Postnatal refinement of auditory nerve projections to the cochlear nucleus in cats

Studies of visual system development have suggested that competition driven by activity is essential for refinement of initial topographically diffuse neuronal projections into their precise adult patterns. This has led to the assertion that this process may shape development of topographic connections throughout the nervous system. Because the cat auditory system is very immature at birth, with auditory nerve neurons initially exhibiting very low or no spontaneous activity, we hypothesized that the auditory nerve fibers might initially form topographically broad projections within the cochlear nuclei (CN), which later would become topographically precise at the time when adult‐like frequency selectivity develops. In this study, we made restricted injections of Neurobiotin, which labeled small sectors (300–500 μm) of the cochlear spiral ganglion, to study the projections of auditory nerve fibers representing a narrow band of frequencies. Results showed that projections from the basal cochlea to the CN are tonotopically organized in neonates, many days before the onset of functional hearing and even prior to the development of spontaneous activity in the auditory nerve. However, results also demonstrated that significant refinement of the topographic specificity of the primary afferent axons of the auditory nerve occurs in late gestation or early postnatal development. Projections to all three subdivisions of the CN exhibit clear tonotopic organization at or before birth, but the topographic restriction of fibers into frequency band laminae is significantly less precise in perinatal kittens than in adult cats. Two injections spaced ≥2 mm apart in the cochlea resulted in labeled bands of projecting axons in the anteroventral CN that were 53% broader than would be expected if they were proportional to those in adults, and the two projections were incompletely segregated in the youngest animals studied. Posteroventral CN (PVCN) projections (normalized for CN size) were 36% broader in neonates than in adults, and projections from double injections in the youngest subjects were nearly fused in the PVCN. Projections to the dorsal division of the CN were 32% broader in neonates than in adults when normalized, but the dorsal CN projections were always discrete, even at the earliest ages studied. J. Comp. Neurol. 448:6–27, 2002. © 2002 Wiley‐Liss, Inc.

[1]  R. Romand,et al.  Myelination kinetics of spiral ganglion cells in kitten , 1982, The Journal of comparative neurology.

[2]  JoAnn McGee,et al.  Long-Term Effects of Sectioning the Olivocochlear Bundle in Neonatal Cats , 1998, The Journal of Neuroscience.

[3]  Larsen Sa,et al.  Postnatal maturation of the cat cochlear nuclear complex. , 1984 .

[4]  P. Dallos,et al.  Developmental alterations in the frequency map of the mammalian cochlea , 1989, Nature.

[5]  K K Osen,et al.  Cytoarchitecture of the cochlear nuclei in the cat , 1969 .

[6]  E. Rouiller,et al.  The central projections of intracellularly labeled auditory nerve fibers in cats: an analysis of terminal morphology. , 1986, The Journal of comparative neurology.

[7]  R. Pujol,et al.  Cochlear receptor development in the rat with emphasis on synaptogenesis , 2004, Anatomy and Embryology.

[8]  G. Flottorp,et al.  A comparative study of the development of hearing and vision in various species commonly used in experiments. , 1974, Acta oto-laryngologica.

[9]  Charles J. Limb,et al.  Development of Primary Axosomatic Endings in the Anteroventral Cochlear Nucleus of Mice , 2000, Journal of the Association for Research in Otolaryngology.

[10]  D. C. Teas,et al.  Postnatal development of physiological responses in auditory nerve fibers. , 1985, The Journal of the Acoustical Society of America.

[11]  R. Snyder,et al.  Topographic organization of the central projections of the spiral ganglion in cats , 1989, The Journal of comparative neurology.

[12]  D. K. Morest,et al.  The neuronal architecture of the cochlear nucleus of the cat , 1974, The Journal of comparative neurology.

[13]  L. Maffei,et al.  Correlation in the discharges of neighboring rat retinal ganglion cells during prenatal life. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[14]  M. Constantine-Paton,et al.  Patterned activity, synaptic convergence, and the NMDA receptor in developing visual pathways. , 1990, Annual review of neuroscience.

[15]  L. Schweitzer,et al.  Morphology of HRP-labelled cochlear nerve axons in the dorsal cochlear nucleus of the developing hamster , 1992, Hearing Research.

[16]  Russell L. Martin,et al.  The development of frequency representation in the inferior colliculus of the kitten , 1991, Hearing Research.

[17]  R. Romand Functional properties of auditory-nerve fibers during postnatal development in the kitten , 2004, Experimental Brain Research.

[18]  L. C. Katz,et al.  Development of ocular dominance columns in the absence of retinal input , 1999, Nature Neuroscience.

[19]  T. Parks,et al.  Functional synapse elimination in the developing avian cochlear nucleus with simultaneous reduction in cochlear nerve axon branching , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[20]  C. Devigne,et al.  Different patterns of cochlear innervation during the development of the kitten , 1978, The Journal of comparative neurology.

[21]  E. Rubel Ontogeny of Structure and Function in the Vertebrate Auditory System , 1978 .

[22]  C. Shatz Impulse activity and the patterning of connections during cns development , 1990, Neuron.

[23]  L. Landmesser,et al.  Polysialic acid in the vertebrate nervous system: a promoter of plasticity in cell-cell interactions , 1996, Trends in Neurosciences.

[24]  M. Liberman The cochlear frequency map for the cat: labeling auditory-nerve fibers of known characteristic frequency. , 1982, The Journal of the Acoustical Society of America.

[25]  C. Shatz Emergence of order in visual system development , 1996, Journal of Physiology-Paris.

[26]  J. McGee,et al.  Paradoxical relationship between frequency selectivity and threshold sensitivity during auditory-nerve fiber development. , 1998, The Journal of the Acoustical Society of America.

[27]  Russell L. Snyder,et al.  Quantitative analysis of spiral ganglion projections to the cat cochlear nucleus , 1997, The Journal of comparative neurology.

[28]  M P Stryker,et al.  Emergence of ocular dominance columns in cat visual cortex by 2 weeks of age , 2001, The Journal of comparative neurology.

[29]  Directional responses by kittens to an auditory stimulus. , 1978, Developmental psychobiology.

[30]  D. K. Morest,et al.  The neuronal architecture of the anteroventral cochlear nucleus of the cat in the region of the cochlear nerve root: Electron microscopy , 1982, Neuroscience.

[31]  D. O'Leary,et al.  Development of topographic order in the mammalian retinocollicular projection , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  L. Maffei,et al.  The action of neurotrophins in the development and plasticity of the visual cortex , 1996, Progress in Neurobiology.

[33]  A. Ryan,et al.  Development of tonotopic representation in the Mongolian gerbil: a 2-deoxyglucose study. , 1988, Brain research.

[34]  C. Shatz,et al.  Prenatal development of retinal ganglion cell axons: segregation into eye-specific layers within the cat's lateral geniculate nucleus , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  V. Montero,et al.  Abnormalities of the cortico‐geniculate pathway in siamese cats , 1978, The Journal of comparative neurology.

[36]  J. McGee,et al.  Postnatal development of auditory nerve and cochlear nucleus neuronal responses in kittens , 1987, Hearing Research.

[37]  Mriganka Sur,et al.  Development of X- and Y-cell retinogeniculate terminations in kittens , 1984, Nature.

[38]  Bradley L. Schlaggar,et al.  Postsynaptic control of plasticity in developing somatosensory cortex , 1993, Nature.

[39]  Terrance Raymond Bourk,et al.  Electrical responses of neural units in the anteroventral cochlear nucleus of the cat , 1976 .

[40]  R. Pujol,et al.  Postnatal maturation in the cochlea of the cat , 1970, The Journal of comparative neurology.

[41]  C. Shatz,et al.  Axon trajectories and pattern of terminal arborization during the prenatal development of the cat's retinogeniculate pathway , 1987, The Journal of comparative neurology.

[42]  B. Norris,et al.  Tonotopic organization of the anteroventral cochlear nucleus of the cat , 1981, Hearing Research.

[43]  P Dallos,et al.  Ontogenetic changes in frequency mapping of a mammalian ear. , 1984, Science.

[44]  S. Larsen Postnatal maturation of the cat cochlear nuclear complex. , 1984, Acta oto-laryngologica. Supplementum.

[45]  J. McGee,et al.  Frequency selectivity in the auditory periphery: similarities between damaged and developing ears. , 1990, American journal of otolaryngology.

[46]  W. S. Rhode,et al.  Physiological study of neurons in the dorsal and posteroventral cochlear nucleus of the unanesthetized cat. , 1987, Journal of neurophysiology.

[47]  J. Fawcett,et al.  Regressive events in neurogenesis. , 1984, Science.

[48]  Russell L. Snyder,et al.  Topography of spiral ganglion projections to cochlear nucleus during postnatal development in cats , 1997, The Journal of comparative neurology.

[49]  Alexander Joseph Book reviewDischarge patterns of single fibers in the cat's auditory nerve: Nelson Yuan-Sheng Kiang, with the assistance of Takeshi Watanabe, Eleanor C. Thomas and Louise F. Clark: Research Monograph no. 35. Cambridge, Mass., The M.I.T. Press, 1965 , 1967 .

[50]  Bernd Fritzsch,et al.  Auditory system development: primary auditory neurons and their targets. , 2002, Annual review of neuroscience.

[51]  P. Dallos,et al.  Ontogenic changes in cochlear characteristic frequency at a basal turn location as reflected in the summating potential , 1985, Hearing Research.

[52]  M. Merzenich,et al.  Topographic organization of the cochlear spiral ganglion demonstrated by restricted lesions of the anteroventral cochlear nucleus , 1992, The Journal of comparative neurology.

[53]  S. Echteler,et al.  Development of ganglion cell topography in the postnatal cochlea , 2000, The Journal of comparative neurology.

[54]  C. Devigne,et al.  Age-related changes in the C57BL/6J mouse cochlea. II. Ultrastructural findings. , 1981, Brain research.

[55]  V S Caviness,et al.  Postnatal changes in arborization patterns of murine retinocollicular axons , 1986, The Journal of comparative neurology.

[56]  I. Whitfield Discharge Patterns of Single Fibers in the Cat's Auditory Nerve , 1966 .

[57]  K. Osen Course and termination of the primary afferents in the cochlear nuclei of the cat. An experimental anatomical study. , 1970, Archives italiennes de biologie.

[58]  R. Pujol Development of tone-burst responses along the auditory pathway in the cat. , 1972, Acta oto-laryngologica.

[59]  D. Ryugo,et al.  Morphology of primary axosomatic endings in the anteroventral cochlear nucleus of the cat: A study of the endbulbs of Held , 1982, The Journal of comparative neurology.

[60]  J. Villablanca,et al.  Development of behavioral audition in the kitten , 1980, Physiology & Behavior.

[61]  J. Puel,et al.  Development of 2ƒ1−ƒ2 otoacoustic emissions in the rat , 1987, Hearing Research.

[62]  B. Lonsbury-Martin,et al.  Postnatal development of 2ƒ1−ƒ2 otoacoustic emissions in pigmented rat , 1990, Hearing Research.

[63]  M. Constantine-Paton,et al.  N-methyl-D-aspartate receptor antagonists disrupt the formation of a mammalian neural map. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[64]  B. Schlaggar,et al.  Early development of the somatotopic map and barrel patterning in rat somatosensory cortex , 1994, The Journal of comparative neurology.

[65]  L. C. Katz,et al.  Early development of ocular dominance columns. , 2000, Science.

[66]  E. Keithley,et al.  Frequency map of the spiral ganglion in the cat. , 1987, The Journal of the Acoustical Society of America.

[67]  C. Shatz,et al.  Transient period of correlated bursting activity during development of the mammalian retina , 1993, Neuron.

[68]  E. Rubel Ontogeny of auditory system function. , 1984, Annual review of physiology.

[69]  C. Shatz,et al.  Developmental mechanisms that generate precise patterns of neuronal connectivity , 1993, Cell.

[70]  S. Easter,et al.  The changing view of neural specificity. , 1985, Science.

[71]  R. Reale,et al.  Sensitivity of auditory cortical neurons of kittens to monaural and binaural high frequency sound , 1988, Hearing Research.

[72]  S. Levay,et al.  Ocular dominance columns and their development in layer IV of the cat's visual cortex: A quantitative study , 1978, The Journal of comparative neurology.

[73]  D. D. Greenwood Critical Bandwidth in Man and Some Other Species in Relation to the Traveling Wave Envelope , 1974 .

[74]  P. Leake,et al.  Postnatal development of the organ of Corti in cats: a light microscopic morphometric study , 1999, Hearing Research.

[75]  E. Rouiller,et al.  The central projections of intracellularly labeled auditory nerve fibers in cats , 1984, The Journal of comparative neurology.

[76]  F. Werblin,et al.  Requirement for Cholinergic Synaptic Transmission in the Propagation of Spontaneous Retinal Waves , 1996, Science.

[77]  N. Woolf,et al.  Functional ontogeny in the central auditory pathway of the mongolian gerbil , 2004, Experimental Brain Research.

[78]  J. Altman,et al.  Development of the brain stem in the rat. III. Thymidine‐radiographic study of the time of origin of neurons of the vestibular and auditory nuclei of the upper medulla , 1980, The Journal of comparative neurology.

[79]  David G Wilkinson,et al.  Eph receptors and ephrins in neural development , 1999, Current Opinion in Neurobiology.

[80]  G. Ehret,et al.  Postnatal development of absolute auditory thresholds in kittens. , 1981, Journal of comparative and physiological psychology.

[81]  E. Rubel,et al.  Embryogenesis of arborization pattern and topography of individual axons in N. Laminaris of the chicken brain stem , 1986, The Journal of comparative neurology.