A tectorin-based matrix and planar cell polarity genes are required for normal collagen-fibril orientation in the developing tectorial membrane.

The tectorial membrane is an extracellular structure of the cochlea. It develops on the surface of the auditory epithelium and contains collagen fibrils embedded in a tectorin-based matrix. The collagen fibrils are oriented radially with an apically directed slant - a feature considered crucial for hearing. To determine how this pattern is generated, collagen-fibril formation was examined in mice lacking a tectorin-based matrix, epithelial cilia or the planar cell polarity genes Vangl2 and Ptk7 In wild-type mice, collagen-fibril bundles appear within a tectorin-based matrix at E15.5 and, as fibril number rapidly increases, become co-aligned and correctly oriented. Epithelial width measurements and data from Kif3acKO mice suggest, respectively, that radial stretch and cilia play little, if any, role in determining normal collagen-fibril orientation; however, evidence from tectorin-knockout mice indicates that confinement is important. PRICKLE2 distribution reveals the planar cell polarity axis in the underlying epithelium is organised along the length of the cochlea and, in mice in which this polarity is disrupted, the apically directed collagen offset is no longer observed. These results highlight the importance of the tectorin-based matrix and epithelial signals for precise collagen organisation in the tectorial membrane.

Temporal bone study of development of the organ of Corti: correlation between auditory function and anatomical structure.

OBJECTIVE: To study the development of the organ of Corti in the human cochlea, and to correlate our findings with the onset of auditory function. MATERIAL AND METHODS: Step sections of 81 human fetal temporal bones were studied, from eight weeks of gestation to full term. RESULTS: By the end of the 10th week, the tectorial membrane primordium could be traced even in the most apical turns. Individual hair cells became identifiable at the basal turn at 14 weeks. At the same time, a small but well formed oval space was observed between the inner and outer hair cells in the basal turn. This does not correspond to the tunnel of Corti, as is erroneously quoted in the literature, as the individual pillar cells develop at later stages. Between 14 and 15 weeks, Hensen's cells were recognised for the first time. Individual pillar cells were identifiable at 17 weeks and the tunnel of Corti opened at 20 weeks. By 25 weeks, the cochlea had reached its adult size, but continued to develop until full term. DISCUSSION AND CONCLUSIONS: A temporal coincidence of different developmental events is responsible for early fetal audition at 20 weeks, including growth of pillar cells, opening of the tunnel of Corti and regression of Kollicker's organ, with the subsequent formation of the inner spiral sulcus and then separation of the tectorial membrane. The fine structures of the organ of Corti continue to develop well after the 25th week, and this may well alter the mechanical properties of the vibrating parts of the cochlea, which may in turn account for the frequency shift observed in preterm infants. These changes will have to be taken into account in the development of prenatal hearing screening tests.

Col11a1 and Col11a2 mRNA expression in the developing mouse cochlea: implications for the correlation of hearing loss phenotype with mutant type XI collagen genotype.

OBJECTIVE: Mutations in the fibrillar collagen genes COL11A1 and COL11A2 can cause sensorineural hearing loss associated with Stickler syndrome. There is a correlation of hearing loss severity, onset, progression and affected frequencies with the underlying mutated collagen gene. We sought to determine whether differences in spatial or temporal expression of these genes underlie this correlation, and to identify the cochlear cell populations expressing these genes and the structures likely to be affected by mutations. MATERIALS AND METHODS: We used in situ hybridization analysis of C57BL/6J mouse temporal bones. RESULTS: Similar, diffuse expression of Col11a1 and Col11a2 mRNA was first observed in the cochlear duct at embryonic Day 15.5, with increasingly focal hybridization being noted at postnatal Days 1 and 5 in the greater epithelial ridge and lateral wall of the cochlea. The greater epithelial ridge appeared to be the main, if not only, source of mRNA encoding Col11a1 and Col11a2 in the tectorial membrane. At postnatal Day 13, Col11a1 and Col11a2 expression became more focal and co-localized in the inner sulcus, Claudius' cells and cells of Boettcher. CONCLUSIONS: We did not observe spatial or temporal differences in mRNA expression that could account for the auditory phenotype genotype correlation. The expression patterns suggest essential roles for Col11a1 and Col11a2 in the basilar or tectorial membranes.

Distribution of glycoconjugates during cochlea development in mice: light microscopic lectin study.

During development, different epithelial cells in the mouse cochlea express different cell surface glycoconjugates, which may reflect membrane specialization. Some of the lectins tested in this study (SBA, succ-WGA, and PSA) labeled the sensory cells of the cochlea around birth. Other lectins (WGA, Con A, RCA-II, and PHA-E) labeled surfaces of the sensory cells, particularly the stereocilia, from early stages of development (gestation day (GD) 16) through 21 days after birth. These may be adhesion molecules needed to attach the newly forming tectorial membrane (TM) to the stereocilia. Lectin staining of the developing TM revealed that the substructures of the TM are biochemically distinct. Lectin staining also showed the temporal sequence of the expression of cytoplasmic glycoconjugates of the cochlear epithelium during development. Biochemical changes during development are probably the result of different cells being involved in the production of glycoconjugates, and may have functional significance, specifically with regard to the expression of adhesion and/or signaling molecules.

Inner ridge cells may be the main source of tectorial membrane type II collagen: evidence from quantitative mRNA in situ hybridization.

In a previous study we showed that COL2A1 mRNA is expressed in both ectodermally and mesodermally derived structures of second trimester human fetal cochlea, whereas type II collagen is present in mesodermally derived structures and in tectorial and basilar membranes. Because the tectorial membrane is acellular and therefore does not make its own proteins, the source of type II collagen and proteoglycans in this membrane has been of interest. We have attempted to address this issue, at least in part, by performing quantitative cRNA mRNA in situ hybridization on second trimester human fetal cochlear sections using a COL2A1 probe. By counting the number of silver grains cell in the interdental cells, inner sulcus cells and inner ridge Kolliker organ cells and by an analysis of variance of these quantitative data. inner ridge cells were found to have significantly higher levels of COL2A1 mRNA than interdental and inner sulcus cells (p < 0.0001). On the basis of significantly higher COL2A1 mRNA levels in inner ridge cells and their higher numbers than interdental and inner sulcus cells we postulate that type II collagen for human fetal tectorial membrane is derived mostly from inner ridge Kolliker organ cells. The lower COL2A1 mRNA in interdental cells appears to provide type II collagen for the spiral limbus and the tectorial membrane. The inner sulcus cells, hair cells. Deiter's and Hensen's cells also appear to contribute lesser amounts of type II collagen to the tectorial membrane. In analogy to these findings it is possible that other tectorial membrane proteins, including proteoglycans and other collagens, are also largely derived from these cells during human fetal development.

Development of the organ of Corti in horseshoe bats: scanning and transmission electron microscopy.

The late prenatal and early postnatal development of the organ of Corti were studied in the horseshoe bat (Rhinolophus rouxi) by using scanning and transmission electron microscopy. Arrangements and dimensions of stereocilia bundles, together with their contacts with the tectorial membrane, were found to be adult-like shortly before birth, and thus before the biological onset of hearing (3-5 days after birth). During the first postnatal week, there were baso-apical gradients in disappearing kinocilia on inner hair cells (IHC), microvillis of supporting cells, and marginal pillars. The lower basal cochlear turn was mature with respect to these regressing structures at 3 days after birth, the apical turn at 10 days after birth. At birth, cytodifferentiation was found to be completed, and the tunnel of Corti and innermost spaces of Nuel had opened. The ultrastructure of IHCs was not markedly different from that at later ages. In outer hair cells (OHC), the adult-like regular arrangement of a single layer of subsurface cisternae and pillars was seen as soon as protrusions of supporting cells had withdrawn from the lateral wall of OHCs (basal turn at birth and throughout the cochlea 2 days after birth). Numerous efferent endings contacted the somata of IHCs up to the second postnatal week. Since the medial olivocochlear system is absent in horseshoe bats, the adult-like innervation pattern of OHCs was established at the biological onset of hearing. During the first 2 postnatal weeks, the cytoskeleton of pillar and Deiters cells, and the specialized Deiters cups developed. The organ of Corti appeared adult-like at 14 days, apart from the persistence of a reduced tympanic cover layer attached to the basilar membrane. Morphological data support physiological findings that the first broadly tuned auditory responses arise from the basal turn. The distinct low to high frequency gradient in development of sensitivity during the first 2 postnatal weeks of the horseshoe bat was not, however, matched by morphological gradients, and it would appear that the development of the cytoskeleton of supporting cells contributed to the establishment of tuning in the auditory fovea. Adult-like morphology of the organ of Corti coincided with the emergence of sharply tuned responses from the auditory fovea, but there was no clear-cut correlate for the shift in tuned foveal frequency representation that occurred during the following 3 weeks.

Development of the tectal cells in the mouse cochlea.

Tectal cells appear at birth in the outer part of the developing organ of Corti. At first they are attached to the basilar membrane, but later they ascend through the auditory epithelium. During the 1st postnatal week (coinciding with the development of the minor tectorial membrane), the newly formed tectal cells show several cytological characteristics suggesting increased metabolic and secretory activities, which include: (1) a large Golgi complex, (2) abundant amorphous material inside the cisterns of rough endoplasmic reticulum, and (3) dense granules inside the mitochondrial matrix. All these features gradually disappear, and by the 14th postnatal day the tectal cells show a dark cytoplasm and few and short microvilli. In addition, tectal cells were stained selectively by some lectins. These findings suggest that tectal cells may participate in the secretion of some components of the minor tectorial membrane, different from those produced by Deiters' cells, Hensen's cells and pillar cells.

SEM analysis of the developing tectorial membrane in the chick cochlea.

The development of the tectorial membrane in the embryonic chick cochlea was studied using scanning electron microscopy. Chick embryos ranged in age from embryonic day 7 (E7) to post-hatching day 15. Our studies revealed that a fine filamentous matrix arose on the apical surface of the basilar papilla at approximately E7. This matrix was secreted by the supporting cells which encircled the hair cells. By E9, the early matrix had increased in volume but remained filamentous in structure, except at the inferior edge of the basilar papilla where it was condensed into a layer of laterally-oriented columns. At E9 the TM exhibited an additional layer of matrix, called the amorphous component. It appeared to originate from the homogene cell population, and attached to the early columnar matrix at the inferior edge of the basilar papilla. The two components of the TM were separated by a longitudinal ridge, called the 'track', which marked the inferior edge of the amorphous component. As the cochlea developed, the basilar papilla increased in width, the columnar component elongated and the track appeared to recede. These morphological findings point to separate developmental origins for the two components of the tectorial membrane.

Gelsolin immunoreactivity and development of the tectorial membrane in the cochlea of normal and hypothyroid rats.

Gelsolin was localized by immunocytochemistry in the developing cochlea of the rat. In normal animals, the protein appeared at 18 th day in utero in cells of the Kölliker's organ, which are involved in the secretion of the tectorial membrane. The Kölliker's organ cells were not immunoreactive after the first postnatal week, which is when they cease their secretory activity. Gelsolin immunoreactivity was similar in thyroid-deficient rats until the second postnatal week but, at this age, Kölliker's organ did not transform and its gelsolin immunoreactivity persisted, together with its secretory activity. As a result, the tectorial membrane was greatly distorted and out of contact with the hair cells, which dramatically impaired the mechanical properties of the organ of Corti. The developing cochlea thus provides an example of the involvement of gelsolin in a secretory process that is of importance in the development of hearing.

Surface aspects of the developing human organ of Corti.

Thirteen cochleas from human fetuses ranging in age from week 9 to week 22 were observed by scanning electron microscopy. The classical 'base-to-apex' and 'internal-to-external' gradients of maturation were confirmed by surface observations of the developing organ of Corti. The tectorial membrane begins to be secreted around week 9, i.e. 2 weeks before the onset of the ciliogenesis. Its structure appears to be first amorphous and then fibrillar. The surface of the organ of Corti looks mature around week 22, but, in fact, its complete maturation, especially at outer hair cell level, probably occurs during the last trimester of pregnancy.

Development of the tectorial membrane.

During development, the organization of the stereociliary bundles undergoes drastic changes from the microvilli-like nascent stereocilia to the 'W' formation of the step-like arrangement of the adult form. During this period the developing tectorial membrane (TM) establishes prescribed attachments with various substructures of the developing sensory ciliary bundles and supporting cells. The TM detaches from the supporting cells and inner hair cell stereociliary bundles as Kölliker's organ matures. The inter-connecting linkage system develops postnatally, and the 'tip-linkages' are already found in one-week-old mice, suggesting that the critical organization of the micromechanics of the stereocilia matures rapidly during the postnatal period. The TM develops in stages, and its development parallels that of the organ of Corti. The major TM is initially secreted by the greater epithelial ridge cells, and the minor TM is produced by the lesser epithelial ridge cells. The substructures of the TM are formed by the participation of a number of different supporting cells. During the active stage of production of the substructures by the supporting cells, these cells are intensely Alcian blue-PAS stained, indicating that the glycoconjugates are locally produced by these cells.

[Formation of the tectorial membrane of the cochlear canal during the embryogenesis of birds]. / Formirovanie pokrovnoi membrany ulitkovogo kanala v émbriogeneze ptits.

By means of electron microscopy formation of the tectorial membrane of the cochlear canal and differentiation of the cells participating in the process (supporting cells of the basilar papilla and anterior homogeneous cells--AHC) have been studied in chick embryos. The AHC, to which the tectorial membrane is fixed, produce fine fibrillar material, included into the composition of the tectorial membrane. The cells mentioned form a number of cytoskeletal structures connected with the mechanical function of the tectorial membrane. Besides the network of the tonofilaments, gradually filling cytoplasm of the AHC, some peculiar attachings in the form of collagenous fibrillar bundles are revealed, they reach the AHC from the sublying connective tissue and have a direct contact with the basal membrane of the cells. The beginning of the tectorial membrane formation precedes the formation of the cytoskeletal structures. The latter appear only when the mass of the tectorial membrane, and hence, the mechanical loading on the AHC is great enough.

Development of the embryonic chick's tectorial membrane.

The nascent tectorial membrane (TM) is identifiable as early as stage 33 (7th day) as thin, wispy material. By stage 37 (11th day), the dense mesh of the immature TM and fibrous webs (subtectorial threads) that attach the TM to the basilar papilla are distinct but scanty. The TM condenses slightly in its upper face. The growth of the columnar cells and basilar papilla during the following days pulls the TM, lifting it upward, and resembling the cables on a suspension bridge in cross-section. As a result, a large hollow wedge forms. During stages 40-44 (14th-18th days), the columnar cells secrete large amounts of fibrous material, which fills the hollow wedge and condenses into the dense meshes. The honeycombed patterns appear at this time. The supporting cells secrete the fibrous webs. Their secretory activity closely corresponds to that of the columnar cells. The secretory material from both cell types remains attached to the apical ends of their respective cells after secretory activity ends. By hatching (stage 46-21 days), the columnar cells have filled with fibrous material and their cytoplasmic organelles are restricted to the apices. The cytoplasm of supporting cells is relatively clear, with few cytoplasmic remnants of their intense secretory activity earlier.

Early aspects of human cochlea development and tectorial membrane histogenesis.

Several human embryos and foetuses cochlea from the first half of pregnancy were studied by light, transmission and scanning electron microscopy. Cochlea development in man is the result of three coexisting processes: First, coiling and maturation of the cartilaginous otic capsule. Second, resorption of the periodic mesenchymal reticulum with the appearance of the labyrinthine fluids. Third, differentiation of the sensory epithelium. Tectorial membrane morphogenesis is closely related to the apocrine secretory activity of the greater and lesser epithelial ridges in the 50 mm c.r.l. specimen. In the 70, 110 and 120 mm c.r.l. specimens the secretory activity rests on the interdental cells of the spiral limbus, the undifferentiated cells of Corti's primordium and in the most external cells of the lesser epithelial ridge.

Cochlea of the human fetus: a scanning electron microscope study.

Fine structures of the human fetal cochlea were observed by scanning electron microscopy. The study aimed to make the knowledge on the developmental microanatomy of the cochlea more accurate. The temporal bones of fetuses were removed and the membranous portions of the cochleas were prepared for observation. In a 14-week 6-day old fetus, the hair cells were arranged mainly in four rows. The sensory hairs differed in appearance from those in the adults. The innermost or first row hair cells corresponded to the inner hair cells and revealed certain characteristic structures. From the second to the third or outermost row, a rather uniform hair pattern with a bud-like appearance was noted. Neither W nor V letter formation of sensory hairs was found. One strong kinocilium was identified with its thick base; it was located lateral to the outermost stereocilia. With older fetuses, 22 weeks 2 days and 24 weeks 0 day of age, the hair patterns closely resembled those of the adult with the exception of the presence of a short kinocilium on the outer hair cells and a slim kinocilium on the inner hair cells. The present study indicates that structures including the sensory hairs and their attachment to the tectorial membrane, the Reissner's membrane and the stria vascularis essentially complete their morphologicjal development in 6 months after gestation.

Embryogenesis of the mammalian inner ear. III. Formation of the tectorial membrane of the CBA/CBA mouse in vivo and in vitro.

The development of the tectorial membrane in the basal coil of the cochlea has started already in the 15th gestational day inner ear and has reached a considerable thickness and maturation at birth. The development of the tectorial membrane occurs synchronously in in vivo labyrinths and the in vitro material cultured to an age corresponding to birth. At least during this part of the development the formation of the tectorial membrane is independent of the specific composition of endolymph. In the in vivo material a secretory maximum was reached on the 18th gestational day, whereafter the secretory activity was low, especially after birth. In the in vitro specimens, however, a rather constant secretion of material occurred also post partum, which indicates a lack of control mechanisms during in vitro conditions. A complete maturation of the tectorial membrane did not occur in vitro. When passing the point of time corresponding to birth, in the in vitro inner ear explants the gross structure of the tectorial membrane is only slightly changed. In vivo a mature configuration of the tectorial membrane is observed on the 14th DAB (day after birth).

The limbus spiralis and its relationship to the developing tectorial membrane in the cochlear duct of the Guinea pig fetus.

The development of the interdental cells of the limbus spiralis and of the inner spiral sulcus cells as well as the formation of the mesenchymal teeth of Huschke are described during fetal life up to the day of birth in the guinea pig. Additionally, the changes of the developing tectorial membrane are studied. The ultrastructural observations allow the conclusion that during fetal development at least a considerable part of the material of the tectorial membrane is secreted by the interdental cells of the limbus spiralis.

Structure of the hairs on cochlear sensory cells.

A study of cochlear sensory hairs has been made using transmission and scanning electron microscopy. The structure of the hairs and the relation to the hair cells and to the tectorial membrane is described. A number of micrographs demonstrate both the inner structure of the hairs and their relation to the surrounding structures.

[Light and electron microscopic studies of the greater epithelial ridge and its relationship to the developing tectorial membrane in the cochlear duct of the guinea pig (author's transl)]. / Licht- und elektronenmikroskopische Untersuchungen des grossen Epithelwulstes und seiner Beziehungen zu der sich entwickelnden Membrana tectoria im Ductus cochlearis von Meerschweinchenfeten.

In early stages of fetal development (36th day, 3rd turn) the thickening of the epithelium at the basal side of the cochlear duct forms two ridges. Later in fetal development the laterally situated lesser epithelial ridge forms the major part of the organ of Corti, whereas the medially situated greater epithelial ridge contributes only a small part to this organ. The medial part of the greater ridge consists of the columnar inner supporting cells, which bear a border of closely packed microvilli at their upper surface. Up to the time of the opening of the internal spiral sulcus in the 48th day of fetal development, there is a close spacial relationship between microvilli and filaments of the tectorial membrane. We conclude that the inner supporting cells contribute to the formation of the tectorial membrane. However, thus far we cannot entirely exclude a different possibility, that the inner supporting cells absorb material of the tectorial membrane. During the opening of the sulcus spiralis internus the inner supporting cells become considerably smaller, some of them undergo complete destruction by cytolysis, with pyknosis and karyorrhexis.