical) midline. In contrast, the majority of centrosomes of FBMNs that are apposed to the ventral basement membrane are in the dorsal half of the cell (72%; n = 36 FBMNs from 4 embryos) and in the anterior or posterior quadrants (28% and 44%, respectively; n = 36 FBMNs from 4 embryos) (Figure 2B, D, E). Chi-squared analysis reveals that the distribution of centrosomes in r5 is significantly different from that in r4 (P < 0.0001). Together, these data form a picture in which FBMNs begin their migration moving slowly ventro-posteriorly with their centrosomes pointing ventro-medially until they reach the basement membrane, where they cease ventral migration, reorient their centrosomes either dorso-anteriorly or dorso-posteriorly, and accelerate in the posterior direction.
PAR-aPKC complex members aPKCλ, aPKCζ, and Pard6gb are required for proper FBMN migration
The above observations led us to speculate that there may be a requirement for proper cell polarity in the migrating FBMNs and/or in the surrounding neuroepithelial progenitors that lay down the basement membrane that appears to be a substrate for migration. Members of the PAR-aPKC complex have been shown to be responsible for both polarity in migrating cells (including centrosome reorientation ), and apical-basal polarity within epithelia . We asked whether PAR-aPKC complex proteins have a role in FBMN migration.
In order to examine the role of aPKC in FBMN migration, we crossed the heart and soul (has/aPKCλm 567) mutant into the Isl1:GFP background. aPKCλm 567mutants exhibit a mild posterior migration defect in which some FBMNs fail to migrate completely, remaining spread along the migratory pathway in r4 and r5 at 48 hpf (Figure 3B). In addition, aPKCλm 567mutants show a novel, partially penetrant phenotype (27%; n = 67) in which a subset of migrating FBMNs deviates from their normal path and mismigrates ventrally (Figure 3F, arrow; Table 1). As aPKCλ and aPKCζ have been shown to function redundantly in zebrafish retinal development, and are both present in the hindbrain , we hypothesized that they were functioning redundantly in this context as well. Single knockdown of either aPKCλ or aPKCζ using previously described morpholino oligonucleotides [24, 25] followed by immunostaining with an antibody that recognizes both gene products , resulted in only a partial reduction in staining (data not shown). Simultaneous knockdown of both aPKCλ and aPKCζ, however, resulted in an absence of detectable aPKC staining in the hindbrain (Figure 3J). While injections of either single morpholino (MO) showed ventral mismigration defects similar in penetrance and severity to the aPKCλm 567mutant embryos (aPKCλ MO = 14%, n = 159; aPKCζ MO = 21%, n = 188), in aPKCλ+ζ double morphant embryos (or in aPKCλm 567mutants injected with aPKCζ MO) the penetrance of migration defects increased to 45% (n = 142) and the severity of defects (assayed by number of mismigrated cells and extent of migration) increased as well (Table 1; Figure 3C, G). In these double morphant embryos, mismigrated FBMNs form an ectopic ventral cluster that is elongated anteriorly, suggesting that FBMNs begin their posterior migration, mismigrate ventrally, then reverse their course and migrate anteriorly (Figure 3G, arrow). This ventral mismigration phenotype can be phenocopied in a dose-dependent manner by the injection of mRNA expressing a dominant negative form of aPKCλ  (Table 1).
We examined cross-sections of aPKCλ+ζ double morphant embryos stained with BODIPY TR methyl ester, a membrane dye . This analysis revealed that the ectopic ventral clusters of FBMNs had escaped the hindbrain entirely, forming ectopia in mesenchyme ventral to the normal migratory path (Figure 3L, arrow). It is also clear from these sections that the architecture of the hindbrain is disrupted in aPKCλ+ζ double knockdown embryos. The cross-sectional area is smaller and rounder and the ventricle has failed to form, both expected outcomes of disrupting neural progenitor cell polarity (see Discussion).
To determine whether removal of other PAR-aPKC complex members resulted in a similar migration phenotype, we examined a pard6gb mutant generated by TILLING  that harbors a nonsense mutation in exon 2 (Figure 4A). We bred this allele into the tg(isl1:GFP) background and examined the incross for defects in FBMN migration. Incrosses produced pard6gbfh 266homozygous mutant embryos with morphological defects identical to those reported for another pard6gb null allele (Figure 4) . As in aPKCλm 567mutant and morphant embryos, FBMNs fail to migrate fully in pard6gbfh 266homozygous mutant embryos, and a subset of pard6gbfh 266mutant FBMNs mismigrate ventrally. This phenotype in pard6gbfh 266mutants is less pronounced than in aPKC knockdown embryos, in that mismigrated FBMNs do not exit the hindbrain (Figure 3H).
aPKC functions cell-nonautonomously to prevent ventral mismigration
In controlling FBMN migration, aPKC may function within the motor neurons, perhaps to determine their polarity during migration, or it may function in the surrounding neuroepithelium that lays down the appropriate boundaries, cues, and substrates for migration. In order to determine if aPKC is required within FBMNs themselves or within the surrounding tissue, we made mosaics by transplanting cells into the presumptive ventral hindbrain territory at the early gastrula stage [29, 30]. When wild-type cells from tg(isl1:GFP) transgenic donors injected only with a rhodamine-tagged lineage dye are transplanted into uninjected tg(isl1:GFP) hosts, the donor-derived (rhodamine+; GFP+) FBMNs migrate along with their host-derived (rhodamine-; GFP+) counterparts to r6 and r7, and are never observed in an ectopic ventral position (Figure 5A, B). In contrast, when wild-type cells are transplanted into aPKCλ+ζ double morphant tg(isl1:GFP) hosts, a subset of both the host-derived FBMNs and donor-derived wild-type FBMNs mismigrates ventrally (Figure 5C, D). This behavior was observed in 10 out of 20 transplants in which donor-derived FBMNs were observed. This is a similar penetrance to that seen in untransplanted aPKCλ+ζ double morphants. This result shows that aPKC is required cell non-autonomously, in the environment of the migrating motor neurons. This non-autonomous function could be in other motor neurons, which serve as guides for donor-derived cells, or it could be in the surrounding neuroepithelium, which provides the substrate and directional cues for migration. We observe that mismigrated clusters of motor neurons can consist largely, if not exclusively, of wild-type donor-derived cells, suggesting that guidance cues from mismigrated host neurons are not required for donor neuron mismigration. Our further results below support a model in which neuroepithelial progenitor cell polarization is essential for normal FBMN migration.
PAR-aPKC complex is required for maintenance of apical-basal polarity in the hindbrain neuroepithelium
Because our mosaic analysis showed that aPKC functions cell-nonautonomously with respect to FBMN migration, we examined the surrounding hindbrain tissue in PAR-aPKC complex mutants and morphants for defects that might explain the FBMN ventral mismigration defect. The earliest migrating FBMNs navigate through a hindbrain composed of neuroepithelial progenitor cells that are polarized apicobasally with their apical domains at the ventricular surface and basal domains at the pial surface. This polarity is reflected in apically localized centrosomes and cellular junctions and a basally localized basement membrane. It has been reported that in aPKCλm 567mutants, apical structures are formed correctly in neural epithelia (retina and neural tube) and are present during the time when the earliest-born FBMNs begin their migration . These structures are not maintained, however, and therefore a loss of apical junctional markers ZO-1 and β-catenin is observed starting at about 40 hpf . aPKCλ and aPKCζ have been shown to function redundantly in the retina , so we looked at markers of apical-basal polarity in aPKCλ+ζ double morphant embryos to determine if this polarity was disrupted in the hindbrain during the time when FBMNs are migrating.
Focusing on the ventral hindbrain where FBMNs are migrating, we found that at 24 hpf in wild-type embryos, the centrosomes of neuroepithelial progenitor cells, visualized by anti-γ-tubulin staining, are localized apically, closely apposed to the ventricle, as is the junction protein ZO1 (Figure 6A, B). ZO1 is typically associated with tight junctions but it has been shown in mammals that tight junctions are disassembled during neurulation and ZO1 becomes associated with adherens junctions in the neuroepithelium  so this staining reflects the localization of whichever apical junctional complexes are present at this stage. In aPKCλ+ζ double morphants at 24 hpf, ZO1 staining is indistinguishable from that in wild type (Figure 6G, L), indicating that apical junctional complexes are formed even in the absence of any detectable aPKC. Anti-γ-tubulin staining of aPKCλ+ζ double morphants, however, reveals that while the majority of centrosomes are localized to the midline as in wild type, there is a small but significant increase in the number of centrosomes located more than 5 μm from the ventricular surface (11% (n = 642 centrosomes from 4 embryos) versus 6% in wild type (n = 633 centrosomes from 4 embryos); t-test, P < 0.05; Figure 6F, arrow). More severe midline defects have been reported in pard6gb mutants  and we also observe these defects in the dorsal hindbrain of pard6gbfh 266mutant embryos but they are less dramatic in the ventral hindbrain where FBMN migration occurs (Figure 5K, L). The mislocalization of progenitor centrosomes in aPKCλ+ζ double morphants and pard6gb mutants suggests that while apical-basal polarity is not abolished, there is a defect in progenitor cells' ability to localize their subcellular components and align apicobasally that results in a defect in neural tube architecture.
Staining of coronal vibratome sections through wild-type 48-hpf embryos at the level of hindbrain rhomobomere 4/5 shows that ZO1 is present at the ventricular surface at 48 hpf (Figure 6E). In both aPKCλ+ζ double morphant and pard6γ b mutant embryos, ZO1 staining is discontinuous and reduced (Figure 6E, J, O), although the amount of staining lost is highly variable. It has been shown that in aPKCλ mutants apical polarity is established correctly but apical structures are gradually lost starting at about 40 hpf in the spinal cord [25, 32]. Our data are consistent with the idea that the PAR-aPKC complex is required for the maintenance of apical structures but that apical-basal polarity is not completely lost in embryos in which aPKC or Pard6gb is removed. These observations are also consistent with the timing of onset of FBMN ventral mismigration as migration in both aPKCλ+ζ double morphant embryos and pard6gbfh 266mutant embryos is normal at 24 hpf (Figure 6A-C, F-H, K-M) while ventral ectopias are observed at 48 hpf (Figure 6I, J, arrows).
Roberts and Appel  reported a reduction of radial glia at 72 hpf in the spinal cord of aPKCλ mutants. We wondered if a disruption of basal glial endfeet could explain the ventral mismigration we observed in aPKCλ+ζ double morphant embryos. Staining for GFAP (Glial fibrillary acidic protein), a glial marker, reveals that basal glial endfeet are formed properly in aPKCλ+ζ double morphants and pard6gbfh 266mutants (Figure 6D, I, N), although the overall architecture and number of radial glia is disrupted due to the altered morphology of the hindbrain. Escaping FBMNs in aPKCλ+ζ double morphant embryos are always located ventro-medially in a region where glial endfeet are absent in both wild type and double morphants (Figure 6D, I, N, asterisk), suggesting that glial endfeet are not responsible for preventing mismigration. The most ventro-medial tissue in these sections is the floorplate, which is also properly formed in aPKCλ+ζ double morphants as seen by Zn5 staining (data not shown).
FBMNs escape the hindbrain through holes in Laminin
In spite of relatively subtle defects in apicobasal polarity in the ventral hindbrain neuroepithelium, migrating FBMNs mismigrate ventrally, frequently escaping the hindbrain altogether. Laminin staining appears normal in whole-mount aPKCλ+ζ double morphants and pard6gb mutants at 24 hpf, indicating that the basal domain is established correctly in these embryos (Figure 6C, H, M). However, by 48 hpf, holes are detected in the Laminin-containing basement membrane through which FBMNs have escaped. A single XY section shows such a discontinuity in the Laminin staining (Figure 7A) while a three-dimensional reconstruction of the same embryo shows that the motor neurons have escaped from a hole of about the size of one cell diameter and then migrated around it outside the ventral surface of the hindbrain (Figure 7B; Additional file 3). These holes occur at various anterior to posterior levels and are never seen in wild-type embryos (data not shown). They do not correspond with the exit points of any of the axons of the isl1:GFP positive branchiomotor nerves or of the abducens motor nerve (data not shown) and are not bilaterally symmetrical, suggesting that their location is likely random.
Ventral mismigration can be phenocopied by Laminin depletion
If ventral mismigration seen in aPKC knockdown is due to a defect in the Laminin-containing ventral basement membrane, we would expect to see similar mismigration if Laminin levels in the basement membrane are reduced. It has been reported that bashful/lamininα1 mutants have a defect in the posterior migration of FBMNs  but the nature of that defect was unclear. In addition, genetic interactions between lama1 and other pathways implicated in FBMN migration have been reported . Cross-sections through either lama1 mutant (baluw 1) or lama1 MO 48-hpf embryos stained with a polyclonal Laminin antibody reveal that while some Laminin staining is preserved at the midline, there are large swaths of Laminin missing ventrally through which large numbers of FBMNs escape, forming large motor neuron ectopia outside the hindbrain (Figure 7C, D, arrow). This phenotype is seen at a higher penetrance than in aPKC double morphant embryos (Table 1) with more FBMNs contributing to these ectopic clusters. Laminin depletion, then, results in basement membrane discontinuities and ventral mismigration of FBMNs similar to that seen upon PAR-aPKC complex depletion. We conclude that the ventral mismigration observed in aPKCλ+ζ double morphant embryos is due to a loss of integrity of the Laminin-containing basement membrane.
In the absence of Laminin, FBMNs fail to speed up and reorient their centrosomes
If the Laminin-containing basement membrane is a substrate for migration that serves to induce the changes in velocity and centrosome orientation that we have observed in wild-type embryos, then we would expect those changes not to occur in the absence of Laminin. In order to test this, we performed live imaging of wild-type and lamininα-/-tg(isl1:GFP) embryos. Counterstaining with BODIPY TR methyl ester dye and imaging in a lateral view allowed us to visualize ventral and posterior migration with respect to the ventral surface of the hindbrain (Figure 8A, B; Additional files 4 and 5). We observed that in both the presence and absence of Laminin, FBMNs undergo ventral migration down to the ventral surface of the hindbrain (Figure 8A, B; Additional files 4 and 5, blue outline). In wild-type embryos we observed that cells that were in contact with the ventral surface of the hindbrain move quickly posteriorly as described in Figure 1 (Figure 8A; Additional file 4, magenta outline). In lamininα1-/- embryos, however, FBMNs continue their ventral migration and exit the hindbrain. Once they are outside the hindbrain they fail to speed up posteriorly (Figure 8B; Additional file 5, magenta outline) and, in some cases, even mismigrate anteriorly (Figure 8B, white outline).
To test whether FBMNs reorient their centrosomes in the absence of Laminin, we stained lamininα1-/-; tg(isl1:GFP) embryos for γ-tubulin and compared the orientation of centrosomes in FBMNs that were inside the hindbrain with those that were outside the hindbrain. Most centrosomes in both FBMNs inside and outside the hindbrain were oriented medially in a distribution that was the same as that seen for wild-type centrosomes that were dorsal to the Laminin-containing basement membrane (compare Figures 2D and 8D). By chi-squared analysis, the distribution of centrosomes inside the hindbrain was not significantly different from that of centrosomes outside the hindbrain (P > 0.2). This suggests that in the absence of Laminin, FBMNs fail to reorient their centrosomes and maintain the polarity of FBMNs in the ventral phase of migration. Together, these data show that the faster, posterior-directed phase of migration with centrosomes oriented along the anterior-posterior axis is dependent on the presence of an intact Laminin-containing basement membrane.
We show here that FBMNs initially migrate ventrally until they come into contact with the Laminin-containing basement membrane, which appears to serve as a substrate for migration. Upon contact with the basement membrane, FBMNs undergo a change in velocity and centrosome orientation. Knockdown of aPKCλ and aPKCζ results in disruption of the basement membrane and a mismigration of FBMNs in which they exit the hindbrain through holes in basal Laminin. This mismigration can be phenocopied by mutation (or knockdown) of Lamininα 1, suggesting that it is the disruption of the basement membrane that is responsible for ventral mismigration. It must be noted, however, that in pard6gbfh 266embryos FBMNs mismigrate ventrally but do not exit the hindbrain, indicating that mismigration can occur without a breach in the integrity of the basement membrane. It is likely, then, that there are other basal structures disrupted in the pard6gbfh 266hindbrain that also serve to prevent ventral mismigration.
What is the nature, then, of the defects in the hindbrain that result in ventral mismigration? Depletion of members of the PAR-aPKC complex aPKCλ, aPKCζ, or Pard6gb results in a disruption in the architecture of the hindbrain resulting in a smaller cross-sectional area and a failure of the ventricle to inflate. Two mechanisms are likely at work here to produce such a phenotype. Munson et al.  report a similar ventricle defect in pard6gbs 441mutants, due to a failure to correctly establish apical identity in neural progenitors. In addition, Roberts and Appel  report that loss of apical-basal polarity in aPKCλm 567mutants results in spindle orientation defects in progenitor cells and premature differentiation. The defects in hindbrain architecture we observe, then, are likely due to a combination of morphogenesis and differentiation defects. We conclude that these defects result, directly or indirectly, in a disruption of the basal structures of the hindbrain, including the basement membrane, that result in ventral mismigration of FBMNs.
The Laminin-containing basement membrane as substrate for migration
The observation that FBMNs reorient their centrosomes and accelerate their posterior migration upon contact with the Laminin-containing basement membrane suggests that the basement membrane is a substrate for migration that allows for more efficient posterior-directed motion. In the absence of Laminin, FBMNs fail to speed up and reorient their centrosomes, suggesting that Laminin is required for the changes in velocity and centrosome reorientation. It remains unclear whether this substrate actively directs migration or simply provides a permissive milieu that allows for faster migration. Signaling between Laminin and Integrin receptors has been shown to be important in a number of neuronal migrations, such as the anterior migration of neuroblasts to the olfactory bulb , and the radial migration that forms the layers of the mammalian cortex . Furthermore, Laminin may be involved directly in the signaling pathways that are required for FBMN migration. Sittaramane et al.  showed pairwise genetic interactions between Lamininα 1, the cell adhesion molecule Tag1, and the transmembrane PCP protein Strabismus in the regulation of FBMN migration, suggesting that there is a direct interaction between Laminin and the adhesion and polarity molecules that control directional migration; however, the molecular mechanism for that interaction is unknown. Both Paulus et al.  and Sittaramane et al.  described the defect in lama1 mutants as a defect in posterior migration and not, as we have described here, as a ventral mismigration. Failure to migrate posteriorly is likely to be a consequence of ventral mismigration and escape from the hindbrain but that does not preclude a role for Laminin as either a permissive or instructive substrate for migration.
The Laminin-containing basement membrane as a boundary that prevents ventral mismigration
Much of the previous work on FBMN migration has focused on the role of the PCP pathway. It is clear from the work of many labs that genes in this pathway are required for the migration of FBMNs [4–7, 37] but the mechanism for this requirement is unclear. Wada and colleagues  observed that in fz3a and celsr2 mutants, FBMNs fail to migrate posteriorly and instead mismigrate dorsally within r4. This observation, along with evidence from genetic mosaics, led them to posit a model in which the PCP pathway is required cell-nonautonomously to restrict FBMN migration to the ventral pial surface [7, 8].
Our analysis of the wild-type behavior of migrating FBMNs is consistent with the idea that the dorsal-ventral position of FBMNs is important for their migration. FBMNs begin their migration traveling ventro-posteriorly but any further ventral migration is blocked by contact with the ventral basement membrane. This initial ventral migration may indeed be due to an exclusion from the more dorsal neuroepithelial progenitor cells as proposed by Wada et al.  or there may be other guidance cues directing FBMNs ventrally. The basement membrane, then, functions as a complementary ventral boundary to the dorsal boundary provided by PCP components, preventing further ventral migration and keeping the migratory pathway sandwiched at an exact dorsal-ventral level. The picture that arises, then, is one in which the dorsal-ventral level of the FBMN migratory pathway is tightly defined by the opposing actions of a signaling pathway on the dorsal side and a physical boundary (that also serves as a substrate for migration) on the ventral side.
FBMN ectopia resembles cobblestone lissencephaly
Cobblestone lissencephaly is a brain malformation found in a number of clinical syndromes, including Walker-Warburg syndrome (WWS), muscle-eye-brain disease and Fukuyama congenital muscular dystrophy. It is characterized by cortical overmigration in which radially migrating cortical neurons migrate past the pial basement membrane, resulting in a cobblestone-like texture in the cortex . Walker-Warburg syndrome and Fukuyama congenital muscular dystrophy have been linked with hypoglycosylation of α-Dystroglycan, which is normally required for Dystroglycan-Laminin binding [39, 40]. In addition, mouse mutations that disrupt cell-basement membrane interactions or basement membrane integrity, such as tissue-specific deletion of integrin-linked kinase or focal adhesion kinase, result in phenotypes that are similar to clinical cobblestone lissencephalies [41, 42]. These defects all show that disruption of the cortical pial basal lamina that serves as the boundary to radial migration results in ectopic migration in which neurons escape the brain.
These cobblestone lissencephaly phenotypes are similar to the motor neuron ectopia described here; however, the underlying genetic causes are different. Whereas mammalian cortical neuron ectopia are caused by the loss of proteins that function directly in the establishment of, or signaling by, the cortical basement membrane, the motor neuron ectopia we describe are due to the loss of PAR-aPKC complex polarity determinants functioning in the environment of the motor neurons. However, we observed discontinuities in the neuroepithelial basement membrane in aPKC mutants and morphants through which FBMNs appear to escape, and these defects were phenocopied by direct knockdown of Laminin itself. We hypothesize that subtle defects in the polarization of neuroepithelial progenitor cells in aPKC mutants causes reduced basal deposition or anchoring of Laminin-containing basement membrane, resulting in holes or weaknesses through which FBMNs escape the hindbrain. It is clear, however, that other models are possible. In addition to midline polarity defects we also observed a decrease in the size of the hindbrain, which is attributable to loss of progenitors as seen by Roberts and Appel . This premature loss of progenitors with neuroepithelial character could result in regions of the pial surface that are lacking a basal surface on which to anchor Laminin polymerization, resulting in the escape of FBMNs.
We have shown that facial branchiomotor neurons undergo a change in velocity and polarity upon contact with the ventral Laminin-containing basement membrane. Disruption of PAR-aPKC complex members results in defects in the basal structures of the neuroepithelium, including the basement membrane, that result in ectopic ventral migration of FBMNs and their escape from the hindbrain. We conclude that the Laminin-containing ventral basement membrane, dependent on the action of the apical PAR-aPKC complex, is both a substrate for migration and a boundary that constrains facial motor neurons to the appropriate migratory path.
Zebrafish (Danio rerio) were maintained as described . tg(isl1:GFP) were used as wild-type controls and crossed into hasm 567 and baluw 1 and pard6gbfh 266mutant backgrounds. Adults and embryos were genotyped by PCR amplification of a region flanking the mutation followed by restriction digest (hasm 567, AGGAACGGCTGGGATGTC and TCTCGAGTCAAAACATCCAAGA, Bfi1 cuts wild-type sequence; pard6gbfh 266, CCATTCCTGCAGTGTTGGCAAATTC and AACAGCACAAGGCAAAACTGGGTCA, BsmA1 cuts wild-type sequence), or by single pair matings followed by morphological identification of mutants (baluw 1). Embryos were raised at 28.5°C. In some cases pigment development was inhibited by the use of phenyl thiourea as described in Westerfield . All of the animal protocols for use of zebrafish in the research described in this paper are in compliance with internationally recognized guidelines for the use of fish in biomedical research. The protocols were approved by the Fred Hutchinson Cancer Research Center Institutional Animal Care and Use Committee, file #1392 'The Genetic Control of Hindbrain Patterning in the Zebrafish', Cecilia Moens PI.
Construction of mutant and transgenic lines
Briefly, the zCREST1 enhancer element  was PCR amplified from the Isl1:GFP construct  with primers that added restriction sites, subcloned through β-Globin-GFP  and into pHSP70  upstream of the HSP70 promoter. memb-mRFP1  was subcloned into zCREST1-HSP70 downstream of the HSP70 promoter. Plasmid DNA was dialyzed against distilled water and microinjected into early one-cell embryos at 50 ng/μl, transient transgenics were raised, and one stably integrated line retained.
Briefly, a PCR product was generated that created a GFP-Kan fusion with 48 bp of krox-20/egr2b on each end that are approximately 1,000 bp apart in the krox-20 coding region. This product was recombined into zebrafish BAC CH211-78A5 using the ET recombination system , creating a fusion gene containing the first ten codons of krox-20 fused in frame to GFP, driven by the endogenous krox-20 promoter region.
A mutant allele of pard6gb was identified by TILLING . The allele contains a nonsense mutation in exon 2 (Q98X) that truncates the protein amino-terminal to its known PDZ protein-protein interaction domain (Figure 4).
Live confocal imaging
Tg(zCREST1:memb-mRFP1); Tg(krox20BAC:GFP) double transgenic embryos at 18 to 24 hpf were embedded in 1.2% agarose in embryo medium in glass bottom dishes (MatTek, Ashland, MA, USA) oriented with their hindbrain against the glass. They were imaged on a Zeiss Pascal inverted confocal microscope using a water immersion 40× objective. Single FBMNs were tracked in Z and time, allowing us to measure, at each timepoint, the distance between the posterior-most extent of a cell's cytoplasm (as determined by the inner edge of membrane fluorescence) and the r4-r5 boundary (determined by krox20:GFP fluorescence in r5). Measurements were made using Zeiss LSM software. Extent of migration (μm) was plotted against time (minutes) and the plots were analyzed for the fit of a bilinear model as described .
Morpholino, mRNA, and dye injections
Zebrafish embryos at the one-cell stage were injected with 1 nl of MO, mRNA, or fixable rhodamine-dextran (Invitrogen, Carlsbad, CA, USA). aPKCλ MO (250 μM)  and aPKCζ MO (2 mM)  were obtained from GeneTools (Philomath, OR, USA). Lama1 MO (1 mM; MO1)  was a gift from Anand Chandrasekhar. pCS2+aPKCi-AA (aPKCλ dominant negative)  was a gift from Salim Abdelilah-Seyfried and was used to make capped mRNA with the mMESSAGE mMACHINE kit (Ambion, Austin TX, USA).
Sectioning and immunohystochemistry
Embryos were fixed in 4% paraformaldehyde overnight at 4°C and either stained in wholemount or equilibrated in 0.3 M sucrose, mounted in 17% gelatin and sectioned to 70 μm using a vibratome followed by staining. Staining was performed as described  except -20°C acetone was used for permeabilization and Roche Western blocking reagent was used for blocking (Roche, Basel Switzerland). Primary antibodies used were: Laminin AB-1 (NeoMarkers, Fremont, CA, USA; 1:200), EphA4 (Upstate, Lake Placid, NY, USA; 1:200), γ-Tubulin (Sigma, St. Louis, MO, USA; 1:2500), aPKC (Santa Cruz C20, (Santa Cruz, CA, USA; 1:1,000), ZO1 (Zymed, San Francisco, CA, USA; 1:1,000), GFAP (Glial fibrillary acidic protein; Dako, Glostrup, Denmark; 1:200), acetylated Tubulin (Sigma; 1:2,000). Secondary antibodies to mouse, rabbit, and goat conjugated with AlexaFluor 405, 488, and 594 used at 1:200 (Invitrogen). When used, BODIPY TR methyl ester dye (Molecular Probes) was added to secondary antibody staining solution at 1:100. Tissue was dehydrated in glycerol then mounted in SlowFade Gold (Invitrogen). Imaging was as above. Three-dimensional reconstructions were performed using 'Three-dimensional opacity' mode in the Volocity software package (Improvision, Boston, MA, USA).
facial branchiomotor neuron
green fluorescent protein
planar cell polarity
Hatten ME: New directions in neuronal migration. Science. 2002, 297: 1660-1663. 10.1126/science.1074572.
Chandrasekhar A: Turning heads: development of vertebrate branchiomotor neurons. Dev Dyn. 2004, 229: 143-161. 10.1002/dvdy.10444.
Lyons DA, Guy AT, Clarke JD: Monitoring neural progenitor fate through multiple rounds of division in an intact vertebrate brain. Development. 2003, 130: 3427-3436. 10.1242/dev.00569.
Bingham S, Higashijima S, Okamoto H, Chandrasekhar A: The Zebrafish trilobite gene is essential for tangential migration of branchiomotor neurons. Dev Biol. 2002, 242: 149-160. 10.1006/dbio.2001.0532.
Jessen JR, Topczewski J, Bingham S, Sepich DS, Marlow F, Chandrasekhar A, Solnica-Krezel L: Zebrafish trilobite identifies new roles for Strabismus in gastrulation and neuronal movements. Nat Cell Biol. 2002, 4: 610-615.
Rohrschneider MR, Elsen GE, Prince VE: Zebrafish Hoxb1a regulates multiple downstream genes including prickle1b. Dev Biol. 2007, 309: 358-372. 10.1016/j.ydbio.2007.06.012.
Wada H, Tanaka H, Nakayama S, Iwasaki M, Okamoto H: Frizzled3a and Celsr2 function in the neuroepithelium to regulate migration of facial motor neurons in the developing zebrafish hindbrain. Development. 2006, 133: 4749-4759. 10.1242/dev.02665.
Wada H, Okamoto H: Roles of planar cell polarity pathway genes for neural migration and differentiation. Dev Growth Differ. 2009, 51: 233-240.
Lowery LA, Sive H: Strategies of vertebrate neurulation and a re-evaluation of teleost neural tube formation. Mech Dev. 2004, 121: 1189-1197. 10.1016/j.mod.2004.04.022.
Suzuki A, Ohno S: The PAR-aPKC system: lessons in polarity. J Cell Sci. 2006, 119: 979-987. 10.1242/jcs.02898.
Munson C, Huisken J, Bit-Avragim N, Kuo T, Dong PD, Ober EA, Verkade H, Abdelilah-Seyfried S, Stainier DY: Regulation of neurocoel morphogenesis by Pard6 gamma b. Dev Biol. 2008, 324: 41-54. 10.1016/j.ydbio.2008.08.033.
Etienne-Manneville S, Hall A: Cdc42 regulates GSK-3beta and adenomatous polyposis coli to control cell polarity. Nature. 2003, 421: 753-756. 10.1038/nature01423.
Solecki DJ, Model L, Gaetz J, Kapoor TM, Hatten ME: Par6alpha signaling controls glial-guided neuronal migration. Nat Neurosci. 2004, 7: 1195-1203. 10.1038/nn1332.
Li S, Edgar D, Fassler R, Wadsworth W, Yurchenco PD: The role of laminin in embryonic cell polarization and tissue organization. Dev Cell. 2003, 4: 613-624. 10.1016/S1534-5807(03)00128-X.
Weir ML, Oppizzi ML, Henry MD, Onishi A, Campbell KP, Bissell MJ, Muschler JL: Dystroglycan loss disrupts polarity and beta-casein induction in mammary epithelial cells by perturbing laminin anchoring. J Cell Sci. 2006, 119: 4047-4058. 10.1242/jcs.03103.
Masuda-Hirata M, Suzuki A, Amano Y, Yamashita K, Ide M, Yamanaka T, Sakai M, Imamura M, Ohno S: Intracellular polarity protein PAR-1 regulates extracellular laminin assembly by regulating the dystroglycan complex. Genes Cells. 2009, 14: 835-850. 10.1111/j.1365-2443.2009.01315.x.
Megason SG, Fraser SE: Digitizing life at the level of the cell: high-performance laser-scanning microscopy and image analysis for in toto imaging of development. Mech Dev. 2003, 120: 1407-1420. 10.1016/j.mod.2003.07.005.
Uemura O, Okada Y, Ando H, Guedj M, Higashijima S, Shimazaki T, Chino N, Okano H, Okamoto H: Comparative functional genomics revealed conservation and diversification of three enhancers of the isl1 gene for motor and sensory neuron-specific expression. Dev Biol. 2005, 278: 587-606. 10.1016/j.ydbio.2004.11.031.
Buchwald P, Sveiczer A: The time-profile of cell growth in fission yeast: model selection criteria favoring bilinear models over exponential ones. Theor Biol Med Model. 2006, 3: 16-10.1186/1742-4682-3-16.
Higashijima S, Hotta Y, Okamoto H: Visualization of cranial motor neurons in live transgenic zebrafish expressing green fluorescent protein under the control of the islet-1 promoter/enhancer. J Neurosci. 2000, 20: 206-218.
Schmoranzer J, Fawcett JP, Segura M, Tan S, Vallee RB, Pawson T, Gundersen GG: Par3 and dynein associate to regulate local microtubule dynamics and centrosome orientation during migration. Curr Biol. 2009, 19: 1065-1074. 10.1016/j.cub.2009.05.065.
Solecki DJ, Trivedi N, Govek EE, Kerekes RA, Gleason SS, Hatten ME: Myosin II motors and F-actin dynamics drive the coordinated movement of the centrosome and soma during CNS glial-guided neuronal migration. Neuron. 2009, 63: 63-80. 10.1016/j.neuron.2009.05.028.
Etienne-Manneville S, Manneville JB, Nicholls S, Ferenczi MA, Hall A: Cdc42 and Par6-PKCzeta regulate the spatially localized association of Dlg1 and APC to control cell polarization. J Cell Biol. 2005, 170: 895-901. 10.1083/jcb.200412172.
Cui S, Otten C, Rohr S, Abdelilah-Seyfried S, Link BA: Analysis of aPKClambda and aPKCzeta reveals multiple and redundant functions during vertebrate retinogenesis. Mol Cell Neurosci. 2007, 34: 431-444. 10.1016/j.mcn.2006.11.016.
Horne-Badovinac S, Lin D, Waldron S, Schwarz M, Mbamalu G, Pawson T, Jan Y, Stainier DY, Abdelilah-Seyfried S: Positional cloning of heart and soul reveals multiple roles for PKC lambda in zebrafish organogenesis. Curr Biol. 2001, 11: 1492-1502. 10.1016/S0960-9822(01)00458-4.
Rohr S, Bit-Avragim N, Abdelilah-Seyfried S: Heart and soul/PRKCi and nagie oko/Mpp5 regulate myocardial coherence and remodeling during cardiac morphogenesis. Development. 2006, 133: 107-115. 10.1242/dev.02182.
Cooper MS, Szeto DP, Sommers-Herivel G, Topczewski J, Solnica-Krezel L, Kang HC, Johnson I, Kimelman D: Visualizing morphogenesis in transgenic zebrafish embryos using BODIPY TR methyl ester dye as a vital counterstain for GFP. Dev Dyn. 2005, 232: 359-368. 10.1002/dvdy.20252.
Draper BW, McCallum CM, Stout JL, Slade AJ, Moens CB: A high-throughput method for identifying N-ethyl-N-nitrosourea (ENU)-induced point mutations in zebrafish. Methods Cell Biol. 2004, 77: 91-112. full_text.
Carmany-Rampey A, Moens CB: Modern mosaic analysis in the zebrafish. Methods. 2006, 39: 228-238. 10.1016/j.ymeth.2006.02.002.
Kemp HA, Carmany-Rampey A, Moens C: Generating chimeric zebrafish embryos by transplantation. J Vis Exp. 2009, 29: pii:1394
Aaku-Saraste E, Hellwig A, Huttner WB: Loss of occludin and functional tight junctions, but not ZO-1, during neural tube closure - remodeling of the neuroepithelium prior to neurogenesis. Dev Biol. 1996, 180: 664-679. 10.1006/dbio.1996.0336.
Roberts RK, Appel B: Apical polarity protein PrkCi is necessary for maintenance of spinal cord precursors in zebrafish. Dev Dyn. 2009, 238: 1638-1648. 10.1002/dvdy.21970.
Paulus JD, Halloran MC: Zebrafish bashful/laminin-alpha 1 mutants exhibit multiple axon guidance defects. Dev Dyn. 2006, 235: 213-224. 10.1002/dvdy.20604.
Sittaramane V, Sawant A, Wolman MA, Maves L, Halloran MC, Chandrasekhar A: The cell adhesion molecule Tag1, transmembrane protein Stbm/Vangl2, and Lamininalpha1 exhibit genetic interactions during migration of facial branchiomotor neurons in zebrafish. Dev Biol. 2009, 325: 363-373. 10.1016/j.ydbio.2008.10.030.
Belvindrah R, Hankel S, Walker J, Patton BL, Muller U: Beta1 integrins control the formation of cell chains in the adult rostral migratory stream. J Neurosci. 2007, 27: 2704-2717. 10.1523/JNEUROSCI.2991-06.2007.
Chen ZL, Haegeli V, Yu H, Strickland S: Cortical deficiency of laminin gamma1 impairs the AKT/GSK-3beta signaling pathway and leads to defects in neurite outgrowth and neuronal migration. Dev Biol. 2009, 327: 158-168. 10.1016/j.ydbio.2008.12.006.
Wada H, Iwasaki M, Sato T, Masai I, Nishiwaki Y, Tanaka H, Sato A, Nojima Y, Okamoto H: Dual roles of zygotic and maternal Scribble1 in neural migration and convergent extension movements in zebrafish embryos. Development. 2005, 132: 2273-2285. 10.1242/dev.01810.
van Reeuwijk J, Brunner HG, van Bokhoven H: Glyc-O-genetics of Walker-Warburg syndrome. Clin Genet. 2005, 67: 281-289. 10.1111/j.1399-0004.2004.00368.x.
Brockington M, Blake DJ, Prandini P, Brown SC, Torelli S, Benson MA, Ponting CP, Estournet B, Romero NB, Mercuri E, Voit T, Sewry CA, Guicheney P, Muntoni F: Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan. Am J Hum Genet. 2001, 69: 1198-1209. 10.1086/324412.
van Reeuwijk J, Janssen M, Elzen van den C, Beltran-Valero de Bernabé D, Sabatelli P, Merlini L, Boon M, Scheffer H, Brockington M, Muntoni F, Huynen MA, Verrips A, Walsh CA, Barth PG, Brunner HG, van Bokhoven H: POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome. J Med Genet. 2005, 42: 907-912. 10.1136/jmg.2005.031963.
Beggs HE, Schahin-Reed D, Zang K, Goebbels S, Nave KA, Gorski J, Jones KR, Sretavan D, Reichardt LF: FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies. Neuron. 2003, 40: 501-514. 10.1016/S0896-6273(03)00666-4.
Niewmierzycka A, Mills J, St-Arnaud R, Dedhar S, Reichardt LF: Integrin-linked kinase deletion from mouse cortex results in cortical lamination defects resembling cobblestone lissencephaly. J Neurosci. 2005, 25: 7022-7031. 10.1523/JNEUROSCI.1695-05.2005.
Westerfield M: The Zebrafish Book. 1995, Eugene, OR: University of Oregon
Woolfe A, Goodson M, Goode DK, Snell P, McEwen GK, Vavouri T, Smith SF, North P, Callaway H, Kelly K, Walter K, Abnizova I, Gilks W, Edwards YJ, Cooke JE, Elgar G: Highly conserved non-coding sequences are associated with vertebrate development. PLoS Biol. 2005, 3: e7-10.1371/journal.pbio.0030007.
Halloran MC, Sato-Maeda M, Warren JT, Su F, Lele Z, Krone PH, Kuwada JY, Shoji W: Laser-induced gene expression in specific cells of transgenic zebrafish. Development. 2000, 127: 1953-1960.
Muyrers JP, Zhang Y, Testa G, Stewart AF: Rapid modification of bacterial artificial chromosomes by ET-recombination. Nucleic Acids Res. 1999, 27: 1555-1557. 10.1093/nar/27.6.1555.
Pollard SM, Parsons MJ, Kamei M, Kettleborough RN, Thomas KA, Pham VN, Bae MK, Scott A, Weinstein BM, Stemple DL: Essential and overlapping roles for laminin alpha chains in notochord and blood vessel formation. Dev Biol. 2006, 289: 64-76. 10.1016/j.ydbio.2005.10.006.
Cooke JE, Kemp HA, Moens CB: EphA4 is required for cell adhesion and rhombomere-boundary formation in the zebrafish. Curr Biol. 2005, 15: 536-542. 10.1016/j.cub.2005.02.019.
The authors wish to thank Anand Chandrasekhar, Mary Halloran, Brian Link, Sean Megason, Hitoshi Okamoto, and Salim Abdelilah-Seyfried for mutant and transgenic fish lines, morpholinos, and DNA constructs. We also thank Aaron Putzke and Greg Walsh for generation and characterization of novel transgenic lines, and members of the Moens lab for critical reading of the manuscript. PKG was supported in part by PHS NRSA T32 GM07270 from NIGMS. This work was supported by NIH grant HD37909. CBM is an Investigator with the Howard Hughes Medical Institute.
The authors declare that they have no competing interests.
PKG conceived of and carried out the experiments and drafted the manuscript. CBM conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Timelapse movie of Tg(zCREST1:memb-mRFP1). The movie was started at 18 hpf. Images were taken every 6 minutes. The movie runs at 4 frames per second. The embryo is shown in dorsal view. (MP4 918 KB)
Additional file 2: Timelapse movie of tg(zCREST1:memb-mRFP1); tg(krox20BAC:GFP) double transgenic. The movie was started at 24 hpf. Images were taken every 6 minutes. The movie runs at 7 frames per second. The embryo is shown in dorsal view. (MP4 2 MB)
Additional file 3: . aPKCλ+ζ double MO tg(isl1:GFP) (green) 48-hpf embryo immunostained for Laminin (red). Cross-section. (MP4 961 KB)
Additional file 4: Timelapse movie of wild-type tg(isl1:GFP) embryo counterstained with BODIPY TR methyl ester dye. The movie was started at 24 hpf. Images were taken every 5 minutes. The movie runs at 2 frames per second. The embryo is shown in lateral view. White line delineates the ventral limit of the hindbrain. The blue outlined cell moves ventrally while the magenta outlined cell moves posteriorly. (MP4 748 KB)
Additional file 5: Timelapse movie of lamininα1-/-; tg(isl1:GFP) embryo counterstained with BODIPY TR methyl ester dye. The movie was started at 24 hpf. Images were taken every 6 minutes. The movie runs at 2 frames per second. The embryo is shown in lateral view. The white line delineates the ventral limit of the hindbrain. The blue outlined cell moves ventrally while the magenta outlined cell fails to move posteriorly and the white outlined cell moves anteriorly. (MP4 1 MB)
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Grant, P.K., Moens, C.B. The neuroepithelial basement membrane serves as a boundary and a substrate for neuron migration in the zebrafish hindbrain. Neural Dev 5, 9 (2010). https://doi.org/10.1186/1749-8104-5-9
- Planar Cell Polarity
- Apical Junctional Complex
- Facial Motor Neuron
- Planar Cell Polarity Pathway
- Posterior Migration