Early Postnatal Development of Spontaneous and Acoustically Evoked Discharge Activity of Principal Cells of the Medial Nucleus of the Trapezoid Body: An In Vivo Study in Mice

The calyx of Held synapse in the medial nucleus of the trapezoid body of the auditory brainstem has become an established in vitro model to study the development of fast glutamatergic transmission in the mammalian brain. However, we still lack in vivo data at this synapse on the maturation of spontaneous and sound-evoked discharge activity before and during the early phase of acoustically evoked signal processing (i.e., before and after hearing onset). Here we report in vivo single-unit recordings in mice from postnatal day 8 (P8) to P28 with a specific focus on developmental changes around hearing onset (P12). Data were obtained from two mouse strains commonly used in brain slice recordings: CBA/J and C57BL/6J. Spontaneous discharge rates progressively increased from P8 to P13, initially showing bursting patterns and large coefficients of variation (CVs), which changed to more continuous and random discharge activity accompanied by gradual decrease of CV around hearing onset. From P12 on, sound-evoked activity yielded phasic-tonic discharge patterns with discharge rates increasing up to P28. Response thresholds and shapes of tuning curves were adult-like by P14. A gradual shortening in response latencies was observed up to P18. The three-dimensional tonotopic organization of the medial nucleus of the trapezoid body yielded a high-to-low frequency gradient along the mediolateral and dorsoventral but not in the rostrocaudal axes. These data emphasize that models of signal transmission at the calyx of Held based on in vitro data have to take developmental changes in firing rates and response latencies up to the fourth postnatal week into account.

[1]  Philip X Joris,et al.  How Secure Is In Vivo Synaptic Transmission at the Calyx of Held? , 2008, The Journal of Neuroscience.

[2]  M. Malmierca,et al.  The medial nucleus of the trapezoid body: Comparative physiology , 2008, Neuroscience.

[3]  J. Jost,et al.  Dynamic coupling of excitatory and inhibitory responses in the medial nucleus of the trapezoid body , 2008, The European journal of neuroscience.

[4]  M. Malmierca,et al.  The medial nucleus of the trapezoid body in rat: spectral and temporal properties vary with anatomical location of the units , 2008, The European journal of neuroscience.

[5]  N. Tritsch,et al.  The origin of spontaneous activity in the developing auditory system , 2007, Nature.

[6]  W. O'Neill,et al.  Age-Related Hearing Loss in C57BL/6J Mice has both Frequency-Specific and Non-Frequency-Specific Components that Produce a Hyperacusis-Like Exaggeration of the Acoustic Startle Reflex , 2007, Journal of the Association for Research in Otolaryngology.

[7]  Olga A. Stakhovskaya,et al.  Spontaneous discharge patterns in cochlear spiral ganglion cells before the onset of hearing in cats. , 2007, Journal of neurophysiology.

[8]  S. Oleskevich,et al.  The role of spontaneous activity in development of the endbulb of Held synapse , 2007, Hearing Research.

[9]  Corné J. Kros,et al.  How to build an inner hair cell: Challenges for regeneration , 2007, Hearing Research.

[10]  H. Taschenberger,et al.  The Role of Physiological Afferent Nerve Activity during In Vivo Maturation of the Calyx of Held Synapse , 2007, The Journal of Neuroscience.

[11]  B. Grothe,et al.  Synaptic transmission at the calyx of Held under in vivo like activity levels. , 2007, Journal of neurophysiology.

[12]  I. Forsythe,et al.  The calyx of Held , 2006, Cell and Tissue Research.

[13]  R. Snyder,et al.  Neonatal deafness results in degraded topographic specificity of auditory nerve projections to the cochlear nucleus in cats , 2006, The Journal of comparative neurology.

[14]  Brian K. Hoffpauir,et al.  Synaptogenesis of the Calyx of Held: Rapid Onset of Function and One-to-One Morphological Innervation , 2006, The Journal of Neuroscience.

[15]  B. Walmsley,et al.  Topographic organization in the auditory brainstem of juvenile mice is disrupted in congenital deafness , 2006, The Journal of physiology.

[16]  D. Sanes,et al.  Early appearance of inhibitory input to the MNTB supports binaural processing during development. , 2005, Journal of neurophysiology.

[17]  T. Yin,et al.  Interaural Phase and Level Difference Sensitivity in Low-Frequency Neurons in the Lateral Superior Olive , 2005, The Journal of Neuroscience.

[18]  Geng-Lin Li,et al.  Presynaptic Na+ Channels: Locus, Development, and Recovery from Inactivation at a High-Fidelity Synapse , 2005, The Journal of Neuroscience.

[19]  Marcus Müller,et al.  A physiological place–frequency map of the cochlea in the CBA/J mouse , 2005, Hearing Research.

[20]  M. Liberman,et al.  Response properties of single auditory nerve fibers in the mouse. , 2005, Journal of neurophysiology.

[21]  K. Henry Males lose hearing earlier in mouse models of late-onset age-related hearing loss; females lose hearing earlier in mouse models of early-onset hearing loss , 2004, Hearing Research.

[22]  R. Rübsamen,et al.  Ontogenesis of auditory fovea representation in the inferior colliculus of the Sri Lankan rufous horseshoe bat, Rhinolophus rouxi , 1990, Journal of Comparative Physiology A.

[23]  J. Willott,et al.  Development of inferior colliculus response properties in C57BL/6J mouse pups , 1979, Experimental Brain Research.

[24]  D. K. Morest,et al.  The growth of synaptic endings in the mammalian brain: A study of the calyces of the trapezoid body , 1968, Zeitschrift für Anatomie und Entwicklungsgeschichte.

[25]  E. Friauf,et al.  Principal cells of the rat medial nucleus of the trapezoid body: an intracellular in vivo study of their physiology and morphology , 2004, Experimental Brain Research.

[26]  R. Rübsamen,et al.  Decreased Temporal Precision of Auditory Signaling in Kcna1-Null Mice: An Electrophysiological Study In Vivo , 2003, The Journal of Neuroscience.

[27]  Stuart L. Johnson,et al.  Developmental changes in the expression of potassium currents of embryonic, neonatal and mature mouse inner hair cells , 2003, The Journal of physiology.

[28]  D. Tollin The Lateral Superior Olive: A Functional Role in Sound Source Localization , 2003, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[29]  R. Rübsamen,et al.  The Medial Nucleus of the Trapezoid Body in the Gerbil Is More Than a Relay: Comparison of Pre- and Postsynaptic Activity , 2003, Journal of the Association for Research in Otolaryngology.

[30]  Edward H. Overstreet,et al.  Passive basilar membrane vibrations in gerbil neonates: mechanical bases of cochlear maturation , 2002, The Journal of physiology.

[31]  Lu-Yang Wang,et al.  Developmental profiles of glutamate receptors and synaptic transmission at a single synapse in the mouse auditory brainstem , 2002, The Journal of physiology.

[32]  Paul A. Fuchs,et al.  Transmitter release at the hair cell ribbon synapse , 2002, Nature Neuroscience.

[33]  J. Borst,et al.  Short-term plasticity at the calyx of held , 2002, Nature Reviews Neuroscience.

[34]  Richard R. Fay,et al.  Integrative Functions in the Mammalian Auditory Pathway , 2002, Springer Handbook of Auditory Research.

[35]  Tom C. T. Yin,et al.  Neural Mechanisms of Encoding Binaural Localization Cues in the Auditory Brainstem , 2002 .

[36]  T. Jones,et al.  Primordial Rhythmic Bursting in Embryonic Cochlear Ganglion Cells , 2001, The Journal of Neuroscience.

[37]  A. Burkitt,et al.  Temporal processing from the auditory nerve to the medial nucleus of the trapezoid body in the rat , 2001, Hearing Research.

[38]  S. Iwasaki,et al.  Developmental regulation of transmitter release at the calyx of Held in rat auditory brainstem , 2001, The Journal of physiology.

[39]  G. Ehret,et al.  Frequency response areas of neurons in the mouse inferior colliculus. I. Threshold and tuning characteristics , 2001, Experimental Brain Research.

[40]  Y. Yoshikawa,et al.  Mitosis and apoptosis in postnatal auditory system of the C3H/He strain 1 1 Published on the World Wide Web on 9 April 2001. , 2001, Brain Research.

[41]  K. Futai,et al.  High-Fidelity Transmission Acquired via a Developmental Decrease in NMDA Receptor Expression at an Auditory Synapse , 2001, The Journal of Neuroscience.

[42]  H. von Gersdorff,et al.  Fine-Tuning an Auditory Synapse for Speed and Fidelity: Developmental Changes in Presynaptic Waveform, EPSC Kinetics, and Synaptic Plasticity , 2000, The Journal of Neuroscience.

[43]  T. Jones,et al.  Spontaneous activity in the statoacoustic ganglion of the chicken embryo. , 2000, Journal of neurophysiology.

[44]  J. Ruppersberg,et al.  Expression of a potassium current in inner hair cells during development of hearing in mice , 1998, Nature.

[45]  T. Yin,et al.  Anatomy and physiology of principal cells of the medial nucleus of the trapezoid body (MNTB) of the cat. , 1998, Journal of neurophysiology.

[46]  S. Iwasaki,et al.  Developmental changes in calcium channel types mediating synaptic transmission in rat auditory brainstem , 1998, The Journal of physiology.

[47]  M. Semple,et al.  Development of ventral cochlear nucleus projections to the superior olivary complex in gerbil , 1995, The Journal of comparative neurology.

[48]  M. Semple,et al.  Development of ectopic projections from the ventral cochlear nucleus to the superior olivary complex induced by neonatal ablation of the contralateral cochlea , 1995, The Journal of comparative neurology.

[49]  P. Dallos,et al.  First appearance and development of electromotility in neonatal gerbil outer hair cells , 1994, Hearing Research.

[50]  W. Lippe,et al.  Rhythmic spontaneous activity in the developing avian auditory system , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[51]  R F Mark,et al.  Patterned neural activity in brain stem auditory areas of a prehearing mammal, the tammar wallaby (Macropus eugenii). , 1994, Neuroreport.

[52]  J. Kaltenbach,et al.  Postnatal development of the hamster coclea. I. Growth of hair cells and the organ of Corti , 1994, The Journal of comparative neurology.

[53]  H. Sohmer,et al.  Development of hearing in neonatal rats: Air and bone conducted ABR thresholds , 1993, Hearing Research.

[54]  E. Friauf,et al.  Pre‐ and postnatal development of efferent connections of the cochlear nucleus in the rat , 1993, The Journal of comparative neurology.

[55]  E. Friauf Tonotopic Order in the Adult and Developing Auditory System of the Rat as Shown by c‐fos Immunocytochemistry , 1992, The European journal of neuroscience.

[56]  Philip H Smith,et al.  Projections of physiologically characterized globular bushy cell axons from the cochlear nucleus of the cat , 1991, The Journal of comparative neurology.

[57]  E Borg,et al.  Age-related loss of auditory sensitivity in two mouse genotypes. , 1991, Acta oto-laryngologica.

[58]  J. Guinan,et al.  Signal processing in brainstem auditory neurons which receive giant endings (calyces of Held) in the medial nucleus of the trapezoid body of the cat , 1990, Hearing Research.

[59]  G. Spirou,et al.  Recordings from cat trapezoid body and HRP labeling of globular bushy cell axons. , 1990, Journal of neurophysiology.

[60]  J. McGee,et al.  Rhythmic discharge properties of caudal cochlear nucleus neurons during postnatal development in cats , 1988, Hearing Research.

[61]  A. Ryan,et al.  Contributions of the middle ear to the development of function in the cochlea , 1988, Hearing Research.

[62]  W. Shofner,et al.  Regularity and latency of units in ventral cochlear nucleus: implications for unit classification and generation of response properties. , 1988, Journal of neurophysiology.

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

[64]  W. S. Rhode,et al.  Characterization of HRP‐labeled globular bushy cells in the cat anteroventral cochlear nucleus , 1987, The Journal of comparative neurology.

[65]  W. A. Cooper,et al.  Development of auditory brainstem response to tone pip stimuli in the rat. , 1987, Brain research.

[66]  B. Ryals,et al.  Development of the Place Principle , 1984, The Journal of the Acoustical Society of America.

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

[68]  A. J. Moffat,et al.  Noise masking of tone responses and critical ratios in single units of the mouse cochlear nerve and cochlear nucleus , 1984, Hearing Research.

[69]  J. Saunders,et al.  Auditory development in the mouse: Structural maturation of the middle ear , 1983, Journal of morphology.

[70]  K R Henry,et al.  Genotypic differences in behavioral, physiological and anatomical expressions of age-related hearing loss in the laboratory mouse. , 1980, Audiology.

[71]  D. Mikaelian Development and degeneration of hearing in the c57/b16 mouse: Relation of electrophysiologic responses from the round window and cochlear nucleus to cochlear anatomy and behavioral responses , 1979, The Laryngoscope.

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

[73]  C. Schneck,et al.  Development of cochlear function in the neonate Mongolian gerbil (Meriones unguiculatus). , 1972, Journal of comparative and physiological psychology.

[74]  N. Kiang,et al.  Spontaneous Activity In The Eighth Cranial Nerve of The Cat , 1972 .

[75]  J. Guinan,et al.  Single Auditory Units in the Superior Olivary Complex: II: Locations of Unit Categories and Tonotopic Organization , 1972 .

[76]  C. Berlin HEARING IN MICE VIA GSR AUDIOMETRY. , 1963, Journal of speech and hearing research.