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The Ames waltzer (av) mouse mutant exhibits auditory and vestibular abnormalities resulting from mutation of protocadherin 15 (Pcdh15). Ames waltzer has been identified as an animal model for inner ear pathology associated with Usher syndrome type 1F. Studies correlating anatomical phenotype with severity of genetic defect in various av alleles are providing better understanding of the role played by Pcdh15 in inner ear development and of sensorineural abnormalities associated with alterations in Pcdh15 protein structure as a result of gene mutation. In this work we present new findings on inner ear pathology in four alleles of av mice with differing mutations of Pcdh15 as well as varying alterations in inner ear morphology. Two alleles with in-frame deletion mutations (Pcdh15av-J and Pcdh15av-2J) and two presumptive functional null alleles (Pcdh15av-3J and Pcdh15av-Tg) were studied. Light and electron microscopic observations demonstrated that the severity of cochlear and vestibular pathology in these animals correlates positively with the extent of mutation in Pcdh15 from embryonic day 18 (E18) up to 12 months. Electron microscopic analysis of immature ears indicated early abnormalities in the arrangement of stereocilia and the inner and outer hair cell cuticular plates, stereocilia rootlets, and the actin meshwork within the cuticular plate. In severe cases, displacement of the kinocilium and alterations in the shape of the cuticular plate was also observed. Mice harboring in-frame deletion mutations showed less disorganization of stereocilia and cuticular plates in the organ of Corti than the presumptive functional null alleles at P0–P10. A slower progression of pathology was also seen via light microscopy in older animals with in-frame deletions, compared to the presumptive functional null mutations. In summary, our results demonstrate that mutation in Pcdh15 affects the initial formation of stereocilia bundles with associated changes in the actin meshwork within the cuticular plate; these effects are more pronounced in the presumed null mutation compared to mutations that only affect the extracellular domain. The positive correlation of severity of effects with extent of mutation can be seen well into adulthood.
Usher's syndrome type 1 (USH1) is a genetically heterogeneous group of recessive disorders that causes deafness in humans at or near birth and blindness by adolescence. Since the original report linking the Ames waltzer (av) mouse mutation to protocadherin 15 (Pcdh15) was published (Alagramam et al. 2001a), several mutations in the human ortholog of Pcdh15 have been linked to human syndromic (USH1F) and nonsyndromic (DFNB23) deafness (Ahmed et al. 2003; Alagramam et al. 2001a,b). More recently, in the Ashkenazi Jewish population, the R245X mutation of PCDH15 was reported to account for 58% of USH1 cases (Ben Yosef et al. 2003). These studies indicate the prevalence of congenital deafness associated with PCDH15 mutation and the importance of understanding PCDH15-associated inner ear pathology as it relates to the nature of the mutation. This knowledge will support optimal rehabilitation of communication in USH1F patients. However, it is difficult, if not impossible, to evaluate the onset and the course of pathology in patients carrying mutations in PCDH15 due to lack of appropriate tissue material. In mice, mutations in Pcdh15av-3J and Pcdh15av-Tg alleles of av result in premature stop codons. Similarly, two USH1F families with mutation in PCDH15 have been identified in which the mutations segregate with the disease phenotype and generate premature stop codons (Alagramam et al. 2001b). Therefore, mice carrying similar genetic lesions in Pcdh15 could serve as a model for inner ear pathology associated with USH1F and DFNB23.
Previously, we characterized different alleles of av, including Pcdh15av-TgN2742Rpw, Pcdh15av-3J, Pcdh15av-2J, and Pcdh15av-J (Alagramam et al. 2000, 2001a,b) (Pcdh15av-TgN2742Rpw is written as Pcdh15av-Tg in this report). Pcdh15 is predicted to code for a transmembrane protein. Pcdh15av-J and Pcdh15av-2J alleles carry in-frame deletions of the coding sequence and are considered to be less deleterious because these mutations would result in the absence of a small number of amino acids in the extracellular domain of the protein. In contrast, Pcdh15av-Tg and Pcdh15av-3J alleles are presumed to be functional null alleles because mutation in these alleles is predicted to code for a Pcdh15 protein lacking the entire transmembrane domain and all of the cytoplasmic domains.
In addition to being a model for inner ear pathology in USH1F and DFNB23 patients, av mice will help provide better understanding of the function of Pcdh15. In all av alleles studied thus far, no auditory evoked potentials can be recorded as early as they can be tested (P15) (Alagramam et al. 1999, 2001a) and all mutant mice display circling behavior by P10, indicative of vestibular dysfunction. This suggests that the mutation in Pcdh15 leads to early functional abnormalities of the mouse inner ear (Alagramam et al. 2005). Studying detailed ultrastructural development of the cochlear sensory epithelia in mutants and correlating that with the nature of the mutation among different alleles of a given mutation should provide additional information about the consequences of the loss of gene function.
In this study, the correlation between genotype and anatomic phenotype was investigated in four av alleles during postnatal development. Early changes in organ of Corti hair cell structure in mice aged P0–P10 were evaluated by electron microscopy. In addition, animals aged P15 to 12 months were studied by light microscopy to determine if the extent of mutation effects the long-term survival of inner ear structures outside the organ of Corti.
Mice The insertional mutant, Pcdh15av-Tg, and methods for genotyping have been described previously (Alagramam et al. 1999). Pcdh15av-J, Pcdh15av-2J, and Pcdh15av-3J alleles were originally obtained from The Jackson Laboratory and subsequently maintained as a breeding colony at Case Western Reserve University. For the all alleles, homozygous males were crossed to heterozygous females; the offspring from these matings were either heterozygous or homozygous for a specific allele. Mice homozygous for an av allele showed circling behavior by P10, compared to heterozygous littermates, which behaved similarly to wild-type mice. For mice younger than P10, a polymerase chain reaction (PCR)-based approach was used to genotype the Jackson alleles (described below). Protocol for animal use was approved by the Animal Care and Use Committee of the Case Western Reserve University.
Genotyping of Pcdh15av-J, Pcdh15av-2J, and Pcdh15av-3J alleles Mice were genotyped by PCR amplification from genomic tail DNA obtained from offspring derived from heterozygous by homozygous mating described above. Genomic DNA (~500 ng/reaction) was amplified under standard reaction conditions using Platinum Taq DNA polymerase (Invitrogen, Carlsbad, CA, USA) for 35 cycles of 94°C for 30 s, 55–58°C (depending on the primer pair used) for 30 s, 72°C for 30 s. Primer pairs and product size are as follows: Pcdh15av-J KA 15, 5′-TTC ACT ACA GCC TGG GGA AC-3′ and KA 16 5′-GTT GAA TGT CGA GGG TGG AC-3′, 156 bp product; Pcdh15av-2J KA26 5′-CTA GGG GAG GAC CAC CAG-3′ and KA27 5′-CGT TTC GAC TCT CTT CAT CA-3′, 72 bp product; Pcdh15av-3J KA 17 5′-GAC GGC AAA CTG CTC GAT A-3′ and KA 18 5′-GGG ATG CAA CAG AGG ATG AT-3′, 190 bp product. The annealing temperature for KA15/16 and 26/27 is 55°C; that annealing temperature for KA17/18 is 58°C. It should be noted that the genotyping scheme for av-J and av-2J is designed to distinguish heterozygous from homozygous offspring derived from crosses between heterozygote and homozygote parents. Primers KA 15/16 and KA 26/27 were designed to sequence DNA contained within the deleted area. For instance, when genotyping for the av-J allele, an amplified band of 156 bp will indicate that the mice are “+/J” and the lack of amplified product (156 bp) band will indicate “J/J” genotype. As a positive control, av-2J primers are added to the av-J genotyping reaction mix. Because av-J mice should carry a wild-type sequence at the “2J” site, the expected size (72 bp) product will be obtained. The same scheme is carried out when genotyping offspring derived from crosses between heterozygote and homozygote av-2J parents. For the av-3J allele, a different scheme is used. This takes advantage of the single nucleotide addition in the av-3J allele (Alagramam et al. 2001a) that results in the introduction of a new restriction site, namely, MboII. The product from the wild-type DNA is 190 bp. Digestion of the 190-bp PCR product with MboII cleaves only the sequence harboring the 3J mutation into 120- and 70-bp fragments, leaving the wild-type sequence undigested. With this approach, +/3J mice allele will show three bands (190, 120, and 70 bp) and mice homozygous for the 3J allele will show two bands (120 and 70 bp).
Histology Inner ear tissue from Pcdh15av-J, Pcdh15av-2J, Pcdh15av-3J, and Pcdh15av-Tg homozygous and heterozygous mice at ages ranging from E18 to 12 months was studied. Tissue specimens were either processed, embedded in glycol methacrylate, then serial-sectioned for light microscopic study of the entire membranous labyrinth or prepared for transmission (TEM) and scanning electron microscopic (SEM) evaluation of the ultrastructure of the endolymphatic surface of organ of Corti.
All study animals were anesthetized and sacrificed by decapitation. The middle and inner ears were opened bilaterally, phosphate-buffered 2.5% glutaraldehyde fixative was flushed through the perilymphatic space, and the tissue was placed in fixative for 14–18 h at 4°C (Alagramam et al. 2000). Tissue was then rinsed in 0.1 M sodium phosphate buffer (pH 7.4–7.5) and stored at 4°C for several days prior to processing for light and electron microscopic viewing.
Specimens from P15 to 12-month Pcdh15av-J, Pcdh15av-2J, Pcdh15av-3J, and Pcdh15av-Tg homozygous and heterozygous mice were prepared for light microscopic study to examine changes in the inner ear structures. Preparation of material for light microscopic examination was as follows: Temporal bones were dissected from the skull and decalcified in 0.35 M EDTA for two to four days at room temperature with agitation, rinsed in saline, dehydrated in a series of alcohols, infiltrated and embedded in glycol methacrylate (JB-4, Polysciences, Warrington, PA, USA) embedding solution. Serial sections at a thickness of 3–5 μm were taken in a plane approximately parallel to the long axis of the modiolus, and every tenth section was stained with toluidine blue, coverslipped, and viewed using a compound microscope. Analysis of each set of sections included the entire cochlea and all vestibular sensory organs.
Organ of Corti samples from E18 to P10 homozygous and heterozygous mice were prepared for either SEM or TEM to examine ultrastructural changes in the cuticular plate. Glutaraldehyde-fixed and buffer-rinsed inner ear samples were stained with 1–1.5% osmium tetroxide, followed by a buffer rinse. Material to be studied by TEM was then decalcified in 0.35 M EDTA, rinsed in buffer, dehydrated in a graded series of ethanols, and embedded in Spurrs resin. The basal turn of the organ of Corti was thin-sectioned either in a plane parallel to the surface of the reticular lamina or in a plane perpendicular to that surface and radial to the modiolus. Sections were then stained with lead citrate and uranyl acetate and viewed using a JEOL 1200EX transmission electron microscope. For SEM, the organs of Corti were exposed via cochlear microdissection and the tissue was dehydrated in a series of ethanols, critical point dried, coated with gold–palladium, and studied using a JEOL 848 scanning electron microscope.
Light and electron microscopic examination of the four av alleles included in this study (see Fig. 1 for deletion sites) revealed a clear difference in the severity of alterations in the organ of Corti depending on the extent of Pcdh15 mutation. Electron microscopic examination of specimens from immature mice showed a more severe phenotype in animals harboring the functional null mutations than in mice harboring in-frame deletion mutations. In addition, light microscopic study of mice ages P15 up to 12 months revealed that the extent of mutation affects the long-term survival of inner ear structures outside the organ of Corti.
No changes in inner ear morphology were detected by light microscopy in temporal bone cross sections from homozygous Pcdh15 mutants at P10 or earlier. This section focuses on electron microscopic findings from mice aged E18–P10 (19 heterozygous controls, 19 presumed functional nulls, 17 in-frame deletions). Light microscopic findings from animals aged 15 days or older are presented in subsequent sections.
Abnormalities in the organ of Corti were observed via SEM in all homozygous mice studied at ages E18–P10 (Figs. 2 and and3).3). Although the most obvious defects were in the outer hair cells (OHCs), the inner hair cells (IHCs) were also affected. The flattened U-shape arrangement of stereocilia on the inner hair cell cuticular plate was close to normal in all animals of all mutations at P10. In the most affected inner hair cells, the arrangement of stereocilia resembled a wavy line more than a “U,” with some splaying of the stereocilia above the point of insertion into the cell (Fig. 2I). The changes in outer hair cell surface ultrastructure were analyzed by extent of mutation and age.
Changes in outer hair cell (OHC) morphology of the functional null alleles were more severe than the in-frame deletion alleles at ages P0–P10 (Fig. 2). The majority of the outer hair cells were abnormal in all the ears examined from the Pcdh15av-Tg and Pcdh15av-3J alleles at this age, with the exception of one ear from a mouse with the Pcdh15av-3J mutation. This ear had a large area near the base of the organ of Corti with normal “W”-shaped arrangement of stereocilia on the surface of the OHCs. Pcdh15av-Tg and Pcdh15av-3J show near-identical results; only data from Pcdh15av-3J are shown here.
E18 ears from heterozygous control and Pcdh15av-3J mice were examined to determine the earliest developmental stage at which abnormalities in the apical surfaces of the hair cells could be observed. In several specimens, differentiation had not proceeded far enough to permit reliable interpretation. However, organs of Corti from three control and three homozygous mice proved mature enough to visualize both inner and outer hair cell surfaces. Examination of these hair cells revealed abnormalities in the mutants at a time when stereocilia are visible in these tissues by SEM (E18; Fig. 3). The surfaces of inner and outer hair cells from control mice were covered with stereocilia and microvilli (Fig. 3A and C). Kinocilia could be seen either in the center or at the periphery of hair cells from both control and mutant mice (arrows, Fig. 3C and D). Alterations observed in the functional null mice at E18 included disorganization of stereocilia and microvilli and the presence of large bare areas on the surfaces of hair cells. Also, the cell surface sometimes had an irregular, rather than round shape (Fig. 3B and D).
Several of the Pcdh15av-3J ears examined from E18 (Fig. 3D) and ears from P5 (Fig. 2F) animals showed no reduction in the number of stereocilia or microvilli. In P10 mice with functional null mutations, alterations in OHC stereocilia arrangement varied from slight deviations in the “W” shape with a normal compliment of stereocilia, to tilted “W,” to clumping stereocilia bundles, or “C”- and “O”-shaped arrangements of stereocilia with a reduction in the number of short stereocilia. This reduction in short stereocilia appears to be attributable to a degradation in the condition of cuticular plates at this stage (P10). Fusion of the stereocilia and bulges on the cuticular plate were not seen in ears from these mutants by P10 (Fig. 2).
Mice harboring in-frame deletions Pchd15av-J and Pcdh15av-2J showed varying degrees of organ of Corti pathology. The Pcdh15av-J specimens were the least affected of the alleles studied. Less than half of the outer hair cells appeared to be abnormal with the extent of pathology varying between animals (P0–P10). At P0, the most common anomaly seen via SEM in the outer hair cells of mice carrying the in-frame deletion mutation was a flattening of the “W”-shaped arrangement of the stereocilia on the cuticular plate (Fig. 2B). In some cases, the cuticular plate also appeared markedly rotated; with the kinocilium located in the 10 o'clock or 2 o'clock position instead of the normal 12 o'clock position. This rotation occurred regardless of whether the “W”-shaped arrangement of the stereocilia continued to orient to the kinocilia. At P5 (Fig. 2E), in cells on which the typical arrangement of stereocilia was disrupted, there was still some organization in the rows of stereocilia of Pcdh15av-J and Pcdh15av-2J mice such that the height of the rows was maintained short to tall. Cell surfaces containing only scattered clumps of stereocilia were rarely seen. A similar, but slightly more severe, effect was observed in Pcdh15av-2J mice (data not shown). Cells on which the stereocilia were shaped more like an “O” than a “W” were also rare in the Pcdh15av-J and Pcdh15av-2J mice. Even in the most affected cells, a full compliment of stereocilia could usually be seen in ears from Pchd15av-J mutants up to P10 (not shown). There was some reduction in numbers of the shorter stereocilia in the more affected of these cells, but fusion of the stereocilia and bulges on the cuticular plate were not seen.
Cochlear tissues from heterozygous and homozygous Pcdh15av-J, Pcdh15av-2J, Pcdh15av-3J, and Pcdh15av-Tg animals aged P0–P10 were examined by TEM for study of the hair cell cuticular plates (20 heterozygous controls, 13 presumed functional nulls, 17 in-frame deletions). The cuticular plate is immature at this age, with a less well-defined structure compared to adult (Figs. 4 and and5).5). However, the basal body, rootlets of the stereocilia, developing cell junctions, and the developing actin meshwork within the cuticular plate could be visualized in both inner and outer hair cells by P2 and are fairly prominent by P10 (Fig. 5G–L). Inner hair cell stereocilia of heterozygous control ears at P2 were already arranged in a flattened “U” shape, oriented to the kinocilia and the lateral aspect of the cuticular plate (Fig. 4A). Inner hair cell cuticular plates in all the homozygous specimens showed disorganization of the stereocilia (Fig. 4B). The arrangement of outer hair cell stereocilia is quite abnormal in Pcdh15av-3J mice at P0 by SEM, but no ultrastructural changes were seen by TEM in cells sectioned perpendicular to the surface of the reticular lamina (Fig. 4C–F). No abnormalities in stereocilia length, thickness, rootlet structure or cuticular plate density were seen in mice as old as P5. Although this material was not fixed in a manner optimum for visualization for lateral links, they appear to be present in cells from both the control and Pcdh15av-3J mice (arrows, Fig. 4E and F). Because of the inability to identify changes by observation with this orientation, majority of TEM data for this study were analyzed in the cross-sectional plane, parallel to the surface of the reticular lamina.
When viewed in cross section, changes were apparent by P0. Outer hair cell stereocilia of control ears at P0 had formed a partial “W”-shaped arrangement at the surface of the cell, which was oriented to the basal body, from which the kinocilium extends during development (Fig. 5A). This shape is more evident by P2 (Fig. 5D), and by P10 the mature stereocilia arrangement was seen on the outer hair cell surface (Fig. 5G), along with a fairly well developed mesh within the cuticular plate (Fig. 5J arrow). Cross sections of homozygous outer hair cells showed the disorganization of stereocilia seen in the SEM samples of ears from mice of the same age and genotype. The arrangement of stereocilia in Pcdh15av-J and Pcdh15av-2J mice at P0 was not markedly different from controls, typically showing only a slight disorganization in the rows of stereocilia (Fig. 5B). Stereocilia on the outer hair cell surface in mice carrying a functional null mutation showed a more dramatic disorganization of stereocilia on hair cells at this early stage of development (Fig. 5C). This disorganization of the stereocilia became more evident as the cells matured (Fig. 5F and I). In addition to changes in stereocilia, several alterations were seen in the cuticular plate itself. The rootlets of the stereocilia were sometimes broken (arrowhead, Fig. 5L) and the dense-staining actin mesh within the cuticular plate disorganized (Fig. 5I and L). In mice carrying functional null mutations, the cuticular plate appeared markedly rotated; with the basal body of the kinocilium located in the 10 o'clock or 2 o'clock position instead of the normal 12 o'clock position (Fig. 5F and I, arrows). This rotation occurred regardless of whether the “W”-shaped arrangement of stereocilia continued to orient to the kinocilia. In some extreme cases, the basal bodies were on the opposite side of the cell and several cells had the poles of the basal body lying parallel to each other instead of the normal perpendicular arrangement. This was also seen in some of the Pcdh15av-J and Pcdh15av-2J mice, but much less often.
Changes in the insertion patterns of stereocilia into the cuticular plate of the inner hair cells could be seen in specimens from homozygous animals by P0 (not shown). Otherwise, no other abnormalities could be seen by TEM in the inner hair cell apices of mutant mice from P0 to P10.
Organ of Corti pathology in homozygous mice becomes severe enough to be obvious by light microscopy at time points of P15 and older. This section describes light microscopic findings relating to the progression of pathology from loss of outer hair cells to loss of spiral ganglion cells and alterations in other inner ear tissues from mice aged 15 days and older.
In heterozygous control mice (N = 11), a slightly short appearance was noted in the basal turn outer hair cells in two of the ears from mice aged P15–P20 and two of the ears from mice aged P25 had small-appearing spiral ganglion cells at the base of the modiolus. All other ears had normal-appearing organs of Corti and spiral ganglion cells for their stage of development. The spiral ligament, spiral limbus, stria vascularis, and vestibular apparatus appeared normal in all animals of this group (Fig. 6A, B, and C).
Conversely, inner ear specimens from homozygous mice at age 15–25 days showed organ of Corti pathology with variation in the degree of pathology depending on the allele. The alleles with in-frame deletions were less affected than the functional null alleles. The morphologic changes are as follows.
Moderate organ of Corti pathology was seen in both Pcdh15av-3J and Pcdh15av-Tg mutants (Fig. 6G) with minimal spiral ganglion changes (Fig. 6I). Changes included patches of organ of Corti damage with inner and outer hair cell loss and collapse, which was seen from base to apex with some associated loss of spiral ganglion cells in the base only. Pathologic changes in the lateral wall, the spiral limbus, or the vestibular apparatus in this age group were limited to a slight thinning of fibrocytes in the apical part of the spiral ligament from one ear and a thinning of the stria vascularis in the apical part of a different ear. Most of the lateral wall tissues, the spiral limbus, and the vestibular apparatus from homozygous animals at this age appeared normal (Fig. 6G–I).
The degree of pathology seen in these specimens ranged from minimal organ of Corti pathology (limited to a shortening or loss of outer hair cells and Deiters' cell swelling at the base of the cochlea with no spiral ganglion changes) in Pcdh15av-J mutants (Fig. 6D and F) to mild/moderate organ of Corti pathology (outer and inner hair cell loss, Deiters' cell swelling, and collapsed tunnel of Corti in the base with some associated loss of spiral ganglion cells) in Pcdh15av-2J mutants. The spiral ligament, spiral limbus, stria vascularis, and vestibular apparatus appear normal in all homozygous animals of this group (Fig. 6D andE).
Inner ears from P30 to P50 heterozygous control mice (N = 4) appeared normal. Inner ear specimens from heterozygous control mice aged 6.5 months (N = 2), showed moderate inner ear alterations (Fig. 7A–C). Scattered loss of outer hair cells was seen at the base of the cochlea with some thinning of spiral limbus fibrocytes and loss of spiral ganglion cells in the basal portion of the cochlea. More than three quarters of the spiral ganglion cells remained intact, with occasional patchy loss and clumping of the cell bodies in the modiolar apex. Occasional thinning of the fibrocytes in the spiral limbus was also seen at the apex of some cochleae. These changes could be a related to aging in the 6.5-month-old ears because they have a C57BL/6J background (Francis et al. 2003; Ichimiya et al. 2000). All control ears had normal-appearing vestibular neuroepithelia (Fig. 7B).
Changes were observed in all alleles of homozygous mice studied by 30–50 days of age (data not shown). By this age, changes in homozygous mice were more pronounced than those in older control ears at age 6.5 months. The pathology in Pcdh15av-J mutants at P50 (N = 3) included complete loss of outer hair cells in the base to patchy loss in the apex. The basal portion of the spiral ganglion had a reduction in cell number by approximately one fifth. No pathology was seen in the spiral limbus, stria vascularis, or spiral limbus. Degenerating otoconia were occasionally found overlying the saccular neuroepithelia. However, no significant changes in the morphology of hair cells were observed in the saccule. The neuroepithelia of the utricle or semicircular canals appeared normal. Some of these findings were reported earlier (Alagramam et al. 2005).
One Pcdh15av-3J mutant and one Pcdh15av-2J mutant showed cuboidal cells replacing the cells of the organ of Corti at the base with collapse of the tunnel of Corti in apical regions. Less than half of spiral ganglion cells remained in the modiolar base with a smaller loss (approximately 20%) in the apex. No pathology was seen in the spiral ligament, stria vascularis, or spiral limbus. Only the condition of the saccular neuroepithelia differed between these two ears, with more changes in saccular otoconia and more hair cell loss seen in the functional null (Pcdh15av-3J) animal. No changes were observed in any of the other vestibular neuroepithelia of P50 mice.
Homozygous alleles ranging in age from 6.5 to 12 months showed a considerable amount of inner ear pathology; however, the degree of pathology seen in the ears of in-frame deletion (Pcdh15av-J) mice appeared to be less than that observed in the ears from functional null alleles Pcdh15av-3J and Pcdh15av-Tg (Fig. 7D–I). The results are as follows.
Inner ear specimens from homozygous Pcdh15av-Tg and Pcdh15av-3J mice, ranging in age from 7 to 12 months, showed a consistent, dramatic loss of organ of Corti with cuboidal-cell scar formation in the basal turn (Fig. 7G), plus patchy scarring and almost complete loss of outer hair cells throughout the rest of the cochlea. Atrophy of spiral ligament fibrocytes wasconsistently seen in the base of the cochlea, sometimes extending into the apex. Atrophy of spiral limbus fibrocytes was consistently limited to the apical region. Less than one tenth of the spiral ganglion cell bodies remained (Fig. 7I) in any of the seven cochleae examined. Patches of strial atrophy were also present in five of seven ears examined. In these ears, very few hair cells remained in the saccular macula (Fig. 7H). There was also obvious vestibular ganglion cell loss in the area of saccular neuroepithelium, whereas the other vestibular neuroepithelia appeared normal by light microscopy.
Ears from the group of Pcdh15av-J mice showed organ of Corti damage ranging from loss of the tunnel of Corti in the base with areas in the apex more or less intact (three of seven ears) to a cuboidal-cell scar formation in the base of the cochlea with inner hair cells and supporting cells remaining in the apex (four of seven ears). Spiral ganglion cell loss ranged from less than one tenth of cells remaining (two of seven ears, Fig.Fig.7F)7F) to more than three quarters of the cells remaining in two of the oldest animals examined. Atrophy of spiral ligament fibrocytes was often seen (Fig. 7D) with more thinning at the base of the cochlea. On the other hand, atrophy of the spiral limbus fibrocytes was restricted to the apex in all cochleae examined in this group. Vestibular changes were limited to degeneration of otoconia in the saccule. No reduction in saccular hair cells was observed in any of these ears. No changes were observed in any other vestibular neuroepithelia (Fig. 7E).
This study focused on morphological alterations of the cochlea and vestibular apparatus in mice harboring mutations in Pcdh15. Inner ear tissues from animals ranging in age from embryonic day 18 to 1 year were examined by light and electron microscopy. It was found that the degree of pathology correlates with the extent of mutation in Pcdh15 in all four alleles included in the investigation. This finding lends support to the contention that the inner ear changes occurring over time in Usher syndrome type 1F are a direct consequence of the mutation in PCDH15. By studying several alleles and evaluating cellular and subcellular changes that correlate with the severity of the mutation, we can better determine the role of Pcdh15 in the development and maintenance of the inner ear, the organ of Corti in particular.
Of the alleles we studied, the Pcdh15av-J mutants consistently showed the smallest degree of inner ear pathology. Pcdh15av-2J mutants, on the other hand, displayed large variations in degree of pathology. The two presumptive functional null mutants, Pcdh15av-3J and Pcdh15av-Tg, showed severe phenotypes that were very similar to one another with regard to severity of inner ear pathology. These animals showed markedly more severe sensory cell changes early in development, which consistently progressed more rapidly than those observed in the in-frame mutants.
The first cadherin domain is believed to be important for the function of protocadherins (Suzuki 2000). Data presented here provide some support for that notion. The Pcdh15av-2J allele is predicted to have 27 amino acids deleted from the first cadherin domain compared to 85 amino acids predicted to be deleted from the 6th, 7th, and 8th cadherin domains in the Pcdh15av-J allele. However, inner ear tissues from animals carrying the Pcdh15av-J mutation tend to be less severely affected than those from Pcdh15av-2J mutants. Thus, mutations in the first cadherin domain result in a more severe phenotype, which supports the contention that the first domain is an important functional component of Pcdh15.
The specific functions of Pcdh15 in the inner ear are not fully understood. The cochlear abnormalities observed to date in Pcdh15 mutants strongly suggest that Pcdh15 is important for the normal development of stereocilia and the cuticular plate. However, it was recently demonstrated that animals carrying presumptive functional null mutations in Pcdh15 show a complete lack of peripheral vestibular function even though stereocilia abnormalities comparable to those in the cochlea are not present in vestibular hair cells (Alagramam et al. 2005, present findings). The distribution of molecules involved in stereocilia function and hair cell transduction was shown to differ between cochlear and other hair cell types (Corey et al. 2004). Therefore, Pcdh15 may not be essential for the structural development of vestibular hair cells. Although Pcdh15 may be essential for the structural development of cochlear hair cells, it may also play a more general role in the transduction process in both cochlear and vestibular organs. More study is needed to determine the role of Pcdh15 in vestibular hair cell function.
Using antibodies to the cytoplasmic domain of Pcdh15, it has been shown that the protein is expressed in the cochlear neuroepithelium and spiral ganglion in mice at P8 (Alagramam et al. 2001a) and in the embryonic ear (Murcia and Woychik 2001). Subsequently, using different antibodies to the cytoplasmic domain of Pcdh15, Ahmed et al. (2003) reported that Pcdh15 is expressed in the inner ear stereocilia from early development into adulthood in mice. They also reported labeling of Pcdh15 in the adult cochlear hair cell cuticular plate. In previous studies, based on stereocilia morphology in Pcdh15 mutants, it was proposed that Pcdh15 plays a role in the morphogenesis of the stereocilia, specifically, in the organization of the stereocilia bundle on the apical surface of hair cells (Alagramam et al. 2001b; Raphael et al. 2001). A more recent report from Ahmed et al. (2003) suggests that Pcdh15 could serve as a component of the lateral link protein. We did not observe lateral link damage in our specimens. However, we did not use methods specifically designed for lateral link preservation and observation. Therefore, direct evidence that Pcdh15 is a component of the link system will require further investigation, perhaps by direct observation of changes in the lateral links in Pcdh15 mutants by TEM and/or immunogold labeling with antibodies to the Pcdh15 extracellular domain.
Based on data from the studies cited above, it is clear that Pcdh15 is present early in hair cell development and is localized so as to suggest a role in the formation and organization of the stereocilia on cochlear hair cells. This is consistent with the present study's findings, which show that different mutations of Pcdh15 alter not only stereocilia development but also formation of the cuticular plate and do so with differing degrees of severity that depends on the nature and extent of gene mutation.
This research was supported by The NIDCD Grant DC05385-01 (KNA). The authors would like to thank Mr. Kunnathu Paulose for assistance in processing tissues. We would also like to thank Dr. Chris Gilpin, Mr. George Lawton, and Mr. Tom Januszewski (UT Southwestern Medical Center, Molecular and Cellular Imaging Facility) for their technical assistance. We would like to thank Jesse Washington III at Case Western Reserve University for technical assistance.