Abstract
Sound information is transduced into graded receptor potential by cochlear hair cells and encoded as discrete action potentials of auditory nerve fibers. In the cochlear nucleus, auditory nerve fibers convey this information through morphologically distinct synaptic terminals onto bushy cells (BCs) and stellate cells (SCs) for processing of different sound features. With expanding use of transgenic mouse models, it is increasingly important to understand the in vivo functional development of these neurons in mice. We characterized the maturation of spontaneous and acoustically evoked activity in BCs and SCs by acquiring single-unit juxtacellular recordings between hearing onset (P12) and young adulthood (P30) of anesthetized CBA/J mice. In both cell types, hearing sensitivity and characteristic frequency (CF) range are mostly adult-like by P14, consistent with rapid maturation of the auditory periphery. In BCs, however, some physiological features like maximal firing rate, dynamic range, temporal response properties, recovery from post-stimulus depression, first spike latency (FSL) and encoding of sinusoid amplitude modulation undergo further maturation up to P18. In SCs, the development of excitatory responses is even more prolonged, indicated by a gradual increase in spontaneous and maximum firing rates up to P30. In the same cell type, broadly tuned acoustically evoked inhibition is immediately effective at hearing onset, covering the low- and high-frequency flanks of the excitatory response area. Together, these data suggest that maturation of auditory processing in the parallel ascending BC and SC streams engages distinct mechanisms at the first central synapses that may differently depend on the early auditory experience.
Highlights
The auditory system decodes complex natural sounds by analyzing the frequency, amplitude and temporal information to master the tasks like sound source localization and discrimination of acoustic objects with extraordinary precision
Primary auditory nerve inputs make central synapses in the anteroventral cochlear nucleus onto the two principal neurons, bushy cells (BCs) and T-stellate cells. They contribute to processing in different auditory pathways: (i) BCs preserve the temporal structure of sound which is crucial for sound source localization in the superior olivary complex (Young et al, 1988; Joris et al, 1994); and (ii) SCs encode the dynamic amplitude profile of sound signals (Blackburn and Sachs, 1990; Frisina et al, 1990) and provide input to the contralateral inferior colliculus (Cant and Benson, 2003)
The present study investigates the functional maturation of BCs and SCs, the two principal neuron types in the AVCN that encode different sound features in segregated afferent brainstem pathways
Summary
The auditory system decodes complex natural sounds by analyzing the frequency, amplitude and temporal information to master the tasks like sound source localization and discrimination of acoustic objects with extraordinary precision. Primary auditory nerve inputs make central synapses in the anteroventral cochlear nucleus onto (among others) the two principal neurons, bushy cells (BCs) and T-stellate cells (further referred to as SCs) They contribute to processing in different auditory pathways: (i) BCs preserve the temporal structure of sound which is crucial for sound source localization in the superior olivary complex (Young et al, 1988; Joris et al, 1994); and (ii) SCs encode the dynamic amplitude profile of sound signals (Blackburn and Sachs, 1990; Frisina et al, 1990) and provide input to the contralateral inferior colliculus (Cant and Benson, 2003). Expanding the use of transgenic mice in auditory research increases the importance of revealing the developmental time course of auditory processing in the cochlear nucleus
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.