RESUMEN
How tissues acquire complex shapes is a fundamental question in biology and regenerative medicine. Zebrafish semicircular canals form from invaginations in the otic epithelium (buds) that extend and fuse to form the hubs of each canal. We find that conventional actomyosin-driven behaviors are not required. Instead, local secretion of hyaluronan, made by the enzymes uridine 5'-diphosphate dehydrogenase (ugdh) and hyaluronan synthase 3 (has3), drives canal morphogenesis. Charged hyaluronate polymers osmotically swell with water and generate isotropic extracellular pressure to deform the overlying epithelium into buds. The mechanical anisotropy needed to shape buds into tubes is conferred by a polarized distribution of actomyosin and E-cadherin-rich membrane tethers, which we term cytocinches. Most work on tissue morphogenesis ascribes actomyosin contractility as the driving force, while the extracellular matrix shapes tissues through differential stiffness. Our work inverts this expectation. Hyaluronate pressure shaped by anisotropic tissue stiffness may be a widespread mechanism for powering morphological change in organogenesis and tissue engineering.
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Espacio Extracelular/química , Ácido Hialurónico/farmacología , Morfogénesis , Especificidad de Órganos , Presión , Canales Semicirculares/citología , Canales Semicirculares/embriología , Actomiosina/metabolismo , Animales , Anisotropía , Conducta Animal , Matriz Extracelular/metabolismo , Ácido Hialurónico/biosíntesis , Modelos Biológicos , Morfogénesis/efectos de los fármacos , Especificidad de Órganos/efectos de los fármacos , Presión Osmótica , Canales Semicirculares/diagnóstico por imagen , Conducta Estereotipada , Pez Cebra/embriología , Proteínas de Pez Cebra/metabolismoRESUMEN
BACKGROUND: Sensorineural hearing loss is an understudied consequence of congenital Zika syndrome, and balance disorders are essentially unreported to date. Also lacking is information about the susceptibility and the pathogenesis of the developing inner ear following Zika virus (ZIKV) exposure. To address this, ZIKV was delivered directly into the otic cup/otocyst of chicken embryos and infection of inner ear tissues was evaluated using immunohistochemistry. RESULTS: After injections on embryonic days 2 to 5, ZIKV infection was observed in 90% of the samples harvested 2 to 8 days later; however, the degree of infection was highly variable across individuals. ZIKV was detected in all regions of the inner ear, associated ganglia, and in the surrounding periotic mesenchyme. Detection of virus peaked earlier in the ganglion and vestibular compartments, and later in the cochlea. ZIKV infection increased cell death robustly in the auditory ganglion, and modestly in the auditory sensory organ. Macrophage accumulation was found to overlap with dense viral infection in some tissues. Additionally, dysmorphogenesis of the semicircular canals and ganglion was observed for a subset of injection conditions. CONCLUSIONS: This article presents evidence of direct ZIKV infection of developing inner ear epithelium and shows previously unknown inner ear dysmorphogenesis phenotypes.
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Oído Interno/embriología , Oído Interno/virología , Pérdida Auditiva Sensorineural/embriología , Infección por el Virus Zika/virología , Virus Zika/metabolismo , Animales , Muerte Celular , Embrión de Pollo , Pollos , Cóclea , Oído Interno/metabolismo , Epitelio/metabolismo , Proteínas de Homeodominio/metabolismo , Humanos , Inmunohistoquímica , Hibridación in Situ , Macrófagos/metabolismo , Fenotipo , Canales Semicirculares/embriología , Canales Semicirculares/metabolismo , Factores de Tiempo , Infección por el Virus Zika/metabolismo , Infección por el Virus Zika/patologíaRESUMEN
Little is known about the role of TBX1 in post-otocyst stages of inner ear development. Here, we report on mice with a missense mutation of Tbx1 that are viable with fully developed but abnormally formed inner ears. Mutant mice are deaf due to an undeveloped stria vascularis and show vestibular dysfunction associated with abnormal semicircular canal formation. We show that TBX1 is expressed in endolymph-producing strial marginal cells and vestibular dark cells of the inner ear and is an upstream regulator of Esrrb, which previously was shown to control the developmental fate of these cells. We also show that TBX1 is expressed in sensory cells of the crista ampullaris, which may relate to the semicircular canal abnormalities observed in mutant mice. Inner ears of mutant embryos have a non-resorbed fusion plate in the posterior semicircular canal and a single ampulla connecting anterior and lateral canals. We hypothesize that the TBX1 missense mutation prevents binding with specific co-regulatory proteins. These findings reveal previously unknown functions of TBX1 during later stages of inner ear development.
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Oído Interno/embriología , Mutación Missense , Canales Semicirculares/embriología , Proteínas de Dominio T Box/genética , Proteínas de Dominio T Box/metabolismo , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Oído Interno/citología , Potenciales Evocados Auditivos del Tronco Encefálico , Femenino , Masculino , Ratones , Ratones Endogámicos C57BL , Modelos Moleculares , Morfogénesis , Receptores de Estrógenos/metabolismo , Canales Semicirculares/anomalías , Estría Vascular/citología , Proteínas de Dominio T Box/química , Técnicas del Sistema de Dos Híbridos , Secuenciación del ExomaRESUMEN
The semicircular canals of the mammalian inner ear are derived from epithelial pouches in which epithelial cells in the central region of each pouch undergo resorption, leaving behind the region at the rim to form a tube-shaped canal. Lack of proliferation at the rim and/or over-clearing of epithelial cells in the center of the pouch can obliterate canal formation. Otic-specific knockout of bone morphogenetic protein 2 (Bmp2) results in absence of all three semicircular canals; however, the common crus and ampullae housing the sensory tissue (crista) are intact. The lack of Bmp2 causes Ntn1 (which encodes netrin 1), which is required for canal resorption, to be ectopically expressed at the canal rim. Ectopic Ntn1 results in reduction of Dlx5 and Lmo4, which are required for rim formation. These phenotypes can be partially rescued by removing one allele of Ntn1 in the Bmp2 mutants, indicating that Bmp2 normally negatively regulates Ntn1 for canal formation. Additionally, non-resorption of the canal pouch in Ntn1-/- mutants is partially rescued by removing one allele of Bmp2 Thus, reciprocal inhibition between Bmp2 and netrin 1 is involved in canal formation of the vestibule.
Asunto(s)
Proteína Morfogenética Ósea 2/genética , Regulación del Desarrollo de la Expresión Génica , Netrina-1/genética , Canales Semicirculares/embriología , Proteínas Adaptadoras Transductoras de Señales/metabolismo , Alelos , Animales , Proteína Morfogenética Ósea 2/metabolismo , Linaje de la Célula , Proliferación Celular , Factores de Transcripción Forkhead/metabolismo , Perfilación de la Expresión Génica , Genotipo , Proteínas de Homeodominio/metabolismo , Proteínas con Dominio LIM/metabolismo , Ratones , Ratones Endogámicos C57BL , Mutación , Proteínas del Tejido Nervioso/metabolismo , Netrina-1/metabolismo , Fenotipo , Unión Proteica , Dominios Proteicos , Vestíbulo del Laberinto/embriologíaRESUMEN
Jawed vertebrates have inner ears with three semicircular canals, the presence of which has been used as a key to understanding evolutionary relationships. Ostracoderms, the jawless stem gnathostomes, had only two canals and lacked the lateral canal1-3. Lampreys, which are modern cyclostomes, are generally thought to possess two semicircular canals whereas the hagfishes-which are also cyclostomes-have only a single canal, which used to be regarded as a more primitive trait1,4. However, recent molecular and developmental analyses have strongly supported the monophyly of cyclostomes5-7, which has left the evolutionary trajectory of the vertebrate inner ear unclear8. Here we show the differentiation of the otic vesicle of the lamprey Lethenteron camtschaticum and inshore hagfish Eptatretus burgeri. This is the first time, to our knowledge, that the development of the hagfish inner ear is reported. We found that canal development in the lamprey starts with two depressions-which is reminiscent of the early developmental pattern of the inner ear in modern gnathostomes. These cyclostome otic vesicles show a pattern of expression of regulatory genes, including OTX genes, that is comparable to that of gnathosomes. Although two depressions appear in the lamprey vesicle, they subsequently fuse to form a single canal that is similar to that of hagfishes. Complete separation of the depressions results in anterior and posterior canals in gnathostomes. The single depression of the vesicle in hagfishes thus appears to be a secondarily derived trait. Furthermore, the lateral canal in crown gnathostomes was acquired secondarily-not by de novo acquisition of an OTX expression domain, but by the evolution of a developmental program downstream of the OTX genes.
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Anguila Babosa/anatomía & histología , Lampreas/anatomía & histología , Organogénesis , Filogenia , Canales Semicirculares/anatomía & histología , Canales Semicirculares/embriología , Vertebrados/anatomía & histología , Vertebrados/embriología , Animales , Regulación del Desarrollo de la Expresión Génica , Anguila Babosa/embriología , Anguila Babosa/genética , Lampreas/embriología , Lampreas/genética , Ratones/anatomía & histología , Ratones/embriología , Organogénesis/genética , Tiburones/anatomía & histología , Tiburones/embriología , Vertebrados/genética , Pez Cebra/anatomía & histología , Pez Cebra/embriologíaRESUMEN
PURPOSE: To describe the ontogeny of vertical semicircular canals using computed tomography. MATERIALS AND METHODS: We have studied 39 human fetuses aged between 17 and 38 weeks of development through multi-helicoidal CT. RESULTS: The first signs of ossification in the semicircular canals, superior and posterior, are from 19 weeks of development, through two primary ossification centers in each canal, which will take part in the formation of the outer cover oriented towards the middle and posterior brain fossae, respectively. In this process it must be added the intervention of the common branch. Internal bone covers are formed by ossification of the fossa subarcuata in the superior semicircular canal, and from the compact center of the labyrinthine capsule into the posterior canal. The tomographic study has allowed us to demonstrate how ossification follows a variable rate, establishing a period between 21 and 26 weeks where there are completely closed canals with others still open to the brain fossae. CONCLUSIONS: The tomographic study of the semicircular canals has enabled us to establish a critical period in its ossification that could explain the etiology of the congenital-type dehiscence.
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Feto/diagnóstico por imagen , Feto/embriología , Canales Semicirculares/diagnóstico por imagen , Canales Semicirculares/embriología , Tomografía Computarizada por Rayos X/métodos , Femenino , Humanos , EmbarazoRESUMEN
The vestibular system of the inner ear detects head position using three orthogonally oriented semicircular canals; even slight changes in their shape and orientation can cause debilitating behavioral defects. During development, the canals are sculpted from pouches that protrude from the otic vesicle, the embryonic anlage of the inner ear. In the center of each pouch, a fusion plate forms where cells lose their epithelial morphology and the basement membrane breaks down. Cells in the fusing epithelia intercalate and are removed, creating a canal. In mice, fusion depends on the secreted protein netrin 1 (Ntn1), which is necessary for basement membrane breakdown, although the underlying molecular mechanism is unknown. Using gain-of-function approaches, we found that overexpression of Ntn1 in the chick otic vesicle prevented canal fusion by inhibiting apoptosis. In contrast, ectopic expression of the same chicken Ntn1 in the mouse otic vesicle, where apoptosis is less prominent, resulted in canal truncation. These findings highlight the importance of apoptosis for tissue morphogenesis and suggest that Ntn1 may play divergent cellular roles despite its conserved expression during canal morphogenesis in chicken and mouse.
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Morfogénesis , Factores de Crecimiento Nervioso/metabolismo , Canales Semicirculares/embriología , Canales Semicirculares/metabolismo , Proteínas Supresoras de Tumor/metabolismo , Alelos , Animales , Apoptosis , Membrana Basal/metabolismo , Pollos , Electroporación , Proteínas Fluorescentes Verdes/metabolismo , Fusión de Membrana , Proteínas de la Membrana/metabolismo , Ratones , Mutación/genética , Netrina-1 , Proteínas Proto-Oncogénicas c-myc/metabolismo , Reproducibilidad de los ResultadosRESUMEN
The inner ear consists of two otocyst-derived, structurally and functionally distinct components: the dorsal vestibular and ventral auditory compartments. BMP signaling is required to form the vestibular compartment, but how it complements other required signaling molecules and acts intracellularly is unknown. Using spatially and temporally controlled delivery of signaling pathway regulators to developing chick otocysts, we show that BMP signaling regulates the expression of Dlx5 and Hmx3, both of which encode transcription factors essential for vestibular formation. However, although BMP regulates Dlx5 through the canonical SMAD pathway, surprisingly, it regulates Hmx3 through a non-canonical pathway involving both an increase in cAMP-dependent protein kinase A activity and the GLI3R to GLI3A ratio. Thus, both canonical and non-canonical BMP signaling establish the precise spatiotemporal expression of Dlx5 and Hmx3 during dorsal vestibular development. The identification of the non-canonical pathway suggests an intersection point between BMP and SHH signaling, which is required for ventral auditory development.
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Proteínas Morfogenéticas Óseas/metabolismo , Oído Interno/embriología , Oído Interno/metabolismo , Regulación del Desarrollo de la Expresión Génica , Transducción de Señal , Animales , Pollos , Cóclea/embriología , Cóclea/metabolismo , Proteínas Quinasas Dependientes de AMP Cíclico/metabolismo , Proteínas de Homeodominio/metabolismo , Factores de Transcripción de Tipo Kruppel/metabolismo , Modelos Biológicos , Proteínas del Tejido Nervioso/metabolismo , Factores de Transcripción Otx/metabolismo , Procesamiento Proteico-Postraduccional , Canales Semicirculares/embriología , Canales Semicirculares/metabolismo , Proteínas Smad/metabolismo , Proteína Gli3 con Dedos de ZincRESUMEN
We describe the development of the human inner ear with the invagination of the otic vesicle at 4 weeks gestation (WG), the growth of the semicircular canals from 5 WG, and the elongation and coiling of the cochlea at 10 WG. As the membranous labyrinth takes shape, there is a concomitant development of the sensory neuroepithelia and their associated structures within. This review details the growth and differentiation of the vestibular and auditory neuroepithelia, including synaptogenesis, the expression of stereocilia and kinocilia, and innervation of hair cells by afferent and efferent nerve fibres. Along with development of essential sensory structures we outline the formation of crucial accessory structures of the vestibular system - the cupula and otolithic membrane and otoconia as well as the three cochlea compartments and the tectorial membrane. Recent molecular studies have elaborated on classical anatomical studies to characterize the development of prosensory and sensory regions of the fetal human cochlea using the transcription factors, PAX2, MAF-B, SOX2, and SOX9. Further advances are being made with recent physiological studies that are beginning to describe when hair cells become functionally active during human gestation. This article is part of a Special Issue entitled
Asunto(s)
Oído Interno/embriología , Células Ciliadas Auditivas/fisiología , Vestíbulo del Laberinto/embriología , Animales , Diferenciación Celular , Linaje de la Célula , Cóclea/embriología , Humanos , Ratones , Neuronas/metabolismo , Órgano Espiral/embriología , Membrana Otolítica/embriología , Factor de Transcripción PAX2/metabolismo , Regeneración , Factor de Transcripción SOX9/metabolismo , Factores de Transcripción SOXB1/metabolismo , Canales Semicirculares/embriología , Sinapsis/metabolismo , Factores de Tiempo , Factores de Transcripción/metabolismo , Vestíbulo del Laberinto/metabolismoRESUMEN
OBJECTIVES: To analyze the ontogeny of the superior semicircular canal and tegmen tympani and determine if there are common embryological factors explaining both associated dehiscence. METHODS: We analyzed 77 human embryological series aged between 6 weeks and newborn. Preparations were serially cut and stained with Masson's trichrome technique. RESULTS: The tegmental prolongation of tegmen tympani and superior semicircular canal originate from the same structure, the otic capsule, and have the same type of endochondral ossification; while the extension of the squamous prolongation of tegmen tympani runs from the temporal squama and ossification is directly of intramembranous type. The nuclei of ossification of the superior and external semicircular canals and accessory of tegmen collaborate in the ossification of the tegmental extension and by growth extend to the tegmental prolongation. This fact plus the fact that both structures share a common layer of external periosteum could explain the coexistence of lack of bone coverage in tegmen and superior semicircular canal. CONCLUSION: The development of the semicircular canal and tegmen tympani could explain the causes of the association of both dehiscences.
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Oído Medio/embriología , Enfermedades del Laberinto/embriología , Canales Semicirculares/embriología , Oído Medio/anomalías , Edad Gestacional , Humanos , Recién Nacido , Osteogénesis , Periostio/anomalías , Periostio/embriología , Rotura Espontánea , Canales Semicirculares/anomalíasRESUMEN
This study examined the external morphology and morphometry of the human embryonic inner ear membranous labyrinth and documented its three-dimensional position in the developing embryo using phase-contrast X-ray computed tomography and magnetic resonance imaging. A total of 27 samples between Carnegie stage (CS) 17 and the postembryonic phase during trimester 1 (approximately 6-10 weeks after fertilization) were included. The otic vesicle elongated along the dorso-ventral axis and differentiated into the end lymphatic appendage and cochlear duct (CD) at CS 17. The spiral course of the CD began at CS18, with anterior and posterior semicircular ducts (SDs) forming prominent circles with a common crus. The spiral course of the CD comprised more than two turns at the postembryonic phase, at which time the height of the CD was evident. A linear increase was observed in the length of anterior, posterior, and lateral SDs, in that order, and the length of the CD increased exponentially over the course of development. Bending in the medial direction was observed between the cochlear and vestibular parts from the latero-caudal view, with the angle decreasing during development. The position of the inner ear was stable throughout the period of observation on the lateral to ventral side of the rhombencephalon, caudal to the pontine flexure, and adjacent to the auditory ganglia. The plane of the lateral semicircular canal was approximately 8.0°-14.6° with respect to the cranial caudal (z-)axis, indicating that the orientation of the inner ear changes during growth to adulthood.
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Oído Interno/diagnóstico por imagen , Oído Interno/embriología , Morfogénesis , Vestíbulo del Laberinto/diagnóstico por imagen , Vestíbulo del Laberinto/embriología , Cóclea/diagnóstico por imagen , Cóclea/embriología , Cóclea/fisiología , Oído Interno/fisiología , Desarrollo Embrionario/fisiología , Humanos , Morfogénesis/fisiología , Canales Semicirculares/diagnóstico por imagen , Canales Semicirculares/embriología , Canales Semicirculares/fisiología , Tomografía Computarizada por Rayos X/métodos , Vestíbulo del Laberinto/fisiologíaRESUMEN
OBJECTIVE: In humans, the inner ear reaches its final configuration and adult size during fetal life. According to the literature, this occurs between 18 and 25 weeks of amenorrhea (WA). The ossification of the otic capsule is believed to arrest any further configuration change. There have, however, been some observations of slight changes in the orientation of the semicircular canals (SCCs) occurring later in fetal life. The present study aim was to examine changes of angulations between bony SCCs during fetal life. PATIENTS: Fifty-four human fetuses aged 22 to 40 WA. INTERVENTION: Computed tomography scanner. MAIN OUTCOME MEASURE: SCC angulation (in degrees) studied with Amira software. RESULTS: We found mean angles between the lateral SCC and anterior SCC, the lateral SCC and posterior SCC, and the anterior SCC and posterior SCC of 88.67, 92.60, and 90.19 degrees, respectively. Inter-SCC angles did not change significantly between the different age groups (22 WA, 24 WA, 26 WA, 29-31 WA, 34-36 WA, 38-40 WA). There was no difference of angulation between males and females and no intraobserver or interobserver variability. CONCLUSION: The absence of correlation of SCC angles with age in our sample of fetuses indicates that the three-dimensional configuration of the SCC has already reached its adult form at 22 WA. As often described in the literature, these angles are close to orthogonality, probably reflecting an optimal vestibular function configuration.
Asunto(s)
Canales Semicirculares/diagnóstico por imagen , Canales Semicirculares/embriología , Femenino , Feto , Humanos , Imagenología Tridimensional , Masculino , Osteogénesis/fisiología , Interpretación de Imagen Radiográfica Asistida por Computador , Tomógrafos Computarizados por Rayos X , Tomografía Computarizada por Rayos X/métodosRESUMEN
Objetivos: Realizar un estudio sobre la ontogénesis del canal semicircular superior con el fin de describir sus peculiaridades. Métodos: Para ello se han analizado 76 series embriológicas humanas de edades comprendidas entre los 32 días (6 mm) y recién nacidos. Las preparaciones estaban cortadas en serie y teñidas con la técnica de tricrómico de Martins. Resultados: En el desarrollo del canal semicircular hemos observado una serie de peculiaridades, como: secuencia cronológica definida de su osteogénesis con un ritmo de osificación variable, cada núcleo de osificación interviene en la formación de una de sus cubiertas, el superior de la superficial y el inferior de la profunda; la aparición de una dehiscencia transitoria, y el cierre del canal por hueso de tipo laminar con un grosor mínimo de 0,1 mm. Conclusión: Las peculiaridades en el desarrollo del canal podrían explicar las causas del origen de la dehiscencia patológica del mismo, ya sean congénitas o adquiridas (AU)
Objective: Our objective was to study the ontogeny of the superior semicircular canal in order to describe its peculiarities. Methods: We analyzed 76 series of human embryos aged between 32 days (6 mm) and newborns. The samples were cut serially and stained using Martin's trichrome technique. Results: In semicircular canal development there were a number of peculiarities, such as: a defined chronological sequence of osteogenesis with a variable rate of ossification; the fact that each nucleus of ossification was involved in the formation of one of its covers (the upper in the superficial and the lower in the deep); the appearance of transitory dehiscence; and canal closure by means of bone with laminar pattern, with a minimum thickness of 0.1 mm. Conclusion: The peculiarities in canal development could explain the origin of pathological dehiscence in the canal, whether congenital or acquired (AU)
Asunto(s)
Humanos , Recién Nacido , Canales Semicirculares/embriología , Morfogénesis/fisiología , Osteogénesis/fisiología , Fijación del Tejido/métodos , Desarrollo Fetal/fisiologíaRESUMEN
Immunoglobulin-like domain containing receptor 1 (ILDR1) is a poorly characterized gene that was first identified in lymphoma cells. Recently, ILDR1 has been found to be responsible for autosomal recessive hearing impairment DFNB42. Patients with ILDR1 mutations cause bilateral non-progressive moderate-to-profound sensorineural hearing impairment. However, the etiology and mechanism of ILDR1-related hearing loss remains to be elucidated. In order to uncover the pathology of DFNB42 deafness, we used the morpholino injection technique to establish an ildr1b-morphant zebrafish model. Ildr1b-morphant zebrafish displayed defective hearing and imbalanced swimming, and developmental delays were seen in the semicircular canals of the inner ear. The gene expression profile and real-time PCR revealed down-regulation of atp1b2b (encoding Na(+)/K(+) transporting, beta 2b polypeptide) in ildr1b-morphant zebrafish. We found that injection of atp1b2b mRNA into ildr1b-knockdown zebrafish could rescue the phenotype of developmental delay of the semicircular canals. Moreover, ildr1b-morphant zebrafish had reduced numbers of lateral line neuromasts due to the disruption of lateral line primordium migration. In situ hybridization showed the involvement of attenuated FGF signaling and the chemokine receptor 4b (cxcr4b) and chemokine receptor 7b (cxcr7b) in posterior lateral line primordium of ildr1b-morphant zebrafish. We concluded that Ildr1b is crucial for the development of the inner ear and the lateral line system. This study provides the first evidence for the mechanism of Ildr1b on hearing in vivo and sheds light on the pathology of DFNB42.
Asunto(s)
Audición/genética , Receptores de Superficie Celular/genética , Canales Semicirculares/embriología , Proteínas de Pez Cebra/genética , Pez Cebra/embriología , Animales , Oído Interno/embriología , Oído Interno/metabolismo , Pérdida Auditiva Sensorineural/embriología , Sistema de la Línea Lateral/embriología , Sistema de la Línea Lateral/metabolismo , Modelos Animales , Receptores de Superficie Celular/metabolismo , Canales Semicirculares/metabolismo , Pez Cebra/metabolismo , Proteínas de Pez Cebra/metabolismoRESUMEN
OBJECTIVE: Our objective was to study the ontogeny of the superior semicircular canal in order to describe its peculiarities. METHODS: We analyzed 76 series of human embryos aged between 32 days (6mm) and newborns. The samples were cut serially and stained using Martin's trichrome technique. RESULTS: In semicircular canal development there were a number of peculiarities, such as: a defined chronological sequence of osteogenesis with a variable rate of ossification; the fact that each nucleus of ossification was involved in the formation of one of its covers (the upper in the superficial and the lower in the deep); the appearance of transitory dehiscence; and canal closure by means of bone with laminar pattern, with a minimum thickness of 0.1mm. CONCLUSION: The peculiarities in canal development could explain the origin of pathological dehiscence in the canal, whether congenital or acquired.
Asunto(s)
Canales Semicirculares/embriología , Canales Semicirculares/crecimiento & desarrollo , Edad Gestacional , Humanos , Recién NacidoRESUMEN
Morphogenesis of the semicircular canal ducts in the vertebrate inner ear is a dramatic example of epithelial remodelling in the embryo, and failure of normal canal development results in vestibular dysfunction. In zebrafish and Xenopus, semicircular canal ducts develop when projections of epithelium, driven by extracellular matrix production, push into the otic vesicle and fuse to form pillars. We show that in the zebrafish, extracellular matrix gene expression is high during projection outgrowth and then rapidly downregulated after fusion. Enzymatic disruption of hyaluronan in the projections leads to their collapse and a failure to form pillars: as a result, the ears swell. We have cloned a zebrafish mutant, lauscher (lau), identified by its swollen ear phenotype. The primary defect in the ear is abnormal projection outgrowth and a failure of fusion to form the semicircular canal pillars. Otic expression of extracellular matrix components is highly disrupted: several genes fail to become downregulated and remain expressed at abnormally high levels into late larval stages. The lau mutations disrupt gpr126, an adhesion class G protein-coupled receptor gene. Expression of gpr126 is similar to that of sox10, an ear and neural crest marker, and is partially dependent on sox10 activity. Fusion of canal projections and downregulation of otic versican expression in a hypomorphic lau allele can be restored by cAMP agonists. We propose that Gpr126 acts through a cAMP-mediated pathway to control the outgrowth and adhesion of canal projections in the zebrafish ear via the regulation of extracellular matrix gene expression.
Asunto(s)
Regulación del Desarrollo de la Expresión Génica/fisiología , Morfogénesis/fisiología , Receptores Acoplados a Proteínas G/metabolismo , Canales Semicirculares/embriología , Proteínas de Pez Cebra/metabolismo , Pez Cebra/embriología , Animales , AMP Cíclico/metabolismo , Matriz Extracelular/metabolismo , Genotipo , Procesamiento de Imagen Asistido por Computador , Inmunohistoquímica , Hibridación in Situ , Repeticiones de Microsatélite/genética , Faloidina , Polimorfismo de Nucleótido Simple/genética , Factores de Transcripción SOXE/metabolismo , Canales Semicirculares/anomalías , Análisis de Secuencia de ADN , Versicanos/metabolismoRESUMEN
The morphogenetic program that shapes the three semicircular canals (SSCs) must be executed with extreme precision to satisfy their complex vestibular function. The SSCs emerge from epithelial outgrowths of the dorsal otocyst, the central regions of which fuse and resorb to leave three fluid-filled canals. The Wnt/ß-catenin signaling pathway is active at multiple stages of otic development, including during vestibular morphogenesis. How Wnt/ß-catenin functionally integrates with other signaling pathways to sculpt the SSCs and their sensory patches is unknown. We used a genetic strategy to spatiotemporally modulate canonical Wnt signaling activity during SSC development in mice. Our findings demonstrate that Wnt/ß-catenin signaling functions in a multifaceted manner during SSC formation. In the early phase, Wnt/ß-catenin signaling is required to preserve the epithelial integrity of the vertical canal pouch perimeter (presumptive anterior and posterior SSCs) by establishing a sensory-dependent signaling relay that maintains expression of Dlx5 and opposes expression of the fusion plate marker netrin 1. Without this Wnt signaling activity the sensory to non-sensory signaling cascade fails to be activated, resulting in loss of vestibular hair and support cells and the anterior and posterior SSCs. In the later phase, Wnt/ß-catenin signaling becomes restricted to the fusion plate where it facilitates the timely resorption of this tissue. Mosaic recombination of ß-catenin in small clusters of canal pouch cells prevents their resorption, causing instead the formation of ectopic SSCs. Together, these disparate functions of the Wnt/ß-catenin pathway in epithelial maintenance and resorption help regulate the size, shape and number of SSCs.
Asunto(s)
Epitelio/embriología , Regulación del Desarrollo de la Expresión Génica/fisiología , Morfogénesis/fisiología , Canales Semicirculares/embriología , Vía de Señalización Wnt/fisiología , beta Catenina/metabolismo , Animales , Bromodesoxiuridina , Regulación del Desarrollo de la Expresión Génica/genética , Proteínas de Homeodominio/metabolismo , Inmunohistoquímica , Hibridación in Situ , Ratones , Factores de Crecimiento Nervioso/metabolismo , Netrina-1 , Proteínas Supresoras de Tumor/metabolismo , beta-GalactosidasaRESUMEN
Macrophage migration inhibitory factor (MIF) plays versatile roles in the immune system. MIF is also widely expressed during embryonic development, particularly in the nervous system, although its roles in neural development are only beginning to be understood. Evidence from frogs, mice and zebrafish suggests that MIF has a major role as a neurotrophin in the early development of sensory systems, including the auditory system. Here we show that the zebrafish mif pathway is required for both sensory hair cell (HC) and sensory neuronal cell survival in the ear, for HC differentiation, semicircular canal formation, statoacoustic ganglion (SAG) development, and lateral line HC differentiation. This is consistent with our findings that MIF is expressed in the developing mammalian and avian auditory systems and promotes mouse and chick SAG neurite outgrowth and neuronal survival, demonstrating key instructional roles for MIF in vertebrate otic development.