- Research article
- Open Access
RBP-J is not required for granule neuron progenitor development and medulloblastoma initiated by Hedgehog pathway activation in the external germinal layer
Neural Development volume 5, Article number: 27 (2010)
The Notch signalling pathway plays crucial roles in neural development, functioning by preventing premature differentiation and promotion of glial cell fates. In the developing cerebellum Notch pathway components are expressed in granule neuron progenitors of the external germinal layer (EGL) but the precise function of Notch in these cells is unclear. The Hedgehog pathway is also crucial in cerebellar development, mainly via control of the cell cycle, and persistent activation of the pathways leads to the cerebellar tumour medulloblastoma. Interactions between Hedgehog and Notch have been reported in normal brain development as well as in Hedgehog pathway induced medulloblastoma but the molecular details of this interaction are not known and we investigate here the role of Notch signalling in the development of the EGL and the intersection between the two pathways in cerebellar granule neuron progenitors and in medulloblastoma.
RBP-J is the major downstream effector of all four mammalian Notch receptors and the RBP-J conditional mouse facilitates inactivation of canonical Notch signals. Patched1 is a negative regulator of Hedgehog signalling and the Patched1 conditional mouse is widely used to activate Hedgehog signalling via Patched1 deletion in specific cell types. The conditional mouse lines were crossed with a Math1-Cre line to delete the two genes in granule neuron progenitors from embryonic day 10.5. While deletion of only Patched1 as well as Patched1 together with RBP-J leads to formation of medulloblastoma concomitant with disorganisation of cell layers, loss of RBP-J from granule neuron progenitors has no obvious effect on overall cerebellar morphology or differentiation and maturation of the different cerebellar cell types.
Our results suggest that even though Notch signalling has been shown to play important roles in cerebellar development, signalling via RBP-J is surprisingly not required in granule neuron progenitors. Furthermore, RBP-J inactivation in these cells does not influence the formation of medulloblastoma initiated by Hedgehog pathway activation. This may suggest a requirement of Notch in cerebellar development at a different developmental stage or in a different cell type than examined here - for example, in the neural stem cells of the ventricular zone. In addition, it remains a possibility that, in granule neuron progenitors, Notch may signal via an alternative pathway without the requirement for RBP-J.
The Notch signalling pathway plays crucial roles in brain development and in the cerebellum in particular. The main function of Notch is preventing (premature) differentiation of neural progenitor cells and at later stages of neural development promoting glial over neuronal cell fates [1–5]. In vitro analyses as well as in vivo murine models have shown that, in the cerebellum, the Notch pathway influences the development of Bergmann glia and the differentiation of granule neuron progenitors (GNPs) [6–10].
There are four Notch receptor paralogues (Notch1-4) in vertebrates, all of which bind transmembrane ligands of the Delta-like and Jagged family [3, 11, 12]. Upon binding of ligand, the Notch receptor is proteolytically cleaved and its intracellular domain translocates to the nucleus where it forms a complex with several co-factors and the DNA binding protein RBP-J (Recombination signal binding protein for immunoglobulin kappa J region; also called CSL for CBF1 in mammalians, Suppressor of Hairless in Drosophila, Lag-1 in C. elegans), the major canonical downstream effector of the Notch pathway [3, 13, 14]. The complex then facilitates the expression of target genes, including basic helix-loop-helix transcription factors, such as Hes1 and Hes5, which act as transcriptional repressors of proneural genes [15–18]. Possible alternative 'non-canonical' downstream pathways of Notch that are RBP-J independent have also been reported [19–22].
Of the Notch receptors, Notch1, Notch2 and Notch3 are most important for cerebellar development and the roles of each receptor vary at different developmental stages [7, 23]. During granule neuron development, Notch2 is expressed predominantly in proliferating GNPs of the external germinal layer (EGL), and Notch1 in postmitotic differentiating cells in the internal granule layer (IGL) [10, 24]. Of the five Notch ligands, Delta-like 3 (Dll3) is mainly expressed in GNPs while Jagged2 is expressed in differentiating and mature neurons of the IGL . The specific expression patterns of Notch receptors and ligands in cerebellar development suggest diverse and cell-type-specific roles for the Notch pathway; however, detailed functions of Notch components in cerebellar cell types are not known. Accordingly, we examine here the role of canonical Notch signalling in cerebellar GNPs.
In addition to its function in normal brain development, the Notch pathway has also been implicated in tumour formation, in particular in medulloblastoma. Notch can act as an oncogene or tumour suppressor and different receptors appear to have varying tumorigenicity . In various mouse models of medulloblastoma initiated by perturbation of the Hedgehog (Hh) pathway, Notch pathway components are upregulated, indicating both a potentially oncogenic role for Notch and possibly an interaction between the two pathways [26, 27]. Hh signalling controls many patterning events of embryonic development via cell cycle regulation, and deregulation of the pathway often results in tumorigenesis. In the absence of Hh ligand the transmembrane receptor Patched1 (Ptc1) inhibits Smoothened (Smo) while Hh binding results in a release of the repression of Smo by Ptc1 and in a cascade of phosphorylation events [28, 29]. Consequently, active Gli transcription factors translocate to the nucleus where they can activate expression of target genes such as Cyclins D1, D2 and E and N-Myc [30–34].
We have shown recently that the Hh and Notch pathways interact during cerebellar development in ventricular zone stem cells but this interaction remains to be defined at other stages of cerebellar development and in other cerebellar cell types . In particular, even though Notch pathway components are clearly expressed in the EGL of the developing cerebellum at a time when GNPs are dividing rapidly and then differentiating under the influence of Purkinje-neuron-derived Sonic hedgehog (Shh), it is not known whether Notch signalling is actually required for appropriate formation of granule neurons.
We addressed the interaction of Notch and Hh signalling during granule neuron development and in medulloblastoma formed from GNPs by adopting a genetic approach in vivo to ablate Notch signalling in the Ptc1 conditional mouse model, which is a widely accepted and relevant model for human medulloblastoma [36–38]. Since the developing EGL expresses multiple components of the Notch signalling pathway, we took the approach to inactivate the common pathway effector RBP-J in order to ablate canonical Notch receptor signalling. This strategy has been previously applied in analyses of Notch signalling and has proved to be highly effective [8, 35, 39, 40]. A Cre-expressing transgenic line facilitated deletion of the two genes in Math1+ cells (Math1-Cre) of the rhombic lip and EGL . Surprisingly, we found no requirement for RBP-J for the proliferation, differentiation or migration of granule neuron precursors. Also, loss of RBP-J concomitant with activation of the Hh pathway in GNPs did not block medulloblastoma formation. Our data suggest that the function of Notch signalling, as distinct from the expression of Notch signalling components during cerebellar development, is restricted to cell types other than GNPs, that is, stem cells of the ventricular zone and cerebellar cells originating from there.
Math1-Cre efficiently inactivates the Patched1 and RBP-Jgenes in the external germinal layer
Math1-Cre results in Cre expression in Math1-positive cells of the rhombic lip from embryonic day 10.5 (E10.5), and in GNPs in the EGL that have not begun to differentiate into mature neurons . To validate the model used in this study, we first confirmed deletion of both the Patched1 and RBP-J alleles by Math1-Cre. GNPs isolated from P7 RBP-Jlox/lox; Math1-Cre mice show high efficiency of floxing by RT-PCR with primers flanking the excised region (exons 6 and 7; Figure 1A). Floxing of RBP-J was confirmed by Taqman and in situ analysis for RBP-J mRNA, which showed significant loss of wild-type RBP-J mRNA in mutant GNPs compared to controls (Figure 1B,C). In addition, we assayed mRNA expression of the direct Notch target gene Hey2 by quantitative real time PCR (Additional file 1). Hey2 mRNA is significantly decreased after RBP-J deletion (P = 0.0157). The Patched1 allele was also deleted with high efficiency by Math1-Cre, as shown by RT-PCR with primers flanking the excised exon 3. Pathway activation due to Patched1 deletion was confirmed by Taqman analysis showing significant upregulation of the universal Hh target Gli1 in Ptc1lox/lox; Math1-Cre GNPs compared to Ptc1lox/lox GNPs (Figure 1D,E). To further validate our model, we performed in situ hybridisation and immunofluorescence staining to characterise the expression of Hh and Notch pathway targets in the mutants. In situ analysis for Gli1 supports Hh activation in the EGL of Ptc1 deleted as well as Ptc1 and RBP-J deleted mice (Figure 2B,D). Interestingly, our in situ analysis also suggests a reduction of Gli1 expression in RBP-Jlox/lox; Math1-Cre cerebella, indicating that RBP-J deleted GNPs might not be able to adequately respond to Shh ligand secreted by Purkinje neurons (Figure 2C). The canonical Notch target Hes1 (Hairy enhancer of split) is expressed in the outer EGL of control mice (Figure 2E). However, Hes1 has also been reported to be a target of Hh signalling [41, 42] and the Hes1-positive area appears expanded in response to Hh activation, with staining throughout the EGL of Ptc1 deleted brains (Figure 2F). RBP-J deletion neither leads to loss of Hes1 nor can it overcome the increase of Hes1-positive cells in the Ptc1 deleted cerebellum (Figure 2G,H). The canonical Notch target Hes5 is expressed in the outer EGL of control mice, with an expansion towards the inner EGL in Hh activated mice, similar to Hes1 (Figure 2I,J). RBP-J deletion results in loss of Hes5 expression; however, some cells of Ptc1lox/lox;RBP-Jlox/lox;Math1-Cre EGL express Hes5, possibly due to proliferation of a small number of GNPs with incomplete deletion of RBP-J in these mutants (Figure 2K,L). Taken together, our data confirm that Math1-Cre efficiently deletes both Patched1 and RBP-J alleles and consequently leads to GNP-specific activation of Hh and inactivation of Notch signalling, respectively.
Loss of RBP-Jin GNPs does not alter cerebellar morphology
To examine the effects of Hh pathway activation and Notch inactivation on the development and differentiation of cerebellar cell types, we first analysed mutant brains at three developmental stages (E18.5, postnatal day 7 (P7) and P21) histologically by haematoxylin and eosin staining. At E18.5 all mutants are morphologically similar to control cerebellum, with a normal appearing EGL and beginning foliation (Figure 3A-D). By P7, control cerebellum has developed ten folia and GNPs have begun to differentiate and form an IGL, which is fully developed by P21 with no EGL remaining (Figure 3E,I). RBP-J deletion has no discernable effect on morphology throughout cerebellar development (Figure 3G,K). Ptc1 deletion results in an increase of GNPs in the EGL and, therefore, a thickening of this region, which develops into medulloblastoma by P21. Foliation appears largely unaffected, with the correct number of lobes present, and some GNPs have been able to differentiate and migrate to form an IGL. The boundaries between the EGL, molecular layer (ML) and IGL appear disturbed, likely due to the excessive expansion of GNPs (Figure 3F,J). Notch inhibition by RBP-J deletion does not alter this phenotype (Figure 3H,L). In summary, GNP-specific deletion of RBP-J does not affect the morphology of the cerebellum with or without Ptc1 deletion.
RBP-Jdeletion does not influence the development of Hedgehog-pathway-induced medulloblastoma
Mice with GNP-specific deletion of the negative Hh regulator Ptc1 develop severe medulloblastoma by P21 in 100% of cases and this phenotype, as well as the overall morphology (Figure 3J,L) are not altered by loss of canonical Notch signalling. We examined tumours of both genotypes (Ptc1lox/lox;Math1-Cre and Ptc1lox/lox;RBP-Jlox/lox;Math1-Cre) in more detail and observed that the tumour mass is made up of small round granular cells interspersed with stroma in both cases (Figure 4A,B), similar to human medulloblastoma and as previously published . Both also stain positively for the granule cell marker Pax6, confirming a GNP origin of the tumours (Figure 4C,D). Staining with proliferating cell nuclear antigen (PCNA) reveals that most cells in both genotypes are actively undergoing proliferation (Figure 4E,F). The universal Hh target Gli1 is expressed in Ptc1 deleted tumours as well as in those with additional loss of RBP-J (Figure 4G,H), as is Hes1, a target of both the Hh and Notch pathways (Figure 4I,J). The canonical Notch target Hes5, however, which requires RBP-J, is expressed in Hh activated tumours but lost in most cells of tumours with activated Hh and inactivated Notch signalling (Figure 4K,L). In conclusion, even though Notch signalling is lost in the majority of cells in Ptc1lox/lox;RBP-Jlox/lox;Math1-Cre tumours, as confirmed by loss of Hes5 mRNA, RBP-J deletion does not appear to influence the characteristics of medulloblastoma initiated by Ptc1 deletion in GNPs.
Differentiation of cerebellar cell types does not depend on canonical Notch signalling via RBP-J
Following the characterisation of Ptc1 and RBP-J deleted medulloblastoma, we investigated cerebellar development in more detail by using immunofluorescence staining with markers specific for different cerebellar cell types. At E18.5, GNPs have migrated from the rhombic lip to form the EGL and neuronal differentiation is in progress. BetaIII-tubulin staining confirmed the presence of immature neurons migrating away from the EGL in control embryos and in all mutants (Figure 5A-D). GNPs in the EGL proliferate in response to Shh, which is secreted by Purkinje neurons, and at P7 the peak of proliferation is reached. PCNA staining confirmed that cells in the outer EGL of the control and RBP-J deleted cerebellum are mitotically active (Figure 5E,G). Ptc1 deletion results in an expansion of the proliferative compartment, which is not influenced by loss of Notch signalling (Figure 5F,H). However, even when Ptc1 deletion is present, GNPs in the inner EGL can differentiate and begin to express betaIII-tubulin in addition to the granule cell marker Pax6 (Figure 5J). The same is evident when the Notch pathway is inhibited in addition to Hh activation (Figure 5L) and differentiation of RBP-Jlox/lox;Math1-Cre GNPs into neurons is initiated normally (Figure 5K,I). GNPs isolated from P7 to P8 cerebellum and stained for PCNA, betaIII-tubulin, NeuN (Neuronal nuclei) and by TUNEL in vitro confirm no obvious difference in proliferation, differentiation and apoptosis rates between RBP-Jlox/lox controls and RBP-Jlox/lox;Math1-Cre mutants (Additional file 2A-H). Culture of GNPs for 3 days in the absence and presence of recombinant Shh-N reveals that RBP-J deletion also has no influence on the proliferative response to Shh as assayed by immunofluorescence for PCNA (Additional file 2I-L) and cell count (Additional file 2M). By P21 most cerebellar differentiation processes are complete and the layering of the mature cerebellum is present. Mature, NeuN-positive neurons populate the IGL while Bergman glial fibres, marked by glial fibrillary acidic protein (GFAP), span the ML in parallel to each other (Figure 5M). Notch ablation does not influence either of these cell types (Figure 5O). Ptc1 deletion, however, results in a severe disorganisation of Bergman glial fibres as well as the presence of NeuN-positive cells in the remainder of the expanded EGL. These cells are likely to be differentiated granule neurons that were hindered from migrating into the IGL by the bulk of proliferating tumour cells (Figure 5N). The same phenotype is evident in Hh-activated cerebella with additional RBP-J deletion (Figure 5P). Purkinje neurons, marked by Calbindin, are organised in a single layer around the surface of the IGL with their fibres reaching into the ML in control brains as well as in Notch deficient cerebella (Figure 5Q,S). In Hh-activated as well as Hh-activated and Notch-inactivated brains the Purkinje neuron layer is disrupted and lacks organisation of cell bodies as well as orientation of their fibres (Figure 5R,T). Overall, the differentiation of cerebellar cell types appears unaffected by RBP-J deletion and the disorganisation of cell layers in medulloblastoma initiated by Ptc1 deletion cannot be overcome by canonical Notch inactivation.
GNP-specific deletion of RBP-J and Ptc1does not influence the cerebellar stem and progenitor cell pool
Next we asked whether Hh activation and/or Notch inactivation in GNPs influences the stem and progenitor cell pool of developing cerebella. To examine cerebellar stem cell properties, we used Sox2, which marks neural stem cells and Bergman glia. In controls as well as all mutants, cerebellar stem cells residing in the ventricular zone (VZ) stain positive for Sox2. In addition, all genotypes show some Sox2-positive cells throughout the cerebellum, Bergman glia originating from the VZ, which are migrating towards the ML (Additional file 3A-D). In Ptc1lox/lox; Math1-Cre mice background staining appears increased, although there is no apparent difference in nuclear Sox2 staining (Additional file 3B). Furthermore, we utilised the neurosphere assay, a widely used tool to examine stem/progenitor cell numbers. The number of colonies counted in this assay is indicative of the number of stem/progenitor cells in the population but it cannot distinguish between the two. No significant difference was observed in colony numbers after deletion of Ptc1 or RBP-J compared to controls after 5 days of incubation of single cell suspensions of P7 cerebella (Additional file 3E). Taken together, GNP-specific deletion of Ptc1 and RBP-J appears to have no effect on the cerebellar stem/progenitor cell pool.
The Notch signalling pathway influences cerebellar development, in particular the differentiation of neurons and glia. Loss of the Notch1 receptor or the ligand Jagged1 in neuroepithelial cells results in premature differentiation of GNPs and defects in neuronal migration, and RBP-J plays a crucial role in the development and migration of Bergman glia [8, 43, 44]. Signalling from the Notch2 receptor appears to have a role opposing that of Notch1 in GNPs, promoting proliferation while inhibiting differentiation [10, 24]. Several studies have also suggested a role for Notch signalling in the formation of medulloblastoma [26, 27, 45]. Multiple components of the Notch pathway are expressed in the EGL, so here we investigate the role of canonical Notch signalling in GNPs by deletion of the common Notch effector RBP-J in Math1+ cells and the consequences of Notch signal inactivation on the initiation and development of Hh-pathway-dependent medulloblastoma.
First we confirmed the validity of our model using RT-PCR, quantitative real-time PCR and in situ analysis, showing high efficiency of floxing for both the Ptc1 and RBP-J alleles, resulting in Hh pathway upregulation and Notch inactivation in GNPs, respectively (Figures 1 and 2; Additional file 1). The overall morphology of cerebella with RBP-J deleted GNPs appeared normal, with foliation and layer formation identical to control cerebella. Hh activation by Ptc1 deletion had no effect until after birth, when GNPs in the EGL excessively proliferate and lead to medulloblastoma formation by P21 in all individuals, as we have shown previously  (Figure 3). Even though RBP-J deletion did not appear to alter overall cerebellar development, we then asked if it had a more subtle impact on differentiation or migration of cerebellar cell lineages. Notch signalling has been shown to be critical for neuronal and glial differentiation and migration in cerebellar development and we therefore examined the different cell types of the cerebellum using lineage-specific markers. We found that loss of RBP-J from GNPs has no effect on neuronal differentiation and migration. This finding appears to be in direct contrast to a report demonstrating defects in granule cell migration after loss of the Notch ligand Jagged1 . However, deletion in the above-mentioned study led to a deficit of Bergman glia, which act as migratory scaffolds for GNPs, and it was therefore found that the GNP defect was likely secondary to the loss of Bergmann glia. Furthermore, GNP-specific RBP-J deletion cannot overcome the cerebellar disorganisation resulting from Ptc1 deletion and medulloblastoma formation (Figures 4 and 5). This raises the question of whether Notch signalling in GNPs is transduced via alternative pathways that are independent of canonical Notch signalling via RBP-J. Indeed, work by Mizutani et al.  indicates that, in contrast to neural stem cells, more committed neural progenitor cells may use alternative Notch pathways without a requirement for RBP-J. In the absence of Notch signals RBP-J could potentially function as a transcriptional repressor, so loss of RBP-J may have an effect even on cells that do not usually require active Notch signalling. It has been suggested that this function of RBP-J does not play a crucial role in mammals and the absence of a phenotype after RBP-J deletion in our model confirms this specifically for GNPs . An alternative explanation for the lack of an effect of RBP-J deletion on GNPs is that Notch signalling may be required at an earlier time point, before commitment to the granule cell lineage. In accordance with this, inactivation of Notch signalling at early embryonic time points has a severe impact on cerebellar development and Notch has also been implicated in controlling the balance between symmetric and asymmetric stem cell division in a number of tissues, including the brain [[3, 44], and our unpublished results]. In addition, we have shown previously that RBP-J deletion in the cerebellar VZ induces an increase in progenitor cell numbers in the niche due to a loss of stem cells and a delay in differentiation . Therefore, we next examined the properties of the cerebellar stem/progenitor cell niche by Sox2 staining and neurosphere assays. Neither approach indicated an effect of RBP-J deletion (Additional file 3), likely due to the specificity of Math1-Cre, which deletes in GNPs after they have left the VZ, the cerebellar stem cell niche, and committed to the granule cell lineage.
In addition to RBP-J deletion having no impact on the differentiation of cerebellar cell types and the stem/progenitor cell niche, we also found that loss of canonical Notch signalling does not influence the formation of Hh-dependent medulloblastoma (Figures 3H,L, 4, and 5D,H,L,P,T). We confirmed loss of Hes5 mRNA in the majority of tumour cells and thereby excluded the possibility that the minority of cells deleted for Ptc1 but not for RBP-J may have had a growth advantage and populated the tumour mass (Figure 4K,L). The absence of any impact of RBP-J deletion on tumour formation was surprising as several studies have noted dysregulation of Notch pathway components in both human and murine medulloblastoma, including the transcription factor targets Hes1 and Hes5, and the expression of Hes1 is associated with poor clinical outcome [24, 26, 27, 45, 47]. Medulloblastoma cell lines treated with γ-secretase inhibitors that block Notch receptor endoproteolysis display reduced growth, clonogenicity and tumorigenicity, and γ-secretase inhibitors have been proposed as a chemotherapeutic approach to treating medulloblastoma [27, 48, 49]. Cerebella of mice with both Ptc1 and RBP-J deletion appear identical in morphology to those with deletion of Ptc1 alone, and expression of cell-type-specific markers and all mutant mice develop severe medulloblastoma by P21. This indicates that canonical Notch signalling is likely not required for the development of medulloblastoma initiated by Hh pathway activation in GNPs. However, we cannot exclude the possibility that there might be some influence of RBP-J deletion on tumour latency, and a more extensive study with a large number of mutant mice of both genotypes would be required to address this question.
We have shown here that canonical Notch signalling via RBP-J is not required in GNPs and Hh-pathway-dependent medulloblastoma. A crucial role for Notch signalling in cerebellar development has been shown previously and we conclude that the involvement of the Notch pathway may be restricted to the stem/progenitor cell niche and loses influence as cells commit to the granule neuron lineage. This is despite the observation that Notch pathway components such as Notch1, Notch2, Notch3, Dll3, Jagged1, Hes1, and Hes5 are expressed in the EGL, underlining the fact that it is important not to confuse detectable expression of a signalling pathway with it necessarily functioning in that tissue. Additional work is required to characterise the role of Notch in cerebellar development, in particular to define the developmental stage(s) when it is required and to identify the utilised downstream effectors.
Materials and methods
All work involving mice was performed with approval and according to guidelines of the University of Queensland Animal Ethics Committee. Mouse models used were Ptc1 conditional mice  and RBP-J conditional mice  crossed with a Math1-Cre line (kindly provided by David Rowitch).
Isolation and culture of granule neuron progenitors
Cerebellar GNPs were isolated from P7 to P8 pups as described previously . In brief, cerebella were dissected and cells dissociated and triturated, followed by centrifugation through a 35 to 65% percoll gradient (Amersham Biosciences, now GE Healthcare Bio-Sciences Corp., Picataway, NJ, USA) in order to segregate granule neurons from astrocytes. Isolated GNPs were washed and used for subsequent experiments.
Culture of GNPs in the presence or absence of 3 μg/ml Shh-N (R&D Systems, Minneapolis, MN, USA) was performed at a density of 5 × 105 cells per well in 12-well plates with poly-L-lysine (Sigma Aldrich, St Louis, MO, USA) coated coverslips in NB-B27 media (Neurobasal with 1 mM sodium pyrovate, 2 mM L-glutamine, penicillin/streptomycin, and B27 supplement, all from Invitrogen, Carlsbad, CA, USA).
RT-PCR and quantitative RT-PCR
RNA was extracted from cells using the RNeasy Mini Kit by QIAgen (Hilden, Germany) according to the manufacturer's manual. Reverse transcription was performed using the Superscript III system by Invitrogen. The following primers were used for PCR detection of the RBP-J floxed allele: forward 5' CATCTCCAAACCCTCCAAAA 3', reverse 5' GTCCAGGAAGCTCCATCGT 3'; and the Patched1 floxed allele: forward 5'-CACCGTAAAGGAGCGTTACCTA-3', reverse 5'-TGGTTGTGGGTCTCCTCATATT-3'. Quantitave PCR was performed with Assays on Demand by Applied Biosystems for RBP-J (Mm00770450_m1), Gli1 (Mm00494645_m1), and Hey2 (Mm00469280_m1) according to the manufacturer's protocol on the ABI Prism 7000 equipment by Applied Biosystems (Austin, TX, USA). Measurements were taken in three technical replicates and data were normalized to the housekeeping gene GAPDH (assay ID 4352339E). Statistical analysis was performed using Graphpad Prism 4 (Graphpad Software, La Jolla, CA, USA) for unpaired t-tests.
Immunofluorescence, TUNEL and haematoxylin and eosin staining
Brains were dissected (after cardiac perfusion for P7 and P21 mice) and fixed in 4% paraformaldehyde overnight. Subsequently, samples were either embedded in paraffin or cryoprotected in 30% sucrose followed by embedding in OCT compound. Antigen retrieval of deparaffinised wax tissue sections or defrosted cryosections was performed by boiling in antigen unmasking solution (Vector Laboratories, Burlingame, CA, USA). Sections were blocked in 4% horse serum, 1% bovine serum albumin and 0.2% Triton-X in phosphate-buffered saline prior to primary antibody incubation overnight at 4°C. Slides were incubated with secondary antibodies for 1 h at room temperature. For immunofluorescence, a DAPI counterstain (1:10,000; Sigma Aldrich) was performed prior to mounting with Fluorescence Mounting Media (Dako, Carpentaria, CA, USA). For histological analysis, deparaffinised and rehydrated sections were stained in haematoxylin (Vector Laboratories) and eosin Y (Sigma Aldrich) and mounted in Entellan. Antibodies used were betaIII-tubulin (1:2,000; Promega Corporation, Madison, WI, USA), Sox2 (1:200; R&D Systems), PCNA (1:100; Invitrogen), GFAP (1:500; Dako), NeuN (1:100; Chemicon, Temecula, CA, USA), Calbindin (1:200; Sigma) and Hes1 (1:400; a gift from R Kageyama, Kyoto, Japan) on paraffin sections, and Pax6 (1:300; Covance, Princeton, NJ, USA), together with betaIII-tubulin on frozen sections. Fluorescent secondary antibodies used were anti-rabbit Alexa555 (1:250; Invitrogen), anti-mouse Alexa488 (1:250; Invitrogen) and anti-goat Cy3 (1:250; Abacus ALS Pty Ltd, Brisbane, Australia). For Sox2 staining, the brightness of all images was increased by the same level to make positive staining better visible. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) was performed with the In Situ Cell Death Detection Kit (Fluorescein; Roche Diagnostics, Mannheim, Germany) according to the manufacturer's protocol.
In situ hybridisation was performed as previously published . In summary, probes were prepared using DIG labelled probe amplification followed by phenol/chloroform extraction and precipitation. Paraffin-embedded sections (6 μm) were treated with 2 μg/ml ProK (Roche Diagnostics) in TE buffer, fixed in 4% paraformaldehyde and acetylated. Hybridisation was performed in hybridisation buffer at 64°C for Gli1 and 65°C for Hes5 and RBP-J over night. A series of saline-sodium citrate (SSC) washes was followed by blocking and washing (DIG block and wash buffer set, Roche) before incubation with anti-DIG-AP antibody (Roche). Colour reaction was performed using 3.5 mg/ml nitroblue tetrazolium (NBT) and 1.75 mg/ml 5-bromo-4-chloro-3-indolyl-phosphate (BCIP) (both Roche) in 10% polyvinylalcohol (PVA) (Sigma). Colour formation was stopped in TE solution followed by counter staining with nuclear fast red (Vector Labs), post-fixation and mounting.
Probes used were Gli1 (a gift from A Joyner, New York, NY, USA), RBP-J (a gift from T Honjo, Kyoto, Japan) and Hes5 (a gift from R Kageyama, Kyoto, Japan).
Light and general fluorescence microscopy were performed using an Olympus BX-51 upright microscope. Confocal images were taken on a Zeiss LSM 510 META.
Stem/progenitor cell analysis
P7 cerebellar cells were harvested and subsequently dissociated. For neurosphere assays, cells were plated at a density of 1 × 105 cells per ml in 200 μl Neurosphere assay media (Neurosphere media containing 10% Neurocult neural stem cell proliferation supplement (Stem Cell Technologies, Tullamarine, VIC), 5% bovine serum albumin (Sigma), 1% penicillin/streptomycin) containing epidermal growth factor (20 ng/ml) in a 96-well plate. For each individual the assay was set up in triplicates. The number of spheres per well was counted 5 days after plating. Statistical analysis was performed using Graphpad Prism 4 for unpaired t-tests.
external germinal layer
glial fibrillary acidic protein
granule neuron progenitor
Hairy enhancer of split 1
internal granule layer
proliferating cell nuclear antigen
Recombination signal binding protein for immunoglobulin kappa J region
terminal deoxynucleotidyl transferase dUTP nick end labelling
Artavanis-Tsakonas S, Rand MD, Lake RJ: Notch signaling: cell fate control and signal integration in development. Science. 1999, 284: 770-776. 10.1126/science.284.5415.770.
Gaiano N, Nye JS, Fishell G: Radial glial identity is promoted by Notch1 signaling in the murine forebrain. Neuron. 2000, 26: 395-404. 10.1016/S0896-6273(00)81172-1.
Louvi A, Artavanis-Tsakonas S: Notch signalling in vertebrate neural development. Nat Rev Neurosci. 2006, 7: 93-102. 10.1038/nrn1847.
Mizutani K, Saito T: Progenitors resume generating neurons after temporary inhibition of neurogenesis by Notch activation in the mammalian cerebral cortex. Development. 2005, 132: 1295-1304. 10.1242/dev.01693.
Taylor MK, Yeager K, Morrison SJ: Physiological Notch signaling promotes gliogenesis in the developing peripheral and central nervous systems. Development. 2007, 134: 2435-2447. 10.1242/dev.005520.
Hatakeyama J, Bessho Y, Katoh K, Ookawara S, Fujioka M, Guillemot F, Kageyama R: Hes genes regulate size, shape and histogenesis of the nervous system by control of the timing of neural stem cell differentiation. Development. 2004, 131: 5539-5550. 10.1242/dev.01436.
Irvin DK, Zurcher SD, Nguyen T, Weinmaster G, Kornblum HI: Expression patterns of Notch1, Notch2, and Notch3 suggest multiple functional roles for the Notch-DSL signaling system during brain development. J Comp Neurol. 2001, 436: 167-181. 10.1002/cne.1059.
Komine O, Nagaoka M, Watase K, Gutmann DH, Tanigaki K, Honjo T, Radtke F, Saito T, Chiba S, Tanaka K: The monolayer formation of Bergmann glial cells is regulated by Notch/RBP-J signaling. Dev Biol. 2007, 311: 238-250. 10.1016/j.ydbio.2007.08.042.
Schuurmans C, Guillemot F: Molecular mechanisms underlying cell fate specification in the developing telencephalon. Curr Opin Neurobiol. 2002, 12: 26-34. 10.1016/S0959-4388(02)00286-6.
Solecki DJ, Liu XL, Tomoda T, Fang Y, Hatten ME: Activated Notch2 signaling inhibits differentiation of cerebellar granule neuron precursors by maintaining proliferation. Neuron. 2001, 31: 557-568. 10.1016/S0896-6273(01)00395-6.
Lathia JD, Mattson MP, Cheng A: Notch: from neural development to neurological disorders. J Neurochem. 2008, 107: 1471-1481. 10.1111/j.1471-4159.2008.05715.x.
Ohishi K, Varnum-Finney B, Bernstein ID: The notch pathway: modulation of cell fate decisions in hematopoiesis. Int J Hematol. 2002, 75: 449-459. 10.1007/BF02982106.
Bray SJ: Notch signalling: a simple pathway becomes complex. Nat Rev Mol Cell Biol. 2006, 7: 678-689. 10.1038/nrm2009.
Hurlbut GD, Kankel MW, Lake RJ, Artavanis-Tsakonas S: Crossing paths with Notch in the hyper-network. Curr Opin Cell Biol. 2007, 19: 166-175. 10.1016/j.ceb.2007.02.012.
Carlson ME, Conboy IM: Regulating the Notch pathway in embryonic, adult and old stem cells. Curr Opin Pharmacol. 2007, 7: 303-309. 10.1016/j.coph.2007.02.004.
Gohlke JM, Armant O, Parham FM, Smith MV, Zimmer C, Castro DS, Nguyen L, Parker JS, Gradwohl G, Portier CJ, Guillemot F: Characterization of the proneural gene regulatory network during mouse telencephalon development. BMC Biol. 2008, 6: 15-10.1186/1741-7007-6-15.
Marino S: Medulloblastoma: developmental mechanisms out of control. Trends Mol Med. 2005, 11: 17-22. 10.1016/j.molmed.2004.11.008.
Kageyama R, Ohtsuka T: The Notch-Hes pathway in mammalian neural development. Cell Res. 1999, 9: 179-188. 10.1038/sj.cr.7290016.
Hori K, Cholewa-Waclaw J, Nakada Y, Glasgow SM, Masui T, Henke RM, Wildner H, Martarelli B, Beres TM, Epstein JA, Magnuson MA, Macdonald RJ, Birchmeier C, Johnson JE: A nonclassical bHLH Rbpj transcription factor complex is required for specification of GABAergic neurons independent of Notch signaling. Genes Dev. 2008, 22: 166-178. 10.1101/gad.1628008.
Liao WR, Hsieh RH, Hsu KW, Wu MZ, Tseng MJ, Mai RT, Wu Lee YH, Yeh TS: The CBF1-independent Notch1 signal pathway activates human c-myc expression partially via transcription factor YY1. Carcinogenesis. 2007, 28: 1867-1876. 10.1093/carcin/bgm092.
Ramain P, Khechumian K, Seugnet L, Arbogast N, Ackermann C, Heitzler P: Novel Notch alleles reveal a Deltex-dependent pathway repressing neural fate. Curr Biol. 2001, 11: 1729-1738. 10.1016/S0960-9822(01)00562-0.
Talora C, Campese AF, Bellavia D, Felli MP, Vacca A, Gulino A, Screpanti I: Notch signaling and diseases: an evolutionary journey from a simple beginning to complex outcomes. Biochim Biophys Acta. 2008, 1782: 489-497.
Mason HA, Rakowiecki SM, Gridley T, Fishell G: Loss of notch activity in the developing central nervous system leads to increased cell death. Dev Neurosci. 2006, 28: 49-57. 10.1159/000090752.
Fan X, Mikolaenko I, Elhassan I, Ni X, Wang Y, Ball D, Brat DJ, Perry A, Eberhart CG: Notch1 and notch2 have opposite effects on embryonal brain tumor growth. Cancer Res. 2004, 64: 7787-7793. 10.1158/0008-5472.CAN-04-1446.
Irvin DK, Nakano I, Paucar A, Kornblum HI: Patterns of Jagged1, Jagged2, Delta-like 1 and Delta-like 3 expression during late embryonic and postnatal brain development suggest multiple functional roles in progenitors and differentiated cells. J Neurosci Res. 2004, 75: 330-343. 10.1002/jnr.10843.
Dakubo GD, Mazerolle CJ, Wallace VA: Expression of Notch and Wnt pathway components and activation of Notch signaling in medulloblastomas from heterozygous patched mice. J Neurooncol. 2006, 79: 221-227. 10.1007/s11060-006-9132-2.
Hallahan AR, Pritchard JI, Hansen S, Benson M, Stoeck J, Hatton BA, Russell TL, Ellenbogen RG, Bernstein ID, Beachy PA, Olson JM: The SmoA1 mouse model reveals that notch signaling is critical for the growth and survival of sonic hedgehog-induced medulloblastomas. Cancer Res. 2004, 64: 7794-7800. 10.1158/0008-5472.CAN-04-1813.
Ingham PW, Taylor AM, Nakano Y: Role of the Drosophila patched gene in positional signalling. Nature. 1991, 353: 184-187. 10.1038/353184a0.
Ingham PW, McMahon AP: Hedgehog signaling in animal development: paradigms and principles. Genes Dev. 2001, 15: 3059-3087. 10.1101/gad.938601.
Adolphe C, Hetherington R, Ellis T, Wainwright B: Patched1 functions as a gatekeeper by promoting cell cycle progression. Cancer Res. 2006, 66: 2081-2088. 10.1158/0008-5472.CAN-05-2146.
Ohlmeyer JT, Kalderon D: Hedgehog stimulates maturation of Cubitus interruptus into a labile transcriptional activator. Nature. 1998, 396: 749-753. 10.1038/25533.
Price MA, Kalderon D: Proteolysis of the Hedgehog signaling effector Cubitus interruptus requires phosphorylation by Glycogen Synthase Kinase 3 and Casein Kinase 1. Cell. 2002, 108: 823-835. 10.1016/S0092-8674(02)00664-5.
Smelkinson MG, Kalderon D: Processing of the Drosophila hedgehog signaling effector Ci-155 to the repressor Ci-75 is mediated by direct binding to the SCF component Slimb. Curr Biol. 2006, 16: 110-116. 10.1016/j.cub.2005.12.012.
Zhang W, Zhao Y, Tong C, Wang G, Wang B, Jia J, Jiang J: Hedgehog-regulated Costal2-kinase complexes control phosphorylation and proteolytic processing of Cubitus interruptus. Dev Cell. 2005, 8: 267-278. 10.1016/j.devcel.2005.01.001.
Julian E, Dave RK, Robson JP, Hallahan AR, Wainwright BJ: Canonical Notch signaling is not required for the growth of Hedgehog pathway induced medulloblastoma. Oncogene. 2010, 29: 3465-3476. 10.1038/onc.2010.101.
Pazzaglia S: Ptc1 heterozygous knockout mice as a model of multi-organ tumorigenesis. Cancer Lett. 2006, 234: 124-134. 10.1016/j.canlet.2005.03.047.
Thomas WD, Chen J, Gao YR, Cheung B, Koach J, Sekyere E, Norris MD, Haber M, Ellis T, Wainwright B, Marshall GM: Patched1 deletion increases N-Myc protein stability as a mechanism of medulloblastoma initiation and progression. Oncogene. 2009, 28: 1605-1615. 10.1038/onc.2009.3.
Yang ZJ, Ellis T, Markant SL, Read TA, Kessler JD, Bourboulas M, Schuller U, Machold R, Fishell G, Rowitch DH, Wainwright BJ, Wechsler-Reya RJ: Medulloblastoma can be initiated by deletion of Patched in lineage-restricted progenitors or stem cells. Cancer Cell. 2008, 14: 135-145. 10.1016/j.ccr.2008.07.003.
Fujikura J, Hosoda K, Iwakura H, Tomita T, Noguchi M, Masuzaki H, Tanigaki K, Yabe D, Honjo T, Nakao K: Notch/Rbp-j signaling prevents premature endocrine and ductal cell differentiation in the pancreas. Cell Metab. 2006, 3: 59-65. 10.1016/j.cmet.2005.12.005.
Imayoshi I, Sakamoto M, Yamaguchi M, Mori K, Kageyama R: Essential roles of notch signaling in maintenance of neural stem cells in developing and adult brains. J Neurosci. 2010, 30: 3489-3498. 10.1523/JNEUROSCI.4987-09.2010.
Ingram WJ, McCue KI, Tran TH, Hallahan AR, Wainwright BJ: Sonic Hedgehog regulates Hes1 through a novel mechanism that is independent of canonical Notch pathway signalling. Oncogene. 2007, 27: 1489-1500. 10.1038/sj.onc.1210767.
Wall DS, Mears AJ, McNeill B, Mazerolle C, Thurig S, Wang Y, Kageyama R, Wallace VA: Progenitor cell proliferation in the retina is dependent on Notch-independent Sonic hedgehog/Hes1 activity. J Cell Biol. 2009, 184: 101-112. 10.1083/jcb.200805155.
Lutolf S, Radtke F, Aguet M, Suter U, Taylor V: Notch1 is required for neuronal and glial differentiation in the cerebellum. Development. 2002, 129: 373-385.
Weller M, Krautler N, Mantei N, Suter U, Taylor V: Jagged1 ablation results in cerebellar granule cell migration defects and depletion of Bergmann glia. Dev Neurosci. 2006, 28: 70-80. 10.1159/000090754.
Yokota N, Mainprize TG, Taylor MD, Kohata T, Loreto M, Ueda S, Dura W, Grajkowska W, Kuo JS, Rutka JT: Identification of differentially expressed and developmentally regulated genes in medulloblastoma using suppression subtraction hybridization. Oncogene. 2004, 23: 3444-3453. 10.1038/sj.onc.1207475.
Mizutani KI, Yoon K, Dang L, Tokunaga A, Gaiano N: Differential Notch signalling distinguishes neural stem cells from intermediate progenitors. Nature. 2007, 449: 351-355. 10.1038/nature06090.
Berman DM, Karhadkar SS, Hallahan AR, Pritchard JI, Eberhart CG, Watkins DN, Chen JK, Cooper MK, Taipale J, Olson JM, Beachy PA: Medulloblastoma growth inhibition by hedgehog pathway blockade. Science. 2002, 297: 1559-1561. 10.1126/science.1073733.
Fan X, Matsui W, Khaki L, Stearns D, Chun J, Li YM, Eberhart CG: Notch pathway inhibition depletes stem-like cells and blocks engraftment in embryonal brain tumors. Cancer Res. 2006, 66: 7445-7452. 10.1158/0008-5472.CAN-06-0858.
Purow B: Notch inhibitors as a new tool in the war on cancer: a pathway to watch. Curr Pharm Biotechnol. 2009, 10: 154-160. 10.2174/138920109787315060.
Ellis T, Smyth I, Riley E, Graham S, Elliot K, Narang M, Kay GF, Wicking C, Wainwright B: Patched 1 conditional null allele in mice. Genesis. 2003, 36: 158-161. 10.1002/gene.10208.
Tanigaki K, Han H, Yamamoto N, Tashiro K, Ikegawa M, Kuroda K, Suzuki A, Nakano T, Honjo T: Notch-RBP-J signaling is involved in cell fate determination of marginal zone B cells. Nat Immunol. 2002, 3: 443-450. 10.1038/ni793.
E Julian is an ANZ Trustees Research Scholar. This work was supported by funds from the National Health and Medical Research Council of Australia, The John Trivett Foundation, the ARC Special Research Centre for Functional and Applied Genomics and the Australian Cancer Research Fund. We thank Professor Tasuku Honjo for RBP-J conditional mice and Professor David Rowitch for Math1-Cre mice. In addition, we are thankful to Professor Ryoichiro Kageyama and Dr Zeng-jie Yang for helpful discussions.
The authors declare that they have no competing financial interests or other conflicts in relation to the work described in this paper.
EJ carried out all experimental work and drafted the manuscript. ARH participated in data analysis and critical reading of the manuscript. BJW conceived of the study, and participated in data analysis and in drafting of the manuscript.
Electronic supplementary material
Additional file 1: Figure S1 - RBP-J deletion in granule neuron precursors leads to loss of Notch target gene expression. Quantitative realtime PCR shows decreased mRNA expression of the direct Notch target Hey2 in RBP-Jlox/lox;Math1-Cre (pool of 3) compared to RBP-Jlox/lox (pool of 4) granule neuron progenitors (statistical analysis on means of three technical replicates for two aliquots of each cDNA pool, P = 0.0157). (TIFF 5 MB)
Additional file 2: Figure S2 - RBP-J deletion does not alter the properties of GNPs in vitro. (A-F) Granule neuron progenitors isolated from 7- to 8-day-old RBP-Jlox/lox (pool of 4) and RBP-Jlox/lox; Math1-Cre (pool of 5) cerebella show no difference in staining for PCNA (A,B) or the neuronal markers betaIII-tubulin (C,D) and NeuN (E,F). (G,H) TUNEL staining also reveals comparable rates of apoptosis in cells of both genotypes. (I-M) Culture of GNPs in the presence of 3 μg/ml Shh results in a modest increase in cells stained positively for PCNA in both genotypes (I,J) compared to untreated cells (K,L); however, the number of cells counted per well is not significantly different (M). Examples of positively stained cells are highlighted by arrows. Nuclei were counterstained with DAPI. Scale bars represent 50 μm. (TIFF 19 MB)
Additional file 3: Figure S3 - RBP-J deletion in granule neuron progenitors does not influence the cerebellar stem cell pool. Neuronal stem cells that reside in the VZ are unaffected by deletion of Ptc1 or RBP-J as shown by Sox2, a marker of neural stem cells and Bergmann glia. (A-D) Sox2 staining appears similar in all genotypes at E18.5, with positive cells in the VZ (magnified insets) and some Sox2-expressing Bergman glia migrating towards the ML, apart from a slight increase in background staining in Ptc1 deleted cerebellum. Nuclei were counterstained with DAPI. Scale bar represents 100 μm. (E) Neurosphere assays of cells isolated from P7 cerebellum also show no significant difference between controls and Ptc1 or RBP-J deleted mutants. For statistical analysis, unpaired t-tests were performed using Graphpad Prism 4. (TIFF 20 MB)
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Julian, E., Hallahan, A.R. & Wainwright, B.J. RBP-J is not required for granule neuron progenitor development and medulloblastoma initiated by Hedgehog pathway activation in the external germinal layer. Neural Dev 5, 27 (2010). https://doi.org/10.1186/1749-8104-5-27
- Proliferate Cell Nuclear Antigen
- Notch Signalling
- Notch Pathway
- Cerebellar Development