Migration, early axonogenesis, and Reelin-dependent layer-forming behavior of early/posterior-born Purkinje cells in the developing mouse lateral cerebellum
© Miyata et al; licensee BioMed Central Ltd. 2010
Received: 3 April 2010
Accepted: 1 September 2010
Published: 1 September 2010
Cerebellar corticogenesis begins with the assembly of Purkinje cells into the Purkinje plate (PP) by embryonic day 14.5 (E14.5) in mice. Although the dependence of PP formation on the secreted protein Reelin is well known and a prevailing model suggests that Purkinje cells migrate along the 'radial glial' fibers connecting the ventricular and pial surfaces, it is not clear how Purkinje cells behave in response to Reelin to initiate the PP. Furthermore, it is not known what nascent Purkinje cells look like in vivo. When and how Purkinje cells start axonogenesis must also be elucidated.
We show that Purkinje cells generated on E10.5 in the posterior periventricular region of the lateral cerebellum migrate tangentially, after only transiently migrating radially, towards the anterior, exhibiting an elongated morphology consistent with axonogenesis at E12.5. After their somata reach the outer/dorsal region by E13.5, they change 'posture' by E14.5 through remodeling of non-axon (dendrite-like) processes and a switchback-like mode of somal movement towards a superficial Reelin-rich zone, while their axon-like fibers remain relatively deep, which demarcates the somata-packed portion as a plate. In reeler cerebella, the early born posterior lateral Purkinje cells are initially normal during migration with anteriorly extended axon-like fibers until E13.5, but then fail to form the PP due to lack of the posture-change step.
Previously unknown behaviors are revealed for a subset of Purkinje cells born early in the posteior lateral cerebellum: tangential migration; early axonogenesis; and Reelin-dependent reorientation initiating PP formation. This study provides a solid basis for further elucidation of Reelin's function and the mechanisms underlying the cerebellar corticogenesis, and will contribute to the understanding of how polarization of individual cells drives overall brain morphogenesis.
The cerebellum plays an essential role in the coordination of posture and locomotion, head and eye movements, and a wide range of motor activities. These functions depend on the structural organization of the cerebellar cortex, in which the Purkinje cells receive input from multiple sources in the central nervous system either directly or via parallel fibers of the granule cells [1–3]. Purkinje cells are generated during the early embryonic period from the ventricular zone (VZ) facing the fourth ventricle [4, 5] and migrate outward towards the pial side to subsequently form a monolayer (Purkinje cell layer) during the early postnatal days [6–10]. Just superficial to the perinatal Purkinje cell layer, there is a transient layer called the external granular layer (EGL) consisting of both differentiating granule neurons and their precursor cells. EGL precursors require Sonic hedgehog, which is supplied by the underlying Purkinje cells, to expand the granule neuron population postnatally . Thus, the arrangement of the Purkinje cells during embryonic development is a key histogenetic event and consequently determines the overall cerebellar volume, the foliation pattern, and the intensity of the Purkinje-granule association, a lifeline of the cerebellar circuitry.
How this arrangement of Purkinje cells is established is only partly understood. In the cerebellum of reeler mice, Purkinje cells cannot form a normal layer under the pial surface and instead are clustered near the deep nuclear (DN) neurons . Reelin, an extracellular glycoprotein encoded by the reelin gene mutated in reeler mice [13–15], begins to be expressed near the pial surface on embryonic day 13.5 (E13.5) by prospective DN neurons [16–18]. At E13.5, these DN neurons are still superficially migrating towards the anterior side from the posterior end of the cerebellum, the rhombic lip (RL) [18–20]. One day later (at E14.5), the arrangement of Purkinje cells into a structure several cells thick (called the Purkinje plate (PP)) is observed in normal cerebella; in reeler cerebella, however, abnormal distribution of Purkinje cells (lack of the PP) is clearly seen [7, 21]. The PP is formed just beneath a Reelin-rich zone to which RL-derived cells are continuously supplied; DN neurons, the first producers of Reelin, are followed by EGL cells [16, 17]. This in vivo spatial relationship between the Reelin-rich zone and Purkinje cells has been reproduced in experimental manipulations of Reelin-producing zones by explant culture and in utero transplantation , suggesting that Reelin may somehow promote or instruct nascent Purkinje cells to take a position close to the Reelin-rich zone. However, our understanding of the cellular scenarios involved in the initiation of PP formation at E14.5 is very limited. Furthermore, it is not known what nascent Purkinje cells look like in vivo.
To elucidate PP formation, there are three specific issues, each of which should be addressed with single-cell resolution studies. First, although a prevailing model suggests that Purkinje cells migrate along the 'radial glial' fibers connecting the ventricular and pial surfaces [6, 10, 23–26], whether or not this model fits with the actual morphology and behavior of Purkinje cells in the formation of the PP should be verified. Second, the key cellular behaviors that initiate or fail to initiate the PP in the presence or absence of Reelin need to be established. Third, whether the migratory and positioning behavior of Purkinje cells is linked with their polarization towards circuit formation should be determined. The time frame and manner in which Purkinje cells begin axonogenesis should also be examined.
By using an adenovirus-mediated pulse-chase method [27, 28] in combination with recently established Purkinje-cell-specific markers [26, 29, 30] and slice culture , the present study focused on the developing mouse lateral cerebellum until E14.5 and unveiled three important behaviors of a subset of Purkinje cells born at E10.5 in the posterior region: tangential migration (at approximately E13.5); early axonogenesis (at approximately E12.5); and Reelin-dependent 'posture' change initiating PP formation (between E13.5 and E14.5).
Purkinje cells that initiate PP formation at E14.5 are born on E10.5 in a posterior VZ
Following in utero injection of adenovirus vectors carrying a membrane-targeted green fluorescent protein (GFP) derivative (lyn-Venus) [32, 33] at E10.5, E11.5, or E12.5, the position of cells double immunostained with anti-GFP and anti-Lhx1/5 antibodies was analyzed in normal cerebella from E12.5 to E16.5 (Additional file 1). While 37% of the total GFP+Lhx1/5+ cells obtained by injection at E10.5 and analyzed at E14.5 were found in a region corresponding to the PP, incorporation of later-born cells into the E14.5 PP was very limited (3% for E11.5-born cells) or not observed (E12.5-born cells), indicating that the Purkinje cells that initiate the PP at E14.5 are generated mainly at E10.5. Histograms for birthdate- and track time-dependent changes of the distance of GFP+Lhx1/5+ cells from the ventricular surface show a general tendency that cells born earlier were seen further from the ventricular surface (Figure 1E). However, not all E10.5-born cells quickly moved towards the pial side to be integrated into the PP; some were still in a deep, periventricular region at E15.5 and E16.5. This result, together with the Lhx1/5 immunoreactivity results, is consistent with the possibility that Purkinje cells born in the VZ of the posterior cerebellar region may be more quickly incorporated into the PP than anterior-born cells. This interpretation was further supported by the observation of individual GFP+Lhx1/5+ cells in normal cerebella at E12.5 and E13.5, as described below.
Early/posterior-born Purkinje cells migrate tangentially in the lateral cerebellar primordium
Purkinje cells begin axonogenesis at E12.5
Collectively, these results suggest that nascent Purkinje cells (not only posterior-born cells, but also more anterior-born ones) may start axonogenesis from E12.5 through the expression of NF and then tau. This timeline, axonogenesis from E12.5, is consistent with a recent suggestion by Joyner's group, using visualization of nascent Purkinje cells by a novel transgenic system (Pcp2-CreER-IRES-hAP), that axonogenesis may begin between E11 and E14 . This interpretation for early axonogenesis is further supported by our observations towards E14.5, as described below.
Migration and axonogenesis are normal in reeler cerebella until E13.5
Purkinje cells form a plate by changing their 'posture' between E13.5 and E14.5 in a Reelin-dependent manner through remodeling of dendrite-like processes
Next, to examine how a Purkinje cell's orientation and polarization at the single cell level contribute to the overall structure of the PP, comparative immunostaining against NF, Corl2, and Lhx1/5 was carried out. In normal cerebella at E14.5, the PP was demarcated (that is, visible as a 'plate' near the pial surface) due to a bundle of NF+ fibers that ran below a group of Purkinje cell somata to form the PP (Figure 8F, G). This suggests that the change in orientation or 'posture' required for each Purkinje cell to make its axon relatively deeper may underlie the emergence of the PP at the population level.
In E14.5 reeler cerebella lacking the PP, a NF+ fiber bundle was observed above the Purkinje cells' somata (just beneath the pial surface; Figure 8H, I), raising the possibility that the lack of a PP is due to a failure to change the orientation or 'posture' of Purkinje cells between E13.5 and E14.5. Indeed, adenovirus-mediated pulse-chase examinations revealed that E10.5-born Purkinje cells in a dorsal region of E14.5 reeler cerebella remained parallel to the pial surface without showing a posture change (Figure 8J, K). While about 40% of the total E10.5-labeled Purkinje cells in normal cerebella (n = 71) were perpendicular to the pial surface (Figure 8E), none of the E10.5-born Purkinje cells adenovirally examined in E14.5 reeler cerebella (0/32 cells) showed the perpendicular orientation seen in normal cerebella.
To better describe this posture-change behavior as a distinct histogenetic step for migratory Purkinje cells, we compared the position of the Golgi apparatus between the most developmentally advanced Purkinje cells that had been incorporated into the PP at E14.5 and younger Purkinje cells exhibiting tangential or radial orientations of the soma in regions deeper than the PP or in E13.5 cerebella. Interestingly, nascent Purkinje cells before and after the formation of the PP distributed their Golgi completely differently (Figure 11E-J). In Purkinje cells displaying morphologies consistent with radial and tangential migration, the Golgi was located in a proximal part of the pially and anteriorly extending axon-like (tau+) fibers. In Purkinje cells from the PP, however, the Golgi was found in the dendrite-like process that was positive for microtubule-associated protein 2 (MAP2) and extended towards the pial side. It is likely, therefore, that the Golgi apparatus was excluded from the axon-like part of Purkinje cells and moved into the non-axon part during a transition from the tangentially oriented phase into the PP-forming step.
We carried out an additional three examinations to find out whether factors other than a Reelin-enriched superficial region and Purkinje cell polarization might also be primarily involved in the emergence of the PP. First, migration of RL-derived cells, which produce Reelin without expressing Reelin receptors and mDab1 (Figure 10A-E), was normal in reeler cerebella at least until E15.5 (as seen for DN cells positive for Tbr1 in Figure 8G, I and EGL cells positive for Pax6 in Additional file 7D, E, N, O). Second, we found that a portion of accumulating NF+ fibers that demarcate the PP in normal E14.5 cerebella did not contain afferent fibers that were labeled with DiI inserted into the cerebellar peduncular region (Additional file 8A). Third, Nestin+ fibers were radially oriented in reeler cerebella at E14.5 (Additional file 8B) in a pattern indistinguishable from that observed in normal E14.5 cerebella (Additional file 7A). These examinations suggest that migration of RL-derived cells, afferent fibers, and radial fiber morphology may not account for the differential Purkinje cell behaviors between normal and reeler cerebella during the E13.5 to 14.5 period.
The present study unveiled three important behaviors of nascent Purkinje cells derived from the posterior lateral cerebellum at E10.5: tangential migration, early axonogenesis, and Reelin-dependent 'posture' change to initiate PP formation. This early/posterior-born subset of Purkinje cells is the main contributor to the initiation of PP at E14.5 (Figure 1), and is a good model to investigate the mechanism through which Purkinje cells can be aligned under the regulation of Reelin.
The tangential mode of migration exhibited by these early/posterior-born Purkinje cells is very similar to that of RL-derived prospective DN neurons moving more superficially. We demonstrated immunohistochemically that the non-superficial, tangentially oriented cells were Purkinje cells. The existence of these cells was well recognized in previous Golgi studies, although they were regarded, together with the superficial cells, to be DN neurons . The tangentially oriented Purkinje cells were negative for markers for RL derivatives (Math1/Atoh1, not shown; Pax6 (Additional file 7; Tbr1 (Figure 8)). Not only E10.5-born but also E11.5-born Purkinje cells exhibited tangential morphologies in a posterior part (Additional file 2E). While E10.5-born DN neurons (GFP+Lhx1/5-) migrated tangentially along the pial surface up to 600 μm from the RL in 2 days, the histogram for the overall E10.5-born Purkinje cells (GFP+Lhx1/5+) showed a peak at 100 μm from the ventricular surface, with the farthest cells around 160 μm at E12.5 (Figure 1E). This suggests a basic rule for the E10.5 to E12.5 period that neuronal migration velocity is much greater in the tangential mode than in the radial mode. Posterior-born Purkinje cells, which are inherently closer to the pial surface than anterior-born cells, seem to be the quickest to reach an outer zone for subsequent initiation of the PP mainly due to their greater dependence on the tangential mode.
According to the previous model [6, 9, 23–26], Purkinje cell behavior prior to initiating the PP could be likened to moving from one side across to another along radial fibers (Figure 12A). We propose here that migration of a population of Purkinje cells born early in the posterior part of the cerebellum is more akin to moving along a triangular perimeter (Figure 12A). The former model was coupled with a speculation that the front (outer extremity) of each migratory Purkinje cell may transform into a dendrite whereas an axon will emerge from the rear (inner extremity). Our results show that the origins of the axons and dendrite-like processes in the early/posterior-born Purkinje cells in the lateral cerebellar primordium are opposite of what is expected in the radial migration model. It is currently unclear whether the pially or anteriorly extended processes, which are ahead of outward migrating Purkinje cells, in cerebella at E12.5 can be immediately defined as axons. However, their traceability later during embryonic development along with the overall increase in number and length, as well as the sequential expression of NF from E12.5 (Figure 5) and tau from E13.5 (Figure 6), strongly suggest that they will directly become mature axons. The axonogenic behavior of Purkinje cells resembles that of neurons outside the neocortex; the extension of a prospective axon to the direction of migration (towards the pial/outer side) is suggested in motor neurons in the developing spinal cord , retinal ganglion cells [41, 42], retinal bipolar cells , tectal ganglion cells , acoustic nuclei neurons , and serotonergic neurons in the hindbrain . Mechanisms regulating the elaboration of a new axon-like pial process from a nascent Purkinje cell (Figure 5C-E) are unknown. But the similarity between the course of axonogenesis by nascent Purkinje cells and that of afferent ingrowth reminds us of an intriguing possibility that afferent fibers might influence Purkinje cell behaviors . Whether some of the axon-like fibers are formed through the inheritance of radial fibers from progenitor cells needs to be determined, as we have observed that progenitor cells in cerebella at E11.5 to E12.5 divide at the ventricular surface while keeping their pial processes (data not shown).
At E13.5, Purkinje cells reach an outer area (150 to 200 μm from the ventricular surface) that underlies the most superficial zone. Although this outer area normally becomes covered with Reelin from this point onward (Figure 10A), it cannot be distinguished between normal and reeler cerebella (Figure 7). The outermost Purkinje cells, which subsequently exhibit the earliest Reelin-dependent behavior, are horizontally oriented at this time-point (Figure 2). Then, differential posture-change behaviors between normal and reeler Purkinje cells are observed by E14.5 (that is, Purkinje cells in normal cerebella change their orientation as if bending upwards, while those in reeler cerebella remain laying down; Figures 8 and 12).
This difference is similar to that previously suggested in E14 to E15 cerebral walls [48, 49]. In the normal cerebral wall, early-born neurons that have migrated to an outer area are oriented vertically, with the dendrites arising from the outer pole of the soma and the axon from the inner pole. The axons extended from these early neurons demarcate these cells' somata above as a plate, forming the cortical plate . In the corresponding outer zone in reeler cerebral walls, many neurons lie horizontally, which is similar to what we observed for Purkinje cells in E14.5 reeler cerebella (Figures 8 and 12). The normal bending up-like posture change of the early/posterior-born Purkinje cells enables the axons to become relatively deep and demarcate their somata above as a plate.
This posture change is likely driven by dynamic extension of dendrite-like processes, coupled with repositioning of Golgi, towards the Reelin-rich zone (Figures 9, 11 and 12). Previous co-culture and transplantation experiments showed that Purkinje cells whose somata were aligned along an artificially provided Reelin-rich zone had extended dendrite-like processes into that zone . Recently, involvement of Reelin in the growth of dendrites has been further demonstrated [36, 37, 51–56]. Taken together, we conclude that the posture change of early/posterior-born Purkinje cells, which drives the PP emergence in the lateral cerebellum, is explained primarily by the action of Reelin immediately above the Purkinje cells during the E13.5 to E14.5 period. Dendritogenesis may be tightly linked with layer formation.
Associated with the extension of the dendrite-like part, the soma moves towards the outer/pial side. The initial somal movement of the early/posterior-born Purkinje cells is oriented towards the anteriorly growing axon-like part (heading away from the posterior ventricular surfaces). The second step of somal movement towards the pial side can be viewed as a reverse or 'switchback'-like behavior (Figure 12), which has been suggested to occur during migration of tectal, acoustic, and facial nuclei neurons [44, 45, 56]. Although the initial migration step until E13.5 is tangential and considered to be independent of radial fibers, this second step between E13.5 and E14.5 is more radial and thus the radial fibers might be involved in this step. Further studies are required to determine whether the migration of Purkinje cells other than the early/posterior-born population is also biphasic (or multi-phasic). Comparison between Lhx1/5 and Nestin immunostaining patterns (Additional file 7) raises the possibility that Purkinje cell behavior after the emergence of the PP (Figure 1) might be explained by the guidance of their second (or final) phase of migration by radial fibers. This could correspond to what has been proposed previously [6, 9, 23–26]. As in the E13.5 to E14.5 period, the most intense extracellular expression of Reelin occurs subpially throughout late embryonic development . Whether the short-range mechanism for Reelin's instruction that we propose for the early/posterior-born Purkinje cells (that is, targeting the action of cells near the Reelin-rich zone) in the lateral cerebellum might be applicable to later-arriving Purkinje cells should be examined further.
It is important to understand how the short-range action mechanism might coincide with other stage- or context-dependent mechanisms. These mechanisms include Reelin's 'encouragement' of migrating or premigratory neurons distant from their final arrangement position , Reelin's effects on radial fibers [58–62], and the Reelin-independent 'community effect' among Purkinje cells . Transgenic mice artificially expressing reelin under the nestin promoter, which works within the VZ (the birthplace of Purkinje cells) until mid-embryonic development, showed an apparently normal arrangement of Purkinje cells by the postnatal period . This may lead to an interpretation that Reelin is not necessarily required at the site of Purkinje cell assembly/alignment, and seemingly contradicts the present short-range action model. Nevertheless, the nestin enhancer/promoter is active not only in the VZ (until around E16.5) but also in glial-like cells radially migrating towards the pial side (from E17.5 onward; our unpublished observation using nestin-enhanced GFP mice ). Our current observations of the course of Purkinje cell migration inferred from Lhx1/5 immunostaining, the orientation of Nestin+ fibers (Additional file 7), and the movement of cells belonging to the glial cell lineage  during the E15.5 to E18.5 period suggests a potential role for glial cells. In reeler cerebella, glial cells can successfully migrate to the subpial region . Reelin artificially provided by glial cells migrating from deep regions to subpial portions in the nestin-reelin transgenic reeler cerebella might have enabled Purkinje cells to approach the subpial position mainly during this late embryonic stage. It would be intriguing to check whether nestin-reelin transgenic reeler cerebella might not have a normal PP at E14.5.
By using an adenovirus-mediated pulse-chase method in combination with recently established Purkinje-cell-specific markers and slice culture, the present study focused on the developing mouse lateral cerebellum until E14.5 and unveiled three important behaviors of early/posterior-born Purkinje cells: tangential migration (at approximately E13.5), early axonogenesis (at approximately E12.5), and Reelin-dependent 'posture' change initiating their layer formation (between E13.5 and E14.5). Early axonogenesis by Purkinje cells contributes to their formation of a discrete layer. Our study provides a solid basis for further elucidation of Reelin's function and the mechanisms underlying the cerebellar corticogenesis, and will contribute to the understanding of how polarization of individual cells drives overall brain morphogenesis.
B6C3Fe-a/a-rl mice (heterozygous for the reeler mutation) were obtained from the Jackson Laboratory. Heterozygous (+/rl) and homozygous (rl/rl) embryos were generated by pairing female heterozygotes and male homozygotes and genotyped as described previously . For 'normal' cerebellar specimens, both the heterozygous mice and ICR mice were used. Only homozygous (rl/rl) mice are called reeler in this paper. The day of vaginal plug identification was defined as E0.5.
Adenoviral construction was carried out as previously described [27, 28]. The adenoviral vector Adex-CAG-Lyn-Venus expresses membrane-targeted Venus under control of the CAG promoter. Lyn-Venus was generated by fusing the sequence of the palmitoylation site of tyrosine kinase Lyn to the amino terminus of Venus [32, 33]. Adenoviral vector solution was injected into the fourth ventricle of embryos at each day from E10.5 to E12.5 using a trans-illumination system of in utero surgery . For histological examination using frozen sections (16 μm), the titer of adenovirus vector solution was set to a level at which <5 labeled cells in each section could be seen. With this dilution, data used for making the histograms in Figure 1E were obtained from three to seven normal (ICR mouse) embryos at each stage. For live imaging on normal cerebellar slices (200 to 250 μm), viral solution was further diluted to ensure sporadic labeling. For comparisons between +/rl and rl/rl littermates at E13.5 (Figure 7C), adenovirus-mediated pulse-chase examination was carried out using a more concentrated viral solution.
Embryos at each day from E13.5 to E18.5 were perfused transcardially with periodate-lysine-paraformaldehyde (PLP) fixative . Younger (E11.5 and E12.5) embryos were fixed by immersion in PLP at 4°C for 2 h. Isolated brains were postfixed in PLP at 4°C for 1 to 2 h, immersed in 20% sucrose, embedded in OCT compound (Miles, Elkhart, IN, USA), and then frozen and sectioned sagittally and in some cases coronally (16 μm). Frozen sections were treated with the following primary antibodies: anti-Lhx1/5 (Lim1/2; mouse, Hybridoma Bank [4F2]); anti-Corl2 (rabbit) ; anti-Nestin (rabbit, gift from Dr Yasuhiro Tomooka) ; RC2 (mouse IgM, gift from Dr Miyuki Mamamoto) ; anti-Neurofilament (mouse, Hybridoma Bank [2H3]; rabbit, BIOMOL, Plymouth Meeting, PA, USA); anti-GFP (rat, Nakarai Tesque, Inc., Kyoto, Japan; rabbit, MBL, Nagoya, Japan, anti-Tbr1 (rabbit, Abcam, Tokyo, Japan), anti-Reelin (mouse [CR50]) [14, 16]; Pax6 (rabbit, Covance, Berkeley, CA, USA); anti-Math1 (Hybridoma Bank); anti-tau (mouse, Chemicon, Billerica, MA, USA); anti-MAP2 (mouse, Sigma, St. Louis, MO, USA); and anti-giantin (rabbit, Covance). For immunostaining of live DiI-labeled cells in cerebellar slices, vibratome sections (50 μm) made after the slices were fixed with 4% paraformaldehyde at 4°C for 20 minutes were treated with antibodies at 4°C overnight.
Cerebellar primordia were isolated from E12.5 or E13.5 embryos that had been infected in utero with GFP-adenovirus at E10.5 and sliced using fine microknives, as previously described for cerebral wall slices [31, 32]. Because the long axis of each cerebellar primordium is roughly perpendicular to the rostorocaudal (anteroposterior) axis of each embryo and bridges both sides of the metencephalon, the plane of each live slice (200 to 250 μm thick, 6 to 8 slices per embryo) was made by sectioning almost perpendicular to the long axis of the isolated primordium and was generally close to the in vivo sagittal plane. In a lateral region, where the cerebellar primordium is more oblique in vivo (less perpendicular to the embryo's long axis), the plane of the live slices was less sagittal. The slices were then transferred to a glass-bottom 35 mm plastic culture dish containing enriched culture medium, a 1:1 mixture of DMEM and Ham's F-12 (phenol red-free) supplemented with insulin (25 μg/ml), transferrin (100 μg/ml), progesterone (20 nM), sodium selenate (30 nM, Sigma), putrescine (60 μM), epidermal growth factor (10 ng/ml), basic fibroblast growth factor (10 ng/ml), horse serum (5%), and fetal calf serum (5%). Up to ten slices were then transferred with 100 to 150 μl of the enriched medium to the center of the dish, then mixed with 100 to 150 μl of 2× type I collagen gel solution (Cellmatrix IA, Nitta Gelatin, Tokyo, Japan; previously diluted to 0.5 to 0.6 mg/ml with distilled water, 5× phenol red-free DMEM, and a neutralizing buffer according to the manufacturer's protocol, and kept on ice until use). The gel (final concentration 0.25 to 0.3 mg/ml) was immediately spread onto the dish base using a pipette tip. After nearly allowing the gel to solidify (about 5 minutes) with the ventricular and pial surfaces of the slices perpendicular to the dish base (arranged with a tungsten needle), the dish was placed in an incubator (37°C, 40% O2 and 5% CO2 ) (Astec, Kasuya, Fukuoka, Japan) to allow further gel solidification (5 to 10 minutes). The enriched medium (0.8 ml) was dropped onto the gel and spread over the entire dish surface.
For on-stage culture, an inverted epifluorescence microscope (IX70, Olympus) equipped with a 10× objective lens (UPlanF1; numerical aperture = 0.30) was used. In this system, slices were continuously cultured in a chamber providing a humidified atmosphere of 5% CO2 and 40% O2 (Tokken, Kashiwa, Chiba, Japan). Imaging was performed at 5-minute intervals using a cooled charge-coupled device (CCD) camera (CoolsnapHQ, Roper Scientific, Tucson, AZ, USA), which was automatically controlled by METAMORPH 6.3r-1 software (Molecular Devices, Silicon Vally, CA, USA) as described previously . Some live images of Venus-labeled cells were captured manually using a different system composed of an inverted epifluorescence microscope (IX71, Olympus) equipped with a 20× objective lens (UPlanApo; numerical aperture = 0.70) and a cooled CCD camera (ORCA-ER, Hamamatsu Photonics, Hamamatsu, Shizuoka, Japan) and IPLab 3.6 software (Scanalytics, Inc., Rockville, MD, USA). The same manual capturing system was used for most of the presented immunofluorescence images. For some of the immunostained specimens, confocal microscopy was performed using a Yokogawa CSU10 (40×, 100×) (Tokyo, Japan) and an Olympus FV1000 (40×) (Tokyo, Japan).
For single cell-level visualization within cerebellar primordia, fine crystals (< 30 μm) of DiI C18(3) (1,1-dioctadecyl-3,3,3,3-tetramethylindocarbocyanine perchlorate; D-282, Molecular Probes, Eugene, OR, USA) were inserted into live cerebella from the pial surface using a small make-up brush, and slices were made and incubated at 37°C (40% O2 and 5% CO2) for 1 to 2 h. After live identification of DiI-labeled cells, slices were fixed and further processed for immunostaining. For labeling of afferent fibers from the vestibular ganglion and those of the cerebellar peduncle, crystals of DiI were inserted into fixed brains using forceps. The DiI-inserted brains were incubated at 37°C for several days, and then vibratome sectioned.
In situ hybridization
Probes to determine the expression of vldlr, apoER2, and mDab1 were designed according to Trommsdorff et al. . Cerebella were fixed with 4% paraformaldehyde at 4°C overnight. Frozen sections (16 μm) were pretreated with 4% paraformaldehyde (5 minutes), 0.1 M triethanolamine/0.25% acetic anhydride (10 minutes), and hybridized at 60°C for 15 h in a solution containing 50% formamide, 0.1% SDS, 0.64 mg/ml tRNA, and 0.5 μg/ml riboprobe.
apolipoprotein E receptor 2
Dulbecco's modified Eagle's medium
external granular layer
green fluorescent protein
very low-density lipoprotein receptor
We are very grateful to T Shimogori for instructing on in utero surgery and critical reading of the manuscript, Y Tomooka, M Yamamoto, M Watanabe for antibodies, E Ito, K Ota, O Noritake, Y Noritake, T Miwa, and S Yamamoto for technical support, and the Developmental Studies Hybridoma Bank at the University of Iowa for monoclonal antibodies. This work was supported by grants from the Japanese Ministry of Education, Science, Sports and Culture (20021016, 21240027), Uehara Memorial Foundation, Brain Science Foundation, and Life Sciences Foundation.
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