PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of wtpaEurope PMCEurope PMC Funders GroupSubmit a Manuscript
 
Development. Author manuscript; available in PMC 2008 September 29.
Published in final edited form as:
PMCID: PMC2555979
EMSID: UKMS2188

An FGF signaling loop sustains the generation of differentiated progeny from stem cells in mouse incisors

Abstract

Rodent incisors grow throughout adult life, but are prevented from becoming excessively long by constant abrasion, which is facilitated by the absence of enamel on one side of the incisor. Here we report that loss-of-function of Sprouty genes, which encode antagonists of receptor tyrosine kinase signaling, leads to bilateral enamel deposition, thus impeding incisor abrasion and resulting in unchecked tooth elongation. We demonstrate that Sprouty genes function to ensure that enamel-producing ameloblasts are generated on only one side of the tooth by inhibiting the formation of ectopic ameloblasts from self-renewing stem cells, and that they do so by preventing the establishment of an epithelial-mesenchymal FGF signaling loop. Interestingly, whilst inactivation of Spry4 alone initiates ectopic ameloblast formation in the embryo, the dosage of another Sprouty gene must also be reduced to sustain it after birth. These data reveal that the generation of differentiated progeny from a particular stem cell population can be differently regulated in the embryo and adult.

Keywords: ameloblast, enamel, FGF signaling, Sprouty genes, stem cells

INTRODUCTION

Rodent incisors are unusual among mammalian teeth in that they grow continuously throughout the life of the animal. This growth is fueled by stem cells in both the mesenchymal and epithelial compartments of the incisor, whose progeny perpetually generate the various cell types in the tooth (Gronthos et al., 2002; Smith and Warshawsky, 1975). Incisor growth is counterbalanced by abrasion, without which the tooth would become excessively long and interfere with feeding. It would be difficult to abrade the incisors if enamel, the hardest component of the tooth, covered the entire surface of the incisor as is does in the molar. However, in rodent incisors enamel is normally present on the labial surface (facing the lip), and is absent on the lingual surface (facing the tongue) (see Fig. 1A). This asymmetry not only facilitates the abrasion that keeps incisor length relatively constant, but also ensures that the tooth will be filed down primarily on one side, thus generating a sharp tip (Addison and Appleton, 1915).

Figure 1
Spry4-/-;Spry2+/- mice develop a ‘tusk’-like incisor due to the presence of enamel on the lingual surface

Little is known about the stem cells that generate enamel-producing ameloblasts (ameloblast stem cells; ASCs), because markers for them have not yet been identified. It has been proposed that ASCs reside in a niche located within a region called the cervical loop (CL) at the posterior end (base) of the incisor (Harada et al., 1999) (see Fig. 1A), but it is not known if ASCs give rise to only ameloblasts or also to the other epithelial cell types that must be continuously generated as the tooth grows. Based on models for the generation of differentiated progeny from stem cells in other tissues, such as the crypt of the intestinal villus (Fuchs et al., 2004), it has further been speculated that ameloblast formation begins when ASC progeny move out of the putative niche and develop into transit-amplifying (T-A) cells that undergo a limited number of cell divisions (Harada et al., 1999; Wang et al., 2007). It is known that once formed, ameloblasts move anteriorly along the length of the incisor (towards the tip) as they differentiate. After producing and depositing enamel, ameloblasts either undergo apoptosis or shrink in size (Smith and Warshawsky, 1975). Genetic analysis has shown that members of the Fibroblast Growth Factor (FGF) family of secreted signaling molecules play a role in regulating ameloblast development or function, as Fgf3-/- mice have defective enamel and Fgf3-/-;Fgf10+/- mice have very thin or no enamel (Wang et al., 2007). Furthermore, based on data from studies of incisors developing in vitro it has been suggested that Fgf10 regulates epithelial stem cell survival (Harada et al., 2002; Yokohama-Tamaki et al., 2006).

In wild-type incisors, the lack of lingual enamel is due to the absence of ameloblasts on that side (Smith and Warshawsky, 1975). However, it is not yet known whether lingual ameloblasts are absent because their formation from ASCs is blocked or because there are no ASCs in the lingual CL. Interestingly, the lingual CL differs in morphology from the labial CL (see Fig. 1A), which might reflect a lack of either T-A cells or ASCs. These morphological differences are correlated with asymmetries in the expression patterns of genes encoding members of the Fibroblast Growth Factor (FGF) family. For example, Fgf3 is detected in the mesenchyme surrounding the labial but not the lingual CL and Fgf10 is expressed at a higher level on the labial than on the lingual side (Harada et al., 1999). Furthermore, ectopic Fgf3 expression in lingual mesenchyme is associated with the formation of lingual ameloblasts in embryos homozygous for a null allele of Follistatin (Fst), which encodes an extracellular inhibitor of signaling by Transforming Growth Factor β (TGFβ) superfamily members (Wang et al., 2007; Wang et al., 2004). Together, the available data suggest that suppression of FGF signaling on the lingual side is necessary to prevent ameloblast formation.

Here we identify Sprouty (Spry) genes, which encode intracellular antagonists of FGF and other receptor-tyrosine kinase signaling pathways (Mason et al., 2006), as essential for establishing and sustaining the asymmetry of enamel deposition necessary to maintain normal incisor length and shape. We provide genetic evidence that Sprouty genes prevent the generation of lingual ameloblasts by inhibiting an FGF-mediated epithelial-mesenchymal signaling loop on the lingual side. Furthermore, our data suggest that the earliest ameloblasts that form in the incisor do not arise from ASCs, but instead are derived from a transient embryonic ameloblast progenitor cell population that does not self-renew.

MATERIALS AND METHODS

Mouse Lines

Mouse lines carrying mutant alleles of Fgf9 (Colvin et al., 2001), Fgf10 (Min et al., 1998), Fst (Matzuk et al., 1995), Spry1 (Basson et al., 2005), Spry2 (Shim et al., 2005), Spry4 (Klein et al., 2006) and the K14-cre (Dassule et al., 2000) and Wnt1-cre (Danielian et al., 1998) transgenes were maintained and genotyped as reported, except that Fst wild-type and null alleles were genotyped using PCR rather than Southern blotting (primer sequences available on request). Age-matched CD1 embryos were used as wild-type controls in all cases.

Gene expression and histological analysis

To stage embryos, noon of the day when a vaginal plug was detected was considered embryonic day (E) 0.5. RNA in situ hybridization was performed according to standard protocols on paraffin sections (10 μm) using digoxigenin-labeled probes. Tissue was prepared for sectioning by fixing embryonic heads in 4% paraformaldehyde (PFA) or postnatal jaws in 4% PFA, and then decalcifying in RNAse-free EDTA for 2-4 days prior to sectioning. For postnatal histology, jaws were fixed in Bouin’s solution, decalcified using a solution of 50% formic acid and 0.7M sodium citrate (mixed 1:1), embedded in paraffin, sectioned at 7 μm, and stained with Heidenhain’s azocarmine-aniline blue (AZAN) stain. For photography of intact adult jaws, mouse heads were boiled for 30 minutes in distilled water and soft tissues were carefully removed.

X-ray computed tomography (XTM)

XTM was used to assess the degree of mineralization as previously described (Kinney et al., 2000). Briefly, mouse incisors (n=5 per group) were scanned at the Advanced Light Source (Lawrence Berkeley National Laboratory) and two-dimensional radiographs were obtained as the specimens were rotated through 180° in 0.5° increments. The radiographs were reconstructed into 1,000 slices by Fourier-filtered back projection with a 10.5 μm resolution. The attenuation coefficient (mm-1) of each pixel is represented by the false colors and relates directly to mineral concentration.

RESULTS

Spry4-/-;Spry2+/- mice have abnormal, ‘tusk-like’ incisors due to ectopic enamel deposition on the lingual side of the tooth

We found that Spry4-/-;Spry2+/- mice, obtained by crossing mice carrying combinations of Spry4 (Klein et al., 2006) and Spry2 (Shim et al., 2005) null alleles, had excessively long and thick mandibular incisors that resembled tusks (Fig. 1B,F). Animals of this genotype will hereafter be referred to as “tusk mutants.” Abnormally long incisors can result from a lack of abrasion when the maxilla and mandible are misaligned. However, we detected no obvious craniofacial abnormalities in tusk mutants, and their incisors were thicker than those found in wild-type mice or in animals we examined in which there was overgrowth due to misalignment (not shown). Thus, we hypothesized that the excessive length and thickness of the tusk-like incisors might be due to deposition of lingual enamel, which would both thicken the mutant incisors and make them resistant to abrasion.

We performed synchrotron X-ray computed tomography (XTM), which measures the relative mineral concentration in calcified tissues and distinguishes enamel from dentin and bone. In adult wild-type and Spry4-/- (Spry4 null) incisors, which were of normal length and thickness, we detected enamel only on the labial surface (Fig. 1C,D). In contrast, tusk mutant incisors had enamel on both labial and lingual surfaces (Fig. 1E, and data not shown). Here we will focus on the phenotype of the mandibular incisors; the maxillary incisors have additional abnormalities, and will be described in a separate study.

Sagittal histological sections of postnatal day (P) 14 tusk mutant incisors confirmed that they had ectopic enamel along much of the anterior-posterior length of the lingual surface (Fig. 1G,H). Underlying this enamel we observed an ectopic layer of columnar cells, which resembled the ameloblasts that are normally found exclusively on the labial side (Fig. 1G-L). In addition to the presence of this ectopic layer of lingual ameloblasts, hereafter referred to as the “lingual ameloblast phenotype,” the morphology of the lingual CL was abnormal. In wild-type incisors the lingual CL is flattened and composed of a cuboidal epithelium (Fig. 1M, and data not shown), whereas in tusk mutants it resembled the labial CL in that it was more bulbous and composed of a columnar epithelium (Fig. 1O and data not shown; compare with Fig. 1N and P). These data indicate that Sprouty genes function in the incisor to prevent ameloblast production on the lingual side, thus facilitating incisor abrasion and preventing excessive incisor length.

Pre-ameloblasts are present on the lingual side of both Spry4-/-;Spry2+/- and Spry4-/- incisors at embryonic stages

Since ameloblasts are continuously lost at the anterior end of the rodent incisor as it grows (Smith and Warshawsky, 1977), and we found that lingual enamel was present throughout the life of the tusk mutants, it follows that ameloblasts must be continuously produced on the lingual side in these mice. To determine when lingual pre-ameloblasts (cells that have not yet begun to produce enamel matrix proteins) first appear in the tusk mutants we assayed for expression of Sonic hedgehog (Shh), which is expressed in ameloblasts from a very early stage in their development and is downregulated as they mature (Bitgood and McMahon, 1995). On the labial side, we detected Shh-expressing cells in wild-type and tusk mutant incisors at E15.5 and E16.5, along the length of the epithelium anterior to the CL (Fig. 2A,B,D,E). At E16.5 we also detected expression of Amelogenin (Amelx), a gene critical for proper enamel formation (Zeichner-David et al., 1995), on the labial side near the anterior end of the incisor (Fig. 2C,F). Thus as expected, we found that cells in the labial epithelium were differentiating along the ameloblast lineage, with those at the anterior end of the incisor at a more advanced stage.

Figure 2
Shh expression reveals the presence of ectopic pre-ameloblasts in Spry4-/-;Spry2+/-, in Spry4-/-, and in Fst-/- embryonic incisors

On the lingual side, Shh-expressing cells were not detected in wild-type or tusk mutant incisors near the cervical loops at E15.5 (Fig. 2D), but by E16.5 Shh-expressing cells were observed in the lingual epithelium of the tusk mutant, in a small domain just anterior to the CL (Fig. 2E). These data suggest that lingual pre-ameloblasts begin to form in tusk mutants between E15.5 and E16.5, at least one day after they are present on the labial side. These lingual pre-ameloblasts go on to differentiate, since Amelx expression was detected in the lingual epithelium of tusk mutants by E18.5 (not shown).

We assumed that Spry4 null incisors would not have lingual ameloblasts, because the incisors in Spry4 null adults were neither excessively long nor thick (not shown) and had no enamel on the lingual side (Fig. 1D). Unexpectedly, we found that lingual Shh-expressing pre-ameloblasts were present in Spry4 null incisors at E16.5 (compare Fig. 2G,H and 2D,E), which matured into Amelx-expressing cells by E18.5 (data not shown). However, lingual ameloblasts ceased to be generated in Spry4 null animals after birth, as discussed below. Pre-ameloblasts were not detected on the lingual side in either Spry4 null heterozygotes, even when they were Spry2 null, or in Spry1-/-;Spry2-/- embryos at E16.5 (not shown). Together, these data show that of the three Sprouty genes known to be expressed in the embryo (Minowada et al., 1999), Spry4 is uniquely required to suppress the generation of pre-ameloblasts on the lingual side of the embryonic incisor, and that both alleles of Spry4 must be inactivated to obtain a lingual ameloblast phenotype.

Previous studies have shown that the incisors in Fst null embryos have lingual ameloblasts (Wang et al., 2004), although it is not known what the postnatal incisor phenotype would be because Fst null embryos die perinatally (Matzuk et al., 1995). Because Fst is the only other gene known to be necessary to suppress the formation of lingual ameloblasts, we were interested to compare pre-ameloblast formation in Fst and Spry4 null embryos. When we assayed Fst null embryos at E16.5, we detected Shh-expressing cells in a domain adjacent to the lingual CL similar to the one we observed in tusk mutant and Spry4 null incisors. However, there was also a second lingual domain of Shh-expressing cells in Fst null incisors, which began a short distance anterior to the first domain and extended anteriorly toward the tip of the tooth (Fig. 2I). These data show that there are two discrete domains in the lingual epithelium, an anterior domain in which the formation of pre-ameloblasts is normally suppressed by FST but not SPRY4, and a posterior domain in which it is suppressed by both genes.

Loss of Sprouty function leads to abnormal FGF gene expression on the lingual side of the incisor

Since Sprouty genes normally function to suppress FGF signaling in different developmental settings (Klein et al., 2006; Shim et al., 2005), we investigated whether loss of Sprouty function affects the expression of targets of FGF signaling, which in the molar include FGF genes themselves (Kettunen et al., 2000; Kratochwil et al., 2002). In wild-type incisors at E16.5, we found that Fgf3 RNA was localized in labial mesenchyme just anterior to the CL (Fig. 3A). Fgf10 RNA was also detected in labial mesenchyme, but was more broadly distributed around the CL, in a domain that extended further anterior and also posterior to the Fgf3 expression domain (Fig. 3D). Fgf9 RNA was localized in a small epithelial domain just anterior to the labial CL (Fig. 3G). In contrast, on the lingual side, only Fgf10 RNA was detected in lingual mesenchyme anterior to and surrounding the CL, but at a much lower level than on the labial side.

Figure 3
FGF genes are upregulated or ectopically expressed on the lingual side of Spry4-/-;Spry2+/- and Spry4-/- embryonic incisors.

In both tusk mutant and Spry4 null incisors the FGF gene expression patterns were indistinguishable from what we observed in wild-type embryos at E15.5 and earlier (not shown). However, by E16.5, Fgf3, Fgf10, and Fgf9 were all abnormally expressed on the lingual side. For Fgf3 and Fgf10, the expression pattern on the lingual side appeared to be a mirror-image of that in labial mesenchyme (Fig. 3B,C,E,F). For Fgf9, lingual expression was limited to a small domain localized slightly more posteriorly than the labial Fgf9 domain, extending into lingual CL epithelium (Fig. 3H,I). This domain was similar to that of the lingual Shh expression domain (see Fig. 2E,H), suggesting that Fgf9 is expressed in lingual pre-ameloblasts. The increase in FGF gene expression detected on the lingual side of the mutant incisors was correlated with a marked alteration in the morphology of the lingual CL, as described for the tusk mutant incisor at P14 (see Fig. 1O); indeed the lingual CL in the E16.5 tusk and Spry4 null mutants appeared to be a mirror-image of the labial CL (see Fig. 3B,C).

We next assayed for expression of Etv4 and Etv5 (previously known as Pea3 and Erm, respectively), which are considered to be direct targets of RTK signaling (O’Hagan and Hassell, 1998; Roehl and Nusslein-Volhard, 2001). In wild-type incisors at E16.5, we detected Etv4 and Etv5 RNAs in both labial mesenchyme and epithelium, anterior to the CL, and on the lingual side, only in the epithelium, in a small domain at the posterior end of the CL (Fig. 3J, and data not shown). In contrast, in tusk mutant incisors, Etv4 and Etv5 RNAs were detected at a high level on both the labial and lingual sides, throughout the posterior epithelium and in the mesenchyme adjacent to the CL (Fig. 3K, and data not shown). These data indicate that loss of Sprouty function results in an increase in RTK signaling in incisor mesenchyme and epithelium on both the labial and lingual sides.

Together these results suggest that the normal function of Sprouty genes is to prevent the establishment of an epithelial-mesenchymal FGF signaling loop on the lingual side of the incisor that can stimulate ameloblast formation from a stem cell population in the CL. We also assayed for expression of a number of other genes that are thought to play a role in tooth development, including Activin, Bmp4, Dll1, Fgf4, Fst, Jag2, Lfng, Notch1, Notch2, Notch3, Runx2, and Twist1, but found no evidence that they were abnormally expressed in tusk mutant incisors (not shown). These observations further suggest that upregulation of FGF gene expression, and consequently FGF signaling, is the primary cause of the observed phenotype in Sprouty loss-of-function mutants.

Continuous formation of lingual ameloblasts in adult mice requires loss of Spry4 function and reduction in the dosage of another Sprouty gene

Although loss of Spry4 function alone results in the formation of ameloblasts on the lingual side of the incisor at E16.5 (Fig. 2), there is no lingual enamel in Spry4 null adults (Fig. 1D). To investigate when the generation of lingual ameloblasts ceases, we examined sections of Spry4 null incisors at P5. In sagittal sections, we observed a long swath of lingual enamel over a layer of ameloblasts (Fig. 4A) extending anteriorly from a point approximately 750 μm anterior to the lingual CL. The region from this point posterior to the CL appeared devoid of ameloblasts (Fig. 4A,B). This absence of ameloblasts was confirmed by examining serial coronal sections (not shown). In contrast, the labial ameloblast layer extended along the entire length of the tooth up to the CL (Fig. 4A,C). These data confirm that the ectopic Shh-expressing pre-ameloblasts detected in Spry4 null incisors at E16.5 subsequently differentiated into functional, enamel-producing ameloblasts, and show that lingual ameloblasts ceased being produced before P5.

Figure 4
Loss of Spry4 function alone is not sufficient to maintain continuous production of ameloblasts on the lingual side of the incisor

To determine whether this change had occurred by P2, we assayed for the expression of two of the genes that we found were affected by loss of Spry4 function at E16.5. Shh was robustly expressed in labial epithelium in all samples (Fig. 4D,E), but very few Shh-expressing cells were detected in the lingual epithelium of Spry4 null incisors (Fig. 4D). In contrast, there was strong lingual expression of Shh in tusk mutant incisors (Fig. 4E). Concomitant with the absence of Shh expression in Spry4 null lingual epithelium, Fgf3 was no longer abnormally expressed in lingual mesenchyme (Fig. 4F), whereas ectopic Fgf3 expression was detected in lingual mesenchyme of tusk mutant incisors at this stage (Fig. 4G). The absence of lingual Fgf3 expression in Spry4 null postnatal incisors was accompanied by a morphological change in the lingual CL from labial-like to lingual-like (Fig. 4D, compare with Fig. 3C). These data show that formation of lingual pre-ameloblasts ceases around the time of birth in Spry4 null incisors, but continues in Spry4 null mice that also lack one copy of Spry2. Interestingly, we found that Spry4-/-;animals that carried one null allele of Spry1 (Basson et al., 2005) likewise displayed a “tusk mutant” phenotype (not shown). Thus, the production of lingual ameloblasts that is initiated prenatally as a result of loss of Spry4 function continues after birth only when the dosage of another Sprouty gene, either Spry1 or Spry2, is reduced.

The lingual ameloblast phenotype can be rescued in the adult by reducing FGF gene dosage

To determine the extent to which lingual ameloblast formation is sensitive to FGF signaling, we produced tusk mutants heterozygous for an Fgf9 null allele (Colvin et al., 2001) (Spry4-/-;Spry2+/-;Fgf9+/- adults), and examined their incisors by XTM. We found that only 14% had lingual enamel, compared with 100% of their Spry4-/-;Spry2+/- littermates (p=<0.01). Likewise, heterozygosity for a null allele of Fgf10 (Min et al., 1998) had a similar although less dramatic effect, in that 37% of Spry4-/-;Spry2+/-;Fgf10+/- adults had lingual enamel, compared with 93% of their Spry4-/-;Spry2+/- littermates (p=<0.01) Fig. 4H). Thus, continuous formation of ameloblasts on the lingual side in Spry4-/-;Spry2+/- adults is dependent on persistent abnormal expression of Fgf9 and Fgf10 at high levels.

In contrast, when we assayed for Shh expression at E16.5, all Sprouty mutant embryos that were heterozygous for an Fgf9 null allele (Spry4-/-;Fgf9+/-, n=4; Spry4-/-;Spry2+/-;Fgf9+/-, n=3) had lingual Shh-expressing pre-ameloblasts (not shown), as was observed in all Spry4 null and tusk mutant incisors in which Fgf9 dosage was normal. Preliminary results on Spry4 null embryos with reduced dosage of Fgf10 were similar. Thus reducing FGF gene dosage in Sprouty mutant embryos did not rescue the prenatal lingual ameloblast phenotype. These data raise the possibility that loss of Sprouty function causes lingual ameloblast formation in embryonic incisors as a consequence of effects on non-FGF-mediated RTK signaling. Alternatively, there may be more FGF signaling in the embryonic than in the adult incisor, and therefore reducing FGF gene dosage by one copy does not sufficiently lower the level of FGF signaling in the embryo to prevent lingual ameloblast formation in the absence of Sprouty gene function.

Spry4 is required in both mesenchyme and epithelium to suppress the initiation of lingual ameloblast formation

To determine where in the embryonic incisor Spry4 might function to suppress the initiation of lingual ameloblast formation, we assessed the expression pattern of Spry4 as well as Spry1 and Spry2 in wild-type embryos. At E14.5, we found significant differences in the expression domains of the three Sprouty genes: Spry1 RNA was detected in both epithelium and mesenchyme (Fig. 5A); Spry2 RNA was detected exclusively in the epithelium (Fig. 5B); and Spry4 RNA was detected exclusively in the mesenchyme (Fig. 5C). However, by E16.5, not only Spry1 and Spry2, but also Spry4 expression was detected in the epithelium on both the labial and lingual sides of the incisor. In the mesenchyme, Spry1 and Spry4, but not Spry2 expression was detected on the labial side, and only Spry4 expression was detected, albeit at a low level, on the lingual side (Fig. 5D-F). Since Spry4 expression was detected in both lingual epithelium and mesenchyme, we next sought to determine in which tissue(s) Spry4 function is required.

Figure 5
Sprouty gene expression and tissue-specific inactivation in the developing incisor

To test whether Spry4 function is required in the epithelium, we performed Cre-mediated conditional loss-of-function experiments using a K14-cre transgene that has previously been used to inactivate floxed alleles in dental epithelium from early stages of tooth development (Dassule et al., 2000). First, we produced K14-cre; Spry4fl/-;Spry2fl/+ embryos, and assayed for Shh, Fgf3, Fgf10, and Fgf9, expression at E17.5, to determine the effect of epithelium-specific inactivation of Spry4 on lingual gene expression. As expected, Spry4 RNA was detected in incisor mesenchyme but not epithelium (Fig. 5G). However, no abnormal lingual gene expression was observed in such embryos (Fig. 5I and data not shown), indicating that a complete loss of Spry4 function in the epithelium, even when the mesenchyme is heterozygous for Spry4, is not sufficient to allow the formation of lingual pre-ameloblasts.

To test whether Spry4 function is required in the mesenchyme, we employed a Wnt1-cre transgene (Danielian et al., 1998) that has previously been used to inactivate floxed alleles in dental mesenchyme from early stages of tooth development (Chai et al., 2000). We produced Wnt1-cre; Spry4fl/fl;Spry2fl/fl embryos, and assayed to determine the effect on lingual gene expression at E16.5. As expected, Spry4 expression was detected in incisor epithelium but not mesenchyme (Fig. 5H). However, despite inactivation of both alleles of Spry4 in the mesenchyme, we detected no lingual expression of Shh or the other genes assayed in these embryos (Fig. 5J and data not shown). Thus, elimination of Spry4 function in only the mesenchyme is not sufficient to cause the formation of lingual pre-ameloblasts.

We next assayed Wnt1-cre; Spry4fl/-;Spry2fl/+ embryos, which inherited one Spry4 null allele and one floxed allele. In these embryos, in which the mesenchyme was null for Spry4 function as a consequence of Wnt1-cre activity, and the epithelium was heterozygous for Spry4, we observed abnormal lingual gene expression (Fig. 5K and data not shown). These data indicate that inactivation of both Spry4 alleles in the mesenchyme and one Spry4 allele in the epithelium is required, when there are two functional Spry2 alleles (floxed and wild-type) in the epithelium, for the generation of Shh-expressing pre-ameloblasts on the lingual side of the embryonic incisor. Because these animals do have two functional Spry2 alleles in the epithelium, they would presumably cease producing ameloblasts after birth and thus would not display the tusk mutant phenotype.

DISCUSSION

In a few mammalian species, teeth have evolved the ability to grow throughout adult life (Tummers and Thesleff, 2003). One such tooth is the rodent incisor, in which continuous growth is coupled with a lack of enamel deposition on the lingual side, thereby providing a means of sharpening the tip and limiting incisor length. Here we demonstrate that in mice, Sprouty genes are essential for ensuring that this vital asymmetry in enamel deposition occurs. Loss of Spry4 function results in the generation of enamel-producing ameloblasts on both the lingual and labial sides of the embryonic incisor. We present evidence that this phenotype is due to the establishment of an ectopic epithelial-mesenchymal FGF signaling loop on the lingual side. Interestingly, we found that this lingual ameloblast phenotype, which is robust in the embryo, is not sustained after birth unless the dosage of an additional Sprouty gene, either Spry1 or Spry2, is reduced. The additive loss of Sprouty function results in ‘tusk-like’ adult incisors that are resistant to abrasion because enamel is deposited on both the lingual and labial side.

FGF signaling regulates the generation of lingual ameloblasts from stem cells

It is now well-established that loss of Sprouty function causes hypersensitivity to FGF and other receptor tyrosine kinase signaling (Mason et al., 2006). Here we provide evidence that in the incisor, Sprouty genes antagonize FGF signaling, and that loss of Sprouty function results in upregulation of FGF gene expression on the lingual side. Three lines of evidence indicate that this increase in FGF gene expression is responsible for the generation of lingual ameloblasts. First, an increase in the level of lingual FGF gene expression is closely correlated with the initiation of Shh expression, a marker for pre-ameloblasts, in the lingual epithelium of late gestation embryos. Second, the reversal of the increase in lingual Fgf3 expression that we observed in Spry4 null incisors shortly after birth is closely correlated with cessation of lingual Shh expression. Third, reducing the dosage of either Fgf9 or Fgf10 substantially rescues the postnatal lingual ameloblast phenotype in tusk mutants, thus providing genetic evidence that high levels of FGF signaling are required to sustain the generation of lingual ameloblasts in adult Sprouty mutants.

Based on the results of our tissue-specific knock-out experiments and gene expression analyses, we propose the following model to explain how Sprouty genes normally function to prevent an increase in FGF gene expression and the consequent establishment of an FGF signaling loop on the lingual side of the incisor between E15.5 and E16.5 (see Fig. 6A). In the epithelium, SPRY4 normally prevents an FGF signal produced in the mesenchyme from inducing/upregulating FGF gene expression in the epithelium. FGF10 is a good candidate for the mesenchymal signal that is antagonized by SPRY4 in the epithelium, since Fgf10 expression is normally detected at a low level in the mesenchyme surrounding the wild-type lingual CL at E16.5. Moreover, FGF10 is known to signal via the b isoform of FGFR2, which is expressed in lingual (and labial) epithelium (Peters et al., 1992). We propose that inactivation of a single allele of Spry4 in the epithelium renders it sufficiently hypersensitive to the small amount of FGF10 normally produced in the mesenchyme such that the expression of Fgf9, a direct or indirect target of FGF10 signaling, is slightly upregulated in the lingual epithelium. However, if the mesenchyme is not sufficiently hypersensitive, as in K14-cre; Spry4fl/-;Spry2fl/+ embryos that retain one functional Spry4 allele in the mesenchyme, then this increase in epithelial Fgf9 expression is presumably transitory because the mesenchymal FGFs are not upregulated in response to the increase in epithelial FGF signal and a positive-feedback signaling loop is therefore not established on the lingual side.

Figure 6
Models for the role of Sprouty genes in controlling FGF signaling in the mouse incisor and for the generation of embryonic ameloblasts

Likewise, in the mesenchyme, SPRY4 prevents an FGF signal produced in the lingual epithelium from upregulating the expression of mesenchymal FGF gene(s). FGF9, which is normally produced in the lingual epithelium at such a low level that its expression is detected only with a radiolabeled probe (Fig. 3G and (Wang et al., 2007), presumably signals via FGFR1, which is expressed throughout the incisor mesenchyme (Peters et al., 1992). Inactivating two alleles of Spry4 in the mesenchyme renders it hypersensitive to the small amount of FGF9 produced in the epithelium, such that the expression of Fgf3 and Fgf10, two direct or indirect targets of FGF9 signaling, is induced/upregulated in the lingual mesenchyme. Thus a positive feedback FGF loop between lingual epithelium and mesenchyme is initiated and maintained for a few days in late-gestation Spry4 mutant incisors. However, if the epithelium is not also sufficiently hypersensitive, as in Wnt1-cre; Spry4fl/fl;Spry2fl/fl embryos with two functional Spry4 alleles in the epithelium, then it will not respond to increases in the level of mesenchymal FGF signals, and a positive-feedback signaling loop will not be initiated.

Although we cannot rule out differences on the labial side between tusk mutant and control incisors, such as more rapid growth, loss of Sprouty function did not appear to cause any gross abnormalities on that side, where Sprouty genes are highly expressed and presumably antagonize the FGF signaling that is required for normal ameloblast development and function. Analogous observations have been made in other developmental settings, where loss of Sprouty function apparently affects only cells that do not normally respond to RTK signaling, but has little or no effect on cells that normally respond to high levels of RTK signaling (Basson et al., 2005; Klein et al., 2006; Shim et al., 2005). Precisely how the dynamics of the negative feedback between RTK signaling and Sprouty-mediated inhibition of that signaling impacts such developmental systems remains to be elucidated.

Comparison of Sprouty and Follistatin mutant incisors suggests that ameloblasts form from two different progenitor populations

The data reported here also must be considered in the context of a larger genetic network that includes TGFβ family members and their antagonists such as Follistatin. Previous studies of the incisor phenotype in Fst null embryos have provided evidence that FST inhibits lingual ameloblast differentiation in the anterior incisor via a direct negative effect on BMP4 signaling (Wang et al., 2004), whereas in the lingual CL region it may do so by negatively regulating Fgf3 expression indirectly via effects on signaling by other TGFβ family members (Wang et al., 2007). Our analysis of Shh expression in Fst null mutants revealed that there are two physically separate domains in which pre-ameloblasts are found in the lingual epithelium at E16.5 (see Fig. 2I). We suggest that these anterior and posterior domains correspond to those in which ameloblast formation is thought to be inhibited by direct and indirect effects on TGFβ signaling, respectively. Significantly, we found that in embryonic Spry4 null incisors, lingual pre-ameloblasts are detected only in the posterior domain (see Fig. 2H), thus providing strong evidence that when ameloblasts form in mutant embryonic lingual epithelium, they do so in two domains that respond differently to increased signaling.

To explain these observations, we propose the model illustrated in Figure 6B. In the anterior domain, ameloblasts are generated from an embryonic ameloblast progenitor (EAP) population capable of giving rise to a limited number of progeny that subsequently differentiate “in situ” into enamel-producing cells. This process is analogous to that by which all ameloblasts in molars are thought to form (Zeichner-David et al., 1995). Development of ameloblasts from EAP cells in the anterior lingual domain is normally inhibited by FST acting to suppress BMP4 signaling, and is not suppressed by Sprouty-mediated inhibition of FGF signaling. In contrast, in the posterior lingual domain, ameloblasts are derived from a self-renewing ameloblast stem cell population located within the nearby CL. The formation of these ameloblasts depends on a high level of FGF signaling, which is normally suppressed by Spry4 function in the epithelium and mesenchyme. However, ameloblast formation in this domain is also suppressed by FST, most likely by an indirect negative effect on Fgf3 expression.

One possible explanation for the observation that loss of function of either Fst or Spry4 leads to the induction of Fgf3 expression in lingual mesenchyme is that Fst and Spry4 act in the same genetic pathway. However, we found that loss of Fst function does not result in a decrease in Spry4 expression or vice versa (not shown), indicating that these genes may instead act in parallel pathways that converge on downstream targets and that can each affect Fgf3 expression. The increase in lingual Fgf3 expression that has been detected in Fst null mutants could sufficiently increase the level of FGF signaling from the mesenchyme to the epithelium such that it overcomes the antagonism by Sprouty genes that normally prevents the establishment of an FGF signaling loop.

We further suggest that ameloblast formation on the labial side likewise occurs by two different mechanisms: the first ameloblasts to form in the embryonic incisor develop from EAP cells; their formation requires BMP4 signaling but may occur independent of FGF signaling. Subsequently, ameloblasts are generated from ASCs in the labial CL, and this process depends on signaling via other TGFβ family members as well as high levels of FGF signaling. Based on these hypotheses, we speculate that a key event in incisor development is the establishment of the ASC population on the labial side between E15.5 and E16.5. Formation of such stem cells would involve the acquisition, perhaps by a subpopulation of EAP cells, of the ability to self-renew as well as to produce progeny that give rise to ameloblasts (and perhaps other epithelial cell types) throughout the life of the animal.

Possible mechanisms by which FGF signaling controls ameloblast formation

Perhaps the most important question raised by our data is: how does an increase in FGF signaling on the lingual side of the incisor result in the formation of ameloblasts? One possibility is that ASCs are not normally present in the lingual CL, and that ectopic FGF signaling functions to induce their formation. Another possibility is that ASCs are present in the lingual CL, but normally they do not give rise to progeny that develop into ameloblasts. If so, then increased FGF signaling might stimulate them to form such progeny, perhaps by promoting the formation and/or expansion of T-A cells that subsequently develop into ameloblasts. With respect to the latter suggestion, it is tempting to speculate that the transformation to a more labial CL-like morphology that occurs in the mutant lingual CL when it begins producing ameloblasts might reflect the presence of an expanded T-A cell population. At present, we are unable to explore these and other possibilities because markers for ASCs and T-A cells have not been identified. However, we are inclined to favor the hypothesis that FGF signaling affects T-A cells, if only because the domains in which ectopic Fgf3 and Fgf9 expression are detected in Spry4 null incisors are localized just anterior to the region in the CL where T-A cells are speculated to reside.

One of our most intriguing findings is that the phenotype that appears to be very robust in the embryo - the generation of an ectopic ameloblast population from stem cells on the linguial side of the incisor due to loss of Spry4 function - is reversed just after birth unless an additional Sprouty gene is inactivated. Based on our genetic rescue data, a likely explanation for this phenomenon is that the normal level of FGF signaling on the lingual side, albeit low, is higher in the embryo than in the adult. Thus the removal of an additional Sprouty gene is required to render the adult epithelium and mesenchyme sufficiently sensitive to the adult level of FGF signaling to sustain the generation of lingual ameloblasts. These data reveal that the generation of differentiated progeny from a particular stem cell population can be differently regulated in the embryo and adult, and illustrate how manipulating levels of signals or their antagonists can provide a mechanism for enhancing the production of differentiated progeny from adult stem cells.

ACKNOWLEDGMENTS

We thank Drs. M. Matzuk, D. Ornitz, L. Reichardt, D. Sheppard, and D. Srivastava for helping us to obtain the mutant mouse lines used in this study, and Drs. P. Denbesten and I. Thesleff for in situ probes. We are grateful to P. Ghatpande, I. Koppova, Z. Markova, A. Nemati, G. Nonomura, L. Prentice, H. Schmidt and E Yu for excellent technical assistance. We also thank Drs. J. Jernvall, B. Kraatz, and I. Thesleff for helpful discussion and advice, as well as M. Kumar, R. Metzger, and our laboratory colleagues for critical reading of the manuscript. The Advanced Light Source is supported by the Director, Office of Basic Energy Sciences, of the U.S. Department of Energy (under Contract No. DE-AC02-05CH11231). O.K. was supported by a Pediatric Scientist Development Program award from the NIH (K12-HD00850). This work was supported by grants from the GACR (304/07/0223) and MSMT CR (project COST B23.002) to R.P. and M.P., the Medical Research Council (G0601104) and the Wellcome Trust (080470) to M.A.B., and the US National Institutes of Health (P01 DE09859) to G.W.M. and (R01 DE17744) to G.R.M..

REFERENCES

  • Addison WH, Appleton JL. The structure and growth of the incisor teeth of the albino rat. J Morph. 1915;26:43–96.
  • Basson MA, Akbulut S, Watson-Johnson J, Simon R, Carroll TJ, Shakya R, Gross I, Martin GR, Lufkin T, McMahon AP, et al. Sprouty1 is a critical regulator of GDNF/RET-mediated kidney induction. Dev Cell. 2005;8:229–39. [PubMed]
  • Bitgood MJ, McMahon AP. Hedgehog and Bmp genes are coexpressed at many diverse sites of cell-cell interaction in the mouse embryo. Dev Biol. 1995;172:126–38. [PubMed]
  • Chai Y, Jiang X, Ito Y, Bringas P, Jr., Han J, Rowitch DH, Soriano P, McMahon AP, Sucov HM. Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis. Development. 2000;127:1671–9. [PubMed]
  • Colvin JS, White AC, Pratt SJ, Ornitz DM. Lung hypoplasia and neonatal death in Fgf9-null mice identify this gene as an essential regulator of lung mesenchyme. Development. 2001;128:2095–106. [PubMed]
  • Danielian PS, Muccino D, Rowitch DH, Michael SK, McMahon AP. Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase. Curr Biol. 1998;8:1323–6. [PubMed]
  • Dassule HR, Lewis P, Bei M, Maas R, McMahon AP. Sonic hedgehog regulates growth and morphogenesis of the tooth. Development. 2000;127:4775–85. [PubMed]
  • Fuchs E, Tumbar T, Guasch G. Socializing with the neighbors: stem cells and their niche. Cell. 2004;116:769–78. [PubMed]
  • Gronthos S, Brahim J, Li W, Fisher LW, Cherman N, Boyde A, DenBesten P, Robey PG, Shi S. Stem cell properties of human dental pulp stem cells. J Dent Res. 2002;81:531–5. [PubMed]
  • Harada H, Kettunen P, Jung HS, Mustonen T, Wang YA, Thesleff I. Localization of putative stem cells in dental epithelium and their association with Notch and FGF signaling. J Cell Biol. 1999;147:105–20. [PMC free article] [PubMed]
  • Harada H, Toyono T, Toyoshima K, Yamasaki M, Itoh N, Kato S, Sekine K, Ohuchi H. FGF10 maintains stem cell compartment in developing mouse incisors. Development. 2002;129:1533–41. [PubMed]
  • Kettunen P, Laurikkala J, Itaranta P, Vainio S, Itoh N, Thesleff I. Associations of FGF-3 and FGF-10 with signaling networks regulating tooth morphogenesis. Dev Dyn. 2000;219:322–32. [PubMed]
  • Kinney JH, Haupt DL, Balooch M, Ladd AJ, Ryaby JT, Lane NE. Three-dimensional morphometry of the L6 vertebra in the ovariectomized rat model of osteoporosis: biomechanical implications. J Bone Miner Res. 2000;15:1981–91. [PubMed]
  • Klein OD, Minowada G, Peterkova R, Kangas A, Yu BD, Lesot H, Peterka M, Jernvall J, Martin GR. Sprouty genes control diastema tooth development via bidirectional antagonism of epithelial-mesenchymal FGF signaling. Dev Cell. 2006;11:181–90. [PMC free article] [PubMed]
  • Kratochwil K, Galceran J, Tontsch S, Roth W, Grosschedl R. FGF4, a direct target of LEF1 and Wnt signaling, can rescue the arrest of tooth organogenesis in Lef1(-/-) mice. Genes Dev. 2002;16:3173–85. [PubMed]
  • Mason JM, Morrison DJ, Basson MA, Licht JD. Sprouty proteins: multifaceted negative-feedback regulators of receptor tyrosine kinase signaling. Trends Cell Biol. 2006;16:45–54. [PubMed]
  • Matzuk MM, Lu N, Vogel H, Sellheyer K, Roop DR, Bradley A. Multiple defects and perinatal death in mice deficient in follistatin. Nature. 1995;374:360–3. [PubMed]
  • Min H, Danilenko DM, Scully SA, Bolon B, Ring BD, Tarpley JE, DeRose M, Simonet WS. Fgf-10 is required for both limb and lung development and exhibits striking functional similarity to Drosophila branchless. Genes Dev. 1998;12:3156–61. [PubMed]
  • Minowada G, Jarvis LA, Chi CL, Neubuser A, Sun X, Hacohen N, Krasnow MA, Martin GR. Vertebrate Sprouty genes are induced by FGF signaling and can cause chondrodysplasia when overexpressed. Development. 1999;126:4465–75. [PubMed]
  • O’Hagan RC, Hassell JA. The PEA3 Ets transcription factor is a downstream target of the HER2/Neu receptor tyrosine kinase. Oncogene. 1998;16:301–10. [PubMed]
  • Peters KG, Werner S, Chen G, Williams LT. Two FGF receptor genes are differentially expressed in epithelial and mesenchymal tissues during limb formation and organogenesis in the mouse. Development. 1992;114:233–43. [PubMed]
  • Roehl H, Nusslein-Volhard C. Zebrafish pea3 and erm are general targets of FGF8 signaling. Curr Biol. 2001;11:503–7. [PubMed]
  • Shim K, Minowada G, Coling DE, Martin GR. Sprouty2, a Mouse Deafness Gene, Regulates Cell Fate Decisions in the Auditory Sensory Epithelium by Antagonizing FGF Signaling. Dev Cell. 2005;8:553–64. [PubMed]
  • Smith CE, Warshawsky H. Cellular renewal in the enamel organ and the odontoblast layer of the rat incisor as followed by radioautography using 3H-thymidine. Anat Rec. 1975;183:523–61. [PubMed]
  • Smith CE, Warshawsky H. Quantitative analysis of cell turnover in the enamel organ of the rat incisor. Evidence for ameloblast death immediately after enamel matrix secretion. Anat Rec. 1977;187:63–98. [PubMed]
  • Tummers M, Thesleff I. Root or crown: a developmental choice orchestrated by the differential regulation of the epithelial stem cell niche in the tooth of two rodent species. Development. 2003;130:1049–57. [PubMed]
  • Wang XP, Suomalainen M, Felszeghy S, Zelarayan LC, Alonso MT, Plikus MV, Maas RL, Chuong CM, Schimmang T, Thesleff I. An integrated gene regulatory network controls stem cell proliferation in teeth. PLoS Biol. 2007;5:e159. [PMC free article] [PubMed]
  • Wang XP, Suomalainen M, Jorgez CJ, Matzuk MM, Werner S, Thesleff I. Follistatin regulates enamel patterning in mouse incisors by asymmetrically inhibiting BMP signaling and ameloblast differentiation. Dev Cell. 2004;7:719–30. [PubMed]
  • Yokohama-Tamaki T, Ohshima H, Fujiwara N, Takada Y, Ichimori Y, Wakisaka S, Ohuchi H, Harada H. Cessation of Fgf10 signaling, resulting in a defective dental epithelial stem cell compartment, leads to the transition from crown to root formation. Development. 2006;133:1359–66. [PubMed]
  • Zeichner-David M, Diekwisch T, Fincham A, Lau E, MacDougall M, Moradian-Oldak J, Simmer J, Snead M, Slavkin HC. Control of ameloblast differentiation. Int J Dev Biol. 1995;39:69–92. [PubMed]