- Research article
- Open Access
Brn3c null mutant mice show long-term, incomplete retention of some afferent inner ear innervation
© Xiang et al; licensee BioMed Central Ltd. 2003
- Received: 22 September 2002
- Accepted: 30 January 2003
- Published: 30 January 2003
Ears of Brn3c null mutants develop immature hair cells, identifiable only by certain molecular markers, and undergo apoptosis in neonates. This partial development of hair cells could lead to enough neurotrophin expression to sustain sensory neurons through embryonic development. We have therefore investigated in these mutants the patterns of innervation and of expression of known neurotrophins.
At birth there is a limited expression of BDNF and NT-3 in the mutant sensory epithelia and DiI tracing shows no specific reduction of afferents or efferents that resembles neurotrophin null mutations. At postnatal day 7/8 (P7/8), innervation is severely reduced both qualitatively and quantitatively. 1% of myosin VIIa-positive immature hair cells are present in the mutant cochlea, concentrated in the base. Around 20% of immature hair cells exist in the mutant vestibular sensory epithelia. Despite more severe loss of hair cells (1% compared to 20%), the cochlea retains many more sensory neurons (46% compared to 15%) than vestibular epithelia. Even 6 months old mutant mice have some fibers to all vestibular sensory epithelia and many more to the cochlear apex which lacks MyoVIIa positive hair cells. Topologically organized central cochlea projections exist at least until P8, suggesting that functional hair cells are not required to establish such projections.
The limited expression of neurotrophins in the cochlea of Brn3c null mice suffices to support many sensory neurons, particularly in the cochlea, until birth. The molecular nature of the long term survival of apical spiral neurons remains unclear.
- ear development
- POU factors and hair cells
- afferent ear innervation
- efferent ear innervation
Brn3c is a POU domain factor that is crucial for inner ear hair cell development. Targeted null Brn3c mutants have no mature hair cells [1, 2]. Close examination has revealed that some 'immature' hair cells form in Brn3c null mutants and express cellular markers such as Myosin VI and VIIa, calretinin and parvalbumin . Furthermore, these immature hair cells of Brn3c null mutants undergo apoptosis in neonates . Consistent with an apparent absence of mature hair cells, initial work suggested that all vestibular and most spiral ganglion cells are lost by postnatal day 14 (P14; ). However, more detailed quantification by others  reported that at P4 about 77% of vestibular neurons and only 29% of spiral neurons are lost. It was suggested that there is possibly a complete loss in adults . Other than these preliminary statements, no data exists concerning the detailed pattern of loss of innervation in Brn3c null mutants.
The initial development and partial differentiation of hair cells in Brn3c mutants could possibly lead to some neurotrophin expression in these cells to sustain sensory neurons through embryonic development and beyond. Data on various single and compound neurotrophin null mutants have shown that the loss of a specific neurotrophin leads to topologically restricted loss of sensory neurons in the embryonic ear [4, 5]. Such selective loss in Brn3c null mutants would therefore indicate reduction of a specific neurotrophin in immature hair cells. Moreover, recent work shows that in embryos NT-3 is primarily expressed in supporting cells, moving only around birth into hair cells [6, 7]. In fact, the selective loss of vestibular as compared to cochlear sensory neurons (77% versus 29%; ) suggests that NT-3 expression may be less downregulated in Brn3c null mutants than BDNF [6, 8, 9], provided that at least some differentiation of supporting cells takes place. In the ear  as well as elsewhere  neurotrophins are progressively downregulated in postnatal mammals and possibly replaced by other factors .
We have investigated in detail the pattern of innervation in the Brn3c mutants, as well as the expression of NT-3 and BDNF. We want to evaluate a possible correlation between the topology of sensory neuron loss and absence of a specific neurotrophin or topological loss of hair cells at birth and in older animals. This information could be important for an in-depth evaluation of the human deafness related to the Pou4f3 gene, DFNA15 .
We report here long term retention of cochlear sensory neurons for at least 6 months, in particular in the cochlear apex, in Brn3c null mutant mice. This retention of afferents and efferents is unrelated to hair cell differentiation as not even immature hair cells can be detected at early postnatal stages with MyoVII immunocytochemistry in this part of the cochlea. This retention of apical spiral neurons is also largely unrelated to neurotrophins which are known to be reduced in their expression in neonatal rodents .
To appreciate the effects of the Brn3c null mutation on the pattern of the inner ear innervation, we first want to present the effects of BDNF and NT-3 null mutations at birth [6, 13, 14]. Null mutants of BDNF or its receptor trkB lose all innervation to the semicircular canals and have a reduced innervation to the utricle, saccule and apical turn of the cochlea. In contrast, null mutations of either NT-3 or its receptor trkC result in loss of spiral neurons in the basal turn with formation of an inner spiral bundle of afferents extending to the basal tip. Our null hypothesis for this study would be that Brn3c null mice show severe compromised production of these neurotrophins and should therefore show a comparable pattern of nerve fiber loss.
Brn3c null mutants at birth (P0)
Consistent with the finding of Xiang et al.  of only a 29% loss of spiral sensory neurons at P4, our data show little difference in the pattern of innervation of the cochlea in P0 Brn3c null mutants (Fig. 2c,2d). No selective loss of spiral neurons is observed in Brn3c null mutants in the basal turn, a feature of either NT-3 or trkC loss [6, 9, 14]. Likewise, the innervation of the apex (Fig. 2f) shows no detectable abnormality in overall pattern of innervation compared to control animals (data not shown), an indication that BDNF could be expressed in the apex . In addition, the pattern of efferent innervation shows no deviation from normal either (Fig. 2e), whereas they show the same pattern of loss as afferent fibers in neurotrophin null mutants . These data suggest that the spiral sensory neurons develop qualitatively normal at least until P0 and therefore allow normal pathfinding of efferents. Most interestingly, there is no increase in radial fiber spacing in the apex, a specific problem of BDNF null mutants [6, 13].
However, there is one qualitative difference not recognized in any single neurotrophin null mutant. Afferents reach all three rows of outer hair cells in the basal turn of control wildtype littermates (Fig. 2c), but both afferent and efferent outgrowth is disorganized to outer hair cells in Brn3c null mutants (Fig. 2d) and does not show any clear organization into three distinct longitudinal fiber bundles paralleling the three rows in the outer hair cell region. These data suggest that fiber organization in the outer hair cell region is partly disrupted in Brn3c null mutant.
Brn3c null mutants at P7/8
The cochlea at P8 shows more qualitative deviations from the normal pattern of innervation. For example, all three rows of outer hair cells now receive both afferent and efferent innervation in the base of control littermates (Fig. 3c). However, no fibers extend to the outer hair cell region in Brn3c null mutants (Figs. 3d,3e,3f). In control animals there is dense innervation of inner hair cells, whereas Brn3c null mutants show a curious aggregation of fibers near focal spots around the habenula perforata. The apex shows less pronounced deviations from normal (Fig. 3f,3g). However, as in the base, afferents and efferents extend sparingly to the outer hair cell region. There is formation of an inner spiral bundle communicating both afferents and efferents between the focal points where fibers appear to pass through the habenula perforata (Fig. 3f,3g). As in newborn animals, efferent fibers closely follow the pattern of innervation displayed by afferents (data not shown).
Numbers of hair cells and sensory neurons in P7 wildtype and Brn3c mutant littermates
% of wild type
6 months Brn3c null mutants
The cochlea, most prominently the apex, receives many afferent fibers, which form an interrupted inner spiral bundle (Fig. 7c). Some of the radial fiber bundles are myelinated (Fig. 7d). Only an occasional fiber extends beyond the inner spiral bundle into the area of the outer hair cells (Fig. 7d). Even at this late stage in maturation there are still numerous spiral neurons present in the apex (Fig. 7c,7d).
In summary, these tracing data suggest that mature hair cells are not necessary to direct fiber outgrowth and to maintain some fibers at least up to 6 months in the apex of the cochlea. Importantly, the spatio-temporal loss of innervation does not follow the pattern of loss known from neurotrophin and neurotrophin receptor null mutations as it starts in Brn3c mutant mice after birth.
In situhybridization confirms neonatal neurotrophin expression
In the saccule, we directly compared the BDNF (Fig. 8c,8d) and NT-3 signal (Fig. 8e,8f) of the Brn3c null mutant (Fig. 8c,8e) and control littermates (Fig. 8d,8f). A strong BDNF signal was found over the hair cells of control animals and an occasional immature hair cell also showed a BDNF signal in the Brn3c null mutants. The NT-3 signal was more diffuse in both the control and the Brn3c null littermates but showed some slightly above background signal in the area of the sensory epithelium even in the Brn3c null mutant.
We will explore five points in this discussion: How the limited expression of neurotrophins relates to the apparent survival of primary neurons until P8; how the known absence of apical hair cells and of classical neurotrophins can be related to the presence of large numbers of apical turn spiral neurons; how absence of differentiated hair cells affects afferent and efferent targeting; and how these data possibly relate to other mutant animals and to children born with profound hearing loss.
Immature hair cells and limited expression of neurotrophins rescue afferent projection until P8
The neurotrophins have long been implicated as the mediators for target mediated cell death. In essence, this theory of regulation of neuronal connections via neurotrophic support implies that only limited quantities of neurotrophins are released by the target tissue to support only properly connected sensory neurons by providing only these with a critical amount of neurotrophins . Past experiments, which eliminated one or more neurotrophins entirely, only partially tested the basic assumption of this theory in vivo. For example, in BDNF heterozygotic animals there is a small decrease in the number of sensory neurons in the ear  but no change in the overall pattern of innervation. Moreover, all of the neurotrophin/neurotrophin receptor null mutants studied to date eliminate expression in both the peripheral target and the brain simultaneously and achieve their effects in late embryos. In contrast, Brn3c is barely expressed during embryogenesis in the CNS  thus arguing that the survival of ear primary neurons depends crucially on the periphery.
We suggest that limited expression of neurotrophins in the immature target leads to retention of primary neurons and their afferent fibers in newborn and early postnatal Brn3c null mice. In agreement with this suggestion, our in situ data show a severe reduction in expression of BDNF (Figs. 8, 9). Despite this reduction, some, apparently biologically significant low levels of neurotrophins are apparently expressed in all sensory epithelia in embryonic Brn3c null mutants. It appears that even these low levels of neurotrophins in the vestibular sensory epithelia can sustain normal fiber outgrowth and a limited maintenance until P0. The comparatively high level of NT-3 expression in Brn3c null mutant cochlea, which has been shown to be the neurotrophin most prominently supporting spiral sensory neurons [6, 9, 14], is in agreement with the normal development of cochlear innervation in newborn Brn3c null mutants.
Since BDNF appears to be exclusively produced by hair cells [6, 7, 20], the lack of terminal differentiation of hair cells appears to be accompanied by only limited expression of BDNF, as is the case in the canal cristae (Fig. 8). Past research has shown that in BDNF and trkB null mutants this innervation to canal cristae is lost before birth [6, 13]. That even these low levels of expression are significant is clear from the fact that all canal sensory epithelia receive an innervation by both afferents and efferents at birth and later (Figs. 2, 3). The situation in the utricle, saccule and cochlea is less clear as both BDNF and NT-3 are expressed [6, 7]. In fact, it appears that the levels of NT-3 expression hardly differ from those in control littermates (Figs. 8, 9). The latter is particularly obvious in the apex of the cochlea. In fact, in the cochlea of embryos and neonates as well as in the saccule and utricle of embryos, NT-3 is predominantly expressed in supporting cells . This expression of NT-3 in supporting cells in embryos and neonates may even preserve in Brn3c null mutants the numerous spiral sensory neurons in the apex of 8-day old animals (Figs. 3, 4).
Long term survival of apical sensory neurons is unrelated to differentiated hair cells and likely is independent of neurotrophins
Past work has shown that BDNF and NT-3 appear to shift in their expression into inner hair cells around birth or are lost in the ear and other parts of the nervous system [6, 10, 20, 23]. It has been suggested that other neurotrophins may come into play in the ear . However, the apex of Brn3c null mutants, which retains most of the spiral neuron afferents at 6-month, shows no formation of mature hair cells at any time surveyed here (P0, P8, P10). Thus the factor(s) cannot be released by differentiated hair cells but there is an unexplored possibility of generalized expression of neurotrophins at low levels in the undifferentiated epithelia. However, known neurotrophins are largely absent in the adult cochleae  and significant amounts of neurotrophin expression appear to develop only in postnatal animals in the CNS . Such expression in the CNS could possibly offset to some extent the peripheral loss of neutrophins in targeted null mutants. This would work only in cases in which the loss of primary neurons would not already be completed long before birth as is the case in the ear [6, 13].
It therefore remains unclear what supports the many afferents in the apex of the Brn3c null mutants until 6 months of age or longer, unknown peripheral neurotrophic substances or neurotrophic support provided by the CNS. Comparable long term retention of apical spiral sensory neurons was described for the deaf white cat  and may also be the case in humans with congenital deafness.
Growth of fibers to the cochlea does not require mature hair cells
Formation of radial fibers that bring peripheral processes of spiral neurons to the organ of Corti seems to be rather normal, even in the apex of the cochlea which does not even develop immature hair cells recognizable by Myo VIIa. This does not preclude that even less differentiated hair cell precursors may form in the apex or that those precursors have died before birth. Interestingly, the growth to outer hair cells is most affected in Brn3c null mutant cochleae. Instead of extending radially through the tunnel of Corti to outer hair cells, afferents appear to stall and extend in longitudinal directions as inner spiral bundles (Figs. 3, 7). It has been shown that the differentiation of pillar cells depends on activation of Fgfr3  by FGF's, probably Fgf8, a factor produced by developing and mature inner hair cells [18, 27]. The formation of supporting cells also appears to depend on the proper expression of various bHLH factors such as Hes 1 and 5 which appear to be regulated by the Notch signaling pathway [17, 28, 29]. It is possible that the apparent inability of fibers to extend along outer hair cells is related to the lack of differentiation of supporting cells in the absence of mature hair cells. Probing for the proper expression of supporting cell specific markers in Brn3c null mutants is necessary to further evaluate these suggestions.
Previous work has suggested that efferent fibers, derived from facial branchial motoneurons, follow afferents and for that reason reflect in detail all connectional deviations of afferents [16, 30–32]. Our data agree with this scenario but extend it. Specifically, efferent fibers may suffer the same loss of their molecularly unknown neurotrophic support as do afferents and therefore show the same spatio-temporal profile of loss (Fig. 3). Alternatively, efferent fibers can sustain established connections only as long as afferent fibers are present. More information on the actual molecular support of efferent fibers in the ear is needed before those two possibilities can be distinguished.
The onset of cochleotopic projections has been investigated in detail in only very few mammals . These data suggest that a cochleotopic projection develops before onset of hearing. Our data show that at least a cochleotopic projection in the cochlear nerve and the cochlear nuclei develops even in Brn 3c null mutants (Fig. 6). Those data are also consistent with the formation of a crude cochleotopic projection in NT-3 null mutants [6, 14]. Those mutants have a much more severely reduced density of innervation in the developing cochlea [6, 14] than the reduction we found in Brn3c null mutants at P0. In this context, it would be interesting to see whether the recently generated transgenic mouse in which BDNF is expressed under NT-3 promoter control  could actually perform an even more pronounced rescue in a Brn3c null mutant background.
Relevance of our findings to other mutations with hair cell loss
Vahava et al.  and Frydman et al.  have demonstrated that mutation in a single human allele of Pou4f3 (Brn3c) results in a late onset of high frequency hearing loss. Thus far no data are available that correlate the late onset of hearing loss with morphological defects in the cochlea. In fact, an investigation of Brn3c heterozygotic mice showed no additional effect on hearing loss due to haploinsufficiency in these mice . Our data on Brn3c null mouse mutants nevertheless suggest that the high to low frequency progressive hearing loss in humans may correlate with the unknown factor(s) that mediate apical spiral neuron survival into adulthood. Quantitative data on human Pou4f3 cochleae is needed to verify that spiral neuron loss is more pronounced in the basal, high frequency area of these hearing-deficient patients. Similar data are also needed for other congenitally deaf children  and in the deaf white cat . Further work on the recently available mutant mice with specific absence of all hair cells , outer hair cells in the base  or apex  could further help to clarify the role of hair cells in forming and maintaining afferent and efferent innervation in these model mice.
The progressive loss of afferent and efferent innervation in Brn3c null mutants shows neither in spatial nor in temporal pattern a resemblance to losses reported in simple BDNF or NT-3 null mutations . Null mutants of ear specific neurotrophins have completed the loss of sensory neurons before birth. In contrast, our results suggest a slow loss of afferent and efferent innervation between P0 and at least 6 months. This late sensory neuron loss is likely not related to known neurotrophin signaling which becomes reduced in neonatal wildtype animals. Other factors, such as GDNF [11, 40] need to be investigated in their expression in these mutants and their functional role needs to be assessed, in particular in the cochlear apex.
The long term retention of afferents in the cochlear apex in the absence of any apparent differentiation of hair cells raises hopes for cochlear implants in deaf-born children. Similar long term retention of apical afferents exists in the deaf white cat  and should be explored in other model systems with embryonic and neonatal hair cell loss [37, 38].
Breeding and genotyping
Brn3c mice were bred as previously described . Mice were genotyped and Brn3c null mutants were raised to a specific age (P0, N = 8; P7, N = 6; P8, N = 6; 6 months old, N = 2). The animals were deeply anesthetized with pentobarbital and transcardially perfused with 4% paraformaldehyde in 0.1 M phosphate buffer (pH 7.4). Ears were postfixed in the same fixative for at least one day prior to dissection.
Tracing of nerve fibers
DiI tracing from the brainstem was performed as previously described . Small filter stripes soaked with saturated DiI were implanted into the efferent fiber bundle near the floor plate or into the ascending or descending afferents in the alar plate . After appropriate diffusion time of the dye, the ears were dissected and mounted flat for visualization in an epifluorescent microscope. Images were taken on black and white film or acquired with a cooled CCD camera and processed using ImagePro software (Media Cybernetics).
Ears were subsequently reacted for acetylated tubulin to reveal the pattern of innervation in addition to the DiI tracing with a different technique as previously described . Briefly, dissected ears were incubated with 1:500 anti-acetylated tubulin antibodies (Sigma, St. Louis) followed by secondary antibodies conjugated to HRP. Dissected inner ears were reacted with DAB and H2O2 for HRP distribution and subsequently viewed as whole mounts.
After photographing as whole mounts, the ears were embedded in epoxy resin and sectioned to reveal the distribution of fibers inside the sensory epithelia in more detail.
Cochleotopic projection was evaluated by inserting DiI soaked filter strips into the base and DiA soaked filter strips into the apical turn of 2 P0 and 4 P8 Brn3c null mutants and a similar number of wildtype littermates. After appropriate diffusion time , the brains with the attached cochlear nerve were embedded in gelatin, hardened in 4% PFA over night, sectioned coronally on a vibratome (100 μm thickness) and viewed with a Biorad Radiance 2000 confocal system attached to a Nikon Eclipse 800 microscope. Image stacks were collapsed to view the entire projection in one section in one focal plane.
Four ears each of Brn3c null mutants (P0 and P8) and control littermates were embedded in paraffin, sectioned and probed for the presence of BDNF and NT-3 mRNA using the in situ technique previously described . Sections were lightly counterstained and viewed with bright and dark field microscopy. Images were acquired with a CCD camera and displayed as false color images as previously described .
Immunocytochemistry of hair cells and quantification of hair cells and neurons
Immunostaining of P7 cochlear whole mounts using the hair cell specific-myosin VII (MyoVIIa) antibody was performed as previously described . Images of labeled organs of Corti were then acquired using a SPOT digital camera (Diagnostic Instruments Inc.) and the number of hair cells was scored from acquired images. To determine the number of hair cells or neurons in vestibular endorgans or sensory ganglia, serial sections were stained with Cresyl Violet and images were similarly acquired and scored. Every other section was scored for each sensory epithelium and every forth section was scored for each ganglion. Only neurons or cells with a clear nucleus and nucleoli were counted and 4–6 samples were counted for each epithelium and ganglion. All data were tested for significance using two-sample Student's t-test with unequal variances.
Supported by the National Eye Institute (EY12020, MX), the March of Dimes Birth Defects Foundation (MX), the Egyptian Government (AM), the Juselius Foundation (UP), the NIDCD (2 P01 DC00215, BF; DC04594, M.X.), the Taub foundation (BF) and NASA (01-OBPR-06; BF).
- Erkman L, McEvilly RJ, Luo L, Ryan AK, Hooshmand F, O'Connell SM, Keithley EM, Rapaport DH, Ryan AF, Rosenfeld MG: Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development. Nature. 1996, 381: 603-606. 10.1038/381603a0.PubMedView ArticleGoogle Scholar
- Xiang M, Gan L, Li D, Chen ZY, Zhou L, O'Malley BW, Klein W, Nathans J: Essential role of POU-domain factor Brn-3c in auditory and vestibular hair cell development. Proc Natl Acad Sci U S A. 1997, 94: 9445-9450. 10.1073/pnas.94.17.9445.PubMedPubMed CentralView ArticleGoogle Scholar
- Xiang M, Gao WQ, Hasson T, Shin JJ: Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells. Development. 1998, 125: 3935-3946.PubMedGoogle Scholar
- Fritzsch B, Pirvola U, Ylikoski J: Making and breaking the innervation of the ear: neurotrophic support during ear development and its clinical implications. Cell Tissue Res. 1999, 295: 369-382. 10.1007/s004410051244.PubMedView ArticleGoogle Scholar
- Rubel EW, Fritzsch B: AUDITORY SYSTEM DEVELOPMENT: Primary Auditory Neurons and Their Targets. Annu Rev Neurosci. 2002, 25: 51-101. 10.1146/annurev.neuro.25.112701.142849.PubMedView ArticleGoogle Scholar
- Farinas I, Jones KR, Tessarollo L, Vigers AJ, Huang E, Kirstein M, de Caprona DC, Coppola V, Backus C, Reichardt LF, Fritzsch B: Spatial shaping of cochlear innervation by temporally regulated neurotrophin expression. J Neurosci. 2001, 21: 6170-6180.PubMedPubMed CentralGoogle Scholar
- Pirvola U, Ylikoski J, Palgi J, Lehtonen E, Arumae U, Saarma M: Brain-derived neurotrophic factor and neurotrophin 3 mRNAs in the peripheral target fields of developing inner ear ganglia. Proc Natl Acad Sci U S A. 1992, 89: 9915-9919.PubMedPubMed CentralView ArticleGoogle Scholar
- Ernfors P, Van De Water T, Loring J, Jaenisch R: Complementary roles of BDNF and NT-3 in vestibular and auditory development. Neuron. 1995, 14: 1153-1164.PubMedView ArticleGoogle Scholar
- Farinas I, Jones KR, Backus C, Wang XY, Reichardt LF: Severe sensory and sympathetic deficits in mice lacking neurotrophin-3. Nature. 1994, 369: 658-661. 10.1038/369658a0.PubMedView ArticleGoogle Scholar
- Cosgaya JM, Chan JR, Shooter EM: The neurotrophin receptor p75NTR as a positive modulator of myelination. Science. 2002, 298: 1245-1248. 10.1126/science.1076595.PubMedView ArticleGoogle Scholar
- Hashino E, Dolnick RY, Cohan CS: Developing vestibular ganglion neurons switch trophic sensitivity from BDNF to GDNF after target innervation. J Neurobiol. 1999, 38: 414-427. 10.1002/(SICI)1097-4695(19990215)38:3<414::AID-NEU9>3.0.CO;2-Y.PubMedView ArticleGoogle Scholar
- Vahava O, Morell R, Lynch ED, Weiss S, Kagan ME, Ahituv N, Morrow JE, Lee MK, Skvorak AB, Morton CC, Blumenfeld A, Frydman M, Friedman TB, King MC, Avraham KB: Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. Science. 1998, 279: 1950-1954. 10.1126/science.279.5358.1950.PubMedView ArticleGoogle Scholar
- Bianchi LM, Conover JC, Fritzsch B, DeChiara T, Lindsay RM, Yancopoulos GD: Degeneration of vestibular neurons in late embryogenesis of both heterozygous and homozygous BDNF null mutant mice. Development. 1996, 122: 1965-1973.PubMedGoogle Scholar
- Fritzsch B, Farinas I, Reichardt LF: Lack of neurotrophin 3 causes losses of both classes of spiral ganglion neurons in the cochlea in a region-specific fashion. J Neurosci. 1997, 17: 6213-6225.PubMedPubMed CentralGoogle Scholar
- Fritzsch B, Silos-Santiago I, Bianchi LM, Farinas I: The role of neurotrophic factors in regulating the development of inner ear innervation. Trends Neurosci. 1997, 20: 159-164. 10.1016/S0166-2236(96)01007-7.PubMedView ArticleGoogle Scholar
- Fritzsch B, Barbacid M, Silos-Santiago I: The combined effects of trkB and trkC mutations on the innervation of the inner ear. Int J Dev Neurosci. 1998, 16: 493-505. 10.1016/S0736-5748(98)00043-4.PubMedView ArticleGoogle Scholar
- Zine A, Aubert A, Qiu J, Therianos S, Guillemot F, Kageyama R, de Ribaupierre F: Hes1 and Hes5 activities are required for the normal development of the hair cells in the mammalian inner ear. J Neurosci. 2001, 21: 4712-4720.PubMedGoogle Scholar
- Pirvola U, Ylikoski J, Trokovic R, Hebert J, McConnell S, Partanen J: FGFR1 Is Required for the Development of the Auditory Sensory Epithelium. Neuron. 2002, 35: 671.PubMedView ArticleGoogle Scholar
- Leake PA, Snyder RL, Hradek GT: Postnatal refinement of auditory nerve projections to the cochlear nucleus in cats. J Comp Neurol. 2002, 448: 6-27. 10.1002/cne.10176.PubMedPubMed CentralView ArticleGoogle Scholar
- Wheeler EF, Bothwell M, Schecterson LC, von Bartheld CS: Expression of BDNF and NT-3 mRNA in hair cells of the organ of Corti: quantitative analysis in developing rats. Hear Res. 1994, 73: 46-56. 10.1016/0378-5955(94)90281-X.PubMedView ArticleGoogle Scholar
- Levi-Montalcini R: The nerve growth factor 35 years later. Science. 1987, 237: 1154-1162.PubMedView ArticleGoogle Scholar
- Xiang M, Gan L, Li D, Zhou L, Chen ZY, Wagner D, O'Malley BW, Klein W, Nathans J: Role of the Brn-3 family of POU-domain genes in the development of the auditory/vestibular, somatosensory, and visual systems. Cold Spring Harb Symp Quant Biol. 1997, 62: 325-336.PubMedView ArticleGoogle Scholar
- Ylikoski J, Pirvola U, Moshnyakov M, Palgi J, Arumae U, Saarma M: Expression patterns of neurotrophin and their receptor mRNAs in the rat inner ear. Hear Res. 1993, 65: 69-78. 10.1016/0378-5955(93)90202-C.PubMedView ArticleGoogle Scholar
- Tierney TS, T PD, Xia G, Moore DR: Development of brain-derived neurotrophic factor and neurotrophin-3 immunoreactivity in the lower auditory brainstem of the postnatal gerbil. Eur J Neurosci. 2001, 14: 785-793. 10.1046/j.0953-816x.2001.01690.x.PubMedView ArticleGoogle Scholar
- Heid S, Hartmann R, Klinke R: A model for prelingual deafness, the congenitally deaf white cat – population statistics and degenerative changes. Hear Res. 1998, 115: 101-112. 10.1016/S0378-5955(97)00182-2.PubMedView ArticleGoogle Scholar
- Colvin JS, Bohne BA, Harding GW, McEwen DG, Ornitz DM: Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3. Nat Genet. 1996, 12: 390-397.PubMedView ArticleGoogle Scholar
- Pirvola U, Spencer-Dene B, Xing-Qun L, Kettunen P, Thesleff I, Fritzsch B, Dickson C, Ylikoski J: FGF/FGFR-2(IIIb) signaling is essential for inner ear morphogenesis. J Neurosci. 2000, 20: 6125-6134.PubMedGoogle Scholar
- Eddison M, Le Roux I, Lewis J: Notch signaling in the development of the inner ear: lessons from Drosophila. Proc Natl Acad Sci U S A. 2000, 97: 11692-11699. 10.1073/pnas.97.22.11692.PubMedPubMed CentralView ArticleGoogle Scholar
- Fritzsch B, Beisel KW, Bermingham NA: Developmental evolutionary biology of the vertebrate ear: conserving mechanoelectric transduction and developmental pathways in diverging morphologies. Neuroreport. 2000, 11: R35-44.PubMedView ArticleGoogle Scholar
- Kim WY, Fritzsch B, Serls A, Bakel LA, Huang EJ, Reichardt LF, Barth DS, Lee JE: NeuroD-null mice are deaf due to a severe loss of the inner ear sensory neurons during development. Development. 2001, 128: 417-426.PubMedPubMed CentralGoogle Scholar
- Karis A, Pata I, van Doorninck JH, Grosveld F, de Zeeuw CI, de Caprona D, Fritzsch B: Transcription factor GATA-3 alters pathway selection of olivocochlear neurons and affects morphogenesis of the ear. J Comp Neurol. 2001, 429: 615-630. 10.1002/1096-9861(20010122)429:4<615::AID-CNE8>3.0.CO;2-F.PubMedView ArticleGoogle Scholar
- Ma Q, Anderson DJ, Fritzsch B: Neurogenin 1 null mutant ears develop fewer, morphologically normal hair cells in smaller sensory epithelia devoid of innervation. J Assoc Res Otolaryngol. 2000, 1: 129-143.PubMedPubMed CentralView ArticleGoogle Scholar
- Coppola V, Kucera J, Palko ME, Martinez-De Velasco J, Lyons WE, Fritzsch B, Tessarollo L: Dissection of NT3 functions in vivo by gene replacement strategy. Development. 2001, 128: 4315-4327.PubMedGoogle Scholar
- Frydman M, Vreugde S, Nageris BI, Weiss S, Vahava O, Avraham KB: Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor. Arch Otolaryngol Head Neck Surg. 2000, 126: 633-637.PubMedView ArticleGoogle Scholar
- Keithley EM, Erkman L, Bennett T, Lou L, Ryan AF: Effects of a hair cell transcription factor, Brn-3.1, gene deletion on homozygous and heterozygous mouse cochleas in adulthood and aging. Hear Res. 1999, 134: 71-76. 10.1016/S0378-5955(99)00070-2.PubMedView ArticleGoogle Scholar
- Yagi M, Kanzaki S, Kawamoto K, Shin B, Shah PP, Magal E, Sheng J, Raphael Y: Spiral ganglion neurons are protected from degeneration by GDNF gene therapy. J Assoc Res Otolaryngol. 2000, 1: 315-325.PubMedPubMed CentralGoogle Scholar
- Bermingham NA, Hassan BA, Price SD, Vollrath MA, Ben-Arie N, Eatock RA, Bellen HJ, Lysakowski A, Zoghbi HY: Math1: an essential gene for the generation of inner ear hair cells. Science. 1999, 284: 1837-1841. 10.1126/science.284.5421.1837.PubMedView ArticleGoogle Scholar
- Liberman MC, Gao J, He DZ, Wu X, Jia S, Zuo J: Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier. Nature. 2002, 419: 300-304. 10.1038/nature01059.PubMedView ArticleGoogle Scholar
- Li S, Price SM, Cahill H, Ryugo DK, Shen MM, Xiang M: Hearing loss caused by progressive degeneration of cochlear hair cells in mice deficient for the Barhl1 homeobox gene. Development. 2002, 129: 3523-3532.PubMedGoogle Scholar
- Qun LX, Pirvola U, Saarma M, Ylikoski J: Neurotrophic factors in the auditory periphery. Ann N Y Acad Sci. 1999, 884: 292-304.PubMedView ArticleGoogle Scholar
- Fritzsch B, Nichols DH: DiI reveals a prenatal arrival of efferents at the differentiating otocyst of mice. Hear Res. 1993, 65: 51-60. 10.1016/0378-5955(93)90200-K.PubMedView ArticleGoogle Scholar
- Fritzsch B, Christensen MA, Nichols DH: Fiber pathways and positional changes in efferent perikarya of 2.5- to 7-day chick embryos as revealed with DiI and dextran amines. J Neurobiol. 1993, 24: 1481-1499.PubMedView ArticleGoogle Scholar
- Maklad A, Fritzsch B: The developmental segregation of posterior crista and saccular vestibular fibers in mice: A carbocyanine tracer study using confocal microscopy. Develop Brain Research. 2002, 135: 1-17. 10.1016/S0165-3806(01)00327-3.View ArticleGoogle Scholar
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