The role of the presynaptic scaffold protein Bassoon in synaptic transmission at the mouse endbulb of Held synapse
by Alejandro Mendoza Schulz
Date of Examination:2013-06-07
Date of issue:2013-06-20
Advisor:Prof. Dr. Tobias Moser
Referee:Prof. Dr. Tobias Moser
Referee:Prof. Dr. Erwin Neher
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Abstract
English
Endbulbs of Held are large calyceal presynaptic terminals of auditory nerve fibers driving bushy cells in the AVCN. These synapses transmit precisely timed auditory signals up to high frequencies that provide the basis for downstream computation of sound localization and for speech perception (Oertel, 1997, 2005). The underlying molecular mechanisms in these ultrafast processes are largely unknown. The presented study analyzed functional and structural changes upon genetic disruption of bassoon, a large presynaptic scaffold protein in the cytomatrix of the active zone by studying the partial deletion mutant Bsn∆Ex4/5 (Altrock et al., 2003). Piccolo expression at active zones was upregulated, and RIM2 and Munc13-1 remained present at mutant active zones. Endbulb terminal and active zones were normal in number; however, postsynaptic densities (PSDs) were enlarged and the vesicle number in close proximity to the presynaptic plasma membrane per µm PSD reduced. In in vitro electrophysiological experiments in auditory brainstem slices, bushy cell miniature EPSCs exhibited larger amplitudes with unchanged kinetics. By applying a minimal stimulation technique, the amplitude of evoked EPSCs recorded from bushy cells was found unaltered while EPSC kinetics was attenuated. Short-term depression in response to train stimulation was increased in the mutants; most pronounced at 100 Hz compared to 200 Hz and 333 Hz. These findings and a reduced rate of recovery after short-term depression suggest that the rate of vesicle replenishment is compromised in the absence of full-length bassoon. The size of the readily releasable pool of vesicles was reduced and release probability was increased as estimated with the method of cumulative EPSCs (Schneggenburger et al., 1999). In consequence, delayed/asynchronous release was increased in the mutant synapses during and after train stimulation. Even though synaptic depression was significantly stronger in mutant synapses, bushy cells compensated for the loss of input and fired with comparable reliability during high frequency stimulation. Auditory brainstem responses from bassoon mutants show synchronous activity from globular bushy cells (as indicated by almost normal wave 2) despite almost complete lack of synchronous activity in the auditory nerve (Khimich et al., 2005; Buran et al., 2010). Additionally to convergence that presumably contributes to this process, restoration of synchronous activity at the level of the AVCN is due to homeostatic plasticity in bushy cells encompassing increased intrinsic excitability and synaptic upscaling. This is manifest in increased mEPSC amplitudes and an enhanced response to depolarizing current injection in mutant bushy cells. In conclusion, the data reported here suggest that bassoon plays an important role in promoting vesicular replenishment and a large standing readily releasable pool. Moreover, bushy cells maintain reliability of transmission in a homeostatic fashion in response to partial auditory deprivation.
Keywords: Bassoon; endbulb of Held; vesicular replenishment; cytomatrix of the active zone; synaptic transmission