Colonizing while migrating: how do individual enteric neural crest cells behave?
© Young et al.; licensee BioMed Central Ltd. 2014
Received: 11 December 2013
Accepted: 21 March 2014
Published: 26 March 2014
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© Young et al.; licensee BioMed Central Ltd. 2014
Received: 11 December 2013
Accepted: 21 March 2014
Published: 26 March 2014
Directed cell migration is essential for normal development. In most of the migratory cell populations that have been analyzed in detail to date, all of the cells migrate as a collective from one location to another. However, there are also migratory cell populations that must populate the areas through which they migrate, and thus some cells get left behind while others advance. Very little is known about how individual cells behave to achieve concomitant directional migration and population of the migratory route. We examined the behavior of enteric neural crest-derived cells (ENCCs), which must both advance caudally to reach the anal end and populate each gut region.
The behavior of individual ENCCs was examined using live imaging and mice in which ENCCs express a photoconvertible protein. We show that individual ENCCs exhibit very variable directionalities and speed; as the migratory wavefront of ENCCs advances caudally, each gut region is populated primarily by some ENCCs migrating non-directionally. After populating each region, ENCCs remain migratory for at least 24 hours. Endothelin receptor type B (EDNRB) signaling is known to be essential for the normal advance of the ENCC population. We now show that perturbation of EDNRB principally affects individual ENCC speed rather than directionality. The trajectories of solitary ENCCs, which occur transiently at the wavefront, were consistent with an unbiased random walk and so cell-cell contact is essential for directional migration. ENCCs migrate in close association with neurites. We showed that although ENCCs often use neurites as substrates, ENCCs lead the way, neurites are not required for chain formation and neurite growth is more directional than the migration of ENCCs as a whole.
Each gut region is initially populated by sub-populations of ENCCs migrating non-directionally, rather than stopping. This might provide a mechanism for ensuring a uniform density of ENCCs along the growing gut.
Neural crest cells are a transient migratory embryonic cell population. Previous imaging studies of cranial neural crest cells in Xenopus and chick embryos have revealed the organization of the cells as they migrate, the rules guiding their behavior and some of the molecular bases of the interactions [1, 2]. In both species, the cells move as a collective from one location to another; in chick embryos, there is a “follow the leader” chain migration in which the spatial order of cells is retained [3–7]. In Xenopus, several concomitant behaviors have been identified including “run and tumble” in which phases of directional migration are interspersed with phases of small random movements, “mutual co-attraction” in which cells retain the same neighbors for long periods of time, and “contact inhibition of locomotion” in which cells polarize and disperse upon contact with each other [8–12].
A sub-population of vagal level (caudal hindbrain) neural crest cells migrates into and along the developing gut, and gives rise to most of the enteric nervous system [13–17]. The neural crest cells that colonize the gut migrate further than other embryonic cells because the gut is growing as the cells migrate [18, 19]. The migration of ENCCs exhibits two important differences from neural crest cell populations that have been examined in detail previously. First, not only must some ENCCs migrate caudally to reach the distal regions of the gut, each gut region through which ENCCs migrate must be populated by ENCCs to ensure there is an even distribution of enteric neurons along the entire gut; this behavior has been termed “directional dispersion” . In contrast, analyses of migrating cranial and trunk neural crest cells have been performed as the entire cell population migrates collectively from one location to another. Studies of ENCC migration to date have focused on the caudal advance of the ENCC wavefront [21–27]. ENCCs migrate in chains with high cell-cell contact [21, 23, 24, 28], and so little is known about how individual ENCCs behave to ensure that all regions of the gut are also evenly populated with ENCCs. We had previously assumed that each gut region is colonized by sub-populations of ENCCs stopping as the wavefront of ENCCs moves caudally . The migration of ENCCs is an excellent model to examine how individual cells behave in a population that both migrates directionally and populates regions along the migratory route.
A second important characteristic of the migration of ENCCs is that a subpopulation of ENCCs starts to differentiate into neurons that project neurites caudally along the same pathways that ENCCs are migrating [29, 30]. The relationship between growing neurites and migrating ENCCs is still unclear, and it is unknown which leads the way at the migratory wavefront.
We used mice in which all ENCCs express the photoconvertible protein, KikGR  and so the behavior of individual ENCCs, their interactions with all other ENCCs, and their location with respect to the migratory wavefront, could be examined. We also examined the role of signaling via endothelin receptor type B (EDNRB) in migratory behavior. Detailed information about the migratory behavior of individual ENCCs at the cellular level is likely to provide clues as to the molecular mechanisms involved, and the data are also essential for the development of models of the colonization of the gut by ENCCs.
Ednrb-hKikGR mice, in which all ENCCs show KikGR fluorescence, were used . KikGR is a photoconvertible protein that changes its emission from green to red following exposure to ultraviolet or violet light . Individual or groups of KikGR cells in explants of embryonic gut were photoconverted from green to red, and then time-lapse imaging was performed in which three-dimensional image z-stacks were collected at two- to five-minute intervals on a confocal microscope. The majority of experiments were performed using explants of gut from E12.5 Ednrb-hKikGR mice because at this age, the ENCC migratory wavefront is in the mid-colon, and the colon is relatively straight ; as a result, the migratory wavefront of ENCCs could be imaged for over 24 hours. In contrast, at E11.5, the ENCC wavefront is difficult to define because of transmesenteric ENCCs, which migrate from the midgut across the mesentery into the proximal colon .
Overall migration direction was defined as the angle between the locations at the beginning and end of imaging relative to the long axis of the gut. Thus, a cell that was directly caudal to its starting position at the end of imaging had an overall migration direction of 0° regardless of its positions at intermediate times. For these analyses, we only used angles between 0° and 180° and did not distinguish between circumferential clockwise (90°) and counterclockwise (270°) migration around the gut. ENCCs that were <150 μm or >750 μm from the wavefront had higher overall migration angles than ENCCs 150 to 600 μm from the wavefront (ANOVA followed by Tukey’s post-hoc test; Figure 1C). Within thick strands oriented parallel to the long axis of the gut, most ENCCs migrated caudally (Additional file 1: Movie 1), and cells about to undergo cell division often continued to advance caudally even after rounding up for division (Figure 2D). However, ENCCs were also regularly observed that migrated in the opposite direction from most ENCCs in a strand, and a cell migrating in one direction could suddenly reverse direction (Figure 2B, cell a, 2F; Additional file 1: Movie 1). Furthermore, some cells followed very circuitous pathways (Figure 2C, cell c; Additional file 2: Movie 2). There was no correlation between speed and angle of migration (R 2 = 0.02; linear regression for entire ENCC population; Figure 2G).
Tortuosity is a measure of the deviation from a straight line and is calculated by dividing the accumulated travel distance by the distance between the first and last points. There was no significant difference in the tortuosities of ENCCs at different locations (ANOVA; Figure 1D). Although tortuosity is a commonly measured parameter in migration studies, it does not take direction into consideration, so it is not very informative for understanding ENCC migration.
The rate of caudal advance was defined as the longitudinal caudal displacement/time of an ENCC, regardless of the route (Figure 2F). Individual ENCCs < 150 μm and > 750 μm from the most caudal cell had significantly lower rates of caudal advance than those 300 to 450 μm from the wavefront (ANOVA followed by Tukey’s post-hoc test; Figure 1E). Consequently, there is considerable local leapfrogging at the wavefront, and we did not observe any “pioneer” ENCCs that remained at the front of the ENCC population for more than two hours (Figure 2E, F).
ENCCs with low rates of caudal advance will populate a region, rather than migrate into new regions. We examined whether the ENCCs that populate a region migrate at the same speed as other ENCCs but non-directionally, or whether they show similar directionality to other ENCCs but migrate slower. Linear regression analyses revealed that for caudal advance versus speed R 2 = 0.24, while for caudal advance versus angle there was an inverse correlation with R 2 = 0.51 (Figure 2H, I). Hence, low directionality appears to play a larger role than decreased speed in reducing caudal advance, and populating gut regions behind the wavefront.
Detailed observations of the interactions between ENCCs are described in Additional file 4: Figures S1 and S2. In brief, ENCCs at the fronts of chains extended filopodia and lamellipodia in a variety of directions into unoccupied regions (Additional file 5: Movie 4) and ENCCs within chains extended processes within and outside of chains (Additional file 4: Figure S1). There was no significant difference between the protrusive activities of ENCCs that were 200 to 400 μm (where new ENCC network is still forming) and 500 to 800 μm (where the network is largely established) from the wavefront (Additional file 4: Figure S1). The predominant type of interaction between chains of ENCCs was adhesive interactions (Additional file 4: Figure S2; Additional file 5: Movie 4).
A sub-population of ENCCs starts to express pan-neuronal markers soon after they enter the gut . Neuron-like cells can occur within 100 μm of the wavefront, and possess a single, persistent caudally-directed neurite . In agreement with our earlier study , neurons migrated slower than non-neuronal ENCCs (neurons: 43 ± 4 μm/h, n = 18; non-neuronal cells: 64 ± 3 μm/h, n = 76; unpaired two-tailed t test; P <0.05; neurons and non-neuronal ENCCs included in this analysis were 200 to 800 μm from the wavefront. The cells are also included in the data shown in Figure 1).
The growth cones at the tips of growing neurites only explored within the ENCC network (Figure 6C). This was in contrast to the lamellipodia and filopodia of ENCCs, which commonly extended outside of the ENCC networks (see Additional file 4: Figure S1). We observed several examples where a growth cone advanced caudally in concert with a particular ENCC for over two hours (Figure 6E). The rate of caudal advance of neurites (measured as the longitudinal distance advanced caudally regardless of the pathway) was 39 ± 5 μm/h (n = 8), which is similar to the rate at which the ENCC population advances caudally (35 to 40 μm/h) [21, 23, 35]. We compared the directionality of neurite extension with that of migrating ENCCs; the neurites were 200 to 800 μm from the wavefront, and the six ENCCs analyzed were all from one preparation and were in a group that was 500 μm from the wavefront. Neurites showed more directional (longitudinal) advance than the ENCCs (Figure 6D; Watson’s U 2 test for angles; ).
When ENCCs are introduced into explants of small intestines lacking ENCCs (from Ret TGM/TGM mice), they migrate equally well rostrally as they do caudally . In the current study we used a similar co-culture system to examine the behavior of neurites in a rostrally-migrating population of ENCCs. Segments of small intestine from Ednrb-hKikGR mice were placed at the rostral and caudal ends of explants of aneural small intestines from Ret TGM/TGM mice (Figure 6F). The ENCC population migrating rostrally was photoconverted from green to red just prior to encountering the caudally-migrating population (Figure 6F). The caudally-migrating (green) and rostrally-migrating (red) ENCCs adhered to each other to form chains of intermingled cells. It was not possible to analyze the effects of collisions between ENCCs migrating in opposite directions on individual cell behavior because high levels of cell-cell contact prevented us from obtaining pre-collision data for individual ENCCs. After forming a network, the red and green ENCCs continued to migrate for at least 22 hours, but non-directionally (Figure 6F). In contrast, red neurites continued to grow rostrally (Figure 6F). We were unable to visualize whether any of the red ENCCs also projected neurites caudally.
Most neuron-like ENCCs in the E11.5 and E12.5 gut project caudally [37, 38]. Four of the movies of the E12.5 colon contained photoconverted ENCCs undergoing neuritogenesis. In all cases, the neurite formed from a thin process that continued to elongate. In two out of four cells, the neurites did not initially emerge from the caudal side of the cell bodies, and in three out of four cells, the neurites did not initially project caudally, but first projected rostrally or circumferentially prior to projecting caudally (Figure 6G). These data suggest that most individual neuron precursors are not polarized prior to extending a neurite.
Most migratory cell populations that have been studied in detail to date migrate as a collective from one location to another. In contrast, the formation of an enteric nervous system along the entire gut requires that some ENCCs advance caudally while others populate each region, which has been termed “directional dispersion” . In this study we showed that a characteristic of ENCCs is their variability in migratory behavior, particularly directionality. Most ENCCs appeared to migrate according to their own individual program while maintaining contact with other ENCCs - for example, ENCCs did not retain their neighbors and cells migrating in opposite directions within the same chain were commonly observed. We suggest that variability in ENCC behavior, but with an overall caudal bias, results in the colonization of each gut region as well as the caudal advance of some ENCCs. Despite the variability, our study shows that ENCCs behave differently when solitary compared to groups, and therefore meet the definition of collective migration . For the majority of time, the behavior of ENCCs did not in general conform to the types of migratory behaviors described previously for neural crest populations that migrate as a collective from one location to another [4, 8–10]. However, some behaviors described for other neural crest populations, including contact inhibition of locomotion, were exhibited occasionally, and we cannot rule out the possibility that non-predominant behaviors play an important role in ENCC migration.
The ENCCs that populate a gut region are those that show the lowest rate of caudal advance. Our data show low ENCC caudal advance is more highly correlated with low directionality than with low speed. Thus, the gut is colonized primarily by ENCCs migrating non-directionally, although ENCCs migrating slower than the rest of the population also contribute to gut colonization. Furthermore, it was not possible to separate the ENCC population in the E12.5 colon into two distinct groups - those that advanced caudally and those that did not.
A recent imaging study using biosensors revealed that ENCC migration speed was positively correlated with Rac1 and Cdc42 activities and inversely correlated with protein kinase A (PKA) activity . Hence the activities of Rac1, Cdc42 and PKA are likely to play a role in determining the rate at which an ENCC advances caudally by regulating ENCC speed. We showed that directionality is also an important determinant in whether an ENCC will advance caudally, and that there was no correlation between direction and speed. Future live imaging of signaling molecule activities in ENCCs are required to reveal whether migration direction is correlated with the activity of signaling molecules at particular subcellular locations within an ENCC, as has been performed in living Xenopus cranial neural crest cells  and fixed ENCCs .
Unexpectedly, most ENCCs were still migratory in regions of the gut that had been colonized for over 24 hours, although they migrated slower than ENCCs closer to the wavefront. Many ENCCs in long-colonized regions migrated circumferentially. This was also surprising as there are prominent longitudinally-oriented neurite bundles in colonized regions of the gut [38, 48], and we showed that ENCCs advancing caudally often use neurites as a migratory substrate. However, we also demonstrated that the thick longitudinally-oriented neurites are located deeper than the un-oriented neurite network associated with most ENCCs. In Ednrb mutant mice where ENCC migration is delayed, the E14.5 mid-colon is colonized by ENCCs migrating circumferentially from a dorsal mesenteric strand . Combined the data suggest that as the gut matures, it favors the circumferential migration of ENCCs. The mechanisms promoting circumferential migration remain to be identified, but are unlikely to be related to the vasculature as the blood vessel network in the mouse intestine is mostly associated with the mucosal crypts and the submucosa [23, 49], whereas the circumferential migration reported in the current study is mainly in the outer mesenchyme where the myenteric plexus will later form. Furthermore, circumferentially migrating ENCCs migrated within the existing ENCC network.
Consistent with our earlier study , we found that the shapes of the ENCC networks first laid down are retained over time. As we now show that most ENCCs continue to migrate after they colonize each gut region, we propose that the ENCC network is maintained by a scaffold of un-oriented neurites that is present at the same level as the majority of ENCCs. In the mature gut, myenteric ganglia are long structures that are oriented parallel to the circular muscle layer. In contrast, the clusters of ENCC present early in ENS development are not oriented in any particular direction and are dynamic in their composition. Hence, major reorganization of the ENCCs occurs prior to mature ganglion formation.
During development of the lateral line in zebrafish, cells migrate collectively along the body of the embryo and deposit cell clusters called rosettes at discrete locations; these are the progenitors of mechanosensory organs . A recent study showed that the deposition of a sub-population of cells to form rosettes during the migration of the collective involves the formation of microtubule-dependent adherens junctions . The formation of mechanosensory organs at distinct intervals in the zebrafish lateral line is, however, different from the directional dispersion of ENCCs, as ENCCs are dispersed evenly along the entire length of the gut. Like ENCCs, other neural crest-derived cell populations, such as Schwann cells and melanocytes, evenly populate structures as they migrate distally. The migratory behavior of these cell types has not yet been examined in detail, but a study of intact skin explants from E14.5 mice showed that melanoblasts remained migratory in regions already colonized . Unlike ENCCs, however, melanocytes are found as solitary cells that exhibit repulsive interactions upon contact with other melanocytes and consequently maintain individual territories .
Earlier studies have shown that ENCCs at the migratory wave front are mainly responsible for populating uncolonized regions of the gut; this process has been termed “frontal advance” [22, 26, 27]. Our data are in agreement with this model but provide some refinements. First, we show that there is considerable local leapfrogging of ENCCs at the wavefront because the most caudal cells on average show low directionality and hence low caudal advance. Thus, within the frontal advance zone, ENCCs do not retain their spatial order. Previous studies in which small regions of mesenchyme in explants of chick gut were replaced with quail gut mesenchyme suggested that the ENCC frontal advance zone is only around 200 to 300 μm long . Our data show that ENCCs advancing caudally are not found in a distinct zone with definable boundaries - ENCCs located 300 to 450 μm from the most caudal cell showed the highest average rate of caudal advance, and the probability that an ENCC would advance caudally decreased caudo-rostrally thereafter so that in the small intestine (> 1.2 mm from the wavefront), there was no significant caudal advance even though most of the cells were still migratory. It is likely that the length of the ENCC frontal advance zone varies with age and species.
Cranial and trunk neural crest cells in the chick migrate in chains with clear leading cells [3, 53, 54]. Even excluding solitary cells, our data show that the extreme wavefront ENCCs migrate with lower directionality than ENCCs that are 150 to 600 μm from the wavefront. Druckenbrod and Epstein (2007)  tracked individual ENCCs in the chick gut that had been labeled with GFP by electroporation and, consistent with the current study, ENCC behavior was shown to be variable, and to vary at different distances from the wavefront. However, ENCCs within 200 μm of the wavefront were observed to show the most directional migration . Hence, there may be some species differences in the behaviors of ENCCs.
We were unable to shed light on the unresolved question of why chains of ENCCs advance into uncolonized regions. Unlike follow-the-leader chain migration of neural crest cells in chicks , our study showed that the protrusive activity of ENCCs does not vary with location. Combined, the data are consistent with the idea that ENCCs cannot detect the polarity of the gut, but preferentially migrate into areas of low ENCC density while retaining contact with other ENCCs.
Our study shows that although ENCCs generally do not maintain the same neighbors for long, there are strong transient adhesive interactions between neighboring ENCCs. The molecular bases of the adhesive interactions between ENCCs are not completely understood but L1CAM and β1 integrins play roles [55–59]. Despite the strong adhesive interactions, ENCCs that are transiently solitary are frequently observed at the migratory wavefront . For follow-the-leader chain migration of cranial and trunk neural crest cells, it has been suggested that cells in a chain follow a path of lesser resistance through the ECM and, therefore, migrate faster than solitary cells . Consistent with this idea, the speed of solitary ENCCs was significantly slower than ENCCs in chains. Furthermore, ENCCs in chains migrated more directionally than solitary ENCCs suggesting that cell-cell contact is essential for ENCCs to respond to environmental cues as has been shown for cranial neural crest cells in Xenopus (see below).
Endothelin-3 (EDN3) acting at EDNRB receptors expressed on ENCCs is essential for the normal colonization of the gut by ENCCs [60–63]. Interpretation of the migratory behavior of ENCCs in Ednrb null mutant mice is difficult because the entry of neural crest-derived cells into the gut is delayed and thus the gut environment through which ENCCs migrate is older than in wildtype mice . Our data, using a pharmacological inhibitor of EDNRB, reveal that EDNRB signaling primarily promotes migration speed, rather than directionality. EDNRB signaling is likely to affect ENCC migration via PKA activity [46, 64]. Although it is well established that EDNRB signaling inhibits ENCC differentiation , we showed that exposure of explants to the EDNRB inhibitor in the timespan of our experiments was not sufficient to result in any detectable changes in neuronal differentiation. Thus the effect of inhibition of EDNRB signaling on ENCC migration cannot be entirely due to an enhancement of neuronal differentiation and our data therefore support the conclusions of a previous study  showing that EDNRB signaling has a direct effect on ENCC migration, as well as an indirect effect via its influence on differentiation. It will be interesting to determine whether the delay in the caudal advance of the ENCC population in other models of Hirschsprung disease is due to perturbed speed or directionality of individual ENCCs.
We showed that neurites within the E12.5 colon advance caudally with overall high directionality, implying that neurites can detect the longitudinal axis and the polarity of the gut. However, when ENCCs were introduced into the caudal end of explants of aneural small intestine, some neurites grew orally. Our data are consistent with the idea that neurites use a property of the gut tube to detect the longitudinal axis of the gut, but the mechanism regulating the direction of neurite growth remains to be determined. We have previously suggested that the direction of neurite growth might be determined by the direction of ENCC migration . However, in the current study, when the orally projecting neurites in the co-cultures encountered a population of ENCCs migrating anally, they continued to grow orally. Furthermore, following pharmacological inhibition of EDNRB signaling, neurites were observed in advance of ENCCs, showing that ENCCs are not required for longitudinal neurite extension. In control explants, the growth cones of the growing neurites did not explore outside of the ENCC network, and thus it appears highly unlikely that neurites normally navigate along longitudinally-oriented structural components of the gut wall, outside of the ENCC network. Mature enteric neurons also include subtypes that project circumferentially or orally . Some circumferentially projecting neurons were observed at E12.5, but only in the small intestine and proximal colon.
Sacral neural crest cells migrate into the hindgut along the axons of extrinsic neurons . Neurites (from intrinsic neurons) are present in close apposition to chains of vagal ENCC, but it was previously unclear whether neurites or ENCCs lead the way; in fixed tissue the most caudal structure is most commonly an ENCC, but it is also not unusual to observe neurites in advance of ENCCs . Our data show that ENCCs lead the way down the gut, with neurites following a short distance behind. Furthermore, the growth cones of neurites only explored within the ENCC network, and as a result, neurites always advanced in concert with chains of ENCCs. Sometimes ENCCs were observed to reverse direction and migrate back along a neurite or to migrate away from a neurite, which explains why neurites are sometimes observed caudal to the most caudal ENCC in fixed tissue. Our data also show that neurites act as substrates for migrating ENCCs. Although neurites are not required for the extension of chains of ENCCs into unpopulated regions, it is possible that longitudinally oriented neurites facilitate the directional migration of ENCCs towards the wavefront. Previous studies have provided evidence both for and against an essential role for neurites in ENCC migration. Humans with mutations in the gene encoding kinesin binding protein (KBP) have Hirschsprung disease , and studies in neuronal cell lines, primary cortical neurons and zebrafish have shown that the main role of KBP appears to be in neurite formation [69–71]. On the other hand, mutant mice with defects in the longitudinal projections of neurites do not exhibit any delay in ENCC migration  showing that longitudinal neurite projections are not essential, or that only a small number of longitudinally oriented neurites is necessary, for normal ENCC migration. To reveal the role of neurites in ENCC migration conclusively, future studies are required in which neurite formation is blocked in differentiating neurons.
A number of molecules that influence the migration of ENCC in vitro are found in gradients along the gut [72–74]. For example, GDNF is chemoattractive to ENCCs in cultured explants, and Gdnf is expressed in a spatial and temporal gradient from the stomach to the cecum coincident with the migration of ENCCs towards the cecum [75, 76]. The side of the cell body from which axons emerge and the initial direction of axon growth of some CNS neurons can be influenced by gradients of guidance factors [77, 78]. We provide two lines of evidence to suggest that individual ENCCs cannot sense the polarity of the gut. First, our data suggest that the polarization of an ENCC cell body required for the initial formation of an axon is random, and that neurites must project for a minimum distance, or exist for a minimum amount of time, before they are able to detect the longitudinal axis of the gut. Second, the migration of solitary ENCCs was consistent with an unbiased random walk. This implies that individual ENCCs are unable to detect chemotactic gradients along the gut. In Xenopus, groups of cranial neural crest cells show a strong chemotactic response towards the chemokine, Sdf1, but single cells respond poorly and thus cell-cell interactions are essential for chemotaxis of cranial neural crest cells towards Sdf1 . It would therefore be very interesting to determine whether solitary ENCCs show a chemotactic response to GDNF.
ENCCs exhibit variable speeds and directionalities, but with a caudal bias, and this results in the population of each gut region as well as the caudal advance of some ENCCs. Hence, the gut is not populated by cells stopping, but by cells migrating non-directionally. ENCCs remain migratory after colonizing each gut region, which might be a mechanism to ensure an even density of cells as the gut grows. Despite the variability in behavior, ENCCs overall behave differently in groups compared to solitary cells and therefore meet the definition of collective migration . Moreover, previous studies have shown that ENCCs can act cooperatively in the regulation of proliferation and migration [60, 79]. Chains of ENCCs appear to advance caudally because they prefer regions with low ENCC density, whereas neurites can detect the longitudinal axis of the gut and exhibit directional growth, although they do not lead the way down the gut. Future studies are needed of other cell populations that exhibit directional dispersion to reveal if the behavior of ENCCs can be generalized.
Ednrb-hKikGR mice, in which all ENCCs express the photoconvertible protein, KikGR,  were used for all experiments. C57BL/6 mice were time-, plug-mated to Ednrb-hKikGR mice. Segments of small intestines from E11.5 Ret TGM/TGM mice  were also used for some experiments. Mice carrying E11.5 or E12.5 embryos were killed by cervical dislocation. All experiments were approved by the Anatomy & Neuroscience, Pathology, Pharmacology and Physiology Animal Ethics Committee of the University of Melbourne.
The guts from E11.5 or E12.5 Ednrb-hKikGR mice weres dissected in DMEM/F12 containing 20 mM glutamine, 10% FBS and penicillin/streptomycin, and attached across a “V” cut into a piece of filter paper as described previously . The filter paper was inverted and placed in a 35-mm coverslip-bottomed dish. A stainless steel ring was placed on the edge of the filter paper support to prevent movement. In some experiments, the culture medium also contained the EDNRB antagonist, BQ-788 (Sigma-Aldrich, Castle Hill, NSW, Australia; 20 μM), which was added three to four hours prior to the commencement of imaging. Co-cultures were also set up in which segments of small intestine from E11.5 Ednrb-hKikGR mice were placed at both the rostral and caudal ends of segments of small intestine from Ret TGM/TGM mice, which lack ENCCs . The co-cultures were grown in an incubator at 37°C with 5% CO2 for 24 to 48 hours prior to imaging. Preparations to be imaged were placed in an environmental chamber, held at 37°C, mounted on an inverted Leica SP5 laser confocal microscope (North Ryde, NSW, Australia). Photoconversion of individual or groups of KikGR + cells was performed using a 405 nm laser and the regions of interest (ROI) function on the confocal microscope. Z-series images were obtained through the ENCC network at 2.5-, 3-, 4- or 5-minute intervals using X10, X20 or X40 oil immersion objectives. Cell tracking (manual and automatic), and measurements of angles and distances, were performed on videos of projected z-series using Axiovision (Zeiss, North Ryde, NSW, Australia) or ImageJ (National Institutes of Health, USA) software. Filopodial extensions were quantified by counting the number of new filopodial extensions outside of the ENCC network in a 100 × 200 μm area at five-minute intervals for three hours. Immunohistochemistry was performed using Tuj1 antibodies (Covance, North Ryde, NSW, Australia) as reported previously .
This fitting procedure allowed us to estimate the drift velocities v x and v y . An unbiased random walk has v x = v y = 0. Our data suggest that the mean drift in the x-direction is v x = 0.020 ± 0.062 μm/minute, and the mean drift in the y-direction is v y = 0.020 ± 0.078 μm/minute. Here we have quantified the uncertainty in our estimates using the sample standard deviation. Since we only have a relatively small number of trajectories, the sample standard deviation is large. In summary, given the large variability in our data, our estimates of v x and v y are sufficiently close to zero to conclude that the motion is, on average, unbiased.
By fitting a straight line to a plot of as a function of log10(t), the least-squares estimate of the slope of that line provided us with an estimate of (α - 1).
endothelin receptor type B
enteric neural crest-derived cells
kinesin binding protein
protein kinase A.
This study was supported by grant and fellowship support from NHMRC Australia to HMY (1047953 and 1002506).
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