Fenestration of the calyx of held occurs sequentially along the tonotopic axis, is influenced by afferent activity, and facilitates glutamate clearance

The calyx of Held is a type of giant glutamatergic presynaptic terminal in the mammalian auditory brainstem that transmits afferent information from the cochlear nucleus to the medial nucleus of the trapezoid body (MNTB). It participates in sound localization, a process that requires very high temporal precision. Consistent with its functional role, the calyx shows a number of specializations for temporal fidelity, one of them being the giant terminal itself with its many release sites. During the first 3 weeks of postnatal development, the calyx transforms from a spoon‐shaped, closed morphology to a highly fenestrated open structure. Calyces in Mongolian gerbils (Meriones unguiculatus) were labeled via injection of fluorescent tracers and their morphology was reconstructed at various timepoints during early postnatal development. We show that the fenestration process does not occur simultaneously in all calyces. Calyces transmitting high‐frequency sound information fenestrate significantly earlier than those transmitting low‐frequency information, such that a temporary developmental gradient along the tonotopic axis is established around the time of hearing onset. Animals that were deprived of afferent activity before hearing onset, either via cochlear removal or administration of ototoxic drugs, do not show this developmental gradient. Glial processes containing glutamate transporters occupy the newly created windows in the calyx and thus could augment the fast clearance of neurotransmitter. The physiological consequences of this faster clearance include a faster decay time course of synaptic currents as well as a lower amount of residual current accumulating during the processing of repeated activity such as stimulus trains. J. Comp. Neurol. 514:92–106, 2009. © 2009 Wiley‐Liss, Inc.

[1]  B. Grothe,et al.  Interaural Time Difference Processing in the Mammalian Medial Superior Olive: The Role of Glycinergic Inhibition , 2008, The Journal of Neuroscience.

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

[3]  J. Borst,et al.  Dynamic development of the calyx of Held synapse , 2008, Proceedings of the National Academy of Sciences.

[4]  B. Walmsley,et al.  Maturation of auditory brainstem projections and calyces in the congenitally deaf (dn/dn) mouse , 2008, The Journal of comparative neurology.

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

[6]  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.

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

[8]  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.

[9]  J. Borst,et al.  Branching of calyceal afferents during postnatal development in the rat auditory brainstem , 2006, The Journal of comparative neurology.

[10]  V. Wimmer,et al.  Donut-Like Topology of Synaptic Vesicles with a Central Cluster of Mitochondria Wrapped into Membrane Protrusions: A Novel Structure–Function Module of the Adult Calyx of Held , 2006, The Journal of Neuroscience.

[11]  B. Walmsley,et al.  Development of a robust central auditory synapse in congenital deafness. , 2005, Journal of neurophysiology.

[12]  E. Neher,et al.  Release kinetics, quantal parameters and their modulation during short‐term depression at a developing synapse in the rat CNS , 2005, The Journal of physiology.

[13]  R. Duvoisin,et al.  Glutamate Transporter Studies Reveal the Pruning of Metabotropic Glutamate Receptors and Absence of AMPA Receptor Desensitization at Mature Calyx of Held Synapses , 2005, The Journal of Neuroscience.

[14]  P. Colditz,et al.  Glial glutamate transporter expression patterns in brains from multiple mammalian species , 2005, Glia.

[15]  G. Awatramani,et al.  Staggered development of GABAergic and glycinergic transmission in the MNTB. , 2005, Journal of neurophysiology.

[16]  E. Rubel,et al.  Avian superior olivary nucleus provides divergent inhibitory input to parallel auditory pathways , 2005, The Journal of comparative neurology.

[17]  G. Awatramani,et al.  Inhibitory Control at a Synaptic Relay , 2004, The Journal of Neuroscience.

[18]  I. Russell,et al.  The Development of a Single Frequency Place in the Mammalian Cochlea: The Cochlear Resonance in the Mustached Bat Pteronotus parnellii , 2003, The Journal of Neuroscience.

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

[20]  M. Vater,et al.  Postnatal development of cochlear function in the mustached bat, Pteronotus parnellii. , 2003, Journal of neurophysiology.

[21]  B. Grothe,et al.  New roles for synaptic inhibition in sound localization , 2003, Nature Reviews Neuroscience.

[22]  Adrian Y. C. Wong,et al.  Distinguishing between Presynaptic and Postsynaptic Mechanisms of Short-Term Depression during Action Potential Trains , 2003, The Journal of Neuroscience.

[23]  B. Sakmann,et al.  Local routes revisited: the space and time dependence of the Ca2+ signal for phasic transmitter release at the rat calyx of Held. , 2003, The Journal of physiology.

[24]  G. Spirou,et al.  Optimizing Synaptic Architecture and Efficiency for High-Frequency Transmission , 2002, Neuron.

[25]  Bert Sakmann,et al.  Three-Dimensional Reconstruction of a Calyx of Held and Its Postsynaptic Principal Neuron in the Medial Nucleus of the Trapezoid Body , 2002, The Journal of Neuroscience.

[26]  Dan H Sanes,et al.  The effect of bilateral deafness on excitatory and inhibitory synaptic strength in the inferior colliculus , 2002, The European journal of neuroscience.

[27]  B. Grothe,et al.  Precise inhibition is essential for microsecond interaural time difference coding , 2002, Nature.

[28]  E. Neher,et al.  Separation of Presynaptic and Postsynaptic Contributions to Depression by Covariance Analysis of Successive EPSCs at the Calyx of Held Synapse , 2002, The Journal of Neuroscience.

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

[30]  T. Ishikawa,et al.  Mechanisms underlying presynaptic facilitatory effect of cyclothiazide at the calyx of Held of juvenile rats , 2001, The Journal of physiology.

[31]  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.

[32]  J. Rho,et al.  Evidence of altered inhibition in layer V pyramidal neurons from neocortex of Kcna1-null mice , 2001, Neuroscience.

[33]  E. Neher,et al.  Quantitative Relationship between Transmitter Release and Calcium Current at the Calyx of Held Synapse , 2001, The Journal of Neuroscience.

[34]  E. Neher,et al.  Combining Deconvolution and Noise Analysis for the Estimation of Transmitter Release Rates at the Calyx of Held , 2001, The Journal of Neuroscience.

[35]  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.

[36]  G. Spirou,et al.  Specialized Synapse-Associated Structures within the Calyx of Held , 2000, The Journal of Neuroscience.

[37]  A. Ryan,et al.  Effects of stimulus frequency and intensity on c‐fos mRNA expression in the adult rat auditory brainstem , 1999, The Journal of comparative neurology.

[38]  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.

[39]  A. Forge,et al.  Postnatal maturation of the organ of Corti in gerbils: Morphology and physiological responses , 1997, The Journal of comparative neurology.

[40]  Laurence O Trussell,et al.  Cellular mechanisms for preservation of timing in central auditory pathways , 1997, Current Opinion in Neurobiology.

[41]  A. Schousboe,et al.  High affinity glutamate transporters: regulation of expression and activity. , 1997, Molecular pharmacology.

[42]  D R Moore,et al.  Susceptibility of developing cochlear nucleus neurons to deafferentation‐induced death abruptly ends just before the onset of hearing , 1997, The Journal of comparative neurology.

[43]  A. Forge,et al.  Postnatal development of membrane specialisations of gerbil outer hair cells , 1995, Hearing Research.

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

[45]  D R Moore,et al.  Afferent reorganisation within the superior olivary complex of the gerbil: Development and induction by neonatal, unilateral cochlear removal , 1995, The Journal of comparative neurology.

[46]  L H Carney,et al.  Enhancement of neural synchronization in the anteroventral cochlear nucleus. I. Responses to tones at the characteristic frequency. , 1994, Journal of neurophysiology.

[47]  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.

[48]  I. Forsythe,et al.  The binaural auditory pathway: excitatory amino acid receptors mediate dual timecourse excitatory postsynaptic currents in the rat medial nucleus of the trapezoid body , 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

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

[50]  P. H. Smith,et al.  Intracellular recordings from neurobiotin-labeled cells in brain slices of the rat medial nucleus of the trapezoid body , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[51]  J. Zook,et al.  Afferents to the medial nucleus of the trapezoid body and their collateral projections , 1991, The Journal of comparative neurology.

[52]  J. Zook,et al.  Classification of the principal cells of the medial nucleus of the trapezoid body , 1991, The Journal of comparative neurology.

[53]  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.

[54]  P. van de Heyning,et al.  Aminoglycoside-induced ototoxicity. , 1990, Toxicology letters.

[55]  R. Helfert,et al.  Immunocytochemical and lesion studies support the hypothesis that the projection from the medial nucleus of the trapezoid body to the lateral superior olive is glycinergic , 1990, Brain Research.

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

[57]  H. Heffner,et al.  Sound localization and use of binaural cues by the gerbil (Meriones unguiculatus). , 1988, Behavioral neuroscience.

[58]  C. K. Henkel,et al.  The projections of principal cells of the medial nucleus of the trapezoid body in the cat , 1985, The Journal of comparative neurology.

[59]  R. Kelly,et al.  Identification of a transmembrane glycoprotein specific for secretory vesicles of neural and endocrine cells , 1985, The Journal of cell biology.

[60]  A. Ryan,et al.  The development of auditory function in the cochlea of the mongolian gerbil , 1984, Hearing Research.

[61]  D. Caspary,et al.  Strychnine blocks binaural inhibition in lateral superior olivary neurons , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[62]  J. T. Hackett,et al.  Organization and development of brain stem auditory nuclei in the chick: Ontogeny of postsynaptic responses , 1982, The Journal of comparative neurology.

[63]  J. T. Hackett,et al.  Synaptic excitation of the second and third order auditory neurons in the avian brain stem , 1982, Neuroscience.

[64]  J. Goldberg,et al.  Response of binaural neurons of dog superior olivary complex to dichotic tonal stimuli: some physiological mechanisms of sound localization. , 1969, Journal of neurophysiology.

[65]  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.

[66]  D. K. Morest,et al.  The collateral system of the medial nucleus of the trapezoid body of the cat, its neuronal architecture and relation to the olivo-cochlear bundle. , 1968, Brain research.

[67]  W. Warr Fiber degeneration following lesions in the anterior ventral cochlear nucleus of the cat. , 1966, Experimental neurology.

[68]  Julie A. Harris,et al.  Development of spontaneous miniature EPSCs in mouse AVCN neurons during a critical period of afferent-dependent neuron survival. , 2007, Journal of neurophysiology.

[69]  泉川 雅彦 Auditory hair cell replacement and hearing improvement by Atoh1 gene therapy in deaf mammals , 2005 .

[70]  R. Klinke,et al.  Processing of binaural stimuli by cat superior olivary complex neurons , 2004, Experimental Brain Research.

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

[72]  D. Oertel The role of timing in the brain stem auditory nuclei of vertebrates. , 1999, Annual review of physiology.

[73]  L. Trussell,et al.  Synaptic mechanisms for coding timing in auditory neurons. , 1999, Annual review of physiology.

[74]  W. Warr Parallel Ascending Pathways from the Cochlear Nucleus: Neuroanatomical Evidence of Functional Specialization , 1995 .

[75]  R. Ruben Development of the inner ear of the mouse: a radioautographic study of terminal mitoses. , 1967, Acta oto-laryngologica.

[76]  Tomoyuki Takahashi,et al.  Cellular/molecular Mechanisms Underlying Developmental Speeding in Ampa-epsc Decay Time at the Calyx of Held , 2022 .