Developmental Morphology of the Mouse Inner Ear: A scanning electron microscopic observation

References

• Anniko M., Nordemar H., Van De Water T. F. Embryogenesis of the inner ear. I. Development and differentiation of the mammalian crista ampullaris in vivo and in vitro. Arch Oto-Rhino-Laryngol 1979a; 224: 285–299
   PubMed Web of Science ®Google Scholar
• Anniko M., Nordemar H., Wersäll J. Genesis and maturation of vestibular hair cells. Adv ORL 1979b; 25: 7–11
   Google Scholar
• Anniko M., Nordemar H. Postnatal maturation of the secretory epithelia of the inner ear in correlation with the elemental composition in the endolymphatic space. Arch Oto-Rhino-Laryng 1980; 229: 281–288
   Google Scholar
• Anniko M. Development of otoconia. Am J Otolaryngol 1980a; 1: 400–410
   PubMedGoogle Scholar
• Anniko M. Embryogenesis of the mammalian inner ear. III. Formation of the tectorial membrane of the CBA/CBA mouse in vivo and in vitro. Anat Embryol 1980b; 160: 301–313
   PubMedGoogle Scholar
• Anniko M., Lundquist P.-G. Temporal bone morphology after systemic arterial perfusion or intralabyrinthine in situ immersion. I. Hair cells of the vestibular organs and the cochlea. Micron 1980; 11: 73–83
   Web of Science ®Google Scholar
• Anniko M. Elemental analysis of the early postnatal tectorial membrane. Hearing Res 1981; 3: 1–9
   Google Scholar
• Anniko M., Wróblewski R. Elemental composition of the developing inner ear. Ann Otol Rhinol Laryngol 1981; 90: 25–32
   PubMed Web of Science ®Google Scholar
• Anniko M., Bagger-Sjöbäck D. Maturation of junctional complexes during embryonic and early postnatal development of inner ear secretory epithelia. Am J Otolaryngol 1982; 3: 242–253
   PubMed Web of Science ®Google Scholar
• Anniko M., Nordemar H. Formation of the cupula cristae ampullaris: Development in vivo and in vitro. Am J Otolaryngol 1982; 3: 31–40
   PubMed Web of Science ®Google Scholar
• Anniko M. Embryonic development of vestibular sense organs and their innervation. Development of auditory and vestibular systems, R. Romand. Academic Press, New York 1983a; 375–423
   Google Scholar
• Anniko M. Maturation of cochlear sensory hairs. Anat Embryol 1983b; 166: 355–368
   PubMedGoogle Scholar
• Anniko M. Cytodifferentiation of cochlear hair cells. Am J Otolaryngol 1983c; 4: 375–388
   PubMed Web of Science ®Google Scholar
• Anniko M., Nordemar H., Sobin A. Principles in embryonic development and differentiation of vestibular hair cells. Otolaryngol Head Neck Surg 1983; 91: 540–549
   PubMed Web of Science ®Google Scholar
• Anniko M., Bagger-Sjöbäck D. The stria vascularis. Ultrastructural atlas of the inner ear, I. Friedmann, J. C. Ballantyne. Butterworths, London 1984; 184–208
   Google Scholar
• Anniko M., Wikström S.-O. Pattern formation of the otic placode and morphogenesis of the otocyst. A scanning electron microscopic study. Am J Otolaryngol 1984; 5: 373–381
   PubMed Web of Science ®Google Scholar
• Bredberg G. The innervation of the organ of Corti: A scanning electron microscopic study. Acta Otolaryngol (Stockh) 1977; 82: 71–78
   Google Scholar
• Curthoys I. S. The development of function of horizontal semicircular canal primary neurons in the rat. Brain Res 1979; 167: 41–52
   PubMed Web of Science ®Google Scholar
• Curthoys I. S. Postnatal developmental changes in the response of rat primary horizontal semicircular canal neurons to sinusoidal angular accelerations. Exp Brain Res 1982; 47: 295–300
   PubMed Web of Science ®Google Scholar
• Curthoys I. S. The development of function of primary vestibular neurons. Development of auditory and vestibular systems, R. Romand. Academic Press, New York 1983; 425–461
   Google Scholar
• Dallos P. Cochlear potentials and cochlear mechanics. Basic mechanisms in hearing, A. R. Møller. Academic Press, New York 1973; 335–376
   Google Scholar
• Deol M. S. Genetic malformation of the inner ear in the mouse and in man. Morphogenesis and malformation of the ear, R. J. Gorlin. Alan R. Liss, Inc., New York 1980; 243–261
   Google Scholar
• Deol M. S. Development of auditory and vestibular systems in mutant mice. Development of auditory and vestibular systems, R. Romand. Academic Press, New York 1983; 309–333
   Google Scholar
• Ehret G. Development of hearing and response behavior to sound stimuli: Behavioral studies. Development of auditory and vestibular systems, R. Romand. Academic Press, New York 1983; 211–237
   Google Scholar
• Engström H., Wersäll J. Myelin sheath structure in nerve fiber demyelinization and branching regions. Exp Cell Res 1958; 14: 414–425
   PubMed Web of Science ®Google Scholar
• Fernández C., Goldberg J. M. Physiology of peripheral neurons innervating semicircular canals of the squirrel monkey. II. Response to sinusoidal stimulation and dynamics of peripheral vestibular system. J Neurophys 1971; 34: 661–675
   PubMed Web of Science ®Google Scholar
• Fernández C., Hinojosa R. Postnatal development of endocochlear potential and stria vascularis in the cat. Acta Otolaryngol (Stockh) 1974; 78: 173–186
   PubMed Web of Science ®Google Scholar
• Geisler C., van Bereijk W., Frishkopf L. The inner ear of the bullfrog. J Morph 1964; 114: 43–58
   PubMed Web of Science ®Google Scholar
• Goldberg J. M., Fernández C. Physiology of peripheral neurons innervating semicircular canals of the squirrel monkey. I. Resting discharge and response to constant angular accelerations. J Neurophys 1971; 34: 635–660
   PubMed Web of Science ®Google Scholar
• Goldberg J. M., Fernández C. Vestibular mechanisms. Ann Rev Physiol 1975; 37: 129–162
   PubMed Web of Science ®Google Scholar
• Hay E. D. Origin and role of collagen in the embryo. Am Zool 1973; 13: 1085–1107
   Google Scholar
• Hillman D. E. Cupular structure and its receptor relationship. Brain Behav Evol 1974; 10: 52–68
   PubMed Web of Science ®Google Scholar
• Hinojosa R. A note on development of Corti's organ. Acta Otolaryngol (Stockh) 1977; 84: 238–251
   PubMed Web of Science ®Google Scholar
• Hunter-Duvar I. M., Hinojosa R. Vestibule: Sensory epithelia. Ultrastructural atlas of the inner ear, I. Friedmann, J. C. Ballantyne. Butterworths, London 1984; 211–244
   Google Scholar
• Kikuchi K., Hilding D. A. The defective organ of Corti in Shaker-I mice. Acta Otolaryngol (Stockh) 1965a; 60: 288–303
   Google Scholar
• Kikuchi K., Hilding D. The development of the organ of Corti in the mouse. Acta Otolaryngol (Stockh) 1965b; 60: 207–222
   PubMedGoogle Scholar
• Kikuchi D., Hilding D. A. The development of the stria vascularis in the mouse. Acta Otolaryngol (Stockh) 1966; 62: 277–291
   PubMedGoogle Scholar
• Kimura R. S. Hairs of the cochlear sensory cells and their attachment to the tectorial membrane. Acta Otolaryngol (Stockh) 1966; 61: 55–72
   PubMedGoogle Scholar
• Knowlton V. Correlation of the development of membranous and bony labyrinths, acoustic ganglia, nerves and brain centers of the chick embryo. J Morph 1967; 121: 179–208
   Web of Science ®Google Scholar
• Kolmer W. Gehörorgan. Handbuch der mikroskopischen Anatomie des Menschen, W. v. Möllendorff. Springer-Verlag, Berlin 1927; 250–478
   Google Scholar
• Kronester-Frei A. Licht- und elektronenmikroskopische Untersuchung der Lagebeziehung der Membrana tectoria zum Cortische Organ in Abhängigkeit von Entwicklungszustand, Fixation und lonenmilieu. Dissertation, Lehrstuhl für Electroakustik der Technischen Universität München. 1977; 1–191
   Google Scholar
• Lewis E. R., Li C. W. Evidence concerning the morphogenesis of saccular receptors in the bullfrog (Rana catesbeiana). J Morph 1973; 139: 351–361
   PubMed Web of Science ®Google Scholar
• Li C. W., McPhee J. Influences on the coiling of the cochlea. Ann Otol Rhinol Laryngol 1979; 88: 280–287
   PubMed Web of Science ®Google Scholar
• Li C. W., Ruben R. J. Further study of the surface morphology of the embryonic mouse cochlear sensory epithelia. Otolaryngol Head Neck Surg 1979; 87: 479–485
   PubMed Web of Science ®Google Scholar
• Lim D. J. Fine morphology of the tectorial membrane: Its relationship to the organ of Corti. Arch Otolaryngol 1972; 96: 199–215
   PubMedGoogle Scholar
• Lim D. J. Fine morphology of the cupula: A scanning electron microscopic observation. Proc. 5th extraordinary meeting of the Bárány Society, M. Morimoto. Bäräny Society, Kyoto 1975; 390–398
   Google Scholar
• Lim D. J. Morphological and physiological correlates in cochlear and vestibular sensory epithelia. Scanning Electron Microscopy 1976a; V: 269–276
   Google Scholar
• Lim D. J. Techniques and application of scanning electron microscopy in otology. Handbook of auditory and vestibular research methods, C. A. Smith, J. D. Vernon. Charles C. Thomas, Springfield, Ill. 1976b; 92–126
   Google Scholar
• Lim D. J. Fine morphology of the tectorial membrane: Fresh and developmental. INSERM Symp (Inner Ear Biology) 1977a; 68: 47–60
   Google Scholar
• Lim D. J. Ultra anatomy of sensory end-organs in the labyrinth and their functional implications. Proceedings of the Shambaugh 5th international workshop on middle ear microsurgery & fluctuant hearing loss, G. E. Shambaugh, Jr, J. J. Shea. Strode Publishers, Inc., Huntsville, Ala. 1977b; 16–27
   Google Scholar
• Lim D. J. Fine morphology of the otoconial membrane and its relationship to the sensory epithelium. Scanning Electron Microscopy 1979; 111: 929–938
   Google Scholar
• Lim D. J., Dunn D. E. Anatomic correlates of noise induced hearing loss. Otolaryngol Clin North Am 1979; 12: 493–513
   PubMed Web of Science ®Google Scholar
• Lim D. J. Cochlear anatomy related to cochlear micromechanics: A review. J Acoust Soc Am 1980; 67: 1686–1695
   PubMed Web of Science ®Google Scholar
• Lim D. J. The development and structure of the otoconia. Ultrastructural atlas of the inner ear, I. Friedmann, J. C. Ballantyne. Butterworths, London 1984; 245–269
   Google Scholar
• Lindeman H. H., Ades H. W., Bredberg G., Engström H. The sensory hairs and the tectorial membrane in the development of the cat's organ of Corti: A scanning electron microscopic study. Acta Otolaryngol (Stockh) 1971; 72: 229–242
   PubMed Web of Science ®Google Scholar
• Lindeman H. H., Ades H., West R. W. Scanning electron microscopy of the vestibular end organs. Proceedings 5th symposium on the vestibular organs in space exploration. NASA, Washington, D.C. 1973; 145–156
   Google Scholar
• Loe P. R., Tomko D. L., Werner G. The neural signal of angular head position in primary afferent vestibular nerve axons. J Physiol (London) 1973; 230: 29–50
   Google Scholar
• Loewenstein O. E. Comparative morphology and physiology. Handbook of sensory physiology, vol. VIII, Vestibular system part I: Basic mechanisms, H. H. Kornhuber. Springer-Verlag, Berlin 1974; 75–120
   Google Scholar
• Malik L. E., Wilson R. B. Evaluation of modified technique for SEM examination of vertebrate specimens without evaporated metal layers. Scanning Electron Microscopy 1975; 269–264
   Google Scholar
• Mikaelian D., Ruben R. J. Development of hearing in the normal CBA-J mouse: Correlation of physiological observation with behavioral responses and with cochlear anatomy. Acta Otolaryngol (Stockh) 1965; 69: 451–461
   Google Scholar
• Murakami T. A revised tannin-osmium method for non-coated scanning electron microscope specimens. Arch Histol Jap 1974; 36: 189–193
   PubMedGoogle Scholar
• Pearson A. A., Jacobsson A. D., Van Calcar R. J., Sauter R. W. The development of the ear. American Academy of Ophthalmology and Otolaryngology, Rochester, Minn. 1967
   Google Scholar
• Pujol R., Carlier E., Devigne C. Different patterns of cochlear innervation during the development of the kitten. J Comp Neurol 1978; 177: 529–536
   PubMed Web of Science ®Google Scholar
• Pujol R., Carlier E., Devigne C. Significance of presynaptic formations in early stages of cochlear synaptogenesis. Neurosci Lett 1979; 15: 97–102
   PubMed Web of Science ®Google Scholar
• Romand R. Development of the cochlea. Development of auditory and vestibular systems, R. Romand. Academic Press, New York 1983; 47–88
   Google Scholar
• Ross M. D., Pote K. G., Rarey K. E., Verma L. M. Microdisc gel electrophoresis in sodium dodecyl sulfate of organic material from rat otoconial complexes. Ann NY Acad Sci 1981; 374: 808–819
   PubMed Web of Science ®Google Scholar
• Ruben R. J. Development of the inner ear of the mouse: A radioautographic study of terminal mitoses. Acta Otolaryngol (Stockh) 1967, Suppl. 220: 1–44
   PubMedGoogle Scholar
• Salamat M. D., Ross M. D., Peacor D. R. Otoconial formation in the fetal rat. Ann Otol Rhinol Laryngol 1980; 89: 229–238
   PubMed Web of Science ®Google Scholar
• Sánchez-Fernández J. M., Rivera-Pomar J. M. A study of the development of utricular and saccular maculae in man and in rat. Am J Otolaryngol 1983; 5: 44–55
   Google Scholar
• Saunders J. C., Garfinkle T. J. Peripheral anatomy and physiology I. The auditory psychobiology of the mouse, J. F. Willott. Charles C. Thomas, Springfield, Ill. 1983; 131–168
   Google Scholar
• Shambaugh G. E. Über Bau und Funktion des Epithels im Sulcus spiralis externus. Arch Ohrenheilkd 1909; 58: 280–287
   Google Scholar
• Sher A. E. The embryonic and postnatal development of the inner ear of the mouse. Acta Otolaryngol (Stockh) 1971, Suppl. 285: 1–77
   Google Scholar
• Shnerson A., Pujol R. Age-related changes in the C57BL/6J mouse cochlea. I. Physiological findings. Dev Brain Res 1982; 2: 65–75
   Google Scholar
• Shnerson A., Devigne C., Pujol R. Age-related changes in the C57BL/6J mouse cochlea. II. Ultrastructural findings. Dev Brain Res 1982; 2: 77–88
   Google Scholar
• Shnerson A., Pujol R. Development: Anatomy, electrophysiology and behavior. The auditory psychobiology of the mouse, J. F. Willott. Charles C. Thomas, Springfield, Ill. 1983; 395–425
   Google Scholar
• Sobin A., Anniko M. Early development of cochlear hair cell stereociliary surface morphology. Arch Oto-Rhino-Laryngol 1984; 241: 53–64
   Google Scholar
• Spoendlin H. Primary neurons and synapses. Ultrastructural atlas of the inner ear, I. Friedmann, J. C. Ballantyne. Butterworths, London 1984; 133–164
   Google Scholar
• Steel K. P., Niaussat M. M., Bock G. R. The genetics of hearing. The auditory psychobiology of the mouse, J. F. Willott. Charles C. Thomas. 1983; 341–394
   Google Scholar
• Tanaka T. Frozen resin cracking method for scanning electron microscopy of biological materials. Naturwiss 1972; 59: 77–78
   PubMedGoogle Scholar
• Tanaka T., Ozeki Y., Aoki T., Ogura Y. Morphological relation of the vestibular sensory hairs to the otolithic membrane and the cupula—A scanning electron microscopic study. Proceedings 5th extraordinary meeting of the Bárány Society, M. Morimoto. Bárány Society, Kyoto 1975; 406–409
   Google Scholar
• Van De Water T. R., Anniko M., Nordemar H., Wersäll J. Embryonic development of the sensory cells in macula utriculae of mouse. INSERM Symp (Inner Ear Biology) 1977; 68: 25–36
   Google Scholar
• Van De Water T. R. The role of epithelio-mesenchymal interactions in development of the mammalian inner ear. Anat Rec 1980; 169: 194A
   Google Scholar
• Van De Water T. R., Li C. W., Ruben R. J., Shea C. A. Ontogenic aspects of mammalian inner ear development. Morphogenesis and malformation of the ear, R. J. Gorlin. Alan R. Liss, Inc., New York 1980; 5–45
   Google Scholar
• Watanuki K. Distribution pattern of the sensory cells in the vestibular otolithic organs. Otologia Fukuoka 1970; 16: 260–262
   Google Scholar
• Weibel E. R. Zur Kenntnis der Differenzierungsvorgánge im Epithel des Ductus cochlearis. Acta Anat (Basel) 1957; 29: 53–90
   PubMedGoogle Scholar
• Vidal J., Jeannerod M., Lifschitz W., Levitan H., Rosenberg J., Segundo K. P. Static and dynamic properties of gravity-sensitive receptors in the cat vestibular system. Kybernetic 1971; 9: 205–215
   PubMedGoogle Scholar
• Wersäll J. Studies on the structure and innervation of the sensory epithelium of the cristae ampullares in the guinea pig. Acta Otolaryngol (Stockh) 1956, Suppl. 126: 1–85
   Google Scholar
• Zajik G., Anniko M., Schacht J. Cellular localization of adenylate cyclase in the developing and mature inner ear of the mouse. Hearing Res 1983; 10: 249–281
   PubMed Web of Science ®Google Scholar