Synaptic boutons sizes are tuned to best fit their physiological performances

  • To truly appreciate the myriad of events which relate synaptic function and vesicle dynamics, simulations should be done in a spatially realistic environment. This holds true in particular in order to explain as well the rather astonishing motor patterns which we observed within in vivo recordings which underlie peristaltic contractionsas well as the shape of the EPSPs at different forms of long-term stimulation, presented both here, at a well characterized synapse, the neuromuscular junction (NMJ) of the Drosophila larva (c.f. Figure 1). To this end, we have employed a reductionist approach and generated three dimensional models of single presynaptic boutons at the Drosophila larval NMJ. Vesicle dynamics are described by diffusion-like partial differential equations which are solved numerically on unstructured grids using the uG platform. In our model we varied parameters such as bouton-size, vesicle output probability (Po), stimulation frequency and number of synapses, to observe how altering these parameters effected bouton function. Hence we demonstrate that the morphologic and physiologic specialization maybe a convergent evolutionary adaptation to regulate the trade off between sustained, low output, and short term, high output, synaptic signals. There seems to be a biologically meaningful explanation for the co-existence of the two different bouton types as previously observed at the NMJ (characterized especially by the relation between size and Po), the assigning of two different tasks with respect to short- and long-time behaviour could allow for an optimized interplay of different synapse types. We can present astonishing similar results of experimental and simulation data which could be gained in particular without any data fitting, however based only on biophysical values which could be taken from different experimental results. As a side product, we demonstrate how advanced methods from numerical mathematics could help in future to resolve also other difficult experimental neurobiological issues.

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Author:Markus Michael Knodel, Dan Bucher, Romina Geiger, Lihao Ge, Alfio Grillo, Gabriel WittumGND, Christoph M. Schuster, Sean Gillian Queisser
URN:urn:nbn:de:hebis:30:3-314394
DOI:https://doi.org/10.1186/1471-2202-14-S1-P138
ISSN:1471-2202
Parent Title (English):BMC neuroscience
Publisher:BioMed Central
Place of publication:London
Document Type:Article
Language:English
Year of Completion:2013
Date of first Publication:2013/07/08
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Contributing Corporation:Twenty Second Annual Computational Neuroscience Meeting: CNS*2013, Paris, France. 13-18 July 2013
Release Date:2013/08/26
Volume:14
Issue:(Suppl 1):P138
Page Number:2
First Page:1
Last Page:2
Note:
© 2013 Knodel et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
HeBIS-PPN:384632556
Institutes:Informatik und Mathematik / Informatik
Wissenschaftliche Zentren und koordinierte Programme / Goethe-Zentrum für Wissenschaftliches Rechnen (G-CSC)
Dewey Decimal Classification:0 Informatik, Informationswissenschaft, allgemeine Werke / 00 Informatik, Wissen, Systeme / 004 Datenverarbeitung; Informatik
6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - Namensnennung 2.0