The Formation of Endoderm-Derived Taste Sensory Organs Requires a -Dependent Expansion of Embryonic Taste Bud Progenitor Cells

Summary

Gustatory perception is an evolutionary ancient sense, and the ability to discriminate toxic and digestible substances is vitally important for all organisms. In mammals, taste perception occurs in taste buds, groups of sensory cells that are housed in various types of taste papillae in the oral cavity. Little is known about the genetic and developmental programs that underlie the different architectures of these papillae. Using mouse models, we identified the transcription factor Pax9 as a major determinant for the development of endoderm-derived taste papillae, which develop in different locations in the back of the oral cavity. In these papillae, Pax9 regulates the expansion of the taste progenitor field, maintains the competence of these progenitors to interact with afferent nerve fibers of the glossopharyngeal nerve, and prevents their differentiation towards epidermal-like epithelial cells. In contrast, Pax9 is not required for the development of ectoderm-derived taste papillae that are distributed over the dorsum of the tongue. Our data reveal that mammals have evolved a specific developmental program to generate taste buds and associated papilla structures in different parts of the oral cavity.

Introduction

Taste buds consist of a group of clustered sensory cells and have been identified in all vertebrates. In the mammalian tongue, taste buds develop in different types of taste papillae: in fungiform papillae (FUP) distributed over the anterior dorsum of the tongue, in circumvallate papillae (CVP) located medially at the back of the tongue, and in foliate papillae (FOP) located laterally at the back of the tongue (Figure 1A). In addition, taste buds form locally without associated papilla structures in the epithelium of the soft palate, throat, epiglottis and upper esophagus. Despite phyletic variations and different distribution patterns of taste papillae, taste buds in the dorsal tongue epithelium develop in all vertebrates, including amphibia, reptiles, birds and mammals. In contrast, larger taste papillae with higher morphological complexity such as the CVP and FOP evolved exclusively in the mammalian lineage [1], [2].

Embryonic induction and development of taste buds have been widely studied in amphibia and rodents (for a recent review, see [3]). These investigations concentrated mainly on the FUPs of mice and rats, which contain taste buds with taste pores that open directly into the oral cavity. FUP development starts around embryonic day 12.5 (E12.5) and involves the formation of an array of epithelial placodes in the anterior two thirds of the tongue. The early patterning of FUP development is regulated by complex signaling processes and involves interactions between the Wnt/β-catenin, Shh and Bmp pathways ([4]–[9]. In mice, each of approximately a total of 90 FUP contains a single taste bud, whereas in some mouse strains the single CVP may house more than 300 taste buds [10], which are located in epithelial trenches that begin to grow into the underlying mesenchyme at E14.5. In addition, small salivary glands (von Ebner's glands) develop together with the CVP and FOP [11] to facilitate gustatory sensation in taste buds located deep in the trenches. Thus, while taste buds of the FUP are formed by epithelial placodes that are established early in development, the placodes of the CVP and FOP undergo substantial morphological changes and intercalate a period of extensive epithelial growth to generate increased taste bud progenitor fields prior to the induction of taste bud cells.

Whereas the CVP and FOP of mammals house the vast majority of taste buds, our understanding of the genetic control of their morphogenesis is surprisingly fragmentary. A single trench was found to develop in the CVP of Tabby mice, which lack ectodysplasin A [12], [13]. A CVP placode is missing altogether in mice lacking a functional Fgf10 gene, which is expressed in the mesenchyme at the pre-placodal stage of CVP development [14]. A malformed CVP or reduction of CVP taste bud number has been described in mice lacking Dystonin, which show insufficient innervation caused by impaired development of the glossopharyngeal cranial nerve [15], as well as in mouse mutants that are compromised in attracting nerve endings due to missing expression of neurotrophins in the CVP epithelium [16]. A recent study revealed a role for Six1 and Six4 in CVP development, however, the morphological abnormalities may partly result from defects during cranial nerve formation, which are seen in Six1/Six4-deficient mice [17]. Thus there are considerable gaps in our knowledge about the developmental mechanisms that regulate the expansion of the early taste bud progenitor cell population in the CVP and FOP epithelium.

The paralogous genes Pax9 and Pax1 evolved from a single ancestral gene in the vertebrate lineage and form a subgroup within a total of nine members of the Pax gene family. Pax9 and Pax1 regulate different aspects of thymus, skeletal and craniofacial development [18]–[22]. Pax genes encode transcription factors and regulate the morphogenesis of a wide range of organs and are key factors for the development of mammalian sensory organs such as the eye (Pax6, Pax2), nose (Pax6) and ears (Pax2, Pax8) (for reviews, see [23], [24]). Here we show that Pax9, previously not implicated in the development of sensory organs, regulates essential steps during the development of endoderm-derived taste papillae.

Results

CVP and FOP development is arrested in Pax9-deficient mice

Epithelial expression of Pax9 in the developing oral apparatus of mice has been documented in the anterior foregut endoderm and its derivatives, as well as in the dorsal epithelium of the tongue [18], [25]. Whole mount X-Gal staining of a developing Pax9^+/LacZ [21] mouse tongue at embryonic day 13.5 (E13.5) indicated that strong Pax9 expression is associated with the localization of placodes forming the CVP and FOP, respectively (Figure 1B). Immunostaining revealed Pax9 expression in the epithelium of placodes and trenches throughout the embryonic period of CVP and FOP development (Figure 1C–J). Pax9 was expressed normally in the region of the developing CVP of E13.5 and E14.5 mouse embryos lacking Fgf10 (Figure S1), a growth factor secreted by the posterior tongue mesenchyme and essential inducer of CVP development [14]. In contrast to the CVP, Pax9 is also expressed in the mesenchyme underlying the FOP epithelium (Figure 1G–J) in cells that are part of two discrete mesenchymal Pax9 expression domains at each side of the tongue (arrowheads in Figure 1B). The expression of Pax9 was down-regulated in some domains of the epithelial trenches at E18.5 (Figure 1F, J), a stage that precedes the early phase of taste bud induction in these papillae. Interestingly, while epithelial cells of the dorsal tongue were also stained, the central regions of placodes forming the FUP were negative for Pax9 at all stages of embryonic development (Figure 1K–N).

A histological analysis of serial sections of the three taste papilla types developing in the mouse tongue revealed that Pax9 is required for the formation of epithelial invaginations in both CVP and FOP. In homozygous Pax9^LacZ/LacZ (for simplicity referred to as Pax9^−/− hereafter) embryos, a CVP placode forms (Figure S2) but the epithelial trenches are growth retarded at E16.5 and E18.5 (Figure 2A–D). Similarly, invaginations of the FOP are missing and keratinocytes of the superficial layers are aberrantly enlarged in the mutant epithelium (Figure 2E–H). Moreover, the thickness of the mesenchymal cell layer was greatly reduced in the mutant FOP at E18.5. In contrast, the morphology of FUP appeared normal in Pax9^−/− embryos (Fig. 2I–L).

To address the role of Pax9 in neural crest cell-derived mesenchymal cells located adjacent to the developing FOP (Figure 1G–J), we inactivated the Pax9 gene in these cells by crossing Pax9^flox (Pax9^fl) mice [26] with transgenic mice expressing Cre under the control of Wnt1 promoter (Wnt1^Cre; [27]). While the Pax9^fl/fl alleles were efficiently recombined in Wnt1^Cre;Pax9^fl/fl embryos, mesenchymal cells underlying the FOP were present and epithelial trenches formed in all (n = 5) mutant FOP of Wnt1^Cre;Pax9^fl/fl embryos (Figure 2M, N). These findings indicate that Pax9 function during FOP development is primarily required in epithelial cells.

Pax9 is dispensable in the developing and adult FUP

Postnatal Pax9 expression continues not only in the FUP epithelium but was also found in a few taste bud cells of the fully differentiated FUP (Figure 3A). Since FUP development is completed postnatally and since taste buds do not form prior to 2 days after birth we asked if Pax9 could be required at these later stages of FUP development. Because Pax9^−/− embryos die at birth, we addressed this question by using transgenic mice expressing Cre under the control of Keratin 14 (K14^Cre) promoter [28]. Previous studies showed that K14 is expressed in basal cells of the tongue epithelium and in FUP but not in actual taste bud cells. However, lineage tracing experiments identified K14-positive epithelial cells located directly adjacent to the taste bud as a niche of stem cells renewing taste bud cells in the adult mouse [29]. X-Gal staining of K14^Cre;ROSAR26 embryos confirmed efficient Cre activity in the dorsal tongue epithelium from E13.5 onwards (Figure S3A,B) and Pax9 immunostaining revealed complete removal of Pax9 protein in both FUP and its associated taste buds in adult K14^Cre;Pax9^fl/fl mouse tongues (Figure 3B). Interestingly, the size and morphology of adult FUPs was not affected and FUP taste buds in these mutants appeared normal and formed taste pores (Figure 3C–F). In addition, the number of FUP visible on the dorsal aspect of K14^Cre;Pax9^fl/fl mouse tongues (30 per tongue, n = 5) did not differ significantly (p>0.79) from the number of FUPs of control mice (31 per tongue, n = 5).

To characterize the differentiation of the adult, Pax9-deficient FUP epithelium, we analyzed the expression of various keratin (K) proteins, which form intermediate filaments in cell type-specific combinations. We found that the keratin pair K1 and K10, which are normally expressed throughout the differentiated suprabasal layers of the epidermis, were strongly up-regulated in the K14^Cre;Pax9^fl/fl FUP epithelium, as well as in the interpapillary epithelium (Figure 3G–J). The expression of K6, which is often seen in hyperproliferative epidermal cells [30], was also up-regulated in the interpapillary epithelium, but not in the FUP epithelium itself (Figure S4A,B). In contrast, the expression of K14 and K5, which are normally found in basal cells of all stratified squamous epithelia, was not changed (Figure 3G,H; Figure S4C,D). Finally, we did not observe changes of the expression of K8, which marks taste bud cells in all taste papillae, as well as of Sox2, a marker of mature taste bud cells and critical regulator for the formation of taste sensory cell [31], in K14^Cre;Pax9^fl/fl mouse tongues (Figure 3K–N). Together, these results indicate that Pax9 is not functionally involved in the development of the mouse FUP. Furthermore, although the Pax9-deficient FUP epithelium shows alterations of keratin expression patterns, these changes are not associated with apparent defects of FUP maturation and FUP maintenance in the adult mouse. In contrast, Pax9 is required for the formation of filiform papillae (FIP), epithelial projections of the dorsal tongue epithelium that do not contain taste buds (Figure 3E,F; [25]).

Unlike the epithelium of the dorsal tongue, we did not detect full K14^Cre activity in the CVP and FOP epithelium during embryonic development (Figure S3A,B). At perinatal stages, K14^Cre activity expands to posterior regions of the tongue (Figure S3C) and while complete inactivation of Pax9 gradually manifests in the CVP and FOP of K14^Cre;Pax9^fl/fl mice, Pax9 deficiency was not associated with obvious morphological defects in these taste papillae (Figure S3D,E). In summary, the data indicate that Pax9 functions are not needed in adult taste papillae and that the requirement for Pax9 is restricted to the early steps of CVP and FOP morphogenesis.

Epithelial differentiation defects of the Pax9-deficient CVP are associated with the absence of proneural induction

While the FOP of Pax9^−/− mutants does not form any epithelial trenches, the CVP exhibits rudimentary invaginations (Figure 2) and we thus chose the latter to characterize the cellular and molecular defects during embryonic CVP morphogenesis. SEM of the posterior tongue region showed that newborn Pax9^−/− mice lack an accumulation of accessory papillae that normally surround the central domain of the CVP (Figure 4A,B). We also noted increased desquamation of the posterior tongue epithelium and diastase-controlled PAS staining revealed strongly increased levels of glycogen in the area in which the CVP trenches normally develop (Figure 4C,D). This differentiation defect is reminiscent of inappropriately increased deposition of glycogen regularly observed in the benign condition glycogenic acanthosis of the esophageal epithelium [32]. Moreover, a barrier assay revealed that only the central domain of the Pax9-deficient CVP was permeable to toluidine blue solution at E18.5, whereas the surrounding mutant tongue epithelium has prematurely established a full barrier (Figure 4E,F). Furthermore, the mutant CVP epithelium expresses high levels of Krt1 (Figure 4G,H), a keratin gene that is normally expressed in the mouse skin and not in the tongue [25] but was found to be up-regulated in oral dysplasia [33]. Together, these findings document the inappropriate differentiation of the Pax9-deficient CVP epithelium.

During mouse CVP development, taste buds become morphologically distinct from the surrounding trench epithelium two days after birth. Thus, to visualize epithelial domains that have started to initiate taste bud formation in the CVP at E18.5, we analyzed the expression of K8 and Prox1, which both mark taste bud primordia at this developmental stage [34], [35]. Both markers identified groups of cells in wild type epithelial trenches but not in the trenches of Pax9-deficient mice (Figure 4I–L). The same result was found using an Ascl1 (previously called Mash1) probe for in situ hybridization (Figure S5). In addition, K8 expression, normally found in loosely aligned cells in the middle of each trench (Figure 4K), was strongly reduced in the mutant CVP (Figure 4L). Interestingly, expression of Prox1 and K8 was also found in the apical domain of the CVP in both wild type (Figure S6A,B) and Pax9-deficient mice at E18.5 (Figure 4J,L; Figure S6C). We did not further investigate these structures, which are likely to represent immature taste buds that lack taste pores [36] and are known to disappear at early postnatal stages [37].

Afferent nerve fiber endings of the glossopharyngeal nerve make contact with the CVP epithelium from E14.5 onwards [38]. To analyze the pattern of CVP innervation, we stained for the neural marker PGP9.5 [39], which revealed a close contact of nerve fibers with the trench epithelium of the wild type CVP (Figure 4M). In contrast, although branches of the glossopharyngeal nerve were present at the Pax9-deficient CVP, we did not detect any penetration of the mutant trench epithelium by nerve endings (Figure 4N).

Disruption of the Shh signaling pathway in Pax9-deficient CVP and FOP

The Shh signaling pathway is active in taste papillae of the developing mouse tongue [40] and its inhibition was found to increase the number of FUP in the dorsal tongue epithelium [6], [7]. At the early stage of CVP development (E13.5), we found Shh expression in the epithelial placode in both control and Pax9-deficient embryos (Figure S2). At E14.5, in addition to the central, dome-like structure of the CVP, a ring of accessory papillae surrounding the center of the CVP was Shh-positive in controls, but not in Pax9^−/− embryos (Figure 5A,B). Similar patterns were obtained with probes for the Shh pathway downstream genes Ptch1 and Gli1, in addition to a strong down-regulation of Gli1 expression in the center of the mutant CVP (Figure 5A,B). In the developing FOP, Shh expression was considerably weaker compared to that of the CVP but expression in an indistinctly delimited area was consistently identified on both sides in the posterior part of the wild type tongue (Figure 5C). In Pax9^−/− mutants, Shh expression levels were below the detection threshold and only very weak expression of Ptch1 and Gli1 was found (Figure 5D). In contrast, consistent with unaffected FUP development, Shh was normally expressed in the dorsal tongue epithelium of Pax9^−/− mutants (Figure 5E, F).

Since the Shh pathway is an important modulator of epithelial morphogenesis during the development of various ectodermal appendages [41]–[43] we speculated that a reduction of Shh pathway activity in the developing CVP could be related to the impaired growth of the trenches in Pax9^−/− embryos. To test this, we cultured mutant embryonic tongues in the presence of purmorphamine, a Shh signaling agonist that targets the Shh pathway effector protein Smoothened [44]. Under culture conditions used in this study, embryonic tongues dissected at E13.5 and cultured for 48 hours in control medium either formed a small CVP or an epithelial bud. In the presence of purmorphamine, the size of the mutant CVP (n = 4) was significantly increased but growth was primarily stimulated in the central, dome-like domain of the CVP (3 out of 4, Figure 5H). A similar response was observed in Pax9-deficient tongues cultured in the presence of a Shh protein-loaded bead placed next to the CVP. However, this result was only seen when the Shh protein-loaded bead was not displaced during culture (Figure S7A,B). In contrast, an enlarged CVP dome or enhanced trench formation was not observed after purmorphamine treatment of explants from wild type embryos (Figure S7C).

Pax1 is a critical target of Pax9 in the proliferating CVP trench epithelium

The incomplete ability of Shh pathway activation to restore epithelial growth of the Pax9-deficient CVP prompted us to search for additional developmental pathways that may be affected in the CVP of Pax9^−/− mutants. To screen for early molecular defects, a genome-wide RNA expression analysis of wild type and Pax9-deficient CVP dissected at E14.5 was carried out. The array data suggested that two genes encoding the transcriptional regulators Sox9 and Pax1 might present early targets of Pax9 in the developing CVP. Immunostaining indeed confirmed that both transcription factors are strongly expressed at the tips of invaginating trenches of the normal CVP, but not in the CVP of Pax9^−/− mutants (Figure 6A–D). Sox9 and Pax1 were shown to regulate epithelial cell proliferation in various developmental systems [45]–[47] and in agreement with these functions, counting of BrdU-positive cells at the tip of the growing trenches revealed a significant reduction of the number of proliferating cells in Pax9^−/− mutants (Figure 6E–G).

Pax1 and Pax9 are paralogous genes and while they have redundant functions during vertebral column development [22], the absence of Pax1 expression in the Pax9-deficient CVP rules out that Pax1 may compensate for the loss of Pax9 during early CVP development. Interestingly, Pax1 itself continues to be expressed and labels most taste bud cells in the wild type CVP and FOP of adult mice (Figure 6H; Figure S8A). In contrast, Pax1 is not expressed in the dorsal tongue epithelium during FUP development or in the FUP of adult mice (Figure S8B,C). Analysis of mouse mutants with a targeted deletion of Pax1 [48] showed that they develop shorter CVP trenches at E18.5 (111 µm in Pax1^−/− mutants, 131 µm in control littermates, n = 8, p<0.01), while the width of the CVP was not significantly changed (Figure 6I,J; Table S1). Histological analysis of the CVP at postnatal day 16 revealed that the CVP of Pax1-deficient mice was noticeably smaller (n = 3; Figure 6K,L). Corresponding with this growth retardation, counting taste buds of a complete series of sections of one Pax1 mutant CVP indicated that the total number of taste buds was reduced by more than 50%. Thus Pax1 expression in the CVP trenches is required for epithelial growth and for the generation of the normal number of taste buds in the mouse CVP.

Taste placodes in the soft palate are missing in Pax9^−/− mutants

The posterior part of the secondary palate forms the soft palate which, in contrast to the hard palate, is movable and not supported by bones. Moreover, the oral mucosa of the soft palate is part of the gustatory system and forms taste buds, however, these taste buds lack supporting papilla structures and are directly embedded in the epithelium (Figure 7D). During soft palate development, Pax9 expression was detected in the mesenchyme as well as in the epithelium prior to palatal shelf elevation (Figure 7A). Taste placodes of the soft palate begin to form as epithelial thickenings at E14.5 and express Shh [49]. Both taste placodes and soft palate epithelium are Pax9-positive, whereas Pax9 is not expressed in the epithelium of the hard palate, which lacks these placodes (Figure 7B,C). In newborn Pax9^−/− mice, no clusters of taste bud progenitors were found in the soft palate epithelium (Figure 7D,E) and complete absence of Shh expression at E14.5 indicates that taste placode induction is not initiated in the soft palate of Pax9^−/− mutants (Figure 7F,G).

Discussion

Taste perception at the back of the mammalian oral cavity serves as a critically important control mechanism to discriminate nutritious ingredients from substances that are potentially toxic to the organism. The formation of epithelial trenches that are rinsed by saliva produced in associated minor salivary glands enables a high concentration of functional taste buds to form in the narrow, posterior part of the tongue. The complex architecture of the CVP and FOP, and the close vicinity of numerous taste buds in these taste papillae predict the activities of developmental programs to differ from those regulating patterning and development of the FUP on the anterior dorsal tongue. Indeed, while loss of Fgf10 signaling in the mouse tongue mesenchyme results in the absence of the CVP, the spacing and size of FUP increased in these mutants [14]. In addition, similar to the differential expression of Pax1 shown in this work, expression of a Bmp4 reporter allele was detected in taste buds of the CVP but not in taste buds of FUP [50]. These fundamental differences may be attributed to the different embryonic origins of various taste papillae. Strong support for an entirely endoderm-derived origin of the CVP and FOP was recently provided by lineage tracing of Sox17-2AiCre/R26R mouse embryos [51],[52]. The study also indicated that the FUP on the dorsal tongue are exclusively derived from ectodermal cells.

During the development of the oral epithelium, expression of Pax9 is not restricted to endoderm-derived structures but is also seen in ectoderm-derived FUP as well as in non-sensory filiform papillae (this work; [25]). Our results clearly demonstrate that Pax9-deficiency does not affect patterning, development or maintenance of the mouse FUP. Although this result was unexpected, it reinforces the conclusion that endoderm-specific developmental pathways regulate the formation of the gustatory system in the posterior region of the oral cavity.

The early steps of CVP morphogenesis follow a sequence that is similar to that typically seen during the development of organs which form by epithelial-mesenchymal interactions. In analogy to the formation of, for example, a mammalian tooth or hair follicle, the CVP placode forms a bud-like epithelial structure that subsequently branches to form lateral invaginations. While the initial branching of the CVP bud is not affected in Pax9 mutant embryos, subsequent invagination of the epithelial trenches is blocked. Interestingly, a characteristic ring of accessory papillae normally surrounding the central dome of the CVP was not established in Pax9-deficient embryos. Whereas the developmental role of the accessory papillae has not been studied thus far, we found that they express Shh, suggesting that they may function as transient signaling centers and thereby contribute to CVP morphogenesis. The mitogenic effect of Shh has been documented in various epithelia [53]–[55] and we here found that activation of the Shh downstream pathway by purmorphamine increased the size of the Pax9-deficient CVP in embryonic tongue cultures. However, epithelial trench formation could not be rescued in these experiments, raising the possibility that precise timing and localization of Shh secretion by accessory papilla cells are required to restrict cell proliferation to the rudimentary trenches. Inhibition of the Shh pathway in rat embryonic tongue cultures was shown to increase the number of FUP [6]. While the external morphology of the CVP was not altered by Shh pathway inhibition, formation and growth of the epithelial trenches was not analyzed in these experiments. Recently, mouse reporter strains mapping the expression of the Shh pathway and its downstream genes in embryonic and adult FUP convincingly demonstrated an association between Shh expression and proliferation in neighboring epithelial cells [29], [56]. Thus, in vivo experiments using genetic tools suitable to inactivate or activate the Shh pathway in the CVP in an inducible manner should help to identify the specific roles of Shh for patterning and morphogenesis during CVP development.

Our analyses identified Pax9 as the first developmental regulator that is directly required for the expansion of taste progenitor cells in the developing mouse CVP. This progenitor field is normally established during a period of epithelial growth between E14.5 and E18.5 and our BrdU-labeling revealed a high proportion of cells that proliferate at the tip of the CVP trenches. Proliferation is significantly reduced in the invaginating epithelial CVP trench cells of Pax9^−/− embryos, and this cellular defect is associated with a drastic down-regulation of Sox9, a known regulator of epithelial cell proliferation in other developing organs [45], [46], [57]. Beside this, Sox9 is necessary to establish the stem cell compartment in the hair follicle [58], raising the possibility that Sox9 could have a similar function in the CVP.

Pax1 and Pax9 exhibit similar expression patterns during embryonic development and function in a redundant manner during the formation of the vertebral column [18], [22]. Similarly, Pax1 and Pax9 both regulate aspects during the development of the thymus, which is derived from the foregut endoderm [20], [21]. Interestingly, while Pax1 is more critically required during vertebral column development, the role of Pax9 is more important in foregut-derived organs, to which the expression of the common Pax9/1 precursor is restricted in early chordates [59]. The moderate CVP phenotype of Pax1^−/− mice identified in this work appears to support this conclusion. Together, these findings suggest that the mammalian Pax9 gene has retained the original function of the common Pax9/1 precursor gene in the foregut endoderm, while Pax1 has acquired a predominant role in the axial skeleton during vertebrate evolution.

Besides their functions in taste papilla formation, the expression of Pax9 and Pax1 in taste buds of adult mice suggests additional roles in the fully matured gustatory system. The absence of isolated, Pax9-positive cells in FUP taste buds after K14Cre-mediated recombination did not cause obvious morphological defects of the taste buds. However, as K14Cre is not active in actual taste bud cells, this finding supports the conclusion that stem cells from adjacent, non-sensory FUP cells contribute to the renewal of FUP taste buds [29]. While the roles of Pax9 and Pax1 in taste buds remain to be elucidated using appropriate genetic tools, it is tempting to speculate that they could be involved in the specification of sub-populations of mature taste bud cells.

Absent expression of K8 and Prox1 and lack of contact by nerve endings in the developing CVP trenches, as well as premature barrier formation indicates a highly defective differentiation program of the posterior tongue epithelium of Pax9-deficient embryos. In the mutants, the arrest of CVP morphogenesis is associated with ectopic expression of Krt1, a keratin gene known to be strongly up-regulated in dysplasia of the oral epithelium [33], as well as with increased levels of glycogen, a feature seen in the benign condition glycogenic acanthosis [32]. It therefore appears likely that premature and inappropriate terminal differentiation of the CVP epithelium accounts, at least in part, for the incompetence of the CVP trench cells to interact with nerve fiber endings and to generate taste bud progenitors.

Our data show that epithelial trench formation in the CVP and FOP is Pax9-dependent. A primary function for Pax9 in the expansion of taste progenitor fields in taste papillae with a higher degree of architectural complexity appears to be supported by the finding that taste papillae on the dorsal tongue, which lack epithelial trenches, develop normally in Pax9-deficient mice. However, although the soft palate epithelium does normally not form any recognizeable taste papilla structures, Pax9 is required for early Shh expression and for the induction of taste progenitor cells in this part of the oral cavity. Interestingly, lack of Shh expression in the taste placodes of the soft palate was also observed in mouse mutants lacking β-Catenin in the epithelium [60], raising the possibility that Pax9 might interact with Wnt-signalling. A complete secondary palate only evolved in the mammalian lineage, whereas the tongue is present in amphibia, reptiles, birds, and mammals [1]. While the molecular mechanisms regulated by Pax9 in the soft palate epithelium remain to be identified, it is conceivable that Pax9 may have acquired an additional, early role for taste placode formation in the soft palate epithelium at a later period during the evolution of tetrapods.

Materials and Methods

Ethics statement

All procedures were carried out under personal and project licenses issued by the Home Office, UK and were approved by the Local Ethics Committee.

Mouse husbandry and genotyping

Mice were housed as described previously [61]. Embryos were staged by taking mid-day on the day of vaginal plug detection as embryonic day 0.5 (E0.5). The following mouse lines were maintained on the indicated genetic background, intercrossed to produce relevant genotypes and PCR genotyped according to references: Pax9^lacZ (C57BL/6; [21]), Pax9^flox (C57BL/6 x 129S2/SvPas; [26]), Wnt1^Cre (C57BL/6; [26]), K14^Cre (FVB/N; [28]), Pax1 (C57BL/6; [48]), ROSA26R (C57BL/6; [62]).

Histology and immunohistochemistry

Mouse tissues were prepared, processed, paraffin-embedded, sectioned, stained with haematoxylin and eosin and photographically documented as described previously [61]. Diastase-controlled Periodic acid-Schiff (D-PAS) staining was performed as described [63]. CVP size was measured using AxioVision software v.4.3 (Carl Zeiss) and statistically analyzed by a two-tailed t-test (Excel software, Microsoft).

Pax9 immunohistochemical staining on paraffin sections was performed as described previously [64] with the following modifications. Antibodies were diluted in antibody diluent (Dako, S3022) and incubated in the following order: rat anti-Pax9 (1∶40), rabbit anti-rat IgG (Dako, Z0494; 1∶50), rat APAAP (Dako, D0488; 1∶50) with three TBS washes in between each step. The last two steps were repeated and alkaline phosphatase activity was visualized using Fast Red (Sigma) as a substrate. Other primary antibodies were detected using the Envision+ System-HRP kit (Dako, K4008 or K4010) according to the manufacturer's instructions. AEC (Dako, K4008) and DAB (Dako, K4010) substrates stain red and brown, respectively. Primary antibodies were used at the following dilutions: rabbit anti-PGP9.5 (7863-0504, AbD Serotec), 1∶200; rabbit anti-Sox2 (C70B1, Cell Signaling), 1∶100; rabbit anti-Sox9 (O9-1, [65]), 1∶1000; rat anti-Pax1 [66], 1∶40. Following incubation with rat anti-Pax1 antibody, HRP-conjugated rabbit anti-rat IgGs (Dako, P0450) were applied at 1∶200 dilution before using the rabbit-specific Envision+ detection system.

To visualize proliferating cells, BrdU labeling and detection was performed as described previously [67]. Serial sections from three wild type (29 sections) and three Pax9-deficient (28 sections) E15.5 CVPs dissected 90 minutes after BrdU injection were prepared and BrdU-positive cells counted in a defined area at the tip of epithelial trenches. Statistical significance was assessed using a two-tailed t-test.

For indirect immunofluorescence analysis, 5 µm cryosections were air-dried on Superfrost ultra plus slides (Thermo Scientific) for 2 hours at room temperature and then fixed for 10 minutes with pre-cooled acetone at −20°C. Immunofluorescence analysis was performed as previously described [68], using the following primary antibodies: rabbit anti-K1 (AF109, Covance), 1∶1000; mouse anti-K10 (DE-K10, Progen), 1∶160; rabbit anti-K5 (Covance), 1∶5000; guinea pig anti-K14 (GPCK14.2, Progen), 1∶50; mouse anti-K6 (Ks6.Ka12, Progen), 1∶10; rat anti-K8 (TROMA-I, Developmental Studies Hybridoma Bank), 1∶50. Nuclei were stained with DAPI (Invitrogen) and secondary antibodies were species-specific fluorochrome-conjugated goat antibodies: Cy3-conjugated anti-mouse and anti-guinea pig, both 1∶200; Alexa 594-conjugated anti-rat and Alexa 488-conjugated anti-rabbit, both 1∶400 (Molecular Probes). Microscopic analysis was performed using a Leica SP2 UV confocal microscope operated through LCS 2.61 software (Leica Microsystems).

Barrier assay, X-Gal staining and scanning electron microscopy (SEM)

Tongue barrier assays and whole-mount X-gal staining were performed as described previously [25], [21]. For SEM, tongues were fixed in 2% glutaraldehyde/PBS, dehydrated through a graded series of ethanol followed by carbon dioxide incubation in a Samdri 780 Critical Point Dryer. The specimens were then mounted on an aluminium stub with Acheson Silver Electrodag (Agar Scientific) and coated with gold using a Polaron SEM coating unit. Specimens were examined and photographed using a Stereoscan 240 scanning electron microscope. SEM images taken from flat-mounted tongues of 4 months old mice were also used to count the number of FUPs that were directly visible on the dorsal tongue surface.

RNA in situ hybridization

RNA in situ hybridization of whole embryonic specimens and of tissue sections using digoxygenin-labelled cRNA probes was performed as described previously [67]. cRNA probes were produced for Shh (0.6 kb; MGI:1327804), Ptch1 (2.2 kb; MGI:3833867), Gli1 (1.7 kb; MGI:12533), Prox1 (0.5 kb; [69]), Ascl1 (0.7 kb; [69]), and Krt1 (0.5 kb; [25]).

Embryonic tongue culture

Embryonic mandibles including tongues were dissected at E13.0 and cultured for two days as described previously [70], [4]. Before culture, the specimens were embedded in growth factor-reduced Matrigel (BD Biosciences, Cat. No. 305128) to prevent them from flattening during culture. To activate the Hh pathway, 4 µM purmorphamine (Calbiochem, Cat.No. 540220) was added to the culture medium. Alternatively, Affi-Gel Blue gel beads (Bio Rad, Cat.No. 153-7302) were soaked in recombinant mouse SHH protein (1.25 mg/mL in PBS; R&D Systems, Cat.No. 461-SH) or BSA for at least an hour and the beads were then placed onto the tongue epithelium close to the developing CVP.

Supporting Information

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