Introduction

With only one axon extending out from the soma, a neuron uses axonal branches to connect with multiple synaptic targets in complex neural circuits. Often axonal branches develop stereotypic patterns that support proper circuit connection and function. This involves not only the generation of new branches at the right location but also the guidance of newly formed branches toward their targets [1, 2]. While extensive knowledge has been gained on the molecular mechanisms of axon guidance and axon branching in the past [3, 4], less attention has been paid to how branches are guided in association with branch formation when precise circuits are assembled.

The central projections of the dorsal root ganglia (DRG) sensory neurons in the spinal cord provide an excellent model to investigate such guidance mechanisms during branch morphogenesis. These projections relay somatosensory information (e.g., pain and touch) collected by their peripheral projection in the skin and muscle to the brain [5-8]. Upon reaching the dorsal spinal cord, they normally bifurcate in a location called the dorsal root entry zone (DREZ) [7, 9]. The bifurcated branches appear to extend in opposite direction along the rostrocaudal axis, generating T-shaped junctions, as part of the dorsal funiculus in the DREZ (Fig. 1E) [1, 8]. The dorsal funiculus is a critical axonal track in the spinal cord that allows information to flow between the periphery nervous system (PNS) and the central nervous system (CNS). Damage to or malformation of this evolutionarily conserved axonal structure in the DREZ can lead to paralysis, as commonly seen after spinal cord injury or in genetic disorders such as Frederick ataxia [10-12]. Thus, understanding the development of DRG axon bifurcation could provide useful insights into the mechanisms that ensure the fidelity of forming branched circuits.

Fig. 1.

Studies in the past have begun to tease out the molecular and cellular mechanisms that generate this stereotypic branch. In mice, after reaching the dorsal spinal cord at embryonic day (E) 10.5 [7, 9], the DRG central projections first generate a new branch in response to the C-type natriuretic peptide (CNP) present in the dorsal spinal cord, and this step requires the CNP receptor Npr2 as well as cGMP signaling [13-16]. The resulting daughter branches are then guided to grow only in the DREZ along the rostrocaudal axis [9], leading to the formation of the T-shaped branch junction. This step is partly controlled by the Slit family of guidance molecules, Slit1 and Slit2, which are expressed next to the DREZ inside the spinal cord, as well as their Robo receptors, which are expressed by DRG neurons [17]. In mouse mutants lacking Slit1 and Slit2 or their receptors Robo1 and Robo2, one of the daughter branches misprojects into the spinal cord. However, the defect only affects ∼50% DRG axons and does not eliminate the dorsal funiculus, suggesting the presence of other molecular mechanisms that guide bifurcating DRG afferents.

In search of additional molecular mechanisms, we re-evaluated the role of Netrin-1 (Ntn1), an extracellular molecule expressed in the spinal cord [18] (S1A-B Fig). Early studies of Ntn1 deletion based on a gene-trap allele (Ntn1^β/β) as well as targeted deletion alleles have identified aberrant entry of sensory axons into the dorsal spinal cord at E11.5 and E12.5 [19-25]. Because of its expression immediately adjacent to the DREZ at E11.5 [18], it has been suggested that Ntn1 prevents premature ingrowth of sensory afferents into the spinal cord via repulsion, an activity that was demonstrated in vitro [19, 26]. However, it is not clear whether Ntn1 is also required for proper DRG axon bifurcation, and if so, whether Ntn1 is needed for forming the second branch or guiding these branches.

Using whole mount immunostaining coupled with tissue clearing [27-30], we examined Ntn1^β/β mutants and found an ingrowth defect at the time of bifurcation, a defect that is different from what has been previously reported [19, 26]. Genetic and dye labeling confirmed that the misprojections are from DRG axons and single cell analysis demonstrated that the defect results from misguidance of otherwise normally bifurcated axons. The misprojections have different trajectories from those found in Slit1;Slit2 mutants [17], and triple deletion of both pathways led to a rare and more severe phenotype with a near loss of the dorsal funiculus. Finally, a similar phenotype was also seen in mice lacking Netrin and Slit receptors. Taken together, these results demonstrate a new role for Ntn1, and more importantly, the presence of multiple guidance mechanisms that confine the bifurcating axons within the DREZ and ensure the precise construction of the dorsal funiculus.

Results

Loss of Ntn1 causes axons to escape from the dorsal funiculus during bifurcation

To determine the role of Ntn1 in early DRG axon development, we first confirmed the expression of Ntn1 in the spinal cord at E10.5, when DRG axons start to bifurcate and form the dorsal funiculus [9, 17]. Consistent with previous published expression data [31], Ntn1 transcripts are found mainly confined to the inside of the spinal cord, including the floor plate, the ventricular zone, and the lateral domain in the dorsal horn below the dorsal funiculus along the pial layer from E10.5 to E11.5 (Fig. S1A-B, arrows). This RNA expression profile is in line with the localization of Ntn1 proteins made by ventricular zone neural progenitor cells and deposited along the pial layer adjacent to the DREZ [24, 32].

To examine the DRG axonal tracts as they are entering the spinal cord at the DREZ, we performed wholemount neurofilament (NF) antibody staining combined with the CUBIC tissue clearing method [27, 28]. Individual DRGs and their central projections in the dorsal funiculus can be seen from the lateral side of the embryos by confocal microscopy. As shown in wild type (WT) embryos, the central DRG axons first extend dorsally, enter the spinal cord, bundle and form the dorsal funiculus that runs along the rostrocaudal axis (Fig. 1A,C). Due to the developmental delay along the rostrocaudal axis, the dorsal funiculus shown as a longitudinal track is thicker near the forelimb (Fig. 1A) than near the hindlimb (Fig. 1C), where it has just begun to form from bifurcated axons. These labeled axons stay within the tract forming tightly bundled fascicles, with few labeled axons extending dorsally from the dorsal funiculus (Fig. 1A). This clear projection pattern can be also seen by traditional NF staining using horseradish peroxidase (HRP)-based immunostaining and BA/BB-based tissue clearing (Fig. S1). When viewed on a stereoscope, the labeled DRG axons appear to stay within the tract, leaving a clear space between left and right dorsal funiculi (Fig. S1C,D,G,H).

Similar to those of WT embryos, DRG projections in Ntn1^β/β mutants also form the dorsal funiculus, which can be seen as a NF-labeled longitudinal tract in the forelimb region (Fig. 1B). However, while some axons remain in the tract, a subpopulation of NF-labeled fibers (Fig. 1B arrows) were found to escape the tract, filling the space above the dorsal funiculus. These misprojecting fiber can be seen in traditional neurofilament staining (Fig. S1E,F,I,J). They appear in the hindlimb region where the dorsal funiculus starts to emerge (Fig. 1D), suggesting that the defect happens at the time of bifurcation.

To quantify the misprojections, we used line scans to determine the number of misprojecting fibers straying away from the dorsal funiculus of a single DRG in the fluorescent wholemount images viewed from the lateral side of the embryo. Lines were placed in three positions - proximal, medial, and distal - that are 75μm apart between the DREZ and the roof plate (Fig. 1B). In WT embryos, almost no fibers were found at any of the three positions, indicating that axons remain inside the dorsal funiculus. In Ntn1^β/β mutants, an average of 22 fibers per DRG were found in the line proximal to the DREZ, 17 fibers/DRG were found in the medial line, and 14 fibers/DRG were found in the distal line that is closest to the midline (Fig. 1F). The presence of NF-fibers in the dorsal midline of the Ntn1mutants suggests that misprojections climb up in the dorsal spinal cord.

To better understand the location of misprojections, we examined transverse sections of E10.5 (Fig. 1G,H K,L) and E11.5 (Fig. 1I,J M,N) embryos stained for NF. In the dorsal spinal cord of WT embryos, NF labels axons that extend from the DRG into the DREZ (Fig. 1G,H, I,J). The DREZ is smaller at E10.5 than E11.5 (Fig. 1G,H vs I,J), but at both ages, the intense NF staining that represents the cross-sections of the dorsal funiculus remains inside the DREZ. However, in Ntn1^β/β mutants, NF-labeled fibers extended out from the DREZ at both ages. More misprojections were found at E11.5, but they all grow along the pia surface (Fig. 1K,L,M,N), consistent with the dorsally extending trajectories seen in the whole mount staining above. Thus, loss of Ntn1 caused NF-labeled axons to escape from the DREZ.

Ntn1 affects DRG branch guidance at the time of bifurcation

Since NF can label axons from different neuronal populations including DRG sensory neurons, commissural neurons, and other spinal cord interneurons [21, 22, 33], we wanted to confirm that the observed misprojections at E10.5 are indeed axons of the DRG sensory neurons. We thus introduced a neural specific CreER^T2 recombinase driver (Neurog1:CreER^T2) and an Ai14 Cre reporter to our Ntn1 mice to label all DRG neurons [34]. After Tamoxifen treatment to activate the Cre recombinase, we used RFP antibody to label the fluorescent protein tdTomato, which is expressed from the Ai14 allele, and examined DRG neurons and their axons in iDISCO-cleared and antibody-stained wholemount embryos.

In WT control embryos, tdTomato labeling is seen in the DRG cell bodies (Fig. 2A, asterisks), the central axons projecting toward the dorsal spinal cord and the dorsal funiculus (Fig. 2A, yellow dotted box), which are also labeled by NF staining (Fig. 2A’). In Ntn1^β/β mutant embryos, tdTomato labeling is seen in DRG central projections as well as misprojections that escape from the DREZ and reach the dorsal spinal cord (Fig. 2B). NF staining similar to Fig. 1 shows the misprojecting fibers (Fig. 2B’) invading the dorsal space. While not all NF misprojections are tdTomato positive, all tdTomato labeled misprojections are NF-positive (Fig. 2B”). This can be demonstrated by closer examination of the region above the DREZ (Fig. 2C) where most misprojecting fibers are stained for both tdTomato and NF (Fig. 2C”, yellow arrows) but only a few are stained for just NF alone (Fig. 2C’,C”, white arrow). Importantly, these tdTomato-labeled misprojections came directly from the DREZ (Fig. 2C). D2 dorsal interneurons inside the spinal cord are known to express Neurog1 [34, 35]. Although they are labeled by tdTomato staining, D2 interneurons are not labeled by NF (see Fig. 2A and 2A”) and thus do not contribute to the NF-labeled misprojections. On the other hand, since Neurog1:CreER^T2 may not be active in all DRG neurons, tdTomato-labeled misprojections likely underrepresent the DRG axon misprojections. Thus, these data support that some if not all NF-labeled misprojections seen above are from the DRG sensory neurons.

Fig. 2.

To further confirm the DRG origin of misprojecting fibers found in Ntn1 mutants and examine the nature of the defect, we next investigated the misprojections at the single axon level. We utilized the leaky recombinase activity of CreER^T2 in the absence of tamoxifen, which leads to tdTomato expression, seemingly at random in a small population of DRG neurons and thus sparsely labels their axons. In iDISCO cleared E10.5 WT embryos, tdTomato labeled axons revealed that DRG axons in the DREZ displayed two types of morphologies of the DRG axon terminals in the DREZ: 1) bifurcated axons (Fig. 2D), which have already reached the DREZ and bifurcated to extend the two branches in the dorsal funiculus that can be visualized by NF co-staining (Fig. 2F); 2) non-bifurcated axons (Fig. 2E), which have not yet bifurcated but reached the spinal cord and turned into the DREZ. Both bifurcated and non-bifurcated axons (n=12 vs 14) stay within the DREZ (Fig. 2I) in the WT spinal cord. Similar bifurcated (n=17) and non-bifurcated (n=13) axons are found in Ntn1^β/βmutants (Fig. 2I). However, although some bifurcated axons exhibit branches that correctly turn at the DREZ and follow the dorsal funiculus tract (Fig. 2G, left branch), others often project dorsally out of the DREZ, indicating misguidance (Fig. 2G, right branch). Non-bifurcated axons often enter the DREZ and project away from the dorsal funiculus (Fig. 2H). For comparison, nearly all axonal terminals stayed within the DREZ of WT embryos (Fig. 2I), whereas ∼55% bifurcated and ∼70% non-bifurcated axons in the Ntn1^β/βmutants misprojected outside of the defined dorsal funiculus (Fig. 2I). These results demonstrate that loss of Ntn1 alters the guidance of DRG axons at the DREZ during bifurcation.

Ntn1 and Slit regulate different aspects of sensory axon guidance during bifurcation

Our previous studies showed that impaired Slit signaling led to misguidance of one of the bifurcated DRG branches, which enter the dorsal spinal cord in the absence of Slit/Robo signaling [17]. Since the misprojections in the Ntn1 mutants appear on the dorsal pial surface and stay outside the spinal cord, we hypothesize that Ntn1 and Slits have different guidance functions that are both required for the formation of the dorsal funiculus. To test this hypothesis, we generated triple mutants (Slit1^-/-;Slit2^-/-;Ntn1^β/β) and examined sensory axons in whole mount embryos using NF staining and tissue clearing as described in Fig. 1. Triple mutants were generated in the Slit1 null background (Slit1^-/-;Slit2^+/+;Ntn1^+/+), which has nearly normal DRG axon projections (Fig. 3A), similar to those in the WT embryos described above (Fig. 1A,C). Once reaching the DREZ, axons form compact bundles that run along the rostrocaudal axis. A few short stray axons, due to the loss of Slit1, enter the normally clear space between the dorsal funiculi of the two sides of the embryo (Fig. 3A). In contrast, NF labeled axons are completely disorganized around the DREZ (dotted-line region) in triple mutants (Slit1^-/-;Slit2^-/-;Ntn1^β/β) (Fig. 3B). DRG axons still grow dorsally extending from the cell body, but rarely turn into the longitudinal track of the DREZ. Most of them continue to grow straight (Fig. 3B, arrows) or veer off slightly after passing the presumptive dorsal funiculus. Examination using traditional DAB staining described earlier also confirms this complete ablation of the funiculus tract in triple mutants (Fig. S2A-D) when viewed in either the forelimb or the hindlimb region. This analysis of triple mutants demonstrates that both Slits and Ntn1 are needed for the formation and integrity of the dorsal funiculus and supports the notion that they have different guidance roles during DRG axon bifurcation.

Fig. 3.

To gain further insights and distinguish the role of Slits and Ntn1, we next compared the trajectory and location of NF-labeled misprojections in embryos lacking Slit1 only, both Slit1 and Slit2, both Slit1 and Ntn1, or all three genes by visualizing them from different angles. First, when viewed from the lateral side of the wholemount embryos as above (Fig. 3C), Slit1 single mutants (Slit1^-/-;Slit2^+/+;Ntn1^+/+) (Fig. 3D) have a compact DREZ with few DRG axons projecting away. In double mutants lacking both Slit1 and Slit2 (Slit1^-/-;Slit2^-/-;Ntn1^+/+), an increased number of DRG axons leave the DREZ (Fig. 3E, arrows) and appear in the proximal region of the dorsal spinal cord (Fig. 3E), similar to those reported previously [17]. The number of misprojections tapers off more distally from the DREZ (Fig. 3E). This can be demonstrated by viewing the misprojections from the dorsal side of the spinal cord (Fig. 3K), as those misprojections maintain a relatively straight trajectory perpendicular to the DREZ. They also reach the midline but stop there without crossing to the contralateral side of the spinal cord. Such a trajectory is consistent with their invasion into the spinal cord, which can be shown on the transverse-section of the spinal cord. There, NF-labeled fibers appear to enter the spinal cord from the DREZ with horizontal trajectories inside the dorsal proper (Fig. 3Q, arrows). These misprojections reach the midline with an average length of 137.8 μm and a summed length of ∼.8 mm, indicating a high number of misprojections (Fig. 3T). For comparison, few misprojections are found in the Slit1^-/- animal on transverse sections, with a summed length of only 0.02 mm (Fig. 3T).

As in Ntn1 mutants, Slit1^-/-;Slit2^+/+;Ntn1^β/βembryos have a large number of dorsal misprojections that spread out in random directions from the DREZ along the dorsal spinal cord when viewed from the side (Fig. 3F, arrowheads). They appear to extend away from the DREZ and reach more distal edge of the spinal cord (Fig. 3F, H), different from that in the Slit1^-/-;Slit2^-/-;Ntn1^+/+mutants. This can be corroborated by the dorsal view, which demonstrates that misprojections are wavy and long, sometimes passing the midline and reaching to the contralateral side of the spinal cord (Fig. 3L). Such pattern is the result of misprojections emerging from the DREZ and growing upward along the pial layer as shown on the transverse section (Fig. 3R). As a consequence, the distance from the midline to the DREZ is reduced to ∼6 μm from ∼69 μm of the Slit1^-/-control animal (Fig. 3T). Although there are similar total numbers of misprojections as those in the Slit1^-/-;Slit2^-/-;Ntn1^+/+animals (Fig. 3T), most of them stay outside the dorsal proper of the spinal cord (Fig. 3R), indicating the different requirements of Ntn1 and Slits in the guidance of bifurcating DRG axons.

The independent roles are further demonstrated in the triple mutant (Slit1^-/-;Slit2^-/-;Ntn1^β/β). In addition to the nearly complete loss of the dorsal funiculus, misprojecting fibers grow in both straight or in randomized directions, which increases their reach to the distal region (Fig. 3C,G, arrows). As result, the defect of the triple mutant is more severe than that in Ntn1^β/β mutants (Fig. 1, Fig. 3F) or Slit1;Slit2 double mutants (Fig. 3E), which is demonstrated by an increase in these dorsally oriented fibers extending at all three proximal-medial-distal locations between the DREZ and the roof plate (Fig. 3H). From the dorsal view, both straight and randomly oriented misprojections co-exist (Fig. 3M), and from the cross section, misprojections are found both inside the dorsal spinal cord and along the pial surface, demonstrating additive defects when both signaling pathways are impaired (Fig. 3H, N, T). In addition, due to few axons turning into the DREZ, the distinct linear line in the DREZ appears uneven and often broken in the dorsal view (Fig. 3M) and the DREZ became elongated in the transverse section (Fig. 3S).

Taken together, these analyses from different views of the DREZ reveal distinct defects in mice lacking Ntn1 and Slit1/2, thus supporting the different guidance roles of these pathways during dorsal funiculus development.

Single axon analysis by DiI indicates neither Ntn1 nor Slit is required for branch formation

To determine whether Ntn1 is required for bifurcation, the process of forming the second branch of DRG sensory axons, we used DiI iontophoresis to label and examine single DRG axons at E12.5, the age when the majority of axons normally have already generated two branches [9, 17]. Spinal cords were removed and imaged from an open book preparation (Fig. 4A). Individuals axons were analyzed from maximum projections that were color coded for depth (Fig. 4B,C) Indeed, in WT embryos, labeled axons properly turn at the DREZ and 26 out of 27 axons have T- or Y-shaped junctions at the DREZ (Fig. 4B,D). In Ntn1^β/β mutants, 32 out of 34 axons analyzed also have two branches (Fig. 4F), indicating that branch formation itself is not affected in the absence of Ntn1. Similarly, 28 out of 29 axons have bifurcated in the Slit1^-/-;Slit2^-/- mutant embryos (Fig. 4E), while 20 out of 21 labeled axons in the triple Slit1^-/-;Slit2^-/-; Ntn1^β/β mutants have two branches (Fig. 4C,G). Since bifurcation remains nearly intact at this age for all these mutants, we conclude neither Ntn1 nor Slit is required for the formation of two branches.

Fig. 4.

Single axon analysis supports that Ntn and Slit are involved in different aspects of guidance at the DREZ

The DiI analysis also allowed us to analyze additional features of bifurcating DRG sensory axons. We examined the single axon trajectories by measuring and comparing two angles between the two branches and the primary axons (Fig. 4D). In WT animals, the angle of bifurcation is on average 115.4° (Fig. 4H), consistent with a more curved trajectory of bifurcation at this age. The average deviation is 10.2° (Fig. 4I) and the difference between two angles from the same axons is 11.8 ° (Fig. 4J), indicating similar projection patterns for the two bifurcated branches. In Slit1^-/-;Slit2^-/- mutant embryos (Fig. 4E), some branches turn normally at the DREZ, while others often fail to properly turn but instead overshoot into the spinal cord, as portrayed by a relatively straight trace. When analyzed together, the average angle is 118.9°, only marginally larger than WT (Fig. 4H), but the angle deviation is increased to 19.5° and the angle difference to 31.6 ° (Fig. 4I, J), reflecting misguidance of one of the two branches (Fig. 4I), consistent with the previous finding [17]. A similar angle difference was found in Ntn1^β/β mutant embryos (Fig. 4F). The average angle of bifurcation is ∼108.0° (Fig. 4H) with a deviation of 17.5° (Fig. 4I) and a difference of 31.8°. However, analysis of Slit1^-/-;Slit2^-/-; Ntn1^β/β triple mutants (Fig. 4G) reveals an enhanced defect with highly deviated trajectories. Although the average angle is similar to that of WT, 110.7° (Fig. 4H), nearly all branches are deviated from the average angle by a margin of 37.8°, significantly different from those seen in either Slit or Ntn1 mutants (Fig. 4I). Some axons in the triple mutants even overshoot the DREZ with 180° angles, turn with a drastic kink, or have an altered axis of turning in the DREZ (Fig. 4G). Moreover, the angle difference is increased dramatically in the triple mutants, reaching 74.6° (Fig. 4J). Taken together, these results demonstrate the additive effects of Ntn1 and Slit and suggest that the guidance of the two branches has different requirements of Ntn1 and Slit.

Role of DCC and Robo receptors in DRG axon guidance during dorsal funiculus formation

To further demonstrate the requirement of the two extracellular signals in guiding DRG sensory axons during bifurcation, we examined mice lacking the Ntn1 receptor DCC, which was previously shown to have a late-ingrowth defect [36]. DCC is expressed at low levels in the DRG by in situ analysis [37](Fig. S3), and recent analysis by single cell RNAseq suggests DCC is expressed in a subset of sensory neurons [37]. Using whole mount analysis of E10.5 DCC mutants, we found similar misprojections as those in the Ntn1 mutants (Fig. 5A,B, arrows). Since the deletion of the Slit receptor Robo1 and Robo2 results in the same overshooting defect as the loss of Slit1 and Slit2 [17], we next generated a triple mutant lacking all three receptors (Robo1Robo2^--/--;DCC^-/-). Fluorescent labeling of sensory axons in E10.5 whole mount embryos reveals extensive dorsal misprojections that fail to form axonal bundles of the dorsal funiculus in the triple mutant when compared with the littermate control (Fig. 5C,D).

Fig. 5.

To characterize the misprojections quantitatively, we examined E11.5 spinal cord transverse-sections and found the same two types of NF-labeled misprojections seen in mutants lacking Slits and Ntn1 above (Fig. 3). In Robo1Robo2^--/-- mutant embryos (Fig. 5G), similar to that in Slit1^-/-;Slit2^-/- cross sections (Fig. 3), the DREZ still forms but some fibers invade the spinal cord with straight trajectories that shoot horizontally in the dorsal spinal cord (Fig. 5I). In DCC^-/- only mutants, the DREZ still forms and the NF-labeled fibers misproject upward along the pial layer (Fig. 5F), leading to a reduced distance between the midline and the DREZ (Fig. 5I), similar to the Ntn1 phenotype (Fig. 1L,M). In Robo1Robo2^--/--;DCC^-/-triple mutants, two types of misprojecting fibers are found, similar to those in Slit1^-/-;Slit2^-/-;Ntn1^β/β embryos (Fig. 3). Both misprojections originate from the DREZ, but some stay dorsally on top of the pial surface (Fig. 5F,H) while others enter the spinal cord horizontally (Fig. 5G,H, arrows). When quantified, mice lacking either Robo1Robo2 or DCC have similar total lengths of horizontal misprojections, but the triple mutants have increased total lengths, reflecting an increased number of misprojections (Fig. 5J). In addition, the gap between the dorsal misprojections and the midline seems to be reduced significantly in all mutants (Fig. 5I). These defects are similar to those found in the analysis of Slit1/2 and Ntn1 mutants above (Fig.3), thus demonstrating that loss of either the ligand or the receptor of both signaling systems has the same impact on DRG axon guidance at the DREZ.

Discussion

Our in vivo analysis of two guidance pathways has identified multiple guidance mechanisms that shape DRG axons bifurcation when forming the dorsal funiculus in the DREZ. We show that development of this stereotyped T-shaped structure requires both Ntn1 and Slits, each regulating different aspects of guidance during bifurcation. These results demonstrate the presence of multiple mechanisms to ensure the proper formation of the dorsal funiculus, a structure that is essential to sensory function in the mammalian spinal cord [38].

Ntn1 signaling is required for guiding bifurcating DRG axons in the DREZ

Our analysis of mouse mutants lacking the secreted molecule Ntn1expanded previous observation of a spinal cord ingrowth defect that was interpreted as the function of Ntn1 in a critical “waiting period” before DRG axons sprout collateral branches [19]. However, our study showed that loss of this molecular pathway also leads to a profound defect at the time of bifurcation, as misprojecting axons were found as early as E10.5, when the dorsal funiculus first forms (Fig. 1). The misprojecting axons do not stop at the DREZ but instead project more dorsally along the pial surface with random paths, supporting the idea that Ntn1 is needed for proper guidance of DRG afferents right at the time when they bifurcate in the DREZ. The origin of the misprojections from DRG neurons is confirmed by both genetic labeling using Neurog1:CreER^T2(Fig. 2) and DiI labeling (Fig. 4). Single axon labeling by both methods further demonstrate the guidance role of Ntn1, which is different from what was suggested from previous studies [19, 26]. Instead of blocking the DRG axons from entering the spinal cord, our data demonstrate that Ntn1 is required for guiding bifurcating axons along the DREZ. Moreover, single axon DiI labeling at later stage rules out the requirement of Ntn1 in bifurcation as the majority of DRG axons in Ntn1 mutants still form two branches (Fig. 4).

The guidance function is further supported by the similar defect found in mice lacking the Ntn1 receptor DCC (Fig. 5). This DCC function is reminiscent to that found in zebrafish DRG axons, which require proper DCC signaling to control actin-mediated invadopodia during the initial entry at the DREZ [39]. It is also possible that Ntn1 proteins present locally outside the DREZ (Fig. S1) [18] provides a permissive cue that encourage the growth of newly bifurcated branches but restrict their trajectory within the DREZ, similar to the recently described role for Ntn1 in confining pontine neuron migration [40]. Such a permissive function matches well with the known function of DCC. However, it is possible that the guidance function is mediated by a repulsive action of Ntn1, which can be mediated by both DCC and the repulsive receptor Unc5C. This is supported by Unc5C expression in DRG neurons as well as the repulsive activity of Ntn1 on E11.5 and E13.5 DRG axons in vitro [19, 26]. Thus, it would be interesting to re-examine Unc5C mutants and determine its role during DRG axon bifurcation and distinguish the potential mechanism for Ntn1 signaling. Nonetheless, our studies demonstrate a key role for Ntn1 signaling in DRG axon guidance right after bifurcation at the DREZ.

Multiple mechanisms are present to regulate DRG axon guidance during bifurcation

One striking result from our studies is the complete disorganization and the loss of axonal bundles in the dorsal funiculus when both Slit and Ntn1 pathways are impaired. This is reflected by the severe sensory misprojections in triple mutants lacking all three genes, Ntn1, Slit1, and Slit2, in which nearly all DRG axons leave the DREZ and grow medially into the dorsal spinal cord (Fig. 3). A similar defect was found in mice lacking the receptors for both pathways (Fig. 5). To our knowledge, this is the first report of such a severe defect of the dorsal funiculus.

Importantly, when the defects were examined more carefully, we found that the guidance defect found in Ntn1 mutants is different from that found in mice lacking Slit [17]. The misprojections due to the loss of Slit signaling tend to enter the spinal cord horizontally whereas those from the loss of Ntn1/DCC grow more dorsally and stay at the pial surface (Fig. 3). In addition, different growth trajectories were found for the misprojections: those in Slit/Robo mutants are relatively straight and parallel whereas those in Ntn1 mutants are wavy and randomly oriented. These phenotypes suggest that Ntn1 and Slit have different actions in guiding DRG axons. This conclusion is further supported by the defects in the triple mutants that exhibit both types of misprojections. Quantitative analysis shows that loss of both pathways resulted in added defects for both horizontally and dorsally invading misprojections (Fig. 3-5), suggesting non-redundant functions of the two mechanisms.

Building on a collateral-couple repulsion model we proposed earlier [17], we suggest that Slit and Ntn1 regulate branch guidance at two different steps during bifurcation (Fig. S4). When the primary axon of DRG neurons first reach the dorsal spinal cord, they are guided by Slits to turn into the DREZ; after turning, the second branch is stimulated to form by CNP; and finally, the two branches continue to grow along the DREZ and their trajectory is regulated by Ntn1. Future analysis at single cell levels would be useful to test this refined model and distinguish the role of these molecules before and after bifurcation. Imaging the growth cone behaviors during bifurcation in vivo would provide additional information of the guidance decision as shown by recent studies in zebrafish and spinal cord explants [39, 41, 42]. Altogether, our new study demonstrates that formation of a simple bifurcation structure requires multiple molecular mechanisms to ensure not only the formation of the second branches but also the correct orientation of both branches.

New insights of guidance regulation at the DREZ

The guidance regulation of DRG axon bifurcation by Slit and Ntn1 may be similar to but overshadowed by their function in midline guidance [43]. However, it is worth noting that midline crossing is defined by the floor plate, a structure that is formed during early spinal cord development and which serves as an intermediate target [43]. However, the DREZ is an evolving structure that is defined not by any preexisting cell types, but rather by the location where DRG sensory axons first bifurcate [43-45]. Therefore, both formation of the second branch and guidance of both bifurcated branches are critical to establishing the DREZ. In combination with our previous studies [13, 17], our data demonstrate a critical role of local cues, including local expression of CNP, Slit, and Ntn1.

Moreover, the formation of DREZ could be influenced by other cell types, including the boundary cap cells [46, 47]. Since these boundary caps are derived from late-born neural crest cells, they are unlikely to shape the DREZ during initial DRG axon bifurcation. However, dorsal interneurons, which migrate ventrally at the time of DRG axon bifurcation, might play a role here, as migration defects have been reported in both Ntn1 and DCC mutant embryos [36, 48]. These cells could produce extracellular factors to control DRG axon guidance. In fact, loss of TAG-1/Axonin-1 from these cells cause similar but not identical afferent defects at the DREZ [49]. To fully understand guidance regulation of DRG axon bifurcation at the PNS-CNS interface [44], it would be important to determine whether Ntn1 acts directly on DRG axons or indirectly to influence DRG bifurcation via interneurons. Thus, our in vivo analysis in various knockout mice provides the first step toward understanding the complex regulation of axonal development at the DREZ, a region pivotal for proper spinal cord function that is disrupted in certain genetic disorders and after injuries [10, 11].

Materials and Methods

Mouse strains

All animal procedures followed the Guidelines for the Care and Use of Laboratory Animals of the National Institutes of Health and the approved IACUC protocols of the Thomas Jefferson University (#01558 and #01559). Mice were maintained in a CD-1 background. Timed pregnancies were determined based on vaginal plugs and the first date was designated as E0.5. Mutant alleles for Ntn1, Slit1 and Slit2 were described previously (Fazeli et al., 1997)(Ma and Tessier-Lavigne, 2007). The transgenic allele Neurog1:CreER^T2 (JAX stock #008529) that express CreER^T2 recombinase from the Neurogenin-1 promoter was described [34] and the Cre-reporter, tdTomato (JAX stock #007914), that expresses the red fluorescent protein from a CAG promoter was described [50]. Homozygous Ntn1^β/β mutants were generated from heterozygous sires and dams. To obtain Slit1^-/-;Slit2^-/-;Ntn1^β/βtriple mutants, mice carrying a single copy of Slit2 and Ntn1 mutant allele in the Slit1^-/- background were first generated and then used to obtain triple mutants. Genotyping of Slit1and Slit2 was done by PCR as previously described [17, 51, 52]; genotyping of tdTomato and Neurog1:CreER^T2 was done by PCR using primers described by JAX. For Ntn1 genotyping, the intensity and kinetics of lacZ staining of embryonic tails were used to determine the copy number of the mutant allele and the resulting Ntn1^β/β mutant exhibited consistent midline crossing phenotype described previously [18]. For tdTomato labeling of DRG axons, pregnant dams at E9.5 were administered via oral gavage a 0.5 mg / 50 ul dose of tamoxifen solution diluted in peanut oil that was warmed at 37°C. Following dissection, tdTomato fluorescent expression was screened using an epifluorescent microscope.

Immunohistochemistry, tissue clearing, and imaging

Embryos (E10.5-E11.5) were fixed overnight in 4% paraformaldehyde (PFA) in phosphate buffered saline (PBS). For wholemount immunostaining, embryo samples were pretreated with methanol dehydration, bleached in 10% hydrogen peroxide o/n at 4°C, then subject to the reverse MeOH gradient re-rehydration treatment followed by staining based on either iDISCO or CUBIC protocols [27-29].

For iDISCO based clearing and staining, re-hydrated samples were washed in 5% DMSO/0.3M Glycine/PTxwH (1X PBS, 0.01% Triton X-100, 0.05% Tween-20, 0.02% NaN3) sequentially for 1 and 2 hours; then washed in PTxwH x3 for 30 min each; and blocked in 3% Donkey Serum (DS)/PTxwH with shaking at 37°C, o/n. Samples were then incubated with primary antibody diluted in blocking solution for 3 days at 37°C; washes done in PTxwH for 1 hour x2, 2 hours x2, then o/n and 1 day; followed by incubation of secondary antibody diluted in blocking solution o/n at 37°C. Washes were done the next day in PTxwH for 1 hour x2, 2 hours x2, then o/n and 1 day. Next, embryos were washed in PBS shaking at RT, 1 hour x2, 2 hours x2, then o/n. For clearing, samples were dehydrated in the MeOH gradient, then washed 3x in 100% MeOH for 15 min each, transferred to 100% dicholoromethane (DCM, Sigma-Aldrich 270997-1L), and finally incubated in DiBenzyl Ether (DBE, Sigma-Aldrich 108014-1KG) until clear [29].

For CUBIC based clearing and staining, embryos were washed after rehydration in 0.1% Triton X-100 for 10-15 min x3, and then transferred to blocking buffer (5% heat-inactivated normal goat serum, 20% DMSO in PBS), at 37°C o/n. Samples were incubated with primary antibodies diluted in blocking buffer for 3 days at 37°C, then washed in 20%DMSO in PBS for 1 hour x6. Secondary antibodies in blocking solution were incubated o/n at 37°C. Embryos were washed 1 hour x6 and then transferred to CUBIC1 solution (25 wt% N,N,N’,N’-tetrakis(2-hydroxypropyl)ethylenediamine (Sigma 122262), 25 wt% urea and 15 wt% Triton X-100) for clearing. Following successful clearing, samples were equilibrated in CUBIC2 solution (50 wt% sucrose, 25 wt% urea, 10 wt% triethanolamine (Sigma T58300), and 0.1 % (v/v) Triton X-100) for imaging [27, 28]

Imaging of cleared embryos was done on a Leica SP8 laser scanning confocal microscope using a 10X objective (NA=1.05). Inverted fluorescent images are 2D projections of confocal sections of the entire stack or the sections surrounding the region of interest.

For immunostaining on tissue sections, PFA-fixed embryos were equilibrated with 30% sucrose in PBS and frozen in the Tissue-Tek OCT embedding medium. Thin sections (16 μm) were cut on a cryostat (Leica) and processed for antibody staining [17]. Cryosections were permeabilized and blocked in blocking buffer (0.1% Triton X-100 and 10% goat serum in PBS) for 1 h at room temperature and overlaid with primary antibodies diluted in blocking buffer overnight at 4°C. Sections were then washed with PBS and 0.1% Triton X-100 x3, blocked again for 2 hours at room temperature and then incubated with secondary antibodies diluted in blocking buffer overnight at 4°C. Sections were then washed with PBS x3 and sealed with cover glass before imaging. Fluorescently labeled tissue sections were imaged on a wide field fluorescence microscope (Zeiss, Inc) or laser confocal systems (Leica SP8 system).

Primary antibodies used to detect tdTomato expression, rabbit anti Red Fluorescent Protein (RFP) polyclonal antibodies (Rockland Antibodies, 200-101-379, 1:1000). For NF staining, a monoclonal mouse antibody (2H3; Developmental Studies Hybridoma Bank, AB_2314897, 1:200) was used. Cy3 (Jackson ImmunoResearch, 711-165-152, 1:500) or Cy5 (Jackson ImmunoResearch, 715-175-150,1:500)-conjugated secondary antibodies were used.

HRP staining in whole mount embryos followed previously described method [17]. Embryos were bleached with hydrogen peroxide overnight, incubated with primary antibodies and then HRP-conjugated secondary antibodies. After converting the 3,3’-diaminobenzidine (DAB) substrate to brownish deposit around labeled axons, the embryos were cleared in a BA/BB solution (benzylalcohol:benzylbenzonate, 2:1) [30], and imaged by the Spot II-RT camera mounted on a Stemi-6 stereoscope (Zeiss, Inc.)

DiI labeling of DRG axons in the spinal cord

For single neuron labeling by DiI, embryos were fixed and then cut open from the ventral side to expose the DRG. A small dye crystal was delivered to the DRG from an ethanol solution of DiI (0.5%) in a glass pipette (1 μm opening) by iontophoresis with a current of ∼5-20 mA as previously described [17]. The dye was allowed to diffuse at 25°C overnight. The floorplate of the spinal cord was cut to create an open-book, which is then laid down in an imaging chamber with the lateral side down. The labeled axons were imaged on a Leica SP8 confocal microscope at 20X objective (NA=.4). Maximum projections were traced and skeletonized in ImageJ using the Neurotrace plugin.

In situ hybridization

Cryosections (16 μm) of E10.5 and E11.5 mouse embryos were processed for in situ analysis following a published procedure [17]. ³⁵S-labeled probes were generated using the following published templates for Netrin-1 [18]. Dark field images were taken on a Zeiss compound microscope.

Experimental design and statistical analysis

Embryos with different genotypes were collected from the same litters and subjected to the immunohistochemical analysis described above. Image comparison was done in the same spinal cord region of embryos with the same age and similar body size. The number of animals analyzed is listed in the figure legends.

To quantify misprojections in whole mount embryos, line scans of pixel intensity were taken from lateral side of whole mount embryos in ImageJ at three regions: proximal (right above the DREZ), medial (75 μm above the DREZ), and distal (150 μm above the DREZ and closest to the dorsal midline). After background subtraction, the peaks representing the labeled axons were counted above each brachial DRG at different regions and used for comparison by one-way ANOVA.

Quantification of misprojections in cross sections was done with the NeuronJ plugin in ImageJ. To quantify horizontal misprojections, the total length of axons projecting centrally were traced and measured on each hemisection. To quantify dorsal misprojections, the distance from the midline to the tip of dorsally projecting axons was measured following the curve of the cross section. Values for multiple hemisections per embryo were summed and then averaged for statistical comparison using one-way ANOVA with post-hoc Tukey’s test.

To quantify DiI labeled single axons, clearly visible axons were first divided into two groups, single or bifurcated. For single axons, we used the neighboring axons as a reference to determine whether they turned into the DREZ. Bifurcated axons that grow in the DREZ are considered normal and those projecting away from the DREZ were considered misguided. Normal and misguided axons were tallied from each spinal cord and used for comparison by t-tests. For quantification of the branching angle for DiI analysis a circle with the radius of 75 um from the branch junction was determined and the angle formed from the main axon shaft and the extending branch was measured. An ANOVA between the varying genotypes was done with Tukey post-hoc test for determining significance.

For all statistical analysis, a minimum of three mice were analyzed. All data are expressed as Mean ± Standard Error of the Mean (SEM), and statistical values are included in figure legends.

Acknowledgements

We thank Zongxiu Zhang and Yonghong Zhou for mouse management. We also thank members of the Ma lab for helpful discussion throughout the study, and Drs. Stephen Tymanskyj and Matthew Dalva for comments on the early version of the manuscript. This work was supported by grants from the National Institutes of Health to KN (F31NS108671), AJ (R01NS095908), LVG (R21DC014916) and LM (R01NS062047 and R01NS112504).